Improved and rapid synthesis of new coumarinyl chalcone derivatives and their antiviral activity
Two closely structurally related coumarins, 4-hydroxy-8-isopropyl-5-methylcoumarin and 4-hydroxy-6-chloro-7-methylcoumarin were acylated at C-3 and further converted to the respective chalcones and two series of eighteen new compounds, which were evaluated for possible antiviral activity.
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Veröffentlicht in: | Tetrahedron letters 2007-11, Vol.48 (48), p.8472-8474 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Two closely structurally related coumarins, 4-hydroxy-8-isopropyl-5-methylcoumarin and 4-hydroxy-6-chloro-7-methylcoumarin were acylated at C-3 and further converted to the respective chalcones and two series of eighteen new compounds, which were evaluated for possible antiviral activity. |
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/j.tetlet.2007.09.175 |