Enantioselective addition of 3-hydroxyquinolin-2(1 H )-one to isatin and pyrazole-4,5-dione derived ketimines
The enantioselective reactivity of 3-hydroxyquinolin-2(1 H )-ones was developed through their addition to isatin and pyrazole-4,5-dione derived ketimines, affording novel architectures featuring multiple natural product scaffolds in high yields with excellent enantioselectivities. Gram-scale synthes...
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Veröffentlicht in: | Organic Chemistry Frontiers 2025-01, Vol.12 (2), p.497-502 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The enantioselective reactivity of 3-hydroxyquinolin-2(1 H )-ones was developed through their addition to isatin and pyrazole-4,5-dione derived ketimines, affording novel architectures featuring multiple natural product scaffolds in high yields with excellent enantioselectivities. Gram-scale synthesis and synthetic transformations further disclosed the potential of the current process. |
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ISSN: | 2052-4129 2052-4110 2052-4129 2052-4110 |
DOI: | 10.1039/D4QO01895H |