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Enantioselective Synthesis of Medium-Sized-Ring Lactones via Iridium-Catalyzed Z -Retentive Asymmetric Allylic Substitution Reaction.

Lu DingHao SongChao ZhengShu-Li You
Published in: Journal of the American Chemical Society (2022)
Medium-sized rings are important structural units, but their synthesis, especially in a highly enantioselective manner, has been a great challenge. Herein we report an enantioselective synthesis of medium-sized-ring lactones by an iridium-catalyzed Z -retentive asymmetric allylic substitution reaction. The reaction features mild conditions and a broad substrate scope. Various eight- to 11-membered-ring lactones can be afforded in moderate to excellent yields (up to 88%) and excellent enantioselectivity (up to 99% ee). The utilization of both Z -allyl precursors and an Ir catalyst is critical for the medium-sized-ring formation.
Keyphrases
  • room temperature
  • ionic liquid
  • high intensity
  • electron transfer
  • amino acid