Radical Cascade Nitro-Cyclization Reaction of Oxygen-Linked 1,7-Dienes for the Synthesis of NO<sub>2</sub>-Substituted Benzoxepines

A series of nitro-benzoxepines were prepared from easily available oxygen-linked 1,7-dienes by using K<sub>2</sub>S<sub>2</sub>O<sub>8</sub> as the oxidant and NaNO<sub>2</sub> as the nitrogen source. This approach features mild conditions, readily accessible reagents, simple operation, and broad substrate applicability. Mechanistic studies suggest that the reaction proceeds through a radical pathway.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-09-12
DOI
https://doi.org/10.1021/acs.joc.5c01739
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.94
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article

Radical Cascade Nitro-Cyclization Reaction of Oxygen-Linked 1,7-Dienes for the Synthesis of NO2-Substituted Benzoxepines

Xiaowei Zhao, A. V. Pan, Nengneng Zhou, Man Zhang et al.
1 citations
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
0.94
article

Radical Cascade Nitro-Cyclization Reaction of Oxygen-Linked 1,7-Dienes for the Synthesis of NO2-Substituted Benzoxepines

Xiaowei Zhao, A. V. Pan, Nengneng Zhou, Man Zhang, Wanqing Zhao, J. Y. C. CHU
article en
1 citations

Abstract

A series of nitro-benzoxepines were prepared from easily available oxygen-linked 1,7-dienes by using K<sub>2</sub>S<sub>2</sub>O<sub>8</sub> as the oxidant and NaNO<sub>2</sub> as the nitrogen source. This approach features mild conditions, readily accessible reagents, simple operation, and broad substrate applicability. Mechanistic studies suggest that the reaction proceeds through a radical pathway.

The Journal of Organic ChemistryVol. 90(38)
Ministry of Education of the People's Republic of China (CN), Ministry of Education (BD), Anhui Normal University (CN)
Openalex Percentile: Top 22%
Catalytic C–H Functionalization Methods
0.94
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