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dc.contributor.authorVijay Nair, G-
dc.contributor.authorSreekumar, V-
dc.contributor.authorBineesh, P B-
dc.contributor.authorVimal Varghese-
dc.contributor.authorPaul, R R-
dc.contributor.authorSuresh, E-
dc.date.accessioned2014-05-22T10:13:54Z-
dc.date.available2014-05-22T10:13:54Z-
dc.date.issued2010-
dc.identifier.citationOrganic & Biomolecular Chemistry 8(21):4861-4866;24 Aug 2010en_US
dc.identifier.issn1477-0520-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1439-
dc.description.abstractHomoenolates generated from alpha,beta-unsaturated aldehydes using NHC catalysis underwent facile addition to dibenzylidene cyclohexanone to afford bicyclic cyclopentenes as single diastereomers.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectN-heterocyclic carbenesen_US
dc.subjectGamma-butyrolactonesen_US
dc.subjectMulticomponent reactionsen_US
dc.subjectStereoselective-synthesisen_US
dc.subjectStetter reactionen_US
dc.subjectConjugate umpolungen_US
dc.subjectAldehydesen_US
dc.subjectHomoenolateen_US
dc.subjectchalconesen_US
dc.titleNHC-catalysed annulation of enals to tethered dienones: efficient synthesis of bicyclic dienesen_US
dc.typeArticleen_US
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