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Application of Oxazaborolidine Catalysts (CBS) on Enantioselective 1,4-Addition of Diarylphosphine Oxides to α,β-Unsaturated Thioesters.

Yinrui ShiLirong ChenQi GaoJiuling LiYafei GuoBaomin Fan
Published in: Organic letters (2023)
Here, we report the first catalytic enantioselective 1,4-addition of diarylphosphine oxides to α,β-unsaturated thioesters. Importantly, the most common and commercial oxazaborolidine (CBS) was employed as a catalyst for its new application without being activated by strong protonic acids or Lewis acids and led to the chiral thioesters in excellent yields and enantioselectivities. Furthermore, this method features mild reaction conditions (room temperature and air-insensitive), good substrate tolerance, and easy scalability.
Keyphrases
  • room temperature
  • ionic liquid
  • highly efficient
  • metal organic framework
  • amino acid
  • transition metal
  • electron transfer