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 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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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. |
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ISSN: | 1477-0520 1477-0539 |
DOI: | 10.1039/c6ob01099g |