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Electrochemical deoxygenative amination of stabilized alkyl radicals from activated alcohols
Nature Communications ( IF 14.7 ) Pub Date : 2024-07-20 , DOI: 10.1038/s41467-024-50596-3 Jia Xu 1 , Yilin Liu 1 , Qing Wang 1 , Xiangzhang Tao 1 , Shengyang Ni 1 , Weigang Zhang 1 , Lei Yu 1 , Yi Pan 1 , Yi Wang 1
中文翻译:
活化醇中稳定烷基的电化学脱氧胺化
更新日期:2024-07-20
Nature Communications ( IF 14.7 ) Pub Date : 2024-07-20 , DOI: 10.1038/s41467-024-50596-3 Jia Xu 1 , Yilin Liu 1 , Qing Wang 1 , Xiangzhang Tao 1 , Shengyang Ni 1 , Weigang Zhang 1 , Lei Yu 1 , Yi Pan 1 , Yi Wang 1
Affiliation
Alkylamine structures represent one of the most functional and widely used in organic synthesis and drug design. However, the general methods for the functionalization of the shielded and deshielded alkyl radicals remain elusive. Here, we report a general deoxygenative amination protocol using alcohol-derived carbazates and nitrobenzene under electrochemical conditions. A range of primary, secondary, and tertiary alkylamines are obtained. This practical procedure can be scaled up through electrochemical continuous flow technique.
中文翻译:
活化醇中稳定烷基的电化学脱氧胺化
烷基胺结构是有机合成和药物设计中功能最丰富、应用最广泛的结构之一。然而,屏蔽和去屏蔽烷基官能化的一般方法仍然难以捉摸。在这里,我们报告了在电化学条件下使用醇衍生的肼基甲酸酯和硝基苯的通用脱氧胺化方案。获得一系列伯、仲和叔烷基胺。该实用程序可以通过电化学连续流技术扩大规模。