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Phosphine-Catalyzed [3 + 2] Cycloaddition Reaction of α-Diazoacetates and β-Trifluoromethyl Enones: A Facile Access to Multisubstituted 4-(Trifluoromethyl)pyrazolines.

Yongfeng LiHuamin WangYuwei SuRunchen LiCao LiLu LiuJunliang Zhang
Published in: Organic letters (2018)
A novel phosphine-catalyzed [3 + 2] cycloaddition of α-diazoacetates and β-trifluoromethyl enones has been developed that provides facile access to multisubstituted 4-(trifluoromethyl)pyrazolines in good to excellent yields at room temperature. In addition, a tandem [3 + 2] cycloaddition/Michael addition is also presented.
Keyphrases
  • room temperature
  • ionic liquid
  • quantum dots
  • reduced graphene oxide
  • highly efficient
  • visible light