School of Chemical Engineering, Zhengzhou University, Zhengzhou 450001, P. R. China.
Chem Commun (Camb). 2020 Apr 25;56(32):4436-4439. doi: 10.1039/d0cc01079k. Epub 2020 Mar 20.
An organoselenium-catalyzed N- and N-selective aza-Wacker reaction of alkenes with benzotriazoles is reported, which provides easy access to N- and N-olefinated benzotriazole derivatives. The wide substrate scope, good functional group tolerance, and facile scale-up of this method are expected to promote its potential application in synthetic chemistry. A preliminary mechanism is proposed to explain the N- and N-selectivities.
报道了一种有机硒催化的烯烃与苯并三唑的 N-和 N-选择性氮杂 Wacker 反应,该反应为 N-和 N-烯基化苯并三唑衍生物的合成提供了一种简便方法。该方法具有广泛的底物范围、良好的官能团耐受性和易于放大的特点,有望促进其在合成化学中的潜在应用。提出了一个初步的反应机理来解释 N-和 N-选择性。