Oxidative decarbonylation coupling of anilines with isocyanates for the synthesis of unsymmetric azobenzenes

This paper presents an efficient strategy for the construction of unsymmetric azobenzene compounds under metal-free and non-acidic conditions. This process employs high-valent iodine to promote the oxidative decarbonylation coupling of anilines and isocyanates. Various anilines and isocyanates are well tolerated, affording the target products in acceptable yields. Additional advantages of this method include the mild reaction conditions, ease of operation, and the use of cost-effective raw materials.

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Publication Details

Journal
Chemical Communications
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cc00708a
Citations
2
Primary Topic
Advanced Computing and Algorithms
Type
article
Field-Weighted Citation Impact
12.35
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article

Oxidative decarbonylation coupling of anilines with isocyanates for the synthesis of unsymmetric azobenzenes

Zhongzhi Zhu, Jiajie Wu, Jie Huang, Xiuwen Chen et al.
2 citations
Chemical Communications
Advanced Computing and Algorithms
12.35
article

Oxidative decarbonylation coupling of anilines with isocyanates for the synthesis of unsymmetric azobenzenes

Zhongzhi Zhu, Jiajie Wu, Jie Huang, Xiuwen Chen, Hao Li, Weijie Ren, Yutong Hu, Jiehao Chen, Xiangya Cai, Wenfang Xiong
article en
2 citations

Abstract

This paper presents an efficient strategy for the construction of unsymmetric azobenzene compounds under metal-free and non-acidic conditions. This process employs high-valent iodine to promote the oxidative decarbonylation coupling of anilines and isocyanates. Various anilines and isocyanates are well tolerated, affording the target products in acceptable yields. Additional advantages of this method include the mild reaction conditions, ease of operation, and the use of cost-effective raw materials.

Chemical CommunicationsVol. 61(36)
Guangdong Medical College (CN), Wuyi University (CN)
Openalex Percentile: Top 3%
Advanced Computing and Algorithms
12.35
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