Rhodium catalysed enantioselective synthesis of mono-(halo)-methyl-cyclopropanes

Org Biomol Chem. 2019 Jan 16;17(3):472-476. doi: 10.1039/c8ob03041c.

Abstract

The catalytic asymmetric synthesis of mono-fluoro-, -chloro- and -bromomethyl-1,2-diaryl cyclopropane ester is described. The reaction, using Rh2((S)-BTPCP)4 as a catalyst, allowed the formation of the desired cyclopropanes in good to excellent yields (up to 99%) and excellent diastereoselectivities (up to >20 : 1) and with a high level of enantioselectivities (up to 98% ee). Finally, the synthetic utility of the chiral cyclopropanes was also demonstrated.