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AU2653200A - Stereoselective synthesis of nucleoside analogues - Google Patents

Stereoselective synthesis of nucleoside analogues

Info

Publication number
AU2653200A
AU2653200A AU26532/00A AU2653200A AU2653200A AU 2653200 A AU2653200 A AU 2653200A AU 26532/00 A AU26532/00 A AU 26532/00A AU 2653200 A AU2653200 A AU 2653200A AU 2653200 A AU2653200 A AU 2653200A
Authority
AU
Australia
Prior art keywords
nucleoside analogues
stereoselective synthesis
stereoselective
synthesis
nucleoside
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.)
Abandoned
Application number
AU26532/00A
Inventor
Alex Cimpoia
Lana Janes
Romas Kazlauskas
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
McGill University
Shire Canada Inc
Original Assignee
IAF BioChem International Inc
Biochem Pharma Inc
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 IAF BioChem International Inc, Biochem Pharma Inc filed Critical IAF BioChem International Inc
Publication of AU2653200A publication Critical patent/AU2653200A/en
Abandoned legal-status Critical Current

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
    • 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)
  • Analytical Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
AU26532/00A 1999-02-11 2000-02-11 Stereoselective synthesis of nucleoside analogues Abandoned AU2653200A (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US11975699P 1999-02-11 1999-02-11
US60119756 1999-02-11
US11988599P 1999-02-12 1999-02-12
US60119885 1999-02-12
PCT/CA2000/000144 WO2000047759A1 (en) 1999-02-11 2000-02-11 Stereoselective synthesis of nucleoside analogues

Publications (1)

Publication Number Publication Date
AU2653200A true AU2653200A (en) 2000-08-29

Family

ID=26817660

Family Applications (1)

Application Number Title Priority Date Filing Date
AU26532/00A Abandoned AU2653200A (en) 1999-02-11 2000-02-11 Stereoselective synthesis of nucleoside analogues

Country Status (5)

Country Link
EP (1) EP1151133A1 (en)
JP (1) JP2002538780A (en)
AU (1) AU2653200A (en)
CA (1) CA2362570A1 (en)
WO (1) WO2000047759A1 (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE269081T1 (en) 1999-09-24 2004-07-15 Shire Biochem Inc DIOXOLANE NUCLEOSIDE ANALOGUES FOR THE TREATMENT AND PREVENTION OF VIRAL INFECTIONS
EP1225899A2 (en) 1999-11-04 2002-07-31 Virochem Pharma Inc. Method for the treatment or prevention of flaviviridae viral infection using nucleoside analogues
EP1265890B1 (en) * 2000-02-11 2007-04-18 Shire BioChem Inc. Stereoselective synthesis of nucleoside analogues
WO2002051852A1 (en) * 2000-12-27 2002-07-04 Mitsui Chemicals, Inc. Process for producing nonnatural saccharide derivative
WO2004048590A1 (en) * 2002-11-18 2004-06-10 Shire Biochem Inc. Stereoselective process for the production of dioxolane nucleoside analogues
DE10335061B4 (en) * 2003-07-31 2005-11-17 Wacker-Chemie Gmbh Process for the preparation of OH-protected [4- (2,6-damino-9H-purin-9-yl) -1,3-dioxolan-2-yl] methanol derivatives
WO2005074654A2 (en) 2004-02-03 2005-08-18 Emory University Methods to manufacture 1,3-dioxolane nucleosides

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5190867A (en) * 1986-05-08 1993-03-02 Shell International Petroleum Company, Ltd. Process for the preparation of R-2,2-R1,R2 -1,3-dioxolane-4-methanol
DD277698A1 (en) * 1988-12-06 1990-04-11 Ve Forschungszentrum Biotechno PROCESS FOR PREPARING SUBSTITUTED (S) -1,3-DIOXOLAN-4-CARBOXYLIC ACID ESTERS FROM THE RACEMATES
US5283346A (en) * 1989-03-23 1994-02-01 Hoffmann-La Roche Inc. Dioxolanes
US5276151A (en) * 1990-02-01 1994-01-04 Emory University Method of synthesis of 1,3-dioxolane nucleosides
GB9525606D0 (en) * 1995-12-14 1996-02-14 Iaf Biochem Int Method and compositions for the synthesis of dioxolane nucleosides with › - configuration

Also Published As

Publication number Publication date
CA2362570A1 (en) 2000-08-17
EP1151133A1 (en) 2001-11-07
WO2000047759A1 (en) 2000-08-17
JP2002538780A (en) 2002-11-19

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Legal Events

Date Code Title Description
MK6 Application lapsed section 142(2)(f)/reg. 8.3(3) - pct applic. not entering national phase