http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4334065-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2ca2e4410855da087e11bf3eea8933fa
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-18
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-18
filingDate 1980-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1982-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f31f72572a296b361b9f45f8addf12f5
publicationDate 1982-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4334065-A
titleOfInvention Cephalosporin intermediates
abstract 7α-(Dimethylamidino)-3-cephem ester 1α-oxides represented by the formula ##STR1## wherein R is hydrogen or acetoxy and R 1 is a carboxy protecting group, are prepared via DBU epimerization of the corresponding 7β-isomer. When R is hydrogen the intermediates are useful in the preparation of the 7β-acylamino-7α-methoxy-1-oxa-β-lactam antibiotics, and when R is acetoxy the compounds are intermediates to 7β-acylamino-7α-methoxy-3-exomethylenecepham compounds.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5824801-A
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4448720-A
priorityDate 1980-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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