DE3686502T2 - Verfahren zur herstellung von optisch aktivem 2-halo-phenyl-ethanol. - Google Patents

Verfahren zur herstellung von optisch aktivem 2-halo-phenyl-ethanol.

Info

Publication number
DE3686502T2
DE3686502T2 DE8686104993T DE3686502T DE3686502T2 DE 3686502 T2 DE3686502 T2 DE 3686502T2 DE 8686104993 T DE8686104993 T DE 8686104993T DE 3686502 T DE3686502 T DE 3686502T DE 3686502 T2 DE3686502 T2 DE 3686502T2
Authority
DE
Germany
Prior art keywords
halo
optically active
producing optically
phenyl ethanol
phenyl
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
DE8686104993T
Other languages
English (en)
Other versions
DE3686502D1 (de
Inventor
Hidetoshi Kutsuki
Ikuo Sawa
Natsuki Mori
Junzo Hasegawa
Kiyoshi Watanabe
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.)
Kanegafuchi Chemical Industry Co Ltd
Original Assignee
Kanegafuchi Chemical Industry 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 JP7911585A external-priority patent/JPS61239893A/ja
Priority claimed from JP20364385A external-priority patent/JPS6265686A/ja
Priority claimed from JP20364485A external-priority patent/JPS6265687A/ja
Application filed by Kanegafuchi Chemical Industry Co Ltd filed Critical Kanegafuchi Chemical Industry Co Ltd
Publication of DE3686502D1 publication Critical patent/DE3686502D1/de
Application granted granted Critical
Publication of DE3686502T2 publication Critical patent/DE3686502T2/de
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00—Preparation of oxygen-containing organic compounds
    • C12P7/02—Preparation of oxygen-containing organic compounds containing a hydroxy group
    • C12P7/22—Preparation of oxygen-containing organic compounds containing a hydroxy group aromatic
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms using fungi
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms using fungi
    • Y10S435/921—Candida
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms using fungi
    • Y10S435/933—Penicillium
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms using fungi
    • Y10S435/94—Saccharomyces
DE8686104993T 1985-04-13 1986-04-11 Verfahren zur herstellung von optisch aktivem 2-halo-phenyl-ethanol. Expired - Fee Related DE3686502T2 (de)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP7911585A JPS61239893A (ja) 1985-04-13 1985-04-13 光学活性（ｓ）−２−ハロ−１−フエニルエタノ−ルの製造法
JP7911485 1985-04-13
JP20364385A JPS6265686A (ja) 1985-09-14 1985-09-14 光学活性（ｓ）−２−ハロ−１−フエニルエタノ−ルの製造法
JP20364485A JPS6265687A (ja) 1985-09-14 1985-09-14 光学活性（ｒ）−２−ハロ−１−フエニルエタノ−ルの製造法

Publications (2)

Publication Number Publication Date
DE3686502D1 DE3686502D1 (de) 1992-10-01
DE3686502T2 true DE3686502T2 (de) 1993-01-28

Family

ID=27466254

Family Applications (1)

Application Number Title Priority Date Filing Date
DE8686104993T Expired - Fee Related DE3686502T2 (de) 1985-04-13 1986-04-11 Verfahren zur herstellung von optisch aktivem 2-halo-phenyl-ethanol.

Country Status (3)

Country Link
US (1) US4857468A (de)
EP (1) EP0198440B1 (de)
DE (1) DE3686502T2 (de)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10248277A1 (de) * 2002-10-16 2004-05-06 X-Zyme Gmbh Verfahren zur Herstellung optisch aktiver Verbindungen

