Electrochemical Oxidative Carbonylation of NH-Sulfoximines
Mingzhe Li1, Mengyu Peng1, Wenxiu Huang1
1Guangxi Key Laboratory of Electrochemical and Magnetochemical Function Materials, College of Chemistry and Bio-engineering, Guilin University of Technology, 12 Jiangan Road, Guilin 541004, China.
Abstract:
The electrochemical synthesis of N-aroylsulfoximines features the use of tetra-n-butylammonium iodide (TBAI) as the medium and a broad substrate scope, thus affording a wide range of N-aroylated sulfoximines in moderate to good yields. The advantages of this electrochemical strategy are augmented by mild reaction conditions that are external oxidant-free, ligand-free, and easy to scale up to gram scale. Both the control experiments and the mechanistic studies revealed that the whole electrochemical process proceeded through a palladium (II/IV/II) catalytic cycle.
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