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Asymmetric [3 + 1]-Cycloaddition Reaction via Diazo Discrimination.

Yong XuZhen WangJiangtao Sun
Published in: Organic letters (2021)
The enantioselective [3 + 1]-cycloaddition of two structurally different diazo compounds has been achieved using chiral bisoxazoline copper(I) complexes as a catalyst, providing a novel route for the synthesis of cyclobutenes containing a quaternary stereocenter. Typically, this reaction represents the first example of asymmetric cross-electrophile coupling of two diazo substrates via carbene discrimination.
Keyphrases
  • room temperature
  • ionic liquid
  • electron transfer
  • solid state
  • reduced graphene oxide
  • capillary electrophoresis
  • carbon dioxide
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  • mass spectrometry
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