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Diastereoselective Synthesis of 1,10-Dihydropyrrolo [ 1,2-a] [1,10]phenanthroline Derivatives via 1,3-Dipolar Cycloaddition Reaction

Diastereoselective Synthesis of 1,10-Dihydropyrrolo [ 1,2-a] phenanthroline Derivatives via 1,3-Dipolar Cycloaddition Reaction

作     者:LIU Zhen-ming FANG Jun YAN Chao-guo 

作者机构:Analysis and Test CenterYangzhou University Yangzhou 225002 P.R.China College of Chemistry & Chemical EngineeringYangzhou University Yangzhou 225002 P.R.China 

出 版 物:《Chemical Research in Chinese Universities》 (高等学校化学研究(英文版))

年 卷 期:2013年第29卷第6期

页      面:1089-1093页

核心收录:

学科分类:081702[工学-化学工艺] 08[工学] 0817[工学-化学工程与技术] 09[农学] 0904[农学-植物保护] 

基  金:the National Natural Science Foundation of China the Priority Academic Program Development of Jiangsu Higher Education Institutions China 

主  题:Pyridinium ylide Phenanthroline Pyrrolo[1,2-a]phenanthroline 1,3-Dipolar cycloaddition Diastereoselectivity 

摘      要:The functionalized 1,10-dihydropyrrolo[1,2-a][1,10]phenanthroline derivatives were synthesized in good yields and with high diastereoselectivity by 1,3-dipolar cycloaddition reactions of N-phenacylphenanthrolinium bromides or N-ethoxycarbonylmethylene phenanthrolinium bromide with various nitrostyrenes in acetonitrile at room temperature in the presence of triethvlamine,

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