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- W1988359051 abstract "2,4-Disubstituted N-tosylpyrrolidines were prepared from olefins 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. 2,4-Disubstituted and 3,4-disubstituted N-tosylpyrrolidines were prepared from olefins." @default.
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- W1988359051 date "1998-04-01" @default.
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- W1988359051 title "Pyrrolidines from olefins via radical cyclization" @default.
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- W1988359051 doi "https://doi.org/10.1016/s0040-4039(98)00217-2" @default.
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