Login / Signup

Organocatalytic diastereo- and enantioselective conjugate addition of pyrazol-3-ones to 3-trifluoroethylidene oxindoles with a newly developed squaramide catalyst.

Zhao HanJiaping JinAlemayehu Gashaw WoldegiorgisXu-Feng Lin
Published in: RSC advances (2022)
An efficient organocatalytic conjugated addition reaction of pyrazol-3-ones with 3-trifluoroethylidene oxindoles has been developed for the synthesis of enantioenriched triflouromethylated indolin-2-ones bearing adjacent tertiary chiral centers in good yields and good to excellent diastereo- and enantioselectivities. The use of a newly developed chiral spirobiindane-derived squaramide catalyst is essential in achieving high diastereo- and enantioselectivities.
Keyphrases
  • ionic liquid
  • room temperature
  • highly efficient
  • reduced graphene oxide
  • capillary electrophoresis
  • carbon dioxide
  • metal organic framework
  • cancer therapy
  • gold nanoparticles
  • drug delivery