Synthetic and Mechanistic Study of the Catalytic Enantioselective Preparation of Primary β-Amino Ketones from Enones and a Fluorinated Gabriel Reagent

The salen μ-oxo complex of aluminum 1 catalyzes the asymmetric 1,4-addition of the novel ammonia equivalent 3,4,5,6-tetrafluorophthalimide to unsaturated ketones. All of the reagents are inexpensive and are readily available. The products are formed in up to 89% yield and up to 96% ee. The tetrafluorophthalimide group is removed under mild chemoselective conditions and in high yields to afford the free primary amines. Mechanistic studies suggest that the reaction occurs through a dual activation mechanism. A pre-equilibrium formation of a 1:1 complex between tetrafluorophthalimide and the catalyst is observed. The rate-determining step is the addition of tetrafluorophthalimide catalyst complex to the catalyst activated enone. These mechanistic studies provide important clues for the further development of catalytic asymmetric reactions. (Chemical Presented).