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Cu-Catalyzed Asymmetric Alkenylation of Enone Diesters with Trialkenylboroxines.

Kento YasumotoNoritaka KunitomoTaichi Kano
Published in: Organic letters (2023)
The Cu-catalyzed asymmetric conjugate addition of trialkenylboroxines to enone diesters is reported. This operationally simple and scalable reaction proceeded at room temperature, and a wide range of enone diesters and boroxines were tolerated under the applied reaction conditions. The practical utility of this approach was demonstrated via the formal synthesis of (+)-methylenolactocin. Mechanistic studies revealed that two different catalytic species work synergistically in the reaction.
Keyphrases
  • room temperature
  • ionic liquid
  • electron transfer
  • single cell
  • aqueous solution
  • solid state