| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278964 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
Polyfluorinated phosphine ligands can be obtained by regioselective nucleophilic aromatic substitution on tetrafluoronaphthalene derivatives. The ligand efficiency has been demonstrated in the room temperature Suzuki coupling reactions of aryl bromides and aryl boronic acids. The described process allows access to a new class of highly versatile fluorinated phosphine ligands.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Shahla Yekta, Lawrence Cheung, Andrei K. Yudin,