Mixed S/N and S/P/N ligands from carbohydrates: Synthesis and application in palladium-catalyzed allylic alkylation

Abstract

A modular synthetic approach to bidentate and tridentate imino-thioglycoside ligands is reported. In only 5 steps from the known glucosamine derivative 1, a conveniently functionalized thioglycoside 5 is obtained, which after imination afforded the desired ligands in excellent yields. The tridentate phosphine imine thioglycoside ligand 10 was found to be a highly efficient catalyst precursor for palladium-(0)-catalysed asymmetric alkylation of 1,3-diphenylpropenylacetate ( 8) with dimethyl malonate. The study of a Pd(II) complex shows that there is an efficient stereochemical control of the sulfur configuration upon coordination to the palladium.