Rhodium(III)-Catalyzed C-C and C-O Coupling of Quinoline N-Oxides with Alkynes: Combination of C-H Activation with O-Atom Transfer

被引:183
作者
Zhang, Xueyun [1 ,2 ]
Qi, Zisong [1 ]
Li, Xingwei [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
[2] Qilu Univ Technol, Sch Chem & Pharmaceut Engn, Jinan 250353, Peoples R China
关键词
alkynes; C-H activation; heterocycles; N-oxides; rhodium; ISOQUINOLONE SYNTHESIS; OXIDATIVE ANNULATION; BOND FORMATION; ALKENYLATION; AMINATION; CLEAVAGE; STRATEGY; ALKENES; RH(III); OXYGEN;
D O I
10.1002/anie.201406747
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
[Cp* Rh-III]-catalyzed C-H activation of arenes assisted by an oxidizing N-O or N-N directing group has allowed the construction of a number of hetercycles. In contrast, a polar N-O bond is well-known to undergo O-atom transfer (OAT) to alkynes. Despite the liability of N-O bonds in both C-H activation and OAT, these two important areas evolved separately. In this report, [Cp* Rh-III] catalysts integrate both areas in an efficient redox-neutral coupling of quinoline N-oxides with alkynes to afford alpha-(8-quinolyl) acetophenones. In this process the N-O bond acts as both a directing group for C-H activation and as an O-atom donor.
引用
收藏
页码:10794 / 10798
页数:5
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