Solid-phase synthesis of C-terminal thio-linked glycopeptides

dc.contributor.author	Falconer, Robert A.	*
dc.contributor.author	Malkinson, J.P.	*
dc.date.accessioned	2009-12-17T15:37:19Z
dc.date.available	2009-12-17T15:37:19Z
dc.date.issued	2002
dc.identifier.citation	Falconer, R.A. and Malkinson, J.P. (2002). Solid-phase synthesis of C-terminal thio-linked glycopeptides. Tetrahedron Letters. Vol. 43, No. 52, pp. 4549-9552.	en
dc.identifier.uri	http://hdl.handle.net/10454/4140
dc.description	No	en
dc.description.abstract	A solid-phase Mitsunobu reaction between a resin-bound 1-thiosugar and an N-Fmoc protected amino alcohol was successfully employed for thio-linked glycopeptide synthesis. Facile cleavage and deprotection in one step afforded the target glycopeptide in good yield and purity.	en
dc.language.iso	en	en
dc.relation.isreferencedby	http://dx.doi.org/10.1016/S0040-4039(02)02419-X	en
dc.subject	Succinate	en
dc.subject	Amino Acid	en
dc.subject	Alcohol	en
dc.subject	Polystyrene	en
dc.subject	Glycosylation	en
dc.subject	Cell Differentiation	en
dc.subject	Cell Adhesion	en
dc.subject	Cell Recognition	en
dc.title	Solid-phase synthesis of C-terminal thio-linked glycopeptides	en
dc.status.refereed	Yes	en
dc.type	Article	en
dc.type.version	No full-text available in the repository	en