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WO2013139949A1 - Compositions comprising a strigolactame compound for enhanced plant growth and yield - Google Patents

Compositions comprising a strigolactame compound for enhanced plant growth and yield Download PDF

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Publication number
WO2013139949A1
WO2013139949A1 PCT/EP2013/056009 EP2013056009W WO2013139949A1 WO 2013139949 A1 WO2013139949 A1 WO 2013139949A1 EP 2013056009 W EP2013056009 W EP 2013056009W WO 2013139949 A1 WO2013139949 A1 WO 2013139949A1
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Prior art keywords
substituted
crc
group
alkyl
halogen atoms
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French (fr)
Inventor
Jean-Marie Beau
François-Didier BOYER
Victor Xiao CHEN
Daniela Portz
Catherine Rameau
Jean-Pierre Vors
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Bayer Intellectual Property GmbH
Centre National de la Recherche Scientifique CNRS
Institut National de la Recherche Agronomique INRA
Universite Paris Sud
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Bayer Intellectual Property GmbH
Centre National de la Recherche Scientifique CNRS
Institut National de la Recherche Agronomique INRA
Universite Paris Sud
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/16—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof the nitrogen atom being part of a heterocyclic ring

Definitions

  • the present invention relates to strigolactame derivatives that are active on plants and to compositions comprising said derivatives.
  • the present invention also relates to the use of said derivatives or compositions for enhancing the plant growth, yield, vigor and/or mycchorization and to corresponding methods.
  • Mycorrhizal symbiosis (or mycchorization) is a common symbiotic relationship between arbuscular mycorrhizal (AM) fungi and plants roots, which is highly beneficial for the plant, its growth, yield and vigor.
  • AM fungi Fungi of the phylum Glomeromycota (AM fungi) penetrate and colonize plant roots, where they differentiate into highly branched structures known as arbuscules and vesicles. AM fungi help plants to capture nutrients such as phosphorus and micronutrients from the soil. More than 80% of lands plants are forming symbiotic associations with AM fungi.
  • Strigolactones have been identified in the root exudates of a variety of plant species, and have been initially disclosed as compounds capable of stimulating the seed germination of parasitic weed species, especially Orobanche sp. and striga sp. (Cook et al., 1 972, J Am Chem Soc, 94, 6198-6199; Hauck et al., 1 992, J Plant Physiol, 139, 474-478; Muller et al., 1 992). Later, it has been shown that strigolactones can stimulate the growth of arbuscular mycorrhizae (AM) fungi (WO 2005/0771 77). More recently, strigolactones have been considered as a new class of plant hormones, exhibiting various biological activities (H. Proust, B. Hoffmann, X. Xie, K. Yoneyama, D. G. Schaefer, K.
  • Natural strigolactones generally possess a chemical structure comprising 4 rings A, B, C, D and share the common configuration indicated below, in which rings A and B can comprise double bond(s) or substituents
  • strigolactone analogues A. J. Humphrey, A. M. Galster, M. H. Beale, Nat. Prod. Rep. 2006, 23, 592-614 and references cited therein ; A. S. Mwakaboko, B. Zwanenburg, Bioorg. Med. Chem. 201 1 , 19, 5006-501 1 ) have been proposed in the last decades to enhance the biological activities and to overcome the low stability of natural strigolactones in aqueous medium.
  • strigolactame derivatives of formula (I) can enhance plant growth, yield, vigor and/or mycchorization of plants.
  • strigolactame derivatives of formula (I) are largely less efficient than strigolactones for promoting the germination of parasitic weed seeds.
  • - Xi, X2, X3, Yi, Y2, Y3 and Z independently represent a hydrogen atom, a halogen atom, a nitro group, a hydroxy group, a cyano group, an amino group, a sulphenyl group, a sulphinyl group, a sulphonyl group, a formyl group, a acetyl group, a formyloxy group, a formylamino group, a carbamoyl group, a N-hydroxycarbamoyl group, a carbamate group, substituted or non- substituted (hydroxyimino)-Ci-C6-alkyl group, substituted or non-substituted Ci-Cs-alkyl, substituted or non-substituted tri(Ci-C8-alkyl)silyl-Ci-C 8 -alkyl, substituted or non-substituted
  • Ci-Cs-cycloalkyl substituted or non-substituted tri(Ci-C8-alkyl)silyl-Ci-C8-cycloalkyl, substituted or non-substituted CrC 8 -halogenoalkyl having 1 to 5 halogen atoms, substituted or non-substituted Ci -C 8 -halogenocycloalkyl having 1 to 5 halogen atoms, a substituted or non- substituted C 2 -C 8 -alkenyl, substituted or non-substituted C 2 -C 8 -alkynyl, substituted or non- substituted Ci -Cs-alkylamino, substituted or non-substituted di-Ci -C 8 -alkylamino, substituted or non-substituted CrC 8 -alkoxy, substituted or non-substituted CrC 8 -halogenoalkoxy having 1 to 5 halogen
  • Ri and R 2 independently represent a hydrogen atom, a halogen atom, a nitro group, a hydroxy group, a cyano group, an amino group, a sulphenyl group, a sulphinyl group, a sulphonyl group, a formyl group, a formyloxy group, a formylamino group, a carbamoyl group, a N-hydroxycarbamoyl group, a carbamate group, substituted or non-substituted (hydroxyimino)-Ci-C 6 -alkyl group, substituted or non-substituted CrC 8 -alkyl, substituted or non-substituted tri(Ci-C 8 -alkyl)silyl-CrC 8 - alkyl, substituted or non-substituted Ci-C 8 -cycloalkyl, substituted or non-substituted tri(Ci-C 8 - alky
  • Ri and R 2 form a saturated or unsaturated, non-aromatic, substituted or non-substituted 4- to 7- membered carbocycle; or Ri and R 2 form a saturated or unsaturated, aromatic or non-aromatic, substituted or non-substituted 4- to 7-membered carbocycle fused to an other saturated or unsaturated, aromatic or non-aromatic, substituted or non-substituted 4- to 7- membered carbocycle; as well as salts, N-oxides, metallic complexes, metalloidic complexes and optically active or geometric isomers thereof;
  • any of the compounds used in the compositions according to the present invention may also exist in one or more geometric isomeric form depending on the number of double bond within the compound.
  • the invention thus equally relates to any geometric isomer and to any possible mixtures thereof, in any proportion.
  • Geometric isomers can be separated according to any method known per se by the man ordinary skilled in the art.
  • Any of the compounds used in the compositions according to the present invention wherein a substituant represents a hydroxy group, a sulphenyl group or an amino group can exist in a tautomeric form resulting from the shift of the proton of said hydroxy group, sulphenyl group or amino group respectively.
  • Such tautomeric forms are also part of the present invention. According to the invention, the following generic terms are generally used with the following meanings:
  • halogen means fluorine, chlorine, bromine or iodine
  • heteroatom can be nitrogen, oxygen or sulphur.
  • a group or a substituent that is substituted according to the invention can be substituted by one or more of the following groups or atoms: a halogen atom, a nitro group, a hydroxy group, a cyano group, an amino group, a sulphenyl group, a sulphinyl group, a sulphonyl group, a formyl group, a formyloxy group, a formylamino group, a carbamoyl group, a N- hydroxycarbamoyl group, a carbamate group, substituted or non-substituted (hydroxyimino)-Ci -C 6 - alkyl group, substituted or non-substituted Ci -C 8 -alkyl, substituted or non-substituted tri(Ci -C 8 - alkyl)silyl-Ci -C 8 -alkyl, substituted or non-substituted Cr
  • Preferred compounds of formula (I) according to the invention are those wherein Xi, X 2 , Yr Y 2 , Y 3 and Z independently represent a hydrogen atom, a halogen atom, a nitro group, a hydroxy group, a cyano group, a substituted or non-substituted CrC 8 -alkyl, a substituted or non-substituted CrC 8 -haloalkyl, a substituted or non-substituted Ci-C 8 -alkoxy, or a substituted or non-substituted Ci-C 8 -haloalkoxy.
  • More preferred compounds of formula (I) according to the invention are those wherein Xi, X 2 , Yi, Y 3 and Z represent a hydrogen atom.
  • Other more preferred compounds of formula (I) are those wherein Y 2 represents a substituted or non- substituted Ci-C 8 -alkyl, or a substituted or non-substituted Ci-C 8 -haloalkyl.
  • Ri and R 2 independently represent a hydrogen atom, a halogen atom, a nitro group, a hydroxy group, a cyano group, a substituted or non-substituted Ci-C 8 -alkyl, a substituted or non-substituted Ci-C 8 -haloalkyl, a substituted or non-substituted Ci-C 8 -alkoxy, or a substituted or non-substituted Ci-C 8 -haloalkoxy; or Ri and R 2 form a saturated or unsaturated, non-aromatic, substituted or non-substituted 4- to 7- membered carbocycle; or
  • Ri and R 2 form a saturated or unsaturated, aromatic or non-aromatic, substituted or non-substituted 4- to 7-membered carbocycle fused to another saturated or unsaturated, aromatic or non-aromatic, substituted or non-substituted 4- to 7-membered carbocycle.
  • Ri and R 2 form a saturated or unsaturated, aromatic or non-aromatic, substituted or non-substituted 4- to 7- membered carbocycle fused to another saturated or unsaturated, aromatic or non-aromatic, substituted or non-substituted 4- to 7-membered carbocycle.
  • Y 2 and Z independently represent a hydrogen atom, a halogen atom, a nitro group, a hydroxy group, a cyano group, a substituted or non-substituted CrC 8 -alkyl, a substituted or non- substituted Ci-C 8 -haloalkyl, a substituted or non-substituted CrC 8 -alkoxy, or a substituted or non- substituted Ci-Cs-haloalkoxy;
  • - represents hydrogen atom, a substituted or non-substituted Ci-C 8 -alkyl, a substituted or non- substituted C 2 -C 8 -alkenyl, a substituted or non-substituted C 2 -C 8 -alkynyl, a substituted or non- substituted arylalkyi, formyl, acetyl, a substituted or non-substituted Ci-C 8 -alkylcarbonyl, a substituted or non-substituted CrC 8 -haloalkylcarbonyl, substituted or non-substituted CrC 8 -alkoxycarbonyl,and
  • - X 3 represents hydrogen atom, a substituted or non-substituted CrC 8 -alkyl, a substituted or non- substituted C 2 -C 8 -alkenyl, a substituted or non-substituted C 2 -C 8 -alkynyl, a substituted or non- substituted arylalkyl, formyl, acetyl, a substituted or non-substituted Ci -C 8 -alkylcarbonyl, a substituted or non-substituted C rC 8 -haloalkylcarbonyl, substituted or non-substituted CrC 8 -alkoxycarbonyl,
  • - Y2 represents a substituted or non-substituted Ci -C 8 -alkyl or a substituted or non-substituted Ci -C 8 - haloalkyl
  • - Ri and R 2 form an unsaturated, non-aromatic substituted or non-substituted 5-membered carbocycle fused to another unsaturated, aromatic, substituted or non-substituted 6-membered carbocycle.
  • X 3 represents hydrogen atom, a substituted or non-substituted CrC 8 -alkyl, a substituted or non-substituted C 2 -C 8 -alkenyl, a substituted or non-substituted C 2 -C 8 -alkynyl, a substituted or non- substituted arylalkyl, formyl, acetyl, a substituted or non-substituted CrC 8 -alkylcarbonyl, a substituted or non-substituted C rC 8 -haloalkylcarbonyl, substituted or non-substituted CrC 8 -alkoxycarbonyl.
  • Step 1 (3afl*,8bS*)-3,3a,4,8b-Tetrahydroindeno[1 ,2-fo]pyrrol-2(1 H)-one
  • the concentrated crude intermediate was directly placed in the next step in presence of thionyl chloride (4.80 g, 40.32 mmol, 1 .1 0 equiv) and pyridine (3.1 9 g, 40.32 mmol, 1 .10 equiv) in CH2CI2 (150 ml_) at 0 °C. After 4 h at room temperature, the reaction mixture was concentrated to dryness under reduced pressure. The crude oil was solubilized in CH2CI2 and washed with water and dried over MgS0 4 .
  • Step 2 tert-Butyl (3aR * ,8bS * )-2-oxo-3,3a, -tetrahydroindeno[1 ,2-b]pyrrole-1 (2H)-carboxylate
  • Boc 2 0 (0.26 g, 1 .1 8 mmol, 2.05 equiv) was added to a solution of previous lactam (1 00.0 mg, 0.58 mmol, 1 equiv) and DMAP (754.0 mg, 0.61 mmol, 1 .05 equiv) in a mixture of triethylamine-acetonitrile (3:1 ) (4 ml_) under argon at room temperature. After 3 h, the reaction mixture was diluted with EtOAc. The organic layer was washed successively with HCI (1 M), saturated aqueous sodium hydrogen carbonate and brine.
  • Step 3
  • Lactam from step 2 (100.0 mg, 0.37 mmol, 1 equiv) was dissolved in tert- butoxybis(dimethylamino)methane (Bredereck's reagent) (0.30 ml_, 1 .46 mmol, 4 equiv) under argon at room temperature. After heating at 75 °C for 3 h, the cooled reaction mixture was diluted with EtOAc, and the resulting mixture was washed with water and brine, and then dried over MgS0 4 .
  • Bredereck's reagent tert- butoxybis(dimethylamino)methane
  • Stepl tert-butyl (3£)-3- ⁇ [(4-methyl-5-oxo-2,5-dihydrofuran-2-yl)oxy]methylene ⁇ -2-oxopyrrolidine-1 - carboxylate
  • Boc 2 0 (2.63 g, 12.05 mmol, 2.05 equiv) diluted was added to a solution pyrrolidinone (500.0 mg, 6.88 mmol, 1 equiv) and DMAP (754.0 mg, 6.1 7 mmol, 1 .05 equiv) in a mixture of triethylamine-acetonitrile (3:1 ) (20 mL) under argon at room temperature. After 3 h, the reaction mixture was diluted with EtOAc. The organic layer was washed successively with HCI (1 M), saturated aqueous sodium hydrogen carbonate solution and brine.
  • the carbamate (250.0 mg, 1 .35 mmol, 1 equiv) was dissolved in tert- butoxybis(dimethylamino)methane (Bredereck reagent) (1 .12 mL, 5.40 mmol, 4 equiv) under argon at room temperature. After heating at 75°C for 3 h, the cooled mixture was diluted with EtOAc, and the organic layer was washed with water and brine, then dried over MgSC .
  • tert- butoxybis(dimethylamino)methane (Bredereck reagent) (1 .12 mL, 5.40 mmol, 4 equiv) under argon at room temperature. After heating at 75°C for 3 h, the cooled mixture was diluted with EtOAc, and the organic layer was washed with water and brine, then dried over MgSC .
  • Step2 (3 £)-3- ⁇ [(4-methyl-5-oxo-2,5-dihydrofuran-2-yl)oxy]methylene ⁇ pyrrolidin-2-one
  • the present invention also relates to a composition comprising an effective and non-phytotoxic amount of an active compound of formula (I).
  • an effective and non-phytotoxic amount means an amount of composition according to the invention that is sufficient for enhancing the plant growth, yield, vigor and/or mycchorization and that does not entail any appreciable symptom of phytotoxicity for the said plant or crop. Such an amount can vary within a wide range depending on the type of crop, the climatic conditions and the compounds included in the composition according to the invention. This amount can be determined by systematic field trials that are within the capabilities of a person skilled in the art.
  • composition comprising, as an active ingredient, an effective amount of a compound of formula (I) as herein defined and an agriculturally acceptable support, carrier or filler.
  • the term "support” denotes a natural or synthetic, organic or inorganic material with which the active material is combined to make it easier to apply, notably to the parts of the plant.
  • This support is thus generally inert and should be agriculturally acceptable.
  • the support may be a solid or a liquid.
  • suitable supports include clays, natural or synthetic silicates, silica, resins, waxes, solid fertilisers, water, alcohols, in particular butanol, organic solvents, mineral and plant oils and derivatives thereof. Mixtures of such supports may also be used.
  • an “effective amount” of the composition is an amount that increases plant growth, yield, vigor and/or mycchorization when compared with the plant growth, yield, vigor and/or mycchorization of plants or seeds that have not been treated with the composition.
  • strigolactame concentration in the composition may range independently from 1 0 4 M to 10 15 M, preferably from 1 0 6 to 1 0 12 M.
  • the agriculturally appropriate solvent is preferably an aqueous solvent, such as water. It may be appropriate to solubilize the compounds in a small volum of organic solvent as acetone, and then to dilute with water.
  • Active ingredients concentration in the composition generally corresponds directly or after dilution to the use rate for this particular active ingredient.
  • the use rate for strigolactame compounds is generally from 1 ⁇ g to 1 g/ha.
  • fertilizers e.g., calcium, nitrogen, potassium, phosphorous
  • micronutrients e.g., copper, aluminum, magnesium, manganese, and zinc ions
  • the composition may be applied to monocot or dicot plants, including legumes and non-legumes.
  • the composition is applied to field-grown plants.
  • the composition is applied to greenhouse-grown plants.
  • the composition may be applied to seeds or foliage of legumes, such as soybeans, peas, chickpeas, dry beans, peanuts, clover, alfalfa, and of non-legumes such as corn, cotton, rice, tomatoes, canola, wheat, barley, sugar beet, and grass.
  • the composition is applied to seeds in a single application, and the seeds may be planted immediately or stored before planting.
  • the composition may be applied to foliage.
  • Foliar application generally consists of spraying the composition on the plant foliage one or more times during the growing period.
  • plant as used herein includes tubers, roots, stems, leaves, flowers, and fruits.
  • the composition may be applied directly to seeds or plants or may be placed in soil in the vicinity of a seed or plant prior to or at the time of planting. In a preferred embodiment, the composition is sprayed on seeds, tubers, or foliage.
  • Seedlings as well as more mature plants, may be treated. Flowers and fruits may also be treated by spraying. Roots of transplants may be sprayed or dipped in the composition prior to planting.
  • composition may also comprise other additional components.
  • the composition may further comprise a surfactant.
  • the surfactant can be an emulsifier, a dispersing agent or a wetting agent of ionic or non-ionic type or a mixture of such surfactants.
  • the presence of at least one surfactant is generally essential when the active material and/or the inert support are water-insoluble and when the vector agent for the application is water.
  • surfactant content may be comprised between 5% and 40% by weight of the composition.
  • Additional components may also be included, e.g. protective colloids, adhesives, thickeners, thixotropic agents, penetration agents, stabilisers, sequestering agents. More generally, the active materials can be combined with any solid or liquid additive, which complies with the usual formulation techniques.
  • composition according to the invention may contain from 0.00000005 to 99% (by weight) of active material, preferably 0.0000001 to 70% by weight.
  • compositions according to the present invention can be used in various forms such as aerosol dispenser, capsule suspension, cold fogging concentrate, dustable powder, emulsifiable concentrate, emulsion oil in water, emulsion water in oil, encapsulated granule, fine granule, flowable concentrate for seed treatment, gas (under pressure), gas generating product, granule, hot fogging concentrate, macrogranule, microgranule, oil dispersible powder, oil miscible flowable concentrate, oil miscible liquid, paste, plant rodlet, powder for dry seed treatment, seed coated with a pesticide, soluble concentrate, soluble powder, solution for seed treatment, suspension concentrate (flowable concentrate), ultra low volume (ulv) liquid, ultra low volume (ulv) suspension, water dispersible granules or tablets, water dispersible powder for slurry treatment, water soluble granules or tablets, water soluble powder for seed treatment and wettable powder.
  • aerosol dispenser capsule suspension, cold fogging concentrate
  • dustable powder emuls
  • compositions include not only compositions which are ready to be applied to the plant or seed to be treated, or in furrow in the soil, by means of a suitable device, such as a spraying or dusting device, but also concentrated commercial compositions which must be diluted before they are applied to the crop.
  • the composition may further comprise a pesticidal active ingredient.
  • pesticides useful in compositions include fungicides, insecticides, bactericides, nematicides, acaricides, molluscicides, attractants, sterilants, growth regulators, herbicides, safeners, semiochemicals pheromone active substance or other compounds with biological activity.
  • the composition may further comprise another active ingredient which enhances the yield, vigor or growth of the plants, which improves the germination of seeds and vitality of seedlings, which acts as seed safener, which improves nutrient uptake or symbiotic interaction by the plant, or which improves the biotic or abiotic environmental stress tolerance of a plant.
  • Examples of said compounds include strigolactone compounds, lipochito-oligosaccharide (LCO) compounds, acyl-homoserine lactone (AHL) compounds, flavonoids (such as flavones, flavanols, flavonols, flavanones, isoflavones, hesperetin, formonometin, genistein, daidzein, naringenin, luteolin, apignenin), chitinous compounds (such as chitin or chitosan), plant activators (such as acibenzolar or probenazole), phytohormones (such as Gibberellic acid), plant growth regulators (such as trinexapac- ethyl, prohexadione-Ca, paclobutrazol, brassinolide, forchlorfenuron, hymexazol, thiametoxam), or other plant regulators (such as benzofluor, buminafo
  • plant growth regulators include, but are not limited to antiauxins (clofibric acid, 2,3,5-tri- iodobenzoic acid), auxins (4-CPA, 2,4-D, 2,4-DB, 2,4-DEP, dichlorprop, fenoprop, IAA, I BA, naphthaleneacetamide, [alpha]-naphthaleneacetic acid, 1 -naphthol, naphthoxyacetic acid, potassium naphthenate, sodium naphthenate, 2,4, 5-T), cytokinins (2iP, benzyladenine, kinetin, zeatin), defoliants (calcium cyanamide, dimethipin, endothal, ethephon, merphos, metoxuron, pentachlorophenol, thidiazuron, tribufos), ethylene inhibitors (aviglycine, 1 - methylcyclopropene), ethylene releasers (ACC, et reviewing the
  • the term additionally includes other active ingredients such as benzofluor, buminafos, carvone, ciobutide, clofencet, cloxyfonac, cyclanilide, cycloheximide, epocholeone, ethychlozate, ethylene, fenridazon, heptopargil, holosulf, inabenfide, karetazan, lead arsenate, methasulfocarb, prohexadione, pydanon, sintofen, triapenthenol, and trinexapac.
  • active ingredients such as benzofluor, buminafos, carvone, ciobutide, clofencet, cloxyfonac, cyclanilide, cycloheximide, epocholeone, ethychlozate, ethylene, fenridazon, heptopargil, holosulf, in
  • Additional plant growth regulators include indolinone derivative plant stimulators described in WO 2005/1 07466; 3,4-disubstituted maleimide derivatives described in WO 2005/1 07465; fused azepinone derivatives described in WO 2005/1 07471 ; and 2-amino-6- oxypurine derivatives described in WO 2005/1 07472.
  • strigolactone compounds examples include, but are not limited to strigol, sorgolactone, alectrol, orobanchol (Cook et al., 1 972, J Am Chem Soc, 94, 6198-6199; Butler, 1 995, Allelopathy: organism, processes and application, 158-1 68; Hauck et al., 1 992, J Plant Physiol, 139, 474-478; Muller et al., 1992, J Plant Growth Regul, 1 1 , 77-84, Siame et al., 1 993, J Agr Food Chem, 41 , 1486- 1491 , Yokota et al., 1 998, Phytochemistry, 49, 1 967-1 973), and the synthetic strigolactones compounds of formula (I) specifically disclosed in WO201 0125065.
  • a lipo-chitooligosaccharide (LCO) compound is a compound having the general LCO structure, i.e. an oligomeric backbone of ⁇ -1 ,4-linked N- acetyl-D-glucosamine residues with a N-linked fatty acyl chain at the non-reducing end, as described in US Pat N ° 5,54971 8; US Pat N ° 5,646,01 8; US Pat N ° 5, 1 75,149; and US Pat N ° 5,321 ,01 1 .
  • This basic structure may contain modifications or substitutions found in naturally occurring LCO's, such as those described in Spaink, Critical Reviews in Plant Sciences 54: 257-288, 2000; D'Haeze and Holsters, Glycobiology 12: 79R-1 05R, 2002.
  • Naturally occurring LCO's are defined as compounds which can be found in nature.
  • This basic structure may also contain modifications or substitutions which have not been found so far in naturally occurring LCO's. Examples of such analogs for which the conjugated amide bond is mimicked by a benzamide bond or which contain a function of benzylamine type are the following compounds of formula (I) which are described in WO2005/063784 and WO2008/071 672, the content of which is incorporated herein by reference.
  • the LCO's compounds may be isolated directly from a particular culture of Rhizobiaceae bacterial strains, synthesized chemically, or obtained chemo-enzymatically. Via the latter method, the oligosaccharide skeleton may be formed by culturing of recombinant bacterial strains, such as Escherichia coli, in a fermenter, and the lipid chain may then be attached chemically.
  • LCO's used in embodiments of the invention may be recovered from natural Rhizobiaceae bacterial strains that produce LCO's, such as strains of Azorhizobium, Bradyrhizobium (including B. japonicum), Mesorhizobium, Rhizobium (including R. leguminosarum), Sinorhizobium (including S. meliloti), or from bacterial strains genetically engineered to produce LCO's. These methods are known in the art and have been described, for example, in U.S. Pat. Nos. 5,549,71 8 and 5,646,018, which are incorporated herein by reference. Hungria and Stacey (Soil Biol. Biochem.
  • LCO's may be utilized in various forms of purity and may be used alone or with rhizobia. Methods to provide only LCO's include simply removing the rhizobial cells from a mixture of LCOs and rhizobia, or continuing to isolate and purify the LCO molecules through LCO solvent phase separation followed by HPLC chromatography as described by Lerouge, et.al (US 5,549,71 8). Purification can be enhanced by repeated H PLC, and the purifed LCO molecules can be freeze-dried for long-term storage. This method is acceptable for the production of LCO's from all genera and species of the Rhizobiaceae.
  • LCO compounds which can be identical or not to naturally occurring LCO's, may also be obtained by chemical synthesis and/or through genetic engineering. Synthesis of precursor oligosaccharide molecules for the construction of LCO by genetically engineered organisms is disclosed in Samain et al., Carbohydrate Research 302: 35-42, 1 997.
  • LCOs compounds wherein the oligosaccharide skeleton is obtained by culturing recombinant bacterial strains, such as recombinant Escherichia coli cells harboring heterologous gene from rhizobia, and wherein the lipid chain is chemically attached is disclosed in WO2005/063784 and WO2008/07167, the content of which is incorporated herein by reference.
  • lipochito-oligosaccharide compounds include, but are not limited to LCO compounds specifically disclosed in WO201 0125065.
  • acyl-homoserine lactone derivatives include, but are not limited to compounds specifically disclosed in EP1 1 35601 1 .4, the content of which is incorporated herein by reference.
  • composition according to the present invention may further comprise a supplementation with different inoculum sources as for example arbuscular mycorrhizal fungi (AM F), Rhizobia or other plant growth promoting bacteria. Said supplementation may be applied simultaneously or sequentially.
  • AMFcould be for example Glomus sp., Gigaspora sp., or other fungi from the group Glomeromycota, while plant growth promoting bacteria others than Rhizobia could be for example Azospirillum sp., Bacillus sp.
  • the dose of active material usually applied is generally and advantageously between 0.00001 and 1000 g/ha, preferably between 0.0001 and 500 g/ha for applications in foliar treatment. If a drench/drip/in furrow application is possible, the dose can be lower, especially in artificial substrates like rockwool or perlite.
  • the dose of active substance applied is generally and advantageously between 0.000001 and 200 g per 100 kg of seed, preferably between 0.00001 and 150 g per 1 00 kg of seed in the case of seed treatment. It is clearly understood that the doses indicated above are given as illustrative examples of the invention. A person skilled in the art will know how to adapt the application doses according to the nature of the crop to be treated.
  • compositions and compounds of the present invention may be used to to increase the yield, growth, vigor and/or mycchorization of the plant and/or for curatively or preventively control pests of crops, as phytopathogenic fungi, insects, nematodes, acarid, and/or for decreasing the needs of fertilizers.
  • the present invention provides a method for increasing the yield, growth, vigor or mycchorization of a plant or crop characterised in that a composition according to the invention is applied via seed treatment, foliar application, stem application, drench/drip application (chemigation) to the seed, the plant or to the fruit of the plant, or to soil, particularly in furrow, and/or to inert substrate (e.g. inorganic substrates (e.g. sand, rockwool, glasswool, expanded minerals (e.g. perlite, vermiculite, zeolite, expanded clay)), Pumice, Pyroclastic materials/tuff, synthetic organic substrates (e.g. Polyurethane), organic substrates (e.g.
  • inert substrate e.g. inorganic substrates (e.g. sand, rockwool, glasswool, expanded minerals (e.g. perlite, vermiculite, zeolite, expanded clay)
  • Pumice Pyroclastic materials/tuff
  • peat e.g. coir, wood fibre/chips, tree bark
  • a liquid substrate e.g. floating hydroponic systems, Nutrient Film Technique, Aeroponics
  • composition as used comprises an effective and non-phytotoxic amount of active compound.
  • the method of treatment according to the present invention is useful to treat propagation material such as tubers or rhizomes, but also seeds, seedlings or seedlings pricking out and plants or plants pricking out. This method of treatment can also be useful to treat roots.
  • the method of treatment according to the present invention can also be useful to treat the overground parts of the plant such as trunks, stems or stalks, leaves, flowers and fruit of the concerned plant.
  • cotton Among the plants that can be treated by the method according to the present invention, mention may be made of cotton; flax; vine; fruit or vegetable crops such as Rosaceae sp. (for instance pip fruit such as apples and pears, but also stone fruit such as apricots, almonds and peaches), Ribesioidae sp., Juglandaceae sp., Betulaceae sp., Anacardiaceae sp., Fagaceae sp., Moraceae sp., Oleaceae sp., Actinidaceae sp., Lauraceae sp., Musaceae sp.
  • Rosaceae sp. for instance pip fruit such as apples and pears, but also stone fruit such as apricots, almonds and peaches
  • Rosaceae sp. for instance pip fruit such as apples and pears, but also stone fruit such as apricots, almonds and peaches
  • Rubiaceae sp. for instance banana trees and plantins
  • Rubiaceae sp. Theaceae sp., Sterculiceae sp., Rutaceae sp. (for instance lemons, oranges and grapefruit); Solanaceae sp. (for instance tomatoes), Liliaceae sp., Asteraceae sp. (for instance lettuces), Umbelliferae sp., Cruciferae sp., Chenopodiaceae sp., Cucurbitaceae sp., Papilionaceae sp. (for instance peas), Rosaceae sp. (for instance strawberries); major crops such as Graminae sp.
  • Asteraceae sp. for instance sunflower
  • Cruciferae sp. for instance oil seed rape
  • Fabacae sp. for instance peanuts
  • Papilionaceae sp. for instance soybean
  • Solanaceae sp. for instance potatoes
  • Chenopodiaceae sp. for instance beetroots
  • horticultural and forest crops as well as genetically modified homologues of these crops.
  • Strigolactame compounds of the invention and compositions comprising said strigolactame compounds, eventually in combination with fungicides, insecticides, or other additives, can be used in the treatment of genetically modified organisms (GMOs), e.g. plants or seeds.
  • GMOs genetically modified organisms
  • heterologous gene essentially means a gene which is provided or assembled outside the plant and when introduced in the nuclear, chloroplastic or mitochondrial genome gives the transformed plant new or improved agronomic or other properties by expressing a protein or polypeptide of interest or by downregulating or silencing other gene(s) which are present in the plant (using for example, antisense technology, cosuppression technology or RNA interference - RNAi - technology).
  • a heterologous gene that is located in the genome is also called a transgene.
  • a transgene that is defined by its particular location in the plant genome is called a transformation or transgenic event.
  • the treatment according to the invention may also result in superadditive (“synergistic") effects.
  • superadditive for example, reduced application rates and/or a widening of the activity spectrum and/or an increase in the activity of the active compounds and compositions which can be used according to the invention, better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or to water or soil salt content, increased flowering performance, easier harvesting, accelerated maturation, higher harvest yields, bigger fruits, larger plant height, greener leaf color, earlier flowering, higher quality and/or a higher nutritional value of the harvested products, higher sugar concentration within the fruits, better storage stability and/or processability of the harvested products are possible, which exceed the effects which were actually to be expected.
  • the active compound combinations according to the invention may also have a strengthening effect in plants. Accordingly, they are also suitable for mobilizing the defense system of the plant against attack by unwanted microorganisms. This may, if appropriate, be one of the reasons of the enhanced activity of the combinations according to the invention, for example against fungi.
  • Plant- strengthening (resistance-inducing) substances are to be understood as meaning, in the present context, those substances or combinations of substances which are capable of stimulating the defense system of plants in such a way that, when subsequently inoculated with unwanted microorganisms, the treated plants display a substantial degree of resistance to these microorganisms.
  • unwanted microorganisms are to be understood as meaning phytopathogenic fungi, bacteria and viruses.
  • the substances according to the invention can be employed for protecting plants against attack by the abovementioned pathogens within a certain period of time after the treatment.
  • the period of time within which protection is effected generally extends from 1 to 21 days, preferably 1 to 14 days, after the treatment of the plants with the active compounds.
  • plants and their parts are treated.
  • wild plant species and plant cultivars or those obtained by conventional biological breeding methods, such as crossing or protoplast fusion, and also parts thereof, are treated.
  • transgenic plants and plant cultivars obtained by genetic engineering methods if appropriate in combination with conventional methods (Genetically Modified Organisms), and parts thereof are treated.
  • the terms "parts” or “parts of plants” or “plant parts” have been explained above. More preferably, plants of the plant cultivars which are commercially available or are in use are treated in accordance with the invention.
  • Plant cultivars are understood to mean plants which have new properties ("traits") and have been obtained by conventional breeding, by mutagenesis or by recombinant DNA techniques. They can be cultivars, varieties, bio- or genotypes.
  • the method of treatment according to the invention can be used in the treatment of genetically modified organisms (GMOs), e.g. plants or seeds.
  • GMOs genetically modified organisms
  • Genetically modified plants are plants of which a heterologous gene has been stably integrated into genome.
  • the expression "heterologous gene” essentially means a gene which is provided or assembled outside the plant and when introduced in the nuclear, chloroplastic or mitochondrial genome gives the transformed plant new or improved agronomic or other properties by expressing a protein or polypeptide of interest or by downregulating or silencing other gene(s) which are present in the plant (using for example, antisense technology, cosuppression technology, RNA interference - RNAi - technology or microRNA - miRNA - technology).
  • a heterologous gene that is located in the genome is also called a transgene.
  • a transgene that is defined by its particular location in the plant genome is called a transformation or transgenic event.
  • the treatment according to the invention may also result in superadditive
  • the active compound combinations according to the invention may also have a strengthening effect in plants. Accordingly, they are also suitable for mobilizing the defense system of the plant against attack by unwanted microorganisms. This may, if appropriate, be one of the reasons of the enhanced activity of the combinations according to the invention, for example against fungi.
  • Plant-strengthening (resistance-inducing) substances are to be understood as meaning, in the present context, those substances or combinations of substances which are capable of stimulating the defense system of plants in such a way that, when subsequently inoculated with unwanted microorganisms, the treated plants display a substantial degree of resistance to these microorganisms.
