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Enantioselective Intermolecular Aminoalkynylation of Styrenes via Copper-Catalyzed Radical Relay.

Zhoumi HuLiang FuPinhong ChenWeiguo CaoGuosheng Liu
Published in: Organic letters (2020)
A novel copper-catalyzed intermolecular aminoalkynylation of alkenes through a radical relay process has been developed in this work, in which N-fluoro-N-alkylsulfonamides (NFASs) are used as nitrogen-centered radical precursors and alkynyltrimethoxysilanes as alkynylating reagents. This method presents an efficient and straightforward approach to various enantioenriched 2-alkynyl-2-arylethylamines in good yields with excellent enantioselectivity, and these products can be readily converted into a series of synthetically useful chiral terminal alkynes, allenes, alkenes, amines, amino acids, and N-heterocycles.
Keyphrases
  • amino acid
  • energy transfer
  • positron emission tomography
  • mass spectrometry
  • capillary electrophoresis