Xiong Biquan, Si Lulu, Liu Yu, Xu Weifeng, Jiang Tao, Cao Fan, Tang Ke-Wen, Wong Wai-Yeung
Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang, 414006, P. R. China.
Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University Hung Hom, Hong Kong, P. R. China.
Chem Asian J. 2022 May 2;17(9):e202200042. doi: 10.1002/asia.202200042. Epub 2022 Mar 24.
An efficient, cheap and green protocol for the highly regioselective 1,6-hydroarylation of para-quinone methides (p-QMs) with indoles at the C-3 position has been established by phosphoric acid catalysis in water under transition-metal-free reaction conditions. A wide range of indole derivatives and para-quinone methides (p-QMs) are compatible for the reaction, affording the corresponding 1,6-hydroarylation products with good to excellent yields. The possible mechanism of the reaction has been explored through step-by-step control experiments. The protocol is convenient for practical applications, leading to a safe, green and feasible way for the formation of C-3 diarylmethyl functionalized indole derivatives.
通过在无过渡金属反应条件下于水中进行磷酸催化,建立了一种高效、廉价且绿色的方法,用于对苯醌甲基化物(p-QMs)与吲哚在C-3位进行高度区域选择性的1,6-氢芳基化反应。多种吲哚衍生物和对苯醌甲基化物(p-QMs)都适用于该反应,能以良好至优异的产率得到相应的1,6-氢芳基化产物。通过逐步控制实验探索了该反应可能的机理。该方法便于实际应用,为形成C-3二芳基甲基官能化吲哚衍生物提供了一种安全、绿色且可行的途径。