http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-8401082-A1

Outgoing Links

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-36
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-36
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filingDate 1982-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1983-12-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-8401082-A1
titleOfInvention A PROCEDURE FOR THE PREPARATION OF NEW CEPHALOSPORINS.
abstract PROCEDURE FOR THE OBTAINING OF CEPHALOSPORINS AND THEIR PHYSIOLOGICALLY COMPATIBLE SALTS, HEMIACETALS AND SALTS, OF FORMULA (I), IN WHICH R4 IS HYDROGEN OR HYDROXY; AND R1, R3, A AND X MAY BE SEVERAL TYPES OF RADICALS.CONSISTENT IN THE REACTION OF ACILATION OF 1-S-OXIDE OF 7-AMINO-3-BROMOMETIL-3-CEFE M-CARBOXYLATE OF T-BUTYL WITH AN ACTIVATED ACID OF FORMULA (II), IN WHICH P IS A PROTECTIVE GROUP AND R1 AND R2 HAVE THE SAME MEANING AS IN FORMULA (I), IN AN APROTIC APOLAR SOLVENT; FOLLOWED BY THE REACTION WITH PIRIDIN-2-TIONA, OR WITH A PIRIDIN-4-TIONA OF FORMULAS (III) OR (IV), IN WHICH R3 AND R4 ARE THE SAME AS IN FORMULA (I), AT A TEMPERATURE BETWEEN 0 and 50JC; AND, FINALLY, SEPARATION OF THE PROTECTIVE GROUPS FOR ACID HYDROLYSIS. THESE COMPOUNDS HAVE PHARMACOLOGICAL APPLICATIONS FOR THEIR ANTIBACTERIAL ACTIVITY.
priorityDate 1981-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Predicate Subject
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Total number of triples: 21.