92014-03-4Relevant academic research and scientific papers
Reaction of 1,2,3-Benzothiadiazoles with Radicophilic Alkenes and Alkynes in Di-tert-butyl Peroxide.
Albertazzi, A.,Leardini, R.,Pedulli, G.F.,Tundo, A.,Zanardi, G.
, p. 4482 - 4486 (2007/10/02)
The reaction of 6-X-1,2,3-benzothiadiazoles (1) with the radicophilic alkenes 1,1-diphenylethylene (2) and 1-cyano-1-(tert-butylthio)ethylene (3) and the alkynes PhCCR (4, R=H or Ph) in di-tert-butyl peroxide (TBP) leads to the cycloadducts 5, 7, and 8.The proposed mechanism involves an initial attack by tert-butoxy radical at the sulfur atom of 1 affording the radical intermediate 9 which is responsible for the formation of all the reaction products.
