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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Year
2025
Type
article
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Qi Lu, Han Chu, Hon‐Wah Man et al. (2025). Copper-Catalyzed Selective N-Sulfenylation of Tryptophan-Containing Peptides. Organic Letters . https://doi.org/10.1021/acs.orglett.5c04752

Identifiers

DOI
10.1021/acs.orglett.5c04752
PMID
41369085

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Data completeness: 77%