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Enantioselective Organocatalytic Transfer Hydrogenation Reactions using Hantzsch Esters

Accounts of Chemical ResearchPublished 1 December 2007
Stéphane G. Ouellet, Abbas M. Walji, David W. C. MacMillan
Citations530
SJR quartileQ1
SJR score5.43
SNIP3.22

TL;DR

A number of bioinspired processes for the enantioselective organocatalytic transfer hydrogenation of alpha,beta-unsaturated carbonyl compounds and imines have been discovered and these topics will be the focus of this Account.

Abstract

Within the realm of catalytic asymmetric hydrogenation, the focus continues to be on the use of chiral metal complexes in conjunction with a hydrogen source. Recently, the widespread development of organocatalysis, including the invention of iminium activation, has led to the discovery of many new enantioselective transformations. Based on this strategy, a number of bioinspired processes for the enantioselective organocatalytic transfer hydrogenation of alpha,beta-unsaturated carbonyl compounds and imines have been discovered. These topics will be the focus of this Account.

Keywords

ChemistryBiochemistry, Genetics and Molecular Biology