68820-09-7Relevant academic research and scientific papers
Pyrrolidines from olefins via radical cyclization
Gupta, Vijay,Besev, Magnus,Engman, Lars
, p. 2429 - 2432 (2007/10/03)
2,4-Disubstituted N-tosylpyrrolidines were prepared from olifeins via N- tosylaziridination, benseneselenolate ring-opening and reductive radical cyclization. Azidoselenation of olefins, followed by reduction, N-tosylation, N-allylation and reductive radical cyclization, afforded 3,4-disubstituted N- tosylpyrrolidines.
