Abstract
An efficient nickel-catalyzed method devoted to the direct formation of functionalized 2-arylpyridines is described avoiding the prior preparation of organometallic species. Various functionalized 2-arylpyridines are obtained in moderate to excellent yields by a one-step chemical procedure from corresponding halides. The NiBr2(2,2′-bipyridine) complex appears to be an extremely suitable catalyst for the activation in the presence of manganese dust of aromatic halides and pyridyl halides functionalized by reactive groups. The versatility of this original process represents a simple alternative to most known methods using organometallic reagents.
| Original language | English |
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| Pages (from-to) | 6141-6146 |
| Number of pages | 6 |
| Journal | Tetrahedron |
| Volume | 65 |
| Issue number | 31 |
| DOIs | |
| Publication status | Published - 1 Aug 2009 |
| Externally published | Yes |