首页> 外文期刊>Monatshefte fur Chemie >Metal-free synthesis of 1,2,3-triazoles by azide-aldehyde cycloaddition under ultrasonic irradiation in TSIL [DBU-Bu]OH and in hydrated IL Bu4NOH under heating
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Metal-free synthesis of 1,2,3-triazoles by azide-aldehyde cycloaddition under ultrasonic irradiation in TSIL [DBU-Bu]OH and in hydrated IL Bu4NOH under heating

机译:在TSIL [DBU-Bu] OH和水合IL Bu4NOH中,在超声辐射下通过叠氮化物-醛环加成反应在无金属条件下合成1,2,3-三唑

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摘要

Efficient and environmentally benign procedures have been reported for the synthesis of 1,4-disubstituted 1,2,3-triazoles by reaction of aryl azides with aldehydes in task-specific basic ionic liquid [DBU-Bu]OH under ultrasonic irradiation and in hydrated ionic liquid tetrabutylammonium hydroxide (Bu4NOH) under conventional heating. These protocols represent simple, general, and efficient approaches in terms of good yields, operational simplicity, easy workup, and shorter reaction time for the synthesis of 1,4-disubstituted 1,2,3-triazoles under metal-free conditions.
机译:据报道,在特定任务的碱性离子液体[DBU-Bu] OH中,在超声波辐射和水合条件下,芳基叠氮化物与醛反应可以合成1,4-二取代的1,2,3-三唑,这种方法对环境有效。常规加热条件下形成离子液体氢氧化四丁基铵(Bu4NOH)。这些协议代表了在无金属条件下合成1,4-二取代1,2,3-三唑的良好收率,操作简便,易于操作以及较短的反应时间的简单,通用和有效的方法。

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