S. Kabashima, T. Okawara, T. Yamasaki
Dec 1, 1991
Citations
0
Influential Citations
12
Citations
Journal
Journal of Heterocyclic Chemistry
Abstract
Chlorocarbonylsulfenyl chloride was allowed to react with 1-alkylidene-4-phenylthiosemicarbazones in the presence of triethylamine to give 1,2,4-triazolines, whereas with 1-arylidene-4-phenylthiosemicarbazones to afford 1,2,4-dithiazolidines. Treatment of diarylidenethiocarbohydrazides and diarylidenaminoguanidines with chlorocarbonylsulfenyl chloride under similar conditions gave 1,2,4-dithiazolidines and 1,2,4-thiadiazolidines, respectively.