| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10588215 | Bioorganic & Medicinal Chemistry Letters | 2012 | 5 Pages |
Abstract
Novel fused 1H-benzo[f]chromen-indole derivatives were synthesized regioselectivly in good to high yields by triethyl amine catalyzed condensation of 3-cyanoacetylindoles, β-naphthol and aryl aldehydes in methanol under ultrasounic irradiations and conventional conditions. The easy work-up of the products, rapidity, and mild reaction conditions are notable features of this protocol. The antibacterial activity of the selected products was examined. Some products showed promising activities.
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Authors
Roghayeh Hossein nia, Manouchehr Mamaghani, Khalil Tabatabaeian, Farhad Shirini, Mehdi Rassa,