多组分反应中的甲醛替代物。

IF 2.2 4区 化学 Q2 CHEMISTRY, ORGANIC
Beilstein Journal of Organic Chemistry Pub Date : 2025-03-13 eCollection Date: 2025-01-01 DOI:10.3762/bjoc.21.45
Cecilia I Attorresi, Javier A Ramírez, Bernhard Westermann
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引用次数: 0

摘要

甲醛是多组分反应的基石,主要因其强劲的反应活性而受到重视。然而,除了这些有益的特性,这种高活性的c1构建块引起了人们的关注,主要是关于它的毒性。一个值得注意的问题是在反应过程中控制不需要的副产物形成的挑战。这篇综述探讨了替代c1构建块作为甲醛的替代品,旨在减轻其在多组分反应中使用的一些挑战。通过确定这些替代品,可以解决毒性问题和改进反应控制,为更有效和可持续的合成方法铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formaldehyde surrogates in multicomponent reactions.

Formaldehyde emerges as a cornerstone in multicomponent reactions, mainly prized for its robust reactivity. Yet, alongside these beneficial traits, this highly reactive C1-building block raises concerns, primarily regarding its toxicity. One notable issue is the challenge of controlling the formation of undesired byproducts during its reactions. This review explores alternative C1-building blocks that serve as surrogates for formaldehyde, aiming to mitigate some of the challenges associated with its use in multicomponent reactions. By identifying these alternatives, toxicity concerns and improved reaction control can be addressed, paving the way for more efficient and sustainable synthetic methodologies.

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来源期刊
CiteScore
4.90
自引率
3.70%
发文量
167
审稿时长
1.4 months
期刊介绍: The Beilstein Journal of Organic Chemistry is an international, peer-reviewed, Open Access journal. It provides a unique platform for rapid publication without any charges (free for author and reader) – Platinum Open Access. The content is freely accessible 365 days a year to any user worldwide. Articles are available online immediately upon publication and are publicly archived in all major repositories. In addition, it provides a platform for publishing thematic issues (theme-based collections of articles) on topical issues in organic chemistry. The journal publishes high quality research and reviews in all areas of organic chemistry, including organic synthesis, organic reactions, natural product chemistry, structural investigations, supramolecular chemistry and chemical biology.
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