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电化学合成二苯并噻吩:通过卤素介导的分子内 C-S 环化反应。

Electrochemical Synthesis of Dibenzothiophenes via Intramolecular C-S Cyclization with a Halogen Mediator.

机构信息

Division of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University, 3-1-1 Tsushima-naka, Kita-ku, Okayama 700-8530, Japan.

出版信息

Org Lett. 2022 Nov 25;24(46):8547-8552. doi: 10.1021/acs.orglett.2c03574. Epub 2022 Nov 11.

Abstract

Electrochemical synthesis of dibenzothiophene derivatives was achieved. Several bis(biaryl) disulfides are efficiently converted to dibenzothiophenes by electrochemical oxidation. The use of BuNBr as a halogen mediator was essential, and wide varieties of dibenzothiophene derivatives were obtained in good yields.

摘要

电化学合成二苯并噻吩衍生物。通过电化学氧化,几种双(联芳基)二硫化物被有效地转化为二苯并噻吩。使用 BuNBr 作为卤素介导物是必不可少的,并且可以以良好的收率获得广泛的二苯并噻吩衍生物。

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