Abstract
Electrochemically induced catalytic multicomponent transformation of isatins, 3-methyl-2-pyrazolin-5-ones and malononitrile in ethanol in an undivided cell in the presence of sodium bromide as an electrolyte results in the formation of spirooxindoles with fused functionalized pyrano[2,3-c]pyrazole system in 78-99} yields. The developed efficient electrocatalytic approach to medicinally relevant spirocyclic [indole-3,4′-pyrano[2,3-c]pyrazoles] is beneficial from the viewpoint of diversity-oriented large-scale processes and represents a novel example of facile environmentally benign synthetic concept for electrocatalytic multicomponent reaction strategy.
Original language | English |
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Pages (from-to) | 47-52 |
Number of pages | 6 |
Journal | Molecular diversity |
Volume | 13 |
Issue number | 1 |
DOIs | |
Publication status | Published - Feb 2009 |
Externally published | Yes |
Keywords
- C-H acids
- Electrocatalysis
- Isatin
- Multicomponent reactions
- Pyranopyrazole
- Spirooxindole