Issue 18, 2023

Recent advances in three-component radical acylative difunctionalization of unsaturated carbon–carbon bonds

Abstract

The radical acylated difunctionalization of unsaturated carbon–carbon bonds, which introduces acyl and other groups simultaneously, represents an attractive approach for the synthesis of functionalized ketones or related derivatives from easily accessible feedstocks. A wide range of acylation reagents, including carbazates, α-keto acid, acyl-1,4-dihydropyridines, aldehydes, oxime esters, oxime oxalate, and carboxylic acid derivatives, etc., can be used to incorporate acyl groups into olefins, dienes, alkynes, 1,3-enynes, cyclopropanes, and allenes. This review highlights the recent advances in this topic and focuses on the mechanistic insights of these transformations.

Graphical abstract: Recent advances in three-component radical acylative difunctionalization of unsaturated carbon–carbon bonds

Article information

Article type
Review Article
Submitted
03 Jūl. 2023
Accepted
03 Aug. 2023
First published
08 Aug. 2023

Org. Chem. Front., 2023,10, 4488-4515

Recent advances in three-component radical acylative difunctionalization of unsaturated carbon–carbon bonds

J. Sun, L. Wang, G. Zheng and Q. Zhang, Org. Chem. Front., 2023, 10, 4488 DOI: 10.1039/D3QO01010D

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