A Chiral Naphthyridine Diimine Ligand Enables Nickel-Catalyzed Asymmetric Alkylidenecyclopropanations

Angew Chem Int Ed Engl. 2020 Sep 14;59(38):16425-16429. doi: 10.1002/anie.202006082. Epub 2020 Jul 10.

Abstract

A novel class of chiral naphthyridine diimine ligands (NDI*) readily accessible from C2 -symmetric 2,6-di-(1-arylethyl)anilines is described. The utility of these ligands, particularly one with fluorinated aryl side arms, is demonstrated by a reductive Ni-catalyzed enantioselective alkylidene transfer reaction from 1,1-dichloroalkenes to olefins. This transformation provides direct access to a broad range of synthetically valuable alkylidenecyclopropanes in high yields and enantioselectivities.

Keywords: alkylidene transfer; asymmetric catalysis; cyclopropanes; naphthyridine diimine (NDI) ligands; nickel.