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Highly Diastereo- and Enantioselective Access to syn-α-Amido β-Hydroxy Esters via Ruthenium-Catalyzed Dynamic Kinetic Resolution-Asymmetric Hydrogenation.

Bin LuXiaoyu WuChengyang LiGuangni DingWanfang LiXiaomin XieZhao-Guo Zhang
Published in: The Journal of organic chemistry (2019)
Dynamic kinetic resolution (DKR) of racemic aryl α-amino β-ketoesters via Ru-diphosphine-catalyzed asymmetric hydrogenation was realized at 70 °C under 50 atm of hydrogen, affording syn α-amido β-hydroxy esters in high yields (up to 96%) with high reactivity (TON up to 940) and diastereo- and enantioselectivities (up to 99:1 dr, 98% ee). These hydrogenation products provide valuable chiral synthons in many natural products and pharmaceuticals. Gram-scale DKR asymmetric hydrogenation (DKR-AH) was also performed with retained reactivity and stereoselectivity, revealing the synthetic utility of this method.
Keyphrases
  • room temperature
  • solid state
  • single molecule
  • dna damage
  • gram negative
  • ionic liquid
  • oxidative stress
  • multidrug resistant
  • capillary electrophoresis
  • quantum dots