A new method for peptide synthesis in the N→C direction: amide assembly through silver-promoted reaction of thioamides

Chem Commun (Camb). 2014 Dec 28;50(100):15963-6. doi: 10.1039/c4cc07601j.

Abstract

The Ag(I)-promoted coupling of amino acids and peptides with amino ester thioamides generates peptide imides without epimerisation. The peptide imides undergo regioselective hydrolysis under mild conditions to generate native peptides. This method was employed to prepare the pentapeptide thymopentin in the N→C direction, in high yield and purity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Hydrolysis
  • Imides / chemistry
  • Peptides / chemical synthesis*
  • Peptides / chemistry
  • Silver / chemistry*
  • Stereoisomerism
  • Thioamides / chemistry*
  • Thymopentin / chemical synthesis
  • Thymopentin / chemistry

Substances

  • Imides
  • Peptides
  • Thioamides
  • Silver
  • Thymopentin