Enantioselective epoxidation of chalcones and naphthoquinones mediated by (+)-norcamphor-derived hydroperoxide
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摘要
(+)-Norcamphor-derived hydroperoxide has been employed in the asymmetric epoxidation of electron poor alkenes such as trans-chalcones and naphthoquinones. Optimization of the reaction conditions required the employment of n-BuLi/THF at 芒芒芒20芒芒C to achieve ees up to 58%. The epoxide of vitamin K3 has now been obtained with the best up to now reported value of enantioselectivity (51%ee).

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