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Molecular-Iodine-Catalyzed Cyclization of 2-Alkynylanilines via Iodocyclization-Protodeiodination Sequence.

Yuichiro TakedaRyota KajiharaNaoko KobayashiKeiichi NoguchiAkio Saito
Published in: Organic letters (2017)
Molecular iodine catalyzes a cyclization of N-aryl-2-alkynylanilines, which proceeds through the iodocyclization of 2-alkynylanilines followed by the protodeiodination of the iodocyclized intermediates at room temperature. Furthermore, the molecular iodine catalysis can be applied to the cascade cyclization of 2-(enynyl)aniline and to the tandem cyclization-addition reaction of 2-alkynylanilines with α,β-enones.
Keyphrases
  • room temperature
  • ionic liquid
  • single molecule
  • magnetic resonance imaging
  • computed tomography
  • magnetic resonance