通过异构催化剂绿色合成具有生物活性的吡咯衍生物,自 2010 年起。

IF 2.9 4区 医学 Q3 CHEMISTRY, MEDICINAL
Berrichi Amina, Bachir Redouane
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引用次数: 0

摘要

众所周知,吡咯衍生物是合成生物化合物和药物的基础材料。合成吡咯的方法有多种,包括汉茨赫(Hantzsch)、帕尔-克诺尔(Paal-Knorr)和二羰基化合物的环加成反应。要获得目标吡咯结构,必须使用纳米颗粒、金属盐和异质催化剂。此外,为了得到更有活性的吡咯化合物,在合成过程中还使用了咪唑等杂环分子或其他环作为胺。本综述介绍了自 2010 年以来通过一锅多组分反应绿色合成生物活性吡咯的异质催化剂。此外,每种合成方法还包括对建议机制的演示。二烷基乙酰二羧酸酯、二羰基、胺、呋喃和乙炔基通过异质催化剂合并生成生物活性吡咯。最后,研究人员还展示了各种对氨基苯甲酸酯的活性,如抗菌、消炎、镇痛和其他重要活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Green Synthesis of Bioactive Pyrrole Derivatives via Heterogeneous Catalysts Since 2010.

Pyrrole derivatives are known as building blocks for the synthesis of biological compounds and pharmaceutical drugs. Several processes were employed to synthesize pyrroles, including Hantzsch, Paal-Knorr, and cycloaddition of dicarbonyl compounds reaction. Using catalysts like nanoparticles, metal salts, and heterogeneous ones was necessary to obtain the targeted pyrrole structure. Also, to afford more active pyrrole compounds, heterocyclic molecules such as imidazole or other rings were used in the synthesis as amines. This review presents heterogeneous catalysts since 2010 for the green synthesis of bioactive pyrroles in a one-pot multi-component reaction. Additionally, each synthetic method included a demonstration of the suggested mechanisms. Diakylacetylenedicarboxylate, dicarbonyl group, amines, furans, and acetylene group are consolidated to yield biological pyrroles through the heterogeneous catalysts. Finally, various parolee-performed activities were displayed, such as antibacterial, anti-inflammatory, analgesic, and other significant activities.

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来源期刊
CiteScore
6.40
自引率
2.90%
发文量
186
审稿时长
3-8 weeks
期刊介绍: Current Topics in Medicinal Chemistry is a forum for the review of areas of keen and topical interest to medicinal chemists and others in the allied disciplines. Each issue is solely devoted to a specific topic, containing six to nine reviews, which provide the reader a comprehensive survey of that area. A Guest Editor who is an expert in the topic under review, will assemble each issue. The scope of Current Topics in Medicinal Chemistry will cover all areas of medicinal chemistry, including current developments in rational drug design, synthetic chemistry, bioorganic chemistry, high-throughput screening, combinatorial chemistry, compound diversity measurements, drug absorption, drug distribution, metabolism, new and emerging drug targets, natural products, pharmacogenomics, and structure-activity relationships. Medicinal chemistry is a rapidly maturing discipline. The study of how structure and function are related is absolutely essential to understanding the molecular basis of life. Current Topics in Medicinal Chemistry aims to contribute to the growth of scientific knowledge and insight, and facilitate the discovery and development of new therapeutic agents to treat debilitating human disorders. The journal is essential for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important advances.
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