首页> 外文期刊>The Journal of Organic Chemistry >Molecular Iodine-Mediated Difunctionalization of Alkenes with Nitriles and Thiols Leading to beta-Acetamido Sulfides
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Molecular Iodine-Mediated Difunctionalization of Alkenes with Nitriles and Thiols Leading to beta-Acetamido Sulfides

机译:分子碘介导的含腈和硫醇的烯烃双官能化反应,导致β-乙酰胺基硫化物

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摘要

A direct difunctionalization protocol of alkenes with nitriles and thiols toward beta-acetamido sulfide derivatives has been proposed under metal-free synthesis conditions. The present protocol provides the facile and highly efficient synthesis of various beta-acetamido sulfides in a scaled-up manner with good to excellent yields simply using inexpensive molecular iodine as a catalyst, DMSO as a mild oxidant, and readily available thiols as thiolating reagents.
机译:在无金属的合成条件下,已经提出了烯烃与腈和硫醇对β-乙酰氨基硫化物衍生物的直接双官能化方案。本方案仅使用廉价的分子碘作为催化剂,使用DMSO作为温和的氧化剂,使用容易获得的硫醇作为硫醇化试剂,即可按规模扩大的方式轻松高效地合成各种β-乙酰氨基硫化物,并具有良好至优异的收率。

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