JPS5931693A - 光学活性オキサゾリジノン誘導体の製造方法 - Google Patents

光学活性オキサゾリジノン誘導体の製造方法

Info

Publication number
JPS5931693A
JPS5931693A JP57141575A JP14157582A JPS5931693A JP S5931693 A JPS5931693 A JP S5931693A JP 57141575 A JP57141575 A JP 57141575A JP 14157582 A JP14157582 A JP 14157582A JP S5931693 A JPS5931693 A JP S5931693A
Authority
JP
Japan
Prior art keywords
compound
manufacturing
substituted
alkyl
microorganism
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.)
Granted
Application number
JP57141575A
Other languages
English (en)
Japanese (ja)
Other versions
JPH0156760B2 (OSRAM
Inventor
Shigeki Hamaguchi
濱口　茂樹
Hiroshi Yamamura
山村　浩
Junzo Hasegawa
淳三 長谷川
Hajime Kawarada
川原田　肇
Kiyoshi Watanabe
清 渡辺
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.)
Kanegafuchi Chemical Industry Co Ltd
Original Assignee
Kanegafuchi Chemical Industry 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 Kanegafuchi Chemical Industry Co Ltd filed Critical Kanegafuchi Chemical Industry Co Ltd
Priority to JP57141575A priority Critical patent/JPS5931693A/ja
Priority to EP19830107962 priority patent/EP0101076B1/en
Priority to DE8383107962T priority patent/DE3378834D1/de
Priority to US06/522,687 priority patent/US4588694A/en
Publication of JPS5931693A publication Critical patent/JPS5931693A/ja
Publication of JPH0156760B2 publication Critical patent/JPH0156760B2/ja
Granted 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
    • 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
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D263/16—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
    • C07D263/18—Oxygen atoms
    • C07D263/20—Oxygen atoms attached in position 2
    • C07D263/24—Oxygen atoms attached in position 2 with hydrocarbon radicals, substituted by oxygen atoms, attached to other ring carbon atoms
    • 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
    • C12P17/14—Nitrogen or oxygen as hetero atom and at least one other diverse hetero ring atom in the same ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (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)
JP57141575A 1982-08-13 1982-08-13 光学活性オキサゾリジノン誘導体の製造方法 Granted JPS5931693A (ja)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP57141575A JPS5931693A (ja) 1982-08-13 1982-08-13 光学活性オキサゾリジノン誘導体の製造方法
EP19830107962 EP0101076B1 (en) 1982-08-13 1983-08-11 Process for production of optically active oxazolidinone derivative
DE8383107962T DE3378834D1 (en) 1982-08-13 1983-08-11 Process for production of optically active oxazolidinone derivative
US06/522,687 US4588694A (en) 1982-08-13 1983-08-12 Process for production of optically active oxazolidinone derivative

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57141575A JPS5931693A (ja) 1982-08-13 1982-08-13 光学活性オキサゾリジノン誘導体の製造方法

Publications (2)

Publication Number Publication Date
JPS5931693A true JPS5931693A (ja) 1984-02-20
JPH0156760B2 JPH0156760B2 (OSRAM) 1989-12-01

Family

ID=15295163

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57141575A Granted JPS5931693A (ja) 1982-08-13 1982-08-13 光学活性オキサゾリジノン誘導体の製造方法

Country Status (2)

Country Link
US (1) US4588694A (OSRAM)
JP (1) JPS5931693A (OSRAM)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60241893A (ja) * 1984-05-15 1985-11-30 Kanegafuchi Chem Ind Co Ltd 光学活性（ｓ）―オキサゾリジノン誘導体の製造方法
JPS6393771A (ja) * 1986-09-12 1988-04-25 ミネソタ　マイニング　アンド　マニユフアクチユアリング　カンパニー フッ素含有オキサゾリジノン化合物

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4870169A (en) * 1985-07-17 1989-09-26 President And Fellows Of Harvard College Intermediates for beta-lactam antibiotics
JP2503994B2 (ja) * 1986-09-02 1996-06-05 味の素株式会社 オキサゾリンカルボン酸誘導体及びその製造法
US5099026A (en) * 1986-09-12 1992-03-24 Crater Davis H Fluorochemical oxazolidinones
IT1198266B (it) * 1986-12-30 1988-12-21 Montedison Spa Processo per la separazione enzimatica degli isomeri ottici di derivati ossazolidinonici racemi
DE3921593A1 (de) * 1989-06-28 1991-01-10 Schering Ag Verfahren zur racemattrennung von 4-aryl-2-oxo-pyrrolidin-3-carbonsaeure-ester
US6403804B1 (en) * 1998-12-07 2002-06-11 Takasago International Corporation Process for preparing optically active oxazolidinone derivative
DE10134366A1 (de) * 2001-07-14 2003-01-23 Aventis Pharma Gmbh Verfahren zur Herstellung der enantiomeren Formen von 2-substituierten 2-(2,5-Dioxoimidazolidin-l-yl)-essigsäure- Derivaten
CN110628743A (zh) * 2019-08-20 2019-12-31 浙江工业大学 一种立体选择性酯酶、编码基因、载体、工程菌与应用

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3607651A (en) * 1968-12-11 1971-09-21 Takasago Perfumery Co Ltd Method for the biochemical isolation of l-menthol
AR207554A1 (es) * 1972-12-02 1976-10-15 Otsuka Pharma Co Ltd Procedimiento para producir derivados de 3-alquil-5-((3,4-dihidro-5-carbostiril)oximetil)-oxazolidinona-(2)
NL7513818A (nl) * 1974-12-13 1976-06-15 Merck & Co Inc Werkwijze voor het scheiden van enantiomere 1-tert.butylamino 2.3-dihydroxypropanen.
IT1113029B (it) * 1979-03-01 1986-01-20 Simes Processo per la separazione dei due isomeri ottici del moprololo e composizioni farmaceutiche dell'antipodo levogiro
IT1125486B (it) * 1979-10-17 1986-05-14 Anic Spa Processo per la preparazione di carbamil derivati di alfa-idrossiacidi e dei corrispondenti alfa-idrossiacidi
JPS5713000A (en) * 1980-06-24 1982-01-22 Ube Ind Ltd Preparation of optical active tryptophane
US4461835A (en) * 1982-07-02 1984-07-24 Wisconsin Alumni Research Foundation Process for preparing optically-active isoprenoid intermediates

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60241893A (ja) * 1984-05-15 1985-11-30 Kanegafuchi Chem Ind Co Ltd 光学活性（ｓ）―オキサゾリジノン誘導体の製造方法
JPS6393771A (ja) * 1986-09-12 1988-04-25 ミネソタ　マイニング　アンド　マニユフアクチユアリング　カンパニー フッ素含有オキサゾリジノン化合物

Also Published As

Publication number Publication date
JPH0156760B2 (OSRAM) 1989-12-01
US4588694A (en) 1986-05-13

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