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Ni-Catalyzed Enantioselective Allylic Alkylation of H-Phosphinates.

Qing ZhangXu-Teng LiuYue WuQing-Wei Zhang
Published in: Organic letters (2021)
The asymmetric synthesis of P-stereogenic phosphinates through allylic alkylation of H-phosphinates has been developed. With H-phosphinates and allylic acetates as the starting materials, a variety of allylic P-chiral phosphinates were accessed in high enantioselectivities of up to 92% ee and generally high yields. In addition, a further study demonstrated the applicability of this protocol, including the scale-up synthesis and facile transformation of chiral products from phosphinates to phosphine oxides with organolithium reagents under mild reaction conditions.
Keyphrases
  • randomized controlled trial
  • ionic liquid
  • capillary electrophoresis
  • mass spectrometry
  • quantum dots
  • solid state