n -杂环的电化学无受体脱氢:释放氢可持续合成芳香族化合物

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC
Shiwen Fu, , , Weihang Li, , , Hangxuan Wu, , , Gongyuan Zhao, , , Zhonghui Sun*, , , Jinsong Peng*, , and , Chunxia Chen*, 
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引用次数: 0

摘要

电化学催化无受体脱氢(ECAD)是一种新兴的绿色有机转化,可以直接合成不饱和化合物。本文首次在环境条件下对n -杂环化合物如二氢嘧啶(dhpm)、二氢嘧啶和二氢嘧啶(DHPs)进行了无电催化剂和无氧化剂的ECAD。通过使用未分裂的电池结构,各种二氢杂环化合物(共40个例子)在阳极有效地转化为相应的产物,收率高达99%,同时在阴极产生分子氢。此外,该方法证明了适用于克尺度合成,突出了其可扩展性和工业实用性。我们提出了一种温和、无金属、可扩展的构建芳香n杂环的策略,为可持续有机合成的进步做出了贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Electrochemical Acceptorless Dehydrogenation of N-Heterocycles: Sustainable Synthesis of Aromatic Compounds with Hydrogen Release

Electrochemical Acceptorless Dehydrogenation of N-Heterocycles: Sustainable Synthesis of Aromatic Compounds with Hydrogen Release

Electrochemical Acceptorless Dehydrogenation of N-Heterocycles: Sustainable Synthesis of Aromatic Compounds with Hydrogen Release

Electrochemical catalytic acceptorless dehydrogenation (ECAD) represents an emerging green organic transformation that enables the direct synthesis of unsaturated compounds. This work describes the first electrocatalyst-free and oxidant-free ECAD of N-heterocycles such as dihydropyrimidinones (DHPMs), dihydropyrimidines, and dihydropyridines (DHPs) under ambient conditions. By utilizing an undivided-cell configuration, various dihydro-heterocycles (40 examples in total) were effectively converted into the corresponding products with yields up to 99% at the anode, while generating molecular hydrogen at the cathode. Furthermore, the methodology demonstrated applicability to gram-scale synthesis, highlighting its scalability and industrial practicality. We present a mild, metal-free, and scalable strategy for constructing aromatic N-heterocycles, contributing to the advancement of sustainable organic synthesis.

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来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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