Gold catalysis in quinoline synthesis

Quinolines are biologically and pharmaceutically important N-heterocyclic aromatic compounds, which have broad applications in medicinal chemistry. Thus, their efficient synthesis has attracted extensive attention, and a broad range of synthetic strategies have been established. Of note, gold-cataly...

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Main Authors: Zhao, Ximei (Author) , Wang, Guanghui (Author) , Hashmi, A. Stephen K. (Author)
Format: Article (Journal)
Language:English
Published: 14 Jun 2024
In: Chemical communications
Year: 2024, Volume: 60, Issue: 55, Pages: 6999-7016
ISSN:1364-548X
DOI:10.1039/D4CC01915F
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1039/D4CC01915F
Verlag, lizenzpflichtig, Volltext: https://pubs.rsc.org/en/content/articlelanding/2024/cc/d4cc01915f
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Author Notes:Ximei Zhao, Guanghui Wang and A. Stephen K. Hashmi
Description
Summary:Quinolines are biologically and pharmaceutically important N-heterocyclic aromatic compounds, which have broad applications in medicinal chemistry. Thus, their efficient synthesis has attracted extensive attention, and a broad range of synthetic strategies have been established. Of note, gold-catalyzed methodologies for the synthesis of quinolines have greatly advanced this field. Various gold-catalyzed intermolecular annulation reactions, such as annulations of aniline derivatives with carbonyl compounds or alkynes, annulations of anthranils with alkynes, and annulations based on A3-coupling reactions, as well as intramolecular cyclization reactions of azide-tethered alkynes, 1,2-diphenylethynes, and 2-ethynyl N-aryl indoles, have been developed. This review provides an overview of this exciting research area. Typical achievements in reaction methodologies and plausible reaction mechanisms are summarized.
Item Description:Gesehen am 19.11.2024
Physical Description:Online Resource
ISSN:1364-548X
DOI:10.1039/D4CC01915F