中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Direct Access to 1,3,5-Trisubstituted 1H-1,2,4-Triazoles from N-Phenylbenzamidines via Copper-Catalyzed Diamination of Aryl Nitriles

文献类型:期刊论文

作者Zhang LT(张路淘)1; Tang D(汤东)1; Gao J(高静)1; Wang J(王静)1; Wu P(吴萍)1; Meng X(孟旭)2; Chen BH(陈保华)1
刊名Synthesis
出版日期2016
卷号48期号:22页码:3924-3930
关键词amination copper heterocycles ring closure tandem reaction
ISSN号0039-7881
通讯作者陈保华
英文摘要

A copper-catalyzed formation of C–N/N–N bonds using N-phenylbenzamidines with aryl nitriles has been developed and affords a route to 1,3,5-trisubstituted 1H-1,2,4-triazoles in moderate to excellent yields. The method is operationally simple and environmentally benign with a large substrate scope available and represents an economical path for numerous C–N/N–N bond formations.

学科主题物理化学与绿色催化
收录类别SCI
资助信息the National Natural Science Foundation of China (No. 21372102;21403256)
语种英语
WOS记录号WOS:000389329100007
源URL[http://210.77.64.217/handle/362003/20720]  
专题兰州化学物理研究所_ERC国家工程研究中心
兰州化学物理研究所_OSSO国家重点实验室
作者单位1.State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, P. R. of China
2.State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000, P. R. of China
推荐引用方式
GB/T 7714
Zhang LT,Tang D,Gao J,et al. Direct Access to 1,3,5-Trisubstituted 1H-1,2,4-Triazoles from N-Phenylbenzamidines via Copper-Catalyzed Diamination of Aryl Nitriles[J]. Synthesis,2016,48(22):3924-3930.
APA Zhang LT.,Tang D.,Gao J.,Wang J.,Wu P.,...&Chen BH.(2016).Direct Access to 1,3,5-Trisubstituted 1H-1,2,4-Triazoles from N-Phenylbenzamidines via Copper-Catalyzed Diamination of Aryl Nitriles.Synthesis,48(22),3924-3930.
MLA Zhang LT,et al."Direct Access to 1,3,5-Trisubstituted 1H-1,2,4-Triazoles from N-Phenylbenzamidines via Copper-Catalyzed Diamination of Aryl Nitriles".Synthesis 48.22(2016):3924-3930.

入库方式: OAI收割

来源:兰州化学物理研究所

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