dc.contributor.author | Bennett, Jack | |
dc.contributor.author | Roux, Amélie | |
dc.contributor.author | Murphy, Paul | |
dc.date.accessioned | 2018-09-20T16:00:53Z | |
dc.date.available | 2018-09-20T16:00:53Z | |
dc.date.issued | 2017-03-19 | |
dc.identifier.citation | Bennett, Jack; Roux, Amélie; Murphy, Paul (2017). Methyl 2,3,6-tri-o-benzoyl-4-o-(tert-butyldimethylsilyl)-β-d-galactopyranoside. Molbank (1), | |
dc.identifier.issn | 1422-8599 | |
dc.identifier.uri | http://hdl.handle.net/10379/10409 | |
dc.description.abstract | Methyl 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.publisher | MDPI AG | |
dc.relation.ispartof | Molbank | |
dc.rights | Attribution-NonCommercial-NoDerivs 3.0 Ireland | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/3.0/ie/ | |
dc.subject | galactose | |
dc.subject | monosaccharide | |
dc.subject | silylation | |
dc.subject | benzoylation | |
dc.subject | nmr | |
dc.subject | anomerization | |
dc.subject | diastereomers | |
dc.subject | inhibitors | |
dc.subject | design | |
dc.subject | sncl4 | |
dc.title | Methyl 2,3,6-tri-o-benzoyl-4-o-(tert-butyldimethylsilyl)-β-d-galactopyranoside | |
dc.type | Article | |
dc.identifier.doi | 10.3390/m935 | |
dc.local.publishedsource | http://www.mdpi.com/1422-8599/2017/1/M935/pdf | |
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