Login / Signup

Synthesis of Unsymmetric Thiosulfonates Starting from N-Substituted O -Thiocarbamates: Easy Access to the S-SO 2 Bond.

Cheng-Li YangXue-Jie GaoXin-Yi JiangZhen ShiEr-Jun HaoZhi-Bing Dong
Published in: The Journal of organic chemistry (2022)
Using phenyliodine diacetate as an oxidant and nickel acetate as a promoter, a wide range of unsymmetric thiosulfonates could be furnished easily in moderate to excellent yields starting from N-substituted O -thiocarbamates and sodium sulfinates. This protocol features mild conditions, short reaction times, and high atomic utilization, which can provide an alternative method for the synthesis of unsymmetric thiosulfonates. In addition, the reaction could be scaled up on a gram scale, showing potential application value in industry.
Keyphrases
  • molecular docking
  • randomized controlled trial
  • dna methylation
  • gene expression
  • transcription factor
  • electron transfer
  • high intensity
  • reduced graphene oxide
  • molecular dynamics simulations