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dc.contributor.authorShanmugam, P-
dc.contributor.authorVaithyanathan, V-
dc.contributor.authorViswambharan, B-
dc.date.accessioned2016-01-18T07:58:49Z-
dc.date.available2016-01-18T07:58:49Z-
dc.date.issued2006-
dc.identifier.citationTetrahedron 62(18):4342-4348; May 2006en_US
dc.identifier.issn0040-4020-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/2170-
dc.description.abstractA facile, high yield stereoselective synthesis of functionalized diastereomeric 3 -spirocyclopropane-2-indolones (10-17a,b) from the isomerised bromo derivatives of Baylis-Hillman adducts of isatin(2-9a,b) by reductive cyclization with sodium borohydride is reporteden_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectIsatinen_US
dc.subjectSpirocyclopropaneen_US
dc.subjectSodium borohydrideen_US
dc.subject2-indalonesen_US
dc.subjectBaylis Hillman adducten_US
dc.subjectVinyl radical cyclizationen_US
dc.subjectDiels alder reactionen_US
dc.subjectStereoselective synthesisen_US
dc.subjectAssisted isomerizationen_US
dc.subjectAlkenesen_US
dc.titleSynthesis of functionalized 3-spirocyclopropane-2-indolones from isomerised Baylis-Hillman adducts of isatinen_US
dc.typeArticleen_US
Appears in Collections:2006

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