Issue 20, 2021, Issue in Progress

Ligand-free copper-catalyzed C(sp3)–H imidation of aromatic and aliphatic methyl sulfides with N-fluorobenzenesulfonimide

Abstract

A novel and efficient process has been developed for copper-catalyzed C(sp3)–H direct imidation of methyl sulfides with N-fluorobenzenesulfonimide(NFSI). Without using any ligands, various methyl sulfides including aromatic and aliphatic methyl sulfides, can be transformed to the corresponding N-((phenylthio)methyl)-benzenesulfonamide derivatives in good to excellent yields.

Graphical abstract: Ligand-free copper-catalyzed C(sp3)–H imidation of aromatic and aliphatic methyl sulfides with N-fluorobenzenesulfonimide

Supplementary files

Article information

Article type
Paper
Submitted
26 Jan 2021
Accepted
20 Mar 2021
First published
25 Mar 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 12136-12140

Ligand-free copper-catalyzed C(sp3)–H imidation of aromatic and aliphatic methyl sulfides with N-fluorobenzenesulfonimide

S. Wang, M. Feng, Y. Ji, W. Han, C. Ke, Q. Zhang and X. Zhang, RSC Adv., 2021, 11, 12136 DOI: 10.1039/D1RA00686J

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