Contemporary Approaches for Amide Bond Formation

IF 4 2区 化学 Q2 CHEMISTRY, APPLIED
Paola Acosta-Guzmán, Andrea Ojeda-Porras, Diego Gamba-Sánchez
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引用次数: 0

Abstract

Amide bond construction has garnered significant interest in recent decades due to amides being one of the most prevalent functional groups among bioactive molecules. Out of the thirty-seven new drugs approved by the FDA in 2022, eleven are small molecules containing at least one amide bond. Additionally, there are nineteen large molecules approved as new drugs, some of which have peptide structures, and therefore, also bear amide bonds. In recent years, multiple teams have embraced the challenge of developing more efficient methods for amide bond formation. This dedication has led to numerous publications appearing monthly in prestigious journals, showcasing significant advancements in this field. The primary goal of this review is to present the most viable strategies for constructing the amide bond. It is crucial to differentiate between amide bond formation and amide synthesis; hence, the focus is on describing specific methods for forming new C(O)−N bonds. In particular, this review concentrates on the methods developed within the last six years. There is a particular emphasis on new approaches that consider the thought process when selecting the starting materials and functional groups. This approach ensures coverage of all the most common chemical transformations that yield new amide bonds.

酰胺键形成的当代方法
近几十年来,酰胺键的构建引起了人们的极大兴趣,因为酰胺是生物活性分子中最普遍的官能团之一。在美国食品药品监督管理局2022年批准的37种新药中,有11种是含有至少一个酰胺键的小分子。此外,有19种大分子被批准为新药,其中一些具有肽结构,因此也带有酰胺键。近年来,多个团队接受了开发更有效的酰胺键形成方法的挑战。这种奉献精神使许多出版物每月出现在著名期刊上,展示了该领域的重大进步。本综述的主要目标是提出构建酰胺键的最可行策略。区分酰胺键的形成和酰胺的合成是至关重要的;因此,重点是描述形成新的C(O)-N键的具体方法。特别是,本次审查的重点是过去六年内制定的方法。在选择起始材料和功能组时,特别强调考虑思维过程的新方法。这种方法确保覆盖所有产生新酰胺键的最常见的化学转化。
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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来源期刊
Advanced Synthesis & Catalysis
Advanced Synthesis & Catalysis 化学-应用化学
CiteScore
9.40
自引率
7.40%
发文量
447
审稿时长
1.8 months
期刊介绍: Advanced Synthesis & Catalysis (ASC) is the leading primary journal in organic, organometallic, and applied chemistry. The high impact of ASC can be attributed to the unique focus of the journal, which publishes exciting new results from academic and industrial labs on efficient, practical, and environmentally friendly organic synthesis. While homogeneous, heterogeneous, organic, and enzyme catalysis are key technologies to achieve green synthesis, significant contributions to the same goal by synthesis design, reaction techniques, flow chemistry, and continuous processing, multiphase catalysis, green solvents, catalyst immobilization, and recycling, separation science, and process development are also featured in ASC. The Aims and Scope can be found in the Notice to Authors or on the first page of the table of contents in every issue.
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