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首页> 外文期刊>Australian Journal of Chemistry: A Journal for the Publication of Original Research in All Branches of Chemistry >A New Synthetic Protocol for One-Pot Preparations of 5-Halo-l ,4-disubstituted-1,2,3-triazoles
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A New Synthetic Protocol for One-Pot Preparations of 5-Halo-l ,4-disubstituted-1,2,3-triazoles

机译:一锅制备5-卤代-1,4-二取代-1,2,3-三唑的新合成方案

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摘要

In this paper, a new synthetic protocol for one-pot preparations of 5-halo-l,4-disubstituted-l,2,3-triazoles is provided by rational combination of a Cu1 catalyzed azide-alkyne cycloaddition (CuAAC) reaction and an oxidative halogenation reaction. Cul- N-chlorosuccinimide (NCS) and CuBr-NCS reaction systems are developed, respectively, for effective preparations of 5-iodo-l,4-disubstituted-l,2,3-triazoles and 5-bromo-l,4-disubstituted-l,2,3-trizoles under mild conditions with a high tolerance of various sensitive groups.
机译:本文通过对Cu1催化的叠氮化物-炔烃环加成反应(CuAAC)的合理组合,为一锅制备5-卤代-1,4-二取代-1,2,3-三唑提供了一种新的合成方案。氧化卤化反应。分别开发了Cul-N-氯代琥珀酰亚胺(NCS)和CuBr-NCS反应体系,以有效制备5-碘-1,4-二取代-1,2,3-三唑和5-溴-1,4-二取代-1、2,3-三唑在温和条件下对各种敏感基团具有较高的耐受性。

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