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 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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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. |
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ISSN: | 0366-7022 1348-0715 |
DOI: | 10.1246/cl.2006.842 |