Dalton Toryn, Greßies Steffen, Das Mowpriya, Niehues Maximilian, Schrader Malte L, Gutheil Christian, Ravoo Bart Jan, Glorius Frank
Organisch-Chemisches Institut, Westfälische Wilhelms-Universität Münster, Corrensstrasse 40, 48149, Münster, Germany.
Angew Chem Int Ed Engl. 2021 Apr 6;60(15):8537-8541. doi: 10.1002/anie.202016268. Epub 2021 Mar 5.
Hydroarylation is an effective strategy to rapidly increase the complexity of organic structures by transforming flat alkene moieties into three-dimensional frameworks. Many strategies have already been developed to achieve the hydroarylation of styrenes, however most of these reports examine the hydroarylation of unpolar, β-mono- or β-unsubstituted styrenes, while exploring mainly electron-rich benzene nucleophiles. Herein, we report a mild and general catalytic system for the selective hydroheteroarylation of multiply substituted styrenes and heteroaromatic styrenes. Mechanistic analysis of the reaction led to the discovery of commercially available 2,2':5',2''-terthiophene as a key reagent.
氢芳基化是一种通过将平面烯烃部分转化为三维骨架来快速增加有机结构复杂性的有效策略。已经开发了许多策略来实现苯乙烯的氢芳基化,然而,这些报道大多研究的是非极性、β-单取代或β-未取代苯乙烯的氢芳基化,同时主要探索富电子的苯亲核试剂。在此,我们报道了一种温和且通用的催化体系,用于多取代苯乙烯和杂芳基苯乙烯的选择性氢杂芳基化。对该反应的机理分析导致发现市售的2,2':5',2''-三联噻吩是关键试剂。