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Trifluoromethylthiolation–arylation of diazocarbonyl compounds by modified Hooz multicomponent coupling

机译:三氟甲基硫醇化-重氮修饰的Hooz多组分偶合使重氮羰基化合物芳基化

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摘要

A new Zn-mediated trifluoromethylthiolation-based bifunctionalization reaction is developed. In this process, simultaneous C–SCF3 and C–C bond formation takes place in a multicomponent reaction, in which an aryl and a SCF3 group arise from different reagents. Our studies show that the reaction mechanism is similar to the Hooz multicomponent coupling. The process involves in situ generation of BAr3, which reacts with a diazocarbonyl compound, and the reaction is terminated by an electrophilic SCF3 transfer. The reaction can also be extended to fluorination based bifunctionalization which proceeds with somewhat lower yield than the analogous trifluoromethylthiolation reaction.
机译:开发了一种新的基于锌的三氟甲基硫醇基双官能化反应。在此过程中,同时发生的C–SCF3和C–C键形成多组分反应,其中芳基和SCF3基团来自不同的试剂。我们的研究表明,反应机理与Hooz多组分偶联相似。该方法涉及原位生成BAr3,其与重氮羰基化合物反应,并通过亲电SCF3转移终止反应。该反应还可以扩展到基于氟化的双官能化,与相似的三氟甲基硫醇化反应相比,该双官能化的产率略低。

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