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Journal articles on the topic 'Glycomonomer'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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1

Ohira, Shuichi, Yu Yasuda, Ikuyoshi Tomita та ін. "Synthesis of end-functionalized glycopolymers containing α(2,8) disialic acids via π-allyl nickel catalyzed coordinating polymerization and their interaction with Siglec-7". Chemical Communications 53, № 3 (2017): 553–56. http://dx.doi.org/10.1039/c6cc07115e.

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2

Adachi, Ryota, Takahiko Matsushita, Tetsuo Koyama, Ken Hatano та Koji Matsuoka. "Use of a Longer Aglycon Moiety Bearing Sialyl α(2→3) Lactoside on the Glycopolymer for Lectin Evaluation". Polymers 15, № 4 (2023): 998. http://dx.doi.org/10.3390/polym15040998.

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A polymerizable alcohol having 9 PEG repeats was prepared in order to mimic an oligosaccharide moiety. Sialyl α(2→3) lactose, which is known as a sugar moiety of GM3 ganglioside, was also prepared, and the polymerizable alcohol was condensed with the sialyl α(2→3) lactose derivative to afford the desired glycomonomer, which was further polymerized with or without acrylamide to give water-soluble glycopolymers. The glycopolymers had higher affinities than those of glycopolymers having sialyl lactose moieties with shorter aglycon moieties.
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3

Bielas, Rafał, Paulina Maksym, Karol Erfurt, et al. "Sugar decorated star-shaped (co)polymers with resveratrol-based core – physicochemical and biological properties." Journal of Materials Science 57, no. 3 (2022): 2257–76. http://dx.doi.org/10.1007/s10853-021-06755-8.

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AbstractStar-shaped glycopolymers due to the attractive combination of the physicochemical, morphological, self-assembly properties along with biological activity have gained increased attention as innovative agents in novel cancer therapies. Unfortunately, the production of these highly desirable biomaterials remains a challenge in modern macromolecular chemistry. The main reason for that is the low polymerizability of ionic glycomonomers originated from their steric congestion and the occurrence of ionic interactions that generally negatively influence the polymerization progress and hinder
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4

Tanaka, Tomonari, Ayane Matsuura, Yuji Aso, and Hitomi Ohara. "Aqueous One-pot Synthesis of Glycopolymers by Glycosidase-catalyzed Glycomonomer Synthesis Using 4,6-Dimetoxy Triazinyl Glycoside Followed by Radical Polymerization." Journal of Applied Glycoscience 67, no. 4 (2020): 119–27. http://dx.doi.org/10.5458/jag.jag.jag-2020_0010.

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5

Iyer, Suri, Shyam Rele, Gabriela Grasa, Steven Nolan, and Elliot L. Chaikof. "Synthesis of a hyaluronan neoglycopolymer by ring-opening metathesis polymerizationElectronic supplementary information (ESI) available: spectral data for compound 11, glycomonomer 14 and glycopolymer [A]. See http://www.rsc.org/suppdata/cc/b3/b301734f/." Chemical Communications, no. 13 (2003): 1518. http://dx.doi.org/10.1039/b301734f.

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6

Adharis, Azis, Dennis Vesper, Nick Koning, and Katja Loos. "Synthesis of (meth)acrylamide-based glycomonomers using renewable resources and their polymerization in aqueous systems." Green Chemistry 20, no. 2 (2018): 476–84. http://dx.doi.org/10.1039/c7gc03023a.

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7

Weaver, Lucy G., Yogendra Singh, Paul L. Burn, and Joanne T. Blanchfield. "Correction: The synthesis and ring-opening metathesis polymerization of glycomonomers." RSC Advances 6, no. 45 (2016): 39015. http://dx.doi.org/10.1039/c6ra90037b.

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8

Chibac, Andreea L., Tinca Buruiana, Violeta Melinte, Ionel Mangalagiu, and Emil C. Buruiana. "Tuning the size and the photocatalytic performance of gold nanoparticles in situ generated in photopolymerizable glycomonomers." RSC Advances 5, no. 110 (2015): 90922–31. http://dx.doi.org/10.1039/c5ra14695j.

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Polymer nanocomposites containing Au NPs in situ photogenerated during the UV-curing process were prepared starting from methacrylated glycomonomers with α-d-glucofuranose or d-mannitol structural units, other mono(di)methacrylates and AuCl<sub>3</sub>.
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9

Weaver, Lucy G., Yogendra Singh, Paul L. Burn, and Joanne T. Blanchfield. "The synthesis and ring-opening metathesis polymerization of glycomonomers." RSC Advances 6, no. 37 (2016): 31256–64. http://dx.doi.org/10.1039/c5ra25732h.

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10

Tanaka, Tomonari. "Protecting-Group-Free Synthesis of Glycomonomers and Glycopolymers from Free Saccharides." Trends in Glycoscience and Glycotechnology 28, no. 164 (2016): E101—E108. http://dx.doi.org/10.4052/tigg.1513.1e.

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11

Tanaka, Tomonari. "Protecting-Group-Free Synthesis of Glycomonomers and Glycopolymers from Free Saccharides." Trends in Glycoscience and Glycotechnology 28, no. 164 (2016): J99—J106. http://dx.doi.org/10.4052/tigg.1513.1j.

