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由异吲哚酮、取代脲和环酮合成螺杂环的三组分反应。

Three-Component Reaction for the Synthesis of Spiro-Heterocycles from Isatins, Substituted Ureas, and Cyclic Ketones.

作者信息

Jiao Yang, Zhu Junyi, Han Niankun, Shen Rongcheng, Zhang Yiru, Rong Liangce, Zhang Jinpeng

机构信息

Jiangsu Engineering Research Center of Biological Data Mining and Healthcare Transformation, Xuzhou Medical University, Xuzhou 221004, Jiangsu, PR China.

Chemistry and Materials Science, Jiangsu Normal University, Xuzhou 221116, Jiangsu, PR China.

出版信息

J Org Chem. 2024 Mar 1;89(5):3441-3452. doi: 10.1021/acs.joc.3c02894. Epub 2024 Feb 20.

Abstract

We reported an efficient three-component reaction to access new spiro heterocycles through the annulation reactions of isatins, substituted ureas, and under normal laboratory conditions, which is another example of isatins being used to build spiro compounds by the ring-opening and recyclization processes. The wide range of substrates, simple operation, normal experimental conditions, and high yields make the approach of high practical value.

摘要

我们报道了一种高效的三组分反应,该反应可在常规实验室条件下通过异吲哚酮、取代脲和[具体反应物未给出]的环化反应来合成新型螺杂环化合物,这是异吲哚酮通过开环和再环化过程用于构建螺环化合物的又一个例子。底物范围广泛、操作简单、实验条件常规以及产率高使得该方法具有很高的实用价值。

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