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3-氨基吲唑作为多功能合成子在氮杂环合成中的最新进展。

Recent advances in 3-aminoindazoles as versatile synthons for the synthesis of nitrogen heterocycles.

机构信息

School of Pharmacy, Xinxiang Medical University, Xinxiang, Henan 453003, P. R. China.

出版信息

Org Biomol Chem. 2022 Sep 21;20(36):7138-7150. doi: 10.1039/d2ob01348g.

Abstract

Nitrogen-based heterocycles are an important class of structural scaffolds distributed in biologically active natural products, medicinal chemistry, and agrochemicals. Hence, there is increasing interest in the development of novel synthetic strategies for the construction of these privileged structural motifs. Recently, 3-aminoindazoles have emerged as versatile synthons participating in a variety of condensation annulation, denitrogenative transannulation and rearrangement ring expansion reactions, which provide efficient synthetic routes for the formation of nitrogen heterocycles. This review systematically highlights for the first time the most recent advances in 3-aminoindazoles to provide a deep understanding of using 3-aminoindazoles as versatile synthons in organic transformations for synthetic and medicinal chemists.

摘要

氮杂环是一类重要的结构骨架,广泛存在于生物活性天然产物、药物化学和农用化学品中。因此,人们越来越感兴趣开发新型合成策略来构建这些优先结构基序。最近,3-氨基吲唑作为多功能的合成子,参与多种缩合环化、脱氮转环和重排环扩张反应,为氮杂环的形成提供了有效的合成途径。本文首次系统地强调了 3-氨基吲唑的最新进展,为合成和药物化学家提供了深入了解将 3-氨基吲唑作为有机转化中多功能合成子的机会。

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