Abstract
In the presence of catalytic amounts of potassium hexamethyldisilazide (KHMDS) and a chiral macrocyclic crown ether, asymmetric 1,4-addition reactions of simple esters with α,β-unsaturated amides proceeded to afford the desired 1,4-adducts in high yields with good stereoselectivities. Mechanistic investigations revealed that proper combination of substrates was a key for the efficient catalytic turnover.
- This article is part of the themed collections: HOT articles in Organic Chemistry Frontiers in 2016 and Celebrating the 75th Birthday of Professor Barry Trost
 
                



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