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Iridium-Catalyzed Asymmetric Transfer Hydrogenation of Alkynyl Ketones Using Sodium Formate and Ethanol as Hydrogen Sources.

Yang-Ming ZhangMing-Lei YuanWei-Peng LiuJian-Hua XieQi-Lin Zhou
Published in: Organic letters (2018)
A green and efficient iridium-catalyzed asymmetric transfer hydrogenation of alkynyl ketones to chiral propargylic alcohols has been developed. By using sodium formate and ethanol as hydrogen sources, a series of alkynyl ketones were hydrogenated by chiral spiro iridium catalyst ( S)-1b to provide optically active chiral propargylic alcohols with up to 98% ee under base-free conditions. This protocol provides a practical and sustainable method for the preparation of optically active propargylic alcohols.
Keyphrases
  • ionic liquid
  • room temperature
  • capillary electrophoresis
  • drinking water
  • visible light
  • randomized controlled trial
  • mass spectrometry
  • solid state
  • carbon dioxide
  • electron transfer