Issue 36, 2023

Transition-metal-free C–S bond cleavage and transformation of organosulfur compounds

Abstract

The activation and transformation of organic chemical bonds is a fundamental scientific problem. In the past several decades, C–S bond cleavage for the construction of C–C and C–heteroatom bonds has received tremendous attention in organic chemistry. Although significant progress has been made in the field of transition metal strategies, a variety of novel transition-metal-free strategies have also been developed using halogenated reagents, oxidants, acids, and bases. Moreover, organic photochemical and electrochemical methods have also been developed to achieve transition-metal-free C–S bond cleavage of organosulfur compounds. To date, however, no comprehensive review of transition-metal-free strategies has been reported. Therefore, we herein provide a comprehensive review of the major advances in the field of the transition-metal-free C–S bond cleavage and transformation of organosulfur compounds, including thioethers, sulfoxides, sulfones, thioacetals, sulfonium salts, and sulfur ylides.

Graphical abstract: Transition-metal-free C–S bond cleavage and transformation of organosulfur compounds

Article information

Article type
Feature Article
Submitted
27 Jan 2023
Accepted
06 Apr 2023
First published
06 Apr 2023

Chem. Commun., 2023,59, 5343-5364

Transition-metal-free C–S bond cleavage and transformation of organosulfur compounds

K. Yang, Q. Li, Z. Li and X. Sun, Chem. Commun., 2023, 59, 5343 DOI: 10.1039/D3CC00377A

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