Ge Fang-Bei, Lu Chuan-Jun, Chen Xiao, Yao Wang, An Mei, Jiang Yu-Kun, Xu Li-Ping, Liu Ren-Rong
College of Chemistry and Chemical Engineering, Qingdao University, Ningxia Road 308#, Qingdao, 266071, China.
School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, China.
Angew Chem Int Ed Engl. 2024 Jun 21;63(26):e202400441. doi: 10.1002/anie.202400441. Epub 2024 May 24.
Nickel-catalyzed transannulation reactions triggered by the extrusion of small gaseous molecules have emerged as a powerful strategy for the efficient construction of heterocyclic compounds. However, their use in asymmetric synthesis remains challenging because of the difficulty in controlling stereo- and regioselectivity. Herein, we report the first nickel-catalyzed asymmetric synthesis of N-N atropisomers by the denitrogenative transannulation of benzotriazones with alkynes. A broad range of N-N atropisomers was obtained with excellent regio- and enantioselectivity under mild conditions. Moreover, density functional theory (DFT) calculations provided insights into the nickel-catalyzed reaction mechanism and enantioselectivity control.
由小分子气体挤出引发的镍催化环化反应已成为高效构建杂环化合物的有力策略。然而,由于难以控制立体和区域选择性,它们在不对称合成中的应用仍然具有挑战性。在此,我们报道了通过苯并三氮唑与炔烃的脱氮环化反应首次实现镍催化的N-N阻转异构体的不对称合成。在温和条件下,以优异的区域和对映选择性获得了多种N-N阻转异构体。此外,密度泛函理论(DFT)计算为镍催化的反应机理和对映选择性控制提供了深入见解。