Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2642
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dc.contributor.authorSankar, Rathinam-
dc.contributor.authorBabu, S.A.-
dc.date.accessioned2020-12-04T05:17:23Z-
dc.date.available2020-12-04T05:17:23Z-
dc.date.issued2017-
dc.identifier.citationAsian Journal of Organic Chemistry, 6(3)en_US
dc.identifier.other10.1002/ajoc.201600596-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/full/10.1002/ajoc.201600596-
dc.identifier.urihttp://hdl.handle.net/123456789/2642-
dc.description.abstractNiII-catalyzed C−N cross-coupling reaction of secondary acyclic amides (2-picolinamides, which were derived from 2-picolinic acid and amines) and aryl halides for the construction of tertiary amides has been reported. Relatively inexpensive NiCl2 was used as the catalyst for the N-arylation of various 2-picolinamides (secondary acyclic amides), in which the 2-picolinamide unit plausibly served as an internal ligand. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.language.isoen_USen_US
dc.publisherWiley-VCH Verlagen_US
dc.subjectamidesen_US
dc.subjectcross-coupling reactionsen_US
dc.subjectpicolinamidesen_US
dc.titleConstruction of Tertiary Amides: NiII-Catalyzed N-Arylation of Secondary Acyclic Amides (2-Picolinamides) with Aryl Halidesen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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