中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Rhenium and base co-catalyzed [3+2] annulations of N-H ketimines and alkynes to access unprotected tertiary indenamines through C-H bond activation

文献类型:期刊论文

作者Jin, Xiqing; Yang, Xiaoxu; Yang, Yunhui; Wang, Congyang
刊名ORGANIC CHEMISTRY FRONTIERS
出版日期2016
卷号3期号:2页码:268-272
英文摘要Herein, a rhenium-catalyzed [3 + 2] carbocyclization of N-H ketimines and alkynes through C-H bond activation to afford unprotected tertiary indenamines is described. Notably, the catalytic use of a cheap base, sodium carbonate, was demonstrated to be crucial to the success of this reaction. The protocol is also highlighted by a high atom-economy, a broad substrate scope, and excellent regioselectivity for unsymmetrical alkynes.
收录类别SCI
语种英语
公开日期2016-05-03
源URL[http://ir.iccas.ac.cn/handle/121111/30135]  
专题化学研究所_分子识别与功能实验室
作者单位Chinese Acad Sci, Inst Chem, CAS Key Lab Mol Recognit & Funct, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
推荐引用方式
GB/T 7714
Jin, Xiqing,Yang, Xiaoxu,Yang, Yunhui,et al. Rhenium and base co-catalyzed [3+2] annulations of N-H ketimines and alkynes to access unprotected tertiary indenamines through C-H bond activation[J]. ORGANIC CHEMISTRY FRONTIERS,2016,3(2):268-272.
APA Jin, Xiqing,Yang, Xiaoxu,Yang, Yunhui,&Wang, Congyang.(2016).Rhenium and base co-catalyzed [3+2] annulations of N-H ketimines and alkynes to access unprotected tertiary indenamines through C-H bond activation.ORGANIC CHEMISTRY FRONTIERS,3(2),268-272.
MLA Jin, Xiqing,et al."Rhenium and base co-catalyzed [3+2] annulations of N-H ketimines and alkynes to access unprotected tertiary indenamines through C-H bond activation".ORGANIC CHEMISTRY FRONTIERS 3.2(2016):268-272.

入库方式: OAI收割

来源:化学研究所

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