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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D503-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D499-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D503-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-43
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D499-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
filingDate 1981-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0749f73fbca929d2c40f48172a1926e3
publicationDate 1981-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0042220-A1
titleOfInvention Process for the preparation of beta-lactam antibiotics
abstract The present invention provides a process for the preparation of a fused bicyclic (β-lactam containing compound having an optionally salified free carboxylic acid group which process comprises the reaction of an ester of the formula (I):n with halide ion; wherein R is the residue of the fused bicyclic (β-lactam containing compound, R' is an alkyl group of 1-6 carbon atoms optionally substituted by an alkoxy group of 1-4 carbon atoms or is an optionally substituted phenyl group or an alkyl group of 1-4 carbon atoms substituted by an optionally substituted phenyl group; and R 2 is a hydrogen atom or an alkyl group of 1-4 carbon atoms or is joined to R 2 to form part of a 5- or 6- membered carbocyclic or heterocyclic ring.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4585638-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4741891-A
priorityDate 1980-06-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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