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A Cu-BOX catalysed enantioselective Mukaiyama-aldol reaction with difluorinated silyl enol ethers and acylpyridine N -oxides.

Amparo Sanz-MarcoDaniel EsperillaMarc Montesinos-MagranerCarlos VilaM Carmen MuñozJosé R PedroGonzalo Blay
Published in: Organic & biomolecular chemistry (2022)
A Cu(II)/BOX complex catalyses the enantioselective addition of difluorinated silyl enol ethers to acylpyridine N -oxides. The reaction provides difluorinated chiral tertiary alcohols of great interest in medicinal chemistry. These compounds are obtained in moderate to excellent yields and with high enantioselectivities. The stereochemical outcome of the reaction has been explained by DFT calculations.
Keyphrases
  • density functional theory
  • transcription factor
  • binding protein
  • electron transfer
  • high intensity
  • molecular dynamics simulations
  • aqueous solution
  • metal organic framework
  • molecular docking
  • drug discovery