Reactions of N-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-carbonyl)-N’-tosylhydrazine with N-, O-nucleophiles
dc.contributor.advisor | Juhasné Tóth , Éva | |
dc.contributor.author | Mudau, Zwivhuya Phoebe | |
dc.contributor.department | DE--Természettudományi és Technológiai Kar--Kémiai Intézet | |
dc.date.accessioned | 2022-11-18T08:53:57Z | |
dc.date.available | 2022-11-18T08:53:57Z | |
dc.date.created | 2022-11-18 | |
dc.description.abstract | At the Chemical Glycobiology Research Group, systematic research has been going on for many years to study the reactivity of C-glycopyranosyl-formaldehyde-tosylhydrazones. In continuation of this topic, the aim of this paper was to synthesize N-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosylcarbonyl)-N'-tosylhydrazine and to study their reactions with different N- and O-nucleophiles. The molecule was reacted in the presence of N-bromosuccinimide with several primary and secondary amines giving the desired N-substituted C-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)formamide derivatives with low to excellent yields (5-86%). We also extended the reaction with several O- nucleophiles however, the C-glucopyranosyl-formamides and formicacid ester type molecules could not be isolated in the case of these nucleophiles. | |
dc.description.course | Chemical Engineering | |
dc.description.degree | BSc/BA | |
dc.format.extent | 23 | |
dc.identifier.uri | https://hdl.handle.net/2437/340996 | |
dc.language.iso | en | |
dc.subject | C-glycopyranosyl-formaldehyde-tosylhydrazones. | |
dc.subject | Carbohydrates | |
dc.subject | N- and O-nucleophiles | |
dc.subject.dspace | DEENK Témalista::Kémia | |
dc.title | Reactions of N-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-carbonyl)-N’-tosylhydrazine with N-, O-nucleophiles |