Issue 9, 2019

Chemoselective N-arylation of aminobenzene sulfonamides via copper catalysed Chan–Evans–Lam reactions

Abstract

Cu-Catalysed Chan–Evans–Lam cross-coupling reactions between unprotected aminobenzene sulfonamides and arylboron nucleophiles are explored herein. Chemoselective N-arylation of aminobenzene sulfonamides could be simply enabled by the adjustment of reaction variables, such as the sources of aerobic oxidative Cu catalysis, solvents and bases. The arylation processes could be well regulated to occur on either amino or sulfonamide nitrogen atoms at room temperature under open flask conditions.

Graphical abstract: Chemoselective N-arylation of aminobenzene sulfonamides via copper catalysed Chan–Evans–Lam reactions

Supplementary files

Article information

Article type
Research Article
Submitted
06 Dec 2018
Accepted
16 Jan 2019
First published
17 Jan 2019

Org. Chem. Front., 2019,6, 1356-1360

Chemoselective N-arylation of aminobenzene sulfonamides via copper catalysed Chan–Evans–Lam reactions

W. Zu, S. Liu, X. Jia and L. Xu, Org. Chem. Front., 2019, 6, 1356 DOI: 10.1039/C8QO01313F

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