Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Vinni H. Lillelund"'
Publikováno v:
Organic & Biomolecular Chemistry. 1:478-482
In order to investigate the hypothesis that the glycosidase inhibitor isofagomine was bound to alpha- or beta-glucosidase in a 1,4B conformation, a number of bicyclic aziridines that adopt the 1,4B or B1,4 conformations were synthesised and investiga
Publikováno v:
Lillelund, V H, Liu, H, Liang, X, Søhoel, H & Bols, M 2003, ' Isofagomine lactams, synthesis and enzyme inhibition ', Organic & Biomolecular Chemistry, vol. 1, pp. 282-287 .
The synthesis of isofagomine lactams (2-oxoisofagomines) corresponding to the biologically important hexoses is presented. The D-glucose/D-mannose analogue (3S,4R,5R)-3,4-dihydroxy-5-hydroxymethylpiperidin-2-one (9) was synthesised in 9 steps from D-
Publikováno v:
Chemical Reviews. 102:515-554
Publikováno v:
ChemInform. 33
Publikováno v:
Liu, H, Lillelund, V H, Andersch, J, Liang, X & Bols, M 2004, ' Synthesis and chemistry of noeuromycin and isofagomine analogues ', J. Carb. Chem, vol. 23, pp. 223-238 .
Several N‐substituted analogues of noeuromycin ((2RS,3S,4R,5R)‐2,3,4‐trihydroxy‐5‐hydroxymethylpiperidine) and isofagomine ((3R,4R,5R)‐3,4‐dihydroxy‐5‐hydroxymethylpiperidine) were synthesised. The isofagomine analogues (3RS,4RS,5RS
Publikováno v:
XXIst International Carbohydrate Symposium 2002.