A metal free, regio and stereoselective syntheses of allylic thioethers using allyl iodides and aryl or alkyl disulfides as coupling partners is described. The densely functionalized allyl iodides having different stereochemistry (E & Z) reacted well with a variety of disulfides in a regio and stereoselective manner providing the resulting allyl aryl thioethers in 62–92% yields.
描述了使用烯丙基
碘和芳基或烷基二
硫化物作为偶联伙伴的无
金属,区域和立体选择性的烯丙基
硫醚的合成。具有不同立体
化学(E&Z)的稠密官能化的烯丙基
碘与多种二
硫化物以区域和立体选择性的方式很好地反应,从而以62-92%的收率得到所得的烯丙基芳基
硫醚。