Nucleophilic halo-Michael addition under Lewis-base activation†
Víctor Laina-Martín,Ignacio Pérez,Jose A. Fernández-Salas
Chemical Communications Pub Date : 10/02/2019 00:00:00 , DOI:10.1039/C9CC07068K
Abstract

A simple and general conjugate nucleophilic halogenation is presented. The THTO/halosilane combination has shown the ability to act as a nucleophilic halide source in the conjugate addition to a variety of Michael acceptors. In addition, a straightforward diastereoselective halogen installation using α,β-unsaturated acyloxazolidinones as platforms has been developed.

Graphical abstract: Nucleophilic halo-Michael addition under Lewis-base activation