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Mendeleev Communications, 1999, Volume 9, Issue 3, Pages 114–116
DOI: https://doi.org/10.1070/MC1999v009n03ABEH001073
(Mi mendc4551)
 

This article is cited in 30 scientific papers (total in 30 papers)

Effect of the nature of protecting group at O-4 on stereoselectivity of glycosylation by 4-O-substituted 2,3-di-O-benzylfucosyl bromides

A. G. Gerbsta, N. E. Ustyuzhaninaa, A. A. Gracheva, D. E. Tsvetkovb, E. A. Khatuntsevab, N. E. Nifantievb

a Higher Chemical College of the Russian Academy of Sciences, D.I. Mendeleev University of Chemical Technology of Russia, Moscow, Russian Federation
b N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract: The effect of the nature of the substituent at O-4 on the stereoselectivity of glycosylation by 2,3-di-O-benzylfucosyl bromides was studied by direct chemical experiments and computer modelling.
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Document Type: Article
Language: English


Citation: A. G. Gerbst, N. E. Ustyuzhanina, A. A. Grachev, D. E. Tsvetkov, E. A. Khatuntseva, N. E. Nifantiev, “Effect of the nature of protecting group at O-4 on stereoselectivity of glycosylation by 4-O-substituted 2,3-di-O-benzylfucosyl bromides”, Mendeleev Commun., 9:3 (1999), 114–116
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  • This publication is cited in the following 30 articles:
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