DE60041143D1 - ENZYMATISCHES VERFAHREN ZUR AUFLöSUNG ENANTIOMERER GEMISCHE VON BETA-LAKTAMEN - Google Patents
ENZYMATISCHES VERFAHREN ZUR AUFLöSUNG ENANTIOMERER GEMISCHE VON BETA-LAKTAMENInfo
- Publication number
- DE60041143D1 DE60041143D1 DE60041143T DE60041143T DE60041143D1 DE 60041143 D1 DE60041143 D1 DE 60041143D1 DE 60041143 T DE60041143 T DE 60041143T DE 60041143 T DE60041143 T DE 60041143T DE 60041143 D1 DE60041143 D1 DE 60041143D1
- Authority
- DE
- Germany
- Prior art keywords
- beta
- resolution
- lactamene
- enantiomeric mixtures
- enzymatic procedure
- 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 - Fee Related
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/06—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D205/08—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with one oxygen atom directly attached in position 2, e.g. beta-lactams
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- C12P17/16—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms containing two or more hetero rings
-
- 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
- C12P41/001—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by metabolizing one of the enantiomers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (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)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US16010399P | 1999-10-18 | 1999-10-18 | |
US09/688,852 US6548293B1 (en) | 1999-10-18 | 2000-10-16 | Enzymatic process for the resolution of enantiomeric mixtures of β-lactams |
PCT/US2000/041204 WO2001029245A2 (en) | 1999-10-18 | 2000-10-17 | ENZYMATIC PROCESS FOR THE RESOLUTION OF ENANTIOMERIC MIXTURES OF β-LACTAMS |
Publications (1)
Publication Number | Publication Date |
---|---|
DE60041143D1 true DE60041143D1 (de) | 2009-01-29 |
Family
ID=26856603
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE60041143T Expired - Fee Related DE60041143D1 (de) | 1999-10-18 | 2000-10-17 | ENZYMATISCHES VERFAHREN ZUR AUFLöSUNG ENANTIOMERER GEMISCHE VON BETA-LAKTAMEN |
Country Status (7)
Country | Link |
---|---|
US (2) | US6548293B1 (de) |
EP (1) | EP1222305B1 (de) |
AT (1) | ATE417934T1 (de) |
AU (1) | AU778711B2 (de) |
CA (1) | CA2386487A1 (de) |
DE (1) | DE60041143D1 (de) |
WO (1) | WO2001029245A2 (de) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6548293B1 (en) * | 1999-10-18 | 2003-04-15 | Fsu Research Foundation, Inc. | Enzymatic process for the resolution of enantiomeric mixtures of β-lactams |
JP4142444B2 (ja) * | 2001-03-07 | 2008-09-03 | 第一三共株式会社 | 2−アゼチジノン誘導体の製造方法 |
BRPI0611959A2 (pt) * | 2005-06-10 | 2011-12-20 | Univ Florida State Res Found | resolução de misturas enantioméricas de beta-lactamas |
WO2009118750A1 (en) * | 2008-03-26 | 2009-10-01 | Council Of Scientific & Industrial Research | Stereoselective hydrolysis for the resolution of racemic mixtures of (+/-) -cis-s-acetoxy-l- (4-methoxyphenyl) -4- (2-furyl) -2-azetidinone, (+/-) -cis-s-acetoxy-l- (4-methoxyphenyl) -4- (2-thienyl) -2-azetidinone, or |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5229526A (en) | 1991-09-23 | 1993-07-20 | Florida State University | Metal alkoxides |
CA2434312A1 (en) | 1992-01-15 | 1993-07-16 | Ramesh N. Patel | Enzymatic processes for resolution of enantiomeric mixtures of compounds useful as intermediates in the preparation of taxanes |
TW397866B (en) | 1993-07-14 | 2000-07-11 | Bristol Myers Squibb Co | Enzymatic processes for the resolution of enantiomeric mixtures of compounds useful as intermediates in the preparation of taxanes |
JP2003517266A (ja) | 1998-02-17 | 2003-05-27 | ジー・ディー・サール・アンド・カンパニー | ラクタムの酵素分割方法 |
US6548293B1 (en) * | 1999-10-18 | 2003-04-15 | Fsu Research Foundation, Inc. | Enzymatic process for the resolution of enantiomeric mixtures of β-lactams |
-
2000
- 2000-10-16 US US09/688,852 patent/US6548293B1/en not_active Expired - Lifetime
- 2000-10-17 WO PCT/US2000/041204 patent/WO2001029245A2/en active IP Right Grant
- 2000-10-17 AT AT00982668T patent/ATE417934T1/de not_active IP Right Cessation
- 2000-10-17 CA CA002386487A patent/CA2386487A1/en not_active Abandoned
- 2000-10-17 EP EP00982668A patent/EP1222305B1/de not_active Expired - Lifetime
- 2000-10-17 DE DE60041143T patent/DE60041143D1/de not_active Expired - Fee Related
- 2000-10-17 AU AU19669/01A patent/AU778711B2/en not_active Ceased
-
2003
- 2003-04-11 US US10/412,114 patent/US7067305B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
AU778711B2 (en) | 2004-12-16 |
US6548293B1 (en) | 2003-04-15 |
WO2001029245A2 (en) | 2001-04-26 |
US7067305B2 (en) | 2006-06-27 |
EP1222305A2 (de) | 2002-07-17 |
EP1222305B1 (de) | 2008-12-17 |
ATE417934T1 (de) | 2009-01-15 |
WO2001029245A8 (en) | 2001-10-04 |
CA2386487A1 (en) | 2001-04-26 |
AU1966901A (en) | 2001-04-30 |
WO2001029245A3 (en) | 2001-06-21 |
EP1222305A4 (de) | 2003-05-28 |
US20030190743A1 (en) | 2003-10-09 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
8364 | No opposition during term of opposition | ||
8339 | Ceased/non-payment of the annual fee |