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Iodine(III)-Mediated Intermolecular Allylic Amination under Metal-Free Conditions

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NIAID Data Ecosystem2026-03-07 收录
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https://figshare.com/articles/dataset/Iodine_III_Mediated_Intermolecular_Allylic_Amination_under_Metal_Free_Conditions/2526751
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资源简介:
A new approach to direct intermolecular allylic amination has been developed using metal-free conditions at room temperature. The reaction employs a hypervalent iodine­(III) reagent as an oxidant and bistosylimide as a nitrogen source. A series of different allylic aminations are presented with up to a 99% yield. Mechanistic studies including isotope labeling and Hammett correlation suggest that depending on the substrate structure two different mechanisms can be operating.
创建时间:
2016-02-21
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