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
Hauptverfasser: Trivedi, Jalpa C., Bariwal, Jitender B., Upadhyay, Kuldip D., Naliapara, Yogesh T., Joshi, Sudhir K., Pannecouque, Christophe C., De Clercq, Erik, Shah, Anamik K.
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Sprache:eng
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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.
ISSN:0040-4039
1873-3581
DOI:10.1016/j.tetlet.2007.09.175