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CuI-Catalyzed Asymmetric [3 + 2] Cycloaddition of Azomethine Ylides with Cyclobutenones.

Javier CorpasAlberto PonceJavier AdrioJuan C Carretero
Published in: Organic letters (2018)
The catalytic asymmetric 1,3-dipolar cycloaddition of cyclobutenones with azomethine ylides provides straightforward access to densely substituted 3-azabicyclo[3.2.0]heptanes. In the presence of CuI/(R)-Fesulphos as the catalytic system, high levels of diastereoselectivity and enantioselectivity were achieved (up to 98% enantiomeric excess (ee)).
Keyphrases
  • solid state
  • crystal structure
  • molecular docking
  • room temperature
  • capillary electrophoresis
  • mass spectrometry