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,