对映选择合成
阿托品
区域选择性
镍
催化作用
化学
组合化学
密度泛函理论
计算化学
立体化学
有机化学
作者
Fang‐Bei Ge,Chuan‐Jun Lu,Xiao Chen,Yao Wang,An Mei,Yukun Jiang,Li‐Ping Xu,Renrong Liu
标识
DOI:10.1002/anie.202400441
摘要
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.
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