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dc.contributor.authorVijay Nair, G-
dc.contributor.authorVimal Varghese-
dc.contributor.authorBeneesh, P B-
dc.contributor.authorSinu, C R-
dc.contributor.authorSuresh, E-
dc.date.accessioned2014-01-07T11:32:55Z-
dc.date.available2014-01-07T11:32:55Z-
dc.date.issued2010-
dc.identifier.citationOrganic & Biomolecular Chemistry 8(4):761-764;2010en_US
dc.identifier.issn1477-0520-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1017-
dc.description.abstractHomoenolate generated from alpha,beta-unsaturated aldehydes by NHC catalysis underwent facile addition to conjugated sulfonimines, generated in situ, and subsequent methanolysis to afford protected GABA derivatives stereoselectively and in high yields, thus constituting a novel pseudo four component reaction.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectChalconesen_US
dc.subjectGlutamateen_US
dc.subjectConjugate umpolungen_US
dc.subjectButyrolactonesen_US
dc.subjectAlpha,beta-unsaturated aldehydesen_US
dc.subjectDirect annulationsen_US
dc.subjectCarbene-catalyzed reactionen_US
dc.subjectStereoselective-synthesisen_US
dc.subjectEnalsen_US
dc.titleA novel pseudo four component reaction involving homoenolate for the synthesis of gamma-aminobutyric acid (GABA) derivativesen_US
dc.typeArticleen_US
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