Artículos de revistas sobre el tema "Guanidinium groups"
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Malinska, Maura, Miroslawa Dauter y Zbigniew Dauter. "Geometry of guanidinium groups in arginines". Protein Science 25, n.º 9 (4 de julio de 2016): 1753–56. http://dx.doi.org/10.1002/pro.2970.
Texto completoGalukhin, Andrey, Ilnaz Imatdinov y Yuri Osin. "p-tert-Butylthiacalix[4]arenes equipped with guanidinium fragments: aggregation, cytotoxicity, and DNA binding abilities". RSC Advances 6, n.º 39 (2016): 32722–26. http://dx.doi.org/10.1039/c6ra04733e.
Texto completoBalos, V., M. Bonn y J. Hunger. "Quantifying transient interactions between amide groups and the guanidinium cation". Physical Chemistry Chemical Physics 17, n.º 43 (2015): 28539–43. http://dx.doi.org/10.1039/c5cp04619j.
Texto completoSzabo, Jan y Gerhard Maas. "Derivatives of the triaminoguanidinium ion, 4. O-Sulfonylation of N,N′,N″-tris(hydroxybenzylidenamino)guanidinium ions". Zeitschrift für Naturforschung B 71, n.º 6 (1 de junio de 2016): 697–703. http://dx.doi.org/10.1515/znb-2016-0035.
Texto completoHanke, Marcel, Niklas Hansen, Emilia Tomm, Guido Grundmeier y Adrian Keller. "Time-Dependent DNA Origami Denaturation by Guanidinium Chloride, Guanidinium Sulfate, and Guanidinium Thiocyanate". International Journal of Molecular Sciences 23, n.º 15 (1 de agosto de 2022): 8547. http://dx.doi.org/10.3390/ijms23158547.
Texto completoMatulková, Irena, Jan Fábry, Václav Eigner, Michal Dušek, Jan Kroupa y Ivan Němec. "Isostructural Crystals of Bis(Guanidinium) Trioxofluoro-Phosphate/Phosphite in the Ratio 1/0, 0.716/0.284, 0.501/0.499, 0.268/0.732, 0/1—Crystal Structures, Vibrational Spectra and Second Harmonic Generation". Crystals 12, n.º 12 (23 de noviembre de 2022): 1694. http://dx.doi.org/10.3390/cryst12121694.
Texto completoBalos, V., M. Bonn y J. Hunger. "Correction: Quantifying transient interactions between amide groups and the guanidinium cation". Physical Chemistry Chemical Physics 18, n.º 2 (2016): 1346–47. http://dx.doi.org/10.1039/c5cp90226f.
Texto completoCui, Yu Fang, Jin Yan Du, Yu Ming Shang, Yao Wu Wang, Jin Hai Wang, Ya Fei Lv y Shu Bo Wang. "Novel Anion Exchange Membranes from Poly(aryl ether)s with Quaternary Guanidinium Groups". Advanced Materials Research 560-561 (agosto de 2012): 864–68. http://dx.doi.org/10.4028/www.scientific.net/amr.560-561.864.
Texto completoDu, Shanshan, Yang Li, Zhilong Chai, Weiguo Shi y Junlin He. "Site-specific functionalization with amino, guanidinium, and imidazolyl groups enabling the activation of 10–23 DNAzyme". RSC Advances 10, n.º 32 (2020): 19067–75. http://dx.doi.org/10.1039/d0ra02226h.
Texto completoTiritiris, Ioannis. "N,N,N′,N′,N′′-Pentamethyl-N′′-[3-(trimethylazaniumyl)propyl]guanidinium bis(tetraphenylborate)". Acta Crystallographica Section E Structure Reports Online 69, n.º 2 (26 de enero de 2013): o292. http://dx.doi.org/10.1107/s1600536813001992.
