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dc.contributor.authorSanthini, P V-
dc.contributor.authorNimisha, G-
dc.contributor.authorJubi John-
dc.contributor.authorSuresh, E-
dc.contributor.authorLuxmi Varma, R-
dc.contributor.authorRadhakrishnan, K V-
dc.date.accessioned2018-07-24T06:02:24Z-
dc.date.available2018-07-24T06:02:24Z-
dc.date.issued2017-02-07-
dc.identifier.citationChemical Communications, 53(11):1848-1851 en_US
dc.identifier.urihttp://10.10.100.66:8080/xmlui/handle/123456789/3199-
dc.description.abstractAn efficient stereoselective route for the synthesis of cyclopentene fused 2-pyrrolines has been established via a Pd-catalyzed C–H activation/oxidative coupling of aryl enamides with diazabicyclic olefins. The proposed two-stage mechanismwas successfully proven by isolating the intermediate trans-disubstituted cyclopentene.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.titlePd-Catalyzed Oxidative Annulation of Enamides with Diazabicyclic Olefins: Rapid Access to Cyclopentene Fused 2-Pyrrolinesen_US
dc.typeArticleen_US
Appears in Collections:2017

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