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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D205-08
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filingDate 1980-07-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1986-02-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber IE-50071-B1
titleOfInvention Preparation of azetidin-2-ones suitable for the synthesis of thienamycin and azetidin-2-ones useful in a synthesis of that kind
abstract Disclosed is a process for the total synthesis of thienamycin from 4-allylazedinone (IIIa) via intermediate (III): R = H, blocking group or salt cation R - H, alkyl, aralkyl, cycloalkyl or cycloalkylalkyl.
priorityDate 1979-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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