| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5266846 | Tetrahedron Letters | 2011 | 5 Pages |
Abstract
Recent advances in the development of the copper facilitated Suzuki-Miyaura reaction are described. Improvements include expansion of substrate scope to include aryl chlorides and polyhalo aryl boronates. It was found that use of S-Phos and X-Phos could accomplish the coupling of 2-pyridyl boronates to aryl chlorides and bromides in shorter reaction times and in higher yield than previously described with DPPF.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Brendan M. Crowley, Craig M. Potteiger, James Z. Deng, Christopher K. Prier, Daniel V. Paone, Christopher S. Burgey,