Excited-State S <sub>N</sub> Ar Reactions of Nitroarenes

substitution, enabling reaction pathways that are inaccessible in the ground state. Following computational evaluation of common nucleophiles, we developed a synthetically practical protocol that enables denitrative substitution across diverse polycyclic arenes. These findings demonstrate that photoexcitation can reshape the aromatic character of arenes, thereby offering a new strategy to access previously inaccessible modes of arene functionalization.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-04-01
DOI
https://doi.org/10.1021/jacs.5c21841
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Excited-State S N Ar Reactions of Nitroarenes

Gui‐Juan Cheng, Zhen Lyu, Tiantian Liang, Fei Ye
Journal of the American Chemical Society
Radical Photochemical Reactions
article

Excited-State S N Ar Reactions of Nitroarenes

Gui‐Juan Cheng, Zhen Lyu, Tiantian Liang, Fei Ye
article en

Abstract

substitution, enabling reaction pathways that are inaccessible in the ground state. Following computational evaluation of common nucleophiles, we developed a synthetically practical protocol that enables denitrative substitution across diverse polycyclic arenes. These findings demonstrate that photoexcitation can reshape the aromatic character of arenes, thereby offering a new strategy to access previously inaccessible modes of arene functionalization.

Journal of the American Chemical SocietyVol. 148(14)
Chinese University of Hong Kong (HK), Central China Normal University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Hubei Province, Basic and Applied Basic Research Foundation of Guangdong Province
Openalex Percentile: Top 29%
Radical Photochemical Reactions
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