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Iridium-Catalyzed ortho-C-H Borylation of Thioanisole Derivatives Using Bipyridine-Type Ligand.

Jialin ZengMorio NaitoTakeru TorigoeMasahiro YamanakaYoichiro Kuninobu
Published in: Organic letters (2020)
A simple iridium catalytic system was developed that allows for a variety of 2-borylthioanisoles to be easily synthesized via ortho-selective C-H borylation of thioanisole derivatives. Once introduced, boryl and methylthio groups were converted by palladium-catalyzed transformations. Density functional theory calculations revealed that weak interactions, such as hydrogen bonding between the C-H bond of the SCH3 group and the oxygen atom of the boryl ligand, control the ortho-selectivity.
Keyphrases
  • density functional theory
  • molecular dynamics
  • structure activity relationship
  • single cell
  • room temperature
  • electron transfer
  • transition metal