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filingDate 1980-04-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_723f98a451fad7458aaf4c742ba5530b
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publicationDate 1981-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S56152479-A
titleOfInvention Optically active cephalosporin analog
abstract NEW MATERIAL:Optically active cephalosporin analogs of formula I (R 1 is H, alkyl, alkenyl; R 2 is H, lower alkyl, lower acyl; R 3 is H, ester residue; the H atoms on the 6 and 7 positions are in cis and OR 1 is insyn) and their salts. n EXAMPLE: ( 4S,6R,7S )-7-[2-(2-Amino-4-thiazolyl)-2-syn-methoxyiminoacetamide]- 4-hydroxy-1-azabicyclo[4,2,0]oct-2-ene-8-one-2-carboxylic acid. n USE: Antibiotic. n PREPARATION: An optically active isomer of formula (V-1) is acylated with a reactive derivative of a compound of formula II (Y is H, amine-protecting group) to give a compound of formula VIII. Then, the protecting groups are removed from the compound of formula VIII and, when necessary, the product is esterified to give the compound of formula I. n COPYRIGHT: (C)1981,JPO&Japio
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