Cu-Catalyzed/mediated synthesis of N-fluoroalkylanilines from arylboronic acids: fluorine effect on the reactivity of fluoroalkylamines.

@article{Wang2018CuCatalyzedmediatedSO,
  title={Cu-Catalyzed/mediated synthesis of N-fluoroalkylanilines from arylboronic acids: fluorine effect on the reactivity of fluoroalkylamines.},
  author={Hui Wang and Yuan-Hong Tu and De-Yong Liu and Xiang-Guo Hu},
  journal={Organic \& biomolecular chemistry},
  year={2018},
  volume={16 36},
  pages={
          6634-6637
        }
}
An oxidative coupling reaction of fluoroalkylamines with arylboronic acids has been achieved for the first time. Fluorine has profound influence on the reactivity and fluoroalkylated amines have the following reactivity trend: difluoroethylamine > trifluoroethylamine > pentafluoropropylamine ≈ heptafluorobutylamine. 
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