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Enantioselective Pictet-Spengler Reaction of Acyclic α-Ketoesters Using Chiral Imidazoline-Phosphoric Acid Catalysts.

Shuichi NakamuraYoichiro MatsudaTsunayoshi TakeharaTakeyuki Suzuki
Published in: Organic letters (2022)
The first enantioselective Pictet-Spengler reaction of acyclic α-ketoesters with tryptamines has been developed. Excellent yields and enantioselectivity were obtained for the reaction using chiral imidazoline-phosphoric acid catalysts. Density functional theory calculations suggested possible transition states that explain the origin of chiral induction. This process provides an efficient route for the synthesis of tetrahydro-β-carboline derivatives.
Keyphrases
  • density functional theory
  • molecular dynamics
  • capillary electrophoresis
  • ionic liquid
  • highly efficient
  • electron transfer
  • metal organic framework
  • monte carlo