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dc.contributor.authorFalconer, Robert A.*
dc.contributor.authorMalkinson, J.P.*
dc.date.accessioned2009-12-17T15:37:19Z
dc.date.available2009-12-17T15:37:19Z
dc.date.issued2002
dc.identifier.citationFalconer, 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.urihttp://hdl.handle.net/10454/4140
dc.descriptionNoen
dc.description.abstractA 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.isoenen
dc.relation.isreferencedbyhttp://dx.doi.org/10.1016/S0040-4039(02)02419-Xen
dc.subjectSuccinateen
dc.subjectAmino Aciden
dc.subjectAlcoholen
dc.subjectPolystyreneen
dc.subjectGlycosylationen
dc.subjectCell Differentiationen
dc.subjectCell Adhesionen
dc.subjectCell Recognitionen
dc.titleSolid-phase synthesis of C-terminal thio-linked glycopeptidesen
dc.status.refereedYesen
dc.typeArticleen
dc.type.versionNo full-text available in the repositoryen


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