High-pressure activation for the solvent- and catalyst-free syntheses of heterocycles, pharmaceuticals and esters.

IF 2.2 4区 化学 Q2 CHEMISTRY, ORGANIC
Beilstein Journal of Organic Chemistry Pub Date : 2025-07-02 eCollection Date: 2025-01-01 DOI:10.3762/bjoc.21.102
Kelsey Plasse, Valerie Wright, Guoshu Xie, R Bernadett Vlocskó, Alexander Lazarev, Béla Török
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引用次数: 0

Abstract

High hydrostatic pressure (HHP) was found to be an efficient activation method in several catalyst- and solvent-free reactions and has found application for the syntheses of heterocycles and the preparation of active pharmaceutical ingredients (APIs) via acylation and acid- and solvent-free esterification. The reactions were carried out at ambient pressure (control) and under HHP (up to 3.8 kbar) conditions. These representative reactions provided higher yields for the products and HHP enabled truly green processes that are catalyst- and solvent-free, to occur with high yields and producing only non-toxic by-products. A computational study accompanies the experimental data to interpret the outcome of the reactions.

高压活化用于无溶剂和无催化剂的杂环、药物和酯的合成。
高静水压力(HHP)在几种无催化剂和无溶剂的反应中被发现是一种有效的活化方法,并已被应用于杂环化合物的合成和通过酰化、无酸和无溶剂酯化制备活性药物成分(api)。反应在环境压力(控制)和高压(高达3.8 kbar)条件下进行。这些具有代表性的反应为产物提供了更高的产率,HHP使真正的绿色工艺成为可能,即无催化剂和溶剂,产率高,只产生无毒副产物。伴随着实验数据的计算研究解释了反应的结果。
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
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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