Abstract

AbstractThe thermal treatment of CuCl2 with N‐(4′‐vinylbenzyl)cinchonidinium chloride (L1) afforded a monomeric discrete homochiral copper(II) complex N‐4′‐(vinylbenzyl)cinchonidinium trichlorocoprate(II) (1). Their applications to the enantioselectively catalytic alkylation reaction of N‐(diphenylmethylidene)glycine tert‐butyl ester (3) show that the higher ee value observed in catalyst 1 than that in the corresponding free ligand L1 is probably due to the rigidity enhancement after the coordination of N atom of quinoline ring to the copper ion.

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