  • the substances according to the invention can be employed for protecting plants against attack by the abovementioned pathogens within a certain period of time after the treatment.
  • the period of time within which protection is effected generally extends from 1 to 1 0 days, preferably 1 to 7 days, after the treatment of the plants with the active compounds.
  • Plants and plant cultivars which are preferably to be treated according to the invention include all plants which have genetic material which impart particularly advantageous, useful traits to these plants (whether obtained by breeding and/or biotechnological means).
  • Plants and plant cultivars which are also preferably to be treated according to the invention are resistant against one or more biotic stresses, i.e. said plants show a better defense against animal and microbial pests, such as against nematodes, insects, mites, phytopathogenic fungi, bacteria, viruses and/or viroids.
  • nematode or insect resistant plants are described in e.g. U.S. Patent Applications 1 1/765,491 , 1 1 /765,494, 10/926,819, 10/782,020, 12/032,479, 10/783,41 7, 10/782,096, 1 1 /657,964, 12/192,904, 1 1 /396,808, 12/166,253, 12/166,239, 12/166,124, 12/166,209, 1 1/762,886, 12/364,335, 1 1 /763,947, 12/252,453, 12/209,354, 12/491 ,396, 12/497,221 , 12/644,632, 12/646,004, 12/701 ,058, 12/718,059, 12/721 ,595, 12/638,591 .
  • Plants and plant cultivars which may also be treated according to the invention are those plants which are resistant to one or more abiotic stresses.
  • Abiotic stress conditions may include, for example, drought, cold temperature exposure, heat exposure, osmotic stress, flooding, increased soil salinity, increased mineral exposure, ozone exposure, high light exposure, limited availability of nitrogen nutrients, limited availability of phosphorus nutrients, shade avoidance.
  • Plants and plant cultivars which may also be treated according to the invention are those plants characterized by enhanced yield characteristics. Increased yield in said plants can be the result of, for example, improved plant physiology, growth and development, such as water use efficiency, water retention efficiency, improved nitrogen use, enhanced carbon assimilation, improved photosynthesis, increased germination efficiency and accelerated maturation.
  • Yield can furthermore be affected by improved plant architecture (under stress and non-stress conditions), including but not limited to, early flowering, flowering control for hybrid seed production, seedling vigor, plant size, internode number and distance, root growth, seed size, fruit size, pod size, pod or ear number, seed number per pod or ear, seed mass, enhanced seed filling, reduced seed dispersal, reduced pod dehiscence and lodging resistance.
  • Further yield traits include seed composition, such as carbohydrate content, protein content, oil content and composition, nutritional value, reduction in anti-nutritional compounds, improved processability and better storage stability.
  • Plants that may be treated according to the invention are hybrid plants that already express the characteristic of heterosis or hybrid vigor which results in generally higher yield, vigor, health and resistance towards biotic and abiotic stresses). Such plants are typically made by crossing an inbred male-sterile parent line (the female parent) with another inbred male-fertile parent line (the male parent). Hybrid seed is typically harvested from the male sterile plants and sold to growers. Male sterile plants can sometimes (e.g. in corn) be produced by detasseling, i.e. the mechanical removal of the male reproductive organs (or males flowers) but, more typically, male sterility is the result of genetic determinants in the plant genome.
  • Male sterile plants can also be obtained by plant biotechnology methods such as genetic engineering.
  • a particularly useful means of obtaining male-sterile plants is described in WO 89/1 0396 in which, for example, a ribonuclease such as barnase is selectively expressed in the tapetum cells in the stamens. Fertility can then be restored by expression in the tapetum cells of a ribonuclease inhibitor such as barstar (e.g. WO 91 /02069).
  • Plants or plant cultivars which may be treated according to the invention are herbicide-tolerant plants, i.e. plants made tolerant to one or more given herbicides. Such plants can be obtained either by genetic transformation, or by selection of plants containing a mutation imparting such herbicide tolerance.
  • Herbicide-resistant plants are for example glyphosate-tolerant plants, i.e. plants made tolerant to the herbicide glyphosate or salts thereof. Plants can be made tolerant to glyphosate through different means. For example, glyphosate-tolerant plants can be obtained by transforming the plant with a gene encoding the enzyme 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS).
  • EPSPS 5-enolpyruvylshikimate-3-phosphate synthase
  • EPSPS genes are the AroA gene (mutant CT7) of the bacterium Salmonella typhimurium (Science 1983, 221, 370-371 ), the CP4 gene of the bacterium Agrobacterium sp. (Curr. Topics Plant Physiol. 1992, 7, 139-145), the genes encoding a Petunia EPSPS (Science 1986, 233, 478-481 ), a Tomato EPSPS (J. Biol. Chem. 1988, 263, 4280-4289), or an Eleusine EPSPS (WO 01 /66704).
  • Glyphosate-tolerant plants can also be obtained by expressing a gene that encodes a glyphosate oxido-reductase enzyme as described in US 5,776,760 and US 5,463,175.
  • Glyphosate-tolerant plants can also be obtained by expressing a gene that encodes a glyphosate acetyl transferase enzyme as described in for example WO 02/036782, WO 03/092360, WO 2005/012515 and WO 2007/024782.
  • Glyphosate-tolerant plants can also be obtained by selecting plants containing naturally-occurring mutations of the above-mentioned genes, as described in for example WO 01 /024615 or WO 03/013226. Plants expressing EPSPS genes that confer glyphosate tolerance are described in e.g. U.S.
  • herbicide resistant plants are for example plants that are made tolerant to herbicides inhibiting the enzyme glutamine synthase, such as bialaphos, phosphinothricin or glufosinate.
  • Such plants can be obtained by expressing an enzyme detoxifying the herbicide or a mutant glutamine synthase enzyme that is resistant to inhibition, e.g. described in U.S. Patent Application 1 1 /760,602.
  • One such efficient detoxifying enzyme is an enzyme encoding a phosphinothricin acetyltransferase (such as the bar or pat protein from Streptomyces species).
  • Plants expressing an exogenous phosphinothricin acetyltransferase are for example described in U.S. Patents 5,561 ,236; 5,648,477; 5,646,024;
  • HPPD hydroxyphenylpyruvatedioxygenase
  • HPPD is an enzyme that catalyze the reaction in which para-hydroxyphenylpyruvate (HPP) is transformed into homogentisate.
  • Plants tolerant to HPPD-inhibitors can be transformed with a gene encoding a naturally-occurring resistant H PPD enzyme, or a gene encoding a mutated or chimeric HPPD enzyme as described in WO 96/38567, WO 99/24585, WO 99/24586, WO 09/144079, WO 02/046387, or US 6,768,044.
  • Tolerance to HPPD- inhibitors can also be obtained by transforming plants with genes encoding certain enzymes enabling the formation of homogentisate despite the inhibition of the native H PPD enzyme by the HPPD- inhibitor. Such plants and genes are described in WO 99/34008 and WO 02/36787. Tolerance of plants to H PPD inhibitors can also be improved by transforming plants with a gene encoding an enzyme having prephenate deshydrogenase (PDH) activity in addition to a gene encoding an H PPD- tolerant enzyme, as described in WO 04/024928. Further, plants can be made more tolerant to HPPD- inhibitor herbicides by adding into their genome a gene encoding an enzyme capable of metabolizing or degrading H PPD inhibitors, such as the CYP450 enzymes shown in WO 2007/103567 and
  • Still further herbicide resistant plants are plants that are made tolerant to acetolactate synthase (ALS) inhibitors.
  • ALS-inhibitors include, for example, sulfonylurea, imidazolinone, triazolopyrimidines, pryimidinyoxy(thio)benzoates, and/or sulfonylaminocarbonyltriazolinone herbicides.
  • Different mutations in the ALS enzyme also known as acetohydroxyacid synthase, AHAS
  • AHAS acetohydroxyacid synthase
  • the production of sulfonylurea-tolerant plants and imidazolinone-tolerant plants is described in U.S.
  • plants tolerant to imidazolinone and/or sulfonylurea can be obtained by induced mutagenesis, selection in cell cultures in the presence of the herbicide or mutation breeding as described for example for soybeans in US 5,084,082, for rice in WO 97/4121 8, for sugar beet in US 5,773,702 and WO 99/057965, for lettuce in US 5, 1 98,599, or for sunflower in WO 01 /065922.
  • Plants or plant cultivars obtained by plant biotechnology methods such as genetic engineering which may also be treated according to the invention are insect-resistant transgenic plants, i.e. plants made resistant to attack by certain target insects. Such plants can be obtained by genetic transformation, or by selection of plants containing a mutation imparting such insect resistance.
  • An "insect-resistant transgenic plant”, as used herein, includes any plant containing at least one transgene comprising a coding sequence encoding:
  • an insecticidal crystal protein from Bacillus thuringiensis or an insecticidal portion thereof such as the insecticidal crystal proteins listed by Crickmore et al. (1998, Microbiology and Molecular Biology Reviews, 62: 807-813), updated by Crickmore et al. (2005) at the Bacillus thuringiensis toxin nomenclature, online at: http://www.lifesci. Hampshire.
  • insecticidal portions thereof e.g., proteins of the Cry protein classes Cryl Ab, Cryl Ac, Cryl B, Cryl C, Cryl D, Cryl F, Cry2Ab, Cry3Aa, or Cry3Bb or insecticidal portions thereof (e.g. EP-A 1 999 141 and WO 2007/107302), or such proteins encoded by synthetic genes as e.g. described in and U.S. Patent Application 12/249,016 ; or
  • a crystal protein from Bacillus thuringiensis or a portion thereof which is insecticidal in the presence of a second other crystal protein from Bacillus thuringiensis or a portion thereof, such as the binary toxin made up of the Cry34 and Cry35 crystal proteins (Nat. Biotechnol. 2001 , 19, 668- 72; Applied Environm. Microbiol. 2006, 71, 1765-1774) or the binary toxin made up of the Cryl A or Cry1 F proteins and the Cry2Aa or Cry2Ab or Cry2Ae proteins (U.S.
  • VIP vegetative insecticidal
  • a secreted protein from Bacillus thunngiensis or Bacillus cereus which is insecticidal in the presence of a second secreted protein from Bacillus thunngiensis or B. cereus, such as the binary toxin made up of the VI P1 A and VI P2A proteins (WO 94/21795); or a hybrid insecticidal protein comprising parts from different secreted proteins from Bacillus thunngiensis or Bacillus cereus, such as a hybrid of the proteins in 1 ) above or a hybrid of the proteins in 2) above; or a protein of any one of 5) to 7) above wherein some, particularly 1 to 10, amino acids have been replaced by another amino acid to obtain a higher insecticidal activity to a target insect species, and/or to expand the range of target insect species affected, and/or because of changes introduced into the encoding DNA during cloning or transformation (while still encoding an insecticidal protein), such as the VI P3Aa protein in cotton event COT102
  • Patent Applications 61 /126083 and 61 /19501 9 or the binary toxin made up of the VI P3 protein and the Cry2Aa or Cry2Ab or Cry2Ae proteins (U.S. Patent Application 12/214,022 and EP-A 2 300 618).
  • an insect-resistant transgenic plant also includes any plant comprising a combination of genes encoding the proteins of any one of the above classes 1 to 10.
  • an insect-resistant plant contains more than one transgene encoding a protein of any one of the above classes 1 to 10, to expand the range of target insect species affected when using different proteins directed at different target insect species, or to delay insect resistance development to the plants by using different proteins insecticidal to the same target insect species but having a different mode of action, such as binding to different receptor binding sites in the insect.
  • an "insect-resistant transgenic plant”, as used herein, further includes any plant containing at least one transgene comprising a sequence producing upon expression a double-stranded RNA which upon ingestion by a plant insect pest inhibits the growth of this insect pest, as described e.g. in WO
  • 2007/080126 WO 2006/129204
  • WO 2007/074405 WO 2007/080127
  • WO 2007/035650 WO 2007/080126
  • Plants or plant cultivars obtained by plant biotechnology methods such as genetic engineering which may also be treated according to the invention are tolerant to abiotic stresses. Such plants can be obtained by genetic transformation, or by selection of plants containing a mutation imparting such stress resistance. Particularly useful stress tolerance plants include:
  • plants which contain a stress tolerance enhancing transgene coding for a plant-functional enzyme of the nicotineamide adenine dinucleotide salvage synthesis pathway including nicotinamidase, nicotinate phosphoribosyltransferase, nicotinic acid mononucleotide adenyl transferase, nicotinamide adenine dinucleotide synthetase or nicotine amide phosphorybosyltransferase as described e.g. in EP-A 1 794 306, WO 2006/133827, WO 2007/107326, EP-A 1 999 263, or WO 2007/107326.
  • Plants or plant cultivars obtained by plant biotechnology methods such as genetic engineering which may also be treated according to the invention show altered quantity, quality and/or storage-stability of the harvested product and/or altered properties of specific ingredients of the harvested product such as:
  • transgenic plants which synthesize a modified starch, which in its physical-chemical characteristics, in particular the amylose content or the amylose/amylopectin ratio, the degree of branching, the average chain length, the side chain distribution, the viscosity behaviour, the gelling strength, the starch grain size and/or the starch grain morphology, is changed in comparison with the synthesised starch in wild type plant cells or plants, so that this is better suited for special applications.
  • a modified starch which in its physical-chemical characteristics, in particular the amylose content or the amylose/amylopectin ratio, the degree of branching, the average chain length, the side chain distribution, the viscosity behaviour, the gelling strength, the starch grain size and/or the starch grain morphology, is changed in comparison with the synthesised starch in wild type plant cells or plants, so that this is better suited for special applications.
  • Said transgenic plants synthesizing a modified starch are disclosed, for example, in EP-A 0 571 427, WO 95/04826, EP-A 0 719 338, WO 96/15248, WO 96/1 9581 , WO 96/27674, WO 97/1 1 188, WO 97/26362, WO 97/32985, WO 97/42328, WO 97/44472, WO 97/45545, WO 98/27212, WO 98/40503, WO 99/58688, WO 99/58690, WO 99/58654, WO 00/08184, WO 00/08185, WO 00/081 75, WO 00/28052, WO 00/77229, WO 01 /12782, WO 01 /12826, WO 02/101 059, WO 03/071 860, WO 04/056999, WO 05/030942, WO 2005/0309
  • WO 2004/078983 WO 01 /19975, WO 95/26407, WO 96/34968, WO 98/20145, WO 99/12950, WO 99/66050, WO 99/53072, US 6,734,341 , WO 00/1 1 192, WO 98/22604, WO 98/32326, WO 01 /98509, WO 01 /98509, WO 2005/002359, US 5,824,790, US 6,013,861 , WO 94/04693, WO 94/09144, WO 94/1 1520, WO 95/35026, WO 97/20936, WO 201 0/012796, WO 2010/003701 ,
  • transgenic plants which synthesize non starch carbohydrate polymers or which synthesize non starch carbohydrate polymers with altered properties in comparison to wild type plants without genetic modification.
  • Examples are plants producing polyfructose, especially of the inulin and levan-type, as disclosed in EP-A 0 663 956, WO 96/01 904, WO 96/21023, WO 98/39460, and WO 99/24593, plants producing alpha- 1 ,4-glucans as disclosed in WO 95/31553, US
  • transgenic plants or hybrid plants such as onions with characteristics such as 'high soluble solids content', low pungency' (LP) and/or long storage' (LS), as described in U.S. Patent Applications 12/020,360 and 61 /054,026.
  • Plants or plant cultivars (that can be obtained by plant biotechnology methods such as genetic engineering) which may also be treated according to the invention are plants, such as cotton plants, with altered fiber characteristics. Such plants can be obtained by genetic transformation, or by selection of plants contain a mutation imparting such altered fiber characteristics and include:
  • Plants such as cotton plants, containing an altered form of cellulose synthase genes as described in WO 98/00549.
  • Plants such as cotton plants, containing an altered form of rsw2 or rsw3 homologous nucleic acids as described in WO 2004/053219.
  • Plants such as cotton plants, with increased expression of sucrose phosphate synth described in WO 01 /17333.
  • Plants, such as cotton plants, having fibers with altered reactivity e.g. through the expression of N- acetylglucosaminetransferase gene including nodC and chitin synthase genes as described in WO
  • Plants or plant cultivars which may also be treated according to the invention are plants, such as oilseed rape or related Brassica plants, with altered oil profile characteristics.
  • plants can be obtained by genetic transformation, or by selection of plants contain a mutation imparting such altered oil profile characteristics and include:
  • Plants or plant cultivars which may also be treated according to the invention are plants, such as oilseed rape or related Brassica plants, with altered seed shattering characteristics.
  • Such plants can be obtained by genetic transformation, or by selection of plants contain a mutation imparting such altered seed shattering characteristics and include plants such as oilseed rape plants with delayed or reduced seed shattering as described in U.S. Patent Application 61 /135,230, WO 2009/068313 and WO
  • Plants or plant cultivars which may also be treated according to the invention are plants, such as Tobacco plants, with altered post-translational protein modification patterns, for example as described in
  • transgenic plants which may be treated according to the invention are plants containing transformation events, or combination of transformation events, that are the subject of petitions for non-regulated status, in the United States of America, to the Animal and Plant Health Inspection Service (APHIS) of the United States Department of Agriculture (USDA) whether such petitions are granted or are still pending.
  • APHIS Animal and Plant Health Inspection Service
  • U RL internet site
  • Transgenic phenotype the trait conferred to the plants by the transformation event.
  • - Transformation event or line the name of the event or events (sometimes also designated as lines or lines) for which nonregulated status is requested.
  • APHIS documents various documents published by APHIS in relation to the Petition and which can be requested with APHIS.
  • Particularly useful transgenic plants which may be treated according to the invention are plants containing transformation events, or a combination of transformation events, and that are listed for example in the databases for various national or regional regulatory agencies including Event 1 143- 14A (cotton, insect control, not deposited, described in WO 2006/128569); Event 1 143-51 B (cotton, insect control, not deposited, described in WO 2006/128570); Event 1 445 (cotton, herbicide tolerance, not deposited, described in US-A 2002-120964 or WO 02/034946); Event 17053 (rice, herbicide tolerance, deposited as PTA-9843, described in WO 201 0/1 17737); Event 1 7314 (rice, herbicide tolerance, deposited as PTA-9844, described in WO 201 0/1 17735); Event 281 -24-236 (cotton, insect control - herbicide tolerance, deposited as PTA-6233, described in WO 2005/103266 or US-A 2005- 21 6969); Event 3006-21 0-23 (cott
  • Event 5307 corn, insect control, deposited as ATCC PTA-9561 , described in WO 2010/07781 6
  • Event ASR-368 leaf, herbicide tolerance, deposited as ATCC PTA-481 6, described in US-A 2006-1 62007 or WO 2004/053062
  • Event B1 6 corn, herbicide tolerance, not deposited, described in US-A 2003-126634
  • Event BPS-CV127-9 sesoybean, herbicide tolerance, deposited as NCIMB No.
  • Event CE43-67B (cotton, insect control, deposited as DSM ACC2724, described in US-A 2009-21 7423 or WO2006/128573); Event CE44-69D (cotton, insect control, not deposited, described in US-A 201 0-0024077); Event CE44-69D (cotton, insect control, not deposited, described in WO 2006/128571 ); Event CE46-02A (cotton, insect control, not deposited, described in WO 2006/128572); Event COT1 02 (cotton, insect control, not deposited, described in US-A 2006-1301 75 or WO 2004/039986); Event COT202 (cotton, insect control, not deposited, described in US-A 2007-067868 or WO 2005/054479) ; Event COT203 (cotton, insect control, not deposited, described in WO 2005/054480); Event DAS40278 (corn, herbicide tolerance, deposited as ATCC PTA-10244
  • Event DP-356043-5 (soybean, herbicide tolerance, deposited as ATCC PTA-8287, described in US-A 201 0-0184079 or WO 2008/002872); Event EE-1 (brinjal, insect control, not deposited, described in WO 2007/091277); Event FI 1 1 7 (corn, herbicide tolerance, deposited as ATCC 209031 , described in US-A 2006-059581 or WO 98/044140); Event GA21 (corn, herbicide tolerance, deposited as ATCC 209033, described in US-A 2005-086719 or WO 98/044140); Event GG25 (corn, herbicide tolerance, deposited as ATCC 209032, described in US-A 2005-1 88434 or WO 98/044140); Event GHB1 1 9 (cotton, insect control - herbicide tolerance, deposited as ATCC PTA-8398, described in WO 2008/151780); Event GHB61 4
  • NCIMB41 658 described in WO 2006/108674 or US-A 2008-320616
  • Event LL55 (soybean, herbicide tolerance, deposited as NCIMB 41660, described in WO 2006/1 08675 or US-A 2008-1 96127);
  • Event LLcotton25 (cotton, herbicide tolerance, deposited as ATCC PTA-3343, described in WO 03/013224 or US-A 2003-097687);
  • Event LLRICE06 rice, herbicide tolerance, deposited as ATCC-23352, described in US 6,468,747 or WO 00/026345) ;
  • Event LLRICE601 (rice, herbicide tolerance, deposited as ATCC PTA-2600, described in US-A 2008-2289060 or WO 00/026356);
  • Event LY038 (corn, quality trait, deposited as ATCC PTA-5623, described in US-A 2007-028322 or WO 2005/061 720);
  • Event MI R1 62 (corn
  • Event MON88913 cotton, herbicide tolerance, deposited as ATCC PTA-4854, described in WO 2004/072235 or US-A 2006-059590
  • Event MON89034 corn, insect control, deposited as ATCC PTA-7455, described in WO 2007/140256 or US-A 2008-260932
  • Event MON89034 corn, insect control, deposited as ATCC PTA-7455, described in WO 2007/140256 or US-A 2008-260932
  • MON89788 (soybean, herbicide tolerance, deposited as ATCC PTA-6708, described in US-A 2006- 282915 or WO 2006/130436); Event MS1 1 (oilseed rape, pollination control - herbicide tolerance, deposited as ATCC PTA-850 or PTA-2485, described in WO 01 /031042); Event MS8 (oilseed rape, pollination control - herbicide tolerance, deposited as ATCC PTA-730, described in WO 01 /041558 or US-A 2003-1 88347); Event NK603 (corn, herbicide tolerance, deposited as ATCC PTA-2478, described in US-A 2007-292854) ; Event PE-7 (rice, insect control, not deposited, described in WO 2008/1 14282); Event RF3 (oilseed rape, pollination control - herbicide tolerance, deposited as ATCC PTA-730, described in WO 01 /041558 or US-A 2003-1 88347); Event
  • Strigolactame derivatives are tested in comparison to strigolactone derivatives, such as GR24, strigol or sorgolactone.
  • Germination stimulation activity assay GR24 and SL analogues were resuspended in acetone at 10 mmol L "1 , then diluted with water at 1 mmol L “1 (water/acetone; v/v; 99/1 ). Dilutions of 1 x1 0 "3 mol L “1 to 1 x10 -15 mol L “1 are then performed in water/acetone (v/v; 99/1 ). Phelipanche ramosa's seeds (St Martin de Fraigneau, France, 2005) were surface-sterilized according to Vieira Dos Santos et al. (C. V. Dos Santos, P. Letousey, P. Delavault, P.
  • methylthiazolyldiphenyl-tetrazolium bromide assays were carried out according to Mossman (T. Mosmann, J. Immunol. Methods 1983, 65, 55-63) with minor modification of the solubilization buffer (Triton X-1 00 1 0%, HCI 0.04 mol L "1 in isopropanol).
  • EC 50 are modeled with a four parameter logistic curve computed with SigmaPlot® 1 0.0.
  • strigolactone derivatives are able to stimulate germination of the weed Phelipanche ramosa seeds with a great efficiency: GR24 is able to germinate 50% of seeds of the weeds Phelipanche ramosa at a concentration of 2.1 1 0 12 M.
  • Other strigolactones such as strigol and sorgolactone, are less efficient than GR24, and need a concentration around 1 0 times higher to get the same results than GR24.
  • Strigolactame derivatives are very significantly less efficient for the germination of parasitic weed species than GR24, but also less efficient than other strigolactones: Strigolactame compound needs a concentration from 500 to 1 600 times higher than GR24 and other tested strigolactones to get the same result.
  • strigolactame derivatives Used as same concentration, strigolactame derivatives will dramatically be less active than strigolactone compounds to stimulate the seed germination of weeds, which is a great advantage for agricultural practices.
  • Test is perfomed in climate chamber, at 27°C. Compounds are dissolved in acetone in a concentration of 10 6 M. Three replicates are done by compounds. The percentage of Glomus intraradices germinated spores is measured after 3 days of incubation. Untreated control and control with the solvent (acetone) only are done in same conditions.
  • Strigolactone derivatives and particularly GR24, are known to stimulate arbuscular mycorrhizae (AM) fungi spore germination and branching of germinating hyphae (Besserer et al., Plant Physiol. 2008, 148(1 ):402-13).
  • AM arbuscular mycorrhizae
  • Several tests, including the test of Glomus intraradices spore germination used here or the measure of branching of germinating Gigaspora margarita hyphae are considered as equivalent for determinate the activity of compounds on AMF fungi and therefore the capability to stimulate mycchorization (Akiyama K. et al., Nature, 2005, 435, 824).
  • P. sativum ccd8 shoot branching mutants of pea are strigolactone deficient plants which show a hyper- branched phenotype.
  • Application of strigolactone directly to the axillary buds is able to restore the wild-type branching phenotype to ccd8 mutants (Gomez-Roldan et al, 2008, Nature, 455, 1 89-194).
  • strigolactone compound GR24 directly to the axillary N4 buds of P. sativum ccd8 mutant restores in a significant amount (more than 80%) the wild-type branching phenotype.
  • Strigolactame derivative compound C restores the wild-type branching phenotype, with an efficiency comparable to the GR24-derived compound.

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Description

COM POSITIONS COMPRISING A STRIGOLACTAM E COMPOUND FOR ENHANCED PLANT
GROWTH AND YI ELD The present invention relates to strigolactame derivatives that are active on plants and to compositions comprising said derivatives. The present invention also relates to the use of said derivatives or compositions for enhancing the plant growth, yield, vigor and/or mycchorization and to corresponding methods. Mycorrhizal symbiosis (or mycchorization) is a common symbiotic relationship between arbuscular mycorrhizal (AM) fungi and plants roots, which is highly beneficial for the plant, its growth, yield and vigor. Fungi of the phylum Glomeromycota (AM fungi) penetrate and colonize plant roots, where they differentiate into highly branched structures known as arbuscules and vesicles. AM fungi help plants to capture nutrients such as phosphorus and micronutrients from the soil. More than 80% of lands plants are forming symbiotic associations with AM fungi.
Strigolactones have been identified in the root exudates of a variety of plant species, and have been initially disclosed as compounds capable of stimulating the seed germination of parasitic weed species, especially Orobanche sp. and striga sp. (Cook et al., 1 972, J Am Chem Soc, 94, 6198-6199; Hauck et al., 1 992, J Plant Physiol, 139, 474-478; Muller et al., 1 992). Later, it has been shown that strigolactones can stimulate the growth of arbuscular mycorrhizae (AM) fungi (WO 2005/0771 77). More recently, strigolactones have been considered as a new class of plant hormones, exhibiting various biological activities (H. Proust, B. Hoffmann, X. Xie, K. Yoneyama, D. G. Schaefer, K.
Yoneyama, F. Nogue, C. Rameau, Development 201 1 , 138, 1531 -1539 ; H. Koltai, New Phytol. 201 1 , 190, 545-549 ; E. Foo, N. W. Davies, Planta 201 1 ).
Natural strigolactones generally possess a chemical structure comprising 4 rings A, B, C, D and share the common configuration indicated below, in which rings A and B can comprise double bond(s) or substituents
Figure imgf000002_0001
Numerous synthetic strigolactone analogues (A. J. Humphrey, A. M. Galster, M. H. Beale, Nat. Prod. Rep. 2006, 23, 592-614 and references cited therein ; A. S. Mwakaboko, B. Zwanenburg, Bioorg. Med. Chem. 201 1 , 19, 5006-501 1 ) have been proposed in the last decades to enhance the biological activities and to overcome the low stability of natural strigolactones in aqueous medium.
In 1981 , A. W. Johnson et al. (A. W. Johnson, G. Gowda, A. Hassanali, J. Knox, S. Monaco, Z.
Razavi, G. Rosebery J. Chem. Soc, Perkin Trans. 1 1981 , 1 734-1 743.) synthesized from the 4-chl 2-methylbut-2-en-4-olide and 3-hydroxymethyleneindolin-2-one, (E)-3-(((4-methyl-5-oxo-2,5- dihydrofuran-2-yl)oxy)methylene)indolin-2-one derivative and three analogs in a poor yield (1 9%).
Figure imgf000003_0001
These four compounds have an aromatic cycle fused to a 5-membered heterocyclic group, and are not embraced by the general formula (I) of the compounds according to the invention.
Surprisingly, we have discovered that strigolactame derivatives of formula (I) can enhance plant growth, yield, vigor and/or mycchorization of plants.
Advantageously, strigolactame derivatives of formula (I) are largely less efficient than strigolactones for promoting the germination of parasitic weed seeds.
Described herein is the invention of new strigolactames of the following formula (I):
Figure imgf000003_0002
(I)
wherein : - Xi, X2, X3, Yi, Y2, Y3 and Z independently represent a hydrogen atom, a halogen atom, a nitro group, a hydroxy group, a cyano group, an amino group, a sulphenyl group, a sulphinyl group, a sulphonyl group, a formyl group, a acetyl group, a formyloxy group, a formylamino group, a carbamoyl group, a N-hydroxycarbamoyl group, a carbamate group, substituted or non- substituted (hydroxyimino)-Ci-C6-alkyl group, substituted or non-substituted Ci-Cs-alkyl, substituted or non-substituted tri(Ci-C8-alkyl)silyl-Ci-C8-alkyl, substituted or non-substituted
Ci-Cs-cycloalkyl, substituted or non-substituted tri(Ci-C8-alkyl)silyl-Ci-C8-cycloalkyl, substituted or non-substituted CrC8-halogenoalkyl having 1 to 5 halogen atoms, substituted or non-substituted Ci -C8-halogenocycloalkyl having 1 to 5 halogen atoms, a substituted or non- substituted C2-C8-alkenyl, substituted or non-substituted C2-C8-alkynyl, substituted or non- substituted Ci -Cs-alkylamino, substituted or non-substituted di-Ci -C8-alkylamino, substituted or non-substituted CrC8-alkoxy, substituted or non-substituted CrC8-halogenoalkoxy having 1 to 5 halogen atoms, substituted or non-substituted C2-C8-alkynyloxy, substituted or non- substituted Ci -C8-alkylsulphenyl, substituted or non-substituted Ci -C8-halogenoalkylsulphenyl having 1 to 5 halogen atoms, substituted or non-substituted C2-C8-alkenyloxy, substituted or non-substituted C2-C8-halogenoalkenyloxy having 1 to 5 halogen atoms, substituted or non- substituted C3-C8-halogenoalkynyloxy having 1 to 5 halogen atoms, substituted or non- substituted CrC8-alkylcarbonyl, substituted or non-substituted CrC8-halogenoalkylcarbonyl having 1 to 5 halogen atoms, substituted or non-substituted CrC8-alkylcarbamoyl, substituted or non-substituted di-CrC8-alkylcarbamoyl, substituted or non-substituted N-C1 -C8- alkyloxycarbamoyl, substituted or non-substituted di-Ci -C8-alkoxycarbamoyl, substituted or non-substituted N-Ci -C8-alkyl-Ci -C8-alkoxycarbamoyl, substituted or non-substituted Ci -C8- alkoxycarbonyl, substituted or non-substituted CrC8-halogenoalkoxycarbonyl having 1 to 5 halogen atoms, substituted or non-substituted CrC8-alkylcarbonyloxy, substituted or non- substituted CrC8-halogenoalkylcarbonyloxy having 1 to 5 halogen atoms, substituted or non- substituted CrC8-alkylcarbonylamino, substituted or non-substituted Ci -C8- halogenoalkylcarbonylamino having 1 to 5 halogen atoms, substituted or non-substituted Ci - C8-alkylaminocarbonyloxy, substituted or non-substituted di-Ci -C8-alkylaminocarbonyloxy, substituted or non-substituted Ci -C8-alkyloxycarbonyloxy, substituted or non-substituted Ci - C8-alkylsulphenyl, substituted or non-substituted CrC8-halogenoalkylsulphenyl having 1 to 5 halogen atoms, substituted or non-substituted Ci -C8-alkylsulphinyl, substituted or non- substituted Ci -C8-halogenoalkylsulphinyl having 1 to 5 halogen atoms, substituted or non- substituted CrC8-alkylsulphonyl, substituted or non-substituted CrC8-halogenoalkylsulphonyl having 1 to 5 halogen atoms, substituted or non-substituted Ci -C8-alkylaminosulfamoyl, substituted or non-substituted di-Ci -C8-alkylaminosulfamoyl, substituted or non-substituted (Ci -C6-alkoxyimino)-Ci -C6-alkyl, substituted or non-substituted (Ci -C6-alkenyloxyimino)-Ci -C6- alkyl, substituted or non-substituted (Ci -C6-alkynyloxyimino)-Ci -C6-alkyl, substituted or non- substituted (benzyloxyimino)-Ci -C6-alkyl, substituted or non-substituted Ci -C8-alkoxyalkyl, substituted or non-substituted CrC8-halogenoalkoxyalkyl having 1 to 5 halogen atoms, a substituted or non-substituted arylalkyi substituted or non-substituted benzyloxy, substituted or non-substituted benzylsulphenyl, substituted or non-substituted benzylamino, substituted or non-substituted phenoxy, substituted or non-substituted phenylsulphenyl, substituted or non- substituted phenylamino, a substituted or non-substituted or a 4-, 5-, 6- or 7-membered heterocycle comprising up to 4 heteroatoms selected in the list consisting of N, O, S]
- Ri and R2 independently represent a hydrogen atom, a halogen atom, a nitro group, a hydroxy group, a cyano group, an amino group, a sulphenyl group, a sulphinyl group, a sulphonyl group, a formyl group, a formyloxy group, a formylamino group, a carbamoyl group, a N-hydroxycarbamoyl group, a carbamate group, substituted or non-substituted (hydroxyimino)-Ci-C6-alkyl group, substituted or non-substituted CrC8-alkyl, substituted or non-substituted tri(Ci-C8-alkyl)silyl-CrC8- alkyl, substituted or non-substituted Ci-C8-cycloalkyl, substituted or non-substituted tri(Ci-C8- alkyl)silyl-Ci-C8-cycloalkyl, substituted or non-substituted CrC8-halogenoalkyl having 1 to 5 halogen atoms, substituted or non-substituted CrC8-halogenocycloalkyl having 1 to 5 halogen atoms, a substituted or non-substituted C2-C8-alkenyl, substituted or non-substituted C2-C8-alkynyl, substituted or non-substituted Ci-C8-alkylamino, substituted or non-substituted di-Ci-C8-alkylamino, substituted or non-substituted Ci-C8-alkoxy, substituted or non-substituted Ci-C8-halogenoalkoxy having 1 to 5 halogen atoms, substituted or non-substituted C2-C8-alkynyloxy, substituted or non-substituted CrC8- alkylsulphenyl, substituted or non-substituted CrC8-halogenoalkylsulphenyl having 1 to 5 halogen atoms, substituted or non-substituted C2-C8-alkenyloxy, substituted or non-substituted C2-C8- halogenoalkenyloxy having 1 to 5 halogen atoms, substituted or non-substituted C3-C8- halogenoalkynyloxy having 1 to 5 halogen atoms, substituted or non-substituted Ci-C8-alkylcarbonyl, substituted or non-substituted Ci-C8-halogenoalkylcarbonyl having 1 to 5 halogen atoms, substituted or non-substituted CrC8-alkylcarbamoyl, substituted or non-substituted di-CrC8-alkylcarbamoyl, substituted or non-substituted N-C1 -C8-alkyloxycarbamoyl, substituted or non-substituted di-Ci-C8- alkoxycarbamoyl, substituted or non-substituted N-Ci-C8-alkyl-Ci-C8-alkoxycarbamoyl, substituted or non-substituted CrC8-alkoxycarbonyl, substituted or non-substituted CrC8-halogenoalkoxycarbonyl having 1 to 5 halogen atoms, substituted or non-substituted Ci-C8-alkylcarbonyloxy, substituted or non-substituted Ci-C8-halogenoalkylcarbonyloxy having 1 to 5 halogen atoms, substituted or non- substituted CrC8-alkylcarbonylamino, substituted or non-substituted CrC8- halogenoalkylcarbonylamino having 1 to 5 halogen atoms, substituted or non-substituted CrC8- alkylaminocarbonyloxy, substituted or non-substituted di-Ci-C8-alkylaminocarbonyloxy, substituted or non-substituted Ci-C8-alkyloxycarbonyloxy, substituted or non-substituted Ci-C8-alkylsulphenyl, substituted or non-substituted CrC8-halogenoalkylsulphenyl having 1 to 5 halogen atoms, substituted or non-substituted CrC8-alkylsulphinyl, substituted or non-substituted Ci-C8-halogenoalkylsulphinyl having 1 to 5 halogen atoms, substituted or non-substituted CrC8-alkylsulphonyl, substituted or non- substituted Ci-C8-halogenoalkylsulphonyl having 1 to 5 halogen atoms, substituted or non-substituted Ci-C8-alkylaminosulfamoyl, substituted or non-substituted di-Ci-C8-alkylaminosulfamoyl, substituted or non-substituted (Ci -alkoxyimino)-Ci -alkyl, substituted or non-substituted alkenyloxyimino)-Ci-C6-alkyl, substituted or non-substituted (Ci -alkynyloxyimino)-Ci-C6-alkyl, substituted or non-substituted (benzyloxyimino)-Ci-C6-alkyl, substituted or non-substituted Ci-C8- alkoxyalkyl, substituted or non-substituted CrC8-halogenoalkoxyalkyl having 1 to 5 halogen atoms, substituted or non-substituted benzyloxy, substituted or non-substituted benzylsulphenyl, substituted or non-substituted benzylamino, substituted or non-substituted phenoxy, substituted or non-substituted phenylsulphenyl, substituted or non-substituted phenylamino, a substituted or non-substituted or a 4-, 5-, 6- or 7-membered heterocycle comprising up to 4 heteroatoms selected in the list consisting of N, O, S]; or
Ri and R2 form a saturated or unsaturated, non-aromatic, substituted or non-substituted 4- to 7- membered carbocycle; or Ri and R2 form a saturated or unsaturated, aromatic or non-aromatic, substituted or non-substituted 4- to 7-membered carbocycle fused to an other saturated or unsaturated, aromatic or non-aromatic, substituted or non-substituted 4- to 7- membered carbocycle; as well as salts, N-oxides, metallic complexes, metalloidic complexes and optically active or geometric isomers thereof;
Any of the compounds used in the compositions according to the present invention may also exist in one or more geometric isomeric form depending on the number of double bond within the compound. The invention thus equally relates to any geometric isomer and to any possible mixtures thereof, in any proportion. Geometric isomers can be separated according to any method known per se by the man ordinary skilled in the art. Any of the compounds used in the compositions according to the present invention wherein a substituant represents a hydroxy group, a sulphenyl group or an amino group can exist in a tautomeric form resulting from the shift of the proton of said hydroxy group, sulphenyl group or amino group respectively. Such tautomeric forms are also part of the present invention. According to the invention, the following generic terms are generally used with the following meanings:
• halogen means fluorine, chlorine, bromine or iodine;
• heteroatom can be nitrogen, oxygen or sulphur.
