Chemistry Letters, Vol.39, No.4, 379-381, 2010
Enantioselective Michael Reaction of Malonates and alpha,beta-Unsaturated Aldehydes Using a trans-4-Hydroxyproline Derived Organocatalyst
Asymmetric Michael addition of malonates to various alpha,beta-unsaturated aldehydes using an organocatalyst derived from trans-4-hydroxyproline in MeOH proceeds smoothly to afford the corresponding Michael adducts in high yields with high to excellent enantioselectivities.