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TMSOTf-Catalyzed [4 + 2] Annulation of Ynamides and β-(2-Aminophenyl)-α,β-ynones for the Synthesis 2-Aminoquinolines.

Chaofan QiXiaoxiao ShenWozheng FangJunbiao ChangXiao-Na Wang
Published in: Organic letters (2024)
A metal-free TMSOTf-catalyzed [4 + 2] annulation of ynamides with β-(2-aminophenyl)-α,β-ynones enables the regiospecific and facile assembly of 2-aminoquinoline frameworks. The catalyst TMSOTf presented a remarkable advancement compared to previously reported transition-metal catalysts. A wide range of 3-aryl/alkyl-substituted 2-aminoquinolines were generated in moderate to excellent yields due to the mild conditions.
Keyphrases
  • transition metal
  • room temperature
  • ionic liquid
  • visible light
  • highly efficient
  • reduced graphene oxide
  • metal organic framework
  • molecular docking
  • high intensity
  • quantum dots
  • gold nanoparticles