Alkylation of α-Oxo-Compounds through C(sp3)-H Functionalization of 2-Methyl Quinolines Under Catalyst- and Solvent-Free Conditions

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Abstract

Highly facile approach of chemoselective alkylation of α-oxo compounds such as α-keto amides, α-keto esters, isatins, and cyclic-α-diketones is developed through C(sp3)-H functionalization of 2-methyl quinolines under solvent and catalyst-free conditions. Further, we complemented the efficacy of this green synthetic protocol by demonstrating the broad substrate diversity, gram-scale synthesis, and new synthetic transformations of the obtained products.

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Rao, Y. S., Latha, D. S., Devunuri, N., Almansour, A. I., Arumugam, N., & Yaragorla, S. (2020). Alkylation of α-Oxo-Compounds through C(sp3)-H Functionalization of 2-Methyl Quinolines Under Catalyst- and Solvent-Free Conditions. European Journal of Organic Chemistry, 2020(27), 4134–4145. https://doi.org/10.1002/ejoc.202000511

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