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Development of Reductive C-S Coupling for Preparing S-Aryl/alkyl Containing Peptides.

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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.
Cite this synthesis DOI: 10.1021/acs.joc.6c02145 ↗
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@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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