Peptide Cyclization Mediated by Metal‐Free S‐Arylation: S‐Protected Cysteine Sulfoxide as an Umpolung of the Cysteine Nucleophile
Author:
Affiliation:
1. Institute of Biomedical Sciences and Graduate School of Pharmaceutical Sciences Tokushima University Shomachi Tokushima 770-8505 Japan
2. Institute of Protein Research Osaka University Suita Osaka 565-0871 Japan
Funder
Japan Agency for Medical Research and Development
Japan Society for the Promotion of Science
Publisher
Wiley
Subject
General Chemistry,Catalysis,Organic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202102420
Reference60 articles.
1. Chemical Protein Modification through Cysteine
2. Studies on peptides. LXXXIII. Behavior of S-substituted cysteine sulfoxides under deprotecting conditions in peptide synthesis.
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4. Metal-free C–H thioarylation of arenes using sulfoxides: a direct, general diaryl sulfide synthesis
5. Direct C2-Functionalization of Indoles Triggered by the Generation of Iminium Species from Indole and Sulfonium Salt
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