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四环吲哚啉的综合方法作为多种吲哚生物碱的多功能构建块。

Synthetic Approaches to Tetracyclic Indolines as Versatile Building Blocks of Diverse Indole Alkaloids.

机构信息

Key Laboratory of Structure-Based Drug Design and Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang, 110016, P. R. China.

Institute of Drug Research in Medicine Capital of China, Benxi, 117000, P. R. China.

出版信息

Chemistry. 2018 Sep 25;24(54):14302-14315. doi: 10.1002/chem.201800775. Epub 2018 Jul 6.

Abstract

Indole alkaloids bearing the tetracyclic indoline scaffolds of 1H-pyrrolo[2,3-d]carbazole have shown fascinating chemical diversity and significant biological activities. The development of efficient synthetic methodologies for such a tetracyclic scaffold remains highly desirable in both synthetic chemistry and medicinal chemistry. This review outlines key strategies for the construction of the tetracyclic indoline scaffolds in total syntheses of many indole alkaloids. The key strategies include nucleophilic additions, Diels-Alder reactions, radical cyclizations, and palladium-catalyzed coupling reactions. The representative examples and their applications in the total syntheses are described here and discussed in depth.

摘要

具有 1H-吡咯并[2,3-d]咔唑四环吲哚啉骨架的吲哚生物碱表现出迷人的化学多样性和显著的生物活性。在合成化学和药物化学中,开发用于此类四环支架的有效合成方法仍然是非常需要的。本文综述了在许多吲哚生物碱的全合成中构建四环吲哚啉支架的关键策略。关键策略包括亲核加成、Diels-Alder 反应、自由基环化和钯催化偶联反应。这里描述了代表性实例及其在全合成中的应用,并进行了深入讨论。

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