Copper-catalyzed aminooxygenation of styrenes with N-fluorobenzenesulfonimide and N-hydroxyphthalimide derivatives

Beilstein Journal of Organic Chemistry
Yan LiQian Zhang

Abstract

A copper-catalyzed aminooxygenation reaction of styrenes with N-fluorobenzenesulfonimide and N-hydroxyphthalimide derivatives has been developed. The aminooxygenation product could be converted into the corresponding alcohol or free amine through the cleavage of the N-O or C-N bond of the N-hydroxyphthalimide moiety.

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Citations

Apr 27, 2016·Journal of the American Chemical Society·Brett N HemricQiu Wang
Jul 7, 2017·Organic Letters·Jiaqiong SunQian Zhang
Apr 19, 2018·Organic & Biomolecular Chemistry·Bowen LeiZiyuan Li
Apr 11, 2018·Chemistry : a European Journal·Weilin WangJing Li
Aug 3, 2016·Chemical Communications : Chem Comm·Shichao RenTeck-Peng Loh
Sep 12, 2018·Beilstein Journal of Organic Chemistry·Igor B KrylovAlexander O Terent'ev
Sep 11, 2020·Organic & Biomolecular Chemistry· SushmitaAkhilesh K Verma
Jan 18, 2018·Angewandte Chemie·Hong-Cheng ShenLiu-Zhu Gong
Oct 23, 2020·Organic & Biomolecular Chemistry·José María Muñoz-MolinaPedro J Pérez
Dec 17, 2016·The Journal of Organic Chemistry·Xiao-Feng XiaYong-Min Liang

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Methods Mentioned

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