Regio- and Enantioselective Baeyer鈥揤illiger Oxidation: Kinetic Resolution of Racemic 2-Substituted Cyclopentanones
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文摘
A kinetic resolution of racemic 2-substituted cyclopentanones via highly regio- and enantioselective Baeyer鈥揤illiger oxidation has been successfully developed. The reaction could afford the normal 6-substituted 未-lactones in up to 98% ee and >19/1 regioselectivity. Meanwhile, the unreacted ketones were recovered in excellent ee values (up to 98%). It represents the best results of the kinetic resolution of racemic 2-substituted cyclopentanones via nonenzymic asymmetric BV oxidation.

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