[go: up one dir, main page]

WO1990012788A3 - ACETALISCH GESCHÜTZTE ENANTIOMERENREINE α-ARYLALKANCARBONSÄUREN, DEREN HERSTELLUNG UND VERWENDUNG - Google Patents

ACETALISCH GESCHÜTZTE ENANTIOMERENREINE α-ARYLALKANCARBONSÄUREN, DEREN HERSTELLUNG UND VERWENDUNG Download PDF

Info

Publication number
WO1990012788A3
WO1990012788A3 PCT/AT1990/000038 AT9000038W WO9012788A3 WO 1990012788 A3 WO1990012788 A3 WO 1990012788A3 AT 9000038 W AT9000038 W AT 9000038W WO 9012788 A3 WO9012788 A3 WO 9012788A3
Authority
WO
WIPO (PCT)
Prior art keywords
acetalically
enantiomer
pure
protected
production
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
PCT/AT1990/000038
Other languages
English (en)
French (fr)
Other versions
WO1990012788A2 (de
Inventor
Christian R Noe
Max Knollmueller
Marion Letschnig
Armin Holzner
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Publication of WO1990012788A2 publication Critical patent/WO1990012788A2/de
Publication of WO1990012788A3 publication Critical patent/WO1990012788A3/de
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C219/00—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton
    • C07C219/02—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having esterified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C219/04—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having esterified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C219/14—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having esterified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having at least one of the hydroxy groups esterified by a carboxylic acid having the esterifying carboxyl group bound to a carbon atom of a six-membered aromatic ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
    • C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C217/06—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted
    • C07C217/08—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to an acyclic carbon atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/93—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems condensed with a ring other than six-membered
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/94—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems condensed with rings other than six-membered or with ring systems containing such rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Die Erfindung betrifft acetalisch geschützte enantiomerenreine α-Arylalkancarbonsäuren der allgemeinen Formel (I), in welcher A, B, C und D Wasserstoff oder eine Methylgruppe in beliebiger Kombination, m und n die Zahlen 0, 1 oder 2 bedeutet, wobei die Summe aus m und n 1 oder 2 sein muss und in welcher Ar substituiertes oder unsubstituiertes Aryl und substituiertes oder unsubstituiertes Heteroaryl in beliebiger Kombination bedeutet, und in welcher R1 verzweigtes und unverzweigtes Alkyl, vorzugsweise nieder Alkyl bedeutet, deren Herstellung und Verwendung.
PCT/AT1990/000038 1989-04-24 1990-04-24 ACETALISCH GESCHÜTZTE ENANTIOMERENREINE α-ARYLALKANCARBONSÄUREN, DEREN HERSTELLUNG UND VERWENDUNG Ceased WO1990012788A2 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
AT96989 1989-04-24
ATA969/89 1989-04-24

Publications (2)

Publication Number Publication Date
WO1990012788A2 WO1990012788A2 (de) 1990-11-01
WO1990012788A3 true WO1990012788A3 (de) 1990-12-13

Family

ID=3503968

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/AT1990/000038 Ceased WO1990012788A2 (de) 1989-04-24 1990-04-24 ACETALISCH GESCHÜTZTE ENANTIOMERENREINE α-ARYLALKANCARBONSÄUREN, DEREN HERSTELLUNG UND VERWENDUNG

Country Status (2)

Country Link
AU (1) AU5527190A (de)
WO (1) WO1990012788A2 (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT396686B (de) * 1992-04-13 1993-11-25 Christian Dr Noe Reagention zur razemattrennung, verfahren zu ihrer herstellung und verwendung

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH291375A (de) * 1950-12-13 1953-06-15 Hommels S Haematogen Ag Verfahren zur Herstellung von a-Phenylbuttersäure-diäthylaminoäthylester.
US3349114A (en) * 1963-05-17 1967-10-24 Hommel Ag Diethylaminoethoxyethyl ester of alpha-phenylbutyric acid and salts thereof
EP0083335A1 (de) * 1981-12-18 1983-07-06 Christian Dipl.-Ing. Dr. Noe Chirale, optisch aktive Verbindungen, Verfahren zu ihrer Herstellung und Verwendung dieser Verbindungen für den Schutz funktioneller -OH, -SH, -NH-Gruppen, zur Racemattrennung, zur Herstellung optisch aktiver Imidoesterhydrochloride sowie optisch aktiver Ester, zur Herstellung optisch angereicherter Alkohole und zur Herstellung optisch aktiver Verbindungen durch asymmetrische Induktion

