Abstract
This study describes the efficacy of P,N-type benzimidazolyl phosphine ligands, which can be easily synthesized from commercially available and inexpensive starting materials. The application of this ligand array in palladium-catalyzed Suzuki-Miyaura coupling reaction of aryl chlorides with potassium aryltrifluoroborates is described. The air stable benzimidazolyl phosphines in combination with a palladium metal precursor provides highly effective catalysts for the Suzuki-Miyaura coupling of unactivated aryl chlorides and can achieve a catalyst loading of only 0.05 mol %.
Original language | English |
---|---|
Pages (from-to) | 3754-3757 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 53 |
Issue number | 29 |
DOIs | |
Publication status | Published - 18 Jul 2012 |
Keywords
- P,N-Type ligand
- Palladium
- Phosphine
- Suzuki coupling
- Trifluoroborate
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry