57239-52-8Relevant academic research and scientific papers
Synthesis of Monofluoromethyl Selenoethers of Aryl and Alkyl from Organoselenocyanate via One-Pot Reaction
Cao, Yuan,Jiang, Lvqi,Yi, Wenbin
supporting information, p. 4360 - 4368 (2019/08/01)
The first practical and feasible approach for the monofluoromethylselenolation of aryl and alkyl halides via one-pot multistep synthesis using KSeCN and ICFH2 is described. Good yields and broad functional group compatibility were obtained. The successful preparation of monofluoromethylselenolated drug-like compounds good practicability of this method. This protocol offered a number of new monofluoromethyl selenoethers, which would accelerate the use of such compounds in the areas of life science. (Figure presented.).
Pronounced activity of aromatic selenocyanates against multidrug resistant ESKAPE bacteria
Nasim, Muhammad Jawad,Witek, Karolina,Kincses, Annamária,Abdin, Ahmad Yaman,?es?awska, Ewa,Mar?, Ma?gorzata Anna,Gajdács, Márió,Spengler, Gabriella,Nitek, Wojciech,Latacz, Gniewomir,Karczewska, El?bieta,Kie?-Kononowicz, Katarzyna,Handzlik, Jadwiga,Jacob, Claus
supporting information, p. 6021 - 6031 (2019/04/16)
Selenocyanates represent an interesting class of organic selenium compounds. Due to their similarity with better known natural (iso-)thiocyanates, they promise high biological activity and may also be metabolized to other Reactive Selenium Species (RSeS),
Selenocyanates and diselenides: A new class of potent antileishmanial agents
Plano, Daniel,Baquedano, Ylenia,Moreno-Mateos, David,Font, María,Jiménez-Ruiz, Antonio,Palop, Juan Antonio,Sanmartín, Carmen
experimental part, p. 3315 - 3323 (2011/08/03)
Thirty five selenocyanate and diselenide compounds were subjected to in vitro screening against Leishmania infantum promastigotes and the most active ones were also tested in an axenic amastigote model. In order to establish the selectivity indexes (SI) t
