Zobrazeno 1 - 3
of 3
pro vyhledávání: '"M. J. Dees"'
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 104:116-119
Penta-O-acetyl-β-D-galactopyranose was converted in two steps into pentabromophenyl 1,2,3,4-tetra-O-acetyl-β-D-galactopyranoside. Short treatment of the latter with tetra-n-butylammonium hydroxide at 20°C, followed by acetylation, afforded crystal
Autor:
C. A. A. Van Boeckel, J. H. Van Boom, M. J. Dees, T. Beetz, H. M. Zuurmond, Cornelis Erkelens, P. Westerduin, P. Smid
Publikováno v:
Journal of Carbohydrate Chemistry. 7:617-644
The preparation of four Rh. Vannielii Lipid A analogues (i.e. compounds 22, 23, 30 and 33) is described. Non-neighbouring group supported introduction of the β-glycosidic linkages was performed by coupling the mannopyranosyl bromide 2 and the 2-azid
Publikováno v:
Chemischer Informationsdienst. 16
Penta-O-acetyl-β-D-galactopyranose was converted in two steps into pentabromophenyl 1,2,3,4-tetra-O-acetyl-β-D-galactopyranoside. Short treatment of the latter with tetra-n-butylammonium hydroxide at 20°C, followed by acetylation, afforded crystal