http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2009322622-B2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D221-28
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D221-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D489-02
filingDate 2009-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9e635b11e5cb5a0ba7cb3beef437e54c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_620ef3444da038377b087ed2413b8548
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publicationDate 2015-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AU-2009322622-B2
titleOfInvention Process for preparing hydrocodone using a super acid
abstract The present disclosure generally relates to a process for converting a fused, tricyclic compound to a fused, tetracyclic compound that includes a furan ring therein. More particularly, the present disclosure related to a process for preparing a hydrocodone compound, or a compound structurally related thereto, and in particular (+)-hydrocodone, by subjecting a structurally corresponding sinomeπine starting compound to a super acid-assisted furan ring closure reaction. Formula I, II. Examples of super acids useful in the processes described herein include, but are not limited to, trifluoromethanesulfonic acid (CF
priorityDate 2008-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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