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Palladium-Catalyzed Aerobic Benzannulation of Amines, Benzaldehydes, and β-Dicarbonyls.

Yujia XiaHua-Wen HuangFeng ZhangXiao-Lan Chen
Published in: Organic letters (2019)
A palladium-catalyzed aerobic multicomponent benzannulation of Hantzsch reactants, i.e., amines, aldehydes, and β-dicarbonyls, has been developed. Hence, a viable entry to highly functionalized anilines has been accessed under solvent-free neat conditions. Mechanistically, the palladium chelating with an imine intermediate was proposed to be the key for this novel carbocyclization.
Keyphrases
  • high intensity
  • quantum dots
  • ionic liquid
  • reduced graphene oxide
  • molecularly imprinted
  • solid phase extraction
  • tandem mass spectrometry