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filingDate 1977-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1982-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber IE-44738-B1
titleOfInvention Cephalosporin synthesis
abstract Cephalosporin sulfoxides are reduced to the corresponding cephalosporin with acyl bromides, e.g., acetyl bromide, in the presence of a bromine scavenger, e.g., an olefin, acetylene, phenol, phenol ether, or an organophosphite. For example, p-nitrobenzyl 7-phenoxyacetamido-3-methyl-3-cephem-4-carboxylate sulfoxide is reduced with acetyl bromide in the presence of amylene to p-nitrobenzyl 7-phenoxyacetamido-3-methyl-3-cephem-4-carboxylate.
priorityDate 1976-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412471889
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID298831
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID783
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID587463
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID67655752
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8882
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID13317102

Total number of triples: 315.