Claus Vanessa, Schukin Michael, Harrer Siegfried, Rudolph Matthias, Rominger Frank, Asiri Abdullah M, Xie Jin, Hashmi A Stephen K
Organisch-Chemisches Institut, Heidelberg University, Im Neuenheimer Feld 270, 69120, Heidelberg, Germany.
Chemistry Department, Faculty of Science, King Abdulaziz University, Jeddah, 21589, Saudi Arabia.
Angew Chem Int Ed Engl. 2018 Sep 24;57(39):12966-12970. doi: 10.1002/anie.201805918. Epub 2018 Sep 3.
We have developed a simple gold-catalyzed procedure for the synthesis of substituted and modifiable azulenes. The azulenes are formed either by the dimerization of push-pull diarylalkynes bearing a fluorine atom in ortho or para position or by the dimerization of a symmetric electron-rich diarylalkyne. In the presence of a cationic gold catalyst, the two alkynes can form a highly reactive vinyl cation. Trapping of this high-energy intermediate by an appropriate aryl unit then delivers substituted azulenes in a single step and in a perfect atom economy.
我们开发了一种简单的金催化方法来合成取代的和可修饰的薁类化合物。薁类化合物可通过在邻位或对位带有氟原子的推拉二芳基炔烃的二聚反应,或者通过对称的富电子二芳基炔烃的二聚反应形成。在阳离子金催化剂存在下,两个炔烃可形成高反应活性的乙烯基阳离子。然后,通过合适的芳基单元捕获这种高能中间体,可一步以完美的原子经济性得到取代的薁类化合物。