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dc.contributor.authorNandi, G C-
dc.contributor.authorKota, S R-
dc.contributor.authorWakchaure, P B-
dc.contributor.authorChinthakindi, P K-
dc.contributor.authorGovender, T-
dc.contributor.authorKruger, H G-
dc.contributor.authorNaicker, T-
dc.contributor.authorArvidsson, P I-
dc.date.accessioned2016-07-14T10:03:30Z-
dc.date.available2016-07-14T10:03:30Z-
dc.date.issued2015-
dc.identifier.citationRSC Advances 5(76):62084-62090; 2015en_US
dc.identifier.urihttp://hdl.handle.net/123456789/2353-
dc.description.abstractN0-Vinyl sulfonimidamides have been synthesized through a Pd-catalyzed C–N cross coupling between the N0-(imine nitrogen) of N0-deprotected sulfonimidamides and vinyl bromides. The hitherto unreported products were obtained in moderate to excellent yield, and the C–C double bond geometry of the vinylic substrates were retained during the course of reaction. Single crystal X-ray crystallographic analysis confirmed the product structure. Furthermore, we demonstrate that the formed N0-vinyl sulfonimidamides could undergo hydrogenation with Pd–C/H2 to provide N0-alkyl sulfonimidamidesen_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.titlePd-catalyzed C-N coupling of vinylbromides and sulfonimidamides: A facile synthesis of N-vinylsulfonimidamidesen_US
dc.typeArticleen_US
Appears in Collections:2015

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