20138-73-2Relevant articles and documents
Electrochemical Oxidative C-H Thiocyanation or Selenocyanation of Imidazopyridines and Arenes
Cui, Ting,Zhang, Xiaofeng,Lin, Jun,Zhu, Zitong,Liu, Ping,Sun, Peipei
, p. 267 - 272 (2021)
Regioselective electrochemical oxidative C-H thiocyanation or selenocyanation of imidazopyridines was achieved by using an undivided electrolytic cell. Transition-metal-and oxidant-free conditions are striking features of this protocol. A library of thioc
Electrochemical Oxidative C-H Thiocyanation or Selenocyanation of Imidazopyridines and Arenes
Cui, Ting,Lin, Jun,Liu, Ping,Sun, Peipei,Zhang, Xiaofeng,Zhu, Zitong
, (2020)
Regioselective electrochemical oxidative C-H thiocyanation or selenocyanation of imidazopyridines was achieved by using an undivided electrolytic cell. Transition-metal- A nd oxidant-free conditions are striking features of this protocol. A library of thi
Catalyst and additive-free regioselective oxidative C-H thio/selenocyanation of arenes and heteroarenes with elemental sulfur/selenium and TMSCN
Feng, Chengtao,Peng, Ya,Ding, Guangrong,Li, Xiangxiao,Cui, Chang,Yan, Yizhe
supporting information, p. 13367 - 13370 (2018/12/13)
A regioselective oxidative C-H thio/selenocyanation of arenes and heteroarenes with TMSCN and elemental sulfur/selenium was demonstrated under catalyst-free and additive-free conditions. Dimethyl sulfoxide (DMSO) was employed as the mild oxidant as well as the solvent. The reaction is operationally simple and scalable with a broad substrate scope.
