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Enantioselective Synthesis of Chiral Phosphonates via Rh/f-spiroPhos Catalyzed Asymmetric Hydrogenation of β,β-Disubstituted Unsaturated Phosphonates.

Chaoqiong WangFang XieQianling GuoChaochao XieGuofu ZiWeiping YeZhangtao ZhouGuohua HouZhanbin Zhang
Published in: The Journal of organic chemistry (2021)
The first asymmetric hydrogenation of β,β-diaryl unsaturated phosphonates has been realized for synthesis of β,β-diaryl chiral phosphonates with excellent enantioselectivities (up to 99.9% ee) catalyzed by the Rh-(R,R)-f-spiroPhos complex. Furthermore, this catalyst also exhibits comparably excellent performance for β-aryl-β-alkyl unsaturated phosphonates providing the corresponding chiral phosphonates with up to 99.9% ee values. This methodology provides a straightforward access to asymmetric synthesis of chiral phosphonates.
Keyphrases
  • ionic liquid
  • room temperature
  • capillary electrophoresis
  • mass spectrometry
  • carbon dioxide