Regioselective Copper-Catalyzed Oxidative Cross-Coupling of Imidazo[1,2-a]pyridines with Methyl Ketones: An Efficient Route for Synthesis of 1,2-Diketones

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Abstract

An efficient copper-catalyzed oxidative coupling of imidazo[1,2-a]pyridines with methyl ketones to directly generate structurally sophisticated 1,2-dicarbonyl imidazo[1,2-a]pyridine derivatives under oxidative conditions is described. The reaction proceeds in good yields using the environmental friendly molecular oxygen as the oxidant. 18O-Labelling experiments unambiguously established that the oxygen of the dicarbonyl products originated from oxygen rather than from water.

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Lei, S., Chen, G., Mai, Y., Chen, L., Cai, H., Tan, J., & Cao, H. (2016). Regioselective Copper-Catalyzed Oxidative Cross-Coupling of Imidazo[1,2-a]pyridines with Methyl Ketones: An Efficient Route for Synthesis of 1,2-Diketones. Advanced Synthesis and Catalysis, 358(1), 67–73. https://doi.org/10.1002/adsc.201500803

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