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DOI: 10.1055/s-0036-1588176
Synthesis of 2,4-Disubstituted Quinoline Derivatives via A3-Coupling: An EcoScale Evaluation
Supported by: National Research Foundation of South Africa Thuthuka Grant (TTK150609119011)Publication History
Received: 10 February 2017
Accepted after revision: 28 March 2017
Publication Date:
26 April 2017 (online)
Abstract
The 2,4-disubstituted quinoline moiety is an important building block for numerous biologically active and industrially useful compounds. These elegant compounds can be synthesised via the three-component coupling between an aldehyde, amine, and alkyne commonly referred to as A3-coupling. This short review aims to give an overview of the progress made towards disubstituted quinoline derivatives using this innovative methodology.
1 Introduction
2 Applications of the Quinoline Moiety
2.1 Antimicrobial Properties
2.2 Anti-inflammatory Properties
2.3 Anticonvulsant Properties
2.4 Photophysical Properties
3 Synthesis Based on A3-Coupling
3.1 Copper-Catalysed Systems
3.2 Iron-Catalysed Systems
3.3 Miscellaneous Systems
3.3.1 Montmorillonite Clays
3.3.2 Polyoxometalates
3.3.3 Rare Earth Metals
3.3.4 Al2O3 Nanoparticles/Methanesulfonic Acid
4 Proposed Reaction Mechanism
5 EcoScale Evaluation
6 Conclusion
7 Appendix
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