Texto completoKanvah, Sriram y Gary B. Schuster. "Effect of positively charged backbone groups on radical cation migration and reaction in duplex DNA". Canadian Journal of Chemistry 89, n.º 3 (febrero de 2011): 326–30. http://dx.doi.org/10.1139/v10-145.
Texto completoSauer, Sven, Sarmenio Saliba, Stefan Tussetschläger, Angelika Baro, Wolfgang Frey, Frank Giesselmann, Sabine Laschat y Willi Kantlehner. "p-Alkoxybiphenyls with guanidinium head groups displaying smectic mesophases". Liquid Crystals 36, n.º 3 (22 de mayo de 2009): 275–99. http://dx.doi.org/10.1080/02678290902850027.
Texto completoRobichon, Alain y Jean Claude Marie. "Chemical modification of guanidinium groups of vasoactive intestinal peptide". Biochimica et Biophysica Acta (BBA) - General Subjects 923, n.º 2 (febrero de 1987): 250–56. http://dx.doi.org/10.1016/0304-4165(87)90010-9.
Texto completoMüller, Gerhard, Jürgen Riede y Franz Peter Schmidtchen. "Host-Guest Bonding of Oxoanions to Guanidinium Anchor Groups". Angewandte Chemie International Edition in English 27, n.º 11 (noviembre de 1988): 1516–18. http://dx.doi.org/10.1002/anie.198815161.
Texto completoRussell, V. A. y M. D. Ward. "Solid-state structure of a layered hydrogen-bonded salt: guanidinium 5-benzoyl-4-hydroxy-2-methoxybenzenesulfonate methanol solvate". Acta Crystallographica Section B Structural Science 52, n.º 1 (1 de febrero de 1996): 209–14. http://dx.doi.org/10.1107/s0108768195009980.
Texto completoKantlehner, Willi, Jochen Mezger, Ralf Kreß, Horst Hartmann, Thorsten Moschny, Ioannis Tiritiris, Boyan Iliev et al. "Orthoamide, LXIX [1]. Beiträge zur Synthese N,N,N´,N´,N´´-peralkylierter Guanidine und N,N,N´,N´,N´´䞲,N´´-persubstituierter Guanidiniumsalze / Orthoamides, LXIX [1]. Contributions to the Synthesis of N, N, N´, N´, N´-peralkylated Guanidines and N, N, N´, N´, N´´, N´´-persubstituted Guanidinium Salts". Zeitschrift für Naturforschung B 65, n.º 7 (1 de julio de 2010): 873–906. http://dx.doi.org/10.1515/znb-2010-0712.
Texto completoWei, Bin. "Dimethylammonium guanidinium naphthalene-1,5-disulfonate". Acta Crystallographica Section E Structure Reports Online 68, n.º 4 (21 de marzo de 2012): o1123. http://dx.doi.org/10.1107/s1600536812011099.
Texto completoVortman, M. Ya, Zh P. Kopteva, A. E. Kopteva, D. R. Abdulina, Yu B. Pysmenna, G. O. Iutynska, A. V. Rudenko, V. V. Tretyak, V. N. Lemeshko y V. V. Shevchenko. "Antibacterial and Fungicidal Activity of Guanidinium Oligomers". Mikrobiolohichnyi Zhurnal 83, n.º 4 (17 de agosto de 2021): 86–97. http://dx.doi.org/10.15407/microbiolj83.04.086.
Texto completoTabujew, Ilja, Ceren Cokca, Leon Zartner, Ulrich S. Schubert, Ivo Nischang, Dagmar Fischer y Kalina Peneva. "The influence of gradient and statistical arrangements of guanidinium or primary amine groups in poly(methacrylate) copolymers on their DNA binding affinity". Journal of Materials Chemistry B 7, n.º 39 (2019): 5920–29. http://dx.doi.org/10.1039/c9tb01269a.
