Issue 82, 2024

Dual transition metal electrocatalysis enables selective C(sp3)–C(sp3) bond cleavage and arylation of cyclic alcohols

Abstract

We report a dual transition metal electrocatalytic approach for C(sp3)–C(sp3) bond cleavage and arylation of cyclic alcohols, providing an efficient and sustainable method for site-specific arylation of ketones. The reaction involves electrophotochemical cerium-catalysed generation of alkoxyl radicals from readily accessible alcohols. Subsequently, homolytic cleavage of the β-C–C bond leads to the generation of carbon-centered radicals that could be effectively utilized by nickel catalysis powered by cathode reduction to deliver the remote arylated ketone products.

Graphical abstract: Dual transition metal electrocatalysis enables selective C(sp3)–C(sp3) bond cleavage and arylation of cyclic alcohols

Supplementary files

Article information

Article type
Communication
Submitted
08 Aug 2024
Accepted
17 Sep 2024
First published
18 Sep 2024

Chem. Commun., 2024,60, 11714-11717

Dual transition metal electrocatalysis enables selective C(sp3)–C(sp3) bond cleavage and arylation of cyclic alcohols

W. Li, R. Zhang, N. Zhou, J. Lu and N. Fu, Chem. Commun., 2024, 60, 11714 DOI: 10.1039/D4CC04036H

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