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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J5-00
filingDate 1983-06-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1984-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_458b4c8f2cb91bc4eeebdbd0f5dfd473
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4deac2ae39ba857067a27d380721e080
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d129d0df90054c0b7d90334ef6631120
publicationDate 1984-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1121267-A1
titleOfInvention Process for preparing 21-hydroxy-16,17alpha-epimino-20-ketostreroyds
abstract 1. METHOD OF OBTAINING 21-OXY§ i-16 i 7cft-3imMHHO-20-KETOCTEPOHHOB forns, it is based on derivatives of pregnerone, characterized in that, with the aim of increasing the yield and inhibiting the process, pregnenolone derivative is used to increase output and inhibit the process. , | 7vS-epiminopregnenolone, which is reacted with iodo-benzene diacetate or iodo-benzozene to methanol
priorityDate 1983-06-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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