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filingDate 1973-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1981-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cb55c1bf46a98e7b550569874ce9ab9b
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publicationDate 1981-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1109860-A
titleOfInvention Process for producing lactol-type cephalosporins
abstract Process for producing Lactol-type Cephalosporins Abstract A 3-hydroxymethylcephalosporin which is not protected at the carboxyl group can be directly oxidized with a hexa-valent chromium compound to give in good yield a lactol type cephalosporin represented by the general formula: wherein R1 is hydrogen or an alkoxy group and R2 is an acylamino, or imido group. The resulting compounds are very useful and important as intermediates for preparing, e.g. 3-alkoxyiminomethyl cephalosporins.
priorityDate 1972-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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