Glycosylation with 1,2-anhydromannofuranose benzyl ether as the glycosyl donor: A comparison between sugar pyranose and furanose acceptors for thelr primary hydroxy activity

Article abstract of DOI:10.1080/07328309908544035

Some 1→5 and 1→6 α-linked furano-disaccharide derivatives were synthesized using 1,2-anhydromannofiiranose as the glycosyl donor. Comparison of the glycosyl acceptors indicated that the activity of primary hydroxyl groups of glycofuranoses was much lower than that of glycopyranoses.

Full text of DOI:10.1080/07328309908544035

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Journal of Carbohydrate Chemistry
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Glycosylation with 1,2-
Anhydromannofuranose Benzyl
Ether as the Glycosyl Donor: A
Comparison Between Sugar Pyranose
and Furanose Acceptors for their
Primary Hydroxy Activity
Xianglan Ding & Fanzuo Kong
a Research Center for Eco-Environmental Science, Academia
Sinica , P.O.Box 2871, Beijing 100085, China
b Research Center for Eco-Environmental Science, Academia
Sinica , P.O.Box 2871, Beijing 100085, China
Published online: 27 Feb 2008.
To cite this article: Xianglan Ding & Fanzuo Kong (1999) Glycosylation with 1,2-
Anhydromannofuranose Benzyl Ether as the Glycosyl Donor: A Comparison Between Sugar
Pyranose and Furanose Acceptors for their Primary Hydroxy Activity, Journal of Carbohydrate
Chemistry, 18:7, 775-787, DOI: 10.1080/07328309908544035
To link to this article: http://dx.doi.org/10.1080/07328309908544035
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