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Manganese(III)-promoted thiocarbonylation of alkylborates with disulfides: synthesis of aliphatic thioesters.

Bo ChenXiao-Feng Wu
Published in: Organic & biomolecular chemistry (2021)
A Mn(III)-promoted thiocarbonylation procedure toward the synthesis of thioesters has been developed. By employing easily available disulfides and potassium alkyltrifluoroborates as the starting materials, and cheap and non-toxic Mn(OAc)3·2H2O as the promotor, a broad range of thioesters were synthesized in good to excellent yields via radical intermediates.
Keyphrases
  • room temperature
  • metal organic framework
  • minimally invasive
  • ionic liquid