New strategy for the synthesis of 2-(N-substituted-amino)-2-deoxy-D-glucono-1,5-lactone arylsemicarbazones

dc.contributor.advisorSándor, Kun
dc.contributor.authorOyun-Erdene, Enkhjin
dc.contributor.departmentDE--Természettudományi és Technológiai Kar--Kémiai Intézet
dc.date.accessioned2024-12-20T08:41:43Z
dc.date.available2024-12-20T08:41:43Z
dc.date.created2024-11-22
dc.description.abstractThis research focuses on synthesizing selective, and potential inhibitor for O-GlcNAcase (OGA), an enzyme linked to diseases including Alzheimer’s, diabetes and cancer. Based on previous research, this study focuses on the synthesis of 2-(N-substituted-amino)-2-deoxy-D-glucono-1,5-lactone arylsemicarbazones. We have designed and performed a five-step synthesis of 2-(N-2,2,2-trichloroethoxycarbonylamino)-3,4,6-tri-O-acetyl-2-deoxy-D-glucono-1,5-lactone 4-phenylsemicarbazone. After selective cleavage of the Troc group, this compound can be used as a starting material for the preparation of new OGA inhibitors.
dc.description.courseChemistry
dc.description.degreeBSc/BA
dc.format.extent27
dc.identifier.urihttps://hdl.handle.net/2437/384083
dc.language.isoen
dc.rights.accessHozzáférhető a 2022 decemberi felsőoktatási törvénymódosítás értelmében.
dc.subjectOGA, Inhibitor, Alzheimer's disease, sugar, carbohydrate chemistry, organic chemistry
dc.subject.dspaceChemistry
dc.titleNew strategy for the synthesis of 2-(N-substituted-amino)-2-deoxy-D-glucono-1,5-lactone arylsemicarbazones
dc.title.translatedUj strategia 2-(N-szubsztitualt-amino)-2-dezoxi-D-glukono-1,5-lakton arilszemikarbazonok eloallitasara
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