作者:Rina Arad-Yellin、Fred Wudl
DOI:10.1016/0022-328x(85)88092-x
日期:1985.1
Reactions of 4,5-dimethyl-1,2,3-selenadiazole with hexaalkylditins or trialkyltin anion followed by quenching with trialkyltin chloride affords only dimethylacetylene and bis(trimethyltin) selenide. Implications of these results in relation to possible syntheses of selenatellurafulvalenes are discussed.
4,5-二甲基-1,2,3-硒代二唑与六烷基二锡或三烷基锡阴离子反应,然后用三烷基氯化锡淬灭,仅得到二甲基乙炔和双(三甲基锡)硒化物。讨论了这些结果与硒代富呋喃烯的可能合成的关系。