Academic literature on the topic 'Glycomonomer'

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Journal articles on the topic "Glycomonomer"

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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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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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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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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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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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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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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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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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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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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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Book chapters on the topic "Glycomonomer"

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von der Ehe, C., F. Kretschmer, C. Weber, et al. "RAFT Copolymerization of Thioglycosidic Glycomonomers withNiPAm and Subsequent Immobilization onto Gold Nanoparticles." In ACS Symposium Series. American Chemical Society, 2015. http://dx.doi.org/10.1021/bk-2015-1188.ch015.

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Adharis, Azis, and Katja Loos. "Synthesis of glycomonomers via biocatalytic methods." In Methods in Enzymology. Elsevier, 2019. http://dx.doi.org/10.1016/bs.mie.2019.04.015.

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