56 research outputs found
Transition metals for the synthesis of glycopolymers and glycopolypeptides
Glycopolymers and glycopolypeptides are an important class of molecules, which can self-assemble to various interesting biohybrid materials. It is envisaged that the glycans impart good immunological response, and the aliphatic or polypeptide backbone can give tertiary structure for the resulting glycopolymers. The major bottleneck in the synthesis of glycopolymers or glycopolypeptides is the access to suitable building blocks and polymerization methods. This review describes methods that have recently been explored for the successful synthesis of many useful glycomonomers that could be polymerized to afford glycopolymers and/or glycopolypeptides. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Efficient isomerization of methyl arabinofuranosides into corresponding arabinopyranosides in presence of pyridine
International audienceFisher glycosylation, the oldest but efficient reaction towards alkyl glycosides, suffers nonetheless from lack of selectivity, especially when dealing with pentoses. In this case, a mixture of the four isomers, namely the furanosides and the pyranosides, is formed. According to previous studies, the rate and selectivity of the reaction depend greatly on the reaction time and the temperature. In this report, another factor was evaluated, the introduction of a weak nucleophilic base. Interestingly, addition of pyridine few hours after the reaction has started allowed rapid isomerization of the methyl pentofuranosides into its pyranoside counterparts. The reaction proceeds with great diastereoselectivity using arabinose, ribose, xylose and lyxose as starting pentoses. Corresponding methyl pyranosides were obtained as the sole isomers with yields ranging from 65% to 75%. © 2016 Elsevier Lt
Gold nanoparticle networks with photoresponsive interparticle spacings
Photoresponsive gold nanoparticle networks were prepared by functionalizing them with azobenzene derivatives. A network can be formed when a linker molecule constituting the azobenzene moiety suitably derivatized on either side with gold surface sensitive groups such as thiols and amines is added to the nanoparticle solution. It is shown that the interparticle spacing in the networks could be controlled by the reversible trans-cis isomerization of the azobenzene moiety induced by UV and visible light, respectively. The photoinduced variation in the interparticle spacings is inferred by the changes in the optical spectra of the gold nanoparticles which display a red or blue shift in the surface plasmon resonance peak depending on a decrease or increase in the interparticle spacing, respectively. Transmission electron microscopy images are in consonance with the evidence from the optical spectra
Dendritic effect of ligand-coated nanoparticles: enhanced apoptotic activity of silica−berberine nanoconjugates
We describe the synthesis and biological characterization of a novel prototype, namely, silica nanoconjugates bearing a covalently linked berberine, a plant alkaloid known to have antiproliferative activity. The effect of synthesized nanoconjugates on cell proliferation, the cell cycle profile, and apoptosis in the human cervical carcinoma cell line (HeLa), human hepatocellular liver carcinoma cell line (HepG2), and human embryonic kidney (HEK) 293T cell line has been studied and compared with the results obtained for free berberine. Our results show that all the nanoconjugates display higher antiproliferative activity than free berberine. The ability of these nanoconjugates to inhibit cellular proliferation is mediated by the cell cycle arrest at the G1 phase. Moreover, silica nanoconugates caused selective apoptotic arrest with a higher efficiency than free berberine followed by apoptotic cell death as shown by quantitative fluorescence-activated cell sorting analyses. Efficiency of the nanoconjugates increases upon an increase in the linker chain length, demonstrating the distinct role of the spacer chain that conjugates nanoparticles and ligands. The actual reason to show enhanced efficiency by the nanoconjugates has not been elucidated in the present study; however, we hypothesize that an increase in local concentration due to the confinement of a ligand on the nanosurface (“dendritic” effect) might have led to the observed effect
Synthesis of Triazole-Linked Glycoconjugates by Copper(I)-Catalyzed Regiospecific Cycloaddition of Alkynes and Azides
The Intermolecular Pauson‐Khand Reaction of Sugar‐Derived Azaenynes: A Case of Total Diastereoselectivity
Influence of Peroxide Impurities in Povidone on the Stability of Selected β-Blockers with the Help of HPLC
Gold-Catalyzed Etherification and Friedel-Crafts Alkylation Using ortho-Alkynylbenzoic Acid Alkyl Ester as an Efficient Alkylating Agent
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