Tetrahedron Letters p. 2429 - 2432 (1998)
Update date:2022-08-05
Topics:
Gupta, Vijay
Besev, Magnus
Engman, Lars
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.
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