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filingDate 1982-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f7ea5cf1961fffe4e63407795c20a4bd
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publicationDate 1986-05-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-188781-B
titleOfInvention Process for producing 3-methyl-2-/2-oxo-4-fluoro-3-phenoxy-acetamido-1-azetidinyl/-3-butenoic-acid-p-nitro-benzyl-ester
abstract 4-Fluoroazetidinones of formula 1 <CHEM> wherein R is a carboxy-substituted or esterified carboxy-substituted butenyl group represented by the formulas <CHEM> and R1 is amino, amido, imido or imidazolidino or a pharmaceutically-acceptable salt thereof obtained from penicillin are useful intermediates in the preparation of beta -lactam antibiotics. 4-Fluoroazetidinones of formula 1 wherein R1 as described above other than amino, benzyloxycarbonylamino, p-nitrobenzyloxycarbonylamino, t-butyloxycarbonylamino, 2,2,2-trichloroethoxycarbonylamino, or p-methoxybenzyloxycarbonylamino; and R is a carboxy-substituted butenyl represented by the formula <CHEM> have antibacterial activity.
priorityDate 1981-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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