SG54231A1 - Enzymatic processes for the resolution of enantiomeric mixtures of compounds useful as intermediates in the preparation of taxanes - Google Patents
Enzymatic processes for the resolution of enantiomeric mixtures of compounds useful as intermediates in the preparation of taxanesInfo
- Publication number
- SG54231A1 SG54231A1 SG1996005278A SG1996005278A SG54231A1 SG 54231 A1 SG54231 A1 SG 54231A1 SG 1996005278 A SG1996005278 A SG 1996005278A SG 1996005278 A SG1996005278 A SG 1996005278A SG 54231 A1 SG54231 A1 SG 54231A1
- Authority
- SG
- Singapore
- Prior art keywords
- taxanes
- intermediates
- resolution
- preparation
- compounds useful
- Prior art date
Links
Classifications
-
- 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
- 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
- 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
- C12P17/04—Oxygen as only ring hetero atoms containing a five-membered hetero ring, e.g. griseofulvin, vitamin C
-
- 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
-
- 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
-
- 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
- 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
- Y10S435/822—Microorganisms using bacteria or actinomycetales
- Y10S435/874—Pseudomonas
-
- 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
- Y10S435/939—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)
- 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 (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US9217093A | 1993-07-14 | 1993-07-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
SG54231A1 true SG54231A1 (en) | 1998-11-16 |
Family
ID=22231980
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG1996005278A SG54231A1 (en) | 1993-07-14 | 1994-07-12 | Enzymatic processes for the resolution of enantiomeric mixtures of compounds useful as intermediates in the preparation of taxanes |
Country Status (12)
Country | Link |
---|---|
US (2) | US5879929A (hu) |
EP (1) | EP0634492A1 (hu) |
JP (1) | JPH0775595A (hu) |
KR (1) | KR960014352A (hu) |
CN (1) | CN1100144A (hu) |
AU (1) | AU688766B2 (hu) |
CA (1) | CA2127972A1 (hu) |
FI (1) | FI943326A (hu) |
HU (1) | HU217790B (hu) |
IL (1) | IL110278A (hu) |
SG (1) | SG54231A1 (hu) |
TW (1) | TW397866B (hu) |
Families Citing this family (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0152437A1 (en) * | 1983-08-11 | 1985-08-28 | CARROLL, Noel | Liquid separating method and apparatus |
US5602272A (en) * | 1994-06-21 | 1997-02-11 | Bristol-Myers Squibb Company | Reduction and resolution methods for the preparation of compounds useful as intemediates for preparing taxanes |
US5635531A (en) * | 1996-07-08 | 1997-06-03 | Bristol-Myers Squibb Company | 3'-aminocarbonyloxy paclitaxels |
EP0855446B1 (en) * | 1997-01-24 | 2003-04-09 | Sumitomo Chemical Company, Limited | Process for producing optically active azetidine-2-carboxylic acid derivative |
GB9714877D0 (en) * | 1997-07-15 | 1997-09-17 | Chiroscience Ltd | Microorganism and its use |
PT1054996E (pt) | 1998-02-17 | 2004-05-31 | Searle & Co | Processo para resolucao enzimatica de lactamas |
JP3757629B2 (ja) * | 1998-07-17 | 2006-03-22 | 住友化学株式会社 | 光学活性n−置換アゼチジン−2−カルボン酸化合物の製造方法 |
AU6049000A (en) | 1999-07-23 | 2001-02-13 | Eli Lilly And Company | Enantioselective acylation of cis racemic azetidinones |
EP1229934B1 (en) | 1999-10-01 | 2014-03-05 | Immunogen, Inc. | Compositions and methods for treating cancer using immunoconjugates and chemotherapeutic agents |
US6548293B1 (en) | 1999-10-18 | 2003-04-15 | Fsu Research Foundation, Inc. | Enzymatic process for the resolution of enantiomeric mixtures of β-lactams |
CO5280224A1 (es) * | 2000-02-02 | 2003-05-30 | Univ Florida State Res Found | Taxanos sustituidos con ester en c7, utiles como agentes antitumorales y composiciones farmaceuticas que los contienen |
