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Access to Chiral β-Boryl δ-Lactones via NHC-Catalyzed [4 + 2] Annulation.

Zhipeng LiJingyang ZhangJian Wang
Published in: Organic letters (2024)
We report a carbene-catalyzed [4 + 2] annulation of activated esters and β-borate enones, providing an efficient method to build enantioenriched organoborones with two consecutive stereogenic centers. It is worth noting that this protocol represents a new organocatalytic manner to generate chiral β-C-B bonds. Moreover, it also greatly enriches the structural diversity of the chiral organoboron compounds.
Keyphrases
  • capillary electrophoresis
  • ionic liquid
  • room temperature
  • randomized controlled trial
  • mass spectrometry