KR100846676B1 - 효소적 방법에 의한 광학활성 2-할로-2-(엔-치환된페닐)아세트산 에스테르와 2-할로-2-(엔-치환된페닐)아세트산의 제조 방법 - Google Patents

효소적 방법에 의한 광학활성 2-할로-2-(엔-치환된페닐)아세트산 에스테르와 2-할로-2-(엔-치환된페닐)아세트산의 제조 방법 Download PDF

Info

Publication number
KR100846676B1
KR100846676B1 KR1020060038183A KR20060038183A KR100846676B1 KR 100846676 B1 KR100846676 B1 KR 100846676B1 KR 1020060038183 A KR1020060038183 A KR 1020060038183A KR 20060038183 A KR20060038183 A KR 20060038183A KR 100846676 B1 KR100846676 B1 KR 100846676B1
Authority
KR
South Korea
Prior art keywords
acetic acid
halo
substituted phenyl
chlorophenyl
candida
Prior art date
Application number
KR1020060038183A
Other languages
English (en)
Korean (ko)
Other versions
KR20070105681A (ko
Inventor
황순욱
정선호
Original Assignee
엔자이텍 주식회사
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 엔자이텍 주식회사 filed Critical 엔자이텍 주식회사
Priority to KR1020060038183A priority Critical patent/KR100846676B1/ko
Priority to PCT/KR2007/002073 priority patent/WO2007126258A1/fr
Publication of KR20070105681A publication Critical patent/KR20070105681A/ko
Application granted granted Critical
Publication of KR100846676B1 publication Critical patent/KR100846676B1/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
    • C12P7/00Preparation of oxygen-containing organic compounds
    • C12P7/40Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
    • C12P7/54Acetic acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/09Preparation of carboxylic acids or their salts, halides or anhydrides from carboxylic acid esters or lactones
    • 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
    • C12P41/005Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions by esterification of carboxylic acid groups in the enantiomers or the inverse reaction
    • 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
    • Y02P20/59Biological synthesis; Biological purification
    • 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
    • Y10S435/911Microorganisms using fungi
    • Y10S435/921Candida
    • 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
    • Y10S435/911Microorganisms using fungi
    • Y10S435/931Mucor
    • 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
    • Y10S435/911Microorganisms using fungi
    • Y10S435/939Rhizopus

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)
  • Genetics & Genomics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
KR1020060038183A 2006-04-27 2006-04-27 효소적 방법에 의한 광학활성 2-할로-2-(엔-치환된페닐)아세트산 에스테르와 2-할로-2-(엔-치환된페닐)아세트산의 제조 방법 KR100846676B1 (ko)

Priority Applications (2)

Application Number Priority Date Filing Date Title
KR1020060038183A KR100846676B1 (ko) 2006-04-27 2006-04-27 효소적 방법에 의한 광학활성 2-할로-2-(엔-치환된페닐)아세트산 에스테르와 2-할로-2-(엔-치환된페닐)아세트산의 제조 방법
PCT/KR2007/002073 WO2007126258A1 (fr) 2006-04-27 2007-04-27 Procédé de fabrication d'esters d'acides 2-halo-2-(n-substitué phényl)acétiques optiquement actifs et acides 2-halo-2-(n-substitué phényl)acétiques par méthode enzymatique

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1020060038183A KR100846676B1 (ko) 2006-04-27 2006-04-27 효소적 방법에 의한 광학활성 2-할로-2-(엔-치환된페닐)아세트산 에스테르와 2-할로-2-(엔-치환된페닐)아세트산의 제조 방법

Publications (2)

Publication Number Publication Date
KR20070105681A KR20070105681A (ko) 2007-10-31
KR100846676B1 true KR100846676B1 (ko) 2008-07-16

Family

ID=38655735

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1020060038183A KR100846676B1 (ko) 2006-04-27 2006-04-27 효소적 방법에 의한 광학활성 2-할로-2-(엔-치환된페닐)아세트산 에스테르와 2-할로-2-(엔-치환된페닐)아세트산의 제조 방법

Country Status (2)

Country Link
KR (1) KR100846676B1 (fr)
WO (1) WO2007126258A1 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107796904A (zh) * 2016-08-31 2018-03-13 武汉武药制药有限公司 一种用hplc分离测定邻氯扁桃酸对映异构体的方法
CN108192932B (zh) * 2017-12-26 2020-09-29 上海皓元生物医药科技有限公司 一种手性醇的酶催化制备方法

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0227078A1 (fr) 1985-12-20 1987-07-01 Wisconsin Alumni Research Foundation Procédé de préparation d'acides S-alpha-méthylarylacétiques
JPS62205797A (ja) 1986-03-05 1987-09-10 Daicel Chem Ind Ltd 光学活性化合物の製造法
US5302528A (en) 1991-04-26 1994-04-12 Ministero Dell `Universita` e Della Ricerca Scientifica e Technologica Process for the enzymatic separation of the optical isomers of alpha-substituted carboxylic acids using esterase from Brevibacterium imperiale

