An efficient palladium-catalyzed enantioselective direct N-alkylation of indoles using a novel type of axially chiral
styrene-phosphine ligand SJTU-PHOS-1 was developed. This
reaction demonstrated good functional group compatibility and a wide
range scope of substrates in mild conditions. Moreover, the DFT calculations
expounded the coordination mode of the metal catalyst and the axially
chiral styrene-phosphine ligand in the enantioselectivity control.