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Acid-mediated synthesis of fully substituted 1,2,3-triazoles: multicomponent coupling reactions, mechanistic study, synthesis of serine hydrolase inhibitor and its derivatives

机译:酸介导的全取代1,2,3-三唑的合成:多组分偶联反应,机理研究,丝氨酸水解酶抑制剂及其衍生物的合成

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摘要

We describe the full details of multicomponent coupling reactions in acid-mediated synthesis of fully substituted 1,2,3-triazoles syntheses, and their applications to bioactive molecule synthesis. For substitution with wide range of nucleophiles, selection of acids or activating reagents was important, and various types of multicomponent coupling reactions were demonstrated, allowing functionalization with alcohols, amines, thiol, azide, and carbon nucleophiles. Four-component couplings including double triazolations were also tested. The efficiency of this method was demonstrated by the synthesis of serine hydrolase inhibitor and its novel substituted derivatives.
机译:我们描述了完全取代的1,2,3-三唑合成物在酸介导的合成中的多组分偶联反应的详细信息,及其在生物活性分子合成中的应用。对于用广泛的亲核试剂进行取代,酸或活化剂的选择很重要,并且已经证明了各种类型的多组分偶联反应,可以用醇,胺,硫醇,叠氮化物和碳亲核试剂进行官能化。还测试了包括双三唑基化在内的四组分偶联。丝氨酸水解酶抑制剂及其新型取代衍生物的合成证明了该方法的有效性。

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