WO2001057033A1 (en) | 2000-02-02 | 2001-08-09 | Florida State University Research Foundation, Inc. | C10 carbamoyloxy substituted taxanes as antitumor agents |
HUP0200651A3 (en) | 2000-02-02 | 2002-10-28 | Univ Florida State Res Found | C7 heterosubstituted acetate taxanes as antitumor agents and pharmaceutical compositions containing them |
NZ514380A (en) | 2000-02-02 | 2005-03-24 | Univ Florida State Res Found | C7 carbonate substituted taxanes as antitumor agents |
SK13632001A3 (sk) * | 2000-02-02 | 2002-06-04 | Florida State University Research Foundation, Inc. | C10 karbonátom substituované taxány ako protinádorové činidlá |
US6649632B2 (en) | 2000-02-02 | 2003-11-18 | Fsu Research Foundation, Inc. | C10 ester substituted taxanes |
IL145639A (en) * | 2000-02-02 | 2007-02-11 | Univ Florida State Res Found | Cetro-converted Texanate acetate in C10 as anti-cancer agents |
AU778991B2 (en) | 2000-02-02 | 2004-12-23 | Florida State University Research Foundation, Inc. | C7 carbamoyloxy substituted taxanes as antitumor agents |
US20040058422A1 (en) * | 2000-11-02 | 2004-03-25 | Chaplin Jennifer Ann | Process for preparing (-)- menthol and similar compounds |
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 |
US7064980B2 (en) * | 2003-09-17 | 2006-06-20 | Sandisk Corporation | Non-volatile memory and method with bit line coupled compensation |
HN2005000054A (es) * | 2004-02-13 | 2009-02-18 | Florida State University Foundation Inc | Taxanos sustituidos con esteres de ciclopentilo en c10 |
EP1737444A4 (en) | 2004-03-05 | 2008-05-21 | Univ Florida State Res Found | C7-LACTYLOXA-SUBSTITUTED TAXANE |
AU2006214498A1 (en) * | 2005-02-14 | 2006-08-24 | Florida State University Research Foundation, Inc. | C10 cyclopropyl ester substituted taxane compositions |
US8242166B2 (en) * | 2008-03-31 | 2012-08-14 | Florida State University Research Foundation, Inc. | C(10) ethyl ester and C(10) cyclopropyl ester substituted taxanes |
Family Cites Families (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4492757A (en) * | 1981-12-28 | 1985-01-08 | Denki Kagaku Kogyo Kabushiki Kaisha | Process for preparing L-threonine |
JPS60248192A (ja) * | 1984-05-23 | 1985-12-07 | Sumitomo Chem Co Ltd | 光学活性なスレオ−3−フエニルセリン誘導体の製造方法 |
FR2629819B1 (fr) * | 1988-04-06 | 1990-11-16 | Rhone Poulenc Sante | Procede de preparation de derives de la baccatine iii et de la desacetyl-10 baccatine iii |
US4943528A (en) * | 1988-11-22 | 1990-07-24 | Nitto Chemical Industry Co., Ltd. | Process for the production of optically active (R)-(-)-3-halo-1,2-propanediol |
JPH02190195A (ja) | 1989-01-19 | 1990-07-26 | Rikagaku Kenkyusho | 光学活性プロピオン酸エステル類化合物の製法 |
JPH02273196A (ja) | 1989-03-08 | 1990-11-07 | Wisconsin Alumni Res Found | ラセミ化合物の生体触媒分割のエナンチオ選択性の改良法 |
AU5674690A (en) * | 1989-05-15 | 1990-12-18 | Schering Corporation | Process for preparing antibacterial compounds and intermediates thereto |
US5175315A (en) * | 1989-05-31 | 1992-12-29 | Florida State University | Method for preparation of taxol using β-lactam |
CA2019484A1 (en) * | 1989-06-21 | 1990-12-21 | Joseph E. Lynch | Nitrogen deprotected 4-acyloxyazetidin-2-ones |
EP0407190A3 (en) * | 1989-07-07 | 1991-03-13 | Schering Corporation | Process for producing antibacterial intermediates via enzyme hydrolysis of racemic substrates |
CA2023645C (fr) * | 1989-08-23 | 2002-03-26 | Jean-Noel Denis | Procede pour la preparation enantioselective de derives de la phenylisoserine |
US5241064A (en) * | 1989-10-02 | 1993-08-31 | Fujisawa Pharmaceutical Co., Ltd. | Enzymatic process for preparing optically active 3-substituted azetidinones |
US5015744A (en) * | 1989-11-14 | 1991-05-14 | Florida State University | Method for preparation of taxol using an oxazinone |
