Sulfonamide synthesis through electrochemical oxidative coupling of amines and thiols

Gabriele Laudadio, E. Barmpoutsis, Christiane Schotten, L.M. Struik, Sebastian M. Govaerts, Duncan Browne, Timothy Noël (Corresponding author)

Onderzoeksoutput: Bijdrage aan tijdschriftTijdschriftartikelAcademicpeer review

34 Citaten (Scopus)
68 Downloads (Pure)


Sulfonamides are key motifs in pharmaceuticals and agrochemicals, spurring the continuous development of novel and efficient synthetic methods to access these functional groups. Herein, we report an environmentally benign electrochemical method which enables the oxidative coupling between thiols and amines, two readily available and inexpensive commodity chemicals. The transformation is completely driven by electricity, does not require any sacrificial reagent or additional catalysts and can be carried out in only 5 min. Hydrogen is formed as a benign byproduct at the counter electrode. Owing to the mild reaction conditions, the reaction displays a broad substrate scope and functional group compatibility.

Originele taal-2Engels
Pagina's (van-tot)5664–5668
Aantal pagina's5
TijdschriftJournal of the American Chemical Society
Nummer van het tijdschrift14
StatusGepubliceerd - 25 mrt 2019

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