Unless indicated otherwise, a group or a substituent that is substituted according to the invention can be substituted by one or more of the following groups or atoms: a halogen atom, a nitro group, a hydroxy group, a cyano group, an amino group, a sulphenyl group, a sulphinyl group, a sulphonyl group, a formyl group, a formyloxy group, a formylamino group, a carbamoyl group, a N- hydroxycarbamoyl group, a carbamate group, substituted or non-substituted (hydroxyimino)-Ci -C6- alkyl group, substituted or non-substituted Ci -C8-alkyl, substituted or non-substituted tri(Ci -C8- alkyl)silyl-Ci -C8-alkyl, substituted or non-substituted CrC8-cycloalkyl, substituted or non-substituted tri(Ci -C8-alkyl)silyl-Ci -C8-cycloalkyl, substituted or non-substituted Ci -C8-halogenoalkyl having 1 to 5 halogen atoms, substituted or non-substituted CrC8-halogenocycloalkyl having 1 to 5 halogen atoms a C2-C8-alkenyl, substituted or non-substituted C2-C8-alkynyl, substituted or non-substituted Ci -C8- alkylamino, substituted or non-substituted di-CrC8-alkylamino, substituted or non-substituted Ci -C8- alkoxy, substituted or non-substituted CrC8-halogenoalkoxy having 1 to 5 halogen atoms, substituted or non-substituted C2-C8-alkenyloxy, substituted or non-substituted C2-C8-alkynyloxy, substituted or non-substituted Ci -C8-alkylsulphenyl, substituted or non-substituted CrC8-halogenoalkylsulphenyl having 1 to 5 halogen atoms, substituted or non-substituted C2-C8-halogenoalkenyloxy having 1 to 5 halogen atoms, substituted or non-substituted C3-C8-alkynyloxy, substituted or non-substituted C3-C8- halogenoalkynyloxy having 1 to 5 halogen atoms, substituted or non-substituted CrC8-alkylcarbonyl, substituted or non-substituted Ci-C8-halogenoalkylcarbonyl having 1 to 5 halogen atoms, substituted or non-substituted Ci-C8-alkylcarbamoyl, substituted or non-substituted di-Ci-C8-alkylcarbamoyl, substituted or non-substituted N-C1 -C8-alkyloxycarbamoyl, substituted or non-substituted di-Ci-C8- alkoxycarbamoyl, substituted or non-substituted N-Ci-C8-alkyl-Ci-C8-alkoxycarbamoyl, substituted or non-substituted CrC8-alkoxycarbonyl, substituted or non-substituted CrC8-halogenoalkoxycarbonyl having 1 to 5 halogen atoms, substituted or non-substituted Ci-C8-alkylcarbonyloxy, substituted or non-substituted Ci-C8-halogenoalkylcarbonyloxy having 1 to 5 halogen atoms, substituted or non- substituted Ci-Cs-alkylcarbonylamino, substituted or non-substituted Ci-C8- halogenoalkylcarbonylamino having 1 to 5 halogen atoms, substituted or non-substituted CrC8- alkylaminocarbonyloxy, substituted or non-substituted di-Ci-C8-alkylaminocarbonyloxy, substituted or non-substituted CrC8-alkyloxycarbonyloxy, substituted or non-substituted CrC8-alkylsulphenyl, substituted or non-substituted CrC8-halogenoalkylsulphenyl having 1 to 5 halogen atoms, substituted or non-substituted Ci-C8-alkylsulphinyl, substituted or non-substituted Ci-C8-halogenoalkylsulphinyl having 1 to 5 halogen atoms, substituted or non-substituted Ci-C8-alkylsulphonyl, substituted or non- substituted CrC8-halogenoalkylsulphonyl having 1 to 5 halogen atoms, substituted or non-substituted Ci-C8-alkylaminosulfamoyl, substituted or non-substituted di-Ci-C8-alkylaminosulfamoyl, substituted or non-substituted (Ci -alkoxyimino)-Ci-C6-alkyl, substituted or non-substituted (Ci-C6- alkenyloxyimino)-Ci-C6-alkyl, substituted or non-substituted (Ci -alkynyloxyimino)-Ci-C6-alkyl, substituted or non-substituted (benzyloxyimino)-Ci -alkyl, substituted or non-substituted Ci-C8- alkoxyalkyl, substituted or non-substituted CrC8-halogenoalkoxyalkyl having 1 to 5 halogen atoms, substituted or non-substituted benzyloxy, substituted or non-substituted benzylsulphenyl, substituted or non-substituted benzylamino, substituted or non-substituted phenoxy, substituted or non-substituted phenylsulphenyl, substituted or non-substituted phenylamino, a substituted or non-substituted or a 4-, 5-, 6- or 7-membered heterocycle comprising up to 4 heteroatoms selected in the list consisting of N, O, S.
Preferred compounds of formula (I) according to the invention are those wherein Xi, X2, Yr Y2, Y3 and Z independently represent a hydrogen atom, a halogen atom, a nitro group, a hydroxy group, a cyano group, a substituted or non-substituted CrC8-alkyl, a substituted or non-substituted CrC8-haloalkyl, a substituted or non-substituted Ci-C8-alkoxy, or a substituted or non-substituted Ci-C8-haloalkoxy.
More preferred compounds of formula (I) according to the invention are those wherein Xi, X2, Yi, Y3 and Z represent a hydrogen atom. Other more preferred compounds of formula (I) are those wherein Y2 represents a substituted or non- substituted Ci-C8-alkyl, or a substituted or non-substituted Ci-C8-haloalkyl.
Other preferred compounds of formula (I) according to the invention are those wherein X3 represents hydrogen atom, a formyl group, a substituted or non-substituted CrC8-alkyl, a substituted or non- substituted Ci-C8-halogenoalkyl having 1 to 5 halogen atoms, a substituted or non-substituted C2-C8- alkenyl, a substituted or non-substituted C2-C8-alkynyl, a substituted or non-substituted arylalkyi, acetyl, a substituted or non-substituted Ci-C8-alkylcarbonyl, a substituted or non-substituted Ci-C8- halogenoalkylcarbonyl, substituted or non-substituted Ci-C8-alkoxycarbonyl, More preferred compounds of formula (I) according to the invention are those wherein X3 represents hydrogen atom, a substituted or non-substituted Ci-C8-alkyl, a substituted or non-substituted C2-C8- alkenyl, a substituted or non-substituted C2-C8-alkynyl, a substituted or non-substituted arylalkyi, formyl, acetyl, a substituted or non-substituted Ci-C8-alkylcarbonyl, a substituted or non-substituted d-Cs-haloalkylcarbonyl, substituted or non-substituted CrC8-alkoxycarbonyl,
Other preferred compounds of formula (I) according to the invention are those wherein Ri and R2 independently represent a hydrogen atom, a halogen atom, a nitro group, a hydroxy group, a cyano group, a substituted or non-substituted Ci-C8-alkyl, a substituted or non-substituted Ci-C8-haloalkyl, a substituted or non-substituted Ci-C8-alkoxy, or a substituted or non-substituted Ci-C8-haloalkoxy; or Ri and R2 form a saturated or unsaturated, non-aromatic, substituted or non-substituted 4- to 7- membered carbocycle; or
Ri and R2 form a saturated or unsaturated, aromatic or non-aromatic, substituted or non-substituted 4- to 7-membered carbocycle fused to another saturated or unsaturated, aromatic or non-aromatic, substituted or non-substituted 4- to 7-membered carbocycle.
Other more preferred compounds of formula (I) according to the invention are those wherein Ri and R2 form a saturated or unsaturated, aromatic or non-aromatic, substituted or non-substituted 4- to 7- membered carbocycle fused to another saturated or unsaturated, aromatic or non-aromatic, substituted or non-substituted 4- to 7-membered carbocycle.
Other even more preferred compounds of formula (I) according to the invention are those wherein Ri and R2 form an unsaturated, non-aromatic, substituted or non-substituted 5-membered carbocycle fused to another unsaturated, aromatic, substituted or non-substituted 6- membered carbocycle. Preferred compound of formula (I) according to the invention are those wherein
- Xi, X2, Yi, Y2 and Z independently represent a hydrogen atom, a halogen atom, a nitro group, a hydroxy group, a cyano group, a substituted or non-substituted CrC8-alkyl, a substituted or non- substituted Ci-C8-haloalkyl, a substituted or non-substituted CrC8-alkoxy, or a substituted or non- substituted Ci-Cs-haloalkoxy;
- represents hydrogen atom, a substituted or non-substituted Ci-C8-alkyl, a substituted or non- substituted C2-C8-alkenyl, a substituted or non-substituted C2-C8-alkynyl, a substituted or non- substituted arylalkyi, formyl, acetyl, a substituted or non-substituted Ci-C8-alkylcarbonyl, a substituted or non-substituted CrC8-haloalkylcarbonyl, substituted or non-substituted CrC8-alkoxycarbonyl,and
- Ri and R2 form an unsaturated, non-aromatic, substituted or non-substituted 5-membered carbocycle fused to another unsaturated, aromatic, substituted or non-substituted 6-membered carbocycle. More preferred compound of formula (I) according to the invention are those wherein
- Xi , X2, Yi , Y3 and Z independently represent a hydrogen atom;
- X3 represents hydrogen atom, a substituted or non-substituted CrC8-alkyl, a substituted or non- substituted C2-C8-alkenyl, a substituted or non-substituted C2-C8-alkynyl, a substituted or non- substituted arylalkyl, formyl, acetyl, a substituted or non-substituted Ci -C8-alkylcarbonyl, a substituted or non-substituted C rC8-haloalkylcarbonyl, substituted or non-substituted CrC8-alkoxycarbonyl,
- Y2 represents a substituted or non-substituted Ci -C8-alkyl or a substituted or non-substituted Ci -C8- haloalkyl; and
- Ri and R2 form an unsaturated, non-aromatic substituted or non-substituted 5-membered carbocycle fused to another unsaturated, aromatic, substituted or non-substituted 6-membered carbocycle.
More preferred compound of formula (I) according to the invention are selected in the list consisting of:
Figure imgf000009_0001
(Id) (le) (If)
wherein X3 represents hydrogen atom, a substituted or non-substituted CrC8-alkyl, a substituted or non-substituted C2-C8-alkenyl, a substituted or non-substituted C2-C8-alkynyl, a substituted or non- substituted arylalkyl, formyl, acetyl, a substituted or non-substituted CrC8-alkylcarbonyl, a substituted or non-substituted C rC8-haloalkylcarbonyl, substituted or non-substituted CrC8-alkoxycarbonyl. We proposed here an access to strigolactames, especially nitrogen analogues of GR24 (example 1 ) and GR5 (example 2).
About the strigolactame analogs of GR24, our synthesis uses a new one-pot four-step route to the known tricyclic compound (A. U. De, B. P. Saha, J. Pharm. Sci. 1973, 62, 1363-1364) and a coupling with the described bromo lactone (G. A. Macalpine, R. A. Raphael, A. Shaw, A. W. Taylor, H. J. Wild J. Chem. Soc, Perkin Trans. 1 1 976, 41 0-41 6) affords the new strigolactames. About the strigolactame analogs of GR5, we synthesize the undescribed 3-enolether of N- Bocpyrrolidinone and link it with the same bromolactone as above.
Example 1 :
Preparation of (3E,3a/?* 8bS*)-3-({[(2/¾-5-hydroxy-4-methyl-2,5-dihydrofuran-2- yl]oxy}methylene)-3,3a,4,8b-tetrahydroindeno[1 ,2-b]pyrrol-2( iH)-one and
(3E,3a/?* 8bS 3-({[(2S)-5-hydroxy-4-methyl-2,5-dihydrofuran-2-yl]oxy}methylene)-3,3a,4,8b- tetrahydroindeno[1 ,2-b]pyrrol-2( 7H)-one
Figure imgf000010_0001
Step 1 : (3afl*,8bS*)-3,3a,4,8b-Tetrahydroindeno[1 ,2-fo]pyrrol-2(1 H)-one
Figure imgf000010_0002
Sodium borohydride (1 .39 g, 36.66 mmol, 1 equiv) was added to a mixture of Ethyl (1 -oxo-2,3-dihydro- 1 H-inden-2-yl)acetate (Mangnus, E. M. ; Dommerholt, F. J. ; Dejong, R. L. P. ; Zwanenburg, B. J. Agric. Food Chem. 1992, 40, 1230 ; Bergmann, E. ; Hoffman, E. J. Org. Chem. 1961 , 26, 3555; Ozaki, S. ; Adachi, M. ; Sekiya, S. ; Kamikawa, R. J. Org. Chem. 2003, 68, 4586) (8.00 g, 36.66 mmol, 1 equiv) in methanol (150 ml_) under argon at -10 °C. After 3 h, the reaction was quenched with water. The resulting mixture was extracted with CH2CI2 (3 x), dried (MgS04), filtered and evaporated under reduce pressure.
The concentrated crude intermediate was directly placed in the next step in presence of thionyl chloride (4.80 g, 40.32 mmol, 1 .1 0 equiv) and pyridine (3.1 9 g, 40.32 mmol, 1 .10 equiv) in CH2CI2 (150 ml_) at 0 °C. After 4 h at room temperature, the reaction mixture was concentrated to dryness under reduced pressure. The crude oil was solubilized in CH2CI2 and washed with water and dried over MgS04.
After evaporation under reduced pressure, the crude oil was dissolved in dry DMF (150 ml_) in presence of sodium azide (5.24 g, 80.64 mmol, 2.20 equiv). After heating at 90 during 3 h, the solvent was removed by evaporation under reduced pressure. The crude product was then dissolved with CH2CI2 and washed with water.
After concentration, it was finally dissolved in methanol (150 ml_) in presence of Pd/C 1 0% (0.92 g, cat) under H2 atmosphere. After stirring for 6 h at room temperature, the reaction mixture was filtered through a celite pad, and after evaporation of the solvent, the crude product was purified on silica gel (heptane/EtOAc 50:50) to afford the desired product (2.03 g, 1 1 .71 mmol, 23%) as an amorphous solid (A. W. Johnson, G. Gowda, A. Hassanali, J. Knox, S. Monaco, Z. Razavi, G. Rosebery J. Chem. Soc, Perkin Trans. 1 1981 , 1 734-1 743).
1 H NMR (300 MHz, CDCI3): δ 7.34-7.23, 6.95, 5.05, 3.40-3.27, 2.94-2.84, 2.74, 2.24.
HRMS (ESI): Calcd for Cn H12NO [M + H]+: 1 74.091 9. Found: 174.091 1 .
Step 2 : tert-Butyl (3aR*,8bS*)-2-oxo-3,3a, -tetrahydroindeno[1 ,2-b]pyrrole-1 (2H)-carboxylate
Figure imgf000011_0001
Boc20 (0.26 g, 1 .1 8 mmol, 2.05 equiv) was added to a solution of previous lactam (1 00.0 mg, 0.58 mmol, 1 equiv) and DMAP (754.0 mg, 0.61 mmol, 1 .05 equiv) in a mixture of triethylamine-acetonitrile (3:1 ) (4 ml_) under argon at room temperature. After 3 h, the reaction mixture was diluted with EtOAc. The organic layer was washed successively with HCI (1 M), saturated aqueous sodium hydrogen carbonate and brine. After drying over MgS04, concentration of the solvent gave a residue, which was purified by flash chromatography on silica gel (EtOAc neat) to afford the pure desired product (1 41 .0 mg, 0.52 mmol, 89%) as a hygroscopic white solid.
1 H NMR (300 MHz, CDCI3): δ 7.51 -7.48, 7.25-7.14, 5.54, 3.16-3.04, 2.75, 2.70, 2.20, 1 .54.
HRMS (ESI): Calcd for C16H19N03Na [M + Na]+: 296.1263. Found: 296.1261 .
Step 3 :
(3E,3aR*,8bS*)-3-({[(2R*)-4-methyl-5-oxo-2,5-dihydrofuran-2-yl]oxy}methylene)-3,3a,4,8b- tetrahydroindeno[1 ,2-b]pyrrol-2(1 H)-one
Figure imgf000011_0002
(3E,3aR*,8bS*)-3-({[(2S*)-4-methyl-5-oxo-2,5-dihydrofuran-2-yl]oxy}methylene)-3,3a,4,8b- tetrahydroindeno[1 ,2-b]pyrrol-2(1 H)-one
Figure imgf000011_0003
Lactam from step 2 (100.0 mg, 0.37 mmol, 1 equiv) was dissolved in tert- butoxybis(dimethylamino)methane (Bredereck's reagent) (0.30 ml_, 1 .46 mmol, 4 equiv) under argon at room temperature. After heating at 75 °C for 3 h, the cooled reaction mixture was diluted with EtOAc, and the resulting mixture was washed with water and brine, and then dried over MgS04. Concentration of the solvent in vacuo gave the crude product, which was directly diluted in a mixture of THF (5 mL) and HCI (1 M) (0.44 mL, 0.44 mmol, 1 .20 equiv) and stirred for 1 h at room temperature. The mixture was neutralized with saturated aqueous sodium hydrogen carbonate solution and diluted with EtOAc. The organic layer was washed with brine and dried over MgS04. Concentration of the solvent in vacuo gave a residue, which was purified by flash chromatography (ChbC /methanol 95:5) to afford the pure desired product enol (96.0 mg, 0.32 mmol, 80%) as an amorphous solid.
To a solution of this enol (45.0 mg, 0.15 mmol, 1 equiv) in
/V-methylpyrrolidone (2 mL) was added potassium carbonate (42.0 mg, 0.31 mmol, 2.05 equiv) at room temperature under argon. To this mixture was added a solution of (±)-4-bromo-2-methyl-2-buten-4-olide ( G. A. Macalpine, R. A. Raphael, A. Shaw, A. W. Taylor, H. J. Wild J. Chem. Soc, Perkin Trans. 1 1 976, 410-41 6) (28.0 mg, 0.1 6 mmol, 1 .05 equiv) in /V-methylpyrrolidone (2 mL). After 3 h, the reaction was quenched with a solution of HCI 1 N and the product was extracted with EtOAc. The organic layer was washed with water, brine and dried on MgS04. After evaporation, the crude product was purified by preparative TLC (heptane/EtOAc 80:20) to afford the two epimers as two pure fractions (F1 , 23.8 mg, 0.06 mmol, 40%; F2, 22.1 mg, 0.06 mmol, 37%) as amorphous white solids.
To a solution of N-Boc F1 (23.8 mg, 0.06 mmol, 1 equiv) in CH2CI2 (5 mL) was added trifluoroacetic acid (1 .83 mL, 24.00 mmol, 400 equiv) at room temperature under argon. After 5 h, the reaction mixture was evaporated to dryness and the crude product was purified on preparative TLC on silica to afford the pure product (2ft*) (14.6 mg, 0.05 mmol, 82%) as a white amorphous solid.
Separately, to a solution of N-Boc F2 (22.1 mg, 0.06 mmol, 1 equiv) in CH2CI2 (5 mL) was added trifluoroacetic acid (1 .70 mL, 22.24 mmol, 400 equiv) at room temperature under argon. After 5 h, the reaction mixture was evaporated to dryness and the crude product was purified on preparative TLC on silica to afford the pure product (2S*) (13.2 mg, 0.04 mmol, 80%) as a white amorphous solid.
(3E,3aft*,8bS*)-3-({[(2ft*)-4-methyl-5-oxo-2,5-dihydrofuran-2-yl]oxy}methylene)-3,3a,4,8b- tetrahydroindeno[1 ,2-b]pyrrol-2(1 H)-one :
1 H NMR (300 MHz, CDCI3): 7.27-7.18, 6.92, 6.68, 6.12, 5.09, 3.92-3.84, 3.41 , 3.05, 2.01 .
HRMS (ESI): Calcd for C17H15N04Na [M + Na]+: 320.0899. Found: 320.0914.
(3E,3aft*,8bS*)-3-({[(2S*)-4-methyl-5-oxo-2,5-dihydrofuran-2-yl]oxy}methylene)-3,3a,4,8b- tetrahydroindeno[1 ,2-b]pyrrol-2(1 H)-one :
1 H NMR (300 MHz, CDCI3): 7.23-7.12, 6.88, 6.67, 6.06, 5.03 , 3.88-3.80, 3.38, 3.00, 1 .96.
HRMS (ESI): Calcd for C17H15N04Na [M + Na]+: 320.0899. Found: 320.0913. Example 2: (3£)-3-{[(4-methyl-5-oxo-2,5-dihydrofuran-2-yl)oxy]methylene}pyrrolidin-2-one
Figure imgf000013_0001
Stepl : tert-butyl (3£)-3-{[(4-methyl-5-oxo-2,5-dihydrofuran-2-yl)oxy]methylene}-2-oxopyrrolidine-1 - carboxylate
Figure imgf000013_0002
Boc20 (2.63 g, 12.05 mmol, 2.05 equiv) diluted was added to a solution pyrrolidinone (500.0 mg, 6.88 mmol, 1 equiv) and DMAP (754.0 mg, 6.1 7 mmol, 1 .05 equiv) in a mixture of triethylamine-acetonitrile (3:1 ) (20 mL) under argon at room temperature. After 3 h, the reaction mixture was diluted with EtOAc. The organic layer was washed successively with HCI (1 M), saturated aqueous sodium hydrogen carbonate solution and brine. After drying over MgS04, concentration of the solvent gave a residue, which was purified by flash chromatography (EtOAc neat) to afford the pure desired carbamate (743.0 mg, 4.01 mmol, 68%) as a pale yellow oil (analyses in accordance with the literature data) (Banfi, L ; Basso, A. ; Cerulli, V. ; Guanti, G.; Riva, R. J. Org. Chem. 2008, 73, 1 608-161 1 ). The carbamate (250.0 mg, 1 .35 mmol, 1 equiv) was dissolved in tert- butoxybis(dimethylamino)methane (Bredereck reagent) (1 .12 mL, 5.40 mmol, 4 equiv) under argon at room temperature. After heating at 75°C for 3 h, the cooled mixture was diluted with EtOAc, and the organic layer was washed with water and brine, then dried over MgSC . Concentration of the solvent in vacuo gave the crude product, which was directly diluted in a mixture of THF (5 mL) and HCI (1 M) (1 .62 mL, 1 .62 mmol, 1 .20 equiv) and stirred for 1 h at room temperature. The reaction mixture was neutralized with saturated aqueous sodium hydrogen carbonate solution and diluted with EtOAc. The organic layer was washed with brine and dried over MgS04. Concentration of the solvent in vacuo gave a residue, which was purified by flash chromatography on silica gel (ChbC /methanol 95:5) to afford the pure desired enol ether (200.0 mg, 0.94 mmol, 69%) as an amorphous solid.
To a solution of previously obtained enol ether (162.0 mg, 0.76 mmol, 1 equiv) in /V-methylpyrrolidone (2 mL) was added potassium carbonate (215.3 mg, 1 .56 mmol, 2.05 equiv) at room temperature under argon. To this mixture was added a solution of (±)-4-bromo-2-methyl-2-buten-4-olideErreur ! Signe, non d6fini- (275.7 mg, 1 .56 mmol, 2.05 equiv) in /V-methylpyrrolidone (2 ml_). After 3 h, the reaction was quenched with a solution of HCI 1 N and the product was extracted with EtOAc. The organic layer was washed with water, brine and dried on MgS04. The crude product was purified on preparative TLC on silica to afford the pure desired product (140.0 mg, 0.42 mmol, 60%) as a white amorphous solid.
1 H NMR (300 MHz, CDCI3): δ 7.37, 6.89, 6.12, 3.69, 2.60, 1 .96, 1 .51 .
HRMS (ESI): Calcd for 0ι5Ηι8ΝΟ6 [M - H]~: 308.1 134. Found: 308.1 143.
Step2 : (3 £)-3-{[(4-methyl-5-oxo-2,5-dihydrofuran-2-yl)oxy]methylene}pyrrolidin-2-one
To a solution of the carbamate (30.0 mg, 0.10 mmol, 1 equiv) in CH2CI2 (5 ml_) was added trifluoroacetic acid (8 μΙ_, 0.1 1 mmol, 1 .1 0 equiv) at room temperature under argon. After 5 h, the reaction mixture was evaporated to dryness and the crude product was purified on preparative TLC on silica to afford the deprotected NH (15.0 mg, 0.07 mmol, 74%) as a white amorphous solid.
1 H NM R (300 M Hz, CDCI3): δ 7.20, 6.85, 6.47, 6.06, 3.39, 2.72, 1 .93. HRMS (ESI): Calcd for C10H12NO4 [M + H]+: 21 0.0766. Found: 21 0.0759. The compound according to the present invention can be prepared according to the processes of preparation described above. It will nevertheless be understood that, on the basis of his general knowledge and of available publications, the skilled worker will be able to adapt the processes of preparation described above according to the specifics of each of the compounds, which it is desired to synthesize.
In a further aspect, the present invention also relates to a composition comprising an effective and non-phytotoxic amount of an active compound of formula (I).
The expression "effective and non-phytotoxic amount" means an amount of composition according to the invention that is sufficient for enhancing the plant growth, yield, vigor and/or mycchorization and that does not entail any appreciable symptom of phytotoxicity for the said plant or crop. Such an amount can vary within a wide range depending on the type of crop, the climatic conditions and the compounds included in the composition according to the invention. This amount can be determined by systematic field trials that are within the capabilities of a person skilled in the art.
Thus, according to the invention, there is provided a composition comprising, as an active ingredient, an effective amount of a compound of formula (I) as herein defined and an agriculturally acceptable support, carrier or filler.
In the present specification, the term "support" denotes a natural or synthetic, organic or inorganic material with which the active material is combined to make it easier to apply, notably to the parts of the plant. This support is thus generally inert and should be agriculturally acceptable. The support may be a solid or a liquid. Examples of suitable supports include clays, natural or synthetic silicates, silica, resins, waxes, solid fertilisers, water, alcohols, in particular butanol, organic solvents, mineral and plant oils and derivatives thereof. Mixtures of such supports may also be used.
An "effective amount" of the composition is an amount that increases plant growth, yield, vigor and/or mycchorization when compared with the plant growth, yield, vigor and/or mycchorization of plants or seeds that have not been treated with the composition. For example, strigolactame concentration in the composition may range independently from 1 0 4 M to 10 15 M, preferably from 1 0 6 to 1 0 12 M. The agriculturally appropriate solvent is preferably an aqueous solvent, such as water. It may be appropriate to solubilize the compounds in a small volum of organic solvent as acetone, and then to dilute with water.
Active ingredients concentration in the composition generally corresponds directly or after dilution to the use rate for this particular active ingredient. The use rate for strigolactame compounds is generally from 1 μg to 1 g/ha.
Other additives that may be applied either simultaneously or sequentially include fertilizers (e.g., calcium, nitrogen, potassium, phosphorous) and micronutrients (e.g., copper, aluminum, magnesium, manganese, and zinc ions).
The composition may be applied to monocot or dicot plants, including legumes and non-legumes. In one embodiment, the composition is applied to field-grown plants. In another embodiment, the composition is applied to greenhouse-grown plants. For example, the composition may be applied to seeds or foliage of legumes, such as soybeans, peas, chickpeas, dry beans, peanuts, clover, alfalfa, and of non-legumes such as corn, cotton, rice, tomatoes, canola, wheat, barley, sugar beet, and grass. In general, for seed treatment, the composition is applied to seeds in a single application, and the seeds may be planted immediately or stored before planting. The composition may be applied to foliage. Foliar application generally consists of spraying the composition on the plant foliage one or more times during the growing period.
The term "plant" as used herein includes tubers, roots, stems, leaves, flowers, and fruits. The composition may be applied directly to seeds or plants or may be placed in soil in the vicinity of a seed or plant prior to or at the time of planting. In a preferred embodiment, the composition is sprayed on seeds, tubers, or foliage.
Seedlings, as well as more mature plants, may be treated. Flowers and fruits may also be treated by spraying. Roots of transplants may be sprayed or dipped in the composition prior to planting.
The composition may also comprise other additional components. In particular, the composition may further comprise a surfactant. The surfactant can be an emulsifier, a dispersing agent or a wetting agent of ionic or non-ionic type or a mixture of such surfactants. Mention may be made, for example, of polyacrylic acid salts, lignosulphonic acid salts, phenolsulphonic or naphthalenesulphonic acid salts, polycondensates of ethylene oxide with fatty alcohols or with fatty acids or with fatty amines, substituted phenols (in particular alkylphenols or arylphenols), salts of sulphosuccinic acid esters, taurine derivatives (in particular alkyl taurates), phosphoric esters of polyoxyethylated alcohols or phenols, fatty acid esters of polyols, and derivatives of the above compounds containing sulphate, sulphonate and phosphate functions. The presence of at least one surfactant is generally essential when the active material and/or the inert support are water-insoluble and when the vector agent for the application is water. Preferably, surfactant content may be comprised between 5% and 40% by weight of the composition.
Additional components may also be included, e.g. protective colloids, adhesives, thickeners, thixotropic agents, penetration agents, stabilisers, sequestering agents. More generally, the active materials can be combined with any solid or liquid additive, which complies with the usual formulation techniques.
In general, the composition according to the invention may contain from 0.00000005 to 99% (by weight) of active material, preferably 0.0000001 to 70% by weight.
Compositions according to the present invention can be used in various forms such as aerosol dispenser, capsule suspension, cold fogging concentrate, dustable powder, emulsifiable concentrate, emulsion oil in water, emulsion water in oil, encapsulated granule, fine granule, flowable concentrate for seed treatment, gas (under pressure), gas generating product, granule, hot fogging concentrate, macrogranule, microgranule, oil dispersible powder, oil miscible flowable concentrate, oil miscible liquid, paste, plant rodlet, powder for dry seed treatment, seed coated with a pesticide, soluble concentrate, soluble powder, solution for seed treatment, suspension concentrate (flowable concentrate), ultra low volume (ulv) liquid, ultra low volume (ulv) suspension, water dispersible granules or tablets, water dispersible powder for slurry treatment, water soluble granules or tablets, water soluble powder for seed treatment and wettable powder.
These compositions include not only compositions which are ready to be applied to the plant or seed to be treated, or in furrow in the soil, by means of a suitable device, such as a spraying or dusting device, but also concentrated commercial compositions which must be diluted before they are applied to the crop.
In another embodiment of the invention, the composition may further comprise a pesticidal active ingredient. Examples of pesticides useful in compositions include fungicides, insecticides, bactericides, nematicides, acaricides, molluscicides, attractants, sterilants, growth regulators, herbicides, safeners, semiochemicals pheromone active substance or other compounds with biological activity.
