Electrosynthesis of a <i>cyclo</i> -N <sub>5</sub> <sup>−</sup> anion <i>via</i> TEMPO-mediated selective C–N bond cleavage in aryl-pentazole

A non-metal and efficient electrochemical strategy for synthesizing a <i>cyclo</i>-N<sub>5</sub><sup>-</sup> anion through TEMPO-catalysed selective C-N bond cleavage in aryl-pentazole has been established. This novel protocol features avoidance of metal catalysts, mild conditions, water as the sole oxygen source, and applicability to other <i>N</i>-arylzoles.

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Publication Details

Journal
Chemical Communications
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cc02899j
Primary Topic
Radical Photochemical Reactions
Type
article
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article

Electrosynthesis of a cyclo -N 5 − anion via TEMPO-mediated selective C–N bond cleavage in aryl-pentazole

Xue‐Hai Ju, Feng Zhao, Chong Zhang
Chemical Communications
Radical Photochemical Reactions
article

Electrosynthesis of a cyclo -N 5 − anion via TEMPO-mediated selective C–N bond cleavage in aryl-pentazole

Xue‐Hai Ju, Feng Zhao, Chong Zhang
article en

Abstract

A non-metal and efficient electrochemical strategy for synthesizing a <i>cyclo</i>-N<sub>5</sub><sup>-</sup> anion through TEMPO-catalysed selective C-N bond cleavage in aryl-pentazole has been established. This novel protocol features avoidance of metal catalysts, mild conditions, water as the sole oxygen source, and applicability to other <i>N</i>-arylzoles.

Chemical CommunicationsVol. 61(68)
Nanjing University of Science and Technology (CN)
Openalex Percentile: Top 87%
Radical Photochemical Reactions
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