Collect. Czech. Chem. Commun.
1989, 54, 2775-2783
https://doi.org/10.1135/cccc19892775
Glycosylation of steroids with silver silicate and 2-deoxy-2-fluoro-α-D-glucopyranosyl bromide triacetate
Ivan Černýa, Petr Novotnýb, Pavel Drašara, Miroslav Havela and Josef Pacákb
a Institute of Organic Chemistry and Biochemistry, Czechoslovak Academy of Sciences, 166 10 Prague 6
b Department of Organic Chemistry, Charles University, 128 40 Prague 2
Abstract
Glycosylation with the title glycosyl bromide I in 1,2-dichloroethane in the presence of silver silicate and a molecular sieves afforded mixtures of 3,4,6-tri-O-acetyl-2-deoxy-2-fluoro-α- and β-D-glucopyranosides (V-X), derived from ethyl (20E)-3β-hydroxy-24-nor-5,20(22)-choladien-23-oate (II), (20E)-3β-hydroxy-5β-pregn-20-ene-21-carboxylate (III) and 3β, 14-dihydroxy-5β, 14β-card-20(22)-enolide (IV, digitoxigenin), in which the β-anomers predominated. Separation and deacetylation furnished the corresponding 2-deoxy-2-fluoroglucosides XI-XVI.
