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C-H键酸度与芳烃亲核性作为双C-H键活化中化学选择性的正交控制

C-H Acidity and Arene Nucleophilicity as Orthogonal Control of Chemoselectivity in Dual C-H Bond Activation.

作者信息

Liu Ji-Ren, Duan Ye-Qing, Zhang Shuo-Qing, Zhu Lu-Jing, Jiang Yuan-Ye, Bi Siwei, Hong Xin

机构信息

Department of Chemistry , Zhejiang University , Hangzhou 310027 , China.

School of Chemistry and Chemical Engineering , Qufu Normal University , Qufu 273165 , China.

出版信息

Org Lett. 2019 Apr 5;21(7):2360-2364. doi: 10.1021/acs.orglett.9b00633. Epub 2019 Mar 20.

Abstract

We discovered a cooperative gold/silver catalysis mechanism in the oxidative cross-coupling reaction between 1,2,4,5-tetrafluorobenzene and N-TIPS-indole, using DFT calculations. A silver(I)-catalyzed CMD mechanism is responsible for the C-H activation of 1,2,4,5-tetrafluorobenzene, and C-H acidity determines the chemoselectivity. A gold(III)-catalyzed S2Ar mechanism is responsible for the C3-H activation of N-TIPS-indole, and arene nucleophilicity determines the chemo- and regioselectivity. The orthogonal chemoselectivity control provides a mechanistic guide for dual C-H activation reactions.

摘要

通过密度泛函理论计算,我们发现了1,2,4,5-四氟苯与N-TIPS-吲哚之间氧化交叉偶联反应中的一种协同金/银催化机制。银(I)催化的CMD机制负责1,2,4,5-四氟苯的C-H活化,而C-H酸度决定了化学选择性。金(III)催化的S2Ar机制负责N-TIPS-吲哚的C3-H活化,芳烃亲核性决定了化学和区域选择性。这种正交化学选择性控制为双C-H活化反应提供了一种机制指导。

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