Login / Signup

Catalytic enantioselective Henry reaction of α-keto esters, 2-acylpyridines and 2-acylpyridine N -oxides.

Feilong HeGuanghui ChenJunxia YangGuojuan LiangPing DengYan XiongHui Zhou
Published in: RSC advances (2018)
A pre-prepared Ni-PyBisulidine complex has been developed for the catalytic asymmetric Henry reaction of α-keto esters, 2-acylpyridines and 2-acylpyridine N -oxides. The corresponding β-nitro-α-hydroxy esters were obtained in good to excellent yields (up to 99%) with a high enantiomeric excess (ee) (up to 94%) with a catalyst loading of 1-2 mol%. The desired products of 2-acylpyridines and 2-acylpyridine N -oxides, which were simple methyl ketones, were obtained in medium to excellent yields (up to 94%) with medium to good ee (up to 86%) by using 2 mol% of catalyst.
Keyphrases
  • metal organic framework
  • room temperature
  • ionic liquid
  • reduced graphene oxide
  • highly efficient
  • carbon dioxide
  • visible light
  • gold nanoparticles
  • electron transfer
  • capillary electrophoresis
  • transition metal