NO20013037L - Fremgangsmåte for fremstilling av optisk aktive 1-amino-4- (hydroksymetyl)-cyklopenten-2-en-derivater - Google Patents

Fremgangsmåte for fremstilling av optisk aktive 1-amino-4- (hydroksymetyl)-cyklopenten-2-en-derivater

Info

Publication number
NO20013037L
NO20013037L NO20013037A NO20013037A NO20013037L NO 20013037 L NO20013037 L NO 20013037L NO 20013037 A NO20013037 A NO 20013037A NO 20013037 A NO20013037 A NO 20013037A NO 20013037 L NO20013037 L NO 20013037L
Authority
NO
Norway
Prior art keywords
hydroxymethyl
amino
cyclopentene
preparation
optically active
Prior art date
Application number
NO20013037A
Other languages
English (en)
Other versions
NO20013037D0 (no
NO326058B1 (no
Inventor
Walter Brieden
Kay-Sara Etter
Michael Petersen
Original Assignee
Lonza 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 Lonza Ag filed Critical Lonza Ag
Publication of NO20013037D0 publication Critical patent/NO20013037D0/no
Publication of NO20013037L publication Critical patent/NO20013037L/no
Publication of NO326058B1 publication Critical patent/NO326058B1/no

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
    • C12P41/00Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • 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
    • C12P41/004Processes 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
    • 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
    • C12P13/00Preparation of nitrogen-containing organic compounds
    • C12P13/02Amides, e.g. chloramphenicol or polyamides; Imides or polyimides; Urethanes, i.e. compounds comprising N-C=O structural element or polyurethanes

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)
NO20013037A 1998-12-23 2001-06-19 Fremgangsmate for fremstilling av optisk aktive 1-amino-4-(hydroksymetyl)-cyklopenten-2-en-derivater NO326058B1 (no)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP98124570 1998-12-23
US14599999P 1999-07-29 1999-07-29
PCT/EP1999/010382 WO2000039324A2 (de) 1998-12-23 1999-12-23 Verfahren zur herstellung von optisch aktiven 1- amino-4- (hydroxymethyl)- cyclopent-2- en-derivaten

Publications (3)

Publication Number Publication Date
NO20013037D0 NO20013037D0 (no) 2001-06-19
NO20013037L true NO20013037L (no) 2001-06-19
NO326058B1 NO326058B1 (no) 2008-09-08

Family

ID=26149931

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20013037A NO326058B1 (no) 1998-12-23 2001-06-19 Fremgangsmate for fremstilling av optisk aktive 1-amino-4-(hydroksymetyl)-cyklopenten-2-en-derivater

Country Status (20)

Country Link
US (1) US6524844B2 (no)
EP (1) EP1141374B1 (no)
JP (1) JP4633934B2 (no)
KR (1) KR100685195B1 (no)
CN (1) CN1189569C (no)
AT (1) ATE253125T1 (no)
AU (1) AU2102600A (no)
CA (1) CA2354382C (no)
CZ (1) CZ301107B6 (no)
DE (1) DE59907569D1 (no)
DK (1) DK1141374T3 (no)
ES (1) ES2211216T3 (no)
HU (1) HUP0104547A3 (no)
IL (1) IL143229A0 (no)
MX (1) MXPA01006428A (no)
NO (1) NO326058B1 (no)
PL (1) PL196857B1 (no)
PT (1) PT1141374E (no)
SK (1) SK285795B6 (no)
WO (1) WO2000039324A2 (no)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4633934B2 (ja) * 1998-12-23 2011-02-16 ロンザ アーゲー 光学活性な1−アミノ−4−(ヒドロキシルメチル)−シクロペンタ−2−エン誘導体の製造方法
GB0306267D0 (en) 2003-03-19 2003-04-23 Ineos Fluor Ltd Process
WO2006117057A1 (en) * 2005-05-02 2006-11-09 Dsm Fine Chemicals Austria Nfg Gmbh & Co Kg Process for preparing enantiomerically enriched e-(2s)- and (2r)-alkyl-5-halopent-4-enecarboxylic acids or their esters

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2756790B2 (ja) * 1988-07-18 1998-05-25 富士薬品工業株式会社 光学活性なシクロペンテノール誘導体の製造方法
GB9108376D0 (en) * 1991-04-19 1991-06-05 Enzymatix Ltd Cyclopentenes
EP0904348B1 (de) 1996-05-30 2004-11-24 Lonza AG Verfahren zur herstellung von aminoalkoholen und derivaten davon
SK285228B6 (sk) 1997-05-13 2006-09-07 Lonza Ag Spôsob výroby racemického alebo opticky aktívnehoderivátu 4-(hydroxymetyl)-2-cyklopenténu a racemicky N-butyryl-1-amino-4- (hydroxymetyl)-2-cyklopentén
SK284594B6 (sk) * 1997-11-27 2005-07-01 Lonza Ag Spôsob výroby derivátov aminoalkoholov a ich soli
JP4633934B2 (ja) * 1998-12-23 2011-02-16 ロンザ アーゲー 光学活性な1−アミノ−4−(ヒドロキシルメチル)−シクロペンタ−2−エン誘導体の製造方法

Also Published As

Publication number Publication date
JP2003520018A (ja) 2003-07-02
DE59907569D1 (de) 2003-12-04
CN1189569C (zh) 2005-02-16
KR20010099861A (ko) 2001-11-09
NO20013037D0 (no) 2001-06-19
PL196857B1 (pl) 2008-02-29
WO2000039324A3 (de) 2000-09-21
MXPA01006428A (es) 2002-06-21
KR100685195B1 (ko) 2007-02-22
CZ20012168A3 (cs) 2001-11-14
CA2354382A1 (en) 2000-07-06
PL349388A1 (en) 2002-07-15
US6524844B2 (en) 2003-02-25
IL143229A0 (en) 2002-04-21
EP1141374A2 (de) 2001-10-10
WO2000039324A2 (de) 2000-07-06
CA2354382C (en) 2010-09-07
DK1141374T3 (da) 2004-02-16
NO326058B1 (no) 2008-09-08
US20020042108A1 (en) 2002-04-11
CZ301107B6 (cs) 2009-11-11
HUP0104547A3 (en) 2003-12-29
SK8812001A3 (en) 2002-01-07
JP4633934B2 (ja) 2011-02-16
PT1141374E (pt) 2004-03-31
ATE253125T1 (de) 2003-11-15
SK285795B6 (sk) 2007-08-02
AU2102600A (en) 2000-07-31
HUP0104547A2 (hu) 2002-03-28
CN1352695A (zh) 2002-06-05
EP1141374B1 (de) 2003-10-29
ES2211216T3 (es) 2004-07-01

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