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Copper-Catalyzed Aerobic Oxidative [3+2] Annulation for the Synthesis of 5-Amino/Imino-Substituted 1,2,4-Thiadiazoles through C-N/N-S Bond Formation.

Wentao YuYubing HuangJianxiao LiXiaodong TangWanqing WuHuan-Feng Jiang
Published in: The Journal of organic chemistry (2018)
A copper-catalyzed aerobic oxidative annulation reaction of 2-aminopyridine/amidine with isothiocyanate has been reported. This strategy involving C-N/N-S bond formations provides various 5-amino/imino-substituted 1,2,4-thiadiazole derivatives under a Cu/O2 catalytic system. This method has demonstrated high reactivity, mild reaction conditions, and a broad substrate scope. Furthermore, the synthetic utilities of the approach are demonstrated by further modifications.
Keyphrases
  • molecular docking
  • electron transfer
  • high intensity
  • transition metal
  • amino acid
  • metal organic framework