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环境友好型铁催化的1,2,4-苯并噻二嗪1,1-二氧化物和喹唑啉酮衍生物的串联合成

Environmentally friendly iron-catalyzed cascade synthesis of 1,2,4-benzothiadiazine 1,1-dioxide and quinazolinone derivatives.

作者信息

Yang Daoshan, Fu Hua, Hu Liming, Jiang Yuyang, Zhao Yufen

机构信息

Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University, Beijing, P. R. China.

出版信息

J Comb Chem. 2009 Jul-Aug;11(4):653-7. doi: 10.1021/cc9000339.

Abstract

We have developed an efficient iron-catalyzed method for the cascade synthesis of 1,2,4-benzothiadiazine 1,1-dioxide and quinazolinone derivatives. The protocol uses inexpensive and environmentally friendly FeCl(3) as the catalyst, and no ligand or additive was required. This is the first example of construction of nitrogen-containing heterocycles via iron-catalyzed N-arylation in the absence of ligand. Therefore, this method is of practical application for the synthesis of the two different nitrogen-containing heterocycles.

摘要

我们已经开发出一种高效的铁催化方法,用于1,2,4-苯并噻二嗪1,1-二氧化物和喹唑啉酮衍生物的级联合成。该方案使用廉价且环境友好的FeCl(3)作为催化剂,无需配体或添加剂。这是在无配体条件下通过铁催化N-芳基化构建含氮杂环的首个实例。因此,该方法在合成这两种不同的含氮杂环方面具有实际应用价值。

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