Issue 9, 2010

Peptide and proteinthioester synthesisvia N→S acyl transfer

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

Article information

Article type
Emerging Area
Submitted
30 Nov 2009
Accepted
29 Jan 2010
First published
18 Feb 2010

Org. Biomol. Chem., 2010,8, 1993-2002

Peptide and protein thioester synthesis via N→S acyl transfer

J. Kang and D. Macmillan, Org. Biomol. Chem., 2010, 8, 1993 DOI: 10.1039/B925075A

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