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dc.contributor.authorParvatkar, P.T.
dc.contributor.authorParameswaran, P.S.
dc.contributor.authorTilve, S.G.
dc.date.accessioned2008-01-30T13:51:13Z
dc.date.available2008-01-30T13:51:13Z
dc.date.issued2007
dc.identifier.citationTetrahedron letters, Vol.48; 7870-7872p.
dc.identifier.urihttp://drs.nio.org/drs/handle/2264/693
dc.description.abstractA new synthesis of the indoloquinoline alkaloid cryptotackieine, isolated from Cryptolepis sanguinolenta, is described which involves a Perkin reaction, a tandem double reduction-double cyclization reaction followed by regioselective methylation at the quinoline nitrogen.
dc.language.isoen
dc.publisherElsevier
dc.rightsAn edited version of the preprint was published by Elsevier. Copyright [2007] Elsevier
dc.subjectaquatic plants
dc.subjectalkaloids
dc.subjectdrugs
dc.subjectreduction
dc.subjectmolecular structure
dc.subjectCryptolepis sanguinolenta
dc.titleDouble reductive cyclization: A facile synthesis of the indoloquinoline alkaloid cryptotackieine
dc.typeJournal Article


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