Mou Rui-Qi, Zhao Mei, Lv Xue-Xin, Zhang Sheng-Yan, Guo Dian-Shun
College of Chemistry, Chemical Engineering and Materials Science, Collaborative Innovation Center of Functionalized Probes for Chemical Imaging in Universities of Shandong, Shandong Normal University Jinan 250014 P. R. China
RSC Adv. 2018 Mar 6;8(17):9555-9563. doi: 10.1039/c8ra01004h. eCollection 2018 Feb 28.
An efficient and green synthesis of 4-ferrocenylquinoline derivatives through a TsOH-catalyzed three-component reaction of aromatic aldehydes, amines and ferrocenylacetylene in water has been successfully developed. This strategy is a powerful method for the construction of diverse ferrocenyl-quinoline conjugates from simple available starting materials as it minimized the use of metal catalyst and organic solvent in the reaction process. The conjugates feature unique structures and excellent electronic properties. Moreover, a plausible mechanism for this TsOH-catalyzed three-component reaction was proposed and assessed.
通过对甲苯磺酸(TsOH)催化的芳香醛、胺和二茂铁乙炔在水中的三组分反应,成功开发了一种高效、绿色合成4-二茂铁基喹啉衍生物的方法。该策略是一种从简单易得的起始原料构建多种二茂铁基喹啉共轭物的有效方法,因为它在反应过程中最大限度地减少了金属催化剂和有机溶剂的使用。这些共轭物具有独特的结构和优异的电子性质。此外,还提出并评估了这种对甲苯磺酸催化的三组分反应的合理机理。