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Catalytic Asymmetric Synthesis of 3,4'-Piperidinoyl Spirooxindoles via [3 + 3] Annulation of 3-Aminobenzofurans and Isatin-Derived Enals.

Lesong LiCongyang LiShuting ZhangXuerui WangPeng FuYang Wang
Published in: The Journal of organic chemistry (2024)
A chiral NHC-catalyzed [3 + 3] cycloaddition reaction of 3-aminobenzofurans with isatin-derived enals has been documented, furnishing 3,4'-piperidinoyl spirooxindoles bearing a quaternary stereocenter with good yields and excellent enantioselectivities. Further gram-scale preparation and synthetic transformation of the cycloadducts to δ-amino acid derivative demonstrated good practicality and applicability of this reaction.
Keyphrases
  • amino acid
  • gram negative
  • room temperature
  • ionic liquid
  • molecularly imprinted
  • capillary electrophoresis
  • mass spectrometry
  • electron transfer
  • high resolution
  • solid state
  • water soluble