Texto completoMetzger, A., W. Peschke y F. P. Schmidtchen. "A Convenient Access to Chiral Monofunctionalized Bicyclic Guanidinium Receptor Groups". Synthesis 1995, n.º 05 (mayo de 1995): 566–70. http://dx.doi.org/10.1055/s-1995-3953.
Texto completoSapse, Anne-Marie, Robert Rothchild y Kyu Rhee. "An ab initio study of the guanidinium groups in saxitoxin". Journal of Molecular Modeling 12, n.º 2 (8 de noviembre de 2005): 140–45. http://dx.doi.org/10.1007/s00894-005-0005-y.
Texto completoLi, Shouchuan, Chunyu Chen, Zhengdong Zhang, Dong Wang y Shanshan Lv. "Illustration and application of enhancing effect of arginine on interactions between nano-clays: self-healing hydrogels". Soft Matter 15, n.º 2 (2019): 303–11. http://dx.doi.org/10.1039/c8sm02188k.
Texto completoGalukhin, Andrey, Anton Erokhin, Ilnaz Imatdinov y Yuri Osin. "Investigation of DNA binding abilities of solid lipid nanoparticles based on p-tert-butylthiacalix[4]arene platform". RSC Advances 5, n.º 42 (2015): 33351–55. http://dx.doi.org/10.1039/c5ra03814f.
Texto completoTiritiris, Ioannis y Willi Kantlehner. "Crystal structure ofN′′-benzyl-N′′-[3-(benzyldimethylazaniumyl)propyl]-N,N,N′,N′-tetramethylguanidinium bis(tetraphenylborate)". Acta Crystallographica Section E Crystallographic Communications 71, n.º 12 (1 de diciembre de 2015): o1086—o1087. http://dx.doi.org/10.1107/s2056989015024639.
Texto completoRichter, Friederike, Liam Martin, Katharina Leer, Elisabeth Moek, Franziska Hausig, Johannes C. Brendel y Anja Traeger. "Tuning of endosomal escape and gene expression by functional groups, molecular weight and transfection medium: a structure–activity relationship study". Journal of Materials Chemistry B 8, n.º 23 (2020): 5026–41. http://dx.doi.org/10.1039/d0tb00340a.
Texto completoCastaneda, C. H., M. J. Scuderi, T. G. Edwards, G. D. Harris Jr., C. M. Dupureur, K. J. Koeller, C. Fisher y J. K. Bashkin. "Improved antiviral activity of a polyamide against high-risk human papillomavirus via N-terminal guanidinium substitution". MedChemComm 7, n.º 11 (2016): 2076–82. http://dx.doi.org/10.1039/c6md00371k.
Texto completoSalama, Ahmed, Mohamed Hasanin y Peter Hesemann. "Synthesis and antimicrobial properties of new chitosan derivatives containing guanidinium groups". Carbohydrate Polymers 241 (agosto de 2020): 116363. http://dx.doi.org/10.1016/j.carbpol.2020.116363.
Texto completoZhu, Xuzhi, Jie Yang y Kirk S. Schanze. "Conjugated polyelectrolytes with guanidinium side groups. Synthesis, photophysics and pyrophosphate sensing". Photochem. Photobiol. Sci. 13, n.º 2 (2014): 293–300. http://dx.doi.org/10.1039/c3pp50288k.
Texto completoSCHMIDTCHEN, F. P., M. BERGER, A. METZGER, K. GLOE y H. STEPHAN. "ChemInform Abstract: Foldable Anion Hosts Based on Bicyclic Guanidinium Anchor Groups". ChemInform 28, n.º 51 (2 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199751316.
Texto completoTanaka, Masato, Hans-Ullrich Siehl, Tillmann Viefhaus, Wolfgang Frey y Willi Kantlehner. "An ONIOM Study of a Guanidinium Salt Ionic Liquid. Experimental and Computational Characterization of N,N,N`,N`,N``-Pentabutyl-N``-benzylguanidinium Bromide". Zeitschrift für Naturforschung B 64, n.º 6 (1 de junio de 2009): 765–72. http://dx.doi.org/10.1515/znb-2009-0624.
