Issue 1, 2021

Using experimental and computational approaches to probe an unusual carbon–carbon bond cleavage observed in the synthesis of benzimidazole N-oxides

Abstract

Experimental and computational studies have been performed in order to investigate an unusual carbon–carbon bond cleavage that occurs in the preparation of certain benzimidazole N-oxides from anilines. The key factor determining the outcome of the reaction was found to be the substituents on the amine functionality of the aniline.

Graphical abstract: Using experimental and computational approaches to probe an unusual carbon–carbon bond cleavage observed in the synthesis of benzimidazole N-oxides

Supplementary files

Article information

Article type
Paper
Submitted
30 Aug 2020
Accepted
03 Nov 2020
First published
06 Nov 2020

Org. Biomol. Chem., 2021,19, 208-215

Using experimental and computational approaches to probe an unusual carbon–carbon bond cleavage observed in the synthesis of benzimidazole N-oxides

F. Politano, A. L. Sandoval, J. G. Uranga, E. I. Buján and N. E. Leadbeater, Org. Biomol. Chem., 2021, 19, 208 DOI: 10.1039/D0OB01797C

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