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Phosphinoyl Radical-Initiated 1,2-Bifunctional Thiocyanodiphenylphosphinoylation of Alkenes.

Ze-Kun TaoCheng-Kun LiPei-Zhi ZhangAdedamola ShoberuJian-Ping ZouWei Zhang
Published in: The Journal of organic chemistry (2018)
1,2-Bifuctional thiocyanodiphenylphosphinoylation of alkenes is established through the phosphinoyl radical addition followed by Cu-catalyzed thiocyanation. This one-pot reaction is applicable to a range of aromatic, aliphatic, and cyclic alkenes to afford thiocyanodiphenylphosphinoylated compounds in satisfactory yields.
Keyphrases
  • room temperature
  • amino acid
  • aqueous solution