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK649787A (da) * 1986-12-23 1988-06-24 Hoffmann La Roche Fremgangsmaade til fremstilling af optisk aktive smoersyrederivater
FR2614038B1 (fr) * 1987-04-17 1989-08-04 Centre Nat Rech Scient Procede electroenzymatique de production de composes de purete enantiomerique controlee
JPH02312593A (ja) * 1989-05-26 1990-12-27 Daito Koeki Kk パン酵母によるケトン類の不斉還元反応方法
DE3942871A1 (de) * 1989-12-23 1991-06-27 Hoechst Ag R-(-)-1-(5-hydroxyhexyl)-3-methyl-7-propylxanthin, verfahren zu dessen herstellung und diese verbindung enthaltende arzneimittel
US5425941A (en) * 1991-08-16 1995-06-20 The United States Of America As Represented By The Secretary Of Agriculture Biological control of diseases of harvested agricultural commodities using strains of the yeast Candida oleophola
EP0538693A3 (en) * 1991-10-23 1994-08-17 Squibb & Sons Inc Stereoselective preparation of halophenyl alcohols
JP3087419B2 (ja) * 1991-11-14 2000-09-11 味の素株式会社 （ｓ）−１−フェニル−１，３−プロパンジオールまたはその誘導体の製造方法
GB9124513D0 (en) * 1991-11-19 1992-01-08 Smithkline Beecham Plc Novel process
JP3279671B2 (ja) * 1992-09-28 2002-04-30 鐘淵化学工業株式会社 チエノチオピラン誘導体の製造方法
CA2103932A1 (en) * 1992-11-05 1994-05-06 Ramesh N. Patel Stereoselective reduction of ketones
US5420337A (en) * 1992-11-12 1995-05-30 E. R. Squibb & Sons, Inc. Enzymatic reduction method for the preparation of compounds useful for preparing taxanes
US5602272A (en) * 1994-06-21 1997-02-11 Bristol-Myers Squibb Company Reduction and resolution methods for the preparation of compounds useful as intemediates for preparing taxanes
JP3529904B2 (ja) * 1995-06-19 2004-05-24 鐘淵化学工業株式会社 光学活性１−ハロ−３−アミノ−４−フェニル−２−ブタノール誘導体の製造法
US5756862A (en) * 1995-08-26 1998-05-26 Nihon Nohyaku Co., Ltd. Production of optically active 2-halo-1-(substituted phenyl)ethanol and substituted styrene oxide
IL132500A0 (en) * 1998-10-29 2001-03-19 Pfizer Prod Inc Stereoselective microbial reduction of a racemic tetralone
JPWO2003033468A1 (ja) * 2001-10-17 2005-02-03 株式会社カネカ （Ｓ）−α−ハロメチルピリジンメタノール誘導体の製造方法
CN104313062A (zh) * 2014-10-30 2015-01-28 青岛科技大学 一种细胞催化生产光活性苯乙醇的方法
CN104328151A (zh) * 2014-10-30 2015-02-04 青岛科技大学 一种细胞催化生产苯并噻吩乙醇的方法
CN106957212A (zh) * 2017-03-09 2017-07-18 康化（上海）新药研发有限公司 一种光学纯五氟苯乙醇的合成方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3076750A (en) * 1959-07-01 1963-02-05 Lever Brothers Ltd Microbiologically reducing keto acids
US4396715A (en) * 1979-04-04 1983-08-02 The Simon Greenberg Foundation Production of gamma-lactone rich flavor additives by pityrosporum species cultured on lipid rich substrates
JPS61289899A (ja) * 1985-06-18 1986-12-19 Kanegafuchi Chem Ind Co Ltd 光学活性２−ハロ−１−フエニルエタノ−ルおよびそのエステルの製造法

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10248277A1 (de) * 2002-10-16 2004-05-06 X-Zyme Gmbh Verfahren zur Herstellung optisch aktiver Verbindungen

Also Published As

Publication number Publication date
EP0198440A3 (en) 1989-02-08
DE3686502D1 (de) 1992-10-01
US4857468A (en) 1989-08-15
EP0198440A2 (de) 1986-10-22
EP0198440B1 (de) 1992-08-26

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Legal Events

Date Code Title Description
8364 No opposition during term of opposition
8339 Ceased/non-payment of the annual fee