How do multivalent glycodendrimers benefit from sulfur chemistry?
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Electrochemistry of nonconjugated proteins and glycoproteins. Toward sensors for biomedicine and glycomicsExpeditive synthesis of trithiotriazine-cored glycoclusters and inhibition of Pseudomonas aeruginosa biofilm formationSynthesis of divalent ligands of β-thio- and β-N-galactopyranosides and related lactosides and their evaluation as substrates and inhibitors of Trypanosoma cruzi trans-sialidaseFullerene sugar balls: a new class of biologically active fullerene derivatives.Design and Synthesis of Galactosylated Bifurcated Ligands with Nanomolar Affinity for Lectin LecA from Pseudomonas aeruginosa.Dendritic glycopolymers based on dendritic polyamine scaffolds: view on their synthetic approaches, characteristics and potential for biomedical applications.Glyconanosynthons as powerful scaffolds and building blocks for the rapid construction of multifaceted, dense and chiral dendrimers.Recent advances in click chemistry applied to dendrimer synthesis.Synthesis of 1D-glyconanomaterials by a hybrid noncovalent-covalent functionalization of single wall carbon nanotubes: a study of their selective interactions with lectins and with live cells.Are glycan biosensors an alternative to glycan microarrays?Inhibition of type 1 fimbriae-mediated Escherichia coli adhesion and biofilm formation by trimeric cluster thiomannosides conjugated to diamond nanoparticles.Exploring the Influence of Shapes and Heterogeneity of Glyco-Gold Nanoparticles on Bacterial Binding for Preventing Infections.Biologically Active Heteroglycoclusters Constructed on a Pillar[5]arene-Containing [2]Rotaxane Scaffold.Assessing the effect of different shapes of glyco-gold nanoparticles on bacterial adhesion and infections.Functionalization of a Rigid Divalent Ligand for LecA, a Bacterial Adhesion Lectin.Orthogonal dual thiol-chloroacetyl and thiol-ene couplings for the sequential one-pot assembly of heteroglycoclustersTBAI-Catalyzed/Water-Assisted Double C-S Bond Formations: An Efficient Approach to Sulfides through Metal-Free Three-Component Reactions.Masked thiol sugars: chemical behavior and synthetic applications of S-glycopyranosyl-N-monoalkyl dithiocarbamates.Stereoretentive Copper-Catalyzed Directed Thioglycosylation of C(sp2 )-H Bonds of Benzamides.Cu0-Loaded organo-montmorillonite with improved affinity towards hydrogen: an insight into matrix-metal and non-contact hydrogen-metal interactions.Core-and-surface-functionalized polyphenylene dendrimers for solution-processed, pure-blue light-emitting diodes through surface-to-core energy transfer.A highly versatile convergent/divergent "onion peel" synthetic strategy toward potent multivalent glycodendrimers.Efficient and accelerated growth of multifunctional dendrimers using orthogonal thiol-ene and SN2 reactions.Functional aqueous assemblies of linear-dendron hybridsSelective S-deacetylation inspired by native chemical ligation: practical syntheses of glycosyl thiols and drug mercapto-analoguesThiol-ene and thiol-yne-based synthesis of glycodendrimers as nanomolar inhibitors of wheat germ agglutinin
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How do multivalent glycodendrimers benefit from sulfur chemistry?
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article científic
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article scientifique
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articol științific
@ro
articolo scientifico
@it
artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
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artículo científico
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name
How do multivalent glycodendrimers benefit from sulfur chemistry?
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type
label
How do multivalent glycodendrimers benefit from sulfur chemistry?
@en
prefLabel
How do multivalent glycodendrimers benefit from sulfur chemistry?
@en
P2093
P2860
P356
P1476
How do multivalent glycodendrimers benefit from sulfur chemistry?
@en
P2093
Myriam Roy
Yoann M Chabre
P2860
P304
P356
10.1039/C3CS60090D
P50
P577
2013-04-30T00:00:00Z