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基于异氰化物的多组分反应在水中:杂环化合物合成的先进绿色工具。

Isocyanide-Based Multicomponent Reactions in Water: Advanced Green Tools for the Synthesis of Heterocyclic Compounds.

机构信息

Department of Organic Chemistry, Shahid Beheshti University, Daneshjou Boulevard Street, Tehran, 1983969411, Iran.

Peoples' Friendship University of Russia, RUDN University, 6, Miklukho-Maklaya Street, Moscow, 117198, Russian Federation.

出版信息

Top Curr Chem (Cham). 2022 Sep 22;380(6):50. doi: 10.1007/s41061-022-00403-8.

Abstract

Reaction rate acceleration using green methods is an intriguing area of research for chemists. In this regard, water as a "green solvent" plays a crucial role in the acceleration of some organic transformations and reveals exclusive selectivity and reactivity in comparison with conventional organic solvents. In particular, multicomponent reactions (MCRs) as sustainable tools lead to the rapid generation of small-molecule libraries in water and aqueous media due to the prominent role of the hydrophobic effect. MCRs, as diversity-oriented synthesis (DOS) methods, have great efficiency with simple operations, atom, pot, and step economy synthesis, and mechanistic beauty. Among diverse classes of MCRs, isocyanide-based multicomponent reactions (I-MCRs), as sustainable and versatile reactions, have gained considerable attention in the synthesis of diverse heterocycle rings, especially in drug design because of the peculiar nature of isocyanide as a particular active reactant. I-MCRs that are performed in water are mild, environmentally friendly, and easily controlled, and have a reduced number of workup, purification, and extraction steps, which fit well with the advantages of "green" chemistry. Performing these powerful organic transformations in water and aqueous media is accompanied by acceleration owing to negative activation volumes, which originate from connecting several reactants together to generate a single product. It should be noted that the combination of MCR strategy and aqueous phase reaction is of growing interest for the development of sustainable synthetic techniques in organic conversions. However, an exclusive account focusing on the recent progress in eco-friendly I-MCRs for the construction of heterocycles in water and aqueous media is particularly lacking. This review highlights the progress of various kinds of I-MCRs in water and aqueous media as benign methods for the efficient construction of vital heterocyclic scaffolds, with a critical discussion of the subject in the period 2000-2021. We hope that this themed collection will be of interest and beneficial for organic and pharmaceutical chemists and will inspire more reaction development in this fascinating field.

摘要

使用绿色方法加速反应速率是化学家研究的一个有趣领域。在这方面,水作为一种“绿色溶剂”在加速某些有机转化中起着至关重要的作用,并且与传统有机溶剂相比表现出独特的选择性和反应性。特别是,多组分反应(MCRs)作为可持续工具,由于疏水效应的突出作用,在水中和水介质中快速生成小分子文库。MCRs 作为多样性导向合成(DOS)方法,具有操作简单、原子经济性、釜式经济性和步骤经济性以及机制美的特点,效率很高。在各种类型的 MCRs 中,基于异氰化物的多组分反应(I-MCRs)作为可持续且多功能的反应,由于异氰化物作为特殊活性反应物的特殊性质,在杂环环的合成中,特别是在药物设计中,引起了相当大的关注。在水中进行的 I-MCRs 温和、环保且易于控制,并且减少了后处理、纯化和提取步骤,这与“绿色”化学的优势非常吻合。由于负的活化体积,这些强大的有机转化在水中和水介质中的进行伴随着加速,这是由于将几个反应物连接在一起生成单个产物所致。应当指出,MCR 策略与水相反应的结合对于开发有机转化中可持续合成技术的发展越来越感兴趣。然而,特别缺乏专门关注在水和水介质中进行环保型 I-MCR 以构建杂环的最新进展的综述文章。这篇综述重点介绍了在水和水介质中作为构建重要杂环骨架的有效方法的各种 I-MCRs 的最新进展,并对 2000-2021 年期间的这一主题进行了批判性讨论。我们希望这个主题集对有机和制药化学家们有兴趣和有益,并激发该迷人领域的更多反应开发。

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