Show simple item record

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.
dc.identifier.urihttp://hdl.handle.net/10454/4140
dc.descriptionNo
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.
dc.language.isoen
dc.subjectSuccinate
dc.subjectAmino Acid
dc.subjectAlcohol
dc.subjectPolystyrene
dc.subjectGlycosylation
dc.subjectCell Differentiation
dc.subjectCell Adhesion
dc.subjectCell Recognition
dc.titleSolid-phase synthesis of C-terminal thio-linked glycopeptides
dc.status.refereedYes
dc.typeArticle
dc.type.versionNo full-text in the repository
dc.identifier.doihttps://doi.org/10.1016/S0040-4039(02)02419-X
dc.openaccess.statusclosedAccess


This item appears in the following Collection(s)

Show simple item record