4695-23-2Relevant academic research and scientific papers
Cycloaddition-elimination reactions of 5-Imino-1,2,4-thiadiazolidin-3-ones and 5-Imino-1,2,4-dithiazolidin-3-ones with electron-rich double bonds
Tittelbach, Franz,Vieth, Siegfried,Schneider, Matthias
, p. 515 - 520 (2007/10/03)
5-Imino-1,2,4-thiadiazolidin-3-ones 1 react with compounds containing electron-rich double bonds such as enamines and ester enolates to afford the 2-iminothiazolidines 3, 4, and 10 in cycloaddition-elimination reactions. The less reactive 5-imino-1,2,4-dithiazolidin-3-ones 2 only give the 2-iminothiazolidines 3 or 4 with enamines; with ester enolates the 5-alkylidene-1,2,4-dithiazolidines 12 are formed. The reaction products with enamines undergo hydrolysis and elimination to form the corresponding hydroxy compounds 5, 6 or the unsaturated compounds 7, 8, depending on the size of the fused ring.
