Chiral β-Iodoamines by Urea-Catalyzed Iodocyclization of Trichloroacetimidates

Chem Sci J. 2013 May 1;4(5):10.1039/C3SC50410G. doi: 10.1039/C3SC50410G.

Abstract

Highly enantioselective vicinal iodoamination of olefins is accomplished through the iodocyclization of alkenyl trichloroacetimidates catalyzed by a new chiral Schiff-base urea derivative. The resulting products are converted readily to a variety of polyfunctional amine-containing chiral building blocks.