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通过电化学自由基级联环化合成磺化4H-3,1-苯并恶嗪。

The synthesis of sulfonated 4H-3,1-benzoxazines via an electro-chemical radical cascade cyclization.

作者信息

He Tian-Jun, Zhong Wei-Qiang, Huang Jing-Mei

机构信息

Key Laboratory of Functional Molecular Engineering of Guangdong Province, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, Guangdong 510640, China.

出版信息

Chem Commun (Camb). 2020 Mar 4;56(18):2735-2738. doi: 10.1039/c9cc09551a. Epub 2020 Feb 5.

DOI:10.1039/c9cc09551a
PMID:32021997
Abstract

A new route for the synthesis of sulfonated 4H-3,1-benzoxazines has been accomplished by electrochemical radical cascade cyclizations of styrenyl amides with sulfonylhydrazines. This process demonstrates a wide substrate scope with diverse functional group compatibility under metal- and external oxidant-free conditions at ambient temperature.

摘要

通过苯乙烯基酰胺与磺酰肼的电化学自由基级联环化反应,实现了一种合成磺化4H-3,1-苯并恶嗪的新路线。该过程在室温下无金属和外部氧化剂的条件下,展示了广泛的底物范围和多样的官能团兼容性。

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