JP2747310B2 - 光学活性２―アリールプロピオン酸の製造方法 - Google Patents

光学活性２―アリールプロピオン酸の製造方法

Info

Publication number
JP2747310B2
JP2747310B2 JP1015207A JP1520789A JP2747310B2 JP 2747310 B2 JP2747310 B2 JP 2747310B2 JP 1015207 A JP1015207 A JP 1015207A JP 1520789 A JP1520789 A JP 1520789A JP 2747310 B2 JP2747310 B2 JP 2747310B2
Authority
JP
Japan
Prior art keywords
racemic
μmol
acid
arylpropionic
arylpropionic acid
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
JP1015207A
Other languages
English (en)
Japanese (ja)
Other versions
JPH01309695A (ja
Inventor
エデイト・セルブロ
ドミニク・ペトレ
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.)
ROONU PUURAN SANTE
Original Assignee
ROONU PUURAN SANTE
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 ROONU PUURAN SANTE filed Critical ROONU PUURAN SANTE
Publication of JPH01309695A publication Critical patent/JPH01309695A/ja
Application granted granted Critical
Publication of JP2747310B2 publication Critical patent/JP2747310B2/ja
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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
    • C12P7/52—Propionic acid; Butyric acids
    • 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
    • C12P41/006—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by reactions involving C-N bonds, e.g. nitriles, amides, hydantoins, carbamates, lactames, transamination reactions, or keto group formation from racemic mixtures
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (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)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
JP1015207A 1988-01-27 1989-01-26 光学活性２―アリールプロピオン酸の製造方法 Expired - Lifetime JP2747310B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR8800923A FR2626288B1 (enExample) 1988-01-27 1988-01-27
FR8800923 1988-01-27

Publications (2)

Publication Number Publication Date
JPH01309695A JPH01309695A (ja) 1989-12-14
JP2747310B2 true JP2747310B2 (ja) 1998-05-06

Family

ID=9362685

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1015207A Expired - Lifetime JP2747310B2 (ja) 1988-01-27 1989-01-26 光学活性２―アリールプロピオン酸の製造方法

Country Status (21)

Country Link
US (1) US5089405A (enExample)
EP (1) EP0330529B1 (enExample)
JP (1) JP2747310B2 (enExample)
KR (1) KR890012004A (enExample)
CN (1) CN1035847A (enExample)
AT (1) ATE87664T1 (enExample)
AU (1) AU616933B2 (enExample)
CA (1) CA1340524C (enExample)
DE (1) DE68905636T2 (enExample)
DK (1) DK174729B1 (enExample)
ES (1) ES2054039T3 (enExample)
FI (1) FI95397C (enExample)
FR (1) FR2626288B1 (enExample)
GR (1) GR3007536T3 (enExample)
HU (1) HU203792B (enExample)
IE (1) IE63391B1 (enExample)
IL (1) IL89089A (enExample)
NZ (1) NZ227742A (enExample)
PT (1) PT89553B (enExample)
RU (1) RU1806201C (enExample)
ZA (1) ZA89641B (enExample)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4962124A (en) * 1987-11-17 1990-10-09 Analgesic Associates Onset-hastened/enhanced antipyretic response
DK314989A (da) * 1988-06-27 1989-12-28 Asahi Chemical Ind Fremgangsmaade til fremstilling af optisk aktive alfa-substituerede organiske syrer, samt mikroorganismer og enzymer anvendelige ved fremgangsmaaden
EP0356912A3 (en) * 1988-08-29 1991-09-18 Idemitsu Kosan Company Limited A method for the preparation of an optically active 2-substituted carboxylic acid
US5238828A (en) * 1988-08-29 1993-08-24 Idemitsu Kosan Company Limited Method for the preparation of an optically active 2-substituted carboxylic acid
DE3910024A1 (de) * 1989-03-28 1990-10-11 Basf Ag Verfahren zur fermentativen herstellung von 2-(4-hydroxipenoxi-)propionsaeure
FR2655660B1 (fr) * 1989-12-11 1992-03-20 Rhone Poulenc Sante Nouveaux polypeptides, sequences d'adn permettant leur expression, procede de preparation et leur utilisation.
DK161690D0 (da) * 1990-07-05 1990-07-05 Novo Nordisk As Fremgangsmaade til fremstilling af enantiomere forbindelser
US5593871A (en) * 1990-09-20 1997-01-14 E. I. Du Pont De Nemours And Company Process for the preparation of enantiometric 2-alkanoic acid amides from nitriles
JP3154721B2 (ja) 1990-09-20 2001-04-09 イー・アイ・デユポン・ドウ・ヌムール・アンド・カンパニー エナンチオマー性２−アルカン酸類の製造方法
DE69126762T2 (de) * 1990-11-14 1997-10-23 Nitto Chemical Industry Co Ltd Biologisches Verfahren zur Herstellung von Alpha-Hydroxyamid und Alpha-Hydroxysäure
FR2669643B1 (fr) * 1990-11-28 1995-04-28 Rhone Poulenc Chimie Procede de synthese enzymatique d'adipate d'ammonium.
US5258305A (en) * 1991-09-13 1993-11-02 Nitto Chemical Industry Co., Ltd. Manufacture of optically active 2-phenylpropionic acid and 2-phenylpropionamide from the nitrile using Rhodococcus equi
FR2687915B1 (fr) * 1992-02-28 1995-05-05 Rhone Poulenc Rorer Sa Composition pharmaceutique utilisable comme analgesique contenant l'acide (benzoyl-3 phenyl)-2 propionique-(r).
US5273895A (en) * 1992-10-26 1993-12-28 Sepracor, Inc. Enantioselective production of chiral carboxylic acids
AU6290594A (en) * 1993-03-09 1994-09-26 Dompe Farmaceutici S.P.A. Salts of 2-(3-benzoylphenyl)propionic acid with achiral and chiral organic bases and pharmaceutical compositions thereof
US5476965A (en) * 1994-02-18 1995-12-19 Genencor International, Inc. Enzymatic resolution of substituted 2-methyl-propionic acid
AU5693996A (en) * 1995-05-08 1996-11-29 Lonza A.G. Biotechnical production process of piperazine r-alpha-carbox ylic acids and piperazine s-alpha-carboxylic acid amide
US6060265A (en) * 1996-12-18 2000-05-09 Cytec Technology Corporation Methods for the detoxification of nitrile and/or amide compounds
US5863750A (en) * 1996-12-18 1999-01-26 Cytec Tech Corp Methods for the detoxification of nitrile and/or amide compounds
CN101892283A (zh) * 2010-06-03 2010-11-24 华东理工大学 红球菌Rhodococcus ruber 4.1187催化制备光学纯(S)-(+)-2-苯基丙酸
CN103789791B (zh) * 2014-02-12 2016-08-17 华东师范大学 一种电化学合成具有光学活性的2-苯丙酸方法
CN109486897A (zh) * 2018-12-04 2019-03-19 湖南理工学院 一种立体选择性酶催化水解拆分2-苯基丙酸对映体的方法

