Department of Chemistry, Colorado State University , Fort Collins, Colorado 80523, United States.
J Am Chem Soc. 2017 Oct 4;139(39):13616-13619. doi: 10.1021/jacs.7b07390. Epub 2017 Sep 19.
Disclosed is a mild, scalable, visible-light-promoted cross-coupling reaction between thiols and aryl halides for the construction of C-S bonds in the absence of both transition metal and photoredox catalysts. The scope of aryl halides and thiol partners includes over 60 examples and therefore provides an entry point into various aryl thioether building blocks of pharmaceutical interest. Furthermore, to demonstrate its utility, this C-S coupling protocol was applied in drug synthesis and late-stage modifications of active pharmaceutical ingredients. UV-vis spectroscopy and time-dependent density functional theory calculations suggest that visible-light-promoted intermolecular charge transfer within the thiolate-aryl halide electron donor-acceptor complex permits the reactivity in the absence of catalyst.
公开了一种在不存在过渡金属和光氧化还原催化剂的情况下,巯基和芳基卤化物之间的温和、可扩展、可见光促进的交叉偶联反应,用于构建 C-S 键。芳基卤化物和硫醇配体的范围包括 60 多个实例,因此为各种具有药物应用价值的芳基硫醚构建块提供了切入点。此外,为了证明其用途,该 C-S 偶联方案已应用于药物合成和活性药物成分的后期修饰。紫外可见光谱和时间依赖密度泛函理论计算表明,可见光促进的硫醇-芳基卤化物电子给体-受体络合物内的分子间电荷转移允许在没有催化剂的情况下进行反应。