Issue 1, 2023

Experimental and computational studies on rhodium-catalyzed C4(5)aryl–H activation/annulation of imidazoles with alkynes: facile synthesis of six types of N-heterocycles

Abstract

C–H annulations at N- and C2-aryls of an imidazole have been researched well, while the annulation on C4(5)-aryls especially the reactivity and site-selectivity among these aryls remains unknown. Herein, a molecular engineering strategy involving six reaction modes based on the rhodium-catalyzed C4(5)aryl–H activation/annulation of imidazoles with alkynes has been developed, giving diverse neutral/cationic N-heterocycles with broad scope (>60 examples) and high selectivity. More importantly, through a series of intramolecular competition experiments and DFT calculations, the reactivity of the peripheral C–H bonds has been studied and ranked for the first time: C2aryl–H > C4(5)aryl–H > C4(5)styryl–H/C2styryl–H > residual C4(5)aryl–H/C4(5)styryl–H. Furthermore, the remote bulky C2-subsituent is found to have a big influence on the regioselectivity of C4(5)aryl–H activation.

Graphical abstract: Experimental and computational studies on rhodium-catalyzed C4(5)aryl–H activation/annulation of imidazoles with alkynes: facile synthesis of six types of N-heterocycles

Supplementary files

Article information

Article type
Research Article
Submitted
01 Sep 2022
Accepted
09 Nov 2022
First published
10 Nov 2022

Org. Chem. Front., 2023,10, 83-91

Experimental and computational studies on rhodium-catalyzed C4(5)aryl–H activation/annulation of imidazoles with alkynes: facile synthesis of six types of N-heterocycles

Y. Tian, S. Lv, L. Huang, C. Wen, Y. Yang, X. Kong, Q. Zhu and S. Li, Org. Chem. Front., 2023, 10, 83 DOI: 10.1039/D2QO01390H

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