| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1267070 | Ultrasonics Sonochemistry | 2010 | 5 Pages |
Abstract
Fused polycyclic 4-aryl-3-methyl-4,7-dihydro-1H-pyrazolo[3,4-b]pyridines were obtained in a three-component regioselective reaction of 5-amino-3-methyl-1H-pyrazole, 2H-indene-1,3-dione and arylaldehydes in ethanol under ultrasound irradiation. This rapid method produced the products in short reaction times (4–5 min) and excellent yields (88–97%).
Related Topics
Physical Sciences and Engineering
Chemistry
Chemistry (General)
Authors
Mohammad Nikpassand, Manouchehr Mamaghani, Farhad Shirini, Khalil Tabatabaeian,
![First Page Preview: A convenient ultrasound-promoted regioselective synthesis of fused polycyclic 4-aryl-3-methyl-4,7-dihydro-1H-pyrazolo[3,4-b]pyridines A convenient ultrasound-promoted regioselective synthesis of fused polycyclic 4-aryl-3-methyl-4,7-dihydro-1H-pyrazolo[3,4-b]pyridines](/preview/png/1267070.png)