Electrocatalytic multicomponent assembling of isatins, 3-methyl-2- pyrazolin-5-ones and malononitrile: Facile and convenient way to functionalized spirocyclic [indole-3,4′-pyrano[2,3-c]pyrazole] system

Michail N. Elinson, Alexander S. Dorofeev, Fedor M. Miloserdov, Gennady I. Nikishin

Research output: Contribution to journalArticleAcademicpeer-review

68 Citations (Scopus)

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 languageEnglish
Pages (from-to)47-52
Number of pages6
JournalMolecular diversity
Volume13
Issue number1
DOIs
Publication statusPublished - Feb 2009
Externally publishedYes

Keywords

  • C-H acids
  • Electrocatalysis
  • Isatin
  • Multicomponent reactions
  • Pyranopyrazole
  • Spirooxindole

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