Enantioselective Epoxidation of Alkenes Catalyzed by 2-Fluoro-<i>N</i>-Carbethoxytropinone and Related Tropinone Derivatives

Several α-substituted N-carbethoxytropinones have been evaluated as catalysts for asymmetric epoxidation of alkenes with Oxone, via a dioxirane intermediate. α-Fluoro-N-carbethoxytropinone (2) has been studied in detail and is an efficient catalyst which does not suffer from Baeyer−Villiger decomposition and can be used in relatively low loadings. This ketone was prepared in enantiomerically pure form using chiral base desymmetrization of N-carbethoxytropinone. Asymmetric epoxidation catalyzed by 2 affords epoxides with up to 83% ee. Among other derivatives tested, the α-acetoxy derivative 7 affords the highest enantioselectivities.