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WO1991000923A3 - Procede de production d'intermediaires bactericides par hydrolyse enzymatique de substrats racemiques - Google Patents

Procede de production d'intermediaires bactericides par hydrolyse enzymatique de substrats racemiques Download PDF

Info

Publication number
WO1991000923A3
WO1991000923A3 PCT/US1990/003688 US9003688W WO9100923A3 WO 1991000923 A3 WO1991000923 A3 WO 1991000923A3 US 9003688 W US9003688 W US 9003688W WO 9100923 A3 WO9100923 A3 WO 9100923A3
Authority
WO
WIPO (PCT)
Prior art keywords
enzyme hydrolysis
via enzyme
producing antibacterial
intermediates via
racemic substrates
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/US1990/003688
Other languages
English (en)
Other versions
WO1991000923A2 (fr
Inventor
Jon E Clark
Doris P Schumacher
Derek Walker
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.)
Merck Sharp and Dohme LLC
Original Assignee
Schering Corp
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 Schering Corp filed Critical Schering Corp
Publication of WO1991000923A2 publication Critical patent/WO1991000923A2/fr
Priority to KR1019910700252A priority Critical patent/KR920701470A/ko
Publication of WO1991000923A3 publication Critical patent/WO1991000923A3/fr
Anticipated expiration legal-status Critical
Ceased 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
    • 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
    • C12P13/00—Preparation of nitrogen-containing organic compounds
    • C12P13/04—Alpha- or beta- amino acids
    • 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
    • C12P41/006—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by reactions involving C-N bonds, e.g. nitriles, amides, hydantoins, carbamates, lactames, transamination reactions, or keto group formation from racemic mixtures
    • C12P41/007—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by reactions involving C-N bonds, e.g. nitriles, amides, hydantoins, carbamates, lactames, transamination reactions, or keto group formation from racemic mixtures by reactions involving acyl derivatives of racemic amines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • General Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biotechnology (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Microbiology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Analytical Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Selon un nouveau procédé de préparation d'intermédiaires bactéricides, par exemple de préparation du composé bactéricide thiamphénicol, on utilise une hydrolase de η-glutamyle afin d'hydrolyser sélectivement un mélange racémique de D-thréophénylsérines et de L-thréophénylsérines.
PCT/US1990/003688 1989-07-07 1990-07-05 Procede de production d'intermediaires bactericides par hydrolyse enzymatique de substrats racemiques Ceased WO1991000923A2 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1019910700252A KR920701470A (ko) 1989-07-07 1991-03-07 라세미 기질의 효소적 가수분해를 통한 항균성 중간물질의 제조방법

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US37644889A 1989-07-07 1989-07-07
US376,448 1989-07-07

Publications (2)

Publication Number Publication Date
WO1991000923A2 WO1991000923A2 (fr) 1991-01-24
WO1991000923A3 true WO1991000923A3 (fr) 1991-03-07

Family

ID=23485070

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1990/003688 Ceased WO1991000923A2 (fr) 1989-07-07 1990-07-05 Procede de production d'intermediaires bactericides par hydrolyse enzymatique de substrats racemiques

Country Status (4)

Country Link
EP (2) EP0407190A3 (fr)
KR (1) KR920701470A (fr)
AU (1) AU6052090A (fr)
WO (1) WO1991000923A2 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5346828A (en) * 1991-03-27 1994-09-13 Celgene Corporation Stereoisomeric enrichment of 2-amino-3-hydroxy-3-phenylpropionic acids using d-threonine aldolase
TW397866B (en) * 1993-07-14 2000-07-11 Bristol Myers Squibb Co Enzymatic processes for the resolution of enantiomeric mixtures of compounds useful as intermediates in the preparation of taxanes
EP0734453A1 (fr) * 1993-12-17 1996-10-02 Dsm N.V. Amides de phenylserine et preparation de phenylserines/amides de phenylserine
US6686296B1 (en) 2000-11-28 2004-02-03 International Business Machines Corp. Nitrogen-based highly polymerizing plasma process for etching of organic materials in semiconductor manufacturing

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3347752A (en) * 1965-03-26 1967-10-17 Merck & Co Inc Microbiological cleavage process for resolving racemic alpha-methyl-beta-(3, 4,-dihydroxyphenyl)-alanine
FR2054852A5 (fr) * 1969-07-29 1971-05-07 Sumitomo Chemical Co
JPS50148326A (fr) * 1974-05-01 1975-11-27
EP0130633A2 (fr) * 1983-06-02 1985-01-09 ZAMBON GROUP S.p.A. Procédé de préparation de dérivés de 1-phényl-1-hydroxy-2-amino-3-fluoro propane
EP0141613A2 (fr) * 1983-11-04 1985-05-15 Zaidan Hojin Biseibutsu Kagaku Kenkyu Kai Procédé de production de 3-(3,4-dihydroxyphényl) sérine optiquement active et son dérivé protégé
JPS60248192A (ja) * 1984-05-23 1985-12-07 Sumitomo Chem Co Ltd 光学活性なスレオ−３−フエニルセリン誘導体の製造方法

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3347752A (en) * 1965-03-26 1967-10-17 Merck & Co Inc Microbiological cleavage process for resolving racemic alpha-methyl-beta-(3, 4,-dihydroxyphenyl)-alanine
FR2054852A5 (fr) * 1969-07-29 1971-05-07 Sumitomo Chemical Co
JPS50148326A (fr) * 1974-05-01 1975-11-27
EP0130633A2 (fr) * 1983-06-02 1985-01-09 ZAMBON GROUP S.p.A. Procédé de préparation de dérivés de 1-phényl-1-hydroxy-2-amino-3-fluoro propane
EP0141613A2 (fr) * 1983-11-04 1985-05-15 Zaidan Hojin Biseibutsu Kagaku Kenkyu Kai Procédé de production de 3-(3,4-dihydroxyphényl) sérine optiquement active et son dérivé protégé
JPS60248192A (ja) * 1984-05-23 1985-12-07 Sumitomo Chem Co Ltd 光学活性なスレオ−３−フエニルセリン誘導体の製造方法

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
CHEMICAL ABSTRACTS, Volume 105, No. 3, 21 July 1986, (Columbus, Ohio, US), see page 537, Abstract No. 23102k & JP, A, 60248192 (Sumitomo Chemical Co., Ltd) 7 December 1985 *
CHEMICAL ABSTRACTS, Volume 85, No. 3, 19 July 1976, (Columbus Ohio, US), see page 736, Abstract No. 21829x & JP, A, 75148326 (Shizuoka Caffeine Industry Co., Ltd) 27 November 1975 *

Also Published As

Publication number Publication date
AU6052090A (en) 1991-02-06
EP0407190A2 (fr) 1991-01-09
EP0481003A2 (en) 1992-04-22
EP0407190A3 (fr) 1991-03-13
KR920701470A (ko) 1992-08-11
WO1991000923A2 (fr) 1991-01-24

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