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Nucleophilic trifluoromethylthiolation of organoselenocyanates with trifluoromethanesulfenamide reagent: Access to CF3SSe-containing compounds
Journal of Fluorine Chemistry ( IF 1.9 ) Pub Date : 2018-03-19 , DOI: 10.1016/j.jfluchem.2018.03.009
Quentin Glenadel , Camille Ayad , Marc-Alexandre D’Elia , Thierry Billard , Fabien Toulgoat

Trifluoromethanesulfenamide reagent, initially designed as electrophilic reagent, can be considered as a trifluoromethylthio anion source in presence of tetrabutylammonium iodide. Herein, we report the reaction of trifluoromethanesulfenamide with organoselenocyanates to prepare under mild conditions compounds bearing a new fluorinated group, namely SeSCF3.



中文翻译:

用三氟甲烷亚磺酰胺试剂对有机硒酸酯进行亲核三氟甲基硫醇化:获得含CF 3 SSe的化合物

最初设计为亲电试剂的三氟甲亚磺酰胺试剂,在存在四丁基碘化铵的情况下,可以视为三氟甲硫基阴离子源。在这里,我们报告三氟甲亚磺酰胺与有机硒酸酯的反应,以在温和的条件下制备带有新的氟化基团,即SeSCF 3的化合物。

更新日期:2018-03-19
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