ES2161942T3 - Resolucion optica de clorhidrina con microorganismos. - Google Patents
Resolucion optica de clorhidrina con microorganismos.Info
- Publication number
- ES2161942T3 ES2161942T3 ES96108451T ES96108451T ES2161942T3 ES 2161942 T3 ES2161942 T3 ES 2161942T3 ES 96108451 T ES96108451 T ES 96108451T ES 96108451 T ES96108451 T ES 96108451T ES 2161942 T3 ES2161942 T3 ES 2161942T3
- Authority
- ES
- Spain
- Prior art keywords
- sup
- active
- optically active
- chlorohidrine
- optimally
- 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 - Lifetime
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
- C12P7/04—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic
- C12P7/18—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic polyhydric
-
- 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
- C12P17/04—Oxygen as only ring hetero atoms containing a five-membered hetero ring, e.g. griseofulvin, vitamin C
-
- 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
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)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
UN NUEVO METODO PARA LA PREPARACION DE UN COMPUESTO DE CLOROHIDRINA OPTICAMENTE ACTIVA Y UN COMPUESTO 1,2-DIOL OPTICAMENTE ACTIVO Y/O 3-HIDROXI-{G}-BUTIROLACTONA OPTICAMENTE ACTIVA LOS CUALES SON UTILES COMO INTERMEDIARIOS PARA PREPARAR MEDICAMENTOS, COMPUESTOS QUIMICOS AGRICOLAS, SUBSTANCIAS FISIOLOGICAMENTE ACTIVAS Y CRISTALES LIQUIDOS FERROELECTRICOS, EL CUAL COMPRENDE TRATAR UN COMPUESTO DE CLOROHIDRINA RACEMICA QUE TIENE LA FORMULA: [EN DONDE R{SUP,1} ES H O UN GRUPO ALQUILO DE CADENA CORTA, Y R{SUB,2} ES UN GRUPO ALQUILO DE CADENA CORTA SUSTITUIDO O NO SUSTITUIDO CUANDO R{SUP,1} ES H, O R{SUP,2} ES H CUANDO R{SUP,1} ES UN GRUPO ALQUILO DE CADENA CORTA] CON UN MICROORGANISMO, DEGRADADO SELECTIVAMENTE DE ESTA FORMA SOLO UNO DE LOS ISOMEROS OPTICOS DE LOS MISMOS, Y RECUPERANDO LA OTRA CLOROHIDRINA RESTANTE OPTICAMENTE ACTIVA Y AISLANDO EL COMPUESTO 1,2-DIOL OPTICAMENTE ACTIVO Y/O EL 3-HIDROXI-{G}-BUTIROLACTONA OPTICAMENTE ACTIVA CONVERTIDA POR LA REACCION.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13018295 | 1995-05-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2161942T3 true ES2161942T3 (es) | 2001-12-16 |
Family
ID=15028033
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES96108451T Expired - Lifetime ES2161942T3 (es) | 1995-05-29 | 1996-05-28 | Resolucion optica de clorhidrina con microorganismos. |
Country Status (4)
Country | Link |
---|---|
US (1) | US5776766A (es) |
EP (1) | EP0745681B1 (es) |
DE (1) | DE69614760T2 (es) |
ES (1) | ES2161942T3 (es) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6395535B1 (en) | 1999-04-05 | 2002-05-28 | Daiso Co., Ltd. | Optical resolution of 4-halogeno-3-alkanoyloxy-butyronitrile |
JP3705046B2 (ja) | 1999-10-26 | 2005-10-12 | ダイソー株式会社 | 微生物による光学活性4−ハロゲノ−1,3−ブタンジオール及びその誘導体の製法 |
JP4197815B2 (ja) * | 1999-11-29 | 2008-12-17 | ダイソー株式会社 | 微生物による(s)−3−ハロゲノ−1,2−プロパンジオールの製法 |
KR20050072066A (ko) * | 2004-01-05 | 2005-07-08 | 다이소 가부시키가이샤 | 미생물을 이용한 광학 활성 3-클로로-2-메틸-1,2-프로판디올의 제조 방법 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1338723C (en) * | 1985-11-25 | 1996-11-19 | Hideyuki Takahashi | Process for preparing 3-chloro-1,2-propanediol |
JPS63251098A (ja) * | 1987-04-07 | 1988-10-18 | Kanegafuchi Chem Ind Co Ltd | (r)−3−ハロゲノ−1,2−プロパンジオ−ルの製造法 |
JPH01247100A (ja) * | 1988-03-30 | 1989-10-02 | Daicel Chem Ind Ltd | 光学活性カルボン酸誘導体の製造方法 |
US5155043A (en) * | 1989-04-06 | 1992-10-13 | Idemitsu Kosan Company Limited | Method for preparing optically active substances |
JP3057197B2 (ja) * | 1990-10-29 | 2000-06-26 | 川研ファインケミカル株式会社 | 光学活性ハロヒドリン誘導体の製造方法 |
JPH04197197A (ja) * | 1990-11-28 | 1992-07-16 | Kawaken Fine Chem Co Ltd | 光学活性ハロヒドリン誘導体の製造方法 |
JP3122767B2 (ja) * | 1992-01-21 | 2001-01-09 | 川研ファインケミカル株式会社 | 光学活性ハロヒドリン誘導体の製造方法 |
JP3155107B2 (ja) * | 1993-01-12 | 2001-04-09 | ダイセル化学工業株式会社 | 光学活性4−ハロ−3−ヒドロキシ酪酸エステルの製造方法 |
JP3077478B2 (ja) * | 1993-11-26 | 2000-08-14 | ダイソー株式会社 | 微生物酵素による光学活性1,2−ジオール類およびハロゲノヒドリン類の製造法 |
-
1996
- 1996-05-21 US US08/651,935 patent/US5776766A/en not_active Expired - Fee Related
- 1996-05-28 EP EP96108451A patent/EP0745681B1/en not_active Expired - Lifetime
- 1996-05-28 ES ES96108451T patent/ES2161942T3/es not_active Expired - Lifetime
- 1996-05-28 DE DE69614760T patent/DE69614760T2/de not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
EP0745681B1 (en) | 2001-08-29 |
US5776766A (en) | 1998-07-07 |
EP0745681A3 (en) | 1997-11-12 |
DE69614760D1 (de) | 2001-10-04 |
EP0745681A2 (en) | 1996-12-04 |
DE69614760T2 (de) | 2002-07-04 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG2A | Definitive protection |
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