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 PDFInfo
- 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
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
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
- C12P7/54—Acetic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/09—Preparation of carboxylic acids or their salts, halides or anhydrides from carboxylic acid esters or lactones
-
- 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
- C12P41/005—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 carboxylic acid groups in the enantiomers or the inverse reaction
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/59—Biological synthesis; Biological purification
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/911—Microorganisms using fungi
- Y10S435/921—Candida
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/911—Microorganisms using fungi
- Y10S435/931—Mucor
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/911—Microorganisms using fungi
- Y10S435/939—Rhizopus
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)
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)
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)
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)
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 |
-
2006
- 2006-04-27 KR KR1020060038183A patent/KR100846676B1/ko not_active IP Right Cessation
-
2007
- 2007-04-27 WO PCT/KR2007/002073 patent/WO2007126258A1/fr active Application Filing
Patent Citations (3)
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 |