摘要
背景:4-官能化异恶唑啉-5-酮(异恶唑酮)作为官能化结构单元的前体引起了广泛的关注,因为它具有多种功能。这些结构特征有助于构建对于新功能材料的开发很重要的大型化合物文库。然而,涉及硝基异恶唑酮的系统综述文章虽然表现出与其他功能化异恶唑酮不同的反应性,但尚未发表。该综述描述了硝基异恶唑酮基序的有趣行为及其在多官能化合物合成中的应用。 方法:收集同行评议的硝基异恶唑酮类化合物研究文献,用标准评价方法对每篇论文进行评价。纳入/排除标准。论文进行了分析,并根据反应模式进行划分。 结果:这个评论由两部分组成。前一部分描述了硝基异恶唑酮吡啶鎓盐的化学反应,后一部分介绍了甲基硝基异恶唑酮的化学反应。这篇评论包括了68篇论文。十二篇论文涉及吡啶鎓盐或其开环产物氰基-aci-硝基乙酸酯。九篇论文提到了甲基硝基异恶唑酮和衍生的硝基烯胺和氧化腈的化学性质。关于各种化学反应的机理和反应机理,引用相关文献进行了讨论。 结论:本综述的结果证实硝基异恶唑酮在合成化学中对多官能化合物的重要性,这些化合物不易通过替代方法获得。本综述将为许多化学家研究合成化学和药物化学提供有用的信息和合成工具。
关键词: 二价阴离子,氧化腈,硝基烯胺,硝基异恶唑酮,假分子内过程,环转化
Current Medicinal Chemistry
Title:Nitroisoxazolones Showing Diverse Chemical Behavior: A Use ful Building Block for Polyfunctionalized Systems
Volume: 24 Issue: 34
关键词: 二价阴离子,氧化腈,硝基烯胺,硝基异恶唑酮,假分子内过程,环转化
摘要: Background: 4-Functionalized isoxazolin-5-ones (isoxazolones) have attracted much attentions as precursors of functionalized building blocks because the multiple functionalities. These structural features facilitate the construction of large compound libraries that is important for development of new functional materials. However, the systematic review article dealing with nitroisoxazolone has not been published although they exhibit different reactivity from other functionalized isoxazolones. This review describes the interesting behavior of the nitroisoxazolone motif and its application to the synthesis of polyfunctionalized compounds.
Methods: Peer-reviewed research literatures describing the chemistry of nitroisoxazolones were collected, and each paper was appraised using standard criteria. inclusion/exclusion criteria. The papers were analyzed, and divided according to the reaction patterns.
Results: This review consists of two parts. In the former part, the chemistry of pyridinium salt of nitroisoxazolone is described, and in the latter part, chemistry of methylnitroisoxazolone is introduced. Sixty-eight papers were included in this review. Twelve papers deal with pyridinium salt or its ring-opened product, cyano-aci-nitroacetate. Nine papers mention the chemistry of methylnitroisoxazolones and derived nitroenamines and nitrile oxide. With regard to each chemistry, reaction mechanism and reactivity are discussed with citing related literatures.
Conclusion: The findings of this review confirm the importance of nitroisoxazolones in synthetic chemistry for polyfunctionalized compounds, which are not readily available by alternative methods. This review will provide useful information and synthetic tools for many chemists studying synthetic chemistry and medicinal chemistry.
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Cite this article as:
Nitroisoxazolones Showing Diverse Chemical Behavior: A Use ful Building Block for Polyfunctionalized Systems, Current Medicinal Chemistry 2017; 24 (34) . https://dx.doi.org/10.2174/0929867324666170714123612
DOI https://dx.doi.org/10.2174/0929867324666170714123612 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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