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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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