Copper-catalyzed three-component radical relay alkenylation of sulfenamides

Abstract

Herein, we report a copper-catalyzed three-component radical relay alkenylation of sulfenamides with Togni reagent and alkynes. This strategy provides a general and efficient route for the synthesis of chiral β-trifluoromethyl alkenyl sulfilimines in good yields with good chemo-, regio- and stereoselectivity. The resulting alkenyl sulfilimine products can be readily oxidized to access the corresponding chiral alkenyl sulfoximines. Mechanistic studies and density functional theory (DFT) calculations support a radical pathway and identify a concerted hydrogen-atom transfer (HAT) and radical coupling (RC) process as the key stereodetermining step.

Graphical abstract: Copper-catalyzed three-component radical relay alkenylation of sulfenamides

Supplementary files

Article information

Article type
Communication
Submitted
04 Mar 2026
Accepted
16 Apr 2026
First published
24 Apr 2026

Chem. Commun., 2026, Advance Article

Copper-catalyzed three-component radical relay alkenylation of sulfenamides

R. Wei, J. Zhong, Q. Wang, Y. Wang, H. Yao and A. Lin, Chem. Commun., 2026, Advance Article , DOI: 10.1039/D6CC01311B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements