Issue 3, 2021

Cp*Ir(iii)- and Cp*Rh(iii)-catalyzed C(sp2)–H amination of arenes using thioethers as directing groups

Abstract

A mild and selective Cp*Ir(III)- and Cp*Rh(III)-catalyzed direct C(sp2)–H amination of arenes and three types of nitrene precursor reagents is reported, with the assistance of a thioether directing group. This redox-neutral protocol proceeds under mild reaction conditions, has a broad substrate scope and high functional-group compatibility and generates the desired aminated products in moderate to excellent yields. The reaction represents the first example of a thioether-directed Cp*Ir(III)- and Cp*Rh(III)-catalyzed C(sp2)–H direct amination reaction. Moreover, azide compounds were employed as a diverse and robust aminating reagent for the first time in a thioether-directed C–H functionalization reaction.

Graphical abstract: Cp*Ir(iii)- and Cp*Rh(iii)-catalyzed C(sp2)–H amination of arenes using thioethers as directing groups

Supplementary files

Article information

Article type
Research Article
Submitted
31 Oct 2020
Accepted
05 Dec 2020
First published
08 Dec 2020

Org. Chem. Front., 2021,8, 635-642

Cp*Ir(III)- and Cp*Rh(III)-catalyzed C(sp2)–H amination of arenes using thioethers as directing groups

H. Xie, M. Zhong, X. Wang, J. Wu, Y. Cai, J. Liu, B. Shu, T. Che and S. Zhang, Org. Chem. Front., 2021, 8, 635 DOI: 10.1039/D0QO01353F

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