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Stereodivergent Construction of 1,3-Chiral Centers via Tandem Asymmetric Conjugate Addition and Allylic Substitution Reaction.

Jia-Hao XieYi-Ming HouZuolijun FengShu-Li You
Published in: Angewandte Chemie (International ed. in English) (2023)
Herein, we report a synthesis of cyclohexanones bearing multi-continuous stereocenters by combining copper-catalyzed asymmetric conjugate addition of dialkylzinc reagents to cyclic enones with iridium-catalyzed asymmetric allylic substitution reaction. Good to excellent yields, diastereoselectivity and enantioselectivity can be obtained. Unlike the stereodivergent construction of adjacent stereocenters (1,2-position) reported in the literature, the current reaction can achieve the stereodivergent construction of nonadjacent stereocenters (1,3-position) by a proper combination of two chiral catalysts with different enantiomers.
Keyphrases
  • capillary electrophoresis
  • solid state
  • systematic review
  • ionic liquid
  • highly efficient
  • mass spectrometry
  • electron transfer
  • drug delivery