Syntese mot glykonjugater med anilin derivater
Abstract
Palladiumkatalysatoren [(2,9-dimetyl-1,10-fenantrolin)Pd(µ-OAc)]2(OTf)2 ble benyttettil 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 utmed anilinderivatene m-anisidin og 3-(Trifluoromethoxy)anilin The palladium catalyst [(2,9-dimetyl-1,10-fenantrolin)Pd(µ-OAc)]2(OTf)2 was used tooxidize methyl-β-D-xylopyranoside in the C-3 posistion. To transform monosacharidesto a UV acitve glycoconjugate by reductive amination with aniline derivates m-anisidinand 3-(Trifluoromethoxy)aniline.