Pd-Catalyzed Stereoselective 1,2-Aryboration of Alkenylarenes

Org Lett. 2019 Oct 4;21(19):8106-8109. doi: 10.1021/acs.orglett.9b03114. Epub 2019 Sep 13.

Abstract

The palladium-catalyzed highly regio- and diastereoselective arylboration of alkenylarenes has been developed. This chemistry afforded the benzylic boronic esters with a broad substrate scope, which are valuable synthetic intermediates for organic synthesis. The chiral anion phase-transfer strategy was designed for this transformation to realize the regio-, diastereo-, and enantioselective control of this reaction simultaneously.