Recent advances in the radical cascade reaction for constructing nitrogen heterocycles using azides as radical acceptors

IF 2.9 3区 化学 Q1 CHEMISTRY, ORGANIC Organic & Biomolecular Chemistry Pub Date : 2024-06-14 DOI:10.1039/D4OB00732H
Dong Xia, Yun Shi, Liying Jiang, Yang Li and Jianfei Kong
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Abstract

Due to the high conversion properties, azide compounds are widely utilized in organic synthesis. For instance, azide compounds readily release nitrogen to form a new N–C bond when they function as radical acceptors for the active intermediates in the reaction. Over the past decade, strategies employing azides as radical acceptors to construct nitrogen heterocycles have been extensively developed. This approach has emerged as a crucial method for synthesizing nitrogen heterocycles. Therefore, this paper provides a review of the research advancements in tandem cyclization reactions using azides as radical acceptors, summarizing the process of reaction design, exploration, reasoning of the mechanism, and prospects for further research of these reactions.

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利用叠氮化物作为自由基受体构建氮杂环的自由基级联反应的最新进展。
由于叠氮化物具有高转化率的特性,因此被广泛应用于有机合成中。例如,叠氮化物作为反应中活性中间体的自由基受体时,很容易释放出氮,形成新的 N-C 键。在过去十年中,人们广泛开发了利用叠氮化物作为自由基受体来构建氮杂环的策略。这种方法已成为合成氮杂环的重要方法。因此,本文综述了以叠氮化物为自由基受体的串联环化反应的研究进展,总结了这些反应的设计、探索、机理推理过程以及进一步研究的前景。
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来源期刊
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry 化学-有机化学
CiteScore
5.50
自引率
9.40%
发文量
1056
审稿时长
1.3 months
期刊介绍: The international home of synthetic, physical and biomolecular organic chemistry.
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