Zhao Yuan, Voloshkin Vladislav A, Martynova Ekaterina A, Maity Bholanath, Cavallo Luigi, Nolan Steven P
Department of Chemistry and Centre for Sustainable Chemistry Ghent University, Krijgslaan 281, S-3, 9000 Ghent, Belgium.
KAUST Catalysis Center (KCC) King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia.
Chem Commun (Camb). 2024 Mar 14;60(23):3174-3177. doi: 10.1039/d4cc00379a.
Photocatalysis involving energy transfer (EnT) has become a valuable technique for building intricate organic frameworks mostly through [2+2]-cycloaddition reactions. Herein, we report a synthetic method leading to functionalized cyclohepta[]indoles, an important structural motif in natural products and pharmaceuticals, using gold-mediated energy transfer photocatalysis. The scope of this operationally simple and atom-economical strategy is presented. Density functional theory studies were employed in order to gain insights into the mechanism of formation of the cyclohepta[]indole core.
涉及能量转移(EnT)的光催化已成为构建复杂有机框架的一项重要技术,主要通过[2+2]环加成反应来实现。在此,我们报道了一种合成方法,该方法利用金介导的能量转移光催化,生成功能化的环庚[ ]吲哚,这是天然产物和药物中一种重要的结构基序。本文展示了这种操作简单且原子经济的策略的适用范围。为了深入了解环庚[ ]吲哚核心的形成机制,我们采用了密度泛函理论研究。