Palladium-Catalyzed Intermolecular C(sp3)-H Amidation

被引:218
作者
Iglesias, Alvaro [2 ]
Alvarez, Rosana [1 ]
de Lera, Angel R. [1 ]
Muniz, Kilian [2 ,3 ]
机构
[1] Univ Vigo, Dept Organ Chem, Vigo 36315, Spain
[2] Inst Chem Res Catalonia ICIQ, Tarragona 43007, Spain
[3] Catalan Inst Res & Adv Studies ICREA, Barcelona 08010, Spain
关键词
amidation; C?H activation; homogeneous catalysis; oxidation; palladium; C-H AMINATION; FORMING REDUCTIVE ELIMINATION; AEROBIC OXIDATIVE AMINATION; TERMINAL ALKENES; BOND-FORMATION; MECHANISM; DIAMINATION; REACTIVITY; COMPLEXES; CARBON;
D O I
10.1002/anie.201108351
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Dual capacity: A new palladium-catalyzed intermolecular sequence consisting of the C-H activation and amidation of methyl groups relies on N-fluorobis(phenylsulfonyl)imide (NFSI) as both the oxidant and the nitrogen source. The reaction provides the corresponding arylamines as bissulfonimides along with HF as the only by-product. Both experimental and computational results suggest the involvement of a monomeric palladium(IV) intermediate. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
引用
收藏
页码:2225 / 2228
页数:4
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