Cyclization of N-Butyl-4-pentenylaminyl: Implications for the Cyclization of Alkenylaminyl Radicals

BJ Maxwell, J Tsanaktsidis

Index: Maxwell, Brendan J.; Tsanaktsidis, John Journal of the American Chemical Society, 1996 , vol. 118, # 18 p. 4276 - 4283

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Citation Number: 23

Abstract

The utility of arenesulfenamides as aminyl radical precursors has been clearly demonstrated. The cyclization of N-butyl-4-pentenylaminyl is shown to be a slow and irreversible process that is accelerated significantly by small amounts of bis (tributyltin) oxide.