posted on 2002-02-13, 00:00authored byHiroshige Koide, Takeshi Hata, Motokazu Uemura
Axially chiral benzamides and anilides were prepared by enantiotopic lithiation at the distinguished
benzylic methyl of prochiral tricarbonylchromium complexes of N,N-diethyl 2,6-dimethylbenzamide
(1) and N-methyl-N-acyl 2,6-dimethylaniline (14 and 21) with a chiral lithium amide base followed
by electrophilic substitution in good yields with high optical purity. The resulting axially chiral
chromium-complexed benzamides and anilides were oxidized under air to give chromium-free axially
chiral benzamides and anilides in an enantiomerically active form without axial bond rotation at
room temperature.