Photocatalytic selective disulfuration of aryl aldehydes and alkenyl aldehydes with dithiosulfonate as a bifunctional disulfur reagent and hydrogen atom acceptor†

Jingchao Jiao , Juan Xu , Jingru Li , Hongru He , Runliang Yang , Xiaorui Ren , Qianwen Gao , Xi Wang
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Abstract

We have developed a highly efficient photocatalytic method for the selective disulfuration of aryl aldehydes and alkenyl aldehydes using a bifunctional dithiosulfonate (ArSO2-SSR), enabling the synthesis of a diverse array of benzoyl disulfides and chroman-4-ones with disulfide moieties. Notably, this method facilitates the synthesis of benzoyl disulfides in the aqueous phase, demonstrating a broad substrate scope and excellent tolerance for various functional groups. Furthermore, it allows for gram-scale production in a continuous-flow blue LED photoreactor and facilitates late-stage functionalization of complex molecules, showcasing its practical applicability in synthetic chemistry.

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以二硫代磺酸盐为双功能二硫试剂和氢原子受体的芳基醛和烯基醛的光催化选择性二硫化反应
我们开发了一种高效的光催化方法,使用双功能二硫代磺酸盐(arso2 -SSR)选择性地对芳基醛和烯基醛进行二硫化反应,从而合成了多种苯甲酰二硫化物和具有二硫基团的铬-4-酮。值得注意的是,该方法有利于在水相中合成苯甲酰二硫化物,显示出广泛的底物范围和对各种官能团的良好耐受性。此外,它允许在连续流蓝色LED光反应器中进行克级生产,并促进复杂分子的后期功能化,展示了其在合成化学中的实际适用性。
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