Stereoselective Synthesis of Sialylated Tumor-Associated Glycosylamino Acids

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Open Access

Field	Value	Language
dc.contributor.author	Corcilius, Leo
dc.contributor.author	Payne, Richard J.
dc.date.accessioned	2020-06-19
dc.date.available	2020-06-19
dc.date.issued	2013-10-25
dc.identifier.uri	https://hdl.handle.net/2123/22614
dc.description.abstract	Suitably protected sialyl TN and 2,6-sialyl T tumor-associated carbohydrate antigen-derived amino acids have been prepared stereoselectively using an oxazolidinone-derived sialoside donor. These glycosylamino acids can be employed directly in the solid-phase synthesis of glycopeptides, as demonstrated by the efficient preparation of tumor-associated MUC1 glycopeptide fragments.	en
dc.language.iso	en_US	en
dc.publisher	American Chemical Society	en
dc.relation	ARC DP120100194	en
dc.rights	Other	en
dc.subject	Peptides and proteins	en
dc.subject	Monomers	en
dc.subject	Organic polymers	en
dc.subject	Antigens	en
dc.title	Stereoselective Synthesis of Sialylated Tumor-Associated Glycosylamino Acids	en
dc.type	Article	en
dc.subject.asrc	FoR::030599 - Organic Chemistry not elsewhere classified	en
dc.subject.asrc	FoR::030499 - Medicinal and Biomolecular Chemistry not elsewhere classified	en
dc.identifier.doi	10.1021/ol402845e
dc.type.pubtype	Author accepted manuscript	en
dc.relation.arc	DP120100194
usyd.faculty	SeS faculties schools::Faculty of Science	en