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Updated: Jan 9, 2026

Constructing Cyclic Peptides Using an On-Tether Sulfonium Center
Published on: September 28, 2022
Copper-Catalyzed Selective N-Sulfenylation of Tryptophan-Containing Peptides
Jian Tang1,2, Qinyu Lu1, Han Chu1
1Key Laboratory of Catalytic Conversion and Clean Energy in Universities of Shandong Province, School of Chemistry and Chemical Engineering, Qufu Normal University, Qufu 273165, P. R. China.
Abstract:
Site-selective modification of peptides is essential for biomedical research; herein, we develop a versatile strategy for the late-stage functionalization of peptides through copper-catalyzed N-sulfenylation of tryptophan residues. This method is quite compatible with a broad range of functional groups and enables the site-selective formation of a N-S bond at the nitrogen atom of tryptophan without the need for directing groups.
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