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Gallium-Catalyzed Scriabine Reaction.

Manish PareekChristophe BourVincent Gandon
Published in: Organic letters (2018)
γ-Aryl enol acetates are easily obtained from diacetoxy alkenes and electron-rich arenes at room temperature using GaCl3 as catalyst. The products can then be converted into β-aryl aldehydes. This method represents the first broadly applicable catalytic version of the Scriabine reaction. DFT computations shed light on the mechanism of this transformation.
Keyphrases
  • room temperature
  • ionic liquid
  • electron transfer
  • crystal structure
  • density functional theory
  • psychometric properties
  • highly efficient