Hefei National Laboratory for Physical Sciences at the Microscale, CAS Key Laboratory of Urban Pollutant Conversion, Anhui Province Key Laboratory of Biomass Clean Energy, iChEM, University of Science and Technology of China, Hefei 230026, China.
Chem Commun (Camb). 2020 Feb 25;56(16):2495-2498. doi: 10.1039/c9cc09654j.
Herein, we report the photocatalytic decarboxylative alkenylation reactions of N-(acyloxy)phthalimide derived from α-amino and α-hydroxy acids with 1,1-diarylethene, and with cinnamic acid derivatives through double decarboxylation, using sodium iodide and triphenylphosphine as redox catalysts. The reaction proceeds under mild irradiation conditions with visible blue light (440 nm or 456 nm) in an acetone solvent without recourse to transition-metal or organic dye based photoredox catalysts. The reaction proceeds via photoactivation of a transiently self-assembled chromophore from N-(acyloxy)phthalimide and NaI/PPh3. Solvation plays a crucial role in the reactivity.
在此,我们报告了 N-(酰氧基)邻苯二甲酰亚胺与 1,1-二芳基乙烯和肉桂酸衍生物通过双脱羧反应的光催化脱羧烯基化反应,使用碘化钠和三苯基膦作为氧化还原催化剂。该反应在温和的光照条件下进行,使用可见蓝光(440nm 或 456nm)在丙酮溶剂中进行,无需过渡金属或有机染料基光氧化还原催化剂。该反应通过 N-(酰氧基)邻苯二甲酰亚胺和 NaI/PPh3 形成的瞬态自组装生色团的光活化进行。溶剂化在反应性中起着至关重要的作用。