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

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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Published in:Mendeleev communications 1999, Vol.9 (3), p.114-116
Main Authors: Gerbst, Alexey G., Ustuzhanina, Nadezhda E., Grachev, Alexey A., Tsvetkov, Dmitry E., Khatuntseva, Elena A., Nifant’ev, Nikolay E.
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Language:English
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cited_by cdi_FETCH-LOGICAL-c379t-f15de072d4fe08a53bfc5c2da509a54c8df1d6e211b9cdcef06ae916119f4ce73
cites cdi_FETCH-LOGICAL-c379t-f15de072d4fe08a53bfc5c2da509a54c8df1d6e211b9cdcef06ae916119f4ce73
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container_title Mendeleev communications
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creator Gerbst, Alexey G.
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description 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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title Effect of the nature of protecting group at O-4 on stereoselectivity of glycosylation by 4-O-substituted 2,3-di- O-benzylfucosyl bromides
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