Modulation of catalyst enantioselectivity through reversible assembly of supramolecular helices

Chem Commun (Camb). 2019 Feb 14;55(15):2162-2165. doi: 10.1039/c8cc09819k.

Abstract

A multi-configurable catalyst, for which the degree of enantioinduction in successive reactions is varied between 6% ee and 52% ee, is achieved by supporting copper centres at the periphery of supramolecular helices. Precise characterization of the co-assemblies corroborates the relation between helix length and catalyst selectivity.