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Copper-Catalyzed Enantioselective Desymmetric Protosilylation of Prochiral Diynes: Access to Optically Functionalized Tertiary Alcohols.

Zhi-Yuan ChenMeng-Wei YangZi-Lu WangYun-He Xu
Published in: Organic letters (2023)
In this protocol, a copper-catalyzed desymmetric protosilylation of prochiral diynes was developed. The corresponding products were obtained in moderate to high yields and enantiomeric ratios. This approach provides a simple method for synthesizing functionalized chiral tertiary alcohols in the presence of a chiral pyridine-bisimidazoline (Pybim) ligand.
Keyphrases
  • capillary electrophoresis
  • quantum dots
  • mass spectrometry
  • ionic liquid
  • molecularly imprinted
  • randomized controlled trial
  • high intensity
  • high resolution
  • simultaneous determination