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Iodine-Catalyzed Regioselective Synthesis of Diphenyl-Substituted Carbazoles via [4 + 2] Annulation of β-Formyl Ketones with Indoles.

Sundaram SureshHung-Sheng ChienChao-Hua ChenHao-Yu TsaiDai-Ru ChungVeerababurao KavalaChing-Fa Yao
Published in: The Journal of organic chemistry (2023)
The [4 + 2] annulation of β-formyl ketones with an indole has been developed for the regioselective synthesis of diphenyl-substituted carbazoles in the presence of a catalytic amount of iodine. The 1,4-dicarbonyl compound containing a phenyl group at the α-position of an aldehyde group reacts more readily with indoles to form carbazole derivatives. Using this method, a variety of carbazole derivatives can be readily accessed under mild reaction conditions.
Keyphrases
  • molecular docking
  • dual energy
  • structure activity relationship
  • computed tomography
  • magnetic resonance imaging
  • magnetic resonance
  • crystal structure
  • ionic liquid