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
Application number
ES96108451T
Other languages
English (en)
Inventor
Naoya Kasai
Toshio Suzuki
Hideaki Idogaki
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.)
Osaka Soda Co Ltd
Original Assignee
Daiso Co Ltd
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 Daiso Co Ltd filed Critical Daiso Co Ltd
Application granted granted Critical
Publication of ES2161942T3 publication Critical patent/ES2161942T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00Preparation of oxygen-containing organic compounds
    • C12P7/02Preparation of oxygen-containing organic compounds containing a hydroxy group
    • C12P7/04Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic
    • C12P7/18Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic polyhydric
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P17/00Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/02Oxygen as only ring hetero atoms
    • C12P17/04Oxygen as only ring hetero atoms containing a five-membered hetero ring, e.g. griseofulvin, vitamin C
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P41/00Processes 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.
ES96108451T 1995-05-29 1996-05-28 Resolucion optica de clorhidrina con microorganismos. Expired - Lifetime ES2161942T3 (es)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

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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