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新型抗癌异噁唑啉基咪唑[1,2-a]吡啶C-核甙类化合物的合成
Synthesis of novel isoxazolinyl substituted imidazo[1,2-a]pyridine C-nucleoside analogs
【摘要】 以异唑啉基环取代呋喃核糖环 (ribosering) ,成功地合成了一系列咪唑 [1 ,2 -a]吡啶C -核甙化合物的衍生物 3和 4 (其中碱基和异唑啉基环之间以C—C化学键方式连接 ) .这两种异构体中N和O原子处于相互交换的位置 ,分别可以利用相应的烯烃和腈氧化物中间体进行偶极环合加成反应制得 ,其中衍生物 4c显示出一定的抗HIV -1活性 .
【Abstract】 Isoxazoline rings have been successfully connected to imidazopyridine derivatives via carbon-carbon bonds for the synthesis of new C-nucleoside analogs 3 and 4. These two isomers, that possess the altered positions of nitrogen and oxygen atoms, can be formed through dipolar cycloaddition reactions of the appropriate olefins and nitrile oxides. And compound 4c shows some moderate anti-HIV-1 activity
【关键词】 异噁唑啉;
C-核甙;
咪唑[1,2-a]吡啶;
抗癌试剂;
【Key words】 isoxazoline; C-nucleoside; imidazopyridine; anticancer and antiviral agents;
【Key words】 isoxazoline; C-nucleoside; imidazopyridine; anticancer and antiviral agents;
- 【文献出处】 东北师大学报(自然科学版) ,Journal of Northeast Normal University (Natural Science Edition) , 编辑部邮箱 ,2001年04期
- 【分类号】O629
- 【被引频次】4
- 【下载频次】123