Multiple Halogenation of Aliphatic C-H Bonds within the Hofmann-Loffler Manifold

被引:19
作者
Del Castillo, Estefania [1 ]
Martinez, Mario D. [1 ]
Bosnidou, Alexandra E. [1 ]
Duhamel, Thomas [1 ,2 ]
O'Broin, Calvin Q. [1 ]
Zhang, Hongwei [1 ]
Escudero-Adan, Eduardo C. [1 ]
Martinez-Belmonte, Marta [1 ]
Muniz, Kilian [1 ,3 ]
机构
[1] Barcelona Inst Sci & Technol, Inst Chem Res Catalonia ICIQ, Ave Paisos Catalans 16, Tarragona 43007, Spain
[2] Univ Oviedo, Fac Quim, E-33006 Oviedo, Spain
[3] Catalan Inst Res & Adv Studies ICREA, Pg Lluis Co 23, Barcelona 08010, Spain
关键词
bromine; C-H functionalization; Hofmann-Loffler reaction; iodine; polyhalogenation; AMINATION; IODINE; BROMINATION; IODINATION; FUNCTIONALIZATION; DICHLORINATION; CHEMISTRY; CATALYSIS; RADICALS; IODIDES;
D O I
10.1002/chem.201804504
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An innovative approach to position-selective polyhalogenation of aliphatic hydrocarbon bonds is presented. The reaction proceeded within the Hofmann-Loffler manifold with amidyl radicals as the sole mediators to induce selective 1,5- and 1,6-hydrogen-atom transfer followed by halogenation. Multiple halogenation events of up to four innate C-H bond functionalizations were accomplished. The broad applicability of this new entry into polyhalogenation and the resulting synthetic possibilities were demonstrated for a total of 27 different examples including mixed halogenations.
引用
收藏
页码:17225 / 17229
页数:5
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