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Transition-Metal-Free Decarboxylation of 3,3,3-Trifluoro-2,2-dimethylpropanoic Acid for the Preparation of C(CF3)Me2-Containing Heteroarenes.

Shuai LiuYangen HuangFeng-Ling QingXiu-Hua Xu
Published in: Organic letters (2018)
The direct synthesis of C(CF3)Me2-substituted heteroarenes by decarboxylative 1,1-dimethyltrifluoroethylation of heteroarenes with 3,3,3-trifluoro-2,2-dimethylpropanoic acid is reported. This method does not need the transition-metal catalyst, and the base is crucial for this reaction. A series of previously unknown C(CF3)Me2-containing heteroarenes were obtained in high yields and have potential applications in the drug discovery process.
Keyphrases
  • transition metal
  • cystic fibrosis
  • drug discovery
  • room temperature
  • molecular docking
  • molecularly imprinted
  • risk assessment
  • mass spectrometry
  • tandem mass spectrometry
  • simultaneous determination