SG48776A1 - Optically active compounds and a process for producing these compounds - Google Patents
Optically active compounds and a process for producing these compoundsInfo
- Publication number
- SG48776A1 SG48776A1 SG1996001565A SG1996001565A SG48776A1 SG 48776 A1 SG48776 A1 SG 48776A1 SG 1996001565 A SG1996001565 A SG 1996001565A SG 1996001565 A SG1996001565 A SG 1996001565A SG 48776 A1 SG48776 A1 SG 48776A1
- Authority
- SG
- Singapore
- Prior art keywords
- compounds
- producing
- optically active
- active compounds
- optically
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title 2
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
- 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
- C12P41/004—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 alcohol- or thiol groups in the enantiomers or the inverse reaction
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D309/08—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D309/10—Oxygen atoms
- C07D309/12—Oxygen atoms only hydrogen atoms and one oxygen atom directly attached to ring carbon atoms, e.g. tetrahydropyranyl ethers
-
- 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
- C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
- C12P17/02—Oxygen as only ring hetero atoms
- C12P17/06—Oxygen as only ring hetero atoms containing a six-membered hetero ring, e.g. fluorescein
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
-
- 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
- Y10S435/822—Microorganisms using bacteria or actinomycetales
- Y10S435/874—Pseudomonas
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63309832A JP2838527B2 (ja) | 1988-12-09 | 1988-12-09 | 光学活性化合物の製造法 |
| JP1101689A JPH02283296A (ja) | 1989-04-24 | 1989-04-24 | 脂肪酸ビニルを用いた光学活性化合物の製造法 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SG48776A1 true SG48776A1 (en) | 1998-05-18 |
Family
ID=26442521
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SG1996001565A SG48776A1 (en) | 1988-12-09 | 1989-12-04 | Optically active compounds and a process for producing these compounds |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US5391494A (de) |
| EP (1) | EP0372891B1 (de) |
| KR (1) | KR920006869B1 (de) |
| DE (1) | DE68925947T2 (de) |
| SG (1) | SG48776A1 (de) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1246264B (it) * | 1990-09-07 | 1994-11-17 | Mini Ricerca Scient Tecnolog | Processo enzimatico per la separazione degli isomeri ottici di 1,2-dioli racemi |
| US20040030160A1 (en) * | 1999-12-24 | 2004-02-12 | Kunihiko Sakano | Process for preparation of tetrahydropyranyoxyamines |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61205230A (ja) * | 1985-03-09 | 1986-09-11 | Nippon Iyakuhin Kogyo Kk | アルキリデンシクロペンテノン誘導体及びその製法 |
| JPH0740956B2 (ja) * | 1986-01-21 | 1995-05-10 | チッソ株式会社 | 生化学的手法による光学活性なアルコ−ルの製造法 |
| US5256569A (en) * | 1986-01-21 | 1993-10-26 | Chisso Corporation | Transesterification process for otereoselection of enantiomers of secondary alcohols using pseudomonas lipase with no added solvent |
| US4916074A (en) * | 1986-10-30 | 1990-04-10 | Chisso Corporation | Process for producing optically active compounds |
| JP2869650B2 (ja) * | 1987-05-15 | 1999-03-10 | チッソ株式会社 | 光学活性化合物およびその製造方法 |
| US4996158A (en) * | 1987-12-26 | 1991-02-26 | Junichi Oda | Optical resolution of racemic alcohols |
-
1989
- 1989-12-04 SG SG1996001565A patent/SG48776A1/en unknown
- 1989-12-04 EP EP89312632A patent/EP0372891B1/de not_active Expired - Lifetime
- 1989-12-04 DE DE68925947T patent/DE68925947T2/de not_active Expired - Fee Related
- 1989-12-07 KR KR1019890018073A patent/KR920006869B1/ko not_active Expired
-
1993
- 1993-08-10 US US08/104,408 patent/US5391494A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| EP0372891A2 (de) | 1990-06-13 |
| US5391494A (en) | 1995-02-21 |
| EP0372891A3 (de) | 1991-01-09 |
| KR920006869B1 (ko) | 1992-08-21 |
| EP0372891B1 (de) | 1996-03-13 |
| KR900009998A (ko) | 1990-07-06 |
| DE68925947D1 (de) | 1996-04-18 |
| DE68925947T2 (de) | 1996-09-12 |
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