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dc.contributor.authorRibeiro Morais, Goreti*
dc.contributor.authorSpringett, Bradley R.*
dc.contributor.authorPauze, Martin*
dc.contributor.authorSchröder, Lisa*
dc.contributor.authorNorthrop, Matthew*
dc.contributor.authorFalconer, Robert A.*
dc.date.accessioned2016-02-10T16:24:09Z
dc.date.available2016-02-10T16:24:09Z
dc.date.issued2016-03
dc.identifier.citationRibeiro Morais G, Springett BR, Pauze M, Schröder L, Northrop M and Falconer RA (2016) Novel strategies for the synthesis of unsymmetrical glycosyl disulfides. Organic & Biomolecular Chemistry, 14: 2749-2754.
dc.identifier.urihttp://hdl.handle.net/10454/7764
dc.descriptionYes
dc.description.abstractNovel strategies for the efficient synthesis of unsymmetrical glycosyl disulfides are reported. Glycosyl disulfides are increasingly important as glycomimetics and molecular probes in glycobiology. Sialosyl disulfides are synthesised directly from the chlorosialoside Neu5Ac2Cl, proceeding via a thiol-disulfide exchange reaction between the sialosyl thiolate and symmetrical disulfides. This methodology was adapted and found to be successfully applicable to the synthesis of unsymmetrical glucosyl disulfides under mild conditions.
dc.language.isoen
dc.rights© 2016 RSC. Reproduced in accordance with the publisher's self-archiving policy.
dc.subjectGlycosyl disulfides
dc.subjectUnsymmetrical glycosyl disulfides
dc.subjectSynthesis
dc.subjectNovel strategies
dc.titleNovel strategies for the synthesis of unsymmetrical glycosyl disulfides
dc.status.refereedYes
dc.typeArticle
dc.type.versionAccepted manuscript
dc.identifier.doihttps://doi.org/10.1039/C6OB00230G
dc.rights.licenseUnspecified
refterms.dateFOA2018-07-25T12:12:40Z
dc.openaccess.statusopenAccess
dc.date.accepted02/02/2016


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