首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Synthesis of [(arylselanyl)alkyl]-1,2,3-triazoles by copper-catalyzed 1,3-dipolar cycloaddition of (arylselanyl)alkynes with benzyl azides
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Synthesis of [(arylselanyl)alkyl]-1,2,3-triazoles by copper-catalyzed 1,3-dipolar cycloaddition of (arylselanyl)alkynes with benzyl azides

机译:用苄基叠氮化铜催化的1,3-偶极环加入的[(芳基Sellanyl)烷基] -1,2,3-三唑酯

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摘要

In the presence of catalytic amounts of copper salts and sodium ascorbate, various (arylselanyl)alkynes underwent click-type 1,3-dipolar cycloaddition reactions with a range of benzyl azides bearing electron-withdrawing or electron-donating groups to give a series of novel [(arylselanyl)alkyl]-1,2,3- triazoles. This click chemistry protocol is an efficient method for synthesizing new selenium-nitrogen compounds that are potentially useful in biological studies.
机译:在存在催化量的铜盐和抗坏血酸钠,各种(芳基)炔烃接受咔哒1,3-偶极环加成反应,通过一系列苄基叠氮化物携带电子 - 叠加或电子捐赠组给一系列新颖 [(芳基)烷基] -1,2,3-三唑。 此咔哒化化学方案是合成诸如在生物学研究中可能有用的新硒 - 氮化合物的有效方法。

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