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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D499-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D235-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D499-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D235-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-72
filingDate 1969-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cfbc692a2dc1340a4d4b206df0f5697d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c0262e8d129830856c8fe896e29080cd
publicationDate 1972-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-1966516-A1
titleOfInvention Cyclopentene compounds
abstract Penicillanic acid derivs. of formulae I and II (where Z = NHR1 or a gp. convertable to NHR1, R1 = H, lower alkyl or phenyl-lower alkyl; R2 and R3= H, lower alkyl, Ph, or CR2R3 together form a lower cycloalkyl ring) are new cmpds. active against gram-negative and gram-positive organisms.They are prepd. by standard methods, functional gps. being protected as necessary, thus condensation of with 6-aminopenicillanic acid (IV) or their derivs., gives I, and subsequent condensation of I (Z = NHR1) with R2R3CO, gives II
priorityDate 1968-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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