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Phototriggered Fluoroalkylation/Cyclization of Unactivated 1-Acryloyl-2-cyanoindoles: Synthesis of RCOCF 2 -Substituted Pyrrolo[1,2- a ]indolediones.

Weixian LvPengyuan YangJin-Wei YuanJiayi LiMengran LiangYitong LiuDongliang XingLiangru Yang
Published in: The Journal of organic chemistry (2024)
A photochemical approach toward RCOCF 2 -substituted pyrrolo[1,2- a ]indolediones was developed by the radical cascade difluoroalkylation/cyclization reaction of unactivated 1-acryloyl-2-cyanoindoles with ethyl iododifluoroacetate or iododifluoramides under visible-light irradiation. This transition-metal- and photosensitizer-free protocol afforded diverse difluoroalkylated pyrrolo[1,2- a ]indolediones in moderate to good yields under mild reaction conditions. Most appealingly, the reaction can proceed smoothly under sunlight irradiation, which opens a new avenue toward difluoroalkylated pyrrolo[1,2- a ]indolediones.
Keyphrases
  • visible light
  • transition metal
  • molecular docking
  • photodynamic therapy
  • radiation induced
  • high intensity
  • electron transfer