Catalytic formal [4 + 1] isocyanide-based cycloaddition: an efficient strategy for the synthesis of 1H-cyclopenta[b]quinolin-1-one derivatives

An unprecedented catalytic isocyanide-based cycloaddition of alkyl and aryl isocyanides with (Z)-2-(2-hydroxy-2-alkylvinyl)quinoline-3-carbaldehydes was developed for the direct and efficient synthesis of 1H-cyclopenta[b]quinolin-1-one derivatives. On the basis of DFT calculations, a mechanism is pr...

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Hauptverfasser: Motaghi, Mila (VerfasserIn) , Rominger, Frank (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2019
In: Organic & biomolecular chemistry
Year: 2018, Jahrgang: 17, Heft: 2, Pages: 275-282
ISSN:1477-0539
DOI:10.1039/C8OB02857E
Online-Zugang:Verlag, Volltext: https://doi.org/10.1039/C8OB02857E
Verlag, Volltext: https://pubs.rsc.org/en/content/articlelanding/2019/ob/c8ob02857e
Volltext
Verfasserangaben:Milad Motaghi, Hormoz Khosravi, Saeed Balalaie and Frank Rominger
Beschreibung
Zusammenfassung:An unprecedented catalytic isocyanide-based cycloaddition of alkyl and aryl isocyanides with (Z)-2-(2-hydroxy-2-alkylvinyl)quinoline-3-carbaldehydes was developed for the direct and efficient synthesis of 1H-cyclopenta[b]quinolin-1-one derivatives. On the basis of DFT calculations, a mechanism is proposed involving formal [4 + 1] cycloaddition of isocyanides, followed by imine-enamine tautomerization and air oxidation.
Beschreibung:First published on 05 Dec 2018
Gesehen am 01.04.2019
Beschreibung:Online Resource
ISSN:1477-0539
DOI:10.1039/C8OB02857E