EP0481003A2 - Process for producing antibacterial intermediates via enzyme hydrolysis of racemic substrates. - Google Patents
Process for producing antibacterial intermediates via enzyme hydrolysis of racemic substrates.Info
- Publication number
- EP0481003A2 EP0481003A2 EP90911357A EP90911357A EP0481003A2 EP 0481003 A2 EP0481003 A2 EP 0481003A2 EP 90911357 A EP90911357 A EP 90911357A EP 90911357 A EP90911357 A EP 90911357A EP 0481003 A2 EP0481003 A2 EP 0481003A2
- Authority
- EP
- European Patent Office
- 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.)
- Pending
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)
- Zoology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Genetics & Genomics (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Analytical Chemistry (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US37644889A | 1989-07-07 | 1989-07-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0481003A2 true EP0481003A2 (en) | 1992-04-22 |
Family
ID=23485070
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP90911357A Pending EP0481003A2 (en) | 1989-07-07 | 1990-07-05 | Process for producing antibacterial intermediates via enzyme hydrolysis of racemic substrates. |
EP19900307347 Withdrawn EP0407190A3 (en) | 1989-07-07 | 1990-07-05 | Process for producing antibacterial intermediates via enzyme hydrolysis of racemic substrates |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19900307347 Withdrawn EP0407190A3 (en) | 1989-07-07 | 1990-07-05 | Process for producing antibacterial intermediates via enzyme hydrolysis of racemic substrates |
Country Status (4)
Country | Link |
---|---|
EP (2) | EP0481003A2 (xx) |
KR (1) | KR920701470A (xx) |
AU (1) | AU6052090A (xx) |
WO (1) | WO1991000923A2 (xx) |
Families Citing this family (4)
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 |
WO1995016786A1 (en) * | 1993-12-17 | 1995-06-22 | Dsm N.V. | Phenylserine amides and the preparation of phenylserines/phenylserine amides |
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 |
Family Cites Families (6)
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 |
US3733352A (en) * | 1969-07-29 | 1973-05-15 | Sumitomo Chemical Co | Preparation of d-threo-1-p-methyl-sulfonylphenyl-2-dichloro-acet-amidopropane-1,3-diol |
JPS5133550B2 (xx) * | 1974-05-01 | 1976-09-20 | ||
EP0677511A3 (en) * | 1983-06-02 | 1996-07-24 | Zambon Spa | Intermediates for the production of 1-phenyl-1-hydroxy-2-amino-3-fluoropropane derivatives. |
JPS6098995A (ja) * | 1983-11-04 | 1985-06-01 | Microbial Chem Res Found | 光学活性3−(3,4−ジヒドロキシフエニル)セリン,およびその誘導体の製造法 |
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 |
-
1990
- 1990-07-05 WO PCT/US1990/003688 patent/WO1991000923A2/en unknown
- 1990-07-05 EP EP90911357A patent/EP0481003A2/xx active Pending
- 1990-07-05 EP EP19900307347 patent/EP0407190A3/en not_active Withdrawn
- 1990-07-05 AU AU60520/90A patent/AU6052090A/en not_active Abandoned
-
1991
- 1991-03-07 KR KR1019910700252A patent/KR920701470A/ko not_active Application Discontinuation
Non-Patent Citations (1)
Title |
---|
See references of WO9100923A2 * |
Also Published As
Publication number | Publication date |
---|---|
EP0407190A3 (en) | 1991-03-13 |
WO1991000923A3 (en) | 1991-03-07 |
AU6052090A (en) | 1991-02-06 |
WO1991000923A2 (en) | 1991-01-24 |
EP0407190A2 (en) | 1991-01-09 |
KR920701470A (ko) | 1992-08-11 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
17P | Request for examination filed |
Effective date: 19911219 |
|
AK | Designated contracting states |
Kind code of ref document: A2 Designated state(s): AT BE CH DE DK ES FR GB IT LI LU NL SE |
|
D17D | Deferred search report published (deleted) | ||
D17P | Request for examination filed (deleted) | ||
DA1 | Application published (deleted) |