Late-Stage Heteroarylation of Hetero(aryl)sulfonium Salts Activated by α-Amino Alkyl Radicals

91Citations
Citations of this article
56Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

We report a late-stage heteroarylation of aryl sulfonium salts through activation with α-amino alkyl radicals in a mechanistically distinct approach from previously reported halogen-atom transfer (XAT). The new mode of activation of aryl sulfonium salts proceeds in the absence of light and photoredox catalysts, engaging a wide range of hetarenes. Furthermore, we demonstrate the applicability of this methodology in synthetically useful cross-coupling transformations.

Cite

CITATION STYLE

APA

Alvarez, E. M., Karl, T., Berger, F., Torkowski, L., & Ritter, T. (2021). Late-Stage Heteroarylation of Hetero(aryl)sulfonium Salts Activated by α-Amino Alkyl Radicals. Angewandte Chemie - International Edition, 60(24), 13609–13613. https://doi.org/10.1002/anie.202103085

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free