http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0201608-A1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C51-377
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C405-0083
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C405-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C401-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-377
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00
filingDate 1985-11-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_500df22f31661f9aa117e582f506d50e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6b7b3efa049e3e52386c4950ed7014df
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7a6e4d21cb2e95b9eaf6302f98329f17
publicationDate 1986-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0201608-A1
titleOfInvention Process for preparing bicyclo ad3.3.0 bdoctenes
abstract A process for preparing bicyclo[3.3.0]octenes represented by general formula (11), wherein R 11 represents H, a mono-equivalent cation or R 1 , R ω , represents R ω' and R 21 represents H or R 2 , from a thiol compound represented by general formula (1), wherein R, represents a C 1-10 alkyl group, a substituted or unsubstituted phenyl group, a substituted or unsubstituted alicyclic group, a substituted or unsubstituted phenyl (C 1-2 ) alkyl group or a tri(C 1-7 hydrocarbyl)silyl group, Ar represents a substituted or unsubstituted aryl group, R ω represents a substituted or unsubstituted C 1-13 alkyl group or a substituted or unsubstituted C 2-13 alkenyl group, and R 2 represents a hydroxy-protecting group. This process enables to obtain isocarbacyclines or synthetic intermediates therefor with industrial advantages.
priorityDate 1984-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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