Shinjo-Nagahara S,
Okada Y,
Hiratsuka G,
Kitano Y,
Chiba K.
*
Tokyo University of Agriculture and Technology, Japan
Improved Electrochemical Peptide Synthesis Enabled by Electron-Rich Triaryl Phosphines.
Chem. Eur. J. 2024;
30: e202402552
Key words
electrochemical synthesis - triaryl phosphine - oligopeptides
Significance
Electrochemical peptide synthesis received considerable attention in peptide chemistry. The authors reported the synthesis of peptides using electron-rich triaryl phosphine under electrochemical conditions. The methodology was examined for a broad range of substrates including oligopeptides.
Comment
The authors developed an improved electrochemical peptide synthesis method using an electron-rich triaryl phosphine that is effective for sterically hindered amino acids and challenging peptides like Rapastinel and Bradykinin. 18O-Labeling experiments suggested the suppression of side reactions, by enabling efficient peptide coupling. This advancement will drive the development of novel peptide synthesis and more efficient synthetic systems for highly hindered amino acids.