Abstract
Protected 3-aminopropyl spacer-armed glycosides that can be further used for the preparation of neoglycoconjugates have been prepared from allyl glycosides using azidophenylselenylation of the double bond as a key step.
References
1.
10.1070/MC1998v008n01ABEH000887_bib1
1994
2.
10.1070/MC1998v008n01ABEH000887_bib2
Magnusson
Neoglycoconjugates: Preparation and Application,
1994
3.
Bovin N.V., Korchagina E.Y., Zemlyanukhina T.V., Byramova N.E., Galanina O.E., Zemlyakov A.E., Ivanov A.E., Zubov V.P., Mochalova L.V.
Glycoconjugate Journal,
1993
4.
Tingoli M., Tiecco M., Chianelli D., Balducci R., Temperini A.
Journal of Organic Chemistry,
1991
5.
Bernstein M.A., Hall L.D.
Carbohydrate Research,
1980
6.
Lee R.T., Lee Y.C.
Carbohydrate Research,
1974
7.
Nashed M.A.
Carbohydrate Research,
1983
8.
9.
L. O. Kononov, A. V. Kornilov, A. A. Sherman, E. V. Zyryanov, A. S. Shashkov, G. V. Zatonsky and N. E. Nifant’ev, Bioorg. Khim., 1998, 24, in press.
10.
10.1070/MC1998v008n01ABEH000887_bib10
Bax
J. Magn. Reson.,
1986
11.
McFarlane W., Wood R.J.
Journal of the Chemical Society Dalton Transactions,
1972
12.
Ercégovic T., Magnusson G.
Journal of Organic Chemistry,
1996