Aluminum tris(2,6-di-tert-butyl-4-methylphenoxide) (ATD) has been succ
essfully utilized as a Lewis acid receptor for effective blocking of c
arbonyl functionality, thereby allowing (1) the conjugate addition of
organolithium reagents to alpha,beta-unsaturated ketones, and (2) sele
ctive reduction of more hindered ketones. The blocking ability of ATD
is evaluated by comparison of the analogous Lewis acid receptors, ATPH
and MAD.