In an embodiment of the invention, the composition may further comprise another active ingredient which enhances the yield, vigor or growth of the plants, which improves the germination of seeds and vitality of seedlings, which acts as seed safener, which improves nutrient uptake or symbiotic interaction by the plant, or which improves the biotic or abiotic environmental stress tolerance of a plant. Examples of said compounds include strigolactone compounds, lipochito-oligosaccharide (LCO) compounds, acyl-homoserine lactone (AHL) compounds, flavonoids (such as flavones, flavanols, flavonols, flavanones, isoflavones, hesperetin, formonometin, genistein, daidzein, naringenin, luteolin, apignenin), chitinous compounds (such as chitin or chitosan), plant activators (such as acibenzolar or probenazole), phytohormones (such as Gibberellic acid), plant growth regulators (such as trinexapac- ethyl, prohexadione-Ca, paclobutrazol, brassinolide, forchlorfenuron, hymexazol, thiametoxam), or other plant regulators (such as benzofluor, buminafos, carvone, ciobutide, clofencet, cloxyfonac, cyanamide, cyclanilide, cycloheximide, cyprosulfamide, epocholeone, ethychlozate, fenridazon, heptopargil, holosulf, inabenfide, karetazan, lead arsenate, methasulfocarb, prohexadione, pydanon, sintofen, triapenthenol).
Examples of said compounds, the way to prepare them from natural sources or to synthetize them, as well as the conditions to use them, are largely disclosed in WO 2005063784, WO2008085958, WO2008152092, WO2009049747, WO2010125065, WO201 1 153442, EP1 1 356001 .5, EP1 135601 1 .4
Examples of plant growth regulators include, but are not limited to antiauxins (clofibric acid, 2,3,5-tri- iodobenzoic acid), auxins (4-CPA, 2,4-D, 2,4-DB, 2,4-DEP, dichlorprop, fenoprop, IAA, I BA, naphthaleneacetamide, [alpha]-naphthaleneacetic acid, 1 -naphthol, naphthoxyacetic acid, potassium naphthenate, sodium naphthenate, 2,4, 5-T), cytokinins (2iP, benzyladenine, kinetin, zeatin), defoliants (calcium cyanamide, dimethipin, endothal, ethephon, merphos, metoxuron, pentachlorophenol, thidiazuron, tribufos), ethylene inhibitors (aviglycine, 1 - methylcyclopropene), ethylene releasers (ACC, etacelasil, ethephon, glyoxime), gibberellins (gibberellic acid, gibberellins, including non-cyclopropene compounds that show gibberellin- like activity, such as, for example, helminthosporic acid, phaseolic acid, kaurenoic acid, and steviol), growth inhibitors (abscisic acid, ancymidol, butralin, carbaryl, chlorphonium, chlorpropham, dikegulac, flumetralin, fluoridamid, fosamine, glyphosine, isopyrimol, jasmonic acid, maleic hydrazide, mepiquat, piproctanyl, prohydrojasmon, propham, 2,3,5-tri-iodobenzoic acid), morphactins (chlorfluren, chlorflurenol, dichlorflurenol, flurenol), growth retardants/modifiers (chlormequat, daminozide, flurprimidol, mefluidide, paclobutrazol, cyproconazole, tetcyclacis, uniconazole, ancymidol, trinexapac-ethyl, and progexadione-CA), growth stimulators (brassinolide, forchlorfenuron, hymexazol, 2-amino-6-oxypurine derivatives, as described below, indolinone derivates, as described below, 3,4-disubstituted maleimide derivatives, as described below, and fused azepinone derivatives, as described below). The term additionally includes other active ingredients such as benzofluor, buminafos, carvone, ciobutide, clofencet, cloxyfonac, cyclanilide, cycloheximide, epocholeone, ethychlozate, ethylene, fenridazon, heptopargil, holosulf, inabenfide, karetazan, lead arsenate, methasulfocarb, prohexadione, pydanon, sintofen, triapenthenol, and trinexapac. Additional plant growth regulators include indolinone derivative plant stimulators described in WO 2005/1 07466; 3,4-disubstituted maleimide derivatives described in WO 2005/1 07465; fused azepinone derivatives described in WO 2005/1 07471 ; and 2-amino-6- oxypurine derivatives described in WO 2005/1 07472.
Examples of natural or synthetic strigolactone compounds include, but are not limited to strigol, sorgolactone, alectrol, orobanchol (Cook et al., 1 972, J Am Chem Soc, 94, 6198-6199; Butler, 1 995, Allelopathy: organism, processes and application, 158-1 68; Hauck et al., 1 992, J Plant Physiol, 139, 474-478; Muller et al., 1992, J Plant Growth Regul, 1 1 , 77-84, Siame et al., 1 993, J Agr Food Chem, 41 , 1486- 1491 , Yokota et al., 1 998, Phytochemistry, 49, 1 967-1 973), and the synthetic strigolactones compounds of formula (I) specifically disclosed in WO201 0125065.
In the meaning of the invention, a lipo-chitooligosaccharide (LCO) compound is a compound having the general LCO structure, i.e. an oligomeric backbone of β-1 ,4-linked N- acetyl-D-glucosamine residues with a N-linked fatty acyl chain at the non-reducing end, as described in US Pat N ° 5,54971 8; US Pat N ° 5,646,01 8; US Pat N ° 5, 1 75,149; and US Pat N ° 5,321 ,01 1 .
This basic structure may contain modifications or substitutions found in naturally occurring LCO's, such as those described in Spaink, Critical Reviews in Plant Sciences 54: 257-288, 2000; D'Haeze and Holsters, Glycobiology 12: 79R-1 05R, 2002. Naturally occurring LCO's are defined as compounds which can be found in nature. This basic structure may also contain modifications or substitutions which have not been found so far in naturally occurring LCO's. Examples of such analogs for which the conjugated amide bond is mimicked by a benzamide bond or which contain a function of benzylamine type are the following compounds of formula (I) which are described in WO2005/063784 and WO2008/071 672, the content of which is incorporated herein by reference. The LCO's compounds may be isolated directly from a particular culture of Rhizobiaceae bacterial strains, synthesized chemically, or obtained chemo-enzymatically. Via the latter method, the oligosaccharide skeleton may be formed by culturing of recombinant bacterial strains, such as Escherichia coli, in a fermenter, and the lipid chain may then be attached chemically.
LCO's used in embodiments of the invention may be recovered from natural Rhizobiaceae bacterial strains that produce LCO's, such as strains of Azorhizobium, Bradyrhizobium (including B. japonicum), Mesorhizobium, Rhizobium (including R. leguminosarum), Sinorhizobium (including S. meliloti), or from bacterial strains genetically engineered to produce LCO's. These methods are known in the art and have been described, for example, in U.S. Pat. Nos. 5,549,71 8 and 5,646,018, which are incorporated herein by reference. Hungria and Stacey (Soil Biol. Biochem. 29: 81 9-830, 1 997) list specific LCO structures that are produced by different rhizobial species. LCO's may be utilized in various forms of purity and may be used alone or with rhizobia. Methods to provide only LCO's include simply removing the rhizobial cells from a mixture of LCOs and rhizobia, or continuing to isolate and purify the LCO molecules through LCO solvent phase separation followed by HPLC chromatography as described by Lerouge, et.al (US 5,549,71 8). Purification can be enhanced by repeated H PLC, and the purifed LCO molecules can be freeze-dried for long-term storage. This method is acceptable for the production of LCO's from all genera and species of the Rhizobiaceae. Commercial products containing LCO's are available, such as OPTIMIZE® (EM D Crop Bioscience). LCO compounds, which can be identical or not to naturally occurring LCO's, may also be obtained by chemical synthesis and/or through genetic engineering. Synthesis of precursor oligosaccharide molecules for the construction of LCO by genetically engineered organisms is disclosed in Samain et al., Carbohydrate Research 302: 35-42, 1 997. Preparation of numerous LCOs compounds wherein the oligosaccharide skeleton is obtained by culturing recombinant bacterial strains, such as recombinant Escherichia coli cells harboring heterologous gene from rhizobia, and wherein the lipid chain is chemically attached is disclosed in WO2005/063784 and WO2008/07167, the content of which is incorporated herein by reference. Examples of lipochito-oligosaccharide compounds include, but are not limited to LCO compounds specifically disclosed in WO201 0125065.
Examples of natural or synthetic acyl-homoserine lactone derivatives (AHLs) include, but are not limited to compounds specifically disclosed in EP1 1 35601 1 .4, the content of which is incorporated herein by reference.
The composition according to the present invention may further comprise a supplementation with different inoculum sources as for example arbuscular mycorrhizal fungi (AM F), Rhizobia or other plant growth promoting bacteria. Said supplementation may be applied simultaneously or sequentially. AMFcould be for example Glomus sp., Gigaspora sp., or other fungi from the group Glomeromycota, while plant growth promoting bacteria others than Rhizobia could be for example Azospirillum sp., Bacillus sp.
When the composition according to the invention comprises a strigolactame derivative of formula (I) and a pesticidal active material, the dose of active material usually applied is generally and advantageously between 0.00001 and 1000 g/ha, preferably between 0.0001 and 500 g/ha for applications in foliar treatment. If a drench/drip/in furrow application is possible, the dose can be lower, especially in artificial substrates like rockwool or perlite. The dose of active substance applied is generally and advantageously between 0.000001 and 200 g per 100 kg of seed, preferably between 0.00001 and 150 g per 1 00 kg of seed in the case of seed treatment. It is clearly understood that the doses indicated above are given as illustrative examples of the invention. A person skilled in the art will know how to adapt the application doses according to the nature of the crop to be treated.
The compositions and compounds of the present invention may be used to to increase the yield, growth, vigor and/or mycchorization of the plant and/or for curatively or preventively control pests of crops, as phytopathogenic fungi, insects, nematodes, acarid, and/or for decreasing the needs of fertilizers.
Thus, according to a further aspect, the present invention provides a method for increasing the yield, growth, vigor or mycchorization of a plant or crop characterised in that a composition according to the invention is applied via seed treatment, foliar application, stem application, drench/drip application (chemigation) to the seed, the plant or to the fruit of the plant, or to soil, particularly in furrow, and/or to inert substrate (e.g. inorganic substrates (e.g. sand, rockwool, glasswool, expanded minerals (e.g. perlite, vermiculite, zeolite, expanded clay)), Pumice, Pyroclastic materials/tuff, synthetic organic substrates (e.g. Polyurethane), organic substrates (e.g. peat, composts, tree waste products (e.g. coir, wood fibre/chips, tree bark) and/or to a liquid substrate (e.g. floating hydroponic systems, Nutrient Film Technique, Aeroponics) wherein the plant is growing or wherein it is desired to grow.
The composition as used comprises an effective and non-phytotoxic amount of active compound.
The method of treatment according to the present invention is useful to treat propagation material such as tubers or rhizomes, but also seeds, seedlings or seedlings pricking out and plants or plants pricking out. This method of treatment can also be useful to treat roots. The method of treatment according to the present invention can also be useful to treat the overground parts of the plant such as trunks, stems or stalks, leaves, flowers and fruit of the concerned plant.
Among the plants that can be treated by the method according to the present invention, mention may be made of cotton; flax; vine; fruit or vegetable crops such as Rosaceae sp. (for instance pip fruit such as apples and pears, but also stone fruit such as apricots, almonds and peaches), Ribesioidae sp., Juglandaceae sp., Betulaceae sp., Anacardiaceae sp., Fagaceae sp., Moraceae sp., Oleaceae sp., Actinidaceae sp., Lauraceae sp., Musaceae sp. (for instance banana trees and plantins), Rubiaceae sp., Theaceae sp., Sterculiceae sp., Rutaceae sp. (for instance lemons, oranges and grapefruit); Solanaceae sp. (for instance tomatoes), Liliaceae sp., Asteraceae sp. (for instance lettuces), Umbelliferae sp., Cruciferae sp., Chenopodiaceae sp., Cucurbitaceae sp., Papilionaceae sp. (for instance peas), Rosaceae sp. (for instance strawberries); major crops such as Graminae sp. (for instance maize, lawn or cereals such as wheat, rice, barley and triticale), Asteraceae sp. (for instance sunflower), Cruciferae sp. (for instance oil seed rape), Fabacae sp. (for instance peanuts),
Papilionaceae sp. (for instance soybean), Solanaceae sp. (for instance potatoes), Chenopodiaceae sp. (for instance beetroots); horticultural and forest crops; as well as genetically modified homologues of these crops.
Strigolactame compounds of the invention, and compositions comprising said strigolactame compounds, eventually in combination with fungicides, insecticides, or other additives, can be used in the treatment of genetically modified organisms (GMOs), e.g. plants or seeds.
Genetically modified plants (or transgenic plants) are plants of which a heterologous gene has been stably integrated into genome. The expression "heterologous gene" essentially means a gene which is provided or assembled outside the plant and when introduced in the nuclear, chloroplastic or mitochondrial genome gives the transformed plant new or improved agronomic or other properties by expressing a protein or polypeptide of interest or by downregulating or silencing other gene(s) which are present in the plant (using for example, antisense technology, cosuppression technology or RNA interference - RNAi - technology). A heterologous gene that is located in the genome is also called a transgene. A transgene that is defined by its particular location in the plant genome is called a transformation or transgenic event.
Depending on the plant species or plant cultivars, their location and growth conditions (soils, climate, vegetation period, diet), the treatment according to the invention may also result in superadditive ("synergistic") effects. Thus, for example, reduced application rates and/or a widening of the activity spectrum and/or an increase in the activity of the active compounds and compositions which can be used according to the invention, better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or to water or soil salt content, increased flowering performance, easier harvesting, accelerated maturation, higher harvest yields, bigger fruits, larger plant height, greener leaf color, earlier flowering, higher quality and/or a higher nutritional value of the harvested products, higher sugar concentration within the fruits, better storage stability and/or processability of the harvested products are possible, which exceed the effects which were actually to be expected.
At certain application rates, the active compound combinations according to the invention may also have a strengthening effect in plants. Accordingly, they are also suitable for mobilizing the defense system of the plant against attack by unwanted microorganisms. This may, if appropriate, be one of the reasons of the enhanced activity of the combinations according to the invention, for example against fungi. Plant- strengthening (resistance-inducing) substances are to be understood as meaning, in the present context, those substances or combinations of substances which are capable of stimulating the defense system of plants in such a way that, when subsequently inoculated with unwanted microorganisms, the treated plants display a substantial degree of resistance to these microorganisms. In the present case, unwanted microorganisms are to be understood as meaning phytopathogenic fungi, bacteria and viruses. Thus, the substances according to the invention can be employed for protecting plants against attack by the abovementioned pathogens within a certain period of time after the treatment. The period of time within which protection is effected generally extends from 1 to 21 days, preferably 1 to 14 days, after the treatment of the plants with the active compounds.
As already mentioned above, it is possible to treat all plants and their parts in accordance with the invention. In a preferred embodiment, wild plant species and plant cultivars, or those obtained by conventional biological breeding methods, such as crossing or protoplast fusion, and also parts thereof, are treated. In a further preferred embodiment, transgenic plants and plant cultivars obtained by genetic engineering methods, if appropriate in combination with conventional methods (Genetically Modified Organisms), and parts thereof are treated. The terms "parts" or "parts of plants" or "plant parts" have been explained above. More preferably, plants of the plant cultivars which are commercially available or are in use are treated in accordance with the invention. Plant cultivars are understood to mean plants which have new properties ("traits") and have been obtained by conventional breeding, by mutagenesis or by recombinant DNA techniques. They can be cultivars, varieties, bio- or genotypes.
The method of treatment according to the invention can be used in the treatment of genetically modified organisms (GMOs), e.g. plants or seeds. Genetically modified plants (or transgenic plants) are plants of which a heterologous gene has been stably integrated into genome. The expression "heterologous gene" essentially means a gene which is provided or assembled outside the plant and when introduced in the nuclear, chloroplastic or mitochondrial genome gives the transformed plant new or improved agronomic or other properties by expressing a protein or polypeptide of interest or by downregulating or silencing other gene(s) which are present in the plant (using for example, antisense technology, cosuppression technology, RNA interference - RNAi - technology or microRNA - miRNA - technology). A heterologous gene that is located in the genome is also called a transgene. A transgene that is defined by its particular location in the plant genome is called a transformation or transgenic event.
Depending on the plant species or plant cultivars, their location and growth conditions (soils, climate, vegetation period, diet), the treatment according to the invention may also result in superadditive
("synergistic") effects. Thus, for example, reduced application rates and/or a widening of the activity spectrum and/or an increase in the activity of the active compounds and compositions which can be used according to the invention, better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or to water or soil salt content, increased flowering performance, easier harvesting, accelerated maturation, higher harvest yields, bigger fruits, larger plant height, greener leaf color, earlier flowering, higher quality and/or a higher nutritional value of the harvested products, higher sugar concentration within the fruits, better storage stability and/or processability of the harvested products are possible, which exceed the effects which were actually to be expected.
At certain application rates, the active compound combinations according to the invention may also have a strengthening effect in plants. Accordingly, they are also suitable for mobilizing the defense system of the plant against attack by unwanted microorganisms. This may, if appropriate, be one of the reasons of the enhanced activity of the combinations according to the invention, for example against fungi. Plant-strengthening (resistance-inducing) substances are to be understood as meaning, in the present context, those substances or combinations of substances which are capable of stimulating the defense system of plants in such a way that, when subsequently inoculated with unwanted microorganisms, the treated plants display a substantial degree of resistance to these microorganisms. In the present case, unwanted microorganisms are to be understood as meaning phytopathogenic fungi, bacteria and viruses. Thus, the substances according to the invention can be employed for protecting plants against attack by the abovementioned pathogens within a certain period of time after the treatment. The period of time within which protection is effected generally extends from 1 to 1 0 days, preferably 1 to 7 days, after the treatment of the plants with the active compounds.
Plants and plant cultivars which are preferably to be treated according to the invention include all plants which have genetic material which impart particularly advantageous, useful traits to these plants (whether obtained by breeding and/or biotechnological means).
Plants and plant cultivars which are also preferably to be treated according to the invention are resistant against one or more biotic stresses, i.e. said plants show a better defense against animal and microbial pests, such as against nematodes, insects, mites, phytopathogenic fungi, bacteria, viruses and/or viroids.
Examples of nematode or insect resistant plants are described in e.g. U.S. Patent Applications 1 1/765,491 , 1 1 /765,494, 10/926,819, 10/782,020, 12/032,479, 10/783,41 7, 10/782,096, 1 1 /657,964, 12/192,904, 1 1 /396,808, 12/166,253, 12/166,239, 12/166,124, 12/166,209, 1 1/762,886, 12/364,335, 1 1 /763,947, 12/252,453, 12/209,354, 12/491 ,396, 12/497,221 , 12/644,632, 12/646,004, 12/701 ,058, 12/718,059, 12/721 ,595, 12/638,591 .
Plants and plant cultivars which may also be treated according to the invention are those plants which are resistant to one or more abiotic stresses. Abiotic stress conditions may include, for example, drought, cold temperature exposure, heat exposure, osmotic stress, flooding, increased soil salinity, increased mineral exposure, ozone exposure, high light exposure, limited availability of nitrogen nutrients, limited availability of phosphorus nutrients, shade avoidance.
Plants and plant cultivars which may also be treated according to the invention, are those plants characterized by enhanced yield characteristics. Increased yield in said plants can be the result of, for example, improved plant physiology, growth and development, such as water use efficiency, water retention efficiency, improved nitrogen use, enhanced carbon assimilation, improved photosynthesis, increased germination efficiency and accelerated maturation. Yield can furthermore be affected by improved plant architecture (under stress and non-stress conditions), including but not limited to, early flowering, flowering control for hybrid seed production, seedling vigor, plant size, internode number and distance, root growth, seed size, fruit size, pod size, pod or ear number, seed number per pod or ear, seed mass, enhanced seed filling, reduced seed dispersal, reduced pod dehiscence and lodging resistance. Further yield traits include seed composition, such as carbohydrate content, protein content, oil content and composition, nutritional value, reduction in anti-nutritional compounds, improved processability and better storage stability.
Plants that may be treated according to the invention are hybrid plants that already express the characteristic of heterosis or hybrid vigor which results in generally higher yield, vigor, health and resistance towards biotic and abiotic stresses). Such plants are typically made by crossing an inbred male-sterile parent line (the female parent) with another inbred male-fertile parent line (the male parent). Hybrid seed is typically harvested from the male sterile plants and sold to growers. Male sterile plants can sometimes (e.g. in corn) be produced by detasseling, i.e. the mechanical removal of the male reproductive organs (or males flowers) but, more typically, male sterility is the result of genetic determinants in the plant genome. In that case, and especially when seed is the desired product to be harvested from the hybrid plants it is typically useful to ensure that male fertility in the hybrid plants is fully restored. This can be accomplished by ensuring that the male parents have appropriate fertility restorer genes which are capable of restoring the male fertility in hybrid plants that contain the genetic determinants responsible for male-sterility. Genetic determinants for male sterility may be located in the cytoplasm. Examples of cytoplasmic male sterility (CMS) were for instance described in Brassica species (WO 92/05251 , WO 95/0991 0, WO 98/27806, WO 05/002324, WO 06/021 972 and US 6,229,072). However, genetic determinants for male sterility can also be located in the nuclear genome. Male sterile plants can also be obtained by plant biotechnology methods such as genetic engineering. A particularly useful means of obtaining male-sterile plants is described in WO 89/1 0396 in which, for example, a ribonuclease such as barnase is selectively expressed in the tapetum cells in the stamens. Fertility can then be restored by expression in the tapetum cells of a ribonuclease inhibitor such as barstar (e.g. WO 91 /02069).
Plants or plant cultivars (obtained by plant biotechnology methods such as genetic engineering) which may be treated according to the invention are herbicide-tolerant plants, i.e. plants made tolerant to one or more given herbicides. Such plants can be obtained either by genetic transformation, or by selection of plants containing a mutation imparting such herbicide tolerance. Herbicide-resistant plants are for example glyphosate-tolerant plants, i.e. plants made tolerant to the herbicide glyphosate or salts thereof. Plants can be made tolerant to glyphosate through different means. For example, glyphosate-tolerant plants can be obtained by transforming the plant with a gene encoding the enzyme 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS). Examples of such EPSPS genes are the AroA gene (mutant CT7) of the bacterium Salmonella typhimurium (Science 1983, 221, 370-371 ), the CP4 gene of the bacterium Agrobacterium sp. (Curr. Topics Plant Physiol. 1992, 7, 139-145), the genes encoding a Petunia EPSPS (Science 1986, 233, 478-481 ), a Tomato EPSPS (J. Biol. Chem. 1988, 263, 4280-4289), or an Eleusine EPSPS (WO 01 /66704). It can also be a mutated EPSPS as described in for example EP 0837944, WO 00/66746, WO 00/66747 or WO 02/26995. Glyphosate-tolerant plants can also be obtained by expressing a gene that encodes a glyphosate oxido-reductase enzyme as described in US 5,776,760 and US 5,463,175. Glyphosate-tolerant plants can also be obtained by expressing a gene that encodes a glyphosate acetyl transferase enzyme as described in for example WO 02/036782, WO 03/092360, WO 2005/012515 and WO 2007/024782. Glyphosate-tolerant plants can also be obtained by selecting plants containing naturally-occurring mutations of the above-mentioned genes, as described in for example WO 01 /024615 or WO 03/013226. Plants expressing EPSPS genes that confer glyphosate tolerance are described in e.g. U.S. Patent Applications 1 1 /517,991 , 10/739,610, 12/139,408, 12/352,532, 1 1 /312,866, 1 1 /315,678, 12/421 ,292, 1 1/400,598, 1 1 /651 ,752, 1 1/681 ,285, 1 1 /605,824, 12/468,205, 1 1 /760,570, 1 1 /762,526, 1 1 /769,327, 1 1/769,255, 1 1 /943801 or 12/362,774. Plants comprising other genes that confer glyphosate tolerance, such as decarboxylase genes, are described in e.g. U.S. Patent Applications 1 1 /588,81 1 , 1 1 /185,342, 12/364,724, 1 1 /185,560 or 12/423,926.
Other herbicide resistant plants are for example plants that are made tolerant to herbicides inhibiting the enzyme glutamine synthase, such as bialaphos, phosphinothricin or glufosinate. Such plants can be obtained by expressing an enzyme detoxifying the herbicide or a mutant glutamine synthase enzyme that is resistant to inhibition, e.g. described in U.S. Patent Application 1 1 /760,602. One such efficient detoxifying enzyme is an enzyme encoding a phosphinothricin acetyltransferase (such as the bar or pat protein from Streptomyces species). Plants expressing an exogenous phosphinothricin acetyltransferase are for example described in U.S. Patents 5,561 ,236; 5,648,477; 5,646,024;
5,273,894; 5,637,489; 5,276,268; 5,739,082; 5,908,81 0 and 7, 1 12,665.
Further herbicide-tolerant plants are also plants that are made tolerant to the herbicides inhibiting the enzyme hydroxyphenylpyruvatedioxygenase (HPPD). HPPD is an enzyme that catalyze the reaction in which para-hydroxyphenylpyruvate (HPP) is transformed into homogentisate. Plants tolerant to HPPD-inhibitors can be transformed with a gene encoding a naturally-occurring resistant H PPD enzyme, or a gene encoding a mutated or chimeric HPPD enzyme as described in WO 96/38567, WO 99/24585, WO 99/24586, WO 09/144079, WO 02/046387, or US 6,768,044. Tolerance to HPPD- inhibitors can also be obtained by transforming plants with genes encoding certain enzymes enabling the formation of homogentisate despite the inhibition of the native H PPD enzyme by the HPPD- inhibitor. Such plants and genes are described in WO 99/34008 and WO 02/36787. Tolerance of plants to H PPD inhibitors can also be improved by transforming plants with a gene encoding an enzyme having prephenate deshydrogenase (PDH) activity in addition to a gene encoding an H PPD- tolerant enzyme, as described in WO 04/024928. Further, plants can be made more tolerant to HPPD- inhibitor herbicides by adding into their genome a gene encoding an enzyme capable of metabolizing or degrading H PPD inhibitors, such as the CYP450 enzymes shown in WO 2007/103567 and
WO 2008/150473.
Still further herbicide resistant plants are plants that are made tolerant to acetolactate synthase (ALS) inhibitors. Known ALS-inhibitors include, for example, sulfonylurea, imidazolinone, triazolopyrimidines, pryimidinyoxy(thio)benzoates, and/or sulfonylaminocarbonyltriazolinone herbicides. Different mutations in the ALS enzyme (also known as acetohydroxyacid synthase, AHAS) are known to confer tolerance to different herbicides and groups of herbicides, as described for example in Tranel and Wright ( Weed Science 2002, 50, 700-712), but also, in U.S. Patents 5,605,01 1 , 5,378,824, 5,141 ,870, and 5,013,659. The production of sulfonylurea-tolerant plants and imidazolinone-tolerant plants is described in U.S.
Patents 5,605,01 1 ; 5,013,659; 5,141 ,870; 5,767,361 ; 5,731 , 180; 5,304,732; 4,761 ,373; 5,331 ,107;
5,928,937; and 5,378,824; and WO 96/33270. Other imidazolinone-tolerant plants are also described in for example WO 2004/040012, WO 2004/106529, WO 2005/020673, WO 2005/093093, WO 2006/007373, WO 2006/015376, WO 2006/024351 , and WO 2006/060634. Further sulfonylurea- and imidazolinone- tolerant plants are also described in for example WO 2007/024782 and U.S. Patent Application 61 /288958. Other plants tolerant to imidazolinone and/or sulfonylurea can be obtained by induced mutagenesis, selection in cell cultures in the presence of the herbicide or mutation breeding as described for example for soybeans in US 5,084,082, for rice in WO 97/4121 8, for sugar beet in US 5,773,702 and WO 99/057965, for lettuce in US 5, 1 98,599, or for sunflower in WO 01 /065922.
Plants or plant cultivars (obtained by plant biotechnology methods such as genetic engineering) which may also be treated according to the invention are insect-resistant transgenic plants, i.e. plants made resistant to attack by certain target insects. Such plants can be obtained by genetic transformation, or by selection of plants containing a mutation imparting such insect resistance.
An "insect-resistant transgenic plant", as used herein, includes any plant containing at least one transgene comprising a coding sequence encoding:
1 ) an insecticidal crystal protein from Bacillus thuringiensis or an insecticidal portion thereof, such as the insecticidal crystal proteins listed by Crickmore et al. (1998, Microbiology and Molecular Biology Reviews, 62: 807-813), updated by Crickmore et al. (2005) at the Bacillus thuringiensis toxin nomenclature, online at: http://www.lifesci. Sussex. ac.uk/Home/Neil_Crickmore/Bt/), or insecticidal portions thereof, e.g., proteins of the Cry protein classes Cryl Ab, Cryl Ac, Cryl B, Cryl C, Cryl D, Cryl F, Cry2Ab, Cry3Aa, or Cry3Bb or insecticidal portions thereof (e.g. EP-A 1 999 141 and WO 2007/107302), or such proteins encoded by synthetic genes as e.g. described in and U.S. Patent Application 12/249,016 ; or
2) a crystal protein from Bacillus thuringiensis or a portion thereof which is insecticidal in the presence of a second other crystal protein from Bacillus thuringiensis or a portion thereof, such as the binary toxin made up of the Cry34 and Cry35 crystal proteins (Nat. Biotechnol. 2001 , 19, 668- 72; Applied Environm. Microbiol. 2006, 71, 1765-1774) or the binary toxin made up of the Cryl A or Cry1 F proteins and the Cry2Aa or Cry2Ab or Cry2Ae proteins (U.S. Patent Application 12/214,022 and EP-A 2 300 618); or 3) a hybrid insecticidal protein comprising parts of different insecticidal crystal proteins from Bacillus thunngiensis, such as a hybrid of the proteins of 1 ) above or a hybrid of the proteins of 2) above, e.g., the Cry1 A.1 05 protein produced by corn event MON89034 (WO 2007/027777); or
4) a protein of any one of 1 ) to 3) above wherein some, particularly 1 to 1 0, amino acids have been replaced by another amino acid to obtain a higher insecticidal activity to a target insect species, and/or to expand the range of target insect species affected, and/or because of changes introduced into the encoding DNA during cloning or transformation, such as the Cry3Bb1 protein in corn events MON863 or MON88017, or the Cry3A protein in corn event MIR604; or
5) an insecticidal secreted protein from Bacillus thunngiensis or Bacillus cereus, or an insecticidal portion thereof, such as the vegetative insecticidal (VIP) proteins listed at:
htt|3j/ www^^ e.g., proteins from the VIP3Aa protein class; or
6) a secreted protein from Bacillus thunngiensis or Bacillus cereus which is insecticidal in the presence of a second secreted protein from Bacillus thunngiensis or B. cereus, such as the binary toxin made up of the VI P1 A and VI P2A proteins (WO 94/21795); or a hybrid insecticidal protein comprising parts from different secreted proteins from Bacillus thunngiensis or Bacillus cereus, such as a hybrid of the proteins in 1 ) above or a hybrid of the proteins in 2) above; or a protein of any one of 5) to 7) above wherein some, particularly 1 to 10, amino acids have been replaced by another amino acid to obtain a higher insecticidal activity to a target insect species, and/or to expand the range of target insect species affected, and/or because of changes introduced into the encoding DNA during cloning or transformation (while still encoding an insecticidal protein), such as the VI P3Aa protein in cotton event COT102; or a secreted protein from Bacillus thunngiensis or Bacillus cereus which is insecticidal in the presence of a crystal protein from Bacillus thunngiensis, such as the binary toxin made up of VI P3 and Cryl A or Cry1 F (U.S. Patent Applications 61 /126083 and 61 /19501 9), or the binary toxin made up of the VI P3 protein and the Cry2Aa or Cry2Ab or Cry2Ae proteins (U.S. Patent Application 12/214,022 and EP-A 2 300 618). a protein of 9) above wherein some, particularly 1 to 10, amino acids have been replaced by another amino acid to obtain a higher insecticidal activity to a target insect species, and/or to expand the range of target insect species affected, and/or because of changes introduced into the encoding DNA during cloning or transformation (while still encoding an insecticidal protein)
Of course, an insect-resistant transgenic plant, as used herein, also includes any plant comprising a combination of genes encoding the proteins of any one of the above classes 1 to 10. In one embodiment, an insect-resistant plant contains more than one transgene encoding a protein of any one of the above classes 1 to 10, to expand the range of target insect species affected when using different proteins directed at different target insect species, or to delay insect resistance development to the plants by using different proteins insecticidal to the same target insect species but having a different mode of action, such as binding to different receptor binding sites in the insect.
An "insect-resistant transgenic plant", as used herein, further includes any plant containing at least one transgene comprising a sequence producing upon expression a double-stranded RNA which upon ingestion by a plant insect pest inhibits the growth of this insect pest, as described e.g. in WO
2007/080126, WO 2006/129204, WO 2007/074405, WO 2007/080127 and WO 2007/035650.
Plants or plant cultivars (obtained by plant biotechnology methods such as genetic engineering) which may also be treated according to the invention are tolerant to abiotic stresses. Such plants can be obtained by genetic transformation, or by selection of plants containing a mutation imparting such stress resistance. Particularly useful stress tolerance plants include:
1 ) plants which contain a transgene capable of reducing the expression and/or the activity of poly(ADP-ribose) polymerase (PARP) gene in the plant cells or plants as described in WO 00/041 73, WO 2006/045633, EP-A 1 807 519, or EP-A 2 018 431 .
2) plants which contain a stress tolerance enhancing transgene capable of reducing the expression and/or the activity of the PARG encoding genes of the plants or plants cells, as described e.g. in WO 2004/090140.
3) plants which contain a stress tolerance enhancing transgene coding for a plant-functional enzyme of the nicotineamide adenine dinucleotide salvage synthesis pathway including nicotinamidase, nicotinate phosphoribosyltransferase, nicotinic acid mononucleotide adenyl transferase, nicotinamide adenine dinucleotide synthetase or nicotine amide phosphorybosyltransferase as described e.g. in EP-A 1 794 306, WO 2006/133827, WO 2007/107326, EP-A 1 999 263, or WO 2007/107326.
