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filingDate 1992-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2000-09-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2d69c90bad13fa87adf3056a64b01ddf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_346f88edbec8942c07ac293b079c95e9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ff7854d31ea227692a34176d31e99cd2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7a7de13bb1688b5a3b993443228e8bda
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_256cd657a287428cdbd6bb67ad0e0a6b
publicationDate 2000-09-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0551034-B1
titleOfInvention Antibiotic cephalosporins having in position 7 a substituted benzyloxyimino radical
abstract New intermediates (III) - (VI) and (VIII) for the preparation of cephalosporins, comprising a substituted benzyloxyimino group in position 7, are new. New intermediates of formulas (III) - (VI) and (VIII) for the preparation of cephalosporins, comprising a substituted benzyloxyimino group in position 7, are new. R1p-R5p = R1-R5 or protected group; R1-R3, R5 = H, halo, OH, 1-4C alkyl (optionally substituted with at least one halo), 1-4C alkoxy, mercapto, 1-4C alkylthio, nitro, cyano, amino (optionally substituted with one 1-4C alkyl), 2-8C dialkylamino, carbamoyl, 2-5C alkylamino-carbonyl, 3-9C dialkylamino-carbonyl, 2-5C alkoxycarbonyl, 1-8C acyloxy or SO2-N(Rx)(Ry); Rx, Ry = H or 1-4C alkyl; R4 = OH or 1-8C acyloxy; R7 = ester residue; R8 = H or protecting group; and provided R3 and R5 are the same as R4 when: (1) R1, R2 or R3, or R2, R4 or R5 is F, Br, I or cyano; or (2) R1 and R5 are both other than H; or (3) R2 and R5 are both Cl.
priorityDate 1991-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 505.