Issue 3, 2022

Cu-catalyzed [2 + 2 + 1] cascade annulation of vinyl iodonium salts with elemental sulfur/selenium for the modular synthesis of thiophenes and selenophenes

Abstract

A [2 + 2 + 1] annulation protocol has been established for the modular synthesis of 2,4-disubstituted thiophenes/selenophenes, with excellent regioselectivity. The reactions have been catalyzed by copper salt with elemental sulfur and selenium serving as the chalcogen source. The mechanistic study has revealed that this process was initiated by a trisulfur radical anion using EPR.

Graphical abstract: Cu-catalyzed [2 + 2 + 1] cascade annulation of vinyl iodonium salts with elemental sulfur/selenium for the modular synthesis of thiophenes and selenophenes

Supplementary files

Article information

Article type
Communication
Submitted
16 Nov 2021
Accepted
07 Dec 2021
First published
08 Dec 2021

New J. Chem., 2022,46, 945-949

Cu-catalyzed [2 + 2 + 1] cascade annulation of vinyl iodonium salts with elemental sulfur/selenium for the modular synthesis of thiophenes and selenophenes

Y. Wu, C. Wu, F. Wang and C. Chen, New J. Chem., 2022, 46, 945 DOI: 10.1039/D1NJ05433C

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