Amination of the Ortho C–H Bonds by the Cu(OAc)2-mediated Reaction of 2-Phenylpyridines with Anilines

The reaction of 2-phenylpyridines with anilines in the presence of Cu(OAc)2 as a promoter results in selective mono-amination of the ortho C–H bonds in 2-phenylpyridines to give amine derivatives in high yields per the conversion. This is the rare example of the functionalization of C–H bonds to C–N...

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Veröffentlicht in:Chemistry letters 2006-08, Vol.35 (8), p.842-843
Hauptverfasser: Uemura, Takeshi, Imoto, Shinya, Chatani, Naoto
Format: Artikel
Sprache:eng
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Zusammenfassung:The reaction of 2-phenylpyridines with anilines in the presence of Cu(OAc)2 as a promoter results in selective mono-amination of the ortho C–H bonds in 2-phenylpyridines to give amine derivatives in high yields per the conversion. This is the rare example of the functionalization of C–H bonds to C–N bonds.
ISSN:0366-7022
1348-0715
DOI:10.1246/cl.2006.842