"Synthetic study of C-Arylglycoside"

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dc.contributor.authorOsman, Dr. Hasnah
dc.date.accessioned2017-06-06T07:01:36Z
dc.date.available2017-06-06T07:01:36Z
dc.date.issued2007
dc.description.abstractThe synthesis of C-arylglycoside have attracted much attention due to the stability towards the enzymatic and acid hydrolysis. In this synthesis, scandium triflate was used as the Lewis acid to promote~ C-glycosylation reactions. The reaction between D-olivoside and 2- naphthol was efficiently catalysed by 0.25 equivalents of scandium triflate with respect to the D-olivoside and afforded a novel 2-hydroxy-1- [3 ',4' -di-0-acetyl-5 '-methyl-2-deoxy-,8-D-arabino-hexopyranosyl]-naphthalene m 75% yield. The synthesised C-glycoside are characterised by IR, 1H-NMR, and 13CNMR spectroscopyen_US
dc.identifier.urihttp://hdl.handle.net/123456789/4001
dc.subjectChemistryen_US
dc.title"Synthetic study of C-Arylglycoside"en_US
dc.typeTechnical Reporten_US
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