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通过非常规炔烃环化反应直接获得功能化薁和伪薁。

Direct Access to Functionalized Azulenes and Pseudoazulenes via Unconventional Alkyne Cyclization Reactions.

机构信息

Chang-Kung Chuang Institute, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, 200241, China.

Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, East China Normal University, Shanghai, 200062, China.

出版信息

Chem Asian J. 2023 Jun 1;18(11):e202300244. doi: 10.1002/asia.202300244. Epub 2023 Apr 27.

Abstract

Owing to the unique chemical structure and photophysical properties of azulene, azulene derivatives show great promise for a wide range of prospective technical applications, such as molecular switching, sensors, solar cells, and biological activities. In addition to functionalization of the existed azulene cores, direct construction of azulenes via condensation with odd-membered carbocycles such as tropolone, 2-oxazulanone, cyclopentadiene, and 6-aminofulvene is another classical method for obtaining azulene derivatives. Although alkynes are widely explored for construction of benzene rings, several unconventional cyclization reactions with alkynes produce azulene, pseudoazulene, or azulenone skeletons. This minireview summarizes these interesting and practical cyclization with a classification based on the function of alkyne in the azulene formation process, aiming at capturing the attention of the scientific community to make efforts in the development of such nonalternant cyclization reactions of alkynes.

摘要

由于薁的独特化学结构和光物理性质,薁衍生物在分子开关、传感器、太阳能电池和生物活性等广泛的潜在技术应用中具有很大的应用前景。除了薁核的功能化之外,通过薁与稠合的奇数碳环(如三唑酮、2-噁唑烷酮、环戊二烯和 6-氨基富烯)的缩合直接构建薁也是获得薁衍生物的另一种经典方法。尽管炔烃广泛用于构建苯环,但一些非常规的炔烃环化反应会产生薁、伪薁或薁酮骨架。这篇综述总结了这些有趣且实用的环化反应,并根据炔烃在薁形成过程中的作用进行了分类,旨在引起科学界的关注,努力开发这种炔烃的非交替环化反应。

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