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FI95931C (fi) * 1988-09-02 1996-04-10 Tanabe Seiyaku Co Menetelmä (2R,3S)-3-(4-metoksifenyyli)glysidiinihapon alemman alkyyliesterin valmistamiseksi
CA2234412C (fr) * 1997-06-09 2008-09-02 Kyowa Hakko Kogyo Co., Ltd. Methode de production d'un compose optiquement actif
ATE309977T1 (de) * 2000-09-29 2005-12-15 Bristol Myers Squibb Co Dynamische trennung von isomeren und getrennte isomere

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0227078A1 (fr) 1985-12-20 1987-07-01 Wisconsin Alumni Research Foundation Procédé de préparation d'acides S-alpha-méthylarylacétiques
JPS62205797A (ja) 1986-03-05 1987-09-10 Daicel Chem Ind Ltd 光学活性化合物の製造法
US5302528A (en) 1991-04-26 1994-04-12 Ministero Dell `Universita` e Della Ricerca Scientifica e Technologica Process for the enzymatic separation of the optical isomers of alpha-substituted carboxylic acids using esterase from Brevibacterium imperiale

Also Published As

Publication number Publication date
WO2007126258A1 (fr) 2007-11-08
KR20070105681A (ko) 2007-10-31

Similar Documents

Publication Publication Date Title
DE602004022929D1 (de) Verfahren zur produktion biologischer substanzen i
WO2005111227A1 (fr) Fabrication de derives d'esters optiquement actifs et de leurs acides provenant d'esters racemiques
JPS63273499A (ja) 光学活性化合物の製造法
KR100846676B1 (ko) 효소적 방법에 의한 광학활성 2-할로-2-(엔-치환된페닐)아세트산 에스테르와 2-할로-2-(엔-치환된페닐)아세트산의 제조 방법
KR100722155B1 (ko) 효소적 방법에 의한 광학활성 2-클로로만델릭산 에스테르와 2-클로로만델릭산의 제조 방법
EP0529085B1 (fr) Procede de production de 3-chloro-1-phenyl-1-propanol optiquement actif et de son derive
KR100758512B1 (ko) 효소적 방법에 의한 광학활성3-히드록시-3-페닐프로피온산과 광학활성3-아실옥시-3-페닐프로피온산의 제조 방법
EP1290208B1 (fr) Procede de resolution optique d'un acide carboxylique heterocyclique alpha-substitue racemique a l'aide d'enzymes
WO1987006266A1 (fr) PROCEDE ENZYMATIQUE POUR LA PREPARATION DE DERIVES DE L'ACIDE 1,2-DIHYDRO-3H-PYROLLO[1,2a]PYRROLE-1-CARBOXYLIQUE OPTIQUEMENT ACTIFS
KR100657204B1 (ko) 효소적 방법에 의한 광학활성 3-히드록시-감마-부티로락톤의 제조 방법
JP2736075B2 (ja) 光学活性1,3−ブタンジオール−1−ベンジルエーテルおよびその誘導体の製造法
JPH01281098A (ja) 光学活性カルボン酸及び光学活性カルボン酸エステルの製造方法
KR100846674B1 (ko) 효소적 방법에 의한 광학활성 트랜스 알코올 화합물 및 그의 에스테르 화합물 제조방법
JP3679819B2 (ja) (s)−3−(2−チエニルチオ)ブタン酸の製造法
JP3970898B2 (ja) 光学活性α−メチルアルカンジカルボン酸−ω−モノエステル及びその対掌体ジエステルを製造する方法
JPH08285A (ja) 光学活性α−メチルアルカンジカルボン酸−ω−モノエステル及びその対掌体ジエステルを製造する方法
KR100973710B1 (ko) 효소적 방법에 의한 광학활성 엔-치환된 페닐글리신 알킬에스테르의 제조 방법
JP2981250B2 (ja) D―パントテノニトリルの製造法
JP2001513628A (ja) 鏡像異性的に純粋なエステルの製造方法
WO2006009338A1 (fr) Procede de preparation d'acide carboxylique chiral substitue
JPH01247100A (ja) 光学活性カルボン酸誘導体の製造方法
WO2001018231A2 (fr) PROCEDE DE FABRICATION DE (R)- OU (S)-HYDROXY-η-BUTYROLACTONE
JP2006328021A (ja) ピリジル酢酸化合物またはその光学活性体
JPS6078585A (ja) 光学活性なシクロペンテノン類およびその製法
JP2006061112A (ja) 光学活性な2−(シクロペンチルメチル)−マロン酸モノエステルの製造方法

Legal Events

Date Code Title Description
A201 Request for examination
E902 Notification of reason for refusal
AMND Amendment
E601 Decision to refuse application
J201 Request for trial against refusal decision
AMND Amendment
E90F Notification of reason for final refusal
B701 Decision to grant
GRNT Written decision to grant
FPAY Annual fee payment

Payment date: 20130108

Year of fee payment: 5

FPAY Annual fee payment

Payment date: 20130709

Year of fee payment: 6

LAPS Lapse due to unpaid annual fee