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 Sept. 2024
First published
18 Sept. 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

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