Autor: |
Alizadeh, Abdolali, Hasanpour, Hamidreza, Rezaiyehraad, Reza |
Předmět: |
|
Zdroj: |
ChemistrySelect; 12/22/2023, Vol. 8 Issue 48, p1-6, 6p |
Abstrakt: |
Extensive studies on the biological activities of several quinone‐fused heterocycles have confirmed their outstanding antitumor activity. Therefore, a new family of 1H‐benzo[f]indole‐4,9‐dione derivatives with the 4‐hydroxycoumarin substitution was prepared by a high‐yield, one‐pot, concise three‐component reaction between arylglyoxals, 4‐hydroxycoumarin, and 2‐aminonaphthalene‐1,4‐dione derivatives under reflux in EtOH. This efficient protocol showed chemoselectivity in addition to facile operation procedure and easy purification. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
|