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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d202e9e866984fe229f6facc38f1d740
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C405-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C405-00
filingDate 1973-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1975-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_10cdb6775b650ef66c0ec12ac2f1cf74
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e31451c2fc498a0d0b0803fd0f14d6fd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_159f89612570e19e41b8a802fbbb3a9a
publicationDate 1975-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3897459-A
titleOfInvention 5-Oxo-1{62 -cyclopentane heptanoic acid derivative
abstract Prostaglandin E1 is totally synthesized with a high degree of stereoselectivity and in good yield at the various steps from 6 Alpha -carboxy-5 Alpha -(1-hydroxyethyl)-2-cyclohexane-1heptanoic acid ester, gamma -lactone; 2 Alpha -carboxy-3 Alpha (1-hydroxyethyl)-5-oxocyclopentaneheptanoic acid ester, gamma lactone; 3 Beta -acetyl-2 Alpha -carboxy-5-oxo-1 Beta cyclopentaneheptanoic acid ester, 5-cyclic ethylene acetal; 3 Beta -acetoxy-5-oxo-2 Alpha -(3-oxo-1-octenyl)-1 Beta cyclopentaneheptanoic acid ester, 5-cyclic acetal; and prostaglandin E1. The end compound has the biological activity of naturally occurring prostaglandin E1.
priorityDate 1972-09-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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