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Cyanide Ion-Promoted Nucleophilic Displacement of Aromatic Nitro Groups: A Mild, One-Pot, Transition Metal-Free Synthesis of Nitrile-Containing Naphthalimide Aryl Ether Derivatives.

Lu ChenXi ChenTingting ZhuHaibing ShaoZhihua ChenYan HuZhen-Jiang LiuChuanxiang Liu
Published in: The Journal of organic chemistry (2021)
Herein we report the novel synthesis of nitrile-containing naphthalimide aryl ether derivatives via transition metal-free cyanide ion-promoted nucleophilic displacement of nitronaphthalimide with alcohols or phenols. The transformation involves a one-pot reaction, which is operationally simple and mild and bereft of transition metal catalysts. This work provides a novel route for the preparation of diaryl ether derivatives.
Keyphrases
  • transition metal
  • fluorescent probe
  • structure activity relationship
  • ionic liquid
  • highly efficient
  • mass spectrometry
  • amino acid
  • high resolution
  • molecularly imprinted