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Electrocatalysis-Enabled Stereoselective Synthesis of Monofluoroalkenes via Hydrodefluorination of gem -Difluoroakenes.

Xiaoying WangJiaxi CaiHaixia SongLe LiuXin-Hua DuanMingyou Hu
Published in: Organic letters (2024)
We report a simple and economical method to synthesize monofluoroalkenes via the electrochemical hydrodefluorination of gem -difluoroalkenes. This reaction proceeds efficiently at room temperature, eliminating the requirement for a costly transition metal catalyst, ligand, and external reducing agent. The monofluoroalkene products can be obtained in medium to good yields and up to 99:1 E / Z selectivity. The reaction is easily scalable to gram scale.
Keyphrases
  • room temperature
  • transition metal
  • ionic liquid
  • electron transfer
  • gram negative
  • gold nanoparticles
  • molecularly imprinted
  • mass spectrometry