Asymmetric Michael addition of formaldehyde N,N-dialkylhydrazones to alkylidene malonates

Chem Commun (Camb). 2002 Mar 7:(5):498-9. doi: 10.1039/b200209b.

Abstract

Enantiopure formaldehyde N,N-dialkylhydrazones 1 smoothly react with prochiral alkylidene malonates 2 in the presence of MgI2 to afford the corresponding Michael adducts 3 in excellent yields and good diastereoselectivities; direct racemization-free BF3.OEt2-catalyzed thiolysis of the hydrazone C=N bond affords the corresponding dithioketals 7 in optically pure or enantiomerically enriched form.