4.4 Review

Click and Multicomponent Reactions Work Together for Polymer Chemistry

期刊

MACROMOLECULAR CHEMISTRY AND PHYSICS
卷 219, 期 16, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/macp.201800163

关键词

Biginelli reactions; click reactions; copper-catalyzed azide-alkyne cycloaddition reactions; Diels-Alder reactions; multicomponent reactions; Passerini reactions; thiol-ene reactions; Ugi reactions

向作者/读者索取更多资源

This article investigates the current combinations of click and multicomponent reactions (MCRs) to produce complex macromolecular structures through polymer-polymer conjugation or hetero-functionalization of polymers. The click and MCRs display similar features covering the equimolarity, fast time scale, high yields, stable compounds, modular, orthogonal and single reaction trajectory. Of classical click reactions, CuAAC, Diels-Alder, thiol-ene (-yne), and nucleophilic substitution on perfluoroaryl groups reactions are combined with MCRs, namely, Passerini, Ugi, or Biginelli reactions. It should be noted that these combinations can afford the target polymer structures, which are not attainable by employing one of these reactions alone.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据