Plants or plant cultivars (obtained by plant biotechnology methods such as genetic engineering) which may also be treated according to the invention show altered quantity, quality and/or storage-stability of the harvested product and/or altered properties of specific ingredients of the harvested product such as:
1 ) transgenic plants which synthesize a modified starch, which in its physical-chemical characteristics, in particular the amylose content or the amylose/amylopectin ratio, the degree of branching, the average chain length, the side chain distribution, the viscosity behaviour, the gelling strength, the starch grain size and/or the starch grain morphology, is changed in comparison with the synthesised starch in wild type plant cells or plants, so that this is better suited for special applications. Said transgenic plants synthesizing a modified starch are disclosed, for example, in EP-A 0 571 427, WO 95/04826, EP-A 0 719 338, WO 96/15248, WO 96/1 9581 , WO 96/27674, WO 97/1 1 188, WO 97/26362, WO 97/32985, WO 97/42328, WO 97/44472, WO 97/45545, WO 98/27212, WO 98/40503, WO 99/58688, WO 99/58690, WO 99/58654, WO 00/08184, WO 00/08185, WO 00/081 75, WO 00/28052, WO 00/77229, WO 01 /12782, WO 01 /12826, WO 02/101 059, WO 03/071 860, WO 04/056999, WO 05/030942, WO 2005/030941 , WO 2005/095632, WO 2005/095617, WO 2005/09561 9, WO 2005/095618, WO 2005/123927, WO 2006/01 8319, WO 2006/103107, WO 2006/108702, WO 2007/009823, WO 00/22140, WO 2006/063862, WO 2006/072603, WO 02/034923, WO 2008/017518, WO 2008/080630, WO 2008/080631 , EP 07090007.1 , WO 2008/090008, WO 01 /14569, WO 02/79410, WO 03/33540,
WO 2004/078983, WO 01 /19975, WO 95/26407, WO 96/34968, WO 98/20145, WO 99/12950, WO 99/66050, WO 99/53072, US 6,734,341 , WO 00/1 1 192, WO 98/22604, WO 98/32326, WO 01 /98509, WO 01 /98509, WO 2005/002359, US 5,824,790, US 6,013,861 , WO 94/04693, WO 94/09144, WO 94/1 1520, WO 95/35026, WO 97/20936, WO 201 0/012796, WO 2010/003701 ,
2) transgenic plants which synthesize non starch carbohydrate polymers or which synthesize non starch carbohydrate polymers with altered properties in comparison to wild type plants without genetic modification. Examples are plants producing polyfructose, especially of the inulin and levan-type, as disclosed in EP-A 0 663 956, WO 96/01 904, WO 96/21023, WO 98/39460, and WO 99/24593, plants producing alpha- 1 ,4-glucans as disclosed in WO 95/31553, US
2002031826, US 6,284,479, US 5,712, 107, WO 97/47806, WO 97/47807, WO 97/47808 and WO 00/14249, plants producing alpha-1 ,6 branched alpha-1 ,4-glucans, as disclosed in WO 00/73422, plants producing alternan, as disclosed in e.g. WO 00/47727, WO 00/73422, EP 06077301 .7, US 5,908,975 and EP-A 0 728 213, 3) transgenic plants which produce hyaluronan, as for example disclosed in WO 2006/032538, WO 2007/039314, WO 2007/039315, WO 2007/039316, JP-A 2006-304779, and WO 2005/012529.
4) transgenic plants or hybrid plants, such as onions with characteristics such as 'high soluble solids content', low pungency' (LP) and/or long storage' (LS), as described in U.S. Patent Applications 12/020,360 and 61 /054,026. Plants or plant cultivars (that can be obtained by plant biotechnology methods such as genetic engineering) which may also be treated according to the invention are plants, such as cotton plants, with altered fiber characteristics. Such plants can be obtained by genetic transformation, or by selection of plants contain a mutation imparting such altered fiber characteristics and include:
a) Plants, such as cotton plants, containing an altered form of cellulose synthase genes as described in WO 98/00549. b) Plants, such as cotton plants, containing an altered form of rsw2 or rsw3 homologous nucleic acids as described in WO 2004/053219.
Plants, such as cotton plants, with increased expression of sucrose phosphate synth described in WO 01 /17333. d) Plants, such as cotton plants, with increased expression of sucrose synthase as described in WO 02/45485. e) Plants, such as cotton plants, wherein the timing of the plasmodesmatal gating at the basis of the fiber cell is altered, e.g. through downregulation of fiber-selective β-1 ,3-glucanase as described in WO 2005/017157, or as described in WO 2009/143995. f) Plants, such as cotton plants, having fibers with altered reactivity, e.g. through the expression of N- acetylglucosaminetransferase gene including nodC and chitin synthase genes as described in WO
2006/136351 .
Plants or plant cultivars (that can be obtained by plant biotechnology methods such as genetic engineering) which may also be treated according to the invention are plants, such as oilseed rape or related Brassica plants, with altered oil profile characteristics. Such plants can be obtained by genetic transformation, or by selection of plants contain a mutation imparting such altered oil profile characteristics and include:
a) Plants, such as oilseed rape plants, producing oil having a high oleic acid content as described e.g. in US 5,969,1 69, US 5,840,946 or US 6,323,392 or US 6,063,947 b) Plants such as oilseed rape plants, producing oil having a low linolenic acid content as described in US 6,270,828, US 6,1 69, 190, or US 5,965,755 c) Plant such as oilseed rape plants, producing oil having a low level of saturated fatty acids as described e.g. in US 5,434,283 or U.S. Patent Application 12/668303
Plants or plant cultivars (that can be obtained by plant biotechnology methods such as genetic engineering) which may also be treated according to the invention are plants, such as oilseed rape or related Brassica plants, with altered seed shattering characteristics. Such plants can be obtained by genetic transformation, or by selection of plants contain a mutation imparting such altered seed shattering characteristics and include plants such as oilseed rape plants with delayed or reduced seed shattering as described in U.S. Patent Application 61 /135,230, WO 2009/068313 and WO
2010/006732.
Plants or plant cultivars (that can be obtained by plant biotechnology methods such as genetic engineering) which may also be treated according to the invention are plants, such as Tobacco plants, with altered post-translational protein modification patterns, for example as described in
WO 2010/121 818 and WO 201 0/145846.
Particularly useful transgenic plants which may be treated according to the invention are plants containing transformation events, or combination of transformation events, that are the subject of petitions for non-regulated status, in the United States of America, to the Animal and Plant Health Inspection Service (APHIS) of the United States Department of Agriculture (USDA) whether such petitions are granted or are still pending. At any time this information is readily available from APHIS (4700 River Road, Riverdale, M D 20737, USA), for instance on its internet site (U RL
http://www. aphis. usda.gov/brs/not_reg. html). On the filing date of this application the petitions for nonregulated status that were pending with APH IS or granted by APHIS were those which contains the following information: - Petition: the identification number of the petition. Technical descriptions of the transformation events can be found in the individual petition documents which are obtainable from APHIS, for example on the APHIS website, by reference to this petition number. These descriptions are herein incorporated by reference. - Extension of Petition: reference to a previous petition for which an extension is requested.
- Institution: the name of the entity submitting the petition.
- Regulated article: the plant species concerned.
- Transgenic phenotype: the trait conferred to the plants by the transformation event.
- Transformation event or line: the name of the event or events (sometimes also designated as lines or lines) for which nonregulated status is requested.
- APHIS documents: various documents published by APHIS in relation to the Petition and which can be requested with APHIS.
Additional particularly useful plants containing single transformation events or combinations of transformation events are listed for example in the databases from various national or regional regulatory agencies (see for example http^gmoinfo. irc.it/qrnp browse. aspx and
http://www.agbios.com/dbase.php).
Particularly useful transgenic plants which may be treated according to the invention are plants containing transformation events, or a combination of transformation events, and that are listed for example in the databases for various national or regional regulatory agencies including Event 1 143- 14A (cotton, insect control, not deposited, described in WO 2006/128569); Event 1 143-51 B (cotton, insect control, not deposited, described in WO 2006/128570); Event 1 445 (cotton, herbicide tolerance, not deposited, described in US-A 2002-120964 or WO 02/034946); Event 17053 (rice, herbicide tolerance, deposited as PTA-9843, described in WO 201 0/1 17737); Event 1 7314 (rice, herbicide tolerance, deposited as PTA-9844, described in WO 201 0/1 17735); Event 281 -24-236 (cotton, insect control - herbicide tolerance, deposited as PTA-6233, described in WO 2005/103266 or US-A 2005- 21 6969); Event 3006-21 0-23 (cotton, insect control - herbicide tolerance, deposited as PTA-6233, described in US-A 2007-143876 or WO 2005/1 03266); Event 3272 (corn, quality trait, deposited as PTA-9972, described in WO 2006/098952 or US-A 2006-230473); Event 4041 6 (corn, insect control - herbicide tolerance, deposited as ATCC PTA-1 1508, described in WO 201 1 /075593) ; Event 43A47 (corn, insect control - herbicide tolerance, deposited as ATCC PTA-1 1509, described in WO
201 1 /075595); Event 5307 (corn, insect control, deposited as ATCC PTA-9561 , described in WO 2010/07781 6); Event ASR-368 (bent grass, herbicide tolerance, deposited as ATCC PTA-481 6, described in US-A 2006-1 62007 or WO 2004/053062); Event B1 6 (corn, herbicide tolerance, not deposited, described in US-A 2003-126634); Event BPS-CV127-9 (soybean, herbicide tolerance, deposited as NCIMB No. 41 603, described in WO 2010/080829); Event CE43-67B (cotton, insect control, deposited as DSM ACC2724, described in US-A 2009-21 7423 or WO2006/128573); Event CE44-69D (cotton, insect control, not deposited, described in US-A 201 0-0024077); Event CE44-69D (cotton, insect control, not deposited, described in WO 2006/128571 ); Event CE46-02A (cotton, insect control, not deposited, described in WO 2006/128572); Event COT1 02 (cotton, insect control, not deposited, described in US-A 2006-1301 75 or WO 2004/039986); Event COT202 (cotton, insect control, not deposited, described in US-A 2007-067868 or WO 2005/054479) ; Event COT203 (cotton, insect control, not deposited, described in WO 2005/054480); Event DAS40278 (corn, herbicide tolerance, deposited as ATCC PTA-10244, described in WO 201 1 /022469); Event DAS-59122-7 (corn, insect control - herbicide tolerance, deposited as ATCC PTA 1 1384 , described in US-A 2006- 070139); Event DAS-59132 (corn, insect control - herbicide tolerance, not deposited, described in WO 2009/1 00188); Event DAS68416 (soybean, herbicide tolerance, deposited as ATCC PTA-10442, described in WO 201 1 /066384 or WO 201 1 /066360); Event DP-098140-6 (corn, herbicide tolerance, deposited as ATCC PTA-8296, described in US-A 2009-137395 or WO 2008/1 12019); Event DP- 305423-1 (soybean, quality trait, not deposited, described in US-A 2008-312082 or WO 2008/054747) ; Event DP-32138-1 (corn, hybridization system, deposited as ATCC PTA-9158, described in US-A
2009-021 0970 or WO 2009/1 03049); Event DP-356043-5 (soybean, herbicide tolerance, deposited as ATCC PTA-8287, described in US-A 201 0-0184079 or WO 2008/002872); Event EE-1 (brinjal, insect control, not deposited, described in WO 2007/091277); Event FI 1 1 7 (corn, herbicide tolerance, deposited as ATCC 209031 , described in US-A 2006-059581 or WO 98/044140); Event GA21 (corn, herbicide tolerance, deposited as ATCC 209033, described in US-A 2005-086719 or WO 98/044140); Event GG25 (corn, herbicide tolerance, deposited as ATCC 209032, described in US-A 2005-1 88434 or WO 98/044140); Event GHB1 1 9 (cotton, insect control - herbicide tolerance, deposited as ATCC PTA-8398, described in WO 2008/151780); Event GHB61 4 (cotton, herbicide tolerance, deposited as ATCC PTA-6878, described in US-A 201 0-050282 or WO 2007/01 7186); Event GJ1 1 (corn, herbicide tolerance, deposited as ATCC 209030, described in US-A 2005-1 88434 or WO 98/044140); Event GM RZ13 (sugar beet, virus resistance , deposited as NCI MB-41 601 , described in WO 2010/076212); Event H7-1 (sugar beet, herbicide tolerance, deposited as NCIMB 41 158 or NCIMB 41 159, described in US-A 2004-1 72669 or WO 2004/074492); Event JOPLI N1 (wheat, disease tolerance, not deposited, described in US-A 2008-064032) ; Event LL27 (soybean, herbicide tolerance, deposited as
NCIMB41 658, described in WO 2006/108674 or US-A 2008-320616); Event LL55 (soybean, herbicide tolerance, deposited as NCIMB 41660, described in WO 2006/1 08675 or US-A 2008-1 96127); Event LLcotton25 (cotton, herbicide tolerance, deposited as ATCC PTA-3343, described in WO 03/013224 or US-A 2003-097687); Event LLRICE06 (rice, herbicide tolerance, deposited as ATCC-23352, described in US 6,468,747 or WO 00/026345) ; Event LLRICE601 (rice, herbicide tolerance, deposited as ATCC PTA-2600, described in US-A 2008-2289060 or WO 00/026356); Event LY038 (corn, quality trait, deposited as ATCC PTA-5623, described in US-A 2007-028322 or WO 2005/061 720); Event MI R1 62 (corn, insect control, deposited as PTA-81 66, described in US-A 2009-300784 or WO 2007/142840); Event M IR604 (corn, insect control, not deposited, described in US-A 2008-167456 or WO 2005/103301 ); Event MON15985 (cotton, insect control, deposited as ATCC PTA-2516, described in US-A 2004-25031 7 or WO 02/1 00163); Event MON81 0 (corn, insect control, not deposited, described in US-A 2002-102582); Event MON863 (corn, insect control, deposited as ATCC PTA-2605, described in WO 2004/01 1601 or US-A 2006-095986); Event MON87427 (corn, pollination control, deposited as ATCC PTA-7899, described in WO 201 1 /062904) ; Event MON87460 (corn, stress tolerance, deposited as ATCC PTA-8910, described in WO 2009/1 1 1263 or US-A 201 1 - 0138504) ; Event MON87701 (soybean, insect control, deposited as ATCC PTA-81 94, described in US-A 2009-130071 or WO 2009/064652) ; Event MON87705 (soybean, quality trait - herbicide tolerance, deposited as ATCC PTA-9241 , described in US-A 201 0-0080887 or WO 201 0/03701 6); Event MON87708 (soybean, herbicide tolerance, deposited as ATCC PTA9670, described in WO 201 1 /034704); Event MON87754 (soybean, quality trait, deposited as ATCC PTA-9385, described in WO 2010/024976); Event MON87769 (soybean, quality trait, deposited as ATCC PTA-891 1 , described in US-A 201 1 -0067141 or WO 2009/102873) ; Event MON8801 7 (corn, insect control - herbicide tolerance, deposited as ATCC PTA-5582, described in US-A 2008-028482 or WO
2005/059103); Event MON88913 (cotton, herbicide tolerance, deposited as ATCC PTA-4854, described in WO 2004/072235 or US-A 2006-059590) ; Event MON89034 (corn, insect control, deposited as ATCC PTA-7455, described in WO 2007/140256 or US-A 2008-260932); Event
MON89788 (soybean, herbicide tolerance, deposited as ATCC PTA-6708, described in US-A 2006- 282915 or WO 2006/130436); Event MS1 1 (oilseed rape, pollination control - herbicide tolerance, deposited as ATCC PTA-850 or PTA-2485, described in WO 01 /031042); Event MS8 (oilseed rape, pollination control - herbicide tolerance, deposited as ATCC PTA-730, described in WO 01 /041558 or US-A 2003-1 88347); Event NK603 (corn, herbicide tolerance, deposited as ATCC PTA-2478, described in US-A 2007-292854) ; Event PE-7 (rice, insect control, not deposited, described in WO 2008/1 14282); Event RF3 (oilseed rape, pollination control - herbicide tolerance, deposited as ATCC PTA-730, described in WO 01 /041558 or US-A 2003-1 88347); Event RT73 (oilseed rape, herbicide tolerance, not deposited, described in WO 02/036831 or US-A 2008-070260) ; Event T227-1 (sugar beet, herbicide tolerance, not deposited, described in WO 02/44407 or US-A 2009-26581 7); Event T25 (corn, herbicide tolerance, not deposited, described in US-A 2001 -029014 or WO 01 /051654); Event T304-40 (cotton, insect control - herbicide tolerance, deposited as ATCC PTA-81 71 , described in US-A 201 0-077501 or WO 2008/122406); Event T342-142 (cotton, insect control, not deposited, described in WO 2006/128568); Event TC1507 (corn, insect control - herbicide tolerance, not deposited, described in US-A 2005-039226 or WO 2004/099447); Event VI P1034 (corn, insect control - herbicide tolerance, deposited as ATCC PTA-3925., described in WO 03/052073), Event 3231 6 (corn, insect control-herbicide tolerance, deposited as PTA-1 1507, described in WO 201 1 /084632), Event 41 14 (corn, insect control-herbicide tolerance, deposited as PTA-1 1506, described in WO 201 1 /084621 ).
EXAMPLES
1. Seed germination of parasitic weed species
Purpose of the test is to determine the EC5o of for strigolactame derivatives, i.e. the concentration of compound which is able to germinate 50% of seeds of the weeds Phelipanche ramosa (= Orobanche ramosa) pathovar C.
Strigolactame derivatives are tested in comparison to strigolactone derivatives, such as GR24, strigol or sorgolactone.
Germination stimulation activity assay: GR24 and SL analogues were resuspended in acetone at 10 mmol L"1 , then diluted with water at 1 mmol L"1 (water/acetone; v/v; 99/1 ). Dilutions of 1 x1 0"3 mol L"1 to 1 x10-15 mol L"1 are then performed in water/acetone (v/v; 99/1 ). Phelipanche ramosa's seeds (St Martin de Fraigneau, France, 2005) were surface-sterilized according to Vieira Dos Santos et al. (C. V. Dos Santos, P. Letousey, P. Delavault, P. Thalouarn, Phytopathology 2003, 93, 451 -457), then resuspended in sterile water (10 g L"1) and distributed in 96-wells plate (50 μΙ_ ~ 1 00 seeds per well). After preconditioning (7 days, 21 °C, in dark, sealed plate), GR24 (1 Ox) or other molecules were added and volumes were adjusted to 1 00 μΙ_ with water (water/acetone; v/v; 999/1 ). Controls were made with water/acetone (v/v; 999/1 ) and without seeds. Plates were incubated for germination as previously described. The methylthiazolyldiphenyl-tetrazolium bromide assays were carried out according to Mossman (T. Mosmann, J. Immunol. Methods 1983, 65, 55-63) with minor modification of the solubilization buffer (Triton X-1 00 1 0%, HCI 0.04 mol L"1 in isopropanol). For each compound tested, dose-reponse curves (A=f(c), A :Absorbance 570 nm ; c : concentration (mol. L-1 )) and EC 50 are modeled with a four parameter logistic curve computed with SigmaPlot® 1 0.0.
EC 50 (M)
Control HO^°^Q 3.7 1 0"6
Compound A 3.5 1 0"9
Compound B 1 .2 1 0"9
Figure imgf000034_0001
As known, strigolactone derivatives are able to stimulate germination of the weed Phelipanche ramosa seeds with a great efficiency: GR24 is able to germinate 50% of seeds of the weeds Phelipanche ramosa at a concentration of 2.1 1 0 12 M. Other strigolactones, such as strigol and sorgolactone, are less efficient than GR24, and need a concentration around 1 0 times higher to get the same results than GR24.
Comparatively, Strigolactame derivatives are very significantly less efficient for the germination of parasitic weed species than GR24, but also less efficient than other strigolactones: Strigolactame compound needs a concentration from 500 to 1 600 times higher than GR24 and other tested strigolactones to get the same result.
Used as same concentration, strigolactame derivatives will dramatically be less active than strigolactone compounds to stimulate the seed germination of weeds, which is a great advantage for agricultural practices.
2. Glomus intraradices spore germination
Test is perfomed in climate chamber, at 27°C. Compounds are dissolved in acetone in a concentration of 10 6M. Three replicates are done by compounds. The percentage of Glomus intraradices germinated spores is measured after 3 days of incubation. Untreated control and control with the solvent (acetone) only are done in same conditions.
% germination
Untreated control 54%
Acetone 56%
Figure imgf000035_0001
Strigolactone derivatives, and particularly GR24, are known to stimulate arbuscular mycorrhizae (AM) fungi spore germination and branching of germinating hyphae (Besserer et al., Plant Physiol. 2008, 148(1 ):402-13). Several tests, including the test of Glomus intraradices spore germination used here or the measure of branching of germinating Gigaspora margarita hyphae are considered as equivalent for determinate the activity of compounds on AMF fungi and therefore the capability to stimulate mycchorization (Akiyama K. et al., Nature, 2005, 435, 824).
Results of the Glomus intraradices spore germination show that strigolactame derivatives are efficient, and in particular as efficient as strigolactone derivatives, to stimulate arbuscular mycorrhizae (AM) fungi spore germination and mycchorization.
3. Test on the inhibition of the axillary bud
P. sativum ccd8 shoot branching mutants of pea are strigolactone deficient plants which show a hyper- branched phenotype. Application of strigolactone directly to the axillary buds is able to restore the wild-type branching phenotype to ccd8 mutants (Gomez-Roldan et al, 2008, Nature, 455, 1 89-194).
Compounds to be tested have been diluted in acetone in desired concentration and applied directly to the axillary N4 buds of P. sativum ccd8 mutant. Length of axillary N3 or N4 bud is measured 1 0 days after treatment and compared to the length observed with a blank (untreated) control. Growth inhibition
Compound C (1 μΜ) ++
GR24 (1 μΜ) +++
GR24-4QH (1 μΜ) ++
++ : 20% < length of axilary treated bud / length of untreated bud < 50%
+++ : length of axilary treated bud / length of untreated bud < 20%
As expected, application of the strigolactone compound GR24 directly to the axillary N4 buds of P. sativum ccd8 mutant restores in a significant amount (more than 80%) the wild-type branching phenotype.
Restoration is also observed with a GR24-derived compound, although with a less efficiency (between 50 and 80 % of restoration).
Strigolactame derivative compound C restores the wild-type branching phenotype, with an efficiency comparable to the GR24-derived compound.

Claims

Claims
1 . A compound of formula (I)
Figure imgf000037_0001
(I)
wherein
Xi , 2, 3, Yi , Y2, Y3 and Z independently represent a hydrogen atom, a halogen atom, a nitro group, a hydroxy group, a cyano group, an amino group, a sulphenyl group, a sulphinyl group, a sulphonyl group, a formyl group, a acetyl group, a formyloxy group, a formylamino group, a carbamoyl group, a N-hydroxycarbamoyl group, a carbamate group, substituted or non- substituted (hydroxyimino)-Ci -C6-alkyl group, substituted or non-substituted CrC8-alkyl, substituted or non-substituted tri(Ci -C8-alkyl)silyl-Ci -C8-alkyl, substituted or non-substituted Ci -C8-cycloalkyl, substituted or non-substituted tri(Ci -C8-alkyl)silyl-Ci -C8-cycloalkyl, substituted or non-substituted CrC8-halogenoalkyl having 1 to 5 halogen atoms, substituted or non-substituted CrC8-halogenocycloalkyl having 1 to 5 halogen atoms, a substituted or non- substituted C2-C8-alkenyl, substituted or non-substituted C2-C8-alkynyl, substituted or non- substituted CrC8-alkylamino, substituted or non-substituted di-Ci -C8-alkylamino, substituted or non-substituted CrC8-alkoxy, substituted or non-substituted CrC8-halogenoalkoxy having 1 to 5 halogen atoms, substituted or non-substituted C2-C8-alkynyloxy, substituted or non- substituted Ci -C8-alkylsulphenyl, substituted or non-substituted CrC8-halogenoalkylsulphenyl having 1 to 5 halogen atoms, substituted or non-substituted C2-C8-alkenyloxy, substituted or non-substituted C2-C8-halogenoalkenyloxy having 1 to 5 halogen atoms, substituted or non- substituted C3-C8-halogenoalkynyloxy having 1 to 5 halogen atoms, substituted or non- substituted CrC8-alkylcarbonyl, substituted or non-substituted CrC8-halogenoalkylcarbonyl having 1 to 5 halogen atoms, substituted or non-substituted CrC8-alkylcarbamoyl, substituted or non-substituted di-CrC8-alkylcarbamoyl, substituted or non-substituted N-C1 -C8- alkyloxycarbamoyl, substituted or non-substituted di-CrC8-alkoxycarbamoyl, substituted or non-substituted N-Ci -C8-alkyl-Ci -C8-alkoxycarbamoyl, substituted or non-substituted Ci -C8- alkoxycarbonyl, substituted or non-substituted CrC8-halogenoalkoxycarbonyl having 1 to 5 halogen atoms, substituted or non-substituted CrC8-alkylcarbonyloxy, substituted or non- substituted CrC8-halogenoalkylcarbonyloxy having 1 to 5 halogen atoms, substituted or non- substituted Ci -C8-alkylcarbonylamino, substituted or non-substituted Ci -C8- halogenoalkylcarbonylamino having 1 to 5 halogen atoms, substituted or non-substituted Ci - Cs-alkylaminocarbonyloxy, substituted or non-substituted di-Ci -C8-alkylaminocarbonyloxy, substituted or non-substituted Ci -C8-alkyloxycarbonyloxy, substituted or non-substituted Ci - Cs-alkylsulphenyl, substituted or non-substituted Ci -C8-halogenoalkylsulphenyl having 1 to 5 halogen atoms, substituted or non-substituted Ci -C8-alkylsulphinyl, substituted or non- substituted Ci -C8-halogenoalkylsulphinyl having 1 to 5 halogen atoms, substituted or non- substituted Ci -Cs-alkylsulphonyl, substituted or non-substituted Ci -C8-halogenoalkylsulphonyl having 1 to 5 halogen atoms, substituted or non-substituted Ci -C8-alkylaminosulfamoyl, substituted or non-substituted di-Ci -C8-alkylaminosulfamoyl, substituted or non-substituted (Ci -C6-alkoxyimino)-Ci -C6-alkyl, substituted or non-substituted (Ci -C6-alkenyloxyimino)-Ci -C6- alkyl, substituted or non-substituted (Ci -C6-alkynyloxyimino)-Ci -C6-alkyl, substituted or non- substituted (benzyloxyimino)-Ci -C6-alkyl, substituted or non-substituted CrC8-alkoxyalkyl, substituted or non-substituted CrC8-halogenoalkoxyalkyl having 1 to 5 halogen atoms, a substituted or non-substituted arylalkyl substituted or non-substituted benzyloxy, substituted or non-substituted benzylsulphenyl, substituted or non-substituted benzylamino, substituted or non-substituted phenoxy, substituted or non-substituted phenylsulphenyl, substituted or non- substituted phenylamino, a substituted or non-substituted or a 4-, 5-, 6- or 7-membered heterocycle comprising up to 4 heteroatoms selected in the list consisting of N, O, S]
- Ri and R2 independently represent a hydrogen atom, a halogen atom, a nitro group, a hydroxy group, a cyano group, an amino group, a sulphenyl group, a sulphinyl group, a sulphonyl group, a formyl group, a formyloxy group, a formylamino group, a carbamoyl group, a N-hydroxycarbamoyl group, a carbamate group, substituted or non-substituted (hydroxyimino)-Ci -C6-alkyl group, substituted or non-substituted CrC8-alkyl, substituted or non-substituted tri(Ci -C8-alkyl)silyl-CrC8- alkyl, substituted or non-substituted Ci -C8-cycloalkyl, substituted or non-substituted tri(Ci -C8- alkyl)silyl-Ci -C8-cycloalkyl, substituted or non-substituted CrC8-halogenoalkyl having 1 to 5 halogen atoms, substituted or non-substituted CrC8-halogenocycloalkyl having 1 to 5 halogen atoms, a substituted or non-substituted C2-C8-alkenyl, substituted or non-substituted C2-C8-alkynyl, substituted or non-substituted CrC8-alkylamino, substituted or non-substituted di-CrC8-alkylamino, substituted or non-substituted CrC8-alkoxy, substituted or non-substituted Ci -C8-halogenoalkoxy having 1 to 5 halogen atoms, substituted or non-substituted C2-C8-alkynyloxy, substituted or non-substituted Ci -C8- alkylsulphenyl, substituted or non-substituted Ci -C8-halogenoalkylsulphenyl having 1 to 5 halogen atoms, substituted or non-substituted C2-C8-alkenyloxy, substituted or non-substituted C2-C8- halogenoalkenyloxy having 1 to 5 halogen atoms, substituted or non-substituted C3-C8- halogenoalkynyloxy having 1 to 5 halogen atoms, substituted or non-substituted CrC8-alkylcarbonyl, substituted or non-substituted Ci -C8-halogenoalkylcarbonyl having 1 to 5 halogen atoms, substituted or non-substituted CrC8-alkylcarbamoyl, substituted or non-substituted di-CrC8-alkylcarbamoyl, substituted or non-substituted N-C1 -C8-alkyloxycarbamoyl, substituted or non-substituted di-Ci -C8- alkoxycarbamoyl, substituted or non-substituted N-Ci -C8-alkyl-Ci -C8-alkoxycarbamoyl, substituted or non-substituted CrC8-alkoxycarbonyl, substituted or non-substituted CrC8-halogenoalkoxycarbonyl having 1 to 5 halogen atoms, substituted or non-substituted Ci -C8-alkylcarbonyloxy, substituted or non-substituted Ci -C8-halogenoalkylcarbonyloxy having 1 to 5 halogen atoms, substituted or non- substituted d-Cs-alkylcarbonylamino, substituted or non-substituted CrC8- halogenoalkylcarbonylamino having 1 to 5 halogen atoms, substituted or non-substituted Ci -C8- alkylaminocarbonyloxy, substituted or non-substituted di-Ci -C8-alkylaminocarbonyloxy, substituted or non-substituted CrC8-alkyloxycarbonyloxy, substituted or non-substituted CrC8-alkylsulphenyl, substituted or non-substituted Ci -Cs-halogenoalkylsulphenyl having 1 to 5 halogen atoms, substituted or non-substituted CrC8-alkylsulphinyl, substituted or non-substituted Ci -C8-halogenoalkylsulphinyl having 1 to 5 halogen atoms, substituted or non-substituted Ci -C8-alkylsulphonyl, substituted or non- substituted Ci -C8-halogenoalkylsulphonyl having 1 to 5 halogen atoms, substituted or non-substituted Ci -C8-alkylaminosulfamoyl, substituted or non-substituted di-Ci -C8-alkylaminosulfamoyl, substituted or non-substituted (Ci -C6-alkoxyimino)-Ci -C6-alkyl, substituted or non-substituted (Ci -C6- alkenyloxyimino)-Ci -C6-alkyl, substituted or non-substituted (Ci -C6-alkynyloxyimino)-Ci -C6-alkyl, substituted or non-substituted (benzyloxyimino)-Ci -C6-alkyl, substituted or non-substituted Ci -C8- alkoxyalkyl, substituted or non-substituted Ci -C8-halogenoalkoxyalkyl having 1 to 5 halogen atoms, substituted or non-substituted benzyloxy, substituted or non-substituted benzylsulphenyl, substituted or non-substituted benzylamino, substituted or non-substituted phenoxy, substituted or non-substituted phenylsulphenyl, substituted or non-substituted phenylamino, a substituted or non-substituted or a 4-, 5-, 6- or 7-membered heterocycle comprising up to 4 heteroatoms selected in the list consisting of N, O, S]; or
Ri and R2 form a saturated or unsaturated, non-aromatic, substituted or non-substituted 4- to 7- membered carbocycle; or
Ri and R2 form a saturated or unsaturated, aromatic or non-aromatic, substituted or non-substituted 4- to 7-membered carbocycle fused to an other saturated or unsaturated, aromatic or non-aromatic, substituted or non-substituted 4- to 7- membered carbocycle. as well as salts, N-oxides, metallic complexes, metalloidic complexes and optically active or geometric isomers thereof.
2. A compound according to claim 1 wherein Xi , X2, Yr Y2, Y3 and Z independently represent a hydrogen atom, a halogen atom, a nitro group, a hydroxy group, a cyano group, a substituted or non- substituted Ci -C8-alkyl, a substituted or non-substituted CrC8-haloalkyl, a substituted or non- substituted Ci -C8-alkoxy, or a substituted or non-substituted CrC8-haloalkoxy.
3. A compound according to claim 2 wherein Xi , X2, Yi , Y3 and Z represent a hydrogen atom.
4. A compound according to any one of claims 1 to 3 wherein Y2 represents a substituted or non- substituted Ci -C8-alkyl, or a substituted or non-substituted Ci -C8-haloalkyl.
5. A compound according to to any one of claims 1 to 4 wherein X3 represents hydrogen atom, a formyl group, a substituted or non-substituted Ci -C8-alkyl, a substituted or non-substituted Ci -C8- halogenoalkyl having 1 to 5 halogen atoms, a substituted or non-substituted C2-C8-alkenyl, a substituted or non-substituted C2-C8-alkynyl, a substituted or non-substituted arylalkyi, acetyl, a substituted or non-substituted Ci -C8-alkylcarbonyl, a substituted or non-substituted Ci -C8- halogenoalkylcarbonyl, substituted or non-substituted CrC8-alkoxycarbonyl.
6. A compound according to claim 5 wherein X3 represents hydrogen atom, a substituted or non- substituted Ci -C8-alkyl, a substituted or non-substituted C2-C8-alkenyl, a substituted or non-substituted C2-C8-alkynyl, a substituted or non-substituted arylalkyi, formyl, acetyl, a substituted or non-substituted Ci -Cs-alkylcarbonyl, a substituted or non-substituted CrC8-haloalkylcarbonyl, substituted or non- substituted Ci -C8-alkoxycarbonyl.
7. A compound according to anyone of claims 1 to 6 wherein Ri and R2 independently represent a hydrogen atom, a halogen atom, a nitro group, a hydroxy group, a cyano group, a substituted or non- substituted Ci -Cs-alkyl, a substituted or non-substituted Ci -C8-haloalkyl, a substituted or non- substituted Ci -C8-alkoxy, or a substituted or non-substituted CrC8-haloalkoxy; or
Ri and R2 form a saturated or unsaturated, non-aromatic, substituted or non-substituted 4- to 7- membered carbocycle; or
Ri and R2 form a saturated or unsaturated, aromatic or non-aromatic, substituted or non-substituted 4- to 7-membered carbocycle fused to another saturated or unsaturated, aromatic or non-aromatic, substituted or non-substituted 4- to 7-membered carbocycle.
8. A compound according to claim 7 wherein Ri and R2 form a saturated or unsaturated, aromatic or non-aromatic, substituted or non-substituted 4- to 7-membered carbocycle fused to another saturated or unsaturated, aromatic or non-aromatic, substituted or non-substituted 4- to 7-membered carbocycle.
9. A compound according to claim 8 wherein Ri and R2 form an unsaturated, non-aromatic, substituted or non-substituted 5-membered carbocycle fused to another unsaturated, aromatic, substituted or non-substituted 6- membered carbocycle.
10. A compound according to any one of claims 1 to 9 wherein
- Xi , X2, Yi , Y2 ,Y3 and Z independently represent a hydrogen atom, a halogen atom, a nitro group, a hydroxy group, a cyano group, a substituted or non-substituted CrC8-alkyl, a substituted or non- substituted CrC8-haloalkyl, a substituted or non-substituted CrC8-alkoxy, or a substituted or non- substituted Ci -C8-haloalkoxy;
- X3 represents hydrogen atom, a substituted or non-substituted CrC8-alkyl, a substituted or non- substituted C2-C8-alkenyl, a substituted or non-substituted C2-C8-alkynyl, a substituted or non- substituted arylalkyi, formyl, acetyl, a substituted or non-substituted CrC8-alkylcarbonyl, a substituted or non-substituted C rC8-haloalkylcarbonyl, substituted or non-substituted CrC8-alkoxycarbonyl,and - Ri and R2 form an unsaturated, non-aromatic, substituted or non-substituted 5-membered carbocycle fused to another unsaturated, aromatic, substituted or non-substituted 6-membered carbocycle.
