Login / Signup

Asymmetric Reductive Amination with Pinacolborane Catalyzed by Chiral SPINOL Borophosphates.

Zhenwei WuHualing HeMinglei ChenLinfei ZhuWeitao ZhengYang CaoJon C Antilla
Published in: Organic letters (2022)
The catalytic asymmetric reductive amination of ketones with pinacolborane employing chiral SPINOL-derived borophosphates as catalysts has been realized. A series of chiral amine derivatives bearing multiple functional groups were obtained in good to excellent yields and enantioselectivities (up to 97% yield, 98% ee) under mild reaction conditions. Moreover, the synthetic applicability of the established method has been demonstrated by the asymmetric synthesis of ( R )-Fendiline.
Keyphrases
  • capillary electrophoresis
  • ionic liquid
  • solid state
  • room temperature
  • highly efficient
  • transition metal