http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CH-613972-A5

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-16
filingDate 1974-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_13991795cd410f1b41612ab0e2ee0f6d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a585cd6259ac332635b157bc1352a0a1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_987eea22ef8b5d53027046238f232696
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bad0f5f18daba5b26ab35ab93ff1db09
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bb755690f02d0d682791576ce4d1da10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_490d747b5f6412e3ab281c41b3d1552e
publicationDate 1979-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-613972-A5
titleOfInvention Process for the preparation of 2- or 3-cephem-4-carboxylic acids with a substituted methyl radical in position 3
abstract Compounds of the formula: <IMAGE> in which A is a thio or sulphinyl group, R<1> is hydrogen or acyl and R<2> is the radical of various thiols, thioamides etc., and their salts and esters are prepared by reacting a corresponding 3-halomethyl or 3-lower-alkanoyloxymethyl compound or a salt or ester thereof with a compound R<2>H in the presence of a quaternary ammonium salt or of a phosphonium salt. If desired, the sulphinyl compounds can be reduced to thio compounds, or a carboxyl group which is protected as a salt or as an ester can be unblocked. The compounds have antibacterial activity.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007503447-A
priorityDate 1973-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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