Academic literature on the topic 'Guanidinylation'

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Journal articles on the topic "Guanidinylation"

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Izawa, Hironori, Mizuki Kinai, Shinsuke Ifuku, Minoru Morimoto, and Hiroyuki Saimoto. "Guanidinylation of Chitooligosaccharides Involving Internal Cyclization of the Guanidino Group on the Reducing End and Effect of Guanidinylation on Protein Binding Ability." Biomolecules 9, no. 7 (2019): 259. http://dx.doi.org/10.3390/biom9070259.

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In order to synthesize a promising material for developing a novel peptide/protein delivery system, guanidinylation of chitooligosaccharides with 1-amidinopyrazole hydrochloride was investigated herein. The production of guanidinylated chitooligosaccharides was demonstrated by infrared spectroscopy (IR), nuclear magnetic resonance (NMR), and elemental analyses. Interestingly, we found that the reducing end in the guanidinylated chitooligosaccharides was converted to a cyclic guanidine structure (2-[(aminoiminomethyl)amino]-2-deoxy-d-glucose structure). This reaction was carefully proven by the
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Bolt, H. L., and S. L. Cobb. "A practical method for the synthesis of peptoids containing both lysine-type and arginine-type monomers." Organic & Biomolecular Chemistry 14, no. 4 (2016): 1211–15. http://dx.doi.org/10.1039/c5ob02279g.

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A practical synthetic procedure to synthesise linear and cyclic peptoids containing both arginine- and lysine-type residues within the same sequence has been developed. The methodology utilises orthogonal N-Boc and N-Dde protection, pyrazole-1-carboxamide as a guanidinylation reagent and is compatible with the sub-monomer method.
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Feichtinger, Konrad, Christoph Zapf, Heather L. Sings, and Murray Goodman. "Diprotected Triflylguanidines: A New Class of Guanidinylation Reagents." Journal of Organic Chemistry 63, no. 12 (1998): 3804–5. http://dx.doi.org/10.1021/jo980425s.

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FEICHTINGER, K., C. ZAPF, H. L. SINGS, and M. GOODMAN. "ChemInform Abstract: Diprotected Triflylguanidines: A New Class of Guanidinylation Reagents." ChemInform 29, no. 45 (2010): no. http://dx.doi.org/10.1002/chin.199845114.

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Feichtinger, Konrad, Heather L. Sings, Tracy J. Baker, Kenneth Matthews, and Murray Goodman. "Triurethane-Protected Guanidines and Triflyldiurethane-Protected Guanidines: New Reagents for Guanidinylation Reactions." Journal of Organic Chemistry 63, no. 23 (1998): 8432–39. http://dx.doi.org/10.1021/jo9814344.

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Witkowska, Ewa, Karolina Kubik, Jolanta Krosnicka, et al. "Microwave-assisted guanidinylation in solid phase peptide synthesis: comparison of various reagents." Tetrahedron Letters 55, no. 45 (2014): 6198–203. http://dx.doi.org/10.1016/j.tetlet.2014.09.056.

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Cortes-Salva, Michelle, Be-Lan Nguyen, Javier Cuevas, Keith R. Pennypacker, and Jon C. Antilla. "Copper-Catalyzed Guanidinylation of Aryl Iodides: The Formation ofN,N′-Disubstituted Guanidines." Organic Letters 12, no. 6 (2010): 1316–19. http://dx.doi.org/10.1021/ol1002175.

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Hammoud, Hassan, Martine Schmitt, Frédéric Bihel, Cyril Antheaume, and Jean-Jacques Bourguignon. "Direct Guanidinylation of Aryl and Heteroaryl Halides via Copper-Catalyzed Cross-Coupling Reaction." Journal of Organic Chemistry 77, no. 1 (2011): 417–23. http://dx.doi.org/10.1021/jo202018w.

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Mattheis, Claudia, Hui Wang, Claus Meister, and Seema Agarwal. "Effect of Guanidinylation on the Properties of Poly(2-aminoethylmethacrylate)-Based Antibacterial Materials." Macromolecular Bioscience 13, no. 2 (2012): 242–55. http://dx.doi.org/10.1002/mabi.201200217.

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Zhao, Xue, Zhen-Zhen Qiao, and Jin-Xin He. "Preparation of Chitosan Biguanidine Hydrochloride and Application in Antimicrobial Finish of Wool Fabric." Journal of Engineered Fibers and Fabrics 5, no. 3 (2010): 155892501000500. http://dx.doi.org/10.1177/155892501000500303.

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Chitosan biguanidine hydrochloride (CGH) has been synthesized by the guanidinylation reaction of chitosan with dicyandiamide. Its synthetic mechanism was discussed. The structures of CGH were characterized by FT-IR and 13CNMR. In this study, we used citric acid (CA) as a crosslinking agent, mixed with CGH to perform a pad-dry-cure treatment on wool fabric to study its antimicrobial effects with the help of scanning electron microscopy (SEM). The result showed that there was no obvious sign that CGH adhered to the wool fabric if the wool fabrics were not oxidized by hydrogen peroxide. The surfa
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Dissertations / Theses on the topic "Guanidinylation"

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Cortes-Salva, Michelle Yolanda. "Guanidines, Amidines and Carbamides as Novel Sigma Receptor Ligands for Post-Stroke Therapeutics." Scholar Commons, 2011. http://scholarcommons.usf.edu/etd/3049.

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Stroke is the 3rd leading cause of death in the United States. For this reason, it has become our goal to find a drug that is capable of reestablishing intracellular and extracellular Ca+2 flux upon direct binding to the sigma receptor, which can be delivered easily and efficiently. Our active research focuses the development of guanidine analogues that can serve as therapeutic drugs which target sigma 1 and sigma 2 receptors having a direct effect on Ca+2 levels on the cell. The use of symmetrical guanidine analogues such as N,N'-di-o-tolyl guanidine (o-DTG) as therapeutic drugs for ischemic
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Zapf, Christoph W. "Novel guanidinylating reagents and heterocyclic structures for peptidomimetic drug design /." Diss., Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC campuses, 2003. http://wwwlib.umi.com/cr/ucsd/fullcit?p3091332.

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Books on the topic "Guanidinylation"

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Ramsden, Philip Dean. A new guanidinylation procedure for the preparation of functionalized guanidines and investigation towards the synthesis of cyclic quanidine compounds. 2003.

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Book chapters on the topic "Guanidinylation"

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Bionda, Nina, and Predrag Cudic. "Solid-Phase Guanidinylation of Peptidyl Amines Compatible with Standard Fmoc-Chemistry: Formation of Monosubstituted Guanidines." In Methods in Molecular Biology. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-652-8_10.

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Musiol, Hans-Jürgen, and Luis Moroder. "Diurethanyl 1H-Benzotriazole-1-carboxamidines as Guanidinylating Reagents." In Peptides: The Wave of the Future. Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0464-0_39.

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Bentham Science Publisher, Bentham Science Publisher. "Diprotected Triflylguanidines: A New Class of Guanidinylation Reagents." In What's Doing? A Tribute to Professor Murray Goodman. BENTHAM SCIENCE PUBLISHERS, 2012. http://dx.doi.org/10.2174/978160805213410501010012.

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