Abstract
(Chemical Equation Presented) Radical transfer hydroaminations have been achieved with 3-aminated 1,4-cyclohexadienes rather than transition-metal reagents (see scheme; DTBP = di-tert-butylperoxide). These functionalized cyclohexadienes are efficient N-radical precursors. Moreover, they are stable and readily prepared, and radical generation occurs under neutral conditions. © 2005 Wiley-VCH Verlag GmbH & Co. KGaA.
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Kemper, J., & Studer, A. (2005). Stable reagents for the generation of N-centered radicals: Hydroamination of norbornene. Angewandte Chemie - International Edition, 44(31), 4914–4917. https://doi.org/10.1002/anie.200463032
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