| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5277786 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
Readily available ferrocenylmethylphosphine was found as an efficient ligand for room temperature Ni(0)-catalyzed Suzuki-Miyaura cross-couplings of aryl arenesulfonates. Ferrocenylmethylphosphine and its polymeric form were also found as useful ligands for Ni(0)-catalyzed Suzuki-Miyaura couplings of deactivated aryl chlorides.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Zhen-Yu Tang, Stephen Spinella, Qiao-Sheng Hu,