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filingDate 1991-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_097cc536c3ddda1b84b3d69836cff019
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publicationDate 1996-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0827168-A
titleOfInvention Carbapenem intermediate
abstract (57) [Summary] [Objective] To provide an intermediate compound useful for the synthesis of carbapenem antibiotics such as thienamycin and a method for producing the same. 【Constitution】 (In the formulae, R 1 , R 2 and R 3 are independently C 1 -C 4 A compound represented by the formula: By reacting with a compound having the formula: wherein L represents a conventional leaving group and R 4 ′ represents a conventional hydroxyl-protecting group. There is obtained a compound of the formula wherein R 4 represents hydrogen or a common hydroxyl protecting group, which is useful as an intermediate in the synthesis of carbapenem antibiotics.
priorityDate 1983-03-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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