The title compounds have been prepared from the reaction of trifluoromethylthiocopper and alkyl mono- and di-haloarsines. This communication describes their synthesis, biological screening and mass spectral fragmentation behavior.
标题化合物是由三
氟甲基
硫代
铜与烷基单和二卤代s啶反应制得的。该交流描述了它们的合成,
生物学筛选和质谱碎片化行为。