Organomediator enabled electrochemically regioselective 1,2-arylalkylation of alkenes with aryl and alkyl halides

Alkene difunctionalization represents an efficient methodology for rapidly accessing complex molecular frameworks. Here, we developed a novel electrochemically intermolecular three-component regioselective 1,2-arylalkylation of alkenes with aryl and alkyl halides assisted by dimethyl terephthalate. This method features mild conditions, a wide substrate scope, and no requirement for noble-metal catalysts, and can be applied to the synthesis of 1,1-diarylalkanes. The protocol offers a pioneering strategy for achieving regioselective 1,2-arylalkylation of alkenes <i>via</i> radical pathways.

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Publication Details

Journal
Chemical Communications
Published
2025-12-23
DOI
https://doi.org/10.1039/d5cc06533j
Primary Topic
Radical Photochemical Reactions
Type
article
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article

Organomediator enabled electrochemically regioselective 1,2-arylalkylation of alkenes with aryl and alkyl halides

Lei Jing, Qian Su, Linhai Jing, Yulin Peng et al.
Chemical Communications
Radical Photochemical Reactions
article

Organomediator enabled electrochemically regioselective 1,2-arylalkylation of alkenes with aryl and alkyl halides

Lei Jing, Qian Su, Linhai Jing, Yulin Peng, Pan Han, Sheng Li
article en

Abstract

Alkene difunctionalization represents an efficient methodology for rapidly accessing complex molecular frameworks. Here, we developed a novel electrochemically intermolecular three-component regioselective 1,2-arylalkylation of alkenes with aryl and alkyl halides assisted by dimethyl terephthalate. This method features mild conditions, a wide substrate scope, and no requirement for noble-metal catalysts, and can be applied to the synthesis of 1,1-diarylalkanes. The protocol offers a pioneering strategy for achieving regioselective 1,2-arylalkylation of alkenes <i>via</i> radical pathways.

Chemical CommunicationsVol. 62(8)
China West Normal University (CN)
Openalex Percentile: Top 33%
Radical Photochemical Reactions
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