Beilstein J. Org. Chem.2011,7, 1115–1123, doi:10.3762/bjoc.7.128
National de la Recherche Scientifique, 91198 Gif-sur-Yvette CEDEX, France Department of Organic Chemistry, Faculty of Chemistry, University of Seville, Prof. García González, 1, 41012 Seville, Spain Glycobiology Institute, Department of Biochemistry, Oxford University, South Parks Road, Oxford, OX1 3QU
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Supporting Information File 214: 1H and 13C NMR spectra of compounds 18–27.
Acknowledgements
IC acknowledges the support of Vetenskapsrådet (the Swedish Research Council). TDB and DSA acknowledge the support of the Glycobiology Institute and Grant No. R01CA125642 from the National Cancer Institute for part
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Graphical Abstract
Scheme 1:
The concept of using allylic reactivity enhancement to facilitate diglycoside synthesis.
Beilstein J. Org. Chem.2010,6, No. 20, doi:10.3762/bjoc.6.20
oligosaccharides is not yet efficient enough for generating oligosaccharide-based libraries that may be useful in the future for the discovery of new therapeutic drugs. Taking into account the increasing importance of glycobiology and the difficulties associated to the synthesis of carbohydrate-based libraries
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Graphical Abstract
Figure 1:
Schematic representation of sugar aminoacids (SAAs) and (pseudo)amide oligosaccharide mimetics.