Tron Gian Cesare, Pirali Tracey, Billington Richard A, Canonico Pier Luigi, Sorba Giovanni, Genazzani Armando A
Dipartimento di Scienze Chimiche, Alimentari, Farmaceutiche e Farmacologiche and Drug and Food Biotechnology Center, Università degli Studi del Piemonte Orientale "A. Avogadro", Via Bovio 6, 28100 Novara, Italy.
Med Res Rev. 2008 Mar;28(2):278-308. doi: 10.1002/med.20107.
In recent years, there has been an ever-increasing need for rapid reactions that meet the three main criteria of an ideal synthesis: efficiency, versatility, and selectivity. Such reactions would allow medicinal chemistry to keep pace with the multitude of information derived from modern biological screening techniques. The present review describes one of these reactions, the 1,3-dipolar cycloaddition ("click-reaction") between azides and alkynes catalyzed by copper (I) salts. The simplicity of this reaction and the ease of purification of the resulting products have opened new opportunities in generating vast arrays of compounds with biological potential. The present review will outline the accomplishments of this strategy achieved so far and outline some of medicinal chemistry applications in which click-chemistry might be relevant in the future.
近年来,对满足理想合成的三个主要标准(效率、通用性和选择性)的快速反应的需求日益增长。此类反应将使药物化学能够跟上源自现代生物筛选技术的大量信息的步伐。本综述描述了其中一种反应,即铜(I)盐催化的叠氮化物与炔烃之间的1,3-偶极环加成反应(“点击反应”)。该反应的简单性以及所得产物的易于纯化,为生成大量具有生物潜力的化合物开辟了新机会。本综述将概述该策略迄今取得的成就,并概述一些点击化学在未来可能相关的药物化学应用。