Issue 1, 1998
From the journal:

Mendeleev Communications

Synthesis of spacer-armed glycosides using azidophenylselenylation of allyl glycosides

Andrei A. Sherman,   Leonid O. Kononov,   Alexander S. Shashkov,   Georgij V. Zatonsky  and  Nikolay E. Nifant'ev  

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.

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Article information

DOI
https://doi.org/10.1070/MC1998v008n01ABEH000887
Article type
Paper

Mendeleev Commun., 1998,8, 9-12

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Synthesis of spacer-armed glycosides using azidophenylselenylation of allyl glycosides

A. A. Sherman, L. O. Kononov, A. S. Shashkov, G. V. Zatonsky and N. E. Nifant'ev, Mendeleev Commun., 1998, 8, 9 DOI: 10.1070/MC1998v008n01ABEH000887

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