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12

Baskaran, Subramanian, Daniel Grande, Xue-Long Sun, Avner Yayon, and Elliot L. Chaikof. "Glycosaminoglycan-Mimetic Biomaterials. 3. Glycopolymers Prepared from Alkene-Derivatized Mono- and Disaccharide-Based Glycomonomers." Bioconjugate Chemistry 13, no. 6 (2002): 1309–13. http://dx.doi.org/10.1021/bc0255485.

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13

Tang, Jo Sing Julia, Sophia Rosencrantz, Lucas Tepper, et al. "Functional Glyco-Nanogels for Multivalent Interaction with Lectins." Molecules 24, no. 10 (2019): 1865. http://dx.doi.org/10.3390/molecules24101865.

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Interactions between glycans and proteins have tremendous impact in biomolecular interactions. They are important for cell–cell interactions, proliferation and much more. Here, we emphasize the glycan-mediated interactions between pathogens and host cells. Pseudomonas aeruginosa, responsible for a huge number of nosocomial infections, is especially the focus when it comes to glycan-derivatives as pathoblockers. We present a microwave assisted protecting group free synthesis of glycomonomers based on lactose, melibiose and fucose. The monomers were polymerized in a precipitation polymerization
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14

Kawaguchi, Asei William, Haruki Okawa та Kazuhiko Hashimoto. "Glycomonomeric and Glycopolymeric Inhibitors for β-Glucuronidase. π–π Stacking Interaction, Polymeric Effect, and Plausible Conformation". Bulletin of the Chemical Society of Japan 84, № 9 (2011): 912–17. http://dx.doi.org/10.1246/bcsj.20110043.

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15

Chen, Jie, Yong Miao, Stéphane Chambert, Julien Bernard, Etienne Fleury та Yves Queneau. "Carboxymethyl glycoside lactone (CMGL) synthons: Scope of the method and preliminary results on step growth polymerization of α-azide-ω-alkyne glycomonomers". Science China Chemistry 53, № 9 (2010): 1880–87. http://dx.doi.org/10.1007/s11426-010-4058-0.

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16

Chen, Jie, Yong Miao, Stephane Chambert, Julien Bernard, Etienne Fleury та Yves Queneau. "ChemInform Abstract: Carboxymethyl Glycoside Lactone (CMGL) Synthons: Scope of the Method and Preliminary Results on Step Growth Polymerization of α-Azide-ω-alkyne Glycomonomers". ChemInform 42, № 10 (2011): no. http://dx.doi.org/10.1002/chin.201110263.

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17

M.S., Mazăre, M. Pană A., M. Ştefan L., et al. "Novel D- glucose Based Glycomonomers Synthesis and Characterization." August 21, 2012. https://doi.org/10.5281/zenodo.1080590.

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In the last decade, carbohydrates have attracted great attention as renewable resources for the chemical industry. Carbohydrates are abundantly found in nature in the form of monomers, oligomers and polymers, or as components of biopolymers and other naturally occurring substances. As natural products, they play important roles in conferring certain physical, chemical, and biological properties to their carrier molecules.The synthesis of this particular carbohydrate glycomonomer is part of our work to obtain biodegradable polymers. Our current paper describes the synthesis and characterization
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18

STEFAN, LILIANA MARINELA, ANA MARIA PANA, MIHAI COSMIN PASCARIU, EUGEN SISU, GEZA BANDUR, and LUCIAN MIRCEA RUSNAC. "Synthesis and characterization of a new methacrylic glycomonomer." Turkish Journal of Chemistry, January 1, 2011. http://dx.doi.org/10.3906/kim-1103-63.

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19

Mahkam, Mehrdad. "Synthesis, characterization and evaluation of poly [glucose acrylate-methacrylic acid] hydrogels for colon-specific drug delivery." e-Polymers 8, no. 1 (2008). http://dx.doi.org/10.1515/epoly.2008.8.1.1831.

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AbstractNew biodegradable polymeric hydrogels based on biocompatible materials, glucose acrylate (GA) and methacrylic acid (MAA) were designed and synthesized. In the first time, the glucose-6-acrylate-1,2,3,4-tetraacetate (GATA) monomer was prepared under mild conditions. The removal of protecting acetate groups from GATA will be carried out before the polymerization and then, the corresponding water soluble glycomonomer (GA) was obtained. This deprotected glycomonomer can be polymerized in aqueous media, which points to a way to obtain polymers with applications in biomedical and biochemical
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20

Nasiri Oskooie, Maryam, Malihe Pooresmaeil та Hassan Namazi. "Design and synthesis of vinylic glycomonomers and glycopolymer based on α-D-glucofuranose moieties". Journal of Polymer Research 26, № 12 (2019). http://dx.doi.org/10.1007/s10965-019-1969-0.

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21

Zhong, Yihong, Lijia Xu, Chen Yang, et al. "Site-selected in situ polymerization for living cell surface engineering." Nature Communications 14, no. 1 (2023). http://dx.doi.org/10.1038/s41467-023-43161-x.

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AbstractThe construction of polymer-based mimicry on cell surface to manipulate cell behaviors and functions offers promising prospects in the field of biotechnology and cell therapy. However, precise control of polymer grafting sites is essential to successful implementation of biomimicry and functional modulation, which has been overlooked by most current research. Herein, we report a biological site-selected, in situ controlled radical polymerization platform for living cell surface engineering. The method utilizes metabolic labeling techniques to confine the growth sites of polymers and de
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