Texto completoGrogg, Marcel, Donald Hilvert, Albert Beck y Dieter Seebach. "Syntheses of Cyanophycin Segments for Investigations of Cell-Penetration". Synthesis 51, n.º 01 (28 de junio de 2018): 31–39. http://dx.doi.org/10.1055/s-0037-1610202.
Texto completoMETZGER, A., W. PESCHKE y F. P. SCHMIDTCHEN. "ChemInform Abstract: A Convenient Access to Chiral Monofunctionalized Bicyclic Guanidinium Receptor Groups." ChemInform 26, n.º 49 (17 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199549189.
Texto completoZhou, Zhe, Cansu Ergene y Edmund F. Palermo. "Guanidinium-Functionalized Photodynamic Antibacterial Oligo(Thiophene)s". MRS Advances 4, n.º 59-60 (2019): 3223–31. http://dx.doi.org/10.1557/adv.2019.359.
Texto completoXue, Boxin, Fen Wang, Jifu Zheng, Shenghai Li y Suobo Zhang. "Highly stable polysulfone anion exchange membranes incorporated with bulky alkyl substituted guanidinium cations". Molecular Systems Design & Engineering 4, n.º 5 (2019): 1039–47. http://dx.doi.org/10.1039/c9me00064j.
Texto completoHildebrandt, Peter, Roman S. Czernuszewicz, Christine A. Grygon y Thomas G. Spiro. "Ultraviolet resonance Raman enhancement of the carboxylate and guanidinium groups in amino acids". Journal of Raman Spectroscopy 20, n.º 10 (octubre de 1989): 645–50. http://dx.doi.org/10.1002/jrs.1250201003.
Texto completoSong, Yongbo, Hongyan Zheng, Yulan Niu, Ying Yao y Rongqian Meng. "Synthesis and Properties of Alkyl Bis-Guanidinium Acetates Surfactants". Tenside Surfactants Detergents 58, n.º 2 (1 de marzo de 2021): 127–35. http://dx.doi.org/10.1515/tsd-2019-2241.
Texto completoKurzmeier, H. y F. P. Schmidtchen. "Abiotic anion receptor functions. A facile and dependable access to chiral guanidinium anchor groups". Journal of Organic Chemistry 55, n.º 12 (junio de 1990): 3749–55. http://dx.doi.org/10.1021/jo00299a013.
Texto completoChen, Xiaoqiang, Jingyun Wang, Shiguo Sun, Jiangli Fan, Song Wu, Jianfeng Liu, Saijian Ma, Lizhu Zhang y Xiaojun Peng. "Efficient enhancement of DNA cleavage activity by introducing guanidinium groups into diiron(III) complex". Bioorganic & Medicinal Chemistry Letters 18, n.º 1 (enero de 2008): 109–13. http://dx.doi.org/10.1016/j.bmcl.2007.11.001.
Texto completoLiu, Fang, Yanhua Wang y Guo-Yuan Lu. "Bilayer Vesicle Formation in Ethanol from Calix[4]arene Derivative with Two Guanidinium Groups". Chemistry Letters 34, n.º 10 (octubre de 2005): 1450–51. http://dx.doi.org/10.1246/cl.2005.1450.
Texto completoSuresh, J., R. V. Krishnakumar y S. Natarajan. "L-Argininium trifluoroacetate". Acta Crystallographica Section E Structure Reports Online 62, n.º 7 (30 de junio de 2006): o3127—o3129. http://dx.doi.org/10.1107/s1600536806024743.
Texto completoSchug, Kevin A. y Wolfgang Lindner. "Noncovalent Binding between Guanidinium and Anionic Groups: Focus on Biological- and Synthetic-Based Arginine/Guanidinium Interactions with Phosph[on]ate and Sulf[on]ate Residues". Chemical Reviews 105, n.º 1 (enero de 2005): 67–114. http://dx.doi.org/10.1021/cr040603j.
