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oaioai:figshare.com:article/2856868

A Diacetate Ketone-Catalyzed Asymmetric Epoxidation of Olefins

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Publication date
26 February 2016
Publisher
Doi

    Abstract

    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 α,β-unsaturated esters as well as certain cis olefins

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    The Francis Crick Institute

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    Last time updated on 16/03/2018

    This paper was published in The Francis Crick Institute.

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    Licence: CC BY-NC 4.0