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Paired Electrolysis Enabled Ni-Catalyzed Unconventional Cascade Reductive Thiolation Using Sulfinates

Jun‐Chen Kang, Zi-Hao Li, Chao Chen, Li-Kun Dong, Shu‐Yu Zhang

2021The Journal of Organic Chemistry26 citationsDOI

Abstract

Herein, we have reported a nickel-catalyzed cascade reductive thiolation of aryl halides with sulfinates driven by paired electrolysis. This protocol uses sulfinates as the sulfur source, and various thioethers could be synthesized under mild conditions. By mechanism exploration, we find that a cascade chemical step is allowed on the electrode interface and could alter the reaction pathway in paired electrolysis, whose findings could help the discovery of novel cascade reactions with unique reactivity.

Topics & Concepts

ChemistryCascadeElectrolysisCatalysisCombinatorial chemistryReactivity (psychology)ArylHalideCascade reactionNickelInorganic chemistryElectrodeOrganic chemistryPhysical chemistryMedicineChromatographyElectrolyteAlkylPathologyAlternative medicineSulfur-Based Synthesis TechniquesRadical Photochemical ReactionsCaching and Content Delivery
Paired Electrolysis Enabled Ni-Catalyzed Unconventional Cascade Reductive Thiolation Using Sulfinates | Litcius