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1,2-Carbonyl migration along the allylic framework: Synthesis of alkenylnaphthoquinones

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dc.contributor.authorChulabhorn Mahidolen_US
dc.contributor.authorYongyut Pinyopronpaniten_US
dc.contributor.authorShuleewan Radviroongiten_US
dc.contributor.authorChachanat Thebtaranonthen_US
dc.contributor.authorYodhathai Thebtaranonthen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-06-14T09:06:26Z
dc.date.available2018-06-14T09:06:26Z
dc.date.issued1988-01-01en_US
dc.description.abstractInstead of undergoing a cyclopentenone annulation, the allylmalonate anion derived from the dicarboxylate (7) rearranges to vinylsuccinate (5), an application of which has led to a convenient synthesis of vinylnaphthoquinones (10).en_US
dc.identifier.citationJournal of the Chemical Society, Chemical Communications. No.20 (1988), 1382-1383en_US
dc.identifier.doi10.1039/C39880001382en_US
dc.identifier.issn00224936en_US
dc.identifier.other2-s2.0-37049077339en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/15496
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=37049077339&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.title1,2-Carbonyl migration along the allylic framework: Synthesis of alkenylnaphthoquinonesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=37049077339&origin=inward

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