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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-34
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filingDate 1982-08-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1985-05-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_61a8cb5ed04a03649f1e6b26138d6186
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_581cde3a17c8cacd3414309a1aed7b1d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bb453a5b84df81f5f81b2d897200e3ae
publicationDate 1985-05-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1155159-A3
titleOfInvention Method of obtaining cephalosporin derivatives or their salts with alkali metals
abstract The method of obtaining cephalosporin derivatives of the general formula C C ONH-pY y Ke N CT l V R, O COORz-SNGSOS | O where RJ is a hydrogen atom or a protecting group forming an ester; R. a. Of hydrogen or a protective group forming an ester; R, a hydrogen atom or methyl; R ,, hydrogen or chlorine atom, methyl, vinyl, methoxy group, methoxymethyl, methylthiomethide or acetoxymethyl, and one of RI and R4 means a hydrogen atom or their salts with alkali metals, when R (and / or Rj is a hydrogen atom, in the form of syn -isomers, about tl and h aJtpsc and also with the fact that the compound of the general formula H, Nr-rV, COOE R and E.L have the indicated values of R. cha VIA, or its reactive derivative in the amino group, or its salt is subjected to interaction with compound of general formula
priorityDate 1981-08-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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