US5136060A (en) * | 1989-11-14 | 1992-08-04 | Florida State University | Method for preparation of taxol using an oxazinone |
DE69127219T2 (de) | 1990-04-12 | 1998-01-15 | Chisso Corp | Verfahren zur Herstellung von optisch aktiven Alkyl-3-aryl-3-hydroxypropionaten |
JPH04258297A (ja) | 1991-02-07 | 1992-09-14 | Ajinomoto Co Inc | 光学活性1−フェニル−1、3−プロパンジオールおよびその誘導体の製造法 |
US5346828A (en) | 1991-03-27 | 1994-09-13 | Celgene Corporation | Stereoisomeric enrichment of 2-amino-3-hydroxy-3-phenylpropionic acids using d-threonine aldolase |
CA2071160A1 (en) * | 1991-07-31 | 1993-02-01 | Vittorio Farina | Asymmetric synthesis of taxol side chain |
ATE134610T1 (de) * | 1991-08-22 | 1996-03-15 | Lonza Ag | Verfahren zur herstellung von optisch aktiven 4- amino-3-hydroxycarbonsäuren |
US5227400A (en) * | 1991-09-23 | 1993-07-13 | Florida State University | Furyl and thienyl substituted taxanes and pharmaceutical compositions containing them |
US5243045A (en) * | 1991-09-23 | 1993-09-07 | Florida State University | Certain alkoxy substituted taxanes and pharmaceutical compositions containing them |
US5250683A (en) * | 1991-09-23 | 1993-10-05 | Florida State University | Certain substituted taxanes and pharmaceutical compositions containing them |
DK0552041T3 (da) * | 1992-01-15 | 2000-10-09 | Squibb & Sons Inc | Enzymatiske fremgangsmåder til spaltning af enantiomerblandinger af forbindelser, der er nyttige som mellemprodukter ved fr |
US5272171A (en) * | 1992-02-13 | 1993-12-21 | Bristol-Myers Squibb Company | Phosphonooxy and carbonate derivatives of taxol |
US5294737A (en) * | 1992-02-27 | 1994-03-15 | The Research Foundation State University Of New York | Process for the production of chiral hydroxy-β-lactams and hydroxyamino acids derived therefrom |
US5294637A (en) * | 1992-07-01 | 1994-03-15 | Bristol-Myers Squibb Company | Fluoro taxols |
US5254580A (en) * | 1993-01-19 | 1993-10-19 | Bristol-Myers Squibb Company | 7,8-cyclopropataxanes |
EP0582469A2 (en) * | 1992-08-06 | 1994-02-09 | Wisconsin Alumni Research Foundation | Process for preparing taxol-type compound from beta-lactam precursors |
MX9308012A (es) * | 1992-12-24 | 1994-08-31 | Bristol Myers Squibb Co | Eteres fosfonooximetilicos de derivados de taxano, solubles en agua y composiciones farmaceuticas que los incluyen. |
-
1994
- 1994-05-16 TW TW083104413A patent/TW397866B/zh not_active IP Right Cessation
- 1994-07-11 IL IL110278A patent/IL110278A/en not_active IP Right Cessation
- 1994-07-12 EP EP94305095A patent/EP0634492A1/en not_active Withdrawn
- 1994-07-12 SG SG1996005278A patent/SG54231A1/en unknown
- 1994-07-12 FI FI943326A patent/FI943326A/fi unknown
- 1994-07-13 KR KR1019940016815A patent/KR960014352A/ko not_active Application Discontinuation
- 1994-07-13 HU HU9402096A patent/HU217790B/hu not_active IP Right Cessation
- 1994-07-13 AU AU67433/94A patent/AU688766B2/en not_active Ceased
- 1994-07-13 CA CA002127972A patent/CA2127972A1/en not_active Abandoned
- 1994-07-14 CN CN94108597A patent/CN1100144A/zh active Pending
- 1994-07-14 JP JP6162145A patent/JPH0775595A/ja active Pending
-
1995
- 1995-06-05 US US08/461,236 patent/US5879929A/en not_active Expired - Fee Related
-
1998
- 1998-11-16 US US09/193,105 patent/US6541242B1/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
FI943326A0 (fi) | 1994-07-12 |
HUT69958A (en) | 1995-09-28 |
EP0634492A1 (en) | 1995-01-18 |
CN1100144A (zh) | 1995-03-15 |
HU217790B (hu) | 2000-04-28 |
US5879929A (en) | 1999-03-09 |
IL110278A0 (en) | 1994-10-21 |
IL110278A (en) | 1998-06-15 |
JPH0775595A (ja) | 1995-03-20 |
FI943326A (fi) | 1995-01-15 |
HU9402096D0 (en) | 1994-09-28 |
TW397866B (en) | 2000-07-11 |
US6541242B1 (en) | 2003-04-01 |
AU688766B2 (en) | 1998-03-19 |
CA2127972A1 (en) | 1995-01-15 |
KR960014352A (ko) | 1996-05-22 |
AU6743394A (en) | 1995-01-27 |
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