化学
芳基
硫酚
六氟丙烯
二聚体
烷基
硫化物
产量(工程)
偶联反应
组合化学
有机化学
计算化学
催化作用
聚合物
四氟乙烯
材料科学
冶金
共聚物
作者
Yu An,Jijun Zeng,X. Charlene Tang,Bo Zhao,Sheng Han,Zhiqiang Yang,Weidong Zhang,Jian Lü
标识
DOI:10.1002/ejoc.202301150
摘要
Abstract Efficient approaches to perfluoroalkyl/alkenyl aryl sulfides were accomplished by a C−S coupling reaction under mild conditions. Hexafluoropropylene dimer was employed as a versatile building block for the perfluoroalkylation and perfluoroalkenylation of thiophenol. The application of the synthetic strategy was demonstrated by the high‐yield transformation of a broad range of aryl derivatives. A plausible mechanistic explanation was proposed to elaborate the differences between the two reaction pathways. The methodology provides straightforward and convenient access to aryl sulfides constituting C 6 perfluoroalkyl and perfluoroalkenyl substituents.
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