文摘
This study describes the application of indolylphosphine ligands with a diphenylphosphino moiety to the palladium-catalyzed borylation of aryl chlorides. The combination of palladium metal precursor with PPh2-Andole-phos, which comprises an inexpensive 鈭扨Ph2 group, provides highly effective catalysts for the borylation of aryl chlorides. A range of functional groups such as 鈭扖N, 鈭扤O2, 鈭扖HO, 鈭扖OMe, 鈭扖OOMe, and 鈭扖F3 was compatible, and the catalyst loading down to 0.025 mol % of Pd can be achieved. The Pd/PPh2-Andole-phos system is able to catalyze both borylation reaction and Suzuki鈥揗iyaura coupling reaction in a one-pot sequential manner for the direct synthesis of biaryl compounds in excellent yields.