YU69399A - Postupak dobijanja obogaćenih enantiomera n-derivata laktama - Google Patents

Postupak dobijanja obogaćenih enantiomera n-derivata laktama

Info

Publication number
YU69399A
YU69399A YU69399A YU69399A YU69399A YU 69399 A YU69399 A YU 69399A YU 69399 A YU69399 A YU 69399A YU 69399 A YU69399 A YU 69399A YU 69399 A YU69399 A YU 69399A
Authority
YU
Yugoslavia
Prior art keywords
derivatised
lactams
enantiomerically enriched
preparing enantiomerically
preparing
Prior art date
Application number
YU69399A
Other languages
English (en)
Inventor
Michael John Dawson
Mahmoud Mahmoudian
Christopher John Wallis
Original Assignee
Glaxo Group Limited
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 Glaxo Group Limited filed Critical Glaxo Group Limited
Publication of YU69399A publication Critical patent/YU69399A/sh
Publication of RS49542B publication Critical patent/RS49542B/sr

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
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/52Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring condensed with a ring other than six-membered
    • 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
    • C12P41/006Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by reactions involving C-N bonds, e.g. nitriles, amides, hydantoins, carbamates, lactames, transamination reactions, or keto group formation from racemic mixtures
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Genetics & Genomics (AREA)
  • Microbiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Hydrogenated Pyridines (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)

Abstract

Ovaj pronalazak se odnosi na postupak dobijanja u osnovi čistih enantiomera intermedijara formule (IV) u kojoj je P aktivirajuća i zaštitna grupa, iz njihovih racemata, tretiranjem smeše sa enzimom acilaze, koji se izdvaja iz soja Bacillus sp.[The present invention relates to a process for the production of substantially enantiomerically pure intermediates of formula (IV), wherein P is an activating and protecting group, from their racemates by treating the mixture with an acylase enzyme derived from i(Bacillus) sp..
YUP-693/99A 1997-08-22 1998-08-20 Postupak dobijanja obogaćenih enantiomera N- derivata laktama RS49542B (sr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB9717928.7A GB9717928D0 (en) 1997-08-22 1997-08-22 Process for the enatioselective hydrolysis of n-derivatised lactams

Publications (2)

Publication Number Publication Date
YU69399A true YU69399A (sh) 2002-06-19
RS49542B RS49542B (sr) 2007-02-05

Family

ID=10817952

Country Status (35)

Country Link
US (1) US6340587B1 (sh)
EP (1) EP1003903B1 (sh)
JP (1) JP3565868B2 (sh)
KR (1) KR100479894B1 (sh)
CN (1) CN1133749C (sh)
AP (1) AP1104A (sh)
AR (1) AR016395A1 (sh)
AT (1) ATE233323T1 (sh)
AU (1) AU738897B2 (sh)
BR (1) BR9810472B1 (sh)
CA (1) CA2295017A1 (sh)
CZ (1) CZ294302B6 (sh)
DE (1) DE69811677T2 (sh)
DK (1) DK1003903T3 (sh)
EA (1) EA001964B1 (sh)
EE (1) EE03934B1 (sh)
ES (1) ES2193568T3 (sh)
GB (1) GB9717928D0 (sh)
HK (1) HK1025796A1 (sh)
HR (1) HRP990408B1 (sh)
HU (1) HU222657B1 (sh)
ID (1) ID25830A (sh)
IL (1) IL133541A (sh)
IN (1) IN183908B (sh)
IS (1) IS2201B (sh)
NO (1) NO320081B1 (sh)
NZ (1) NZ501880A (sh)
PL (1) PL191108B1 (sh)
PT (1) PT1003903E (sh)
RS (1) RS49542B (sh)
SI (1) SI1003903T1 (sh)
SK (1) SK282782B6 (sh)
TR (1) TR199903210T2 (sh)
TW (1) TW589301B (sh)
WO (1) WO1999010519A1 (sh)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU5280399A (en) * 1998-07-09 2000-02-01 Lonza A.G. Method for producing (1r,4s)-2-azabicylco(2.2.1)hept-5-en-3-on derivatives
DE19962543A1 (de) * 1999-12-23 2001-07-05 Degussa Chromatographische Enantiomerentrennung von bicyclischen Lactamen
US6780635B2 (en) * 2001-12-27 2004-08-24 Council Of Scientific And Industrial Research Process for the preparation of optically active azabicyclo heptanone derivatives
DE60211646T2 (de) * 2002-03-28 2007-05-24 Council Of Scientific And Industrial Research Verfahren zur Herstellung von optisch aktiven Azabicycloheptanone-Derivaten
HU227663B1 (en) * 2007-07-09 2011-10-28 Univ Szegedi Resolution process
NZ627826A (en) 2010-01-27 2016-01-29 Viiv Healthcare Co Antiviral combinations involving (3s,11ar)-n-[(2,4-difluorophenyl)methyl]-2,3,5,7,11,11a-hexahydro-6-hydroxy-3-methyl-5,7-dioxo-oxazolo[3,2-a]pyrido[1,2-d]pyrazine-8-carboxamide
CN103695495B (zh) * 2014-01-14 2014-08-27 营口三征新科技化工有限公司 一种制备(1R,4s)-(-)-2-氮杂双环[2,2,1]庚-5-烯-3-酮的方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE118208T1 (de) * 1989-10-16 1995-02-15 Chiroscience Ltd Chirale azabicycloheptanone und verfahren zu ihrer herstellung.
GB9108384D0 (en) 1991-04-19 1991-06-05 Enzymatix Ltd Bicycloheptanes
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

