Catalytic and highly enantioselective selenolactonization

Organic Letters
Wenxue Niu, Ying-Yeung Yeung

Abstract

An enantioselective selenolactonization of olefinic acids has been developed using (DHQD)2PHAL as the catalyst. Structurally simple and commercially available N-phenylselenophthalimide was used as the electrophilic selenium reagent. The corresponding selenolactones could be obtained with up to 96% ee.

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Citations

Jul 23, 2015·Journal of the American Chemical Society·Yusuke SuzukiMasato Kitamura
Apr 12, 2016·Journal of the American Chemical Society·Yu KawamataKeiji Maruoka
Apr 27, 2016·Journal of the American Chemical Society·Brett N HemricQiu Wang
Apr 5, 2018·Organic & Biomolecular Chemistry·Shilong LuoHailong Yan
Mar 7, 2019·Organic & Biomolecular Chemistry·Jonathan BockUlrich Hennecke
Jul 26, 2019·Journal of Physics. Condensed Matter : an Institute of Physics Journal·Zhi Ping Niu

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