Recent Advances in the Synthesis of Pyrazole Derivatives: A Review

Reactions Pub Date : 2023-09-05 DOI:10.3390/reactions4030029
Issam Ameziane El Hassani, Khouloud Rouzi, Hamza Assila, K. Karrouchi, M. Ansar
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引用次数: 2

Abstract

Pyrazole, characterized by a five-membered heterocyclic structure featuring two neighboring nitrogen atoms, serves as a core element. Pyrazoles hold a privileged status as versatile frameworks in various sectors of the chemical industry, including medicine and agriculture. Previous reviews have extensively highlighted the significance of pyrazoles and their diverse biological activities, encompassing roles such as antituberculosis, antimicrobial, antifungal, anti-inflammatory, anticancer, and antidiabetic agents. Consequently, they have garnered substantial interest from researchers. The aim of this review is to offer a comprehensive overview of the published research related to the synthesis of pyrazole derivatives, encompassing a discussion of diverse methods for accessing the pyrazole moiety. These methods span from utilizing transition-metal catalysts and photoredox reactions to employing one-pot multicomponent processes, novel reactants, and innovative reaction types. It encompasses studies conducted by numerous scientists worldwide, showcasing collective efforts in advancing the methodologies and applications of pyrazole derivatives.
吡唑衍生物的合成研究进展
吡唑具有五元杂环结构,具有两个相邻的氮原子,是核心元素。吡唑类化合物在包括医药和农业在内的化学工业的各个部门中作为多功能框架具有特殊地位。以往的综述广泛强调了吡唑的重要性及其多种生物活性,包括抗结核、抗菌、抗真菌、抗炎、抗癌和降糖药等作用。因此,它们引起了研究人员的极大兴趣。本综述的目的是提供有关吡唑衍生物合成的已发表的研究的全面概述,包括对获取吡唑部分的各种方法的讨论。这些方法包括利用过渡金属催化剂和光氧化还原反应,采用一锅多组分工艺,新型反应物和创新的反应类型。它包含了由世界各地众多科学家进行的研究,展示了在推进吡唑衍生物的方法和应用方面的集体努力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
2.70
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0.00%
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