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dc.contributor.authorShanmugam, P-
dc.contributor.authorVaithyanathan, V-
dc.contributor.authorBaby Viswambharan-
dc.date.accessioned2014-08-09T04:33:16Z-
dc.date.available2014-08-09T04:33:16Z-
dc.date.issued2006-
dc.identifier.citationTetrahedron Letters 47(38):6851-6855;18 Sep 2006en_US
dc.identifier.issn0040-4039-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1612-
dc.description.abstractA facile method for activation of the NC-H bond of N-methylisatin and Baylis-Hillman adducts of N-methylisatin with cerium ammonium nitrate (CAN) and saturated and unsaturated alcohols is reported. Adducts bearing an ester group at the activated alkene afford functionalized ethers, while those with a nitrile afforded ethers and nitrated aromatic products in good yield.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectBaylis Hillman adducten_US
dc.subjectCH-activationen_US
dc.subjectIsatinen_US
dc.subjectFunctionalized ethersen_US
dc.subjectCerium(iv) ammonium-nitrateen_US
dc.subjectVinyl radical cyclizationen_US
dc.subjectStereoselective synthesisen_US
dc.subjectIsomerizationen_US
dc.subjectHydroxylationen_US
dc.titleActivation of the NC-H bond of Baylis-Hillman adducts of N-methylisatin with CAN/ROHen_US
dc.typeArticleen_US
Appears in Collections:2006

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