The absolute configurations of ino)3-(1-hydroxy-1-methylethyl)cyclopen
t-1-en-1-yl phenyl ketone, C23H27NO2, and -(alpha-methylbenzylamino)-1
-phenyl-2-hepten-1-one monohydrate, C24H31NO2. H2O, Obtained by a dire
cted enantioselective aldol condensation, have been ascertained to be
(alpha R, 3S) and (alpha R, 4S, 5S), respectively. While in the first
cyclic delta-hydroxy-beta-enamino ketone the enaminic N atom is hydrog
en bonded to the carbonyl O atom, in the second acyclic compound, the
N atom is hydrogen bonded to the hydroxyl group.