57239-46-0Relevant academic research and scientific papers
Solvent free nucleophilic selenocyanation with [bmim][SeCN]. Direct access to perfluoroalkylselenide compounds
De-Zordo Banliat, Arnaud,Grollier, Kévin,Damond, Aurélie,Billard, Thierry,Dagousset, Guillaume,Magnier, Emmanuel,Pégot, Bruce
, (2021/11/08)
Available online-1-n-butyl-3-methylimidazolium selenocyanate ([bmim][SeCN]) proved to be a very efficient reagent for selenocyanation of alkyl halides. As part of an eco-friendly process, no organic solvents were used during the transformation and reaction times are reduced by using microwave as a heating source. The ionic liquid was carefully recycled in two different ways. Selenocyanate compounds were successfully transformed into trifluoromethylselenides in a one-pot two step procedure.
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),