1 1 . A compound according to claim 1 0 wherein
- Xi , X2, Yi , Y3 and Z independently represent a hydrogen atom;
- X3 represents hydrogen atom, a substituted or non-substituted Ci -C8-alkyl, a substituted or non- substituted C2-C8-alkenyl, a substituted or non-substituted C2-C8-alkynyl, a substituted or non- substituted arylalkyi, formyl, acetyl, a substituted or non-substituted Ci -C8-alkylcarbonyl, a substituted or non-substituted C rC8-haloalkylcarbonyl, substituted or non-substituted CrC8-alkoxycarbonyl, - Y2 represents a substituted or non-substituted CrC8-alkyl or a substituted or non-substituted CrC8- haloalkyl; and
- Ri and R2 form an unsaturated, non-aromatic substituted or non-substituted 5-membered carbocycle fused to another unsaturated, aromatic, substituted or non-substituted 6-membered carbocycle.
12. A compound according to any one of claims 1 to 10 selected in the list consisting of
Figure imgf000041_0001
(Id) (le) (If)
wherein X3 represents hydrogen atom, a substituted or non-substituted CrC8-alkyl, a substituted or non-substituted C2-C8-alkenyl, a substituted or non-substituted C2-C8-alkynyl, a substituted or non- substituted arylalkyi, formyl, acetyl, a substituted or non-substituted CrC8-alkylcarbonyl, a substituted or non-substituted C i-C8-haloalkylcarbonyl, substituted or non-substituted Ci-C8-alkoxycarbonyl.
13. Composition characterized by a content of at least one compound of the formula (I) according to Claim 1 or 2, in addition to at least one further active ingredient selected from the group of the insecticides, attractants, sterilants, bactericides, acaricides, nematicides, fungicides, growth regulators, herbicides, fertilizers, safeners and semiochemicals.
14. A method for enhancing the growth, yield, vigor and/or mycchorization of a plant, characterized in that an agronomically effective quantity of a compound according to claims 1 to 12 is applied to the soil where plants grow or are capable of growing, to the leaves and/or the fruit of plants or to the seeds of plants.
15. The use of a compound as claimed in any one of claims 1 to 12 for improving the plant growth and/or for enhancing the yield and/or decreasing the needs for fertilizers.
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20150189876A1 (en) * 2012-06-11 2015-07-09 Syngenta Participations Ag Crop enhancement compositions
WO2015128321A1 (en) * 2014-02-26 2015-09-03 Syngenta Participations Ag Plant growth regulating compounds
WO2016193290A1 (en) * 2015-06-03 2016-12-08 Syngenta Participations Ag Plant growth regulating compounds
WO2018145979A1 (en) * 2017-02-09 2018-08-16 Syngenta Participations Ag Germination promoters
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WO2019175025A1 (en) * 2018-03-16 2019-09-19 Syngenta Participations Ag Plant growth regulator compounds
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Citations (283)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2036008A (en) 1934-11-07 1936-03-31 White Martin Henry Plug fuse
US2289060A (en) 1940-03-12 1942-07-07 Merkle Corp Method of and apparatus for utilizing dry ice
US4761373A (en) 1984-03-06 1988-08-02 Molecular Genetics, Inc. Herbicide resistance in plants
WO1989010396A1 (en) 1988-04-28 1989-11-02 Plant Genetic Systems N.V. Plants with modified stamen cells
WO1991002069A1 (en) 1989-08-10 1991-02-21 Plant Genetic Systems N.V. Plants with modified flowers
US5013659A (en) 1987-07-27 1991-05-07 E. I. Du Pont De Nemours And Company Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase
US5084082A (en) 1988-09-22 1992-01-28 E. I. Du Pont De Nemours And Company Soybean plants with dominant selectable trait for herbicide resistance
WO1992005251A1 (en) 1990-09-21 1992-04-02 Institut National De La Recherche Agronomique Dna sequence imparting cytoplasmic male sterility, mitochondrial genome, nuclear genome, mitochondria and plant containing said sequence and process for the preparation of hybrids
US5175149A (en) 1991-10-04 1992-12-29 The University Of Tennessee Research Corporation Pentasaccharide phytohormones and methods for their use
US5198599A (en) 1990-06-05 1993-03-30 Idaho Resarch Foundation, Inc. Sulfonylurea herbicide resistance in plants
EP0571427A1 (en) 1991-02-13 1993-12-01 Hoechst Schering AgrEvo GmbH Plasmids containing dna-sequences that cause changes in the carbohydrate concentration and the carbohydrate composition in plants, as well as plant cells and plants containing these plasmids
US5273894A (en) 1986-08-23 1993-12-28 Hoechst Aktiengesellschaft Phosphinothricin-resistance gene, and its use
US5276268A (en) 1986-08-23 1994-01-04 Hoechst Aktiengesellschaft Phosphinothricin-resistance gene, and its use
WO1994004693A2 (en) 1992-08-26 1994-03-03 Zeneca Limited Novel plants and processes for obtaining them
US5304732A (en) 1984-03-06 1994-04-19 Mgi Pharma, Inc. Herbicide resistance in plants
WO1994009144A1 (en) 1992-10-14 1994-04-28 Zeneca Limited Novel plants and processes for obtaining them
WO1994011520A2 (en) 1992-11-09 1994-05-26 Zeneca Limited Novel plants and processes for obtaining them
US5321011A (en) 1991-10-04 1994-06-14 The University Of Tennessee Research Corporation Pentasaccharide phytohormones and methods for their use
US5331107A (en) 1984-03-06 1994-07-19 Mgi Pharma, Inc. Herbicide resistance in plants
EP0607730A1 (en) 1992-12-24 1994-07-27 International Business Machines Corporation Method of direct transferring of electrically conductive elements into a substrate
WO1994021795A1 (en) 1993-03-25 1994-09-29 Ciba-Geigy Ag Novel pesticidal proteins and strains
US5378824A (en) 1986-08-26 1995-01-03 E. I. Du Pont De Nemours And Company Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase
WO1995004826A1 (en) 1993-08-09 1995-02-16 Institut Für Genbiologische Forschung Berlin Gmbh Debranching enzymes and dna sequences coding them, suitable for changing the degree of branching of amylopectin starch in plants
WO1995009910A1 (en) 1993-10-01 1995-04-13 Mitsubishi Corporation Gene that identifies sterile plant cytoplasm and process for preparing hybrid plant by using the same
US5434283A (en) 1990-04-04 1995-07-18 Pioneer Hi-Bred International, Inc. Edible endogenous vegetable oil extracted from rapeseeds of reduced stearic and palmitic saturated fatty acid content
EP0663956A1 (en) 1992-08-12 1995-07-26 Hoechst Schering AgrEvo GmbH Dna sequences which lead to the formation of polyfructans (levans), plasmids containing these sequences as well as a process for preparing transgenic plants
WO1995026407A1 (en) 1994-03-25 1995-10-05 National Starch And Chemical Investment Holding Corporation Method for producing altered starch from potato plants
US5463175A (en) 1990-06-25 1995-10-31 Monsanto Company Glyphosate tolerant plants
WO1995031553A1 (en) 1994-05-18 1995-11-23 Institut Für Genbiologische Forschung Berlin Gmbh DNA SEQUENCES CODING FOR ENZYMES CAPABLE OF FACILITATING THE SYNTHESIS OF LINEAR α-1,4 GLUCANS IN PLANTS, FUNGI AND MICROORGANISMS
WO1995035026A1 (en) 1994-06-21 1995-12-28 Zeneca Limited Novel plants and processes for obtaining them
WO1996001904A1 (en) 1994-07-08 1996-01-25 Stichting Scheikundig Onderzoek In Nederland Production of oligosaccharides in transgenic plants
EP0709000A1 (en) 1993-07-15 1996-05-01 Siemens Ag METHOD AND DEVICE FOR CONTROLLING A PULSE INVERTER DEVICE COMPRISING A MASTER INVERTER AND AT LEAST ONE SLAVE INVERTER
WO1996015248A1 (en) 1994-11-10 1996-05-23 Hoechst Schering Agrevo Gmbh Dna molecules that code for enzymes involved in starch synthesis, vectors, bacteria, transgenic plant cells and plants containing said molecules
WO1996019581A1 (en) 1994-12-22 1996-06-27 Hoechst Schering Agrevo Gmbh Dna molecules coding for debranching enzymes derived from plants
EP0719338A1 (en) 1993-09-09 1996-07-03 Hoechst Schering AgrEvo GmbH Combination of dna sequences which enable the formation of modified starch in plant cells and plants, processes for the production of these plants and the modified starch obtainable therefrom
WO1996021023A1 (en) 1995-01-06 1996-07-11 Centrum Voor Plantenveredelings- En Reproduktieonderzoek (Cpro - Dlo) Dna sequences encoding carbohydrate polymer synthesizing enzymes and method for producing transgenic plants
US5549718A (en) 1990-04-06 1996-08-27 Centre National De La Recherche Scientifique (C.N.R.S.) Substance with lipo-oligosaccharide structure capable of acting as plant-specific symbiotic signals, processes for producing them and their applications
EP0728213A1 (en) 1993-11-09 1996-08-28 E.I. Du Pont De Nemours And Company Transgenic fructan accumulating crops and methods for their production
WO1996027674A1 (en) 1995-03-08 1996-09-12 Hoechst Schering Agrevo Gmbh Modified starch from plants, plants synthesizing this starch, and process for its preparation
US5561236A (en) 1986-03-11 1996-10-01 Plant Genetic Systems Genetically engineered plant cells and plants exhibiting resistance to glutamine synthetase inhibitors, DNA fragments and recombinants for use in the production of said cells and plants
WO1996033270A1 (en) 1995-04-20 1996-10-24 American Cyanamid Company Structure-based designed herbicide resistant products
WO1996034968A2 (en) 1995-05-05 1996-11-07 National Starch And Chemical Investment Holding Corporation Improvements in or relating to plant starch composition
WO1996038567A2 (en) 1995-06-02 1996-12-05 Rhone-Poulenc Agrochimie Dna sequence of a gene of hydroxy-phenyl pyruvate dioxygenase and production of plants containing a gene of hydroxy-phenyl pyruvate dioxygenase and which are tolerant to certain herbicides
US5605011A (en) 1986-08-26 1997-02-25 E. I. Du Pont De Nemours And Company Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase
WO1997011188A1 (en) 1995-09-19 1997-03-27 Planttec Biotechnologie Gmbh Plants which synthesise a modified starch, process for the production thereof and modified starch
US5637489A (en) 1986-08-23 1997-06-10 Hoechst Aktiengesellschaft Phosphinothricin-resistance gene, and its use
WO1997020936A1 (en) 1995-12-06 1997-06-12 Zeneca Limited Modification of starch synthesis in plants
US5646018A (en) 1992-06-29 1997-07-08 Institut National De La Recherche Agronomique - I.N.R.A. Broad host spectrum rhizobiaceae nodulation signals
WO1997026362A1 (en) 1996-01-16 1997-07-24 Planttec Biotechnologie Gmbh Nucleic acid molecules from plants coding enzymes which participate in the starch synthesis
WO1997032985A1 (en) 1996-03-07 1997-09-12 Planttec Biotechnologie Gmbh Forschung & Entwicklung Nucleic acid molecules coding for debranching enzymes from maize
WO1997041218A1 (en) 1996-04-29 1997-11-06 Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College Herbicide resistant rice
WO1997042328A1 (en) 1996-05-06 1997-11-13 Planttec Biotechnologie Gmbh Nucleic acid molecules which code the potato debranching enzyme
WO1997044472A1 (en) 1996-05-17 1997-11-27 Planttec Biotechnologie Gmbh Nucleic acid molecules coding soluble maize starch synthases
WO1997045545A1 (en) 1996-05-29 1997-12-04 Hoechst Schering Agrevo Gmbh Nucleic acid molecules encoding enzymes from wheat which are involved in starch synthesis
WO1997047807A1 (en) 1996-06-12 1997-12-18 Pioneer Hi-Bred International, Inc. Substitutes for modified starch in paper manufacture
WO1997047808A1 (en) 1996-06-12 1997-12-18 Pioneer Hi-Bred International, Inc. Substitutes for modified starch in paper manufacture
WO1997047806A1 (en) 1996-06-12 1997-12-18 Pioneer Hi-Bred International, Inc. Substitutes for modified starch in paper manufacture
WO1998000549A1 (en) 1996-06-27 1998-01-08 The Australian National University MANIPULATION OF CELLULOSE AND/OR β-1,4-GLUCAN
US5712107A (en) 1995-06-07 1998-01-27 Pioneer Hi-Bred International, Inc. Substitutes for modified starch and latexes in paper manufacture
US5731180A (en) 1991-07-31 1998-03-24 American Cyanamid Company Imidazolinone resistant AHAS mutants
US5739082A (en) 1990-02-02 1998-04-14 Hoechst Schering Agrevo Gmbh Method of improving the yield of herbicide-resistant crop plants
EP0837944A2 (en) 1995-07-19 1998-04-29 Rhone-Poulenc Agrochimie Mutated 5-enol pyruvylshikimate-3-phosphate synthase, gene coding for said protein and transformed plants containing said gene
WO1998020145A2 (en) 1996-11-05 1998-05-14 National Starch And Chemical Investment Holding Corporation Improvements in or relating to starch content of plants
WO1998022604A1 (en) 1996-11-20 1998-05-28 Pioneer Hi-Bred International, Inc. Methods of producing high-oil seed by modification of starch levels
WO1998027212A1 (en) 1996-12-19 1998-06-25 Planttec Biotechnologie Gmbh Novel nucleic acid molecules from maize and their use for the production of modified starch
US5773702A (en) 1996-07-17 1998-06-30 Board Of Trustees Operating Michigan State University Imidazolinone herbicide resistant sugar beet plants
WO1998027806A1 (en) 1996-12-24 1998-07-02 Pioneer Hi-Bred International, Inc. Oilseed brassica containing an improved fertility restorer gene for ogura cytoplasmic male sterility
WO1998032326A2 (en) 1997-01-24 1998-07-30 Pioneer Hi-Bred International, Inc. Methods for $i(agrobacterium)-mediated transformation
WO1998039460A1 (en) 1997-03-04 1998-09-11 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. Nucleic acid molecules from artichoke ($i(cynara scolymus)) encoding enzymes having fructosyl polymerase activity
WO1998040503A1 (en) 1997-03-10 1998-09-17 Planttec Biotechnologie Gmbh Nucleic acid molecules encoding starch phosphorylase from maize
WO1998044140A1 (en) 1997-04-03 1998-10-08 Dekalb Genetics Corporation Glyphosate resistant maize lines
US5824790A (en) 1994-06-21 1998-10-20 Zeneca Limited Modification of starch synthesis in plants
US5840946A (en) 1987-12-31 1998-11-24 Pioneer Hi-Bred International, Inc. Vegetable oil extracted from rapeseeds having a genetically controlled unusually high oleic acid content
WO1999012950A2 (en) 1997-09-06 1999-03-18 National Starch And Chemical Investment Holding Corporation Improvements in or relating to stability of plant starches
WO1999024585A1 (en) 1997-11-07 1999-05-20 Aventis Cropscience S.A. Mutated hydroxy-phenyl pyruvate dioxygenase, dna sequence and method for obtaining herbicide-tolerant plants containing such gene
WO1999024593A1 (en) 1997-11-06 1999-05-20 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. Nucleic acid molecules which encode proteins having fructosyl transferase activity and methods for producing long-chain inulin
US5908810A (en) 1990-02-02 1999-06-01 Hoechst Schering Agrevo Gmbh Method of improving the growth of crop plants which are resistant to glutamine synthetase inhibitors
WO1999034008A1 (en) 1997-12-24 1999-07-08 Aventis Cropscience S.A. Method for enzymatic preparation of homogentisate
US5928937A (en) 1995-04-20 1999-07-27 American Cyanamid Company Structure-based designed herbicide resistant products
US5965755A (en) 1993-10-12 1999-10-12 Agrigenetics, Inc. Oil produced from the Brassica napus
US5969169A (en) 1993-04-27 1999-10-19 Cargill, Incorporated Non-hydrogenated canola oil for food applications
WO1999053072A1 (en) 1998-04-09 1999-10-21 E.I. Du Pont De Nemours And Company Starch r1 phosphorylation protein homologs
WO1999058688A2 (en) 1998-05-08 1999-11-18 Aventis Cropscience Gmbh Nucleic acid molecules which code for enzymes derived from wheat and which are involved in the synthesis of starch
WO1999058690A2 (en) 1998-05-08 1999-11-18 Aventis Cropscience Gmbh Nucleic acid molecules which code for enzymes derived from wheat and which are involved in the synthesis of starch
WO1999058654A2 (en) 1998-05-13 1999-11-18 Planttec Biotechnologie Gmbh Forschung & Entwicklung Transgenic plants with a modified activity of a plastidial adp/atp translocator
WO1999057965A1 (en) 1998-05-14 1999-11-18 Aventis Cropscience Gmbh Sulfonylurea-tolerant sugar beet mutants
WO1999066050A1 (en) 1998-06-15 1999-12-23 National Starch And Chemical Investment Holding Corporation Improvements in or relating to plants and plant products
US6013861A (en) 1989-05-26 2000-01-11 Zeneca Limited Plants and processes for obtaining them
WO2000004173A1 (en) 1998-07-17 2000-01-27 Aventis Cropscience N.V. Methods and means to modulate programmed cell death in eukaryotic cells
WO2000008184A1 (en) 1998-07-31 2000-02-17 Aventis Cropscience Gmbh Plants which synthesize a modified starch, methods for producing the plants, their use, and the modified starch
WO2000008185A1 (en) 1998-07-31 2000-02-17 Aventis Cropscience Gmbh Nucleic acid molecule coding for beta-amylase, plants synthesizing a modified starch, method of production and applications
WO2000008175A2 (en) 1998-07-31 2000-02-17 Aventis Cropscience Gmbh Nucleic acid module coding for alpha glucosidase, plants that synthesize modified starch, methods for the production and use of said plants, and modified starch
WO2000011192A2 (en) 1998-08-25 2000-03-02 Pioneer Hi-Bred International, Inc. Plant glutamine: fructose-6-phosphate amidotransferase nucleic acids
WO2000014249A1 (en) 1998-09-02 2000-03-16 Planttec Biotechnologie Gmbh Nucleic acid molecules encoding an amylosucrase
WO2000022140A1 (en) 1998-10-09 2000-04-20 Planttec Biotechnologie Gmbh Forschung & Entwicklung NUCLEIC ACID MOLECULES WHICH CODE A BRANCHING ENZYME FROM BACTERIA OF THE GENUS NEISSERIA, AND A METHOD FOR PRODUCING α-1,6-BRANCHED α-1,4-GLUCANS
WO2000026345A1 (en) 1998-11-03 2000-05-11 Aventis Cropscience N.V. Glufosinate tolerant rice
WO2000026356A1 (en) 1998-11-03 2000-05-11 Aventis Cropscience N. V. Glufosinate tolerant rice
US6063947A (en) 1996-07-03 2000-05-16 Cargill, Incorporated Canola oil having increased oleic acid and decreased linolenic acid content
WO2000028052A2 (en) 1998-11-09 2000-05-18 Planttec Biotechnologie Gmbh Nucleic acid molecules from rice encoding an r1 protein and their use for the production of modified starch
WO2000047727A2 (en) 1999-02-08 2000-08-17 Planttec Biotechnologie Gmbh Forschung & Entwicklung Nucleic acid molecules encoding alternansucrase
WO2000066746A1 (en) 1999-04-29 2000-11-09 Syngenta Limited Herbicide resistant plants
WO2000066747A1 (en) 1999-04-29 2000-11-09 Syngenta Limited Herbicide resistant plants
WO2000073422A1 (en) 1999-05-27 2000-12-07 Planttec Biotechnologie Gmbh Genetically modified plant cells and plants with an increased activity of an amylosucrase protein and a branching enzyme
WO2000077229A2 (en) 1999-06-11 2000-12-21 Aventis Cropscience Gmbh R1 protein from wheat and the use thereof for the production of modified strach
WO2001012826A2 (en) 1999-08-11 2001-02-22 Aventis Cropscience Gmbh Nucleic acid molecules derived from plants which code for enzymes which are involved in the synthesis of starch
WO2001012782A2 (en) 1999-08-12 2001-02-22 Aventis Cropscience Gmbh Transgenically modified plant cells and plants having modified gbssi- and be-protein activity
WO2001014569A2 (en) 1999-08-20 2001-03-01 Basf Plant Science Gmbh Increasing the polysaccharide content in plants
WO2001017333A1 (en) 1999-09-10 2001-03-15 Texas Tech University Transgenic fiber producing plants with increased expression of sucrose phosphate synthase
WO2001019975A2 (en) 1999-09-15 2001-03-22 National Starch And Chemical Investment Holding Corporation Plants having reduced activity in two or more starch-modifying enzymes
WO2001024615A1 (en) 1999-10-07 2001-04-12 Valigen (Us), Inc. Non-transgenic herbicide resistant plants
WO2001031042A2 (en) 1999-10-29 2001-05-03 Aventis Cropscience N.V. Male-sterile brassica plants and methods for producing same
US6229072B1 (en) 1995-07-07 2001-05-08 Adventa Technology Ltd Cytoplasmic male sterility system production canola hybrids
WO2001041558A1 (en) 1999-12-08 2001-06-14 Aventis Cropscience N.V. Hybrid winter oilseed rape and methods for producing same
WO2001051654A2 (en) 2000-01-11 2001-07-19 Bayer Cropscience N.V. Methods and kits for identifying elite event gat-zm1 in biological samples
US6270828B1 (en) 1993-11-12 2001-08-07 Cargrill Incorporated Canola variety producing a seed with reduced glucosinolates and linolenic acid yielding an oil with low sulfur, improved sensory characteristics and increased oxidative stability
US6284479B1 (en) 1995-06-07 2001-09-04 Pioneer Hi-Bred International, Inc. Substitutes for modified starch and latexes in paper manufacture
WO2001066704A2 (en) 2000-03-09 2001-09-13 Monsanto Technology Llc Methods for making plants tolerant to glyphosate and compositions thereof
WO2001065922A2 (en) 2000-03-09 2001-09-13 E. I. Du Pont De Nemours And Company Sulfonylurea-tolerant sunflower plants
EP1135600A1 (en) 1999-10-06 2001-09-26 Robert Bosch Gmbh Fuel high pressure accumulator
EP1135601A1 (en) 1998-11-12 2001-09-26 Volvo Lastvagnar AB Fuel delivery system
US6323392B1 (en) 1999-03-01 2001-11-27 Pioneer Hi-Bred International, Inc. Formation of brassica napus F1 hybrid seeds which exhibit a highly elevated oleic acid content and a reduced linolenic acid content in the endogenously formed oil of the seeds
WO2001098509A2 (en) 2000-06-21 2001-12-27 Syngenta Participations Ag Grain processing method and transgenic plants useful therein
WO2002026995A1 (en) 2000-09-29 2002-04-04 Syngenta Limited Herbicide resistant plants
WO2002034946A2 (en) 2000-10-25 2002-05-02 Monsanto Technology Llc Cotton event pv-ghgt07(1445) and compositions and methods for detection thereof
WO2002034923A2 (en) 2000-10-23 2002-05-02 Bayer Cropscience Gmbh Monocotyledon plant cells and plants which synthesise modified starch
WO2002036787A2 (en) 2000-10-30 2002-05-10 Bayer Cropscience S.A. Herbicide-tolerant plants through bypassing metabolic pathway
WO2002036782A2 (en) 2000-10-30 2002-05-10 Maxygen, Inc. Novel glyphosate n-acetyltransferase (gat) genes
WO2002036831A2 (en) 2000-10-30 2002-05-10 Monsanto Technology Llc Canola event pv-bngt04(rt73) and compositions and methods for detection thereof
WO2002044407A2 (en) 2000-11-30 2002-06-06 Ses Europe N.V. Glyphosate resistant transgenic sugar beet characterised by a specific transgene insertion (t227-1), methods and primers for the detection of said insertion
WO2002046387A2 (en) 2000-12-07 2002-06-13 Syngenta Limited Plant derived hydroxy phenyl pyruvate dioxygenases (hppd) resistant against triketone herbicides and transgenic plants containing these dioxygenases
WO2002045485A1 (en) 2000-12-08 2002-06-13 Commonwealth Scienctific And Industrial Research Organisation Modification of sucrose synthase gene expression in plant tissue and uses therefor
US20020102582A1 (en) 2000-09-13 2002-08-01 Levine Elaine B. Corn event MON810 and compositions and methods for detection thereof
WO2002079410A2 (en) 2001-03-30 2002-10-10 Basf Plant Science Gmbh Glucan chain length domains
WO2002100163A2 (en) 2001-06-11 2002-12-19 Monsanto Technology Llc Cotton event moni5985 and compositions and methods for detection
WO2002101059A2 (en) 2001-06-12 2002-12-19 Bayer Cropscience Gmbh Transgenic plants synthesising high amylose starch
WO2003013224A2 (en) 2001-08-06 2003-02-20 Bayer Bioscience N.V. Herbicide tolerant cotton plants and methods for producing and identifying same
WO2003013226A2 (en) 2001-08-09 2003-02-20 Cibus Genetics Non-transgenic herbicide resistant plants
WO2003033540A2 (en) 2001-10-17 2003-04-24 Basf Plant Science Gmbh Starch
WO2003052073A2 (en) 2001-12-17 2003-06-26 Syngenta Participations Ag Novel corn event
US20030126634A1 (en) 1990-08-09 2003-07-03 Dekalb Genetics Corporation Methods and compositions for the increase of yield in plants
WO2003071860A2 (en) 2002-02-26 2003-09-04 Bayer Cropscience Gmbh Method for generating maize plants with an increased leaf starch content, and their use for making maize silage
WO2003092360A2 (en) 2002-04-30 2003-11-13 Verdia, Inc. Novel glyphosate-n-acetyltransferase (gat) genes
WO2004011601A2 (en) 2002-07-29 2004-02-05 Monsanto Technology, Llc Corn event pv-zmir13 (mon863) plants and compositions and methods for detection thereof
WO2004024928A2 (en) 2002-09-11 2004-03-25 Bayer Cropscience S.A. Transformed plants with enhanced prenylquinone biosynthesis
US6734341B2 (en) 1999-09-02 2004-05-11 Pioneer Hi-Bred International, Inc. Starch synthase polynucleotides and their use in the production of new starches
WO2004039986A1 (en) 2002-10-29 2004-05-13 Syngenta Participations Ag Cot102 insecticidal cotton
WO2004040012A2 (en) 2002-10-29 2004-05-13 Basf Plant Science Gmbh Compositions and methods for identifying plants having increased tolerance to imidazolinone herbicides
WO2004053219A2 (en) 2002-12-05 2004-06-24 Jentex Corporation Abrasive webs and methods of making the same
WO2004053062A2 (en) 2002-12-05 2004-06-24 Monsanto Technology Llc Bentgrass event asr-368 and compositions and methods for detection thereof
WO2004056999A1 (en) 2002-12-19 2004-07-08 Bayer Cropscience Gmbh Plant cells and plants which synthesize a starch with an increased final viscosity
US6768044B1 (en) 2000-05-10 2004-07-27 Bayer Cropscience Sa Chimeric hydroxyl-phenyl pyruvate dioxygenase, DNA sequence and method for obtaining plants containing such a gene, with herbicide tolerance
WO2004072235A2 (en) 2003-02-12 2004-08-26 Monsanto Technology Llc Cotton event mon 88913 and compositions and methods for detection thereof
US20040172669A1 (en) 2003-02-28 2004-09-02 Josef Kraus Glyphosate tolerant sugar beet
WO2004074492A1 (en) 2003-02-20 2004-09-02 Kws Saat Ag Glyphosate tolerant sugar beet
WO2004078983A2 (en) 2003-03-07 2004-09-16 Basf Plant Science Gmbh Enhanced amylose production in plants
WO2004090140A2 (en) 2003-04-09 2004-10-21 Bayer Bioscience N.V. Methods and means for increasing the tolerance of plants to stress conditions
WO2004099447A2 (en) 2003-05-02 2004-11-18 Dow Agrosciences Llc Corn event tc1507 and methods for detection thereof
WO2004106529A2 (en) 2003-05-28 2004-12-09 Basf Aktiengesellschaft Wheat plants having increased tolerance to imidazolinone herbicides
WO2005002359A2 (en) 2003-05-22 2005-01-13 Syngenta Participations Ag Modified starch, uses, methods for production thereof
WO2005002324A2 (en) 2003-07-04 2005-01-13 Institut National De La Recherche Agronomique Method of producing double low restorer lines of brassica napus having a good agronomic value
WO2005012515A2 (en) 2003-04-29 2005-02-10 Pioneer Hi-Bred International, Inc. Novel glyphosate-n-acetyltransferase (gat) genes
WO2005012529A1 (en) 2003-07-31 2005-02-10 Toyo Boseki Kabushiki Kaisha Plant producing hyaluronic acid
WO2005017157A1 (en) 2003-08-15 2005-02-24 Commonwealth Scientific And Industrial Research Organisation (Csiro) Methods and means for altering fiber characteristics in fiber-producing plants
WO2005020673A1 (en) 2003-08-29 2005-03-10 Instituto Nacional De Technologia Agropecuaria Rice plants having increased tolerance to imidazolinone herbicides
WO2005030941A1 (en) 2003-09-30 2005-04-07 Bayer Cropscience Gmbh Plants with increased activity of a class 3 branching enzyme
WO2005030942A1 (en) 2003-09-30 2005-04-07 Bayer Cropscience Gmbh Plants with reduced activity of a class 3 branching enzyme
WO2005054480A2 (en) 2003-12-01 2005-06-16 Syngenta Participations Ag Insect resistant cotton plants and methods of detecting the same
WO2005054479A1 (en) 2003-12-01 2005-06-16 Syngenta Participations Ag Insect resistant cotton plants and methods of detecting the same
WO2005059103A2 (en) 2003-12-15 2005-06-30 Monsanto Technology Llc Corn plant mon88017 and compositions and methods for detection thereof
WO2005061720A2 (en) 2003-12-11 2005-07-07 Monsanto Technology Llc High lysine maize compositions and methods for detection thereof
WO2005063784A1 (en) 2003-12-30 2005-07-14 Bayer Cropscience Sa Synthetic compounds useful as nodulation agents of leguminous plants and preparation processes thereof
WO2005077177A2 (en) 2004-02-10 2005-08-25 Universite Paul Sabatier Toulouse Iii Modulators of the development of mychorrizal fungi with arbuscules, and uses thereof
US20050216969A1 (en) 2004-03-26 2005-09-29 Dow Agrosciences Llc Cry1F and Cry1AC transgenic cotton lines and event-specific identification thereof
WO2005093093A2 (en) 2004-03-22 2005-10-06 Basf Aktiengesellschaft Methods and compositions for analyzing ahasl genes
WO2005095618A2 (en) 2004-03-05 2005-10-13 Bayer Cropscience Gmbh Plants with reduced activity of the starch phosphorylating enzyme phosphoglucan, water dikinase
WO2005095619A1 (en) 2004-03-05 2005-10-13 Bayer Cropscience Gmbh Plants with increased activity of multiple starch phosphorylating enzymes
WO2005095632A2 (en) 2004-03-05 2005-10-13 Bayer Cropscience Gmbh Methods for identifying proteins with starch phosphorylating enzymatic activity
WO2005095617A2 (en) 2004-03-05 2005-10-13 Bayer Cropscience Gmbh Plants with increased activity of a starch phosphorylating enzyme
WO2005103301A2 (en) 2004-03-25 2005-11-03 Syngenta Participations Ag Corn event mir604
WO2005107471A1 (en) 2004-05-12 2005-11-17 Bayer Cropscience Gmbh Plant growth regulation
WO2005107466A1 (en) 2004-05-12 2005-11-17 Bayer Cropscience Gmbh Plant growth regulation
WO2005107465A1 (en) 2004-05-12 2005-11-17 Bayer Cropscience Gmbh Plant growth regulation
WO2005107472A1 (en) 2004-05-12 2005-11-17 Bayer Cropscience Gmbh Plant growth regulation
WO2005123927A1 (en) 2004-06-21 2005-12-29 Bayer Cropscience Gmbh Plants that produce amylopectin starch with novel properties
WO2006007373A2 (en) 2004-06-16 2006-01-19 Basf Plant Science Gmbh Polynucleotides encoding mature ahasl proteins for creating imidazolinone-tolerant plants
WO2006015376A2 (en) 2004-08-04 2006-02-09 Basf Plant Science Gmbh Monocot ahass sequences and methods of use
WO2006018319A1 (en) 2004-08-18 2006-02-23 Bayer Cropscience Gmbh Plants with increased plastidic activity of r3 starch-phosphorylating enzyme
WO2006021972A1 (en) 2004-08-26 2006-03-02 Dhara Vegetable Oil And Foods Company Limited A novel cytoplasmic male sterility system for brassica species and its use for hybrid seed production in indian oilseed mustard brassica juncea
WO2006024351A1 (en) 2004-07-30 2006-03-09 Basf Agrochemical Products B.V. Herbicide-resistant sunflower plants, plynucleotides encoding herbicide-resistant acetohydroxy acid synthase large subunit proteins, and methods of use
WO2006032538A1 (en) 2004-09-23 2006-03-30 Bayer Cropscience Gmbh Methods and means for producing hyaluronan
US20060070139A1 (en) 2004-09-29 2006-03-30 Pioneer Hi-Bred International, Inc. Corn event DAS-59122-7 and methods for detection thereof
WO2006045633A1 (en) 2004-10-29 2006-05-04 Bayer Bioscience N.V. Stress tolerant cotton plants
WO2006060634A2 (en) 2004-12-01 2006-06-08 Basf Agrochemical Products, B.V. Novel mutation involved in increased tolerance to imidazolinone herbicides in plants
WO2006063862A1 (en) 2004-12-17 2006-06-22 Bayer Cropscience Ag Transformed plant expressing a dextransucrase and synthesizing a modified starch
