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dc.contributor.authorSelvakumar, K-
dc.contributor.authorVaithiyanathan, V-
dc.contributor.authorShanmugam, P-
dc.date.accessioned2014-01-07T09:07:44Z-
dc.date.available2014-01-07T09:07:44Z-
dc.date.issued2010-
dc.identifier.citationChemical Communications 46(16):2826-2828;2010en_US
dc.identifier.issn1359-7345-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1006-
dc.description.abstractThe chemistry phosphorus and sulfur ylides have been exploited for a facile, short and efficient synthesis of 3-spirocyclopentene- and 3-spiropyrazole-2-oxindoles from E- and Z-isomers of bromo derivatives of Morita-Baylis-Hillman adducts of isatin with Ph(3)P/activated alkene/K(2)CO(3) and Me(2)S/DEAD/K(2)CO(3), respectively, via [3 + 2]-annulation strategy.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectDerivativesen_US
dc.subjectAnnulationen_US
dc.subjectMarine-derived fungusen_US
dc.subjectBaylis-hillman reactionen_US
dc.subjectAllylic compoundsen_US
dc.subjectSpirocyclic oxindolesen_US
dc.subjectNatural-productsen_US
dc.subjectSpiro compoundsen_US
dc.subjectRing expansionen_US
dc.subjectCitrinadin-Aen_US
dc.titleAn efficient stereoselective synthesis of 3-spirocyclopentene- and 3-spiropyrazole-2-oxindoles via 1,3-dipolar cycloaddition reactionen_US
dc.typeArticleen_US
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