http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100523146-B1

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filingDate 1996-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2005-10-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2005-10-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-100523146-B1
titleOfInvention Process for preparation of 7 alpha-carboxyl 9, 11-epoxy steroids and intermediates useful therein and a general process for the epoxidation of olefinic double bonds
abstract Formula In n n n n n n n Formula IIIn n n n n n n n Several novel schemes, new process steps and novel intermediates are provided for the synthesis of epoxymexrenone and other compounds of formula (I), where -AA- represents a group -CHR 4 -CHR 5 -or -CR 4 = CR 5- . R 3 , R 4 and R 5 are independently selected from the group consisting of hydrogen, halo, hydroxy, lower alkyl, lower alkoxy, hydroxyalkyl, alkoxyalkyl, hydroxycarbonyl, cyano, aryloxy, R 1 represents an α-oriented lower alkoxycarbonyl or hydroxycarbonyl radical, -BB- represents a group -CHR 6 -CHR 7 -or an α- or β-alignment group of formula III, and R 6 and R 7 Is independently selected from the group consisting of hydrogen, halo, lower alkoxy, acyl, hydroxyalkyl, alkoxyalkyl, hydroxycarbonyl, alkyl, alkoxycarbonyl, acyloxyalkyl, cyano, aryloxy, R 8 and R 9 is hydrogen, halo, lower alkoxy, acyl, hydroxyalkyl, alkoxyal Independently selected from the group consisting of chel, hydroxycarbonyl, alkyl, alkoxycarbonyl, acyloxyalkyl, cyano, aryloxy, or R 8 and R 9 together form a carbocyclic or heterocyclic ring structure, or R 8 or R 9 together with R 6 or R 7 form a carbocyclic or heterocyclic ring structure condensed into a 5-ring D ring.
priorityDate 1995-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID796328
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID5547
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID36822
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID4837
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID43767
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393625
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID1766
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID2587408
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID447798631
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID101105
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2735122
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID46936193
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414326734
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419490720
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID1873719
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID454397067
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419523364
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11595250
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419592827
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID1911

Total number of triples: 314.