[go: up one dir, main page]

PT1943211E - Processo para a preparação de compostos de dimetil-(3-arilbutil)- amina substituídos por meio de catálise homogénea - Google Patents

Processo para a preparação de compostos de dimetil-(3-arilbutil)- amina substituídos por meio de catálise homogénea Download PDF

Info

Publication number
PT1943211E
PT1943211E PT06840923T PT06840923T PT1943211E PT 1943211 E PT1943211 E PT 1943211E PT 06840923 T PT06840923 T PT 06840923T PT 06840923 T PT06840923 T PT 06840923T PT 1943211 E PT1943211 E PT 1943211E
Authority
PT
Portugal
Prior art keywords
arylbutyl
amine compounds
homogeneous catalysis
preparing substituted
substituted dimethyl
Prior art date
Application number
PT06840923T
Other languages
English (en)
Inventor
Felix Spindler
Helmut Buschmann
Wolfgang Hell
Markus Kegel
Hans-Joachim Drexler
Detlef Heller
Original Assignee
Gruenenthal Gmbh
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Gruenenthal Gmbh filed Critical Gruenenthal Gmbh
Publication of PT1943211E publication Critical patent/PT1943211E/pt

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
    • C07C213/08—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reactions not involving the formation of amino groups, hydroxy groups or etherified or esterified hydroxy groups
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • B01J31/2409—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring with more than one complexing phosphine-P atom
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • B01J31/2419—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising P as ring member
    • B01J31/2428—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising P as ring member with more than one complexing phosphine-P atom
    • B01J31/2433—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising P as ring member with more than one complexing phosphine-P atom comprising aliphatic or saturated rings
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • B01J31/2419—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising P as ring member
    • B01J31/2438—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising P as ring member and further hetero atoms as ring members, excluding the positions adjacent to P
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • B01J31/2442—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems
    • B01J31/2447—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as substituents on a ring of the condensed system or on a further attached ring
    • B01J31/2452—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as substituents on a ring of the condensed system or on a further attached ring with more than one complexing phosphine-P atom
    • B01J31/2457—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as substituents on a ring of the condensed system or on a further attached ring with more than one complexing phosphine-P atom comprising aliphatic or saturated rings, e.g. Xantphos
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • B01J31/2442—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems
    • B01J31/2461—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as ring members in the condensed ring system or in a further ring
    • B01J31/2471—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as ring members in the condensed ring system or in a further ring with more than one complexing phosphine-P atom
    • B01J31/2476—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as ring members in the condensed ring system or in a further ring with more than one complexing phosphine-P atom comprising aliphatic or saturated rings
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • B01J31/2442—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems
    • B01J31/249—Spiro-condensed ring systems
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/60—Reduction reactions, e.g. hydrogenation
    • B01J2231/64—Reductions in general of organic substrates, e.g. hydride reductions or hydrogenations
    • B01J2231/641—Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes
    • B01J2231/645—Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes of C=C or C-C triple bonds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/02—Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0261—Complexes comprising ligands with non-tetrahedral chirality
    • B01J2531/0263—Planar chiral ligands, e.g. derived from donor-substituted paracyclophanes and metallocenes or from substituted arenes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/02—Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0261—Complexes comprising ligands with non-tetrahedral chirality
    • B01J2531/0266—Axially chiral or atropisomeric ligands, e.g. bulky biaryls such as donor-substituted binaphthalenes, e.g. "BINAP" or "BINOL"
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/02—Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0269—Complexes comprising ligands derived from the natural chiral pool or otherwise having a characteristic structure or geometry
    • B01J2531/0272—Complexes comprising ligands derived from the natural chiral pool or otherwise having a characteristic structure or geometry derived from carbohydrates, including e.g. tartrates or DIOP
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82—Metals of the platinum group
    • B01J2531/821—Ruthenium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82—Metals of the platinum group
    • B01J2531/822—Rhodium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82—Metals of the platinum group
    • B01J2531/827—Iridium

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
PT06840923T 2005-11-02 2006-10-30 Processo para a preparação de compostos de dimetil-(3-arilbutil)- amina substituídos por meio de catálise homogénea PT1943211E (pt)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE102005052588A DE102005052588A1 (de) 2005-11-02 2005-11-02 Verfahren zur Herstellung substituierter Dimethyl-(3-aryl-butyl)-amin-Verbindungen mittels homogener Katalyse

Publications (1)

Publication Number Publication Date
PT1943211E true PT1943211E (pt) 2011-09-06

Family

ID=37709627

Family Applications (1)

Application Number Title Priority Date Filing Date
PT06840923T PT1943211E (pt) 2005-11-02 2006-10-30 Processo para a preparação de compostos de dimetil-(3-arilbutil)- amina substituídos por meio de catálise homogénea

Country Status (11)

