dc.contributor.advisor | Simic, Nebojsa | |
dc.contributor.advisor | Nervik, Sondre | |
dc.contributor.author | Alsaker, Nicolai Etwin | |
dc.date.accessioned | 2019-09-11T10:36:12Z | |
dc.date.created | 2018-05-25 | |
dc.date.issued | 2018 | |
dc.identifier | ntnudaim:16099 | |
dc.identifier.uri | http://hdl.handle.net/11250/2615649 | |
dc.description.abstract | Towards 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.language | eng | |
dc.publisher | NTNU | |
dc.subject | Chemistry, Organisk kjemi | en |
dc.title | Synthesis of Selectively Fully Protected Glucose Derivatives via a Furanose-to-Pyranose Rearrangement Method | en |
dc.type | Master thesis | en |
dc.source.pagenumber | 194 | |
dc.contributor.department | Norges teknisk-naturvitenskapelige universitet, Fakultet for naturvitenskap,Institutt for kjemi | nb_NO |