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Solvent-free 1,6-conjugate arylation of para-quinone methides: A greener approach to unsymmetrical triarylmethanes
Journal of Saudi Chemical Society ( IF 5.6 ) Pub Date : 2021-08-02 , DOI: 10.1016/j.jscs.2021.101320
Yu Hu 1 , Min Tang 2 , Jia-Xuan Chen 1 , Shi-Qian Wei 1 , Yi Tian 1 , Liang-Dong Zhang 3 , Zhang-Qin Liu 3
Affiliation  

A highly efficient arylation of para-quinone methides (p-QMs) with N,N-dimethylaniline under solvent free condition has been developed, which proceeded via a para-toluenesulfonic acid (TsOH)-promoted 1,6-conjugated addition pathway. This methodology provided a green and sustainable methodology to construct various novel unsymmetrical triarylmethanes (TAMs) with the advantages of good functional group tolerance, scalability, and regioselectivity.



中文翻译:

对醌甲基化物的无溶剂 1,6-共轭芳基化:一种更环保的不对称三芳基甲烷方法

已开发出在无溶剂条件下对-醌甲基化物 ( p- QMs) 与N,N-二甲基苯胺的高效芳基化反应,该反应通过对-甲苯磺酸 (TsOH) 促进的 1,6-共轭加成途径进行。该方法为构建各种新型不对称三芳基甲烷(TAM)提供了一种绿色和可持续的方法,具有良好的官能团耐受性、可扩展性和区域选择性等优点。

更新日期:2021-08-19
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