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Organocatalytic Stereoselective Epoxidation of Trisubstituted Acrylonitriles

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NIAID Data Ecosystem2026-03-06 收录
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https://figshare.com/articles/dataset/Organocatalytic_Stereoselective_Epoxidation_of_Trisubstituted_Acrylonitriles/2697181
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The first diastereospecific and enantioselective epoxidation of trans-2-aroyl-3-arylacrylonitriles by means of the commercially available diaryl l-prolinol/tert-butyl hydroperoxide system has been developed. These diversely functionalized epoxides were obtained in excellent yield (up to 99%), complete diastereoselectivity for the trans-isomer, and good enantioselectivity (up to 84% ee). Highly enantioenriched epoxides can be easily obtained after a single crystallization (ee > 90%).
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2011-01-21
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