KR900009998A - 광학 활성 화합물 및 이의 제조방법 - Google Patents

광학 활성 화합물 및 이의 제조방법

Info

Publication number
KR900009998A
KR900009998A KR1019890018073A KR890018073A KR900009998A KR 900009998 A KR900009998 A KR 900009998A KR 1019890018073 A KR1019890018073 A KR 1019890018073A KR 890018073 A KR890018073 A KR 890018073A KR 900009998 A KR900009998 A KR 900009998A
Authority
KR
South Korea
Prior art keywords
preparation
active compound
optically active
optically
compound
Prior art date
Application number
KR1019890018073A
Other languages
English (en)
Other versions
KR920006869B1 (ko
Inventor
가즈토시 미야자와
나오유키 요시다
Original Assignee
칫소가부시키가이샤
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
Priority claimed from JP63309832A external-priority patent/JP2838527B2/ja
Priority claimed from JP1101689A external-priority patent/JPH02283296A/ja
Application filed by 칫소가부시키가이샤 filed Critical 칫소가부시키가이샤
Publication of KR900009998A publication Critical patent/KR900009998A/ko
Application granted granted Critical
Publication of KR920006869B1 publication Critical patent/KR920006869B1/ko

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
    • C12P41/00Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • 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
    • C12P41/003Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions
    • C12P41/004Processes 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02Heterocyclic 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
    • C07D309/08Heterocyclic 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
    • C07D309/10Oxygen atoms
    • C07D309/12Oxygen atoms only hydrogen atoms and one oxygen atom directly attached to ring carbon atoms, e.g. tetrahydropyranyl ethers
    • 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
    • C12P17/06Oxygen as only ring hetero atoms containing a six-membered hetero ring, e.g. fluorescein
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00Chemistry: molecular biology and microbiology
    • Y10S435/8215Microorganisms
    • Y10S435/822Microorganisms using bacteria or actinomycetales
    • Y10S435/874Pseudomonas

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)
KR1019890018073A 1988-12-09 1989-12-07 광학 활성 화합물 및 이의 제조방법 KR920006869B1 (ko)

Applications Claiming Priority (4)

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
JP309832 1988-12-09
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
JP101689 1989-04-24

Publications (2)

Publication Number Publication Date
KR900009998A true KR900009998A (ko) 1990-07-06
KR920006869B1 KR920006869B1 (ko) 1992-08-21

Family

ID=26442521

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019890018073A KR920006869B1 (ko) 1988-12-09 1989-12-07 광학 활성 화합물 및 이의 제조방법

Country Status (5)

Country Link
US (1) US5391494A (ko)
EP (1) EP0372891B1 (ko)
KR (1) KR920006869B1 (ko)
DE (1) DE68925947T2 (ko)
SG (1) SG48776A1 (ko)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
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
DE60010516T2 (de) * 1999-12-24 2005-05-12 Mitsubishi Rayon Co., Ltd. Verfahren zur herstellung von tetrahydropyranyloxyaminen

Family Cites Families (6)

* Cited by examiner, † Cited by third party
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

Also Published As

Publication number Publication date
EP0372891A3 (en) 1991-01-09
US5391494A (en) 1995-02-21
KR920006869B1 (ko) 1992-08-21
EP0372891B1 (en) 1996-03-13
EP0372891A2 (en) 1990-06-13
DE68925947D1 (de) 1996-04-18
DE68925947T2 (de) 1996-09-12
SG48776A1 (en) 1998-05-18

Similar Documents

Publication Publication Date Title
BR1100580A (pt) Composto e complexo
MC2034A1 (fr) Preparations
KR910700249A (ko) 신규 치료학적 활성 화합물 및 그의 제조 방법
IT1229451B (it) Mieti-trebbia
IT1224421B (it) Galattomannani modificati e realtivo procedimento di preparazione
KR910001409A (ko) 광부품 및 그 제조방법
DK540389D0 (da) Immunstimulerende praeparat
KR920700043A (ko) 알부민 제제 및 이의 제조방법
KR900009790A (ko) 모노-n-알킬화된 폴리아자마크로사이클의 제조방법
FI896091A0 (fi) Korkeatoimiset polarisaattorit
DK84489A (da) Praeparater
DE68929086T2 (de) Mähmaschine
KR900009879A (ko) 결정형 염료 및 그의 제조방법
FI91488B (fi) Seula
DK570289A (da) Insekticide midler
DK570189D0 (da) Insekticide midler
KR900009998A (ko) 광학 활성 화합물 및 이의 제조방법
ATA58988A (de) Optisch aktive oxo-isoindolinylderivate
KR900004691A (ko) 페닐피리딘 및 이의 제조방법
DK606288D0 (da) Praeparat
DK143889D0 (da) Saerlig fremgangsmaade
IT8847653A0 (it) Sizzante comprendente 5 - idroscomposizione farmaceutica anoressitrpofano
DK343689A (da) Herbicidt praeparat
KR900007843A (ko) 신규 6-플루오로퓨린화합물과 그 제조방법
TR23156A (tr) Lif-tepkin ftalosiyanin-monoazo bilesikler ve bunlarin hazirlanmalarina mahsus usul

Legal Events

Date Code Title Description
A201 Request for examination
G160 Decision to publish patent application
E701 Decision to grant or registration of patent right
GRNT Written decision to grant
FPAY Annual fee payment

Payment date: 19970730

Year of fee payment: 6

LAPS Lapse due to unpaid annual fee