Encounter of Organic Electrochemical Reactions and Liquid-Phase Peptide Synthesis: Development of Electrochemical Peptide Synthesis

Our group has been developing organic electrochemical reactions (since 1994) and liquid-phase peptide synthesis (since 2002) mostly independently of each other. The merger of electrochemistry and peptides had been a long-cherished goal of our group, yet apart from the limited example of electrochemical disulfide bond formation, the two had never encountered. Herein, we describe electrochemical peptide synthesis using triarylphophines as recyclable “coupling reagents,” where electrochemistry and peptides are merged.

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Publication Details

Journal
Journal of Synthetic Organic Chemistry Japan
Published
2026-05-01
DOI
https://doi.org/10.5059/yukigoseikyokaishi.84.443
Primary Topic
Radical Photochemical Reactions
Type
article
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article

Encounter of Organic Electrochemical Reactions and Liquid-Phase Peptide Synthesis: Development of Electrochemical Peptide Synthesis

Kazuhiro Chiba, Yohei Okada
Journal of Synthetic Organic Chemistry Japan
Radical Photochemical Reactions
article

Encounter of Organic Electrochemical Reactions and Liquid-Phase Peptide Synthesis: Development of Electrochemical Peptide Synthesis

Kazuhiro Chiba, Yohei Okada
article en

Abstract

Our group has been developing organic electrochemical reactions (since 1994) and liquid-phase peptide synthesis (since 2002) mostly independently of each other. The merger of electrochemistry and peptides had been a long-cherished goal of our group, yet apart from the limited example of electrochemical disulfide bond formation, the two had never encountered. Herein, we describe electrochemical peptide synthesis using triarylphophines as recyclable “coupling reagents,” where electrochemistry and peptides are merged.

Journal of Synthetic Organic Chemistry JapanVol. 84(5)
Tokyo University of Agriculture (JP), Tokyo University of Agriculture and Technology (JP)
Openalex Percentile: Top 10%
Radical Photochemical Reactions
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