Development of Reductive C-S Coupling for Preparing S-Aryl/alkyl Containing Peptides.
Key Insights
- Herein, we report a robust reductive coupling of cysteine thiosulfonate derivatives with aryl/alkyl halides, enabling chemoselective modification of peptides.
- Using zinc as the reducing agent, it provides a divergent platform for construction of Csp3/Csp2─S bonds, featuring base-free reaction condit.
Show formatted citation
@misc{ acaciamarkets-research-development-of-reductive-c-s-coupling-for-preparing-s-aryl-a,
title = { Development of Reductive C-S Coupling for Preparing S-Aryl/alkyl Containing Peptides. },
author = { J Wang, Q Fan, C Wang et al. },
year = { 2026 },
doi = { 10.1021/acs.joc.6c02145 },
url = { https://pubmed.ncbi.nlm.nih.gov/42895049/ },
note = {Summarized and classified by AcaciaFund}
}
TY - GEN TI - Development of Reductive C-S Coupling for Preparing S-Aryl/alkyl Containing Peptides. AU - J Wang, Q Fan, C Wang et al. PY - 2026 DO - 10.1021/acs.joc.6c02145 UR - https://pubmed.ncbi.nlm.nih.gov/42895049/ ER -
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Overview
Herein, we report a robust reductive coupling of cysteine thiosulfonate derivatives with aryl/alkyl halides, enabling chemoselective modification of peptides. Using zinc as the reducing agent, it provides a divergent platform for construction of Csp3/Csp2─S bonds, featuring base-free reaction conditions, operational simplicity, and broad substrate compatibility.
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