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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >A straightforward and versatile approach to the synthesis of 1,4,5-trisubstituted 1,2,3-triazoles from alkyl halides via a one-pot, three-component reaction
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A straightforward and versatile approach to the synthesis of 1,4,5-trisubstituted 1,2,3-triazoles from alkyl halides via a one-pot, three-component reaction

机译:一种简单,通用的方法,可通过一锅三组分反应从烷基卤化物合成1,4,5-三取代的1,2,3-三唑

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摘要

The preparation of 1,4,5-trisubstituted 1,2,3-triazoles by the coupling of three components (alkyl halides, sodium azide, and active ketones) through an azide-enolate [3+2] cycloaddition (Dimroth cycloaddition) has been developed for the first time. A wide variety of halides (including chlorides, bromides, and iodides as well as primary and secondary derivatives) have demonstrated the versatility of this method, which is based on a one-pot system under mild reaction conditions. (C) 2015 Elsevier Ltd. All rights reserved.
机译:通过将三组分(卤代烷,叠氮化钠和活性酮)通过叠氮化物-烯酸酯[3 + 2]环加成反应(Dimroth环加成反应)制备1,4,5-三取代的1,2,3-三唑是第一次开发。多种卤化物(包括氯化物,溴化物和碘化物以及一元和二级衍生物)已证明了该方法的多功能性,该方法基于在温和反应条件下的一锅法系统。 (C)2015 Elsevier Ltd.保留所有权利。

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