NIMBE, CEA, CNRS, Université Paris-Saclay, CEA Saclay, 91191, Gif-sur-Yvette cedex, France.
Angew Chem Int Ed Engl. 2017 May 8;56(20):5616-5619. doi: 10.1002/anie.201702311. Epub 2017 Apr 12.
The conversion of SO into arylsulfones under metal-free conditions was achieved for the first time by reacting SO with (hetero)arylsilanes and alkylhalides in the presence of a fluoride source. The mechanism of this transformation was elucidated based on DFT calculations, which highlight the influence of SO in promoting C-Si bond cleavage.
首次在无金属条件下通过 SO 与(杂)芳基硅烷和卤代烷烃在氟源存在下反应实现了芳基砜的转化。基于 DFT 计算阐明了这种转化的机制,该计算突出了 SO 在促进 C-Si 键断裂方面的影响。