DE602004019523D1 - Verfahren zur herstellung von optisch aktivem chroman-carbonsäureester - Google Patents
Verfahren zur herstellung von optisch aktivem chroman-carbonsäureesterInfo
- Publication number
- DE602004019523D1 DE602004019523D1 DE602004019523T DE602004019523T DE602004019523D1 DE 602004019523 D1 DE602004019523 D1 DE 602004019523D1 DE 602004019523 T DE602004019523 T DE 602004019523T DE 602004019523 T DE602004019523 T DE 602004019523T DE 602004019523 D1 DE602004019523 D1 DE 602004019523D1
- Authority
- DE
- Germany
- Prior art keywords
- production
- carboxylic acid
- acid esters
- optically active
- active chroman
- 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
Links
- SFLFCQJQOIZMHF-UHFFFAOYSA-N 3,4-dihydro-2h-chromene-2-carboxylic acid Chemical class C1=CC=C2OC(C(=O)O)CCC2=C1 SFLFCQJQOIZMHF-UHFFFAOYSA-N 0.000 title 1
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
- C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
- C12P17/02—Oxygen as only ring hetero atoms
- C12P17/06—Oxygen as only ring hetero atoms containing a six-membered hetero ring, e.g. fluorescein
-
- 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
- C12P41/004—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 alcohol- or thiol groups in the enantiomers or the inverse reaction
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)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2003159353 | 2003-06-04 | ||
| PCT/JP2004/007851 WO2004108944A1 (ja) | 2003-06-04 | 2004-05-31 | 光学活性クロマンカルボン酸エステルの製造方法 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE602004019523D1 true DE602004019523D1 (de) | 2009-04-02 |
Family
ID=33508511
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE602004019523T Expired - Lifetime DE602004019523D1 (de) | 2003-06-04 | 2004-05-31 | Verfahren zur herstellung von optisch aktivem chroman-carbonsäureester |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US20060141591A1 (de) |
| EP (1) | EP1634958B1 (de) |
| JP (1) | JPWO2004108944A1 (de) |
| DE (1) | DE602004019523D1 (de) |
| WO (1) | WO2004108944A1 (de) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4826132B2 (ja) * | 2005-04-28 | 2011-11-30 | 三菱瓦斯化学株式会社 | ６−ヒドロキシ−２，５，７，８−テトラメチルクロマン−２−カルボン酸及びその製造方法 |
| JP4826133B2 (ja) * | 2005-04-28 | 2011-11-30 | 三菱瓦斯化学株式会社 | Ｓ−（−）−６−ヒドロキシ−２，５，７，８−テトラメチルクロマン−２−カルボン酸及びその製造方法 |
| WO2008050829A1 (fr) * | 2006-10-26 | 2008-05-02 | Mitsubishi Gas Chemical Company, Inc. | Procédé de fabrication de l'acide s -(-)-6-hydroxy-2,5,7,8-tétraméthylchromane-2-carboxylique et produit obtenu par le procédé |
| JP5092465B2 (ja) * | 2007-03-13 | 2012-12-05 | 三菱瓦斯化学株式会社 | ピペコリン酸の立体選択的なエステル化方法 |
| JP5092466B2 (ja) * | 2007-03-13 | 2012-12-05 | 三菱瓦斯化学株式会社 | 光学活性ピペコリン酸またはその誘導体の製造方法。 |
| WO2010050499A1 (ja) | 2008-10-29 | 2010-05-06 | 三菱瓦斯化学株式会社 | 光学活性有機カルボン酸の製造方法 |
| FR2986231B1 (fr) * | 2012-01-26 | 2014-07-04 | Centre Nat Rech Scient | Derives de thiazolidinedione, leur preparation et leur utilisation dans le traitement des cancers |
| FR2986804A1 (fr) * | 2012-02-09 | 2013-08-16 | Servier Lab | Procede de synthese enzymatique de l'acide (7s) 3,4-dimethoxybicyclo[4.2.0]octa-1,3,5-triene 7-carboxylique ou de ses esters, et application a la synthese de l'ivabradine et de ses sels |
| EP2953938B1 (de) | 2014-02-07 | 2017-08-02 | Novogen Ltd. | Funktionalisierte benzopyranverbindungen und verwendung davon |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5037747A (en) * | 1988-01-26 | 1991-08-06 | Hoffmann-La Roche Inc. | Production of benzopyran-2-carboxylic acids and esters by enzymatic hydrolysis |
| CA2023856A1 (en) * | 1989-09-26 | 1991-03-27 | Jeffrey M. Howell | Enzymatic resolution process |
| US5089637A (en) * | 1990-03-21 | 1992-02-18 | Pfizer Inc. | Process and intermediates for 2r-benzyl-chroman-6-carbaldehyde |
| US5658796A (en) * | 1995-06-07 | 1997-08-19 | Seprachem, Inc. | Optical resolution of alkyl chroman-2-carboxylates |
| JPH11206398A (ja) * | 1997-07-18 | 1999-08-03 | Mitsui Chem Inc | 光学活性クロマン−３−酢酸類及びそのエステルの製造法 |
| JP3913329B2 (ja) * | 1997-09-11 | 2007-05-09 | 株式会社クラレ | （±）−クロマンカルボン酸の光学分割法 |
| JP2001128694A (ja) * | 1999-11-05 | 2001-05-15 | Daiso Co Ltd | 光学活性エステルの製造方法 |
| JP2002167381A (ja) * | 2000-08-03 | 2002-06-11 | Kuraray Co Ltd | （±）−６−ヒドロキシ−２，５，７，８−テトラメチルクロマン−２−カルボン酸の光学分割法 |
| CN100379867C (zh) * | 2000-08-31 | 2008-04-09 | 巴斯福股份公司 | 丁炔醇ⅰ酯酶 |
| JP2002335991A (ja) * | 2001-05-11 | 2002-11-26 | Toyotama Koryo Kk | 新規シクロペンタデカン誘導体及びその製造法 |
| JP2003144190A (ja) * | 2001-11-14 | 2003-05-20 | Mitsubishi Gas Chem Co Inc | 光学活性ｓ−６−ヒドロキシ−２，５，７，８−テトラメチルクロマン−２−カルボン酸の製造方法 |
-
2004
- 2004-05-31 EP EP04735497A patent/EP1634958B1/de not_active Expired - Lifetime
- 2004-05-31 US US10/559,577 patent/US20060141591A1/en not_active Abandoned
- 2004-05-31 WO PCT/JP2004/007851 patent/WO2004108944A1/ja active Application Filing
- 2004-05-31 DE DE602004019523T patent/DE602004019523D1/de not_active Expired - Lifetime
- 2004-05-31 JP JP2005506801A patent/JPWO2004108944A1/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| EP1634958B1 (de) | 2009-02-18 |
| EP1634958A1 (de) | 2006-03-15 |
| WO2004108944A1 (ja) | 2004-12-16 |
| EP1634958A4 (de) | 2008-01-02 |
| JPWO2004108944A1 (ja) | 2006-07-20 |
| US20060141591A1 (en) | 2006-06-29 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8364 | No opposition during term of opposition |