Single-Isomer Trisubstituted Olefins from a Novel Reaction of (E)-β-Chloro-α-iodo-α,β-unsaturated Esters and Amides
journal contributionposted on 01.08.2008 by Julie Simard-Mercier, Jojo Liu Jiang, Michael L. Ho, Alison B. Flynn, William W. Ogilvie
Any type of content formally published in an academic journal, usually following a peer-review process.
(E)-β-Chloro-α-iodo-α,β-unsaturated esters are converted to single isomer trisubstituted olefins bearing three different carbon substituents by cross-coupling under reflux. Mechanistic investigations suggest that this process transfers a hydrogen from the boronic acid to the α-position of the substrate and then introduces an aryl group to the β-position of the intermediate template while replacing chloride. The reaction is highly stereoselective, showing preference for the E-isomer. The process proceeds through (E)-β-chloro-α-aryl-α,β-unsaturated esters that are transformed efficiently into the corresponding E-products through stereoselective Suzuki-type reactions giving single isomers. The observed stereochemistry is apparently enabled by the intermediacy of a palladium allenoate. The reaction involves a catalytic cycle in which PdII is reduced to Pd0 through the formation of biaryl-coupled products.