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Indium-Catalyzed Denitrogenative Transannulation of Pyridotriazoles: Synthesis of Pyrido[1,2- a]indoles.

Deepa RawatChitrakar RaviAbhisek JoshiEringathodi SureshKalyanashis JanaBishwajit GangulySubbarayappa Adimurthy
Published in: Organic letters (2019)
Pyrido[1,2- a]indoles are known for medicinally and pharmaceutically important compounds; however, the efficient synthetic routes are scarce in the literature. We report herein a convenient and efficient route to synthesize these molecules through indium-catalyzed transannulation of pyridotriazoles with arenes. A library of compounds have been synthesized employing the method developed with various substituted pyrido[1,2- a]indole derivatives in moderate to good yields. The density functional theory study using SMDDCB-M06/6-31++G(d,p)/LANL2DZ//B3LYP/6-31G(d)/LANL2DZ method suggests that the reactions proceed via indium-carbenoid complex.
Keyphrases
  • density functional theory
  • room temperature
  • molecular dynamics
  • systematic review
  • molecular docking
  • high intensity
  • ionic liquid