Issue 20, 2022

C-centered radical-initiated cyclization by directed C(sp3)–H oxidative functionalization

Abstract

The development of C(sp3)–H functionalization has been proved to be challenging and therefore is attracting constant attention. This provides an opportunity to obviate the requirement of a preexisting functional handle with high atom- and step-economy, which are often complementary to traditional methods. The C-centered radical strategy with considerable potential has been established as a powerful toolbox for chemists to construct molecules with comprehensive value from various organic functional groups via oxidation, avoiding the difficulty of removing or converting directing groups and the limitations of utilizing metals or harsh temperature. The selection of an oxidation system requires the cooperation of multiple parameters, which provides great freedom for the application of substrates and the optimization of conditions. Based on our long-term interest in radical oxidative cyclization, herein, we focus on C-centered radical-initiated cyclization strategies by directed C(sp3)–H oxidative functionalization since 2012. The typical routes are intramolecular and intermolecular cyclization, where intermolecular cyclization is further classified according to the type of addition to the unsaturated bonds of alkenes, acrylamides, alkynes, eneynes, isonitriles and C(sp) or C(sp2) bonds in other substrates. These studies not only pave the way to C(sp3)–H oxidative functionalization but also provide insight into the exploration of new reaction modes for radical chemistry.

Graphical abstract: C-centered radical-initiated cyclization by directed C(sp3)–H oxidative functionalization

Article information

Article type
Review Article
Submitted
15 iyl 2022
Accepted
22 avq 2022
First published
23 avq 2022

Org. Chem. Front., 2022,9, 5726-5757

C-centered radical-initiated cyclization by directed C(sp3)–H oxidative functionalization

J. Li, L. Mei, X. Yu, L. Wang, X. Cai, T. Li and W. Wei, Org. Chem. Front., 2022, 9, 5726 DOI: 10.1039/D2QO01128J

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