A rare γ-pyranopyrazole skeleton: design, one-pot synthesis and computational study

Drawing upon a consecutive amide coupling and intramolecular cyclisation pathway, a one-pot, straightforward synthetic route has been developed for a range of pyrazole fused γ-pyrone derivatives. The reaction mechanism proposed for the chemoselective formation of γ-pyranopyrazole is furthermore full...

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Veröffentlicht in:Organic & biomolecular chemistry 2016-01, Vol.14 (31), p.749-7494
Hauptverfasser: Üçüncü, Muhammed, Cantürk, Ceren, Karaku, Erman, Zeybek, Hüseyin, Bozkaya, U ur, Soyda, Emine, ahin, Ertan, Emrullaho lu, Mustafa
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Sprache:eng
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Zusammenfassung:Drawing upon a consecutive amide coupling and intramolecular cyclisation pathway, a one-pot, straightforward synthetic route has been developed for a range of pyrazole fused γ-pyrone derivatives. The reaction mechanism proposed for the chemoselective formation of γ-pyranopyrazole is furthermore fully supported by experimental and computational studies. A base mediated one-pot, two-step synthetic method for constructing γ-pyranopyrazoles.
ISSN:1477-0520
1477-0539
DOI:10.1039/c6ob01099g