Login / Signup

CuH-Catalyzed Asymmetric Intramolecular Reductive Coupling of Allenes to Enones.

Yun-Xuan TanXiao-Qi TangPing LiuDe-Shen KongYa-Li ChenPing TianGuo-Qiang Lin
Published in: Organic letters (2017)
The CuH-catalyzed asymmetric intramolecular reductive coupling of allenes to enones is successfully realized, providing cis-hydrobenzofurans with promising yields and excellent enantioselectivities. Such brilliant enantioselectivities are partially contributed by CuH-catalyzed favorable kinetic resolution of the cyclization products. This protocol tolerates a broad range of functional groups, allowing for further construction of tricyclic and bridged-ring structures. Moreover, the meta-chiral functionalization of 4-substituted phenol and asymmetric dearomatization modification of phenol-contained bioactive molecules are also described.
Keyphrases
  • room temperature
  • ionic liquid
  • solid state
  • randomized controlled trial
  • energy transfer
  • molecular docking
  • high resolution
  • single molecule
  • tissue engineering