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filingDate 1991-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5024b837a009872b7ec2edf554fb2dba
publicationDate 1992-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H04273875-A
titleOfInvention Cleavage of ester group of cephalosporins
abstract PURPOSE: To cleave ester group mildly in one step with minimum decomposition of cephalosporins bringing a specific substrate into contact with lithium iodide in the reaction mixture which contains a substantial concentration of acetonitrile. n CONSTITUTION: The compound of formula II (X is CH 2 or S; R 1 is H or an amino protecting group, etc.; R 2 is Cl, Br or methyl; R 3 is H or a 1-4C alkoxy, etc.) is obtained by bringing the substrate of formula I (R 4 is methyl or ethyl) into contact with lithium iodide in the reaction mixture which contains a substantial concentration of acetonitrile. The amount of lithium iodide to be added is 2-7 mole per mole of objective product, and the solvent used for reaction is comprised of 0-20% of an aprotic solvent and 80-100% of acetonitrile. n COPYRIGHT: (C)1992,JPO
priorityDate 1990-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 28.