Fedorov Oleg V, Scherbinina Sofya I, Levin Vitalij V, Dilman Alexander D
N. D. Zelinsky Institute of Organic Chemistry , Leninsky prosp. 47 , 119991 Moscow , Russian Federation.
Higher Chemical College , D. Mendeleev University of Chemical Technology of Russia , Miusskaya sq. 9 , 125047 Moscow , Russian Federation.
J Org Chem. 2019 Sep 6;84(17):11068-11079. doi: 10.1021/acs.joc.9b01649. Epub 2019 Aug 26.
The atom transfer radical addition reaction catalyzed by triphenylphosphine and copper(I) halide is described. The reaction proceeds under irradiation with 365 nm light using a light-emitting diode and was performed in regular glassware. The proposed mechanism involves the formation of quaternary phosphonium salt, which undergoes single electron reduction by copper(I) salt via photo-induced electron transfer. The method works well for terminal alkenes and activated organic halides such as esters of bromo- and iodoacetic acid and bromoacetonitrile. -Difluorinated styrenes, for which atom transfer reactions are rare, also proved to be good substrates for this phosphine-/copper-catalyzed protocol.
描述了由三苯基膦和卤化亚铜催化的原子转移自由基加成反应。该反应在使用发光二极管的365nm光照射下进行,并在普通玻璃器皿中进行。提出的机理涉及季鏻盐的形成,其通过光诱导电子转移被亚铜盐进行单电子还原。该方法对末端烯烃和活性有机卤化物如溴乙酸酯、碘乙酸酯和溴乙腈效果良好。原子转移反应很少见的二氟苯乙烯也被证明是这种膦/铜催化反应的良好底物。