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Photochemical reductive deamination of alpha-amino aryl alkyl ketones.

Ji-Yuan LiangYi-Wen SuYou-Quan Zou
Published in: Chemical communications (Cambridge, England) (2023)
Photochemical reductive deamination of alpha-amino aryl alkyl ketones under photosensitizer-free conditions is presented. This protocol features high efficiency and selectivity. A plausible reaction pathway is proposed based on ultraviolet-visible absorption investigation, control experiments and deuterium-labelling studies. Mechanistic study reveals that the alpha-hydrogen atom of the ketone product originated from water.
Keyphrases
  • high efficiency
  • ionic liquid
  • photodynamic therapy
  • randomized controlled trial
  • molecular dynamics
  • electron transfer