21731-34-0Relevant academic research and scientific papers
Metal-Free Thiocyanation of Imidazoheterocycles through Visible Light Photoredox Catalysis
Mitra, Shubhanjan,Ghosh, Monoranjan,Mishra, Subhajit,Hajra, Alakananda
, p. 8275 - 8281 (2015)
A visible light mediated, metal-free process for the thiocyanation of imidazoheterocycles has been developed using eosin Y as a photoredox catalyst under ambient air at room temperature. A library of 3-(thiocyanato)imidazo[1,2-a]pyridines with broad funct
Electrochemical Oxidative C-H Thiocyanation or Selenocyanation of Imidazopyridines and Arenes
Cui, Ting,Zhang, Xiaofeng,Lin, Jun,Zhu, Zitong,Liu, Ping,Sun, Peipei
supporting information, p. 267 - 272 (2021/02/03)
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
supporting information, (2020/12/01)
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
Investigation on the effects of antimicrobial imidazo[2,1-b]Thiazole derivatives on the genitourinary microflora
Morigi, Rita,Vitali, Beatrice,Prata, Cecilia,Palomino, Rogers A. ?.,Graziadio, Alessandra,Locatelli, Alessandra,Rambald, Mirella,Leoni, Alberto
, p. 311 - 319 (2018/05/17)
Background: Fused five-membered heterocyclic rings containing bridgehead nitrogen atom are particularly versatile in the field of medicinal chemistry because of their different biological activities. Among them, the imidazo[2,1-b]thiazole is an attractive
Highly Efficient and Practical Thiocyanation of Imidazopyridines Using an N-Chlorosuccinimide/NaSCN Combination
Zhang, Hailei,Wei, Qian,Wei, Shiqiang,Qu, Jingping,Wang, Baomin
, p. 3373 - 3379 (2016/07/23)
A direct C–H thiocyanation of imidazo[1,2-a]pyridines, and a practical sequential one-pot condensation/C–H thiocyanation process, using a combination of N-chlorosuccinimide/NaSCN for the synthesis of 3-thiocyanatoimidazo[1,2-a]pyridines have been develope
