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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Doi:10.1139/v74-496
(1974)Doi:10.1016/S0008-6215(00)81199-4
(1968)Doi:10.1021/ic9716161
(1998)Doi:10.1021/jm00287a007
(1971)Doi:10.1016/S0040-4039(98)02486-1
(1999)Doi:10.1248/cpb.22.2108
(1974)
