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Ni-Catalyzed Reductive Allylation of α-Chloroboronates to Access Homoallylic Boronates.

Yixian LouJian QiuKai YangFeng ZhangChenglan WangQiuling Song
Published in: Organic letters (2021)
The transition-metal-catalyzed allylation reaction is an efficient strategy for the construction of new carbon-carbon bonds alongside allyl or homoallylic functionalization. Herein we describe a Ni-catalyzed reductive allylation of α-chloroboronates to efficiently render the corresponding homoallylic boronates, which could be readily converted into valuable homoallylic alcohols or amines or 1,4-diboronates. This reaction features a broad substrate scope with good functional group compatibility that is complementary to the existing methods for the preparation of homoallylic boronates.
Keyphrases
  • transition metal
  • room temperature
  • molecularly imprinted
  • mass spectrometry
  • amino acid
  • electron transfer
  • liquid chromatography
  • tandem mass spectrometry