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首页> 外文期刊>Comptes Rendus Chimie >An efficient and economical synthesis of 5-substituted 1H-tetrazoles via Pb(II) salt catalyzed [3+2] cycloaddition of nitriles and sodium azide
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An efficient and economical synthesis of 5-substituted 1H-tetrazoles via Pb(II) salt catalyzed [3+2] cycloaddition of nitriles and sodium azide

机译:通过Pb(II)盐催化腈和叠氮化钠的[3 + 2]环加成反应,可高效经济地合成5-取代的1H-四唑

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摘要

A simple, mild and efficient method is developed for the synthesis of 5-substituted 1H-tetrazoles. Out of three used Pb(II) catalysts, lead chloride (PbCl2) has been found to be an efficient catalyst for [3+2] cycloaddition of NaN3 with aromatic and aliphatic nitriles to afford 5-substituted 1H-tetrazoles. The catalyst is reusable up to four cycles with consistent activity. The cost effectiveness and easy availability of the catalyst, simple methodology, excellent yield and easy work-up are the additional advantages. (C) 2015 Academie des sciences. Published by Elsevier Masson SAS. All rights reserved.
机译:开发了一种简单,温和且有效的方法来合成5-取代的1H-四唑。在三种使用过的Pb(II)催化剂中,氯化铅(PbCl2)被发现是NaN3与芳族和脂族腈进行[3 + 2]环加成反应以提供5取代的1H-四唑的有效催化剂。该催化剂可重复使用多达四个周期,且具有一致的活性。催化剂的成本效益和易得性,简单的方法,优异的收率和后处理是另外的优点。 (C)2015年科学研究院。由Elsevier Masson SAS发布。版权所有。

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