http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3897459-A
Outgoing Links
Predicate | Object |
---|---|
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 |
Incoming Links
Total number of triples: 76.