Peptide Ligation–Desulfurization Chemistry at Arginine

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Open Access

Field	Value	Language
dc.contributor.author	Malins, Lara R.
dc.contributor.author	Cergol, Katie M.
dc.contributor.author	Payne, Richard J.
dc.date.accessioned	2020-05-11
dc.date.available	2020-05-11
dc.date.issued	2013-02-20
dc.identifier.uri	https://hdl.handle.net/2123/22249
dc.description.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.	en
dc.language.iso	en_US	en
dc.publisher	Wiley	en
dc.relation	ARC DP130101984	en
dc.rights	Other	en
dc.subject	Arginine	en
dc.subject	Desulfurization	en
dc.subject	glycopeptide	en
dc.subject	Ligation	en
dc.subject	peptides	en
dc.title	Peptide Ligation–Desulfurization Chemistry at Arginine	en
dc.type	Article	en
dc.subject.asrc	FoR::030599 - Organic Chemistry not elsewhere classified	en
dc.identifier.doi	10.1002/cbic.201300049
dc.type.pubtype	Author accepted manuscript	en
dc.relation.arc	DP130101984
usyd.faculty	SeS faculties schools::Faculty of Science	en