http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2482597-A2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-14
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-545
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-14
filingDate 1980-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_793e76c17265fee7cb737a4e73db56df
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_38536b96860c5c7a8bd63b8286c07484
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4685a5fd755c32965b95b1b097dfc258
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publicationDate 1981-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber FR-2482597-A2
titleOfInvention NEW DERIVATIVES OF VINYL-3 CEPHALOSPORINS AND THEIR PREPARATION
abstract NEW DERIVATIVES OF VINYL-3 CEPHALOSPORINS OF GENERAL FORMULA I IN THE FORM BICYCLOOCTENE-2 OR -3, IN WHICH R IS A RADICAL OF GENERAL FORMULA II IN WHICH R IS VINYL, CYANOMETHYL OR METHOXY-2 AND R IS A RADICAL R PROTECTIVE OR BIGENE WHERE ALKYL AND R IS FORMYL OR TRIFLUOROACETYL, R IS A PROTECTIVE RADICAL OR A RADICAL ELIMINABLE BY ENZYMATIC ROUTE AND R AND R, IDENTICAL OR DIFFERENT, REPRESENT ALCOYL (POSSIBLY SUBSTITUTED BY HYDROXY, ALCOYLENAMOYLOXY, OR DIALOYLOXY, OR ALCOYLOXY ALCOHYLOXY, OR ALCOYLOXY, OR DIALOY, ORALCOYL, OR ALCOYLOXY, OR ALCOYLOXY, OR DIALOY TOGETHER WITH THE NITROGEN ATOM A 5 OR 6-CHAIN SATURATED HETEROCYCLE CONTAINING ANOTHER HETEROATOM, THEIR E AND Z FORMS AND THEIR MIXTURES, AS WELL AS THEIR PREPARATION. THESE NEW PRODUCTS ARE USEFUL AS INTERMEDIARIES FOR THE PREPARATION OF BIOLOGICALLY ACTIVE CEPHALOSPORINS.
priorityDate 1980-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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