Electrochemical Approach Toward Mesoionic 1,2,3‐Triazole 1‐Imines

Abstract Synthetic electrochemistry may establish direct routes to a preparation of a plethora of organic substances, which are hardly accessible by conventional experimental techniques. Herein, we present an electrochemically‐driven method for an assembly of a broad range of rare heterocyclic mesoionic entities –1,2,3‐triazole 1‐imines. These nitrogen heterocycles were prepared through a transition‐metal‐ and exogenous oxidant‐free strategy using a C/Ni electrode pair. Over 30 examples of thus synthesized 1,2,3‐triazole 1‐imines illustrate selectivity and practical utility of this approach. Key solvent‐controlled reactivity patterns for the formation of the triazole imine scaffold were revealed indicating a modulation ability of the developed approach. These experimental findings were additionally justified based on cyclic voltammetry (CV) data and density functional theory (DFT) calculations. Moreover, according to differential scanning calorimetry (DSC) data, some of the prepared 1,2,3‐triazole 1‐imines correspond to the thermally stable species with an onset decomposition temperature up to 190 °C.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2024-08-21
DOI
https://doi.org/10.1002/adsc.202400761
Citations
5
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
1.25
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article

Electrochemical Approach Toward Mesoionic 1,2,3‐Triazole 1‐Imines

Alexander D. Shuvaev, Fedor E. Teslenko, Леонид Л. Ферштат, Matvey A. Feoktistov
5 citations
Advanced Synthesis & Catalysis
Radical Photochemical Reactions
1.25
article

Electrochemical Approach Toward Mesoionic 1,2,3‐Triazole 1‐Imines

Alexander D. Shuvaev, Fedor E. Teslenko, Леонид Л. Ферштат, Matvey A. Feoktistov
article en
5 citations

Abstract

Abstract Synthetic electrochemistry may establish direct routes to a preparation of a plethora of organic substances, which are hardly accessible by conventional experimental techniques. Herein, we present an electrochemically‐driven method for an assembly of a broad range of rare heterocyclic mesoionic entities –1,2,3‐triazole 1‐imines. These nitrogen heterocycles were prepared through a transition‐metal‐ and exogenous oxidant‐free strategy using a C/Ni electrode pair. Over 30 examples of thus synthesized 1,2,3‐triazole 1‐imines illustrate selectivity and practical utility of this approach. Key solvent‐controlled reactivity patterns for the formation of the triazole imine scaffold were revealed indicating a modulation ability of the developed approach. These experimental findings were additionally justified based on cyclic voltammetry (CV) data and density functional theory (DFT) calculations. Moreover, according to differential scanning calorimetry (DSC) data, some of the prepared 1,2,3‐triazole 1‐imines correspond to the thermally stable species with an onset decomposition temperature up to 190 °C.

Advanced Synthesis & CatalysisVol. 366(24)
Lomonosov Moscow State University (RU), N.D. Zelinsky Institute of Organic Chemistry (RU)
Openalex Percentile: Top 23%
Radical Photochemical Reactions
1.25
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Electrochemical Approach Toward Mesoionic 1,2,3‐Triazole 1‐Imines — Alexander D. Shuvaev, Fedor E. Teslenko, et al. · Advanced Synthesis & Catalysis (2024) | TGRS Research Map | TGRS