Synthesis of Quinoxalin-2(1 H)-ones and Hexahydroquinoxalin-2(1 H)-ones via Oxidative Amidation-Heterocycloannulation

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Abstract

A metal-catalyst-free synthesis of substituted quinoxalin-2-ones from 2,2-dibromo-1-arylethanone by employing an oxidative amidation-heterocycloannulation protocol is reported. The substrate scope of the reaction has been demonstrated and a possible mechanism for this reaction has also been proposed.

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Raghunadh, A., Tadiparthi, K., Meruva, S. B., Murthy, V. N., Rao, L. V., & Kumar, U. K. S. (2020). Synthesis of Quinoxalin-2(1 H)-ones and Hexahydroquinoxalin-2(1 H)-ones via Oxidative Amidation-Heterocycloannulation. SynOpen, 4(3), 55–61. https://doi.org/10.1055/s-0040-1707203

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