Electrochemical One-Pot Diverse C(sp3)–X Bond (Including C–H, C–C, C–N, and C–O) Transformations and C(sp2)–H Acyloxylation of Alkylarenes

Abstract In this study, an electrochemical one-pot cleavage of diverse C(sp3)–X bonds and acyloxylation of C(sp2)–H were reported. Based on the experimental results, we discovered for the first time that NH3 can strongly promote electrolyte dissolution and significantly increase the conductivity of a solution. Unlike previous C(sp2)–H acetoxylation reactions in which AcO– functions as a nucleophile, this reaction undergoes an acetoxy radical mechanism and prevents decarboxylation of the acetoxy radical. This reaction is advantageous because it is transition-metal-free, external-oxidant-free, atom- and step-economical, and applicable to diverse substrates; additionally, it uses mild reaction conditions and green and nontoxic solvents.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-09-30
DOI
https://doi.org/10.1021/acs.joc.6c01447
Primary Topic
Radical Photochemical Reactions
Type
article
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Electrochemical One-Pot Diverse C(sp3)–X Bond (Including C–H, C–C, C–N, and C–O) Transformations and C(sp2)–H Acyloxylation of Alkylarenes

Hui Gao, Pei-Long Wang, Li-Xue Zhou, Yu-Wei Jiang et al.
The Journal of Organic Chemistry
Radical Photochemical Reactions
article

Electrochemical One-Pot Diverse C(sp3)–X Bond (Including C–H, C–C, C–N, and C–O) Transformations and C(sp2)–H Acyloxylation of Alkylarenes

Hui Gao, Pei-Long Wang, Li-Xue Zhou, Yu-Wei Jiang, Jia-Di Ren
article en

Abstract

Abstract In this study, an electrochemical one-pot cleavage of diverse C(sp3)–X bonds and acyloxylation of C(sp2)–H were reported. Based on the experimental results, we discovered for the first time that NH3 can strongly promote electrolyte dissolution and significantly increase the conductivity of a solution. Unlike previous C(sp2)–H acetoxylation reactions in which AcO– functions as a nucleophile, this reaction undergoes an acetoxy radical mechanism and prevents decarboxylation of the acetoxy radical. This reaction is advantageous because it is transition-metal-free, external-oxidant-free, atom- and step-economical, and applicable to diverse substrates; additionally, it uses mild reaction conditions and green and nontoxic solvents.

The Journal of Organic Chemistry
Huaibei Normal University (CN)
Openalex Percentile: Top 22%
Radical Photochemical Reactions
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Electrochemical One-Pot Diverse C(sp3)–X Bond (Including C–H, C–C, C–N, and C–O) Transformations and C(sp2)–H Acyloxylation of Alkylarenes — Hui Gao, Pei-Long Wang, et al. · The Journal of Organic Chemistry (2026) | TGRS Research Map | TGRS