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JOURNALS
// Mendeleev Communications
// Archive
Mendeleev Commun.,
1998
Volume 8,
Issue 1,
Pages
9–12
(Mi mendc4629)
This article is cited in
8
papers
Synthesis of spacer-armed glycosides using azidophenylselenylation of allyl glycosides
A. A. Sherman
,
L. O. Kononov
,
A. S. Shashkov
,
G. V. Zatonsky
,
N. E. Nifantiev
N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
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.
Language:
English
DOI:
10.1070/MC1998v008n01ABEH000887
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