CA2065433A1 - Synthese d'arylalcanediols de grande purete optique - Google Patents

Synthese d'arylalcanediols de grande purete optique

Info

Publication number
CA2065433A1
CA2065433A1 CA2065433A CA2065433A CA2065433A1 CA 2065433 A1 CA2065433 A1 CA 2065433A1 CA 2065433 A CA2065433 A CA 2065433A CA 2065433 A CA2065433 A CA 2065433A CA 2065433 A1 CA2065433 A1 CA 2065433A1
Authority
CA
Canada
Prior art keywords
ester
acid
phenyl
optical purity
yield
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
CA2065433A
Other languages
English (en)
Other versions
CA2065433C (fr
Inventor
Neil Warren Boaz
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.)
Eastman Chemical Co
Original Assignee
Individual
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 Individual filed Critical Individual
Publication of CA2065433A1 publication Critical patent/CA2065433A1/fr
Application granted granted Critical
Publication of CA2065433C publication Critical patent/CA2065433C/fr
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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
    • C12P7/42Hydroxy-carboxylic acids
    • 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
    • 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
    • Y10S435/876Pseudomonas fluorescens

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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
CA002065433A 1989-09-25 1990-09-17 Synthese d'arylalcanediols de grande purete optique Expired - Fee Related CA2065433C (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US07/412,260 US4921798A (en) 1989-09-25 1989-09-25 Synthesis of (aryl or arylalkyl)-3-hydroxy propionic acids and aryl alkanediols having high optical purity
US412,260 1989-09-25

Publications (2)

Publication Number Publication Date
CA2065433A1 true CA2065433A1 (fr) 1991-03-26
CA2065433C CA2065433C (fr) 1997-04-29

Family

ID=23632290

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002065433A Expired - Fee Related CA2065433C (fr) 1989-09-25 1990-09-17 Synthese d'arylalcanediols de grande purete optique

Country Status (6)

Country Link
US (1) US4921798A (fr)
EP (1) EP0494203B1 (fr)
JP (1) JPH05500754A (fr)
CA (1) CA2065433C (fr)
DE (1) DE69005121T2 (fr)
WO (1) WO1991004334A1 (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3919029A1 (de) * 1989-06-10 1990-12-13 Hoechst Ag Verfahren zur enzymatischen spaltung von 2-arylpropionsaeure-vinylester
US5342780A (en) * 1990-01-26 1994-08-30 University Of New Mexico Methods of enzymatically separating stereoisomers of a racemic mixture of a reactive ester
US5126268A (en) * 1990-03-30 1992-06-30 Eastman Kodak Company Alcohol-ester sparation by reaction with acetate
US5445963A (en) * 1990-03-30 1995-08-29 Eastman Chemical Company Alcohol-ester separation by recrystallization
SG48774A1 (en) * 1990-04-12 1998-05-18 Chisso Corp Optically active alkyl 3-aryl-3-hydroxypropionate and a method for producing thereof
WO1992002631A1 (fr) * 1990-08-10 1992-02-20 Daicel Chemical Industries, Ltd. Procede de production d'un compose 3-phenyl-1,3-propanediol optiquement actif
JP3087419B2 (ja) * 1991-11-14 2000-09-11 味の素株式会社 (s)−1−フェニル−1,3−プロパンジオールまたはその誘導体の製造方法
EP0704419B1 (fr) * 1994-04-19 2001-07-25 Kanegafuchi Kagaku Kogyo Kabushiki Kaisha Procede de production de 2-aryl-3-acyloxy-1,2-propanediols optiquement actifs

