| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5279945 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
The selective alkylation of functionalized 2-(1H-imidazol-1-yl)pyridines 1 furnishes 3-methyl-1-pyridinyl-1H-imidazolium salts 2, which can be deprotonated to deliver strongly electron-donating bidentate N-heterocyclic carbene ligands (NHC). The synthesis of these ligands and their application in the iridium-catalyzed C-H activated borylation of arenes with its current scope and limitations are reported.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Martin Peters, Rolf Breinbauer,
