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Oxidative Cyclization of 4-(2-Aminophenyl)-4-oxo-2-phenylbutanenitriles into 2-(3-Oxoindolin-2-ylidene)acetonitriles.

Nicolai A AksenovAlexander V AksenovLidiya A PritykoDmitrii A AksenovDaria S AksenovaMezvah A NobiMichael Rubin
Published in: ACS omega (2022)
A facile and highly efficient method for the preparation of 2-(3-oxoindolin-2-ylidene)acetonitriles from 4-(2-aminophenyl)-4-oxo-2-phenylbutanenitriles is described. The featured transformation operates via nucleophilic intramolecular cyclization and involves oxidation of the aniline moiety. Overall, this modification allowed for the improvement of yields and expansion of the reaction scope.
Keyphrases
  • highly efficient
  • electron transfer
  • hydrogen peroxide
  • molecularly imprinted
  • energy transfer
  • high resolution
  • gold nanoparticles
  • liquid chromatography
  • metal organic framework