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Silver-Catalyzed Asymmetric Desymmetrization of Cyclohexadienones via Van Leusen Pyrrole Synthesis.

Mohamed Ahmed AbozeidHun Young KimKyungsoo Oh
Published in: Organic letters (2022)
A catalytic asymmetric desymmetrization of cyclohexadienones was accomplished via Van Leusen pyrrole synthesis in the presence of a chiral silver catalyst. The ready access to chiral-fused pyrrole derivatives is attributed to the identification of a suitable isocyanomethyl sulfone surrogate, NasMIC. The current Ag(I)-chiral phosphino-carboamide ligand system can be extended to the kinetic resolution of racemic cyclohexadienones, capitalizing on the differentiated reactivity of chiral quaternary complexes from AgSbF 6 , chiral ligand ( L *), cyclohexadienone, and NasMIC.
Keyphrases
  • ionic liquid
  • capillary electrophoresis
  • gold nanoparticles
  • room temperature
  • mass spectrometry
  • highly efficient
  • quantum dots
  • silver nanoparticles
  • single molecule
  • solid state
  • carbon dioxide
  • visible light