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dc.contributor.authorVijay Nair, G-
dc.contributor.authorBeneesh, P B-
dc.contributor.authorSreekumar, V-
dc.contributor.authorSuresh, E-
dc.date.accessioned2016-01-18T06:53:09Z-
dc.date.available2016-01-18T06:53:09Z-
dc.date.issued2008-
dc.identifier.citationChemical Communications (6):747-749;2008en_US
dc.identifier.issn1359-7345-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/2099-
dc.description.abstractHomoenolates generated from enals by nucleophilic heterocyclic carbene (NHC) catalysis undergo a conjugate addition/cyclization sequence with cyclic dienones, culminating in the efficient synthesis of spirocyclopentanones.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectDiels-alder reactionsen_US
dc.subjectGamma-butyrolactonesen_US
dc.subjectHomoenolate reagentsen_US
dc.subjectAlpha,beta-unsaturated aldehydesen_US
dc.subjectAsymmetric reactionsen_US
dc.subjectNucleophilic carbenesen_US
dc.subjectDirect annulationsen_US
dc.subjectConjugate additionsen_US
dc.subjectDeprotonationen_US
dc.subjectEstersen_US
dc.titleStereoselective synthesis of spirocyclopentanones via N-heterocyclic carbene-catalyzed reactions of enals and dienonesen_US
dc.typeArticleen_US
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