Enantioselective synthesis of 2,2-disubstituted terminal epoxides via catalytic asymmetric corey-chaykovsky epoxidation of ketones

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Abstract

Catalytic asymmetric Corey-Chaykovsky epoxidation of various ketones with dimethyloxosulfonium methylide using a heterobimetallic La-Li3-BINOL complex (LLB) is described. The reaction proceeded smoothly at room temperature in the presence of achiral phosphine oxide additives, and 2,2-disubstituted terminal epoxides were obtained in high enantioselectivity (97%-91% ee) and yield (>99%-88%) from a broad range of methyl ketones with 1-5 mol% catalyst loading. Enantioselectivity was strongly dependent on the steric hindrance, and other ketones, such as ethyl ketones and propyl ketones resulted in slightly lower enantioselectivity (88%-67% ee).

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Sone, T., Yamaguchi, A., Matsunaga, S., & Shibasaki, M. (2012). Enantioselective synthesis of 2,2-disubstituted terminal epoxides via catalytic asymmetric corey-chaykovsky epoxidation of ketones. Molecules, 17(2), 1617–1634. https://doi.org/10.3390/molecules17021617

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