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filingDate 1973-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2c04eb0c466a4e1de57010d584f7b767
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publicationDate 1974-01-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BE-807179-A
titleOfInvention NEW CEPHALOSPORINS AND METHODS FOR THEIR PREPARATION
abstract Compounds of formula (I) and salts, esters and lactones (where Y=OH) thereof are new: (R4=H or acyl; B=H, CH3, CH3O, or SR; R=aryl or lower alkyl; Y=-CH(A)R5 or is R'; R5=1-3C alkyl; A=H, halo, opt. substd. OH or SH, N3, CN, opt. substd. amino, acyloxy, opt. substd. carbamoyloxy or quaternary ammonium; R'= opt. substd. phenyl or heterocyclyl). Intermediates of formulae (II), (III), (IV), (V) and (VI) are also new: (R1= blocking gp., B'=B other than H; B"=H). (I) are antibiotics active against gram positive and negative bacteria; (II)-(VI) are intermediates to (I). They are used in human or veterinary medicine, as animal feed additives, disinfectants etc. gave dl-3-(1-acetoxy-ethyl)-7beta-(2-thienylacetamido)-3-cephem-4-carb- oxylic acid.
priorityDate 1972-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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