4.7 Article

A Diacetate Ketone-Catalyzed Asymmetric Epoxidation of Olefins

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JOURNAL OF ORGANIC CHEMISTRY
卷 74, 期 10, 页码 3986-3989

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AMER CHEMICAL SOC
DOI: 10.1021/jo900330n

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  1. General Medical Sciences of the National Institutes of Health [GM59705-08]

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A fructose-derived diacetate ketone has been shown to be an effective catalyst for asymmetric epoxidation. High ee values have been obtained for a variety of trans and trisubstituted olefins. including electron-deficient alpha,beta-unsaturated esters as well as certain cis olefins.

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