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Asymmetric 1,4-Addition of Diarylphosphine Oxides to α, β-Unsaturated 2-Acyl Imidazoles.

Lirong ChenGuiyong WangXiufei NongWendi ShaoJiuling LiYafei GuoBaomin Fan
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2024)
Here we introduce a metal-free, catalytic and enantioselective strategy from α,β-unsaturated 2-acyl imidazoles to the chiral phosphorous 2-acyl imidazoles. Interestingly, this methodology was catalyzed by the classical and commercial oxazaborolidine under mild conditions. This strategy features a wide range of substrates scope with good yields and excellent enantioselectivities. The possible mechanism further suggests the key of this reaction through the cleavage of diarylphosphine oxides using Frustrated Lewis Pairs theory.
Keyphrases
  • fatty acid
  • room temperature
  • ionic liquid
  • dna binding
  • capillary electrophoresis
  • mass spectrometry