Rh(III)-Catalyzed intramolecular redox-neutral cyclization of alkenes via C-H activation

被引:97
|
作者
Shi, Zhuangzhi [1 ]
Boultadakis-Arapinis, Melissa [1 ]
Koester, Dennis C. [1 ]
Glorius, Frank [1 ]
机构
[1] Univ Munster, Inst Organ Chem, D-48149 Munster, Germany
基金
欧洲研究理事会;
关键词
AROMATIC IMINES; EFFICIENT SYNTHESIS; BOND ACTIVATION; ANNULATION; INDOLIZIDINE; HYDROARYLATION; AGONIST; ALKYNES; ACID;
D O I
10.1039/c4cc00029c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Biologically interesting fused oligocyclic lactams have been prepared via an intramolecular redox-neutral cyclization process. By the proper choice of the substrates with a wide variety of tethered olefins, the less favored C-H bond can be activated and functionalized. This C-H activation proceeds under mild conditions, obviates the need for external oxidants, and displays a broad scope with respect to the substituents.
引用
收藏
页码:2650 / 2652
页数:3
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