http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2010072864-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C13-553
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C13-553
filingDate 2009-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a68e8c5a34475a3aee5da30056fb379b
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publicationDate 2010-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2010072864-A1
titleOfInvention Method for preparing synthesis intermediates that can be used in the preparation of taiwaniaquinoids
abstract The invention relates to a method for obtaining taiwaniaquinoids having general formula (13), which can be used as synthesis intermediates in the production of other taiwaniaquinoids and derivatives. The method comprises the condensation between α-cyclocitral or β-cyclocitral and a halogenated derivative having formula (11) in order to obtain a compound having formula (12), which is subsequently cyclized and dehydrated by means of acid treatment to produce the tricyclic structure [6-5-6] of the taiwaniaquinoids.
priorityDate 2008-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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