Peptide and proteinthioester synthesisvia N→S acyl transfer†‡
Jaskiranjit Kang,Derek Macmillan
Organic & Biomolecular Chemistry Pub Date : 02/18/2010 00:00:00 , DOI:10.1039/B925075A
Abstract

Peptide and protein thioesters are playing an increasingly prominent role in the chemical toolbox for protein assembly and modification through Native Chemical Ligation (NCL). In this Emerging Area we highlight recent developments in a somewhat surprising route to thioesters: selective disruption of amides, the more stable carboxylic acid derivatives.

Graphical abstract: Peptide and protein thioester synthesis via N→S acyl transfer