| dc.contributor.advisor | Kenneth Aase Kristoffersen | |
| dc.contributor.advisor | Yngve Stenstrøm | |
| dc.contributor.author | Myrvold, Ida Eline Nes | |
| dc.date.accessioned | 2024-04-10T16:27:19Z | |
| dc.date.available | 2024-04-10T16:27:19Z | |
| dc.date.issued | 2024 | |
| dc.identifier | no.nmbu:wiseflow:6983034:57368018 | |
| dc.identifier.uri | https://hdl.handle.net/11250/3125880 | |
| dc.description.abstract | Palladiumkatalysatoren [(2,9-dimetyl-1,10-fenantrolin)Pd(µ-OAc)]2(OTf)2 ble benyttet
til å selektiv oksidere metyl-β-D-xylopyranosid i C-3 posisjonen, og reagere denne forbindelsen videre til ulike UV-aktive glykokonjugat. Reduktiv aminering ble testet ut
med anilinderivatene m-anisidin og 3-(Trifluoromethoxy)anilin | |
| dc.description.abstract | The palladium catalyst [(2,9-dimetyl-1,10-fenantrolin)Pd(µ-OAc)]2(OTf)2 was used to
oxidize methyl-β-D-xylopyranoside in the C-3 posistion. To transform monosacharides
to a UV acitve glycoconjugate by reductive amination with aniline derivates m-anisidin
and 3-(Trifluoromethoxy)aniline. | |
| dc.language | nob | |
| dc.publisher | Norwegian University of Life Sciences | |
| dc.title | Syntese mot glykonjugater med anilin derivater | |
| dc.type | Master thesis | |
