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Boons Geert-Jan
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http://hub.abes.fr/oup/periodical/glycob/2006/volume_16/issue_8/101093glycobcwj125/authorship/3
http://hub.abes.fr/oup/periodical/glycob/2009/volume_19/issue_6/101093glycobcwp036/authorship/8
http://hub.abes.fr/acs/periodical/joceah/1998/volume_63/issue_14/101021jo9808728/authorship/3
http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_16/101021jo010345f/authorship/3
http://hub.abes.fr/acs/periodical/chreay/2000/volume_100/issue_12/101021cr990313g/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/2002/volume_124/issue_44/101021ja020536f/authorship/5
http://hub.abes.fr/acs/periodical/jacsat/1999/volume_121/issue_35/101021ja991319q/authorship/6
http://hub.abes.fr/acs/periodical/joceah/1997/volume_62/issue_23/101021jo971233k/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/2002/volume_124/issue_12/101021ja0153161/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/2007/volume_129/issue_16/101021ja068922a/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/2000/volume_122/issue_41/101021ja001930l/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1999/volume_64/issue_21/101021jo990836o/authorship/4
http://hub.abes.fr/acs/periodical/joceah/1996/volume_61/issue_13/101021jo960131b/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/2006/volume_128/issue_36/101021ja0629817/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/2003/volume_125/issue_24/101021ja029759w/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/2002/volume_124/issue_21/101021ja0169771/authorship/5
http://hub.abes.fr/acs/periodical/jacsat/2003/volume_125/issue_20/101021ja029316s/authorship/5
http://hub.abes.fr/acs/periodical/joceah/2005/volume_70/issue_5/101021jo048443z/authorship/4
http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_8/101021jo001477w/authorship/2
http://hub.abes.fr/acs/periodical/bichaw/2003/volume_42/issue_28/101021bi034189d/authorship/3
http://hub.abes.fr/acs/periodical/joceah/2000/volume_65/issue_11/101021jo991685s/authorship/6
http://hub.abes.fr/acs/periodical/jacsat/2001/volume_123/issue_33/101021ja0104655/authorship/6
http://hub.abes.fr/acs/periodical/jacsat/2001/volume_123/issue_49/101021ja004315q/authorship/6
http://hub.abes.fr/acs/periodical/jacsat/2008/volume_130/issue_28/101021ja711248y/authorship/7
http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_34/101021ja052548h/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/2006/volume_128/issue_25/101021ja061216p/authorship/5
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A Novel and Efficient Synthesis of a Dimeric LexOligosaccharide on Polymeric Support
Involvement of Water in Carbohydrate−Protein Binding
Synthesis and Biological Evaluation of Rhizobium sin-1Lipid A Derivatives
Multivalency and the Mode of Action of Bacterial Sialidases
A Highly Convergent Synthesis of a Complex OligosaccharideDerived from Group B Type III Streptococcus
Vinyl Glycosides in Oligosaccharide Synthesis. 2. The Use of Allyland Vinyl Glycosides in Oligosaccharide Synthesis
Recent Advances in O-Sialylation
Stereochemical Dependence of the Self-Assembly of theImmunoadjuvants Pam3Cys and Pam3Cys-Ser
High-Avidity, Low-Affinity Multivalent Interactions and theBlock to Polyspermy in Xenopus laevis
Modulation of Innate Immune Responses with Synthetic LipidA Derivatives
Glycopeptides as versatile tools for glycobiology
Secondary cell wall polysaccharides of Bacillus anthracis are antigens that contain specific epitopes which cross-react with three pathogenic Bacillus cereus strains that caused severe disease, and other epitopes common to all the Bacillus cereus strains tested
Probing the Substrate Specificity of Golgi α-Mannosidase II by Use of Synthetic Oligosaccharides and a Catalytic Nucleophile Mutant
Synthesis of Proteophosphoglycans of Leishmania major andLeishmania mexicana
A General Strategy for Stereoselective Glycosylations
Structural Basis of the Inhibition of Golgi α-Mannosidase II byMannostatin A and the Role of the Thiomethyl Moiety inLigand−Protein Interactions
Application of the 2,5-Dimethylpyrrole Groupas a New and Orthogonal Amine-ProtectingGroup in Oligosaccharide Synthesis
Glycosyltransferase Activity Can Be Modulated by Small ConformationalChanges of Acceptor Substrates
Synthesis and Proinflammatory Effects ofPeptidoglycan-Derived Neoglycopeptide Polymers
Practical Approach for the Stereoselective Introduction ofβ-Arabinofuranosides
Chemoselective Glycosylations. 2. Differences in Size ofAnomeric Leaving Groups Can Be Exploited in ChemoselectiveGlycosylations
Synthesis and Supramolecular Characterization of a Novel Classof Glycopyranosyl-Containing Amphiphiles
α-(2,6)-Sialyltransferase-Catalyzed Sialylations ofConformationally Constrained Oligosaccharides
Chemoselective Glycosylation Strategy for the ConvergentAssembly of Phytoalexin-Elicitor Active Oligosaccharides andTheir Photoreactive Derivatives
Glycochemistry: Principles, Synthesis andApplications Edited by Peng George Wang (WayneState University) and Carolyn R. Bertozzi (HowardHughes Medical Institute and University of California,Berkeley). Marcel Dekker, Inc. New York, Basel. 2001.xvi + 682 pp. $195.00. ISBN: 0-8247-0538-6.
A Stereoselective Approach for the Synthesis of α-Sialosides
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