Issue 50, 2022

Ir(iii)-catalyzed quadruple C–H activation of N-arylimidazolium and diaryliodonium salts: facile access to polysubstituted imidazo[1,2-f]phenanthridiniums

Abstract

Herein, N-heterocyclic carbene-directed Ir(III)-catalyzed cascade C–H arylation/annulation of N-arylimidazolium with diaryliodonium salts has been accomplished for the first time via a quadruple C–H activation strategy to construct imidazo[1,2-f]phenanthridinium structures. This protocol overcomes the compatibility of three kinds of different C–H activations with high catalytic efficiency, which allows ortho-unhindered N-arylimidazoliums to undergo a diarylation/annulation reaction, affording a variety of polysubstituted imidazo[1,2-f]phenanthridiniums. Neutral imidazo[1,2-f]phenanthridines are also prepared via a demethylation reaction of imidazo[1,2-f]phenanthridiniums.

Graphical abstract: Ir(iii)-catalyzed quadruple C–H activation of N-arylimidazolium and diaryliodonium salts: facile access to polysubstituted imidazo[1,2-f]phenanthridiniums

Supplementary files

Article information

Article type
Communication
Submitted
22 Mar 2022
Accepted
23 May 2022
First published
24 May 2022

Chem. Commun., 2022,58, 7042-7045

Ir(III)-catalyzed quadruple C–H activation of N-arylimidazolium and diaryliodonium salts: facile access to polysubstituted imidazo[1,2-f]phenanthridiniums

Z. Liu, Q. Li, C. Yang, X. Zheng, D. Wu, G. Gao and J. Lan, Chem. Commun., 2022, 58, 7042 DOI: 10.1039/D2CC01646J

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