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dc.contributor.authorBennett, Jack
dc.contributor.authorRoux, Amélie
dc.contributor.authorMurphy, Paul
dc.date.accessioned2018-09-20T16:00:53Z
dc.date.available2018-09-20T16:00:53Z
dc.date.issued2017-03-19
dc.identifier.citationBennett, Jack; Roux, Amélie; Murphy, Paul (2017). Methyl 2,3,6-tri-o-benzoyl-4-o-(tert-butyldimethylsilyl)-β-d-galactopyranoside. Molbank (1),
dc.identifier.issn1422-8599
dc.identifier.urihttp://hdl.handle.net/10379/10409
dc.description.abstractMethyl 2,3,6-tri-O-benzoyl-4-O-(tert-butyldimethylsilyl)-beta-D-galactopyranoside was synthesized in 47% yield by the silylation of a partially benzoylated galactose derivative, prepared from methyl beta-D-galactopyranoside. The product was characterized by H-1-NMR, C-13-NMR, IR and mass spectrometry.
dc.publisherMDPI AG
dc.relation.ispartofMolbank
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Ireland
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/3.0/ie/
dc.subjectgalactose
dc.subjectmonosaccharide
dc.subjectsilylation
dc.subjectbenzoylation
dc.subjectnmr
dc.subjectanomerization
dc.subjectdiastereomers
dc.subjectinhibitors
dc.subjectdesign
dc.subjectsncl4
dc.titleMethyl 2,3,6-tri-o-benzoyl-4-o-(tert-butyldimethylsilyl)-β-d-galactopyranoside
dc.typeArticle
dc.identifier.doi10.3390/m935
dc.local.publishedsourcehttp://www.mdpi.com/1422-8599/2017/1/M935/pdf
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Attribution-NonCommercial-NoDerivs 3.0 Ireland
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Ireland