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首页> 外文期刊>Journal of Fluorine Chemistry >Copper catalyzed 1,3-dipolar cycloaddition reaction of azides with N-(2-trifluoroacetylaryl)propargylamines A mild entry to novel 1,4-disubstituted-[1,2,3]-triazole derivatives
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Copper catalyzed 1,3-dipolar cycloaddition reaction of azides with N-(2-trifluoroacetylaryl)propargylamines A mild entry to novel 1,4-disubstituted-[1,2,3]-triazole derivatives

机译:铜与叠氮化物与N-(2-三氟乙酰芳基)炔丙基胺的1,3-偶极环加成反应新型1,4-二取代-[1,2,3]-三唑衍生物的温和进入

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摘要

The synthesis of N-(2-trifluoroacetylaryl)propargylamines 10-14 and 17 is presented. The copper(I) catalyzed cycloaddition reaction of these propargylamines (dipolarophiles) with a series of azides (1,3-dipoles) 18-20,21 and 24 was found to proceed smoothly in dimethylsulfoxide at room temperature, to furnish the corresponding 1,4-disubstituted-[ 1,2,3]triazole derivatives 26-36 in moderate to good yields.
机译:提出了N-(2-三氟乙酰基芳基)炔丙基胺10-14和17的合成。发现这些炔丙基胺(偶极亲子)与一系列叠氮化物(1,3-偶极)18-20,21和24的铜(I)催化的环加成反应在室温下于二甲基亚砜中顺利进行,得到相应的1, 4-二取代的[[1,2,3]三唑衍生物26-36,产率中等至良好。

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