CA2065550A1 - Process for the enzymatic hydrolysis of a carboxylic acid derivative - Google Patents

Process for the enzymatic hydrolysis of a carboxylic acid derivative

Info

Publication number
CA2065550A1
CA2065550A1 CA002065550A CA2065550A CA2065550A1 CA 2065550 A1 CA2065550 A1 CA 2065550A1 CA 002065550 A CA002065550 A CA 002065550A CA 2065550 A CA2065550 A CA 2065550A CA 2065550 A1 CA2065550 A1 CA 2065550A1
Authority
CA
Canada
Prior art keywords
water
organic
carboxylic acid
process according
hydrolase
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.)
Abandoned
Application number
CA002065550A
Other languages
English (en)
French (fr)
Inventor
Maria Buchner
Robert Estermann
Herbert Mayrhofer
Gerald Banko
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.)
Patheon Austria GmbH and Co KG
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 CA2065550A1 publication Critical patent/CA2065550A1/en
Abandoned 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
    • C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • C12P41/003—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions
    • C12P41/005—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions by esterification of carboxylic acid groups in the enantiomers or the inverse reaction
    • 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
    • C12P7/04—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic
    • 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
    • C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Microbiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biotechnology (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Analytical Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
CA002065550A 1991-04-29 1992-04-07 Process for the enzymatic hydrolysis of a carboxylic acid derivative Abandoned CA2065550A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
AT0088691A AT398081B (de) 1991-04-29 1991-04-29 Verfahren zur enzymatischen hydrolyse eines carbonsäurederivates
ATA886/91 1991-04-29

Publications (1)

Publication Number Publication Date
CA2065550A1 true CA2065550A1 (en) 1992-10-30

Family

ID=3502090

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002065550A Abandoned CA2065550A1 (en) 1991-04-29 1992-04-07 Process for the enzymatic hydrolysis of a carboxylic acid derivative

Country Status (12)

Country Link
US (1) US5278054A (https=)
EP (1) EP0511526A1 (https=)
JP (1) JPH05130881A (https=)
AT (1) AT398081B (https=)
AU (1) AU662134B2 (https=)
CA (1) CA2065550A1 (https=)
CZ (1) CZ130992A3 (https=)
DK (1) DK0511526T3 (https=)
HU (1) HUT62940A (https=)
NZ (1) NZ242279A (https=)
SK (1) SK130992A3 (https=)
ZA (1) ZA923072B (https=)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3228513B2 (ja) * 1991-12-23 2001-11-12 ジェンザイム・リミテッド ホモキラル性の２−ヒドロキシ酸の合成
DE4328231C1 (de) * 1993-08-23 1994-07-28 Basf Ag Verfahren zur Herstellung von (L)-2-Chlorpropionsäure und deren Salzen
DE19501452A1 (de) * 1995-01-19 1996-07-25 Basf Ag Verfahren zur Herstellung von optisch aktiven 2-Halogenpropionsäuren
US6022977A (en) * 1997-03-26 2000-02-08 Dupont Pharmaceuticals Company Dynamic resolution of isoxazoline thioesters to isoxazoline carboxylic acids
DE60143262D1 (de) * 2000-06-01 2010-11-25 Sk Holdings Co Ltd Verfahren zur optischen auflösung einer razemischen alpha-substituierten, heterozyklischen karbonsäure unter enzymverwendung
KR100378741B1 (ko) * 2000-06-01 2003-04-07 에스케이 주식회사 효소를 이용하여 R-폼 또는 S-폼의 α-치환 헤테로싸이클릭 카르복실산 및 이와 상반되는 광학특성을 갖는 α-치환 헤테로싸이클릭 카르복실산 에스테르를 제조하는 방법
JP5266875B2 (ja) * 2008-05-23 2013-08-21 三菱瓦斯化学株式会社 有機カルボン酸エステルからの光学活性有機カルボン酸の製造方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4601987A (en) * 1985-02-27 1986-07-22 Massachusetts Institute Of Technology Enzymatic production of optical isomers of 2-halopropionic acids
US4668628A (en) * 1985-04-01 1987-05-26 Stauffer Chemical Company Resolution of racemic mixtures of aliphatic acid esters
EP0257716A3 (en) * 1986-08-22 1989-11-08 Stauffer Chemical Company Improved process for conducting lipase enzyme hydrolysis
US5032523A (en) * 1987-01-14 1991-07-16 Lion Corporation Preparation of optically active esters
US4800162A (en) * 1987-04-01 1989-01-24 Sepracor, Inc. Method for resolution of steroisomers in multiphase and extractive membrane reactors
US5057427A (en) * 1988-04-07 1991-10-15 Sepracor, Inc. Method for resolution of stereoisomers
US5108916A (en) * 1989-06-05 1992-04-28 Rhone-Poulenc Rorer, S.A. Process for stereoselectively hydrolyzing, transesterifying or esterifying with immobilized isozyme of lipase from candida rugosa

Also Published As

Publication number Publication date
ATA88691A (de) 1994-01-15
EP0511526A1 (de) 1992-11-04
ZA923072B (en) 1992-12-30
AT398081B (de) 1994-09-26
AU662134B2 (en) 1995-08-24
US5278054A (en) 1994-01-11
HUT62940A (en) 1993-06-28
DK0511526T3 (https=) 1992-11-04
SK130992A3 (en) 1995-08-09
CZ130992A3 (en) 1994-01-19
HU9201412D0 (en) 1992-07-28
JPH05130881A (ja) 1993-05-28
AU1502492A (en) 1992-11-05
NZ242279A (en) 1993-02-25

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Legal Events

Date Code Title Description
FZDE Discontinued