Inverse electron-demand Diels–Alder reactions of 3-(β-D-glucopyranosyl)-6-(het)aryl-1,2,4,5-tetrazines

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dc.contributor.advisorBokor, Éva
dc.contributor.authorDabian, Akram
dc.contributor.departmentDE--Természettudományi és Technológiai Kar--Kémiai Intézethu_HU
dc.date.accessioned2021-12-14T11:48:43Z
dc.date.available2021-12-14T11:48:43Z
dc.date.created2021-12-09
dc.description.abstractThe ring transformation of C-glucosyl-1,2,4,5-tetrazines by means of inverse electron-demand Diels-Alder reactions with Norbonadiene and BCN conjugates was explored. These reactions afforded good yields of O-perbenzoylated 3-(beta-d-glucopyranosyl)-6-(het)aryl-pyridazines and fluorescent anellated C-(beta-d-glucopyranosyl)-6-(het)aryl-pyridazines.hu_HU
dc.description.courseChemistryhu_HU
dc.description.degreeMSc/MAhu_HU
dc.format.extent34hu_HU
dc.identifier.urihttp://hdl.handle.net/2437/326361
dc.language.isoenhu_HU
dc.subjectBioorthogonal, IEDDA, Carbohydratehu_HU
dc.subjectTetrazine, Diels-Alder Reactionhu_HU
dc.subject.dspaceDEENK Témalista::Kémiahu_HU
dc.titleInverse electron-demand Diels–Alder reactions of 3-(β-D-glucopyranosyl)-6-(het)aryl-1,2,4,5-tetrazineshu_HU
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