WO2006072603A2 (en) 2005-01-10 2006-07-13 Bayer Cropscience Ag Transformed plant expressing a mutansucrase and synthesizing a modified starch
WO2006098952A2 (en) 2005-03-16 2006-09-21 Syngenta Participations Ag Corn event 3272 and methods of detection thereof
WO2006103107A1 (en) 2005-04-01 2006-10-05 Bayer Cropscience Ag Phosphorylated waxy potato starch
WO2006108702A1 (en) 2005-04-08 2006-10-19 Bayer Cropscience Ag High-phosphate starch
WO2006108674A2 (en) 2005-04-08 2006-10-19 Bayer Bioscience N.V. Elite event a2704-12 and methods and kits for identifying such event in biological samples
WO2006108675A2 (en) 2005-04-11 2006-10-19 Bayer Bioscience N.V. Elite event a5547-127 and methods and kits for identifying such event in biological samples
JP2006304779A (en) 2005-03-30 2006-11-09 Toyobo Co Ltd Hexosamine high production plant
WO2006128573A2 (en) 2005-06-02 2006-12-07 Syngenta Participations Ag Ce43- 67b, insecticidal transgenic cotton expressing cry1ab
WO2006129204A2 (en) 2005-05-31 2006-12-07 Devgen Nv Rnai for control of insects and arachnids
WO2006128569A2 (en) 2005-06-02 2006-12-07 Syngenta Participations Ag 1143-14a, insecticidal transgenic cotton expressing cry1ab
WO2006130436A2 (en) 2005-05-27 2006-12-07 Monsanto Technology Llc Soybean event mon89788 and methods for detection thereof
WO2006128568A2 (en) 2005-06-02 2006-12-07 Syngenta Participations Ag T342-142, insecticidal transgenic cotton expressing cry1ab
WO2006128571A2 (en) 2005-06-02 2006-12-07 Syngenta Participations Ag Ce44-69d , insecticidal transgenic cotton expressing cry1ab
WO2006128572A1 (en) 2005-06-02 2006-12-07 Syngenta Participations Ag Ce46-02a insecticidal cotton
WO2006128570A1 (en) 2005-06-02 2006-12-07 Syngenta Participations Ag 1143-51b insecticidal cotton
WO2006133827A2 (en) 2005-06-15 2006-12-21 Bayer Bioscience N.V. Methods for increasing the resistance of plants to hypoxic conditions
WO2006136351A2 (en) 2005-06-24 2006-12-28 Bayer Bioscience N.V. Methods for altering the reactivity of plant cell walls
WO2007009823A1 (en) 2005-07-22 2007-01-25 Bayer Cropscience Ag Overexpression of starch synthase in plants
WO2007017186A1 (en) 2005-08-08 2007-02-15 Bayer Bioscience N.V. Herbicide tolerant cotton plants and methods for identifying same
WO2007024782A2 (en) 2005-08-24 2007-03-01 Pioneer Hi-Bred International, Inc. Compositions providing tolerance to multiple herbicides and methods of use thereof
WO2007027777A2 (en) 2005-08-31 2007-03-08 Monsanto Technology Llc Nucleotide sequences encoding insecticidal proteins
WO2007035650A2 (en) 2005-09-16 2007-03-29 Monsanto Technology Llc Methods for genetic control of insect infestations in plants and compositions thereof
WO2007039314A2 (en) 2005-10-05 2007-04-12 Bayer Cropscience Ag Plants with increased hyaluronan production
WO2007039315A1 (en) 2005-10-05 2007-04-12 Bayer Cropscience Ag Plants with an increased production of hyaluronan ii
WO2007039316A1 (en) 2005-10-05 2007-04-12 Bayer Cropscience Ag Improved methods and means for producings hyaluronan
EP1794306A2 (en) 2004-09-24 2007-06-13 Bayer BioScience N.V. Stress resistant plants
WO2007074405A2 (en) 2005-09-16 2007-07-05 Devgen Nv Dsrna as insect control agent
WO2007080127A2 (en) 2006-01-12 2007-07-19 Devgen N.V. Dsrna as insect control agent
WO2007080126A2 (en) 2006-01-12 2007-07-19 Devgen N.V. Dsrna as insect control agent
WO2007091277A2 (en) 2006-02-10 2007-08-16 Maharashtra Hybrid Seeds Company Limited (Mahyco) TRANSGENIC BRINJAL (SOLANUM MELONGENA) EXPRESSING THE CRYlAC GENE
WO2007103567A2 (en) 2006-03-09 2007-09-13 E. I. Dupont De Nemours & Company Polynucleotide encoding a maize herbicide resistance gene and methods for use
WO2007107302A2 (en) 2006-03-21 2007-09-27 Bayer Bioscience N.V. Novel genes encoding insecticidal proteins
WO2007107326A1 (en) 2006-03-21 2007-09-27 Bayer Bioscience N.V. Stress resistant plants
WO2007140256A1 (en) 2006-05-26 2007-12-06 Monsanto Technology, Llc Corn plant and seed corresponding to transgenic event mon89034 and methods for detection and use thereof
WO2007142840A2 (en) 2006-06-03 2007-12-13 Syngenta Participations Ag Corn event mir162
US20070292854A1 (en) 2000-06-22 2007-12-20 Behr Carl F Corn event PV-ZMGT32(nk603) and compositions and methods for detection thereof
WO2008002872A2 (en) 2006-06-28 2008-01-03 Pioneer Hi-Bred International, Inc. Soybean event 3560.4.3.5 and compositions and methods for the identification and/or detection thereof
WO2008007167A1 (en) 2006-07-07 2008-01-17 Societe Bic Writing instrument with cushioning device
WO2008017518A1 (en) 2006-08-09 2008-02-14 Bayer Cropscience Ag Genetically modified plants which synthesize a starch having increased swelling power
US20080064032A1 (en) 2006-09-13 2008-03-13 Syngenta Participations Ag Polynucleotides and uses thereof
WO2008054747A2 (en) 2006-10-31 2008-05-08 E. I. Du Pont De Nemours And Company Soybean event dp-305423-1 and compositions and methods for the identification and/or detection thereof
WO2008071672A2 (en) 2006-12-12 2008-06-19 Bayer Cropscience Sa Pesticidal composition comprising a synthetic compound useful as nodulation agent of leguminous plants and a fungicide compound
WO2008080631A1 (en) 2006-12-29 2008-07-10 Bayer Cropscience Ag Process for modifying the thermal and/or digestion properties of corn starches and corn flours
WO2008080630A1 (en) 2006-12-29 2008-07-10 Bayer Cropscience Ag Corn starch and also corn flours and food comprising this corn starch
WO2008085958A1 (en) 2007-01-09 2008-07-17 Merck Patent Gmbh Lipo-chitooligosaccharide combination compositions for enhanced plant growth and yield
WO2008090008A1 (en) 2007-01-26 2008-07-31 Bayer Cropscience Ag Genetically modified plants which synthesize a low amylose starch with increased swelling power
WO2008112019A2 (en) 2006-10-30 2008-09-18 Pioneer Hi-Bred International, Inc. Maize event dp-098140-6 and compositions and methods for the identification and/or detection thereof
WO2008114282A2 (en) 2007-03-19 2008-09-25 Maharashtra Hybrid Seeds Company Limited Transgenic rice (oryza sativa) comprising pe-7 event and method of detection thereof
WO2008122406A1 (en) 2007-04-05 2008-10-16 Bayer Bioscience N.V. Insect resistant cotton plants and methods for identifying same
WO2008150473A2 (en) 2007-05-30 2008-12-11 Syngenta Participations Ag Cytochrome p450 genes conferring herbicide resistance
WO2008152091A2 (en) * 2007-06-15 2008-12-18 Bayer Cropscience Sa Pesticidal composition comprising a strigolactone derivative and an insecticide compound
WO2008151780A1 (en) 2007-06-11 2008-12-18 Bayer Bioscience N.V. Insect resistant cotton plants comprising elite event ee-gh6 and methods for identifying same
WO2008152092A2 (en) 2007-06-15 2008-12-18 Bayer Cropscience Sa Pesticidal composition comprising a strigolactone derivative and an fungicide compound
EP2018431A2 (en) 2006-05-12 2009-01-28 Bayer BioScience N.V. Novel stress-related microrna molecules and uses thereof
WO2009049747A2 (en) 2007-10-16 2009-04-23 Merck Patent Gmbh Lipo-chitooligosaccharide and flavonoid combination for enhanced plant growth and yield
US20090130071A1 (en) 2007-11-15 2009-05-21 Ai-Guo Gao Soybean Plant And Seed Corresponding To Transgenic Event MON87701 And Methods For Detection Thereof
US20090137395A1 (en) 2006-10-30 2009-05-28 Pioneer Hi-Bred International, Inc. Maize event DP-098140-6 and compositions and methods for the identification and/or detection thereof
WO2009068313A2 (en) 2007-11-28 2009-06-04 Bayer Bioscience N.V. Brassica plant comprising a mutant indehiscent allele
WO2009100188A2 (en) 2008-02-08 2009-08-13 Dow Agrosciences Llc Methods for detection of corn event das-59132
WO2009102873A1 (en) 2008-02-15 2009-08-20 Monsanto Technology Llc Soybean plant and seed corresponding to transgenic event mon87769 and methods for detection thereof
US20090210970A1 (en) 2008-02-14 2009-08-20 Pioneer Hi-Bred International, Inc. Plant Genomic DNA Flanking SPT Event and Methods for Identifying SPT Event
WO2009111263A1 (en) 2008-02-29 2009-09-11 Monsanto Technology Llc Corn plant event mon87460 and compositions and methods for detection thereof
WO2009144079A1 (en) 2008-04-14 2009-12-03 Bayer Bioscience N.V. New mutated hydroxyphenylpyruvate dioxygenase, dna sequence and isolation of plants which are tolerant to hppd inhibitor herbicides
WO2009143995A1 (en) 2008-05-26 2009-12-03 Bayer Bioscience N.V. Methods and means to modify fiber strength in fiber-producing plants
WO2010003701A1 (en) 2008-07-10 2010-01-14 Bayer Cropscience Ag Wheat starch and wheat flours and foodstuffs containing these wheat starch/wheat flours
WO2010006732A2 (en) 2008-07-17 2010-01-21 Bayer Bioscience N.V. Brassica plant comprising a mutant indehiscent allelle
WO2010012796A1 (en) 2008-08-01 2010-02-04 Bayer Bioscience N.V. A method for increasing photosynthetic carbon fixation in rice
WO2010024976A1 (en) 2008-08-29 2010-03-04 Monsanto Technology Llc Soybean plant and seed corresponding to transgenic event mon87754 and methods for detection thereof
US20100080887A1 (en) 2008-09-29 2010-04-01 Monsanto Technology Llc Soybean Transgenic Event MON87705 and Methods for Detection Thereof
WO2010077816A1 (en) 2008-12-16 2010-07-08 Syngenta Participations Ag Corn event 5307
WO2010076212A1 (en) 2008-12-19 2010-07-08 Syngenta Participations Ag Transgenic sugar beet event gm rz13
WO2010080829A1 (en) 2009-01-07 2010-07-15 Basf Agrochemical Products B.V. Soybean event 127 and methods related thereto
WO2010117737A1 (en) 2009-03-30 2010-10-14 Monsanto Technology Llc Rice transgenic event17053 and methods of use thereof
WO2010117735A1 (en) 2009-03-30 2010-10-14 Monsanto Technology Llc Transgenic rice event17314 and methods of use thereof
WO2010121818A1 (en) 2009-04-22 2010-10-28 Bayer Bioscience N.V. Production of multi-antennary n-glycan structures in plants
WO2010125065A2 (en) 2009-04-28 2010-11-04 Bayer Cropscience Ag Compositions comprising a strigolactone compound and a chito-oligosaccharide compound for enhanced plant growth and yield
WO2010145846A1 (en) 2009-06-15 2010-12-23 Bayer Bioscience N.V. Nicotiana benthamiana plants deficient in xylosyltransferase activity
WO2011022469A2 (en) 2009-08-19 2011-02-24 Dow Agrosciences Llc Aad-1 event das-40278-9, related transgenic corn lines, and event-specific identification thereof
WO2011034704A1 (en) 2009-09-17 2011-03-24 Monsanto Technology Llc Soybean transgenic event mon 87708 and methods of use thereof
EP2300618A1 (en) 2008-06-13 2011-03-30 Bayer BioScience N.V. Bollworm insect resistance management in transgenic plants
WO2011062904A1 (en) 2009-11-23 2011-05-26 Monsanto Technology Llc Transgenic maize event mon 87427 and the relative development scale
WO2011066384A1 (en) 2009-11-24 2011-06-03 Dow Agrosciences Llc Aad-12 event 416, related transgenic soybean lines, and event-specific identification thereof
WO2011066360A1 (en) 2009-11-24 2011-06-03 Dow Agrosciences Llc Detection of aad-12 soybean event 416
WO2011075593A1 (en) 2009-12-17 2011-06-23 Pioneer Hi-Bred International, Inc. Maize event dp-040416-8 and methods for detection thereof
WO2011075595A1 (en) 2009-12-17 2011-06-23 Pioneer Hi-Bred International, Inc. Maize event dp-043a47-3 and methods for detection thereof
WO2011084621A1 (en) 2009-12-17 2011-07-14 Pioneer Hi-Bred International, Inc. Maize event dp-004114-3 and methods for detection thereof
WO2011084632A1 (en) 2009-12-17 2011-07-14 Pioneer Hi-Bred International, Inc. Maize event dp-032316-8 and methods for detection thereof
EP2380876A1 (en) * 2008-12-19 2011-10-26 Nippon Soda Co., Ltd. 1-heterodiene derivative and harmful organism control agent
WO2011153442A1 (en) 2010-06-04 2011-12-08 Syngenta Participations Ag Plant irrigation methods

Patent Citations (335)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2036008A (en) 1934-11-07 1936-03-31 White Martin Henry Plug fuse
US2289060A (en) 1940-03-12 1942-07-07 Merkle Corp Method of and apparatus for utilizing dry ice
US4761373A (en) 1984-03-06 1988-08-02 Molecular Genetics, Inc. Herbicide resistance in plants
US5304732A (en) 1984-03-06 1994-04-19 Mgi Pharma, Inc. Herbicide resistance in plants
US5331107A (en) 1984-03-06 1994-07-19 Mgi Pharma, Inc. Herbicide resistance in plants
US7112665B1 (en) 1986-03-11 2006-09-26 Bayer Bioscience N.V. Genetically engineered plant cells and plants exhibiting resistance to glutamine synthetase inhibitors, DNA fragments and recombinants for use in the production of said cells and plants
US5561236A (en) 1986-03-11 1996-10-01 Plant Genetic Systems Genetically engineered plant cells and plants exhibiting resistance to glutamine synthetase inhibitors, DNA fragments and recombinants for use in the production of said cells and plants
US5646024A (en) 1986-03-11 1997-07-08 Plant Genetic Systems, N.V. Genetically engineered plant cells and plants exhibiting resistance to glutamine synthetase inhibitors, DNA fragments and recombinants for use in the production of said cells and plants
US5648477A (en) 1986-03-11 1997-07-15 Plant Genetic Systems, N.V. Genetically engineered plant cells and plants exhibiting resistance to glutamine synthetase inhibitors, DNA fragments and recombinants for use in the production of said cells and plants
US5273894A (en) 1986-08-23 1993-12-28 Hoechst Aktiengesellschaft Phosphinothricin-resistance gene, and its use
US5276268A (en) 1986-08-23 1994-01-04 Hoechst Aktiengesellschaft Phosphinothricin-resistance gene, and its use
US5637489A (en) 1986-08-23 1997-06-10 Hoechst Aktiengesellschaft Phosphinothricin-resistance gene, and its use
US5605011A (en) 1986-08-26 1997-02-25 E. I. Du Pont De Nemours And Company Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase
US5378824A (en) 1986-08-26 1995-01-03 E. I. Du Pont De Nemours And Company Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase
US5013659A (en) 1987-07-27 1991-05-07 E. I. Du Pont De Nemours And Company Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase
US5141870A (en) 1987-07-27 1992-08-25 E. I. Du Pont De Nemours And Company Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase
US5840946A (en) 1987-12-31 1998-11-24 Pioneer Hi-Bred International, Inc. Vegetable oil extracted from rapeseeds having a genetically controlled unusually high oleic acid content
WO1989010396A1 (en) 1988-04-28 1989-11-02 Plant Genetic Systems N.V. Plants with modified stamen cells
US5084082A (en) 1988-09-22 1992-01-28 E. I. Du Pont De Nemours And Company Soybean plants with dominant selectable trait for herbicide resistance
US6013861A (en) 1989-05-26 2000-01-11 Zeneca Limited Plants and processes for obtaining them
WO1991002069A1 (en) 1989-08-10 1991-02-21 Plant Genetic Systems N.V. Plants with modified flowers
US5908810A (en) 1990-02-02 1999-06-01 Hoechst Schering Agrevo Gmbh Method of improving the growth of crop plants which are resistant to glutamine synthetase inhibitors
US5739082A (en) 1990-02-02 1998-04-14 Hoechst Schering Agrevo Gmbh Method of improving the yield of herbicide-resistant crop plants
US5434283A (en) 1990-04-04 1995-07-18 Pioneer Hi-Bred International, Inc. Edible endogenous vegetable oil extracted from rapeseeds of reduced stearic and palmitic saturated fatty acid content
US5549718A (en) 1990-04-06 1996-08-27 Centre National De La Recherche Scientifique (C.N.R.S.) Substance with lipo-oligosaccharide structure capable of acting as plant-specific symbiotic signals, processes for producing them and their applications
US5198599A (en) 1990-06-05 1993-03-30 Idaho Resarch Foundation, Inc. Sulfonylurea herbicide resistance in plants
US5776760A (en) 1990-06-25 1998-07-07 Monsanto Company Glyphosate tolerant plants
US5463175A (en) 1990-06-25 1995-10-31 Monsanto Company Glyphosate tolerant plants
US20030126634A1 (en) 1990-08-09 2003-07-03 Dekalb Genetics Corporation Methods and compositions for the increase of yield in plants
WO1992005251A1 (en) 1990-09-21 1992-04-02 Institut National De La Recherche Agronomique Dna sequence imparting cytoplasmic male sterility, mitochondrial genome, nuclear genome, mitochondria and plant containing said sequence and process for the preparation of hybrids
EP0571427A1 (en) 1991-02-13 1993-12-01 Hoechst Schering AgrEvo GmbH Plasmids containing dna-sequences that cause changes in the carbohydrate concentration and the carbohydrate composition in plants, as well as plant cells and plants containing these plasmids
US5767361A (en) 1991-07-31 1998-06-16 American Cyanamid Company Imidazolinone resistant AHAS mutants
US5731180A (en) 1991-07-31 1998-03-24 American Cyanamid Company Imidazolinone resistant AHAS mutants
US5175149A (en) 1991-10-04 1992-12-29 The University Of Tennessee Research Corporation Pentasaccharide phytohormones and methods for their use
US5321011A (en) 1991-10-04 1994-06-14 The University Of Tennessee Research Corporation Pentasaccharide phytohormones and methods for their use
US5646018A (en) 1992-06-29 1997-07-08 Institut National De La Recherche Agronomique - I.N.R.A. Broad host spectrum rhizobiaceae nodulation signals
EP0663956A1 (en) 1992-08-12 1995-07-26 Hoechst Schering AgrEvo GmbH Dna sequences which lead to the formation of polyfructans (levans), plasmids containing these sequences as well as a process for preparing transgenic plants
WO1994004693A2 (en) 1992-08-26 1994-03-03 Zeneca Limited Novel plants and processes for obtaining them
WO1994009144A1 (en) 1992-10-14 1994-04-28 Zeneca Limited Novel plants and processes for obtaining them
WO1994011520A2 (en) 1992-11-09 1994-05-26 Zeneca Limited Novel plants and processes for obtaining them
EP0607730A1 (en) 1992-12-24 1994-07-27 International Business Machines Corporation Method of direct transferring of electrically conductive elements into a substrate
WO1994021795A1 (en) 1993-03-25 1994-09-29 Ciba-Geigy Ag Novel pesticidal proteins and strains
US5969169A (en) 1993-04-27 1999-10-19 Cargill, Incorporated Non-hydrogenated canola oil for food applications
EP0709000A1 (en) 1993-07-15 1996-05-01 Siemens Ag METHOD AND DEVICE FOR CONTROLLING A PULSE INVERTER DEVICE COMPRISING A MASTER INVERTER AND AT LEAST ONE SLAVE INVERTER
WO1995004826A1 (en) 1993-08-09 1995-02-16 Institut Für Genbiologische Forschung Berlin Gmbh Debranching enzymes and dna sequences coding them, suitable for changing the degree of branching of amylopectin starch in plants
EP0719338A1 (en) 1993-09-09 1996-07-03 Hoechst Schering AgrEvo GmbH Combination of dna sequences which enable the formation of modified starch in plant cells and plants, processes for the production of these plants and the modified starch obtainable therefrom
WO1995009910A1 (en) 1993-10-01 1995-04-13 Mitsubishi Corporation Gene that identifies sterile plant cytoplasm and process for preparing hybrid plant by using the same
US6169190B1 (en) 1993-10-12 2001-01-02 Agrigenetics Inc Oil of Brassica napus
US5965755A (en) 1993-10-12 1999-10-12 Agrigenetics, Inc. Oil produced from the Brassica napus
US5908975A (en) 1993-11-09 1999-06-01 E. I. Du Pont De Nemours And Company Accumulation of fructans in plants by targeted expression of bacterial levansucrase
EP0728213A1 (en) 1993-11-09 1996-08-28 E.I. Du Pont De Nemours And Company Transgenic fructan accumulating crops and methods for their production
US6270828B1 (en) 1993-11-12 2001-08-07 Cargrill Incorporated Canola variety producing a seed with reduced glucosinolates and linolenic acid yielding an oil with low sulfur, improved sensory characteristics and increased oxidative stability
WO1995026407A1 (en) 1994-03-25 1995-10-05 National Starch And Chemical Investment Holding Corporation Method for producing altered starch from potato plants
WO1995031553A1 (en) 1994-05-18 1995-11-23 Institut Für Genbiologische Forschung Berlin Gmbh DNA SEQUENCES CODING FOR ENZYMES CAPABLE OF FACILITATING THE SYNTHESIS OF LINEAR α-1,4 GLUCANS IN PLANTS, FUNGI AND MICROORGANISMS
WO1995035026A1 (en) 1994-06-21 1995-12-28 Zeneca Limited Novel plants and processes for obtaining them
US5824790A (en) 1994-06-21 1998-10-20 Zeneca Limited Modification of starch synthesis in plants
WO1996001904A1 (en) 1994-07-08 1996-01-25 Stichting Scheikundig Onderzoek In Nederland Production of oligosaccharides in transgenic plants
WO1996015248A1 (en) 1994-11-10 1996-05-23 Hoechst Schering Agrevo Gmbh Dna molecules that code for enzymes involved in starch synthesis, vectors, bacteria, transgenic plant cells and plants containing said molecules
WO1996019581A1 (en) 1994-12-22 1996-06-27 Hoechst Schering Agrevo Gmbh Dna molecules coding for debranching enzymes derived from plants
WO1996021023A1 (en) 1995-01-06 1996-07-11 Centrum Voor Plantenveredelings- En Reproduktieonderzoek (Cpro - Dlo) Dna sequences encoding carbohydrate polymer synthesizing enzymes and method for producing transgenic plants
WO1996027674A1 (en) 1995-03-08 1996-09-12 Hoechst Schering Agrevo Gmbh Modified starch from plants, plants synthesizing this starch, and process for its preparation
WO1996033270A1 (en) 1995-04-20 1996-10-24 American Cyanamid Company Structure-based designed herbicide resistant products
US5928937A (en) 1995-04-20 1999-07-27 American Cyanamid Company Structure-based designed herbicide resistant products
WO1996034968A2 (en) 1995-05-05 1996-11-07 National Starch And Chemical Investment Holding Corporation Improvements in or relating to plant starch composition
WO1996038567A2 (en) 1995-06-02 1996-12-05 Rhone-Poulenc Agrochimie Dna sequence of a gene of hydroxy-phenyl pyruvate dioxygenase and production of plants containing a gene of hydroxy-phenyl pyruvate dioxygenase and which are tolerant to certain herbicides
US5712107A (en) 1995-06-07 1998-01-27 Pioneer Hi-Bred International, Inc. Substitutes for modified starch and latexes in paper manufacture
US20020031826A1 (en) 1995-06-07 2002-03-14 Nichols Scott E. Glucan-containing compositions and paper
US6284479B1 (en) 1995-06-07 2001-09-04 Pioneer Hi-Bred International, Inc. Substitutes for modified starch and latexes in paper manufacture
US6229072B1 (en) 1995-07-07 2001-05-08 Adventa Technology Ltd Cytoplasmic male sterility system production canola hybrids
EP0837944A2 (en) 1995-07-19 1998-04-29 Rhone-Poulenc Agrochimie Mutated 5-enol pyruvylshikimate-3-phosphate synthase, gene coding for said protein and transformed plants containing said gene
WO1997011188A1 (en) 1995-09-19 1997-03-27 Planttec Biotechnologie Gmbh Plants which synthesise a modified starch, process for the production thereof and modified starch
WO1997020936A1 (en) 1995-12-06 1997-06-12 Zeneca Limited Modification of starch synthesis in plants
WO1997026362A1 (en) 1996-01-16 1997-07-24 Planttec Biotechnologie Gmbh Nucleic acid molecules from plants coding enzymes which participate in the starch synthesis
WO1997032985A1 (en) 1996-03-07 1997-09-12 Planttec Biotechnologie Gmbh Forschung & Entwicklung Nucleic acid molecules coding for debranching enzymes from maize
WO1997041218A1 (en) 1996-04-29 1997-11-06 Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College Herbicide resistant rice
WO1997042328A1 (en) 1996-05-06 1997-11-13 Planttec Biotechnologie Gmbh Nucleic acid molecules which code the potato debranching enzyme
WO1997044472A1 (en) 1996-05-17 1997-11-27 Planttec Biotechnologie Gmbh Nucleic acid molecules coding soluble maize starch synthases
WO1997045545A1 (en) 1996-05-29 1997-12-04 Hoechst Schering Agrevo Gmbh Nucleic acid molecules encoding enzymes from wheat which are involved in starch synthesis
WO1997047807A1 (en) 1996-06-12 1997-12-18 Pioneer Hi-Bred International, Inc. Substitutes for modified starch in paper manufacture
WO1997047808A1 (en) 1996-06-12 1997-12-18 Pioneer Hi-Bred International, Inc. Substitutes for modified starch in paper manufacture
WO1997047806A1 (en) 1996-06-12 1997-12-18 Pioneer Hi-Bred International, Inc. Substitutes for modified starch in paper manufacture
WO1998000549A1 (en) 1996-06-27 1998-01-08 The Australian National University MANIPULATION OF CELLULOSE AND/OR β-1,4-GLUCAN
US6063947A (en) 1996-07-03 2000-05-16 Cargill, Incorporated Canola oil having increased oleic acid and decreased linolenic acid content
US5773702A (en) 1996-07-17 1998-06-30 Board Of Trustees Operating Michigan State University Imidazolinone herbicide resistant sugar beet plants
WO1998020145A2 (en) 1996-11-05 1998-05-14 National Starch And Chemical Investment Holding Corporation Improvements in or relating to starch content of plants
WO1998022604A1 (en) 1996-11-20 1998-05-28 Pioneer Hi-Bred International, Inc. Methods of producing high-oil seed by modification of starch levels
WO1998027212A1 (en) 1996-12-19 1998-06-25 Planttec Biotechnologie Gmbh Novel nucleic acid molecules from maize and their use for the production of modified starch
WO1998027806A1 (en) 1996-12-24 1998-07-02 Pioneer Hi-Bred International, Inc. Oilseed brassica containing an improved fertility restorer gene for ogura cytoplasmic male sterility
WO1998032326A2 (en) 1997-01-24 1998-07-30 Pioneer Hi-Bred International, Inc. Methods for $i(agrobacterium)-mediated transformation
WO1998039460A1 (en) 1997-03-04 1998-09-11 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. Nucleic acid molecules from artichoke ($i(cynara scolymus)) encoding enzymes having fructosyl polymerase activity
WO1998040503A1 (en) 1997-03-10 1998-09-17 Planttec Biotechnologie Gmbh Nucleic acid molecules encoding starch phosphorylase from maize
US20050188434A1 (en) 1997-04-03 2005-08-25 Michael Spencer Method for plant breeding
US20060059581A1 (en) 1997-04-03 2006-03-16 Dekalb Genetics Corporation Method of breeding glyphosate resistant plants
US20050086719A1 (en) 1997-04-03 2005-04-21 Michael Spencer Glyphosate resistant maize lines
WO1998044140A1 (en) 1997-04-03 1998-10-08 Dekalb Genetics Corporation Glyphosate resistant maize lines
WO1999012950A2 (en) 1997-09-06 1999-03-18 National Starch And Chemical Investment Holding Corporation Improvements in or relating to stability of plant starches
WO1999024593A1 (en) 1997-11-06 1999-05-20 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. Nucleic acid molecules which encode proteins having fructosyl transferase activity and methods for producing long-chain inulin
WO1999024586A1 (en) 1997-11-07 1999-05-20 Aventis Cropscience S.A. Chimeric hydroxy-phenyl pyruvate dioxygenase, dna sequence and method for obtaining plants containing such a gene, with herbicide tolerance
WO1999024585A1 (en) 1997-11-07 1999-05-20 Aventis Cropscience S.A. Mutated hydroxy-phenyl pyruvate dioxygenase, dna sequence and method for obtaining herbicide-tolerant plants containing such gene
WO1999034008A1 (en) 1997-12-24 1999-07-08 Aventis Cropscience S.A. Method for enzymatic preparation of homogentisate
WO1999053072A1 (en) 1998-04-09 1999-10-21 E.I. Du Pont De Nemours And Company Starch r1 phosphorylation protein homologs
WO1999058690A2 (en) 1998-05-08 1999-11-18 Aventis Cropscience Gmbh Nucleic acid molecules which code for enzymes derived from wheat and which are involved in the synthesis of starch
WO1999058688A2 (en) 1998-05-08 1999-11-18 Aventis Cropscience Gmbh Nucleic acid molecules which code for enzymes derived from wheat and which are involved in the synthesis of starch
WO1999058654A2 (en) 1998-05-13 1999-11-18 Planttec Biotechnologie Gmbh Forschung & Entwicklung Transgenic plants with a modified activity of a plastidial adp/atp translocator
WO1999057965A1 (en) 1998-05-14 1999-11-18 Aventis Cropscience Gmbh Sulfonylurea-tolerant sugar beet mutants
WO1999066050A1 (en) 1998-06-15 1999-12-23 National Starch And Chemical Investment Holding Corporation Improvements in or relating to plants and plant products
WO2000004173A1 (en) 1998-07-17 2000-01-27 Aventis Cropscience N.V. Methods and means to modulate programmed cell death in eukaryotic cells
WO2000008185A1 (en) 1998-07-31 2000-02-17 Aventis Cropscience Gmbh Nucleic acid molecule coding for beta-amylase, plants synthesizing a modified starch, method of production and applications
WO2000008175A2 (en) 1998-07-31 2000-02-17 Aventis Cropscience Gmbh Nucleic acid module coding for alpha glucosidase, plants that synthesize modified starch, methods for the production and use of said plants, and modified starch
WO2000008184A1 (en) 1998-07-31 2000-02-17 Aventis Cropscience Gmbh Plants which synthesize a modified starch, methods for producing the plants, their use, and the modified starch
WO2000011192A2 (en) 1998-08-25 2000-03-02 Pioneer Hi-Bred International, Inc. Plant glutamine: fructose-6-phosphate amidotransferase nucleic acids
WO2000014249A1 (en) 1998-09-02 2000-03-16 Planttec Biotechnologie Gmbh Nucleic acid molecules encoding an amylosucrase
WO2000022140A1 (en) 1998-10-09 2000-04-20 Planttec Biotechnologie Gmbh Forschung & Entwicklung NUCLEIC ACID MOLECULES WHICH CODE A BRANCHING ENZYME FROM BACTERIA OF THE GENUS NEISSERIA, AND A METHOD FOR PRODUCING α-1,6-BRANCHED α-1,4-GLUCANS
US6468747B1 (en) 1998-11-03 2002-10-22 Plant Genetic System, N.V. Glufosinate tolerant rice
WO2000026356A1 (en) 1998-11-03 2000-05-11 Aventis Cropscience N. V. Glufosinate tolerant rice
WO2000026345A1 (en) 1998-11-03 2000-05-11 Aventis Cropscience N.V. Glufosinate tolerant rice
WO2000028052A2 (en) 1998-11-09 2000-05-18 Planttec Biotechnologie Gmbh Nucleic acid molecules from rice encoding an r1 protein and their use for the production of modified starch
EP1135601A1 (en) 1998-11-12 2001-09-26 Volvo Lastvagnar AB Fuel delivery system
WO2000047727A2 (en) 1999-02-08 2000-08-17 Planttec Biotechnologie Gmbh Forschung & Entwicklung Nucleic acid molecules encoding alternansucrase
US6323392B1 (en) 1999-03-01 2001-11-27 Pioneer Hi-Bred International, Inc. Formation of brassica napus F1 hybrid seeds which exhibit a highly elevated oleic acid content and a reduced linolenic acid content in the endogenously formed oil of the seeds
WO2000066746A1 (en) 1999-04-29 2000-11-09 Syngenta Limited Herbicide resistant plants
WO2000066747A1 (en) 1999-04-29 2000-11-09 Syngenta Limited Herbicide resistant plants
WO2000073422A1 (en) 1999-05-27 2000-12-07 Planttec Biotechnologie Gmbh Genetically modified plant cells and plants with an increased activity of an amylosucrase protein and a branching enzyme
WO2000077229A2 (en) 1999-06-11 2000-12-21 Aventis Cropscience Gmbh R1 protein from wheat and the use thereof for the production of modified strach
WO2001012826A2 (en) 1999-08-11 2001-02-22 Aventis Cropscience Gmbh Nucleic acid molecules derived from plants which code for enzymes which are involved in the synthesis of starch
WO2001012782A2 (en) 1999-08-12 2001-02-22 Aventis Cropscience Gmbh Transgenically modified plant cells and plants having modified gbssi- and be-protein activity
WO2001014569A2 (en) 1999-08-20 2001-03-01 Basf Plant Science Gmbh Increasing the polysaccharide content in plants
