DE69512002T2 - Verfahren zur Herstellung von optisch aktiven Carbinolen - Google Patents

Verfahren zur Herstellung von optisch aktiven Carbinolen

Info

Publication number
DE69512002T2
DE69512002T2 DE69512002T DE69512002T DE69512002T2 DE 69512002 T2 DE69512002 T2 DE 69512002T2 DE 69512002 T DE69512002 T DE 69512002T DE 69512002 T DE69512002 T DE 69512002T DE 69512002 T2 DE69512002 T2 DE 69512002T2
Authority
DE
Germany
Prior art keywords
production
optically active
carbinols
active carbinols
optically
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.)
Expired - Fee Related
Application number
DE69512002T
Other languages
English (en)
Other versions
DE69512002D1 (de
Inventor
Kenji Saito
Norio Kometani
Azusa Fujiwara
Yukio Yoneyoshi
Gohfu Suzukamo
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.)
Sumika Fine Chemicals Co Ltd
Original Assignee
Sumika Fine Chemicals Co Ltd
Sumitomo Chemical Co Ltd
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
Priority claimed from JP15607295A external-priority patent/JP3687138B2/ja
Priority claimed from JP17616995A external-priority patent/JPH08225475A/ja
Priority claimed from JP17617095A external-priority patent/JPH08176039A/ja
Application filed by Sumika Fine Chemicals Co Ltd, Sumitomo Chemical Co Ltd filed Critical Sumika Fine Chemicals Co Ltd
Publication of DE69512002D1 publication Critical patent/DE69512002D1/de
Application granted granted Critical
Publication of DE69512002T2 publication Critical patent/DE69512002T2/de
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
    • C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
    • C07D317/54—Radicals substituted by oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
    • C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
    • C07C29/143—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of ketones
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07—Optical isomers
DE69512002T 1994-10-28 1995-10-27 Verfahren zur Herstellung von optisch aktiven Carbinolen Expired - Fee Related DE69512002T2 (de)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
JP28908994 1994-10-28
JP33579294 1994-12-20
JP15607295A JP3687138B2 (ja) 1995-06-22 1995-06-22 光学活性アルコール類の製法
JP17616995A JPH08225475A (ja) 1994-12-20 1995-07-12 光学活性ハロメチルフェニルカルビノール類の製造方法
JP17617095A JPH08176039A (ja) 1994-10-28 1995-07-12 光学活性ハロメチルフェニルカルビノール類の製造法

Publications (2)

Publication Number Publication Date
DE69512002D1 DE69512002D1 (de) 1999-10-14
DE69512002T2 true DE69512002T2 (de) 2000-05-25

Family

ID=27528098

Family Applications (1)

Application Number Title Priority Date Filing Date
DE69512002T Expired - Fee Related DE69512002T2 (de) 1994-10-28 1995-10-27 Verfahren zur Herstellung von optisch aktiven Carbinolen

Country Status (3)

Country Link
US (2) US5831132A (de)
EP (1) EP0713848B1 (de)
DE (1) DE69512002T2 (de)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPWO2002051781A1 (ja) * 2000-12-25 2004-04-22 味の素株式会社 光学活性ハロヒドリン化合物の製造方法
BR0214863A (pt) * 2001-12-11 2004-12-14 Wyeth Corp Processo para a sìntese de beta-aminoálcoois quiralmente puros
TW200843642A (en) * 2007-03-08 2008-11-16 Du Pont Liquid sulfonylurea herbicide formulations
WO2011132194A1 (en) * 2010-04-19 2011-10-27 Hetero Research Foundation Process for the preparation of raloxifene hydrochloride
DE102010040187A1 (de) 2010-09-02 2012-03-08 Bayer Schering Pharma Aktiengesellschaft Substituierte N-Phenethyl-triazolonacetamide und ihre Verwendung
CN102584536B (zh) * 2012-01-18 2014-06-11 广西新晶科技有限公司 不对称催化合成(r)-(+)-3-氯-苯丙醇的方法
CN110015944A (zh) * 2019-05-06 2019-07-16 福建康鸿生物科技有限公司 一种高选择性的卢立康唑中间体的合成方法

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5041651A (en) * 1983-04-04 1991-08-20 Sumitomo Chemical Company, Limited Asymmetrically modified boron hydride type compound and a method for producing an optically active alcohol derivative by the use thereof
HU202873B (en) * 1983-04-04 1991-04-29 Sumitomo Chemical Co Process for producing asymmetrically modified boron hydride type compounds
WO1985004401A1 (en) * 1984-04-03 1985-10-10 Sumitomo Chemical Company, Limited PROCESS FOR PREPARING OPTICALLY ACTIVE alpha, beta-UNSATURED ALCOHOL
US4943635A (en) * 1987-08-27 1990-07-24 President & Fellows Of Harvard College Enantioselective reduction of ketones
US5144039A (en) * 1989-01-30 1992-09-01 Sumitomo Electric Company, Limited Process for producing optically active alcohol
JPH06329679A (ja) * 1993-01-20 1994-11-29 Nissan Chem Ind Ltd 光学活性β−アミノアルコキシボラン錯体
TW416958B (en) * 1993-05-14 2001-01-01 Pfizer Enantioselective oxazaborolidine catalysts
JP3498332B2 (ja) * 1993-10-07 2004-02-16 住友化学工業株式会社 不斉還元剤、および該不斉還元剤を用いる光学活性体の製造方法
ATE159706T1 (de) * 1993-11-30 1997-11-15 Pfizer Verfahren zur herstellung von chiralen tetralonen
US5495054A (en) * 1994-05-31 1996-02-27 Sepracor, Inc. Tetrahydroindeno[1,2-D][1,3,2]oxazaboroles and their use as enantioselective catalysts
US5801280A (en) * 1995-04-07 1998-09-01 Sumitomo Chemical Company, Limited Processes for preparing optically active alcohols and optically active amines

Also Published As

Publication number Publication date
US6156940A (en) 2000-12-05
EP0713848B1 (de) 1999-09-08
DE69512002D1 (de) 1999-10-14
US5831132A (en) 1998-11-03
EP0713848A1 (de) 1996-05-29

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Legal Events

Date Code Title Description
8364 No opposition during term of opposition
8327 Change in the person/name/address of the patent owner

Owner name: SUMIKA FINE CHEMICAL CO. LTD., OSAKA, JP

8339 Ceased/non-payment of the annual fee