Panja Subir, Ahsan Salman, Pal Tanay, Kolb Simon, Ali Wajid, Sharma Sulekha, Das Chandan, Grover Jagrit, Dutta Arnab, Werz Daniel B, Paul Amit, Maiti Debabrata
IIT Bombay, Department of Chemistry and IDP, Climate Studies Powai Mumbai 400076 India
Indian Institute of Science Education and Research (IISER) Bhopal, Department of Chemistry Bhopal Madhya Pradesh 462066 India
Chem Sci. 2022 Aug 5;13(32):9432-9439. doi: 10.1039/d2sc03288k. eCollection 2022 Aug 17.
The Fujiwara-Moritani reaction is a powerful tool for the olefination of arenes by Pd-catalysed C-H activation. However, the need for superstoichiometric amounts of toxic chemical oxidants makes the reaction unattractive from an environmental and atom-economical view. Herein, we report the first non-directed and regioselective olefination of simple arenes an electrooxidative Fujiwara-Moritani reaction. The versatility of this operator-friendly approach was demonstrated by a broad substrate scope which includes arenes, heteroarenes and a variety of olefins. Electroanalytical studies suggest the involvement of a Pd(ii)/Pd(iv) catalytic cycle a Pd(iii) intermediate.
藤原-森谷反应是通过钯催化的C-H活化实现芳烃烯基化的有力工具。然而,从环境和原子经济性的角度来看,需要使用超化学计量的有毒化学氧化剂使得该反应缺乏吸引力。在此,我们报道了首例简单芳烃的非导向区域选择性烯基化反应——电氧化藤原-森谷反应。这种操作简便的方法的通用性通过广泛的底物范围得到了证明,该底物范围包括芳烃、杂芳烃和各种烯烃。电分析研究表明涉及Pd(ii)/Pd(iv)催化循环以及一个Pd(iii)中间体。