Electrochemical Synthesis of 3-(Sulfonyl)quinol-4-ones from <i>o</i>-Alkynyl-<i>N</i>-(formyl)anilides and Sulfinates

Electrolysis of <i>o</i>-alkynyl-<i>N</i>-(formyl)anilides and sodium sulfinates on graphite electrodes delivers biologically sound 3-(sulfonyl)quinol-4-ones with moderate to good yields. The reaction is carried out in an undivided cell in the presence of silver(I) oxide with potassium iodide or sodium tetrafluoroborate as the supporting electrolyte. The reaction tolerates variously substituted anilides as well as aryl and alkyl sulfinates. The transformation proceeds as a domino sequence of oxysulfonylation and cyclocondensation steps.

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Publication Details

Journal
Organic Letters
Published
2024-12-25
DOI
https://doi.org/10.1021/acs.orglett.4c04209
Citations
1
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.25

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article

Electrochemical Synthesis of 3-(Sulfonyl)quinol-4-ones from o-Alkynyl-N-(formyl)anilides and Sulfinates

Vladimir A. Kokorekin, А. В. Варламов, Alexey А. Festa, Vladimir L. Bondarev et al.
1 citations
Organic Letters
Sulfur-Based Synthesis Techniques
0.25
article

Electrochemical Synthesis of 3-(Sulfonyl)quinol-4-ones from o-Alkynyl-N-(formyl)anilides and Sulfinates

Vladimir A. Kokorekin, А. В. Варламов, Alexey А. Festa, Vladimir L. Bondarev, Leonid G. Voskressensky, Olga А. Storozhenko, Anton P. Novikov
article en
1 citations

Abstract

Electrolysis of <i>o</i>-alkynyl-<i>N</i>-(formyl)anilides and sodium sulfinates on graphite electrodes delivers biologically sound 3-(sulfonyl)quinol-4-ones with moderate to good yields. The reaction is carried out in an undivided cell in the presence of silver(I) oxide with potassium iodide or sodium tetrafluoroborate as the supporting electrolyte. The reaction tolerates variously substituted anilides as well as aryl and alkyl sulfinates. The transformation proceeds as a domino sequence of oxysulfonylation and cyclocondensation steps.

Organic LettersVol. 27(1)
Peoples' Friendship University of Russia (RU), Sechenov University (RU), Frumkin Institute of Physical Chemistry and Electrochemistry Russian Academy of Sciences (RU)
Russian Science Foundation
Openalex Percentile: Top 45%
Sulfur-Based Synthesis Techniques
0.25
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