Country Link
US (1) US8791300B2 (pt)
EP (1) EP1943211B1 (pt)
CN (1) CN101351441B (pt)
AT (1) ATE520648T1 (pt)
DE (1) DE102005052588A1 (pt)
ES (1) ES2368946T3 (pt)
IL (1) IL191162A (pt)
PL (1) PL1943211T3 (pt)
PT (1) PT1943211E (pt)
SI (1) SI1943211T1 (pt)
WO (1) WO2007051576A1 (pt)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102005052588A1 (de) 2005-11-02 2007-05-10 Grünenthal GmbH Verfahren zur Herstellung substituierter Dimethyl-(3-aryl-butyl)-amin-Verbindungen mittels homogener Katalyse
CZ2010997A3 (cs) * 2010-12-30 2012-02-08 Zentiva, K.S. Zpusob výroby (2R,3R)-N,N-dimethyl-3-(3-hydroxyfenyl)-2-methylpentylaminu (tapentadolu)
WO2012089181A1 (en) * 2010-12-30 2012-07-05 Zentiva, K.S. O-substituted (2r,3r)-3-(3-hydroxyphenyl)-2-methyl-4-pentenoic acids and a method of obtaining the same
EP2842423B1 (en) 2011-03-24 2018-07-18 Enviro Tech Chemical Services Inc. Method for the generation of peracetic acid on site at the point-of-use.
EP2674414A1 (en) 2012-06-15 2013-12-18 Siegfried AG Method for the preparation of 1-aryl-1-alkyl-3-dialkylaminopropane compounds
US9090539B2 (en) * 2013-05-24 2015-07-28 Ampac Fine Chemicals Llc Compounds and methods for preparing substituted 3-(1-amino-2-methylpentane-3-yl)phenyl compounds

Family Cites Families (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT322534B (de) 1972-03-16 1975-05-26 Thomae Gmbh Dr K Verfahren zur herstellung von neuen optisch aktiven 1-(4'-amino-3'-halogenphenyl)-2-aminoäthanolen und deren säureadditionssalzen
US4012456A (en) 1974-11-19 1977-03-15 Chaplits Donat N Method for separation of isobutylene from C4 hydrocarbon fractions
DD124521A1 (pt) 1976-03-16 1977-03-02
US4276195A (en) 1979-12-20 1981-06-30 Iowa State University Research Foundation, Inc. Converting homogeneous to heterogeneous catalysts
US6022637A (en) 1984-10-23 2000-02-08 Wilson; John T. R. High temperature battery
JPH0690934B2 (ja) 1987-08-07 1994-11-14 日本電信電話株式会社 二次電池およびその製造方法
US5446844A (en) 1987-10-05 1995-08-29 Unisys Corporation Peripheral memory interface controller as a cache for a large data processing system
DE59309554D1 (de) 1992-04-02 1999-06-10 Novartis Ag Ferrocenyldiphosphine als Liganden für homogene Katalysatoren
SG42938A1 (en) * 1993-02-26 1997-10-17 Ciba Geigy Ag Ferrocenc diphosphines as ligands for homogeneous catalysts
DE59408655D1 (de) 1993-10-01 1999-09-30 Novartis Ag Mit Fluoralkyl substituierte Ferrocenyldiphosphine als Liganden für homogene Katalysatoren
JP3833699B2 (ja) 1994-02-02 2006-10-18 シンジェンタ パーティシペーションズ アクチェンゲゼルシャフト イミンの水素化法
JPH07326372A (ja) 1994-05-30 1995-12-12 Yuasa Corp 固体電解質電池
DE4426245A1 (de) 1994-07-23 1996-02-22 Gruenenthal Gmbh 1-Phenyl-3-dimethylamino-propanverbindungen mit pharmakologischer Wirkung
DE59609584D1 (de) 1995-02-24 2002-10-02 Syngenta Participations Ag An Seitenketten von Polymeren gebundene Diphosphine und deren Metall-Komplexe
ATE195525T1 (de) * 1995-02-24 2000-09-15 Novartis Ag Silylierte ferrocenyldiphosphine, an anorganische oder polymere organische träger gebundene silylierte ferrocenyldiphosphine sowie metallkomplexe davon, ihre herstellung und verwendung
DE19609847A1 (de) 1996-03-13 1997-09-18 Gruenenthal Gmbh Dimethyl-(3-aryl-but-3-enyl)-aminverbindungen als pharmazeutische Wirkstoffe
US6337156B1 (en) 1997-12-23 2002-01-08 Sri International Ion battery using high aspect ratio electrodes
JPH11345629A (ja) 1998-03-31 1999-12-14 Canon Inc 二次電池及びその製造方法
DE10000311A1 (de) * 2000-01-05 2001-07-12 Gruenenthal Gmbh Aminomethyl-Phonyl-Cyclohexanonderivate
JP4951809B2 (ja) 2000-11-21 2012-06-13 日油株式会社 二次電池用電解質および二次電池
JP4777593B2 (ja) 2002-11-29 2011-09-21 株式会社オハラ リチウムイオン二次電池の製造方法
JP4366101B2 (ja) 2003-03-31 2009-11-18 キヤノン株式会社 リチウム二次電池
WO2004089920A2 (de) * 2003-04-07 2004-10-21 Solvias Ag Amin-substituierte diphenyldiphosphine und deren verwendung in metallkomplexen für asymmetrische synthesen
DE10326097A1 (de) * 2003-06-06 2005-01-05 Grünenthal GmbH Verfahren zur Herstellung von Dimethyl-(3-aryl-butyl)-aminverbindungen
DE10328316A1 (de) 2003-06-23 2005-01-20 Grünenthal GmbH Verfahren zur Herstellung von Dimethyl-(3-aryl-buthyl)-aminverbindungen als pharmazeutische Wirkstoffe
JP2009519212A (ja) 2005-10-26 2009-05-14 イーライ リリー アンド カンパニー 選択的ｖｐａｃ２受容体ペプチドアゴニスト
DE102005052588A1 (de) 2005-11-02 2007-05-10 Grünenthal GmbH Verfahren zur Herstellung substituierter Dimethyl-(3-aryl-butyl)-amin-Verbindungen mittels homogener Katalyse

