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http://hdl.handle.net/123456789/2642
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DC Field | Value | Language |
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dc.contributor.author | Sankar, Rathinam | - |
dc.contributor.author | Babu, S.A. | - |
dc.date.accessioned | 2020-12-04T05:17:23Z | - |
dc.date.available | 2020-12-04T05:17:23Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | Asian Journal of Organic Chemistry, 6(3) | en_US |
dc.identifier.other | 10.1002/ajoc.201600596 | - |
dc.identifier.uri | https://onlinelibrary.wiley.com/doi/full/10.1002/ajoc.201600596 | - |
dc.identifier.uri | http://hdl.handle.net/123456789/2642 | - |
dc.description.abstract | NiII-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, Weinheim | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | Wiley-VCH Verlag | en_US |
dc.subject | amides | en_US |
dc.subject | cross-coupling reactions | en_US |
dc.subject | picolinamides | en_US |
dc.title | Construction of Tertiary Amides: NiII-Catalyzed N-Arylation of Secondary Acyclic Amides (2-Picolinamides) with Aryl Halides | en_US |
dc.type | Article | en_US |
Appears in Collections: | Research Articles |
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