Organocatalytic regioselective Michael additions of cyclic enones via asymmetric phase transfer catalysis

Org Biomol Chem. 2006 Dec 7;4(23):4281-4. doi: 10.1039/b612606e. Epub 2006 Oct 30.

Abstract

Cyclohexanone and cycloheptanone can be enantioselectively functionalized in the 3-position with up to 92% ee and 87% ee, respectively, by the base-promoted dimerization of the corresponding enones using 3,4,5-tribenzyloxybenzyl cinchoninium bromide, as a new effective catalyst.