http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5037975-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2ca2e4410855da087e11bf3eea8933fa
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D463-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D205-085
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D463-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D205-085
filingDate 1990-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1991-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7f9ee8114ee876108393bd30f88c1aa7
publicationDate 1991-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5037975-A
titleOfInvention Cephalosporin free radical compounds
abstract The invention provides a free radical process for preparing 1-carba(1-dethia)cephalosporin antibiotics with 2-substituted methylcephalosporin 1,1-dioxides wherein the substituent on the 2-methylene group is a free radical precursor group such as a phenyl or alkylseleno group. The latter dioxides are treated with a free radical initiator, e.g., a trialkyltin hydride or actinic radiation at 40 DEG C. to 150 DEG C. to provide the 1-carba-3-cephem and 1-carba-2-cephem products. The invention also provides free radical compounds formed as intermediates in the process.
priorityDate 1988-09-16-04:00^^<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/CID19816472
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127537863
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID57378924
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22793890
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226487520

Total number of triples: 313.