Also Published As

Publication number Publication date
BR9810472B1 (pt) 2011-01-11
EA199901059A1 (ru) 2000-08-28
NO996368L (no) 2000-02-21
IL133541A0 (en) 2001-04-30
HU222657B1 (hu) 2003-09-29
ATE233323T1 (de) 2003-03-15
DE69811677T2 (de) 2003-10-16
DE69811677D1 (de) 2003-04-03
AU9738698A (en) 1999-03-16
AU738897B2 (en) 2001-09-27
JP3565868B2 (ja) 2004-09-15
TW589301B (en) 2004-06-01
IN183908B (sh) 2000-05-13
SK184499A3 (en) 2000-09-12
SI1003903T1 (en) 2003-08-31
HUP0002661A3 (en) 2001-12-28
IL133541A (en) 2003-10-31
DK1003903T3 (da) 2003-06-10
NO320081B1 (no) 2005-10-17
WO1999010519A1 (en) 1999-03-04
IS2201B (is) 2007-02-15
KR100479894B1 (ko) 2005-03-30
AR016395A1 (es) 2001-07-04
PL337647A1 (en) 2000-08-28
JP2001504354A (ja) 2001-04-03
ID25830A (id) 2000-11-09
AP9901721A0 (en) 1999-12-31
BR9810472A (pt) 2000-09-19
US6340587B1 (en) 2002-01-22
EP1003903B1 (en) 2003-02-26
PL191108B1 (pl) 2006-03-31
CA2295017A1 (en) 1999-03-04
EP1003903A1 (en) 2000-05-31
EE200000075A (et) 2000-10-16
PT1003903E (pt) 2003-06-30
CZ294302B6 (cs) 2004-11-10
ES2193568T3 (es) 2003-11-01
CZ471699A3 (cs) 2000-06-14
HK1025796A1 (en) 2000-11-24
HRP990408B1 (en) 2006-05-31
EA001964B1 (ru) 2001-10-22
HRP990408A2 (en) 2000-04-30
TR199903210T2 (xx) 2000-07-21
NO996368D0 (no) 1999-12-21
RS49542B (sr) 2007-02-05
AP1104A (en) 2002-09-04
EE03934B1 (et) 2002-12-16
IS5297A (is) 1999-12-14
HUP0002661A2 (hu) 2000-12-28
KR20010014078A (ko) 2001-02-26
NZ501880A (en) 2001-08-31
SK282782B6 (sk) 2002-12-03
CN1261405A (zh) 2000-07-26
CN1133749C (zh) 2004-01-07
GB9717928D0 (en) 1997-10-29

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