Two series of new bidentate P-N ligands have been synthesized. Application
of these ligands in the palladium catalysed allylic alkylation of crotyl ch
loride and cinnamyl chloride leads to the preferential formation of the bra
nched product. A larger bite angle of the ligand leads to higher regioselec
tivity. Stoichiometric alkylation of the complex [Pd(C4H7){p-MeOC6H4C=N(CH2
)(4)OPPh2}][O3SCF3] proceeds with 88% regioselectivity to the branched prod
uct.