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH628009A5 (de) * 1977-07-26 1982-02-15 Hoffmann La Roche Verfahren zur herstellung von optisch aktiven alpha-hydroxycarbonsaeuren.
EP0130752B1 (fr) * 1983-07-04 1991-02-27 Mitsubishi Rayon Co., Ltd. Procédé de préparation d'acides carboxyliques optiquement actifs et de leurs esters antipodes
EP0144832A3 (fr) * 1983-12-06 1987-01-21 F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft Procédé de production de dérivés optiquement actifs de l'acide 3-hydroxypropionique substitué en alpha
IT1201408B (it) * 1985-03-22 1989-02-02 Montedison Spa Processo per la preparazione biotecnologica di acidi alfa-arilalcanoici otticamente attivi
JPS61227797A (ja) * 1985-04-01 1986-10-09 Kanegafuchi Chem Ind Co Ltd 光学活性グリコ−ル類の製造方法
US4668628A (en) * 1985-04-01 1987-05-26 Stauffer Chemical Company Resolution of racemic mixtures of aliphatic acid esters
GB2179651A (en) * 1985-08-29 1987-03-11 Inst Organicheskogo Sinteza Ak S(-)2-(4-carboxy-3-hydroxybutyl)cyclopent-2-ene-1-one and a process for producing same
JPS6488894A (en) * 1987-09-30 1989-04-03 Tokyo Electric Co Ltd Order register
EP0325971A3 (fr) * 1988-01-26 1990-07-25 F. Hoffmann-La Roche Ag Procédé de préparation d'acides hydroxyarylalcanoiques optiquement purs et des esters correspondants

Also Published As

Publication number Publication date
US4921798A (en) 1990-05-01
WO1991004334A1 (fr) 1991-04-04
EP0494203B1 (fr) 1993-12-08
DE69005121T2 (de) 1994-07-07
CA2065433C (fr) 1997-04-29
EP0494203A1 (fr) 1992-07-15
JPH05500754A (ja) 1993-02-18
DE69005121D1 (de) 1994-01-20

Similar Documents

Publication Publication Date Title
CA2065433A1 (fr) Synthese d'arylalcanediols de grande purete optique
EP0044158B1 (fr) Dérivés de l'imidazolidin-2-one optiquement actifs et leur préparation
US4435423A (en) Anti-ulcer composition comprising terpenoid containing two functional groups and method of treating ulcers
JPH03228694A (ja) 光学活性ヒドロキシラクトン類の製造方法
JPH0436195A (ja) 光学活性α―ヒドロキシエステル類の製造方法
RU2108393C1 (ru) Способ стереоспецифического гидролиза производных пиперидиндиона
JPS63284184A (ja) 光学活性化合物およびその製造方法
EP0448254B1 (fr) Procédé et intermédiaires pour 2R-benzylchromane-6-carbaldehyde
US5447865A (en) Method of resolution of hydroxy substituted cyclopentanone enantiomers using lipase and lithium salt complexation
EP0271433B1 (fr) Dédoublement de racemates de 7 alpha-acyloxy-6-bêta-hydroxy-méthyl-2-oxabicyclo[3.3.0]octan-3-ones par hydrolyse stéréospécifique et enzymatique d'acétate
EP0765857A1 (fr) Derive d'acide carboxylique optiquement actif a substitution alpha et procede de production dudit derive
US4468458A (en) Two-functional-group-containing terpenoids, processes for the preparation of the same, and anti-ulcer agents containing the same
US3927084A (en) Process for the production of 2(4-alkylphenyl)propionic acid
JPH06256278A (ja) 光学活性α−カルバモイルアルカン酸誘導体およびその製法
Sakai et al. Convenient synthesis of optically active abscisic acid and xanthoxin
US5256800A (en) Optically active 2,2-dimethyl-1,3-dioxin-4-ones and method for preparing same
JP2808320B2 (ja) 光学活性なシクロペンテノール類
US5049497A (en) Novel process for the synthesis of the enantiomers of bicyclo(4.2.0)oct-2-en-7-one and derivatives
IN170240B (fr)
WO2007126258A1 (fr) 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
US5605833A (en) Process for preparation of D-lactic acid from D,L lactic acid ester using wheat germ or pancreatic lipase
US5654440A (en) Method for production of optically active (+)-4,4,4-trifluoro-3-(indole-3-)butyric acid
CA2054773A1 (fr) Methode de protection de la fonction hydroxyde lors de la separation d'alcool et d'ester
JP2609922B2 (ja) 2′―ケトパントテン酸エステル
EP0627396B1 (fr) Dérivés du cyclohexanediol

Legal Events

Date Code Title Description
EEER Examination request
MKLA Lapsed