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One-step catalytic synthesis of alkyl-substituted quinolines
Journal article   Peer reviewed

One-step catalytic synthesis of alkyl-substituted quinolines

Courtney E Meyet and Catharine H Larsen
Journal of organic chemistry, Vol.79(20), pp.9835-9841
17/10/2014
PMID: 25229642

Abstract

Aldehydes - chemistry Alkynes - chemistry Aniline Compounds - chemistry Catalysis Ligands Mesylates - chemistry Molecular Structure Quinolines - chemical synthesis Quinolines - chemistry
Difficult-to-access alkyl-substituted quinolines are formed directly from commercially available anilines, aldehydes, and alkynes bearing a variety of substituents. Copper(II) triflate catalyzes this three-component coupling without ligand, cocatalyst, solvent, or inert atmosphere. In addition, a two-component Povarov reaction forms 2,3-dialkyl quinolines under the same green conditions that enable the selective three-component synthesis of 2-alkyl quinolines as well as more common aryl quinolines.

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