Olefin Oxyamination with Unfunctionalized N-Alkylanilines

被引:10
|
作者
Gao, Shuang [1 ]
Niggeman, Meike [1 ]
机构
[1] Rhein Westfal TH Aachen, Inst Organ Chem, Landoltweg 1, D-52074 Aachen, Germany
关键词
N-centered radicals; aminium radical cations; olefin oxyamination; oxidation of secondary amines; C-N bond formation; LIGHT PHOTOREDOX CATALYSIS; ALPHA-AMINOALKYL RADICALS; CENTERED RADICALS; RECENT PROGRESS; RATE CONSTANTS; GENERATION; FUNCTIONALIZATION; METHODOLOGY; HYDRAZONYL; CHEMISTRY;
D O I
10.1002/adsc.201801407
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
N-Alkylanilines have rarely been used in oxyamination reactions, due to the normally necessary pre-functionalization of the N-atom. Also, the formation of aminium radical cations (ARCs) of anilines bearing alkyl substituents is plagued by the ARC's tendency to instantaneously convert to alpha-amino radicals or iminium ions. We present a readily available reagent combination that addresses both challenges, and thus allows for an oxyamination with N-alkylanilines via ARCs as the crucial reactive intermediates and excellent diastereoselectivity.
引用
收藏
页码:1549 / 1553
页数:5
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