Robust synthesis of C-terminal cysteine-containing peptide acids through a peptide hydrazide-based strategy

Org Biomol Chem. 2019 Jun 12;17(23):5698-5702. doi: 10.1039/c9ob01114e.

Abstract

A new robust strategy was reported for the epimerization-free synthesis of C-terminal Cys-containing peptide acids through mercaptoethanol-mediated hydrolysis of peptide thioesters prepared in situ from peptide hydrazides. This simple-to-operate and highly efficient method avoids the use of derivatization reagents for resin modification, thus providing a practical avenue for the preparation of C-terminal Cys-containing peptide acids.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acids / chemical synthesis*
  • Amino Acid Sequence
  • Cysteine / chemistry*
  • Peptides / chemical synthesis*
  • Peptides / chemistry
  • Protein Conformation

Substances

  • Acids
  • Peptides
  • Cysteine