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Recyclable fluorous cinchona organocatalysts for asymmetric synthesis of biologically interesting compounds.

Xin HuangWei Zhang
Published in: Chemical communications (Cambridge, England) (2021)
Organocatalysis has unique modes of activation, mild reaction conditions, and good catalyst structural amenability. The integration of green techniques such as catalyst recovery and one-pot reactions makes organocatalysis more efficient and attractive. Presented in this article are the recyclable cinchona alkaloid-catalyzed reactions including fluorination and Michael addition-initiated cascade reactions in asymmetric synthesis of functionalized compounds of biological interest.
Keyphrases
  • room temperature
  • ionic liquid
  • reduced graphene oxide
  • highly efficient
  • carbon dioxide
  • metal organic framework
  • quantum dots
  • solid state
  • mass spectrometry
  • molecularly imprinted