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Photocatalytic α-Acylation of Ethers.

Zhongdong SunNaoya KumagaiMasakatsu Shibasaki
Published in: Organic letters (2017)
Direct coupling of ethers and acyl halides was promoted by a binary catalytic system comprising an Ir-based photocatalyst and a Ni complex under blue-light irradiation. Photocatalysts with high triplet energy directed the catalysis, and the reaction likely proceeded by triplet-triplet energy transfer from the excited photocatalysts. Chlorine radicals generated from an excited Ni complex bearing a Ni-Cl bond would be responsible for generating α-oxy radicals leading to the α-acylated ethers.
Keyphrases
  • energy transfer
  • visible light
  • transition metal
  • quantum dots
  • metal organic framework
  • electron transfer
  • room temperature
  • ionic liquid
  • radiation induced
  • highly efficient