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH291375A (de) * 1950-12-13 1953-06-15 Hommels S Haematogen Ag Verfahren zur Herstellung von a-Phenylbuttersäure-diäthylaminoäthylester.
US3349114A (en) * 1963-05-17 1967-10-24 Hommel Ag Diethylaminoethoxyethyl ester of alpha-phenylbutyric acid and salts thereof
EP0083335A1 (de) * 1981-12-18 1983-07-06 Christian Dipl.-Ing. Dr. Noe Chirale, optisch aktive Verbindungen, Verfahren zu ihrer Herstellung und Verwendung dieser Verbindungen für den Schutz funktioneller -OH, -SH, -NH-Gruppen, zur Racemattrennung, zur Herstellung optisch aktiver Imidoesterhydrochloride sowie optisch aktiver Ester, zur Herstellung optisch angereicherter Alkohole und zur Herstellung optisch aktiver Verbindungen durch asymmetrische Induktion

Also Published As

Publication number Publication date
AU5527190A (en) 1990-11-16
WO1990012788A2 (de) 1990-11-01

Similar Documents

Publication Publication Date Title
CA2033392A1 (en) A-nor-steroid-3-carboxylic acid derivatives
CA2123052A1 (en) Monomeric bile acid derivatives, processes for their preparation and the use of these compounds as medicaments
EP0955340A3 (de) Flüssige Silikon-Ester
CA2011294A1 (en) Carbonylation catalyst system
ATE105285T1 (de) Salicylaldehyd- und salicylsaeurederivate sowie deren schwefelanaloge, verfahren zu ihrer herstellung und ihre verwendung als herbizide und bioregulatoren.
IE892272L (en) Novel fused heterocyclic compounds
EP0952151A3 (de) Zwischenverbindungen zur Herstellung von neunen Pyridoncarbonsäurederivate oder deren Salzen
CA2135751A1 (en) 4-Mercaptoacetylamino-[2] Benzazepinone(3) Derivatives, and Use as Enkephalinase Inhibitors
CA2206754A1 (en) Benzimidazole derivatives with antihistaminic activity
FI911910A0 (fi) 5,5-bis(perfluorialkyyliheterometyyli)-2-hydroksi-2-okso-1,3,2-dioksafosforinaanit, niiden asykliset fosforihapokejohdannaiset sekä suolat tai esterit
CA2038848A1 (en) Hydantoin derivatives
MY131693A (en) Arylacetic acid derivatives
AU1614492A (en) New peptide compound and a process for the preparation thereof
GR3004988T3 (de)
CA2020474A1 (en) Antiinflammatory and/or antiallergic composition
CA2164642A1 (en) Novel compounds having a benzisoselen-azoline and -azine structure, method for preparing same and therapeutic uses thereof
ES2191364T3 (es) Agente tixotropico basado en una resina alquidica.
WO1990012788A3 (de) ACETALISCH GESCHÜTZTE ENANTIOMERENREINE α-ARYLALKANCARBONSÄUREN, DEREN HERSTELLUNG UND VERWENDUNG
AU625627B2 (en) Triazinic compounds
FI941149A7 (fi) 2,4-diamino-3-hydroksikarboksyylihapon johdannaisia
EP0712393A1 (de) Substituierte 4-carbamoyl-pyrrolin-2-on- und -dihydrofuran-2-on-derivate und deren verwendung als schädlingsbekämpfungsmittel
IE851486L (en) CYCLOPENTA (b) THIOPHENE-6-CARBOXYLIC ACIDS
GB2321459A (en) Synthesis of carboxylic acid derivatives
PL312966A1 (en) Derivatives of thiocarbamoil
WO1995006473A3 (en) Medical use of polysulfonic acid compound

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A2

Designated state(s): AU CA HU JP KR SU US

AL Designated countries for regional patents

Kind code of ref document: A2

Designated state(s): AT BE CH DE DK ES FR GB IT LU NL SE

AK Designated states

Kind code of ref document: A3

Designated state(s): AU CA HU JP KR SU US

AL Designated countries for regional patents

Kind code of ref document: A3

Designated state(s): AT BE CH DE DK ES FR GB IT LU NL SE

NENP Non-entry into the national phase in:

Ref country code: CA