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Photoinduced Deaminative Borylation of Unreactive Aromatic Amines Enhanced by CO2.

Akira ShiozukaKohei SekineYoichiro Kuninobu
Published in: Organic letters (2021)
Herein, direct unreactive C-N borylation of aromatic amines by a photocatalyst was achieved. The C-N borylation of aromatic amines with bis(pinacolato)diboron (B2pin2) proceeded using a pyrene catalyst under light irradiation to afford desired borylated products and aminoborane as a byproduct. The yield of the borylated product improved under a CO2 atmosphere which probably reduced the inhibitory effect of aminoborane. Mechanistic studies suggested that the C-N bond cleavage and C-B bond formation proceeded via a concerted pathway.
Keyphrases
  • amino acid
  • ionic liquid
  • highly efficient
  • visible light
  • electron transfer
  • room temperature
  • case control
  • gold nanoparticles
  • transition metal
  • dna binding
  • transcription factor
  • metal organic framework
  • carbon dioxide