Also Published As

Publication number Publication date
ATE520648T1 (de) 2011-09-15
EP1943211B1 (de) 2011-08-17
PL1943211T3 (pl) 2012-01-31
CN101351441A (zh) 2009-01-21
HK1121131A1 (en) 2009-04-17
ES2368946T3 (es) 2011-11-23
IL191162A (en) 2013-10-31
US20090043132A1 (en) 2009-02-12
US8791300B2 (en) 2014-07-29
DE102005052588A1 (de) 2007-05-10
EP1943211A1 (de) 2008-07-16
SI1943211T1 (sl) 2011-10-28
IL191162A0 (en) 2008-12-29
WO2007051576A1 (de) 2007-05-10
CN101351441B (zh) 2012-11-14

Similar Documents

Publication Publication Date Title
IL191162A0 (en) Process for preparing substituted dimethyl (3-arylbutyl)amine compounds by means of homogeneous catalysis
Lo et al. Gold (III)(C^ N) complex-catalyzed synthesis of propargylamines via a three-component coupling reaction of aldehydes, amines and alkynes
Miura et al. Nickel‐Catalyzed Regio‐and Enantioselective Annulation Reactions of 1, 2, 3, 4‐Benzothiatriazine‐1, 1 (2H)‐dioxides with Allenes
Abdur‐Rashid et al. Synthesis of ruthenium hydride complexes containing beta‐aminophosphine ligands derived from amino acids and their use in the H2‐hydrogenation of ketones and imines
MX2013008560A (es) Metodo para preparar derivados de 2-aminobenzamida.
JP5847386B2 (ja) アミン化合物の製造方法
LeCloux et al. Synthesis and transition metal complexation of an enantiomerically pure tris (pyrazolyl) hydroborate ligand
MY172034A (en) Intermediate for producing bicyclic ?-amino acid derivative
IL205378A0 (en) Process for preparing 2 - amino - 5 - cyanobenzoic acid derivatives
Ortega-Moreno et al. Synthesis, properties, and some rhodium, iridium, and platinum complexes of a series of bulky m-terphenylphosphine ligands
MX2010013939A (es) Derivados de n-oxido pirazina sustituidos.
Kawano et al. Syntheses and Reactivity of Cationic Borane− Ruthenium Complexes [(η5-C5R5) Ru (PMe3) 2 (η1-BH3⊙ EMe3)][BAr f 4](R= H, Me; E= N, P; BAr f 4=[B {3, 5-C6H3 (CF3) 2} 4])
García‐Álvarez et al. Arene‐Ruthenium (II) and Bis (allyl)‐Ruthenium (IV) Complexes Containing 2‐(Diphenylphosphanyl) pyridine Ligands: Potential Catalysts for Nitrile Hydration Reactions?
MXPA02012678A (es) Complejos de rutenio-difosfina y su uso como catalizadores.
CA2385927A1 (en) Carbon monoxide source for the preparation of transition metal carbonyl complexes
Haasnoot et al. X-ray structure and reactivity of bis (2, 2'-bipyridine) carbonylhydridoruthenium hexafluorophosphate hemi (acetone), a possible intermediate in the water-gas shift reaction catalyzed by ruthenium polypyridyl complexes
IL171765A (en) Substituted ferrocenyldiphosphines as ligands for homogeneous hydrogenation catalysts
TW200724547A (en) Bidentate C, P chiral phosphine ligands
Kitamura et al. Mechanistic insight into NOYORI asymmetric hydrogenations
WO2008148202A8 (en) Method for the preparation of aminophosphine ligands and their use in metal catalysts
WO2006100169A3 (en) Unsymmetrically substituted phospholane catalysts
PT1191030E (pt) Fosfinetes-oxazolinas e complexos metalicos
IL164915A0 (en) Process for hydrogenating unactivated imines usines using ruthenium complexes as catalysts
IL196178A0 (en) Diphosphine ligands
IL207020A0 (en) Process for preparing substituted biphenylanilides