首页> 外文期刊>The Journal of Organic Chemistry >Regio- and stereospecific synthesis of beta-sulfonamidodisulfides and beta-sulfonamidosulfides from aziridines using tetrathiomolybdate as a sulfur transfer reagent
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Regio- and stereospecific synthesis of beta-sulfonamidodisulfides and beta-sulfonamidosulfides from aziridines using tetrathiomolybdate as a sulfur transfer reagent

机译:使用四硫代钼酸盐作为硫转移试剂,从氮丙啶区域和立体定向合成β-磺酰胺基二硫化物和β-磺酰胺基硫化物

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摘要

A comprehensive study of a general and effective one-step procedure for the synthesis of beta-sulfonamidodisulfides directly from N-tosyl aziridines in a regio- and stereospecific manner under neutral conditions without the use of any Lewis acid or base has been reported. This methodology is extended to the synthesis of an optically pure cyclic seven-membered disulfide 29. Synthesis of a variety of beta-sulfonamidosulfides involving tandem, multistep reactions in one pot is also reported.
机译:已经报道了在中性条件下不使用任何路易斯酸或碱的情况下,以区域和立体特异性方式直接由N-甲苯磺酰基氮丙啶直接合成β-磺酰胺基二硫化物的一般有效步骤的综合研究。该方法扩展到光学纯的环状七元二硫键29的合成。还报道了在一个反应​​釜中进行串联,多步反应的多种β-磺酰胺基硫化物的合成。

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