US6734341B2 (en) 1999-09-02 2004-05-11 Pioneer Hi-Bred International, Inc. Starch synthase polynucleotides and their use in the production of new starches
WO2001017333A1 (en) 1999-09-10 2001-03-15 Texas Tech University Transgenic fiber producing plants with increased expression of sucrose phosphate synthase
WO2001019975A2 (en) 1999-09-15 2001-03-22 National Starch And Chemical Investment Holding Corporation Plants having reduced activity in two or more starch-modifying enzymes
EP1135600A1 (en) 1999-10-06 2001-09-26 Robert Bosch Gmbh Fuel high pressure accumulator
WO2001024615A1 (en) 1999-10-07 2001-04-12 Valigen (Us), Inc. Non-transgenic herbicide resistant plants
WO2001031042A2 (en) 1999-10-29 2001-05-03 Aventis Cropscience N.V. Male-sterile brassica plants and methods for producing same
US20030188347A1 (en) 1999-12-08 2003-10-02 Both Greta De Hybrid winter oilseed rape and methods for producing same
WO2001041558A1 (en) 1999-12-08 2001-06-14 Aventis Cropscience N.V. Hybrid winter oilseed rape and methods for producing same
WO2001051654A2 (en) 2000-01-11 2001-07-19 Bayer Cropscience N.V. Methods and kits for identifying elite event gat-zm1 in biological samples
US20010029014A1 (en) 2000-01-11 2001-10-11 Beuckeleer Marc De Methods and kits for identifying elite event GAT-ZM1 in biological samples
WO2001066704A2 (en) 2000-03-09 2001-09-13 Monsanto Technology Llc Methods for making plants tolerant to glyphosate and compositions thereof
WO2001065922A2 (en) 2000-03-09 2001-09-13 E. I. Du Pont De Nemours And Company Sulfonylurea-tolerant sunflower plants
US6768044B1 (en) 2000-05-10 2004-07-27 Bayer Cropscience Sa Chimeric hydroxyl-phenyl pyruvate dioxygenase, DNA sequence and method for obtaining plants containing such a gene, with herbicide tolerance
WO2001098509A2 (en) 2000-06-21 2001-12-27 Syngenta Participations Ag Grain processing method and transgenic plants useful therein
US20070292854A1 (en) 2000-06-22 2007-12-20 Behr Carl F Corn event PV-ZMGT32(nk603) and compositions and methods for detection thereof
US20020102582A1 (en) 2000-09-13 2002-08-01 Levine Elaine B. Corn event MON810 and compositions and methods for detection thereof
WO2002026995A1 (en) 2000-09-29 2002-04-04 Syngenta Limited Herbicide resistant plants
WO2002034923A2 (en) 2000-10-23 2002-05-02 Bayer Cropscience Gmbh Monocotyledon plant cells and plants which synthesise modified starch
WO2002034946A2 (en) 2000-10-25 2002-05-02 Monsanto Technology Llc Cotton event pv-ghgt07(1445) and compositions and methods for detection thereof
US20020120964A1 (en) 2000-10-25 2002-08-29 Rangwala Tasneem S. Cotton event PV-GHGT07(1445) and compositions and methods for detection thereof
WO2002036782A2 (en) 2000-10-30 2002-05-10 Maxygen, Inc. Novel glyphosate n-acetyltransferase (gat) genes
US20080070260A1 (en) 2000-10-30 2008-03-20 Rachel Krieb Canola event PV-BNGT04(RT73) and compositions and methods for detection thereof
WO2002036787A2 (en) 2000-10-30 2002-05-10 Bayer Cropscience S.A. Herbicide-tolerant plants through bypassing metabolic pathway
WO2002036831A2 (en) 2000-10-30 2002-05-10 Monsanto Technology Llc Canola event pv-bngt04(rt73) and compositions and methods for detection thereof
US20090265817A1 (en) 2000-11-30 2009-10-22 Ses Europe N.V./S.A. T227-1 flanking sequence
WO2002044407A2 (en) 2000-11-30 2002-06-06 Ses Europe N.V. Glyphosate resistant transgenic sugar beet characterised by a specific transgene insertion (t227-1), methods and primers for the detection of said insertion
WO2002046387A2 (en) 2000-12-07 2002-06-13 Syngenta Limited Plant derived hydroxy phenyl pyruvate dioxygenases (hppd) resistant against triketone herbicides and transgenic plants containing these dioxygenases
WO2002045485A1 (en) 2000-12-08 2002-06-13 Commonwealth Scienctific And Industrial Research Organisation Modification of sucrose synthase gene expression in plant tissue and uses therefor
WO2002079410A2 (en) 2001-03-30 2002-10-10 Basf Plant Science Gmbh Glucan chain length domains
WO2002100163A2 (en) 2001-06-11 2002-12-19 Monsanto Technology Llc Cotton event moni5985 and compositions and methods for detection
US20040250317A1 (en) 2001-06-11 2004-12-09 Huber Scott A Cotton event moni5985 and compositions and methods for detection thereof
WO2002101059A2 (en) 2001-06-12 2002-12-19 Bayer Cropscience Gmbh Transgenic plants synthesising high amylose starch
US20030097687A1 (en) 2001-08-06 2003-05-22 Linda Trolinder Herbicide tolerant cotton plants and methods for producing and identifying same
WO2003013224A2 (en) 2001-08-06 2003-02-20 Bayer Bioscience N.V. Herbicide tolerant cotton plants and methods for producing and identifying same
WO2003013226A2 (en) 2001-08-09 2003-02-20 Cibus Genetics Non-transgenic herbicide resistant plants
WO2003033540A2 (en) 2001-10-17 2003-04-24 Basf Plant Science Gmbh Starch
WO2003052073A2 (en) 2001-12-17 2003-06-26 Syngenta Participations Ag Novel corn event
WO2003071860A2 (en) 2002-02-26 2003-09-04 Bayer Cropscience Gmbh Method for generating maize plants with an increased leaf starch content, and their use for making maize silage
WO2003092360A2 (en) 2002-04-30 2003-11-13 Verdia, Inc. Novel glyphosate-n-acetyltransferase (gat) genes
US20060095986A1 (en) 2002-07-29 2006-05-04 Cavato Tracey A Corn event pv-zmir13 (mon863) plants and compositions and methods for detection thereof
WO2004011601A2 (en) 2002-07-29 2004-02-05 Monsanto Technology, Llc Corn event pv-zmir13 (mon863) plants and compositions and methods for detection thereof
WO2004024928A2 (en) 2002-09-11 2004-03-25 Bayer Cropscience S.A. Transformed plants with enhanced prenylquinone biosynthesis
WO2004040012A2 (en) 2002-10-29 2004-05-13 Basf Plant Science Gmbh Compositions and methods for identifying plants having increased tolerance to imidazolinone herbicides
US20060130175A1 (en) 2002-10-29 2006-06-15 Ellis Daniel M Cot102 insecticidal cotton
WO2004039986A1 (en) 2002-10-29 2004-05-13 Syngenta Participations Ag Cot102 insecticidal cotton
US20060162007A1 (en) 2002-12-05 2006-07-20 Monsanto Technology Llc Bentgrass event asr-368 and compositions and methods for detection thereof
WO2004053062A2 (en) 2002-12-05 2004-06-24 Monsanto Technology Llc Bentgrass event asr-368 and compositions and methods for detection thereof
WO2004053219A2 (en) 2002-12-05 2004-06-24 Jentex Corporation Abrasive webs and methods of making the same
WO2004056999A1 (en) 2002-12-19 2004-07-08 Bayer Cropscience Gmbh Plant cells and plants which synthesize a starch with an increased final viscosity
WO2004072235A2 (en) 2003-02-12 2004-08-26 Monsanto Technology Llc Cotton event mon 88913 and compositions and methods for detection thereof
US20060059590A1 (en) 2003-02-12 2006-03-16 Monsanto Technology Llc Cotton event mon 88913 and compositions and methods for detection thereof
WO2004074492A1 (en) 2003-02-20 2004-09-02 Kws Saat Ag Glyphosate tolerant sugar beet
US20040172669A1 (en) 2003-02-28 2004-09-02 Josef Kraus Glyphosate tolerant sugar beet
WO2004078983A2 (en) 2003-03-07 2004-09-16 Basf Plant Science Gmbh Enhanced amylose production in plants
WO2004090140A2 (en) 2003-04-09 2004-10-21 Bayer Bioscience N.V. Methods and means for increasing the tolerance of plants to stress conditions
WO2005012515A2 (en) 2003-04-29 2005-02-10 Pioneer Hi-Bred International, Inc. Novel glyphosate-n-acetyltransferase (gat) genes
US20050039226A1 (en) 2003-05-02 2005-02-17 Dow Agrosciences Llc Corn event TC1507 and methods for detection thereof
WO2004099447A2 (en) 2003-05-02 2004-11-18 Dow Agrosciences Llc Corn event tc1507 and methods for detection thereof
WO2005002359A2 (en) 2003-05-22 2005-01-13 Syngenta Participations Ag Modified starch, uses, methods for production thereof
WO2004106529A2 (en) 2003-05-28 2004-12-09 Basf Aktiengesellschaft Wheat plants having increased tolerance to imidazolinone herbicides
WO2005002324A2 (en) 2003-07-04 2005-01-13 Institut National De La Recherche Agronomique Method of producing double low restorer lines of brassica napus having a good agronomic value
WO2005012529A1 (en) 2003-07-31 2005-02-10 Toyo Boseki Kabushiki Kaisha Plant producing hyaluronic acid
WO2005017157A1 (en) 2003-08-15 2005-02-24 Commonwealth Scientific And Industrial Research Organisation (Csiro) Methods and means for altering fiber characteristics in fiber-producing plants
WO2005020673A1 (en) 2003-08-29 2005-03-10 Instituto Nacional De Technologia Agropecuaria Rice plants having increased tolerance to imidazolinone herbicides
WO2005030942A1 (en) 2003-09-30 2005-04-07 Bayer Cropscience Gmbh Plants with reduced activity of a class 3 branching enzyme
WO2005030941A1 (en) 2003-09-30 2005-04-07 Bayer Cropscience Gmbh Plants with increased activity of a class 3 branching enzyme
WO2005054480A2 (en) 2003-12-01 2005-06-16 Syngenta Participations Ag Insect resistant cotton plants and methods of detecting the same
WO2005054479A1 (en) 2003-12-01 2005-06-16 Syngenta Participations Ag Insect resistant cotton plants and methods of detecting the same
US20070067868A1 (en) 2003-12-01 2007-03-22 Negrotto David V Insect resistant cotton plants and methods of detecting the same
US20070028322A1 (en) 2003-12-11 2007-02-01 Dizigan Mark A High lysine maize compositions and methods for detection thereof
WO2005061720A2 (en) 2003-12-11 2005-07-07 Monsanto Technology Llc High lysine maize compositions and methods for detection thereof
US20080028482A1 (en) 2003-12-15 2008-01-31 Beazley Kim A Corn Plant Mon88017 and Compositions and Methods for Detection Thereof
WO2005059103A2 (en) 2003-12-15 2005-06-30 Monsanto Technology Llc Corn plant mon88017 and compositions and methods for detection thereof
WO2005063784A1 (en) 2003-12-30 2005-07-14 Bayer Cropscience Sa Synthetic compounds useful as nodulation agents of leguminous plants and preparation processes thereof
WO2005077177A2 (en) 2004-02-10 2005-08-25 Universite Paul Sabatier Toulouse Iii Modulators of the development of mychorrizal fungi with arbuscules, and uses thereof
WO2005095618A2 (en) 2004-03-05 2005-10-13 Bayer Cropscience Gmbh Plants with reduced activity of the starch phosphorylating enzyme phosphoglucan, water dikinase
WO2005095619A1 (en) 2004-03-05 2005-10-13 Bayer Cropscience Gmbh Plants with increased activity of multiple starch phosphorylating enzymes
WO2005095632A2 (en) 2004-03-05 2005-10-13 Bayer Cropscience Gmbh Methods for identifying proteins with starch phosphorylating enzymatic activity
WO2005095617A2 (en) 2004-03-05 2005-10-13 Bayer Cropscience Gmbh Plants with increased activity of a starch phosphorylating enzyme
WO2005093093A2 (en) 2004-03-22 2005-10-06 Basf Aktiengesellschaft Methods and compositions for analyzing ahasl genes
WO2005103301A2 (en) 2004-03-25 2005-11-03 Syngenta Participations Ag Corn event mir604
US20080167456A1 (en) 2004-03-25 2008-07-10 Syngenta Participations Ag Corn Event MIR604
US20070143876A1 (en) 2004-03-26 2007-06-21 Dow Agrosciences Llc Cry1F and Cry1Ac transgenic cotton lines and event-specific identification thereof
WO2005103266A1 (en) 2004-03-26 2005-11-03 Dow Agrosciences Llc Cry1f and cry1ac transgenic cotton lines and event-specific identification thereof
US20050216969A1 (en) 2004-03-26 2005-09-29 Dow Agrosciences Llc Cry1F and Cry1AC transgenic cotton lines and event-specific identification thereof
WO2005107471A1 (en) 2004-05-12 2005-11-17 Bayer Cropscience Gmbh Plant growth regulation
WO2005107466A1 (en) 2004-05-12 2005-11-17 Bayer Cropscience Gmbh Plant growth regulation
WO2005107472A1 (en) 2004-05-12 2005-11-17 Bayer Cropscience Gmbh Plant growth regulation
WO2005107465A1 (en) 2004-05-12 2005-11-17 Bayer Cropscience Gmbh Plant growth regulation
WO2006007373A2 (en) 2004-06-16 2006-01-19 Basf Plant Science Gmbh Polynucleotides encoding mature ahasl proteins for creating imidazolinone-tolerant plants
WO2005123927A1 (en) 2004-06-21 2005-12-29 Bayer Cropscience Gmbh Plants that produce amylopectin starch with novel properties
WO2006024351A1 (en) 2004-07-30 2006-03-09 Basf Agrochemical Products B.V. Herbicide-resistant sunflower plants, plynucleotides encoding herbicide-resistant acetohydroxy acid synthase large subunit proteins, and methods of use
WO2006015376A2 (en) 2004-08-04 2006-02-09 Basf Plant Science Gmbh Monocot ahass sequences and methods of use
WO2006018319A1 (en) 2004-08-18 2006-02-23 Bayer Cropscience Gmbh Plants with increased plastidic activity of r3 starch-phosphorylating enzyme
WO2006021972A1 (en) 2004-08-26 2006-03-02 Dhara Vegetable Oil And Foods Company Limited A novel cytoplasmic male sterility system for brassica species and its use for hybrid seed production in indian oilseed mustard brassica juncea
WO2006032538A1 (en) 2004-09-23 2006-03-30 Bayer Cropscience Gmbh Methods and means for producing hyaluronan
EP1794306A2 (en) 2004-09-24 2007-06-13 Bayer BioScience N.V. Stress resistant plants
US20060070139A1 (en) 2004-09-29 2006-03-30 Pioneer Hi-Bred International, Inc. Corn event DAS-59122-7 and methods for detection thereof
WO2006045633A1 (en) 2004-10-29 2006-05-04 Bayer Bioscience N.V. Stress tolerant cotton plants
EP1807519A1 (en) 2004-10-29 2007-07-18 Bayer BioScience N.V. Stress tolerant cotton plants
WO2006060634A2 (en) 2004-12-01 2006-06-08 Basf Agrochemical Products, B.V. Novel mutation involved in increased tolerance to imidazolinone herbicides in plants
WO2006063862A1 (en) 2004-12-17 2006-06-22 Bayer Cropscience Ag Transformed plant expressing a dextransucrase and synthesizing a modified starch
WO2006072603A2 (en) 2005-01-10 2006-07-13 Bayer Cropscience Ag Transformed plant expressing a mutansucrase and synthesizing a modified starch
US20060230473A1 (en) 2005-03-16 2006-10-12 Syngenta Participations Ag Corn event 3272 and methods for detection thereof
WO2006098952A2 (en) 2005-03-16 2006-09-21 Syngenta Participations Ag Corn event 3272 and methods of detection thereof
JP2006304779A (en) 2005-03-30 2006-11-09 Toyobo Co Ltd Hexosamine high production plant
WO2006103107A1 (en) 2005-04-01 2006-10-05 Bayer Cropscience Ag Phosphorylated waxy potato starch
WO2006108674A2 (en) 2005-04-08 2006-10-19 Bayer Bioscience N.V. Elite event a2704-12 and methods and kits for identifying such event in biological samples
WO2006108702A1 (en) 2005-04-08 2006-10-19 Bayer Cropscience Ag High-phosphate starch
US20080320616A1 (en) 2005-04-08 2008-12-25 Bayer Bioscience N.V. Elite Event A2407-12 and Methods and Kits for Identifying Such Event in Biological Samples
US20080196127A1 (en) 2005-04-11 2008-08-14 Bayer Bioscience N.V. Elite Event A5547-127 and Methods and Kits For Identifying Such Event in Biological Samples
WO2006108675A2 (en) 2005-04-11 2006-10-19 Bayer Bioscience N.V. Elite event a5547-127 and methods and kits for identifying such event in biological samples
WO2006130436A2 (en) 2005-05-27 2006-12-07 Monsanto Technology Llc Soybean event mon89788 and methods for detection thereof
US20060282915A1 (en) 2005-05-27 2006-12-14 Monsanto Technology Llc Soybean event MON89788 and methods for detection thereof
WO2006129204A2 (en) 2005-05-31 2006-12-07 Devgen Nv Rnai for control of insects and arachnids
WO2006128568A2 (en) 2005-06-02 2006-12-07 Syngenta Participations Ag T342-142, insecticidal transgenic cotton expressing cry1ab
US20100024077A1 (en) 2005-06-02 2010-01-28 Syngenta Participations Ag Ce44-69d insecticidal cotton
WO2006128571A2 (en) 2005-06-02 2006-12-07 Syngenta Participations Ag Ce44-69d , insecticidal transgenic cotton expressing cry1ab
WO2006128569A2 (en) 2005-06-02 2006-12-07 Syngenta Participations Ag 1143-14a, insecticidal transgenic cotton expressing cry1ab
US20090217423A1 (en) 2005-06-02 2009-08-27 Cayley Patricia J Ce43-67b insecticidal cotton
WO2006128570A1 (en) 2005-06-02 2006-12-07 Syngenta Participations Ag 1143-51b insecticidal cotton
WO2006128573A2 (en) 2005-06-02 2006-12-07 Syngenta Participations Ag Ce43- 67b, insecticidal transgenic cotton expressing cry1ab
WO2006128572A1 (en) 2005-06-02 2006-12-07 Syngenta Participations Ag Ce46-02a insecticidal cotton
WO2006133827A2 (en) 2005-06-15 2006-12-21 Bayer Bioscience N.V. Methods for increasing the resistance of plants to hypoxic conditions
WO2006136351A2 (en) 2005-06-24 2006-12-28 Bayer Bioscience N.V. Methods for altering the reactivity of plant cell walls
WO2007009823A1 (en) 2005-07-22 2007-01-25 Bayer Cropscience Ag Overexpression of starch synthase in plants
US20100050282A1 (en) 2005-08-08 2010-02-25 Bayer Bioscience N.V. Herbicide Tolerant Cotton Plants and Methods for Identifying the Same
WO2007017186A1 (en) 2005-08-08 2007-02-15 Bayer Bioscience N.V. Herbicide tolerant cotton plants and methods for identifying same
WO2007024782A2 (en) 2005-08-24 2007-03-01 Pioneer Hi-Bred International, Inc. Compositions providing tolerance to multiple herbicides and methods of use thereof
WO2007027777A2 (en) 2005-08-31 2007-03-08 Monsanto Technology Llc Nucleotide sequences encoding insecticidal proteins
WO2007074405A2 (en) 2005-09-16 2007-07-05 Devgen Nv Dsrna as insect control agent
WO2007035650A2 (en) 2005-09-16 2007-03-29 Monsanto Technology Llc Methods for genetic control of insect infestations in plants and compositions thereof
WO2007039316A1 (en) 2005-10-05 2007-04-12 Bayer Cropscience Ag Improved methods and means for producings hyaluronan
WO2007039315A1 (en) 2005-10-05 2007-04-12 Bayer Cropscience Ag Plants with an increased production of hyaluronan ii
WO2007039314A2 (en) 2005-10-05 2007-04-12 Bayer Cropscience Ag Plants with increased hyaluronan production
WO2007080126A2 (en) 2006-01-12 2007-07-19 Devgen N.V. Dsrna as insect control agent
WO2007080127A2 (en) 2006-01-12 2007-07-19 Devgen N.V. Dsrna as insect control agent
WO2007091277A2 (en) 2006-02-10 2007-08-16 Maharashtra Hybrid Seeds Company Limited (Mahyco) TRANSGENIC BRINJAL (SOLANUM MELONGENA) EXPRESSING THE CRYlAC GENE
WO2007103567A2 (en) 2006-03-09 2007-09-13 E. I. Dupont De Nemours & Company Polynucleotide encoding a maize herbicide resistance gene and methods for use
WO2007107326A1 (en) 2006-03-21 2007-09-27 Bayer Bioscience N.V. Stress resistant plants
WO2007107302A2 (en) 2006-03-21 2007-09-27 Bayer Bioscience N.V. Novel genes encoding insecticidal proteins
EP1999263A1 (en) 2006-03-21 2008-12-10 Bayer BioScience N.V. Stress resistant plants
EP1999141A2 (en) 2006-03-21 2008-12-10 Bayer BioScience N.V. Novel genes encoding insecticidal proteins
EP2018431A2 (en) 2006-05-12 2009-01-28 Bayer BioScience N.V. Novel stress-related microrna molecules and uses thereof
US20080260932A1 (en) 2006-05-26 2008-10-23 Anderson Heather M Corn Plant and Seed Corresponding to Transgenic Event MON89034 and Methods For Detection and Use Thereof
WO2007140256A1 (en) 2006-05-26 2007-12-06 Monsanto Technology, Llc Corn plant and seed corresponding to transgenic event mon89034 and methods for detection and use thereof
US20090300784A1 (en) 2006-06-03 2009-12-03 Syngenta Participations Ag Corn event mir162
WO2007142840A2 (en) 2006-06-03 2007-12-13 Syngenta Participations Ag Corn event mir162
WO2008002872A2 (en) 2006-06-28 2008-01-03 Pioneer Hi-Bred International, Inc. Soybean event 3560.4.3.5 and compositions and methods for the identification and/or detection thereof
US20100184079A1 (en) 2006-06-28 2010-07-22 Pioneer Hi-Bred International, Inc. Soybean event 3560.4.3.5 and compositions and methods for the identification and detection thereof
WO2008007167A1 (en) 2006-07-07 2008-01-17 Societe Bic Writing instrument with cushioning device
WO2008017518A1 (en) 2006-08-09 2008-02-14 Bayer Cropscience Ag Genetically modified plants which synthesize a starch having increased swelling power
US20080064032A1 (en) 2006-09-13 2008-03-13 Syngenta Participations Ag Polynucleotides and uses thereof
WO2008112019A2 (en) 2006-10-30 2008-09-18 Pioneer Hi-Bred International, Inc. Maize event dp-098140-6 and compositions and methods for the identification and/or detection thereof
US20090137395A1 (en) 2006-10-30 2009-05-28 Pioneer Hi-Bred International, Inc. Maize event DP-098140-6 and compositions and methods for the identification and/or detection thereof
US20080312082A1 (en) 2006-10-31 2008-12-18 Kinney Anthony J Soybean event dp-305423-1 and compositions and methods for the identification and/or detection thereof
WO2008054747A2 (en) 2006-10-31 2008-05-08 E. I. Du Pont De Nemours And Company Soybean event dp-305423-1 and compositions and methods for the identification and/or detection thereof
WO2008071672A2 (en) 2006-12-12 2008-06-19 Bayer Cropscience Sa Pesticidal composition comprising a synthetic compound useful as nodulation agent of leguminous plants and a fungicide compound
WO2008080631A1 (en) 2006-12-29 2008-07-10 Bayer Cropscience Ag Process for modifying the thermal and/or digestion properties of corn starches and corn flours
WO2008080630A1 (en) 2006-12-29 2008-07-10 Bayer Cropscience Ag Corn starch and also corn flours and food comprising this corn starch
WO2008085958A1 (en) 2007-01-09 2008-07-17 Merck Patent Gmbh Lipo-chitooligosaccharide combination compositions for enhanced plant growth and yield
WO2008090008A1 (en) 2007-01-26 2008-07-31 Bayer Cropscience Ag Genetically modified plants which synthesize a low amylose starch with increased swelling power
WO2008114282A2 (en) 2007-03-19 2008-09-25 Maharashtra Hybrid Seeds Company Limited Transgenic rice (oryza sativa) comprising pe-7 event and method of detection thereof
US20100077501A1 (en) 2007-04-05 2010-03-25 Bayer Bioscience N.V. Insect resistant cotton plants and methods for identifying same
WO2008122406A1 (en) 2007-04-05 2008-10-16 Bayer Bioscience N.V. Insect resistant cotton plants and methods for identifying same
WO2008150473A2 (en) 2007-05-30 2008-12-11 Syngenta Participations Ag Cytochrome p450 genes conferring herbicide resistance
WO2008151780A1 (en) 2007-06-11 2008-12-18 Bayer Bioscience N.V. Insect resistant cotton plants comprising elite event ee-gh6 and methods for identifying same
WO2008152091A2 (en) * 2007-06-15 2008-12-18 Bayer Cropscience Sa Pesticidal composition comprising a strigolactone derivative and an insecticide compound
WO2008152092A2 (en) 2007-06-15 2008-12-18 Bayer Cropscience Sa Pesticidal composition comprising a strigolactone derivative and an fungicide compound
WO2009049747A2 (en) 2007-10-16 2009-04-23 Merck Patent Gmbh Lipo-chitooligosaccharide and flavonoid combination for enhanced plant growth and yield
WO2009064652A1 (en) 2007-11-15 2009-05-22 Monsanto Technology Llc Soybean plant and seed corresponding to transgenic event mon87701 and methods for detection thereof
US20090130071A1 (en) 2007-11-15 2009-05-21 Ai-Guo Gao Soybean Plant And Seed Corresponding To Transgenic Event MON87701 And Methods For Detection Thereof
WO2009068313A2 (en) 2007-11-28 2009-06-04 Bayer Bioscience N.V. Brassica plant comprising a mutant indehiscent allele
WO2009100188A2 (en) 2008-02-08 2009-08-13 Dow Agrosciences Llc Methods for detection of corn event das-59132
US20090210970A1 (en) 2008-02-14 2009-08-20 Pioneer Hi-Bred International, Inc. Plant Genomic DNA Flanking SPT Event and Methods for Identifying SPT Event
WO2009103049A2 (en) 2008-02-14 2009-08-20 Pioneer Hi-Bred International, Inc. Plant genomic dna flanking spt event and methods for identifying spt event
WO2009102873A1 (en) 2008-02-15 2009-08-20 Monsanto Technology Llc Soybean plant and seed corresponding to transgenic event mon87769 and methods for detection thereof
US20110067141A1 (en) 2008-02-15 2011-03-17 Byron Froman Soybean plant and seed corresponding to transgenic event mon87769 and methods for detection thereof
WO2009111263A1 (en) 2008-02-29 2009-09-11 Monsanto Technology Llc Corn plant event mon87460 and compositions and methods for detection thereof
US20110138504A1 (en) 2008-02-29 2011-06-09 Monsanto Technology Llc Corn plant event mon87460 and compositions and methods for detection thereof
WO2009144079A1 (en) 2008-04-14 2009-12-03 Bayer Bioscience N.V. New mutated hydroxyphenylpyruvate dioxygenase, dna sequence and isolation of plants which are tolerant to hppd inhibitor herbicides
WO2009143995A1 (en) 2008-05-26 2009-12-03 Bayer Bioscience N.V. Methods and means to modify fiber strength in fiber-producing plants
EP2300618A1 (en) 2008-06-13 2011-03-30 Bayer BioScience N.V. Bollworm insect resistance management in transgenic plants
WO2010003701A1 (en) 2008-07-10 2010-01-14 Bayer Cropscience Ag Wheat starch and wheat flours and foodstuffs containing these wheat starch/wheat flours
WO2010006732A2 (en) 2008-07-17 2010-01-21 Bayer Bioscience N.V. Brassica plant comprising a mutant indehiscent allelle
WO2010012796A1 (en) 2008-08-01 2010-02-04 Bayer Bioscience N.V. A method for increasing photosynthetic carbon fixation in rice
WO2010024976A1 (en) 2008-08-29 2010-03-04 Monsanto Technology Llc Soybean plant and seed corresponding to transgenic event mon87754 and methods for detection thereof
US20100080887A1 (en) 2008-09-29 2010-04-01 Monsanto Technology Llc Soybean Transgenic Event MON87705 and Methods for Detection Thereof
WO2010037016A1 (en) 2008-09-29 2010-04-01 Monsanto Technology Llc Soybean transgenic event mon87705 and methods for detection thereof
WO2010077816A1 (en) 2008-12-16 2010-07-08 Syngenta Participations Ag Corn event 5307
EP2380876A1 (en) * 2008-12-19 2011-10-26 Nippon Soda Co., Ltd. 1-heterodiene derivative and harmful organism control agent
WO2010076212A1 (en) 2008-12-19 2010-07-08 Syngenta Participations Ag Transgenic sugar beet event gm rz13
WO2010080829A1 (en) 2009-01-07 2010-07-15 Basf Agrochemical Products B.V. Soybean event 127 and methods related thereto
WO2010117735A1 (en) 2009-03-30 2010-10-14 Monsanto Technology Llc Transgenic rice event17314 and methods of use thereof
WO2010117737A1 (en) 2009-03-30 2010-10-14 Monsanto Technology Llc Rice transgenic event17053 and methods of use thereof
WO2010121818A1 (en) 2009-04-22 2010-10-28 Bayer Bioscience N.V. Production of multi-antennary n-glycan structures in plants
WO2010125065A2 (en) 2009-04-28 2010-11-04 Bayer Cropscience Ag Compositions comprising a strigolactone compound and a chito-oligosaccharide compound for enhanced plant growth and yield
WO2010145846A1 (en) 2009-06-15 2010-12-23 Bayer Bioscience N.V. Nicotiana benthamiana plants deficient in xylosyltransferase activity
WO2011022469A2 (en) 2009-08-19 2011-02-24 Dow Agrosciences Llc Aad-1 event das-40278-9, related transgenic corn lines, and event-specific identification thereof
WO2011034704A1 (en) 2009-09-17 2011-03-24 Monsanto Technology Llc Soybean transgenic event mon 87708 and methods of use thereof
WO2011062904A1 (en) 2009-11-23 2011-05-26 Monsanto Technology Llc Transgenic maize event mon 87427 and the relative development scale
WO2011066384A1 (en) 2009-11-24 2011-06-03 Dow Agrosciences Llc Aad-12 event 416, related transgenic soybean lines, and event-specific identification thereof
WO2011066360A1 (en) 2009-11-24 2011-06-03 Dow Agrosciences Llc Detection of aad-12 soybean event 416
WO2011075593A1 (en) 2009-12-17 2011-06-23 Pioneer Hi-Bred International, Inc. Maize event dp-040416-8 and methods for detection thereof
WO2011075595A1 (en) 2009-12-17 2011-06-23 Pioneer Hi-Bred International, Inc. Maize event dp-043a47-3 and methods for detection thereof
WO2011084621A1 (en) 2009-12-17 2011-07-14 Pioneer Hi-Bred International, Inc. Maize event dp-004114-3 and methods for detection thereof
WO2011084632A1 (en) 2009-12-17 2011-07-14 Pioneer Hi-Bred International, Inc. Maize event dp-032316-8 and methods for detection thereof
WO2011153442A1 (en) 2010-06-04 2011-12-08 Syngenta Participations Ag Plant irrigation methods

Non-Patent Citations (38)

* Cited by examiner, † Cited by third party
Title
A. J. HUMPHREY; A. M. GALSTER; M. H. BEALE, NAT. PROD. REP., vol. 23, 2006, pages 592 - 614
A. S. MWAKABOKO; B. ZWANENBURG, BIOORG. MED. CHEM., vol. 19, 2011, pages 5006 - 5011
A. U. DE; B. P. SAHA, J. PHARM. SCI., vol. 62, 1973, pages 1363 - 1364
A. W. JOHNSON; G. GOWDA; A. HASSANALI; J. KNOX; S. MONACO; Z. RAZAVI; G. ROSEBERY, J. CHEM. SOC., PERKIN TRANS. 1, 1981, pages 1734 - 1743
A. W. JOHNSON; G. GOWDA; A. HASSANALI; J. KNOX; S. MONACO; Z. RAZAVI; G. ROSEBERY, J. CHEM. SOC., PERKIN TRANS., vol. 1, 1981, pages 1734 - 1743
AKIYAMA K. ET AL., NATURE, vol. 435, 2005, pages 824
APPLIED ENVIRONM. MICROBIOL, vol. 71, 2006, pages 1765 - 1774
BANFI, L; BASSO, A.; CERULLI, V.; GUANTI, G.; RIVA, R., J. ORG. CHEM., vol. 73, 2008, pages 1608 - 1611
BERGMANN, E.; HOFFMAN, E., J. ORG. CHEM., vol. 26, 1961, pages 3555
BESSERER ET AL., PLANT PHYSIOL., vol. 148, no. 1, 2008, pages 402 - 13
BUTLER, ALLELOPATHY: ORGANISM, PROCESSES AND APPLICATION, 1995, pages 158 - 168
C. V. DOS SANTOS; P. LETOUSEY; P. DELAVAULT; P. THALOUARN, PHYTOPATHOLOGY, vol. 93, 2003, pages 451 - 457
COOK ET AL., J AM CHEM SOC, vol. 94, 1972, pages 6198 - 6199
CRICKMORE ET AL., MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, vol. 62, 1998, pages 807 - 813
CURR. TOPICS PLANT PHYSIOL, vol. 7, 1992, pages 139 - 145
D'HAEZE; HOLSTERS, GLYCOBIOLOGY, vol. 12, 2002, pages 79R - 105R
E. FOO; N. W. DAVIES, PLANTA, 2011
G. A. MACALPINE; R. A. RAPHAEL; A. SHAW; A. W. TAYLOR; H. J. WILD, J. CHEM. SOC., PERKIN TRANS. 1, 1976, pages 410 - 416
G. A. MACALPINE; R. A. RAPHAEL; A. SHAW; A. W. TAYLOR; H. J. WILD, J. CHEM. SOC., PERKIN TRANS., vol. 1, 1976, pages 410 - 416
GOMEZ-ROLDAN ET AL., NATURE, vol. 455, 2008, pages 189 - 194
H. KOLTAI, NEW PHYTOL, vol. 190, 2011, pages 545 - 549
H. PROUST; B. HOFFMANN; X. XIE; K. YONEYAMA; D. G. SCHAEFER; K. YONEYAMA; F. NOGUE; C. RAMEAU, DEVELOPMENT, vol. 138, 2011, pages 1531 - 1539
HAUCK ET AL., J PLANT PHYSIOL, vol. 139, 1992, pages 474 - 478
HUNGRIA; STACEY, SOIL BIOL. BIOCHEM., vol. 29, 1997, pages 819 - 830
J. BIOL. CHEM., vol. 263, 1988, pages 4280 - 4289
JOHNSSON A W ET AL: "THE PREPARATION OF SYNTHETIC ANALOGUES OF STRIGOL", JOURNAL OF THE CHEMICAL SOCIETY, PERKIN TRANSACTIONS 1, CHEMICAL SOCIETY, LETCHWORTH; GB, no. 6, 1 January 1981 (1981-01-01), pages 1734 - 1743, XP002024940, ISSN: 0300-922X, DOI: 10.1039/P19810001734 *
MANGNUS, E. M.; DOMMERHOLT, F. J.; DEJONG, R. L. P.; ZWANENBURG, B., J. AGRIC. FOOD CHEM., vol. 40, 1992, pages 1230
MULLER ET AL., J PLANT GROWTH REGUL, vol. 11, 1992, pages 77 - 84
NAT. BIOTECHNOL., vol. 19, 2001, pages 668 - 72
OZAKI, S.; ADACHI, M.; SEKIYA, S.; KAMIKAWA, R., J. ORG. CHEM., vol. 68, 2003, pages 4586
SAMAIN ET AL., CARBOHYDRATE RESEARCH, vol. 302, 1997, pages 35 - 42
SCIENCE, vol. 221, 1983, pages 370 - 371
SCIENCE, vol. 233, 1986, pages 478 - 481
SIAME ET AL., J AGR FOOD CHEM, vol. 41, 1993, pages 1486 - 1491
SPAINK, CRITICAL REVIEWS IN PLANT SCIENCES, vol. 54, 2000, pages 257 - 288
T. MOSMANN, J. IMMUNOL. METHODS, vol. 65, 1983, pages 55 - 63
WEED SCIENCE, vol. 50, 2002, pages 700 - 712
YOKOTA ET AL., PHYTOCHEMISTRY, vol. 49, 1998, pages 1967 - 1973

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