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一种由芳基甲醇和脒通过钌催化脱氢高效合成2,4,6-三芳基-1,3,5-三嗪的方法。

An efficient ruthenium-catalyzed dehydrogenative synthesis of 2,4,6-triaryl-1,3,5-triazines from aryl methanols and amidines.

作者信息

Xie Feng, Chen Mengmeng, Wang Xiaoting, Jiang Huanfeng, Zhang Min

机构信息

School of Chemical & Material Engineering, Jiangnan University, Wuxi 214122, People's Republic of China.

出版信息

Org Biomol Chem. 2014 May 7;12(17):2761-8. doi: 10.1039/c3ob42589d.

Abstract

By using [RuCl2(p-Cymene)]2/Cs2CO3 as an efficient catalyst system, the readily available, inexpensive aryl methanols were firstly employed for dehydrogenative synthesis of aryl substituted 1,3,5-triazine derivatives. Due to the inherent stability of alcohols in contrast with aldehydes, our synthetic protocol is adaptable to a broad substrate scope, there is no need for stringent protection during the whole operation process, and it has the potential to prepare valuable products that are currently inaccessible or challenging to prepare using conventional methods. It is a significantly important complement to the conventional synthetic methodologies.

摘要

通过使用[RuCl2(p-异丙基苯)]2/Cs2CO3作为高效催化体系,首次将易于获得且价格低廉的芳基甲醇用于芳基取代的1,3,5-三嗪衍生物的脱氢合成。由于醇类相对于醛类具有固有的稳定性,我们的合成方案适用于广泛的底物范围,在整个操作过程中无需严格的保护措施,并且有潜力制备目前难以通过传统方法获得或制备具有挑战性的有价值产物。这是对传统合成方法的一个非常重要的补充。

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