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吲哚 C2-功能化的最新进展:反转策略

Recent Advances on the C2-Functionalization of Indole via Umpolung.

机构信息

Department of Applied Sciences, GUIST, Gauhati University, Guwahati, Assam, 781014, India.

出版信息

Top Curr Chem (Cham). 2020 Feb 7;378(2):22. doi: 10.1007/s41061-020-0287-7.

Abstract

Heterocyclic compounds having a nitrogen atom in the ring exhibit very interesting biological activities. Indole is the core structure of many bioactive compounds owing to its high affinity to bind with most biological targets. Indole is an electron-rich compound and generally prefers electrophilic rather than nucleophilic substitution. Hence, many important indole derivatives are difficult to synthesize through the conventional reactivity of indole. This limitation can be avoided by using the umpolung, from the German word meaning polarity inversion. In umpolung, the indole molecule, especially the C2 and C3 positions, behave as an electrophile. As C2-functionalized indoles have substantial importance in synthetic and pharmaceutical chemistry, this review focuses on the C2 umpolung of indoles via the indirect approach which is less explored. Unlike direct approaches of indole umpolung, indirect methods have several advantages and therefore a number of research articles have been published in this field. But no review is available up till now. This is the first review on this topic and we believe that it will surely motivate the readers to work in this area further.

摘要

具有环氮原子的杂环化合物表现出非常有趣的生物活性。吲哚是许多生物活性化合物的核心结构,因为它与大多数生物靶标具有很高的亲和力。吲哚是一种富电子化合物,通常更喜欢亲电而不是亲核取代。因此,许多重要的吲哚衍生物很难通过吲哚的常规反应性来合成。这种限制可以通过使用反转极性来避免,这个德语单词的意思是极性反转。在反转极性中,吲哚分子,特别是 C2 和 C3 位置,表现为亲电试剂。由于 C2 功能化吲哚在合成和药物化学中具有重要意义,因此本综述重点介绍了通过间接方法实现的 C2 吲哚反转极性,因为这种方法尚未得到充分探索。与吲哚反转极性的直接方法不同,间接方法具有几个优点,因此在该领域发表了许多研究文章。但到目前为止,还没有综述。这是关于该主题的第一篇综述,我们相信它肯定会激励读者在该领域进一步研究。

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