Cinchona-Diaminomethylenemalononitrile Organocatalyst for the Highly Enantioselective Hydrophosphonylation of Ketones and Enones

Org Lett. 2018 Sep 21;20(18):5569-5572. doi: 10.1021/acs.orglett.8b02241. Epub 2018 Sep 10.

Abstract

The use of diaminomethylenemalononitrile (DMM) organocatalyst to promote the challenging 1,2-hydrophosphonylation of simple ketones and enones, which are also called α,β-unsaturated ketones, is proposed and validated. This reaction provided the corresponding chiral α-hydroxy phosphonates in high to excellent yields and with enantioselectivity up to 96% ee.

Publication types

  • Research Support, Non-U.S. Gov't