Abstract
A new electrophilic sulfoximidation of thiols has been developed. Using sodium hydride as a base, the treatment of sulfoximidoyl-containing hypervalent iodine(III) reagents with thiols affords the corresponding N-ulfenylsulfoximines (N-thiosulfoximines) in good to excellent yields. A plausible mechanism is proposed.
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APA
Wang, H., Zhang, D., Cao, M., & Bolm, C. (2018). Electrophilic Sulfoximidations of Thiols by Hypervalent Iodine Reagents. Synthesis (Germany), 51(1), 271–275. https://doi.org/10.1055/s-0037-1610369
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