http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1157012-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_97a285d8ecd0184a7e5d89a1e4e07997
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-16
filingDate 1983-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1983-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2f81359cbf93393d32bac58754239518
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_135bffe6572a4acc22d407cb4376c1de
publicationDate 1983-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1157012-A
titleOfInvention Process for the preparation of (subtituted)-2- carbamoyloxymethylpenam and (substituted)-3- carbamoyloxycepham
abstract ABSTRACT Penicillin sulfoxide esters are reacted with an iso-cyanate to produce the corresponding (substituted)-2-carbamoyl-oxymethylpenam, The corresponding (substituted)-3-carbamoyl-oxycepham or the corresponding 3-methylcephem. The 6- or 7-side-chain of these products may be cleaved to give the corresponding 6-amino (penams) or 7-amino (cephams and cephems) compounds, and the latter may be reacylated to produce different 6-acyl-2-carbamoyloxymethyl penams, 7-acyl-3-carbamoyloxy cephams and 7-acyl-3-mothylcephams. The substituent groups may be removed from the (substituted)-2-carbamoyloxypenams or the (substituted)-3-carbamoyloxycephams to give the corresponding free 2-carbamoyloxymethylpenams or 3-carbamoyloxycephams, respectively. Novel penams and cephams provided by the present invention (after removal of the carboxyl-protecting group to produce the free acid) are active against various Gram-positive and Gram-negative organisms and, accordingly, are useful antibacterial agents for the treatment of diseases caused by such organisms in animals, including man.
priorityDate 1978-04-03-04:00^^<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/compound/CID7937
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID416154439
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID76400
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID27970
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID139265241
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID13649181
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419723178
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10665
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20283241
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411306435
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12668337
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID172266
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393346
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6327678
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410437678
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419545381
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12300404
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12668338
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11715415
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID107602
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID430868451
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415758710
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419516651
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393684
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21904465
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419576080
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456029861
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415814991

Total number of triples: 328.