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1157237B (de) * 1961-09-16 1963-11-14 Bayer Ag Verfahren zur Herstellung von optisch aktiven Phenoxyessigsaeuren
FR1342844A (fr) * 1961-09-16 1963-11-15 Bayer Ag Procédé de préparation d'acides phénoxyacétiques substitués, optiquement actifs
JPS4913989A (enExample) * 1972-05-19 1974-02-06
FR2245585B1 (enExample) * 1973-09-19 1976-05-14 Anvar
JPS5446887A (en) * 1977-09-19 1979-04-13 Nitto Chem Ind Co Ltd Preparation of acrylic acid or methacrylic acid
FR2447359A1 (fr) * 1979-01-24 1980-08-22 Anvar Procede de preparation d'acides a-amines optiquement actifs par hydrolyse biologique de nitriles ou d'amides a-amines
US4366250A (en) * 1980-09-24 1982-12-28 Anvar Preparation process of optically active α-aminated acids by biological hydrolysis of nitriles
NL8400312A (nl) * 1984-02-02 1985-09-02 Stamicarbon Optisch aktief gesubstitueerd boterzuuramide alsmede werkwijze voor de optische scheiding van gesubstitueerd boterzuuramide.
JPS61162191A (ja) * 1985-01-11 1986-07-22 Nitto Chem Ind Co Ltd 微生物による有機酸類の製造法
DK261685A (da) * 1985-06-11 1986-12-12 Novo Industri As Fremgangsmaade til fremstilling af optisk aktive, organiske forbindelser
EP0227078A1 (en) * 1985-12-20 1987-07-01 Wisconsin Alumni Research Foundation Process for preparing (S)-alpha-methylarylacetic acids
GB8600245D0 (en) * 1986-01-07 1986-02-12 Shell Int Research Preparation of 2-arylpropionic acids
AU599438B2 (en) * 1986-12-01 1990-07-19 Gist-Brocades N.V. Process for the preparation of 2-arylpropionic acids
AU619249B2 (en) * 1988-02-25 1992-01-23 Istituto Guido Donegani S.P.A. Process for the continuous biotechnological preparation of optical isomer s(+) of 2-(6-methoxy-2-naphthyl) propionic acid

Also Published As

Publication number Publication date
DE68905636T2 (de) 1993-09-23
AU2882889A (en) 1989-08-10
FR2626288A1 (enExample) 1989-07-28
CA1340524C (fr) 1999-05-04
DK33889D0 (da) 1989-01-26
DE68905636D1 (de) 1993-05-06
JPH01309695A (ja) 1989-12-14
HUT52821A (en) 1990-08-28
PT89553A (pt) 1989-10-04
US5089405A (en) 1992-02-18
AU616933B2 (en) 1991-11-14
GR3007536T3 (enExample) 1993-08-31
FI95397B (fi) 1995-10-13
ZA89641B (en) 1989-10-25
EP0330529B1 (fr) 1993-03-31
EP0330529A1 (fr) 1989-08-30
KR890012004A (ko) 1989-08-23
IL89089A (en) 1992-11-15
ATE87664T1 (de) 1993-04-15
FI890388L (fi) 1989-07-28
NZ227742A (en) 1991-10-25
DK174729B1 (da) 2003-10-06
IL89089A0 (en) 1989-08-15
CN1035847A (zh) 1989-09-27
HU203792B (en) 1991-09-30
DK33889A (da) 1989-07-28
RU1806201C (ru) 1993-03-30
IE63391B1 (en) 1995-04-19
ES2054039T3 (es) 1994-08-01
FR2626288B1 (enExample) 1990-05-18
FI95397C (fi) 1996-01-25
FI890388A0 (fi) 1989-01-26
IE890238L (en) 1989-07-27
PT89553B (pt) 1994-02-28

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