Palladium-Catalyzed C−H Iodination of N-(8-Quinolinyl)benzamide Derivatives Under Electrochemical and Non-Electrochemical Conditions

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Abstract

Palladium-catalyzed ortho-selective C−H iodination of N-(8-quinolinyl)benzamides proceeded using I2 under both electrochemical and non-electrochemical conditions. The C−H iodination at 90 °C under base-free conditions provided high yields of the iodination products. The use of anodic oxidation increased the efficiency of the iodination at sterically-hindered positions.

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Sano, K., Kimura, N., Kochi, T., & Kakiuchi, F. (2018). Palladium-Catalyzed C−H Iodination of N-(8-Quinolinyl)benzamide Derivatives Under Electrochemical and Non-Electrochemical Conditions. Asian Journal of Organic Chemistry, 7(7), 1311–1314. https://doi.org/10.1002/ajoc.201800202

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