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dc.contributor.advisorSimic, Nebojsa
dc.contributor.advisorNervik, Sondre
dc.contributor.authorAlsaker, Nicolai Etwin
dc.date.accessioned2019-09-11T10:36:12Z
dc.date.created2018-05-25
dc.date.issued2018
dc.identifierntnudaim:16099
dc.identifier.urihttp://hdl.handle.net/11250/2615649
dc.description.abstractTowards the total synthesis of a natural anti-inflammatory compound present in the plant Sclerochloa dura, three full protection strategies were developed for selectively full protected glucose derivatives, available for subsequent 1,3,6- functionalization. Difficulty of distinguishing secondary carbohydrate hydroxyls for 3-O protection was overcome by employing a furanose-to-pyranose rearrangement method, affording allyl 3-O-benzyl-D-glucopyranoside. The three protection strategies were based on this shared intermediate.en
dc.languageeng
dc.publisherNTNU
dc.subjectChemistry, Organisk kjemien
dc.titleSynthesis of Selectively Fully Protected Glucose Derivatives via a Furanose-to-Pyranose Rearrangement Methoden
dc.typeMaster thesisen
dc.source.pagenumber194
dc.contributor.departmentNorges teknisk-naturvitenskapelige universitet, Fakultet for naturvitenskap,Institutt for kjeminb_NO


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