Synthesis and Reactions of Some Derivatives Of (3,6 S,9 R,10 R,11 S)-1,4,7-Trioxaspiro[5,5]Undecane-3,9,10,11-Tetrol: Novel Quasi-Saccharides 1 Presented at the 2nd International Meeting of the Portuguese Carbohydrate Chemistry Group, Porto, Portugal, 21–25 September 1997. 1

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dc.contributor.authorRegeling, Henk
dc.contributor.authorSunghwa, Fortunatus
dc.contributor.authorZwanenburg, Binne
dc.contributor.authorde Gelder, Rene
dc.contributor.authorChittenden, Gordon J. F.
dc.date.accessioned2016-07-21T18:26:36Z
dc.date.available2016-07-21T18:26:36Z
dc.date.issued1998-10
dc.descriptionFull text can be accessed at http://www.sciencedirect.com/science/article/pii/S0144861798000782en_US
dc.description.abstractThe title compound was obtained by reductive ozonolysis of allyl β-d-fructopyranoside. The synthesis and characterization of a number of C-3-substituted derivatives using conventional carbohydrate procedures is described. Some of the products may be of biological interest as carbohydrate mimics. The structures of two of the basic products (8 and 9) were substantiated by X-ray diffraction studies. Do you want to read the rest of this article?Access full-texten_US
dc.identifier.citationRegeling, H., Sunghwa, F., Zwanenburg, B., de Gelder, R. and Chittenden, G.J., 1998. Synthesis and reactions of some derivatives of (3, 6S, 9R, 10R, 11S)-1, 4, 7-trioxaspiro [5, 5] undecane-3, 9, 10, 11-tetrol: novel quasi-saccharides. Carbohydrate polymers, 37(3), pp.323-333.en_US
dc.identifier.doi10.1016/S0144-8617(98)00078-2
dc.identifier.urihttp://hdl.handle.net/20.500.11810/3372
dc.language.isoenen_US
dc.subjectSpiro-fructosides-quasisaccharidesen_US
dc.subjectCarbohydrates mimicsen_US
dc.subjectX-ray diffractionen_US
dc.titleSynthesis and Reactions of Some Derivatives Of (3,6 S,9 R,10 R,11 S)-1,4,7-Trioxaspiro[5,5]Undecane-3,9,10,11-Tetrol: Novel Quasi-Saccharides 1 Presented at the 2nd International Meeting of the Portuguese Carbohydrate Chemistry Group, Porto, Portugal, 21–25 September 1997. 1en_US
dc.typeJournal Articleen_US
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