Texto completoWang, Sheng Qin, Mohit Sharma y Yew Wei Leong. "Polyamide 11/Clay Nanocomposite Using Polyhedral Oligomeric Silsesquioxane Surfactants". Advanced Materials Research 1110 (junio de 2015): 65–68. http://dx.doi.org/10.4028/www.scientific.net/amr.1110.65.
Texto completoMORILLAS, Manuel, Martin L. GOBLE y Richard VIRDEN. "The kinetics of acylation and deacylation of penicillin acylase from Escherichia coli ATCC 11105: evidence for lowered pKa values of groups near the catalytic centre". Biochemical Journal 338, n.º 1 (8 de febrero de 1999): 235–39. http://dx.doi.org/10.1042/bj3380235.
Texto completoGrijalvo, Santiago, Montserrat Terrazas, Anna Aviñó y Ramón Eritja. "Stepwise synthesis of oligonucleotide–peptide conjugates containing guanidinium and lipophilic groups in their 3′-termini". Bioorganic & Medicinal Chemistry Letters 20, n.º 7 (abril de 2010): 2144–47. http://dx.doi.org/10.1016/j.bmcl.2010.02.049.
Texto completoAndreyko, Elena A., Joshua B. Puplampu, Patricia A. Ignacio-De Leon, Ilya Zharov y Ivan I. Stoikov. "p-tert-Butylthiacalix[4]arenes containing guanidinium groups: synthesis and self-assembly into nanoscale aggregates". Supramolecular Chemistry 31, n.º 7 (16 de junio de 2019): 473–83. http://dx.doi.org/10.1080/10610278.2019.1628231.
Texto completoAït-Haddou, Hassan, Jun Sumaoka, Sheryl L. Wiskur, J. Frantz Folmer-Andersen y Eric V. Anslyn. "Remarkable Cooperativity between a ZnII Ion and Guanidinium/Ammonium Groups in the Hydrolysis of RNA". Angewandte Chemie International Edition 41, n.º 21 (4 de noviembre de 2002): 4013–16. http://dx.doi.org/10.1002/1521-3773(20021104)41:21<4013::aid-anie4013>3.0.co;2-y.
Texto completoVORTMAN, M. YA, V. N. LEMESHKO, L. A. GONCHARENKO, S. M. KOBYLINSKIY, V. V. SHEVCHENKO y S. N. OSTAPIUK. "OLIGOMERIC GUANIDINE-CONTAINING PROTON CATIONIC IONIC LIQUID". Polymer journal 43, n.º 4 (26 de noviembre de 2021): 304–10. http://dx.doi.org/10.15407/polymerj.43.04.304.
Texto completoRoig, Victoria y Ulysse Asseline. "Oligo-2‘-deoxyribonucleotides Containing Uracil Modified at the 5-Position with Linkers Ending with Guanidinium Groups". Journal of the American Chemical Society 125, n.º 15 (abril de 2003): 4416–17. http://dx.doi.org/10.1021/ja029467v.
Texto completoPerreault, Denise M., Larry A. Cabell y Eric V. Anslyn. "Using guanidinium groups for the recognition of RNA and as catalysts for the hydrolysis of RNA". Bioorganic & Medicinal Chemistry 5, n.º 6 (junio de 1997): 1209–20. http://dx.doi.org/10.1016/s0968-0896(97)00051-5.
Texto completoDeng, Qiliang, Jianhua Wu, Yang Chen, Zhijun Zhang, Yang Wang, Guozhen Fang, Shuo Wang y Yukui Zhang. "Guanidinium functionalized superparamagnetic silica spheres for selective enrichment of phosphopeptides and intact phosphoproteins from complex mixtures". J. Mater. Chem. B 2, n.º 8 (2014): 1048–58. http://dx.doi.org/10.1039/c3tb21540g.
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