IL158586A0 - Process for the preparation of substituted carboxylic acid esters by enzymatic hydrolysis - Google Patents

Process for the preparation of substituted carboxylic acid esters by enzymatic hydrolysis

Info

Publication number
IL158586A0
IL158586A0 IL15858602A IL15858602A IL158586A0 IL 158586 A0 IL158586 A0 IL 158586A0 IL 15858602 A IL15858602 A IL 15858602A IL 15858602 A IL15858602 A IL 15858602A IL 158586 A0 IL158586 A0 IL 158586A0
Authority
IL
Israel
Prior art keywords
halogenpent
alkyl
ene carboxylic
carboxylic esters
enzymatic hydrolysis
Prior art date
Application number
IL15858602A
Other languages
English (en)
Original Assignee
Speedel Pharma Ag
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 Speedel Pharma Ag filed Critical Speedel Pharma Ag
Publication of IL158586A0 publication Critical patent/IL158586A0/xx

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
    • C12P7/62Carboxylic acid esters
    • 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

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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
IL15858602A 2001-05-15 2002-04-26 Process for the preparation of substituted carboxylic acid esters by enzymatic hydrolysis IL158586A0 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH8952001 2001-05-15
PCT/EP2002/004640 WO2002092828A2 (en) 2001-05-15 2002-04-26 Process for the preparation of substituted carboxylic acid estersby enzymatic hydrolysis

Publications (1)

Publication Number Publication Date
IL158586A0 true IL158586A0 (en) 2004-05-12

Family

ID=4546156

Family Applications (2)

Application Number Title Priority Date Filing Date
IL15858602A IL158586A0 (en) 2001-05-15 2002-04-26 Process for the preparation of substituted carboxylic acid esters by enzymatic hydrolysis
IL158586A IL158586A (en) 2001-05-15 2003-10-23 Process for the preparation of esters of carboxylic acid 2 (S) -alkyl-5-halogenate-4-an by enzymatic hydrolysis

Family Applications After (1)

Application Number Title Priority Date Filing Date
IL158586A IL158586A (en) 2001-05-15 2003-10-23 Process for the preparation of esters of carboxylic acid 2 (S) -alkyl-5-halogenate-4-an by enzymatic hydrolysis

Country Status (14)

Country Link
US (1) US7153675B2 (de)
EP (1) EP1412514B1 (de)
JP (1) JP4252803B2 (de)
KR (1) KR100897597B1 (de)
CN (1) CN1279178C (de)
AT (1) ATE458066T1 (de)
AU (1) AU2002310883A1 (de)
BR (1) BR0209657B1 (de)
CA (1) CA2445014C (de)
DE (1) DE60235374D1 (de)
IL (2) IL158586A0 (de)
MX (1) MXPA03010394A (de)
PT (1) PT1412514E (de)
WO (1) WO2002092828A2 (de)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2507944C (en) * 2002-12-09 2012-04-17 Asahi Glass Company, Limited Process for producing (4e)-5-chloro-2-isopropyl-4-pentenoate and optically active form thereof
EP1626093A1 (de) 2004-08-11 2006-02-15 Dow Global Technologies Inc. Verfahren zur Herstellung von (S)-5-Clor-2-Isopropylpent-4-Encarbonsäureestern
JP2008536810A (ja) * 2005-03-09 2008-09-11 ディーエスエム ファイン ケミカルズ オーストリア エヌエフジー ゲーエムベーハー ウント ツェーオー カーゲー エナンチオピュアなe−(2s)−アルキル−5−ハロペンタ−4−エン酸およびエステルの製造方法
DE102005052195A1 (de) 2005-10-28 2007-05-03 Reuter Chemischer Apparatebau Kg Verfahren zur Herstellung von chiralen Octensäurederivaten
AT502992B1 (de) * 2005-12-27 2008-04-15 Dsm Fine Chem Austria Gmbh Verfahren zur herstellung von enantiomerenangereicherten 2-alkyl-5-halogen-pent-4-en-carbonsäuren bzw. -carbonsäureestern
EP1958666A1 (de) 2007-02-13 2008-08-20 Speedel Experimenta AG Heterozyklische substituierte Alkanamide als therapeutische Verbindungen
DE102007049039A1 (de) 2007-10-11 2009-04-16 Reuter Chemischer Apparatebau Kg Verfahren zur Herstellung von 8-Hydrazino-8-Aryl-Octanoylderivaten und deren Verwendung
WO2011051853A1 (en) 2009-10-29 2011-05-05 CarboDesign LLC Manufacturing process for preparing enaniomerically pure 8- aryloctanoic acid derivatives such as aliskiren
US8703976B2 (en) 2011-10-02 2014-04-22 Milan Soukup Manufacturing process for 8-aryloctanoic acids such as Aliskiren

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MY119161A (en) 1994-04-18 2005-04-30 Novartis Ag Delta-amino-gamma-hydroxy-omega-aryl-alkanoic acid amides with enzyme especially renin inhibiting activities
US5658796A (en) 1995-06-07 1997-08-19 Seprachem, Inc. Optical resolution of alkyl chroman-2-carboxylates
DE19809649A1 (de) * 1998-03-06 1999-09-09 Hoechst Marion Roussel De Gmbh Verfahren zur enzymatischen Enantiomeren-Trennung von 3(R)- und 3(S)-Hydroxy-1-methyl-4-(2,4,6-trimethoxyphenyl)-1,2,3,6-tetrahydro-pyridin bzw. der Carbonsäureester
WO2001009079A1 (de) 1999-07-29 2001-02-08 Speedel Pharma Ag 2-alkyl-5-halogen-pent-4-encarbonsäuren und deren herstellung

Also Published As

Publication number Publication date
EP1412514B1 (de) 2010-02-17
ATE458066T1 (de) 2010-03-15
WO2002092828A3 (en) 2004-02-26
BR0209657A (pt) 2004-04-20
CN1279178C (zh) 2006-10-11
IL158586A (en) 2008-08-07
KR100897597B1 (ko) 2009-05-14
US20040132148A1 (en) 2004-07-08
JP2004524860A (ja) 2004-08-19
AU2002310883A1 (en) 2002-11-25
JP4252803B2 (ja) 2009-04-08
CA2445014C (en) 2011-10-11
CA2445014A1 (en) 2002-11-21
CN1520461A (zh) 2004-08-11
MXPA03010394A (es) 2004-03-09
KR20040026655A (ko) 2004-03-31
EP1412514A2 (de) 2004-04-28
DE60235374D1 (de) 2010-04-01
WO2002092828A2 (en) 2002-11-21
WO2002092828A9 (en) 2004-05-06
BR0209657B1 (pt) 2014-10-21
PT1412514E (pt) 2010-04-27
US7153675B2 (en) 2006-12-26

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