Alkylation of α-Oxo-Compounds through C(sp < sup > 3 < /sup > )-H Functionalization of 2-Methyl Quinolines Under Catalyst- and Solvent-Free Conditions
Alkylation of α-Oxo-Compounds through C(sp < sup > 3 < /sup > )-H Functionalization of 2-Methyl Quinolines Under Catalyst- and Solvent-Free Conditions
No Thumbnail Available
Date
2020-07-23
Authors
Rao, Yadavalli Subba
Latha, Dandugula Sneha
Devunuri, Nagaraju
Almansour, Abdulrahman I.
Arumugam, Natarajan
Yaragorla, Srinivasarao
Journal Title
Journal ISSN
Volume Title
Publisher
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.
Description
Keywords
Alkylation Carbonyl compounds C–H activation Heterocycles Synthetic methods
Citation
European Journal of Organic Chemistry. v.2020(27)