Luo Renshi, Tong Jinghui, Ouyang Lu, Liu Liang, Liao Jianhua
College of Chemistry and Environmental Engineering, Shaoguan University Shaoguan 512005 P. R. China.
School of Pharmaceutical Sciences, Gannan Medical University Ganzhou 341000 Jiangxi Province P. R. China
RSC Adv. 2023 Oct 9;13(42):29607-29612. doi: 10.1039/d3ra05736d. eCollection 2023 Oct 4.
The formation of C-N bond is a vital synthetic tool for establishing molecular diversity, which is highly sought after in a wide range of biologically active natural products and drugs. Herein, we present a new strategy for the synthesis of secondary amines iridium-catalyzed one-pot reductive amination of carbonyl compounds with nitro compounds. This method is demonstrated for a variety of carbonyl compounds, including miscellaneous aldehydes and ketones, which are compatible with this catalytic system, and deliver the desired products in good yields under mild conditions. In this protocol, the reduction of nitro compounds occurs first, followed by reductive amination to form amine products, providing a new one-pot procedure for amine synthesis.
碳氮键的形成是构建分子多样性的重要合成手段,在众多具有生物活性的天然产物和药物中备受青睐。在此,我们报道了一种合成仲胺的新策略——铱催化羰基化合物与硝基化合物的一锅法还原胺化反应。该方法适用于多种羰基化合物,包括各种醛和酮,它们与该催化体系兼容,并能在温和条件下以良好的产率得到所需产物。在此反应中,硝基化合物首先发生还原反应,随后进行还原胺化反应生成胺产物,为胺的合成提供了一种新的一锅法流程。