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dc.contributor.authorRibeiro Morais, Goreti*
dc.contributor.authorHumphrey, Andrew J.*
dc.contributor.authorFalconer, Robert A.*
dc.date.accessioned2010-12-21T16:32:24Z
dc.date.available2010-12-21T16:32:24Z
dc.date.issued2008
dc.identifier.citationRibeiro Morais, G., Humphrey, A.J. and Falconer, R.A. (2008). Application of HOF.CH3CN to the synthesis of glycosyl sulphones. Tetrahedron. Vol. 64, No. , pp. 7426-7431.en
dc.identifier.urihttp://hdl.handle.net/10454/4617
dc.descriptionNoen
dc.description.abstractA fast, complete and clean conversion of thioglycosides into glycosyl sulfones under mild acidic conditions is described, using the HOF·CH3CN complex at room temperature. This methodology affords glycosyl sulfones in high yields and in excellent purity.en
dc.language.isoenen
dc.subjectGlycosyl Sulfonesen
dc.subjectOxidationen
dc.subjectThioglycosidesen
dc.titleApplication of HOF.CH3CN to the synthesis of glycosyl sulphonesen
dc.status.refereedyesen
dc.typeArticleen
dc.type.versionNo full-text available in the repositoryen
dc.identifier.doihttps://doi.org/10.1016/j.tet.2008.05.033


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