http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1092575-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_dc2f7134efa50484bb359fda73782848
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S8-924
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C49-423
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J75-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B1-34
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B1-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-423
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J75-00
filingDate 1965-08-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1967-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1092575-A
titleOfInvention í¸-3-oxo-14ª‰-hydroxy-androstenes
abstract The novel D 4-3,17-dioxo-14b -hydroxy-androstane and the corresponding 17b -ol and its esters and ethers are prepared by the methods disclosed in Specification 1,092,574. D 4 - 3 - oxo - 14a - hydroxy - 17b - acetoxy-androstene is prepared by acetylating D 3,5-3-ethoxy - 14a ,17b - dihydroxy - androstadiene (prepared by reduction of the 17-one, itself prepared by enol esterification of the D 4-3,17-dione) to give the 17b -acetoxy compound, and hydrolysing the enol ester group.
priorityDate 1963-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419501829
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11273

Total number of triples: 19.