Year: 2013
Type: article
Abstract: The utility of a new β-thiol arginine building block in ligation-desulfurization chemistry has been demonstrated through reactions and kinetic studies with a range of peptide thioesters. Application of the method is highlighted by a one-pot, kinetically controlled, rapid ligation to generate a 7 kDa MUC1 glycopeptide.
Source: ChemBioChem
Institution: The University of Sydney
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: green
Funder: Australian Research Council
OpenAlex ID: W2080220870
