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Copper-Catalyzed Asymmetric Boroprotonation of Phosphinylallenes.

Huijun LiLong ChengGuiqin LiTongyu XuShengjun ZhangFanlong Zeng
Published in: Organic letters (2023)
Synthesis of chiral phosphorus compounds from readily available substrates by a facile method is an attractive strategy. In this study, an efficient route for copper-catalyzed asymmetric boroprotonation of phosphinylallenes with bis(pinacolato)diboron with high regioselectivity was developed, affording chiral allylphosphine oxides in high yields with high enantioselectivities of up to 98% ee. The synthetic utility was further demonstrated by the facile transformation of the chiral allylphosphine oxides to several stereospecific products.
Keyphrases
  • ionic liquid
  • capillary electrophoresis
  • quantum dots
  • reduced graphene oxide
  • mass spectrometry
  • risk assessment
  • metal organic framework
  • heavy metals