Issue 33, 2020

Copper catalysed oxidative α-sulfonylation of branched aldehydes using the acid enhanced reactivity of manganese(iv) oxide

Abstract

The oxidative coupling of secondary aldehydes and sulfinate salts is achieved using copper catalysis to form α-sulfonyl aldehydes. The use of an acidic co-solvent is important to adjust the oxidation potential of MnO2 as an oxidant. A broad range of sulfonylated aldehydes is prepared, and their further functionalisation is demonstrated. A dual ionic/radical pathway mechanism is proposed.

Graphical abstract: Copper catalysed oxidative α-sulfonylation of branched aldehydes using the acid enhanced reactivity of manganese(iv) oxide

Supplementary files

Article information

Article type
Communication
Submitted
28 Feb 2020
Accepted
17 Mar 2020
First published
17 Mar 2020
This article is Open Access
Creative Commons BY license

Chem. Commun., 2020,56, 4587-4590

Copper catalysed oxidative α-sulfonylation of branched aldehydes using the acid enhanced reactivity of manganese(IV) oxide

J. I. Higham and J. A. Bull, Chem. Commun., 2020, 56, 4587 DOI: 10.1039/D0CC01576H

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