芳基
化学
卤化物
催化作用
药物化学
联轴节(管道)
卤代芳基
金属
偶联反应
表面改性
高分子化学
金属卤化物
替代(逻辑)
过渡金属
键裂
还原消去
转化(遗传学)
铜
光化学
反应条件
立体化学
衍生工具(金融)
组合化学
作者
Jaime Ponce‐de‐León,Markus D. Schoetz,Amit Dahiya,Susanna L. Kirsten,Kristina Deckers,Steffen Benkhoff,Franziska Schoenebeck
摘要
Aryl germanes have emerged as robust and orthogonal coupling partners, but the chemistry enabling their functionalization is still in its infancy. Herein, we report the first C─S bond formation of aryl germanes. In contrast to conventional C─S cross-couplings of prefunctionalized arenes that largely rely on transition-metal catalysis, this transformation proceeds in the absence of a metal catalyst at room temperature and tolerates air and moisture. The reaction is orthogonal to common coupling handles, including aryl halides and aryl silanes, enabling selective thiolations in multifunctional molecules. Mechanistic studies support a radical-based aromatic substitution pathway.
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