Journal
PROCESSES
Volume 11, Issue 8, Pages -Publisher
MDPI
DOI: 10.3390/pr11082262
Keywords
peptide; ynamide; addition reaction
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Peptide modification is an important topic in academia and the pharmaceutical industry, with a focus on the diversification of amines, thiols, and alcohols. However, the direct and chemoselective modification of acid residues in peptides is relatively underdeveloped. In this study, a novel and efficient method for the direct functionalization of acid residues in peptides is reported, using ynamides as reaction partners. This approach shows excellent chemoselectivity and a broad scope for various dipeptides containing unprotected Trp or Tyr residue and free Ser or Gln residue.
Peptide modification has emerged as an important topic in the academic community and pharmaceutical industry. However, they are primarily focused on the diversification of amines, thiols, and alcohols. Direct and chemoselective modification of acid residues in peptides is relatively underdeveloped. In this context, we report a novel and efficient method for the direct functionalization of acid residues in peptides. By using ynamides as reaction partners, the adducts are rapidly obtained in moderate to excellent yields at room temperature in water. This approach shows excellent chemoselectivity and a broad scope including dipeptides bearing unprotected Trp or Tyr residue and free Ser or Gln residue.
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