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Phosphine-Catalyzed Asymmetric Tandem Isomerization/Annulation of Allyl Amines with Allenoates: Enantioselective Annulation of a Saturated C-N Bond.

Leijie ZhouXue ZhangQijun WangMin LiuWei WangYongjun WuLiezhong ChenHongchao Guo
Published in: Organic letters (2021)
Under catalysis by chiral phosphine, an asymmetric isomerization/annulation cascade reaction of allylamines with allenoates was realized. A wide range of γ-substituted allenoates were tolerated to afford chiral pyrroline derivatives in high yields with excellent enantioselectivities. In the reaction, isomerization of readily available N-allylamines to reactive aliphatic imines through a 1,4-proton shift is a key step, which circumvents the isolation of highly unstable alkyl N-sulfonylimines.
Keyphrases
  • ionic liquid
  • electron transfer
  • capillary electrophoresis
  • room temperature
  • solid state
  • molecular docking
  • visible light
  • mass spectrometry