Inverse Electron Demand Diels Alder Reaction of Aza‑o‑Quinone Methides and Enaminones: Accessing 3‑Aroyl Quinolines and Indeno[1,2‑b]quinolinones

We have developed a Diels Alder cycloaddition route toward 3-aroyl quinolines from enaminones and in situ generated aza-o-quinone methides. The reaction was found to be general with a range of substituted enaminones and aza-o-quinone methides, and we could validate the applicability of the methodolo...

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Veröffentlicht in:	Journal of organic chemistry 2022-11, Vol.87 (21), p.13708-13714
Hauptverfasser:	P, Rahul, S, Veena, John, Jubi
Format:	Artikel
Sprache:	eng
Schlagworte:	Cycloaddition Reaction Electrons Indolequinones Quinolones
Online-Zugang:	Volltext
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