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filingDate 1968-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f06dc83bdf835fd7028b730dabf301fc
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publicationDate 1972-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-522679-A
titleOfInvention Process for the preparation of new cephalosporin derivatives
abstract (A) Compounds salts and esters. R = carboxylic acyl; P = Cl, Br, I, formyloxy, isothiocyanato, or haloacetoxy. Preferred compounds have R = - (B) Compounds B = alkyls or B and the attached N atom represent an opt. subst. thiazole ring. - (C) Compounds - A together with the attached N atom = opt. subst. pyrazole ring. - Broad spectrum antibiotics. - Reaction of ceph-3-em-4-carboxylic acids or derivs. having an RNH group in 7-position and the group -CH2X in 3-position where the acid HX has a pKa or not greater than 4.0 and X does not contain an SH group, with a compound having a nucleophilic group in suitable conditions to displace X.
priorityDate 1967-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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