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铱催化、弱配位辅助的(杂)芳基羧酸的邻位炔基化反应,无环化。

Iridium-Catalyzed, Weakly Coordination-Assisted Ortho-Alkynylation of (Hetero)aromatic Carboxylic Acids without Cyclization.

机构信息

Frontier Institute of Science and Technology, Xi'an Jiaotong University , Xi'an 710054, China.

Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University , Chengdu 610064, China.

出版信息

Org Lett. 2017 May 19;19(10):2474-2477. doi: 10.1021/acs.orglett.7b00581. Epub 2017 May 2.

Abstract

It is reported a weakly coordination-assisted alkynylation of aryl and heteroaryl carboxylic acids with iridium catalysis. The reaction is catalyzed by [{Cp*IrCl}] complex without cyclization, forming ortho-alkynylated aryl and heteroaryl carboxylic acids, and features high functional group tolerance and broad substrate scope under an air atmosphere. 2-(Hetero)aryl-substituted acetic acids were amenable to the alkynylation by forming an unusual six-membered ring cycloiridiated intermediate.

摘要

据报道,在铱催化作用下,芳基和杂芳基羧酸可进行弱配位辅助的炔基化反应。该反应在无需环化的情况下由[{Cp*IrCl}]配合物催化,生成邻位炔基化的芳基和杂芳基羧酸,在空气氛围中具有高官能团容忍度和广泛的底物范围。2-(杂)芳基取代的乙酸可通过形成不寻常的六元环环铱化中间体进行炔基化。

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