Artigos de revistas sobre o tema "Tautomeric constant"
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KOSAR, BASAK. "THERMODYNAMIC AND SECOND-ORDER NON-LINEAR OPTICAL PROPERTIES OF TAUTOMERIC FORMS OF (E)-4-METHOXY-2-[(4-NITROPHENYL)IMINOMETHYL]PHENOL: A DENSITY FUNCTIONAL STUDY". Journal of Theoretical and Computational Chemistry 10, n.º 03 (junho de 2011): 279–95. http://dx.doi.org/10.1142/s021963361100644x.
Texto completo da fonteScrypynets, Yu V., G. O. Fedosenko, G. V. Maltsev, I. I. Chebotars'ka, D. I. Aleksandrova, S. N. Kashutskуy e A. V. Yegorova. "DETERMINATION OF THE IONIZATION CONSTANT OF FAVIPIRAVIR API". Odesa National University Herald. Chemistry 28, n.º 2(85) (12 de setembro de 2023): 52–61. http://dx.doi.org/10.18524/2304-0947.2023.2(85).286603.
Texto completo da fonteBabu, Numbury Surendra, e Didugu Jayaprakash. "Computational Study of the Stability of Tautomers and equilibrium constants of Cyanuric acid (CA) in Different solvents." JOURNAL OF ADVANCES IN CHEMISTRY 11, n.º 2 (22 de janeiro de 2015): 3485–97. http://dx.doi.org/10.24297/jac.v11i2.6691.
Texto completo da fonteHallé, Jean-Claude, Jacques Lelievre e François Terrier. "Solvent effect on preferred protonation sites in nicotinate and isonicotinate anions". Canadian Journal of Chemistry 74, n.º 4 (1 de abril de 1996): 613–20. http://dx.doi.org/10.1139/v96-065.
Texto completo da fonteMchedlov-Petrossyan, Nikolay O., e Natalya A. Vodolazkaya. "Protolytic Equilibria in Organized Solutions: Ionization and Tautomerism of Fluorescein Dyes and Related Indicators in Cetyltrimethylammonium Chloride Micellar Solutions at High Ionic Strength of the Bulk Phase". Liquids 1, n.º 1 (20 de fevereiro de 2021): 1–24. http://dx.doi.org/10.3390/liquids1010001.
Texto completo da fonteNishimura, N., K. Danjo, Y. Sueishi e S. Yamamoto. "Solvent and Pressure Effects on the Tautomeric Equilibrium of 4-Phenylazo-1-naphthol". Australian Journal of Chemistry 41, n.º 6 (1988): 863. http://dx.doi.org/10.1071/ch9880863.
Texto completo da fonteLopez, Concepcion, Rosa Ma Claramunt, Swiatoslaw Trofimenko e José Elguero. "A 13C NMR spectroscopy study of the structure of N-H pyrazoles and indazoles". Canadian Journal of Chemistry 71, n.º 5 (1 de maio de 1993): 678–84. http://dx.doi.org/10.1139/v93-092.
Texto completo da fonteNěmcová, Irena, Oldřich Valcl e Jiří Makovička. "The interactions of tensides with calconalide I". Collection of Czechoslovak Chemical Communications 56, n.º 10 (1991): 2100–2106. http://dx.doi.org/10.1135/cccc19912100.
Texto completo da fonteAcree, William E., e Sheryl A. Tucker. "Thermochemical Investigations of Tautomeric Equilibrium. Variation of the Calculated Equilibrium Constant with Binary Solvent Composition". Physics and Chemistry of Liquids 20, n.º 2-3 (setembro de 1989): 135–45. http://dx.doi.org/10.1080/00319108908036400.
Texto completo da fonteMoskaeva, Elena, Ahina Mosharenkova, Sergey Shekhovtsov e Nikolay Mchedlov-Petrossyan. "PROTOLYTIC EQUILIBRIUM OF TETRA- AND PENTANITROFLUORESCEINS IN A BINARY SOLVENT ACETONITRILE – DIMETHYL SULFOXIDE (MASS RATIO 96 : 4)". Ukrainian Chemistry Journal 87, n.º 5 (25 de junho de 2021): 25–37. http://dx.doi.org/10.33609/2708-129x.87.05.2021.25-37.
Texto completo da fonteHarris, Victoria H., Clifford L. Smith, W. Jonathan Cummins, Alan L. Hamilton, Harry Adams, Mark Dickman, David P. Hornby e David M. Williams. "The Effect of Tautomeric Constant on the Specificity of Nucleotide Incorporation during DNA Replication: Support for the Rare Tautomer Hypothesis of Substitution Mutagenesis". Journal of Molecular Biology 326, n.º 5 (março de 2003): 1389–401. http://dx.doi.org/10.1016/s0022-2836(03)00051-2.
Texto completo da fonteRaczyńska, Ewa D. "Influence of Substituent on Tautomeric Equilibrium Constant in 5(6)-Substituted Benzimidazoles in the Gas Phase". Journal of Chemical Research, n.º 11 (1998): 704–5. http://dx.doi.org/10.1039/a802613k.
Texto completo da fonteCHARIF, I. E., S. M. MEKELLECHE e D. VILLEMIN. "SOLVENT EFFECTS ON THE KETO-ENOL TAUTOMERIC EQUILIBRIUM OF TETRONIC AND ETHYL ACETOACETATE CARBON ACIDS: A THEORETICAL STUDY". Journal of Theoretical and Computational Chemistry 09, n.º 06 (dezembro de 2010): 1021–32. http://dx.doi.org/10.1142/s0219633610006171.
Texto completo da fonteRamírez-Galicia, G. "A new model for the theoretical tautomeric constant (KT) calculation of 2-, 3- and 4-substituted pyridines". Journal of Molecular Structure: THEOCHEM 542, n.º 1-3 (15 de junho de 2001): 1–6. http://dx.doi.org/10.1016/s0166-1280(00)00649-7.
Texto completo da fonteObukhova, Olena M., Nikolay O. Mchedlov-Petrossyan, Natalya A. Vodolazkaya, Leonid D. Patsenker e Andrey O. Doroshenko. "Stability of Rhodamine Lactone Cycle in Solutions: Chain–Ring Tautomerism, Acid–Base Equilibria, Interaction with Lewis Acids, and Fluorescence". Colorants 1, n.º 1 (24 de fevereiro de 2022): 58–90. http://dx.doi.org/10.3390/colorants1010006.
Texto completo da fonteCristiani, Franco, Francesco A. Devillanova, Angelo Diaz, Francesco Isaia, Gaetano Verani, Francesco Demartin e Giuseppe Saba. "2-S-Methyl-5,5-dimethylimidazolin-4-one: chemical behaviour and crystal structure of its Δ1 tautomer". Canadian Journal of Chemistry 69, n.º 3 (1 de março de 1991): 383–90. http://dx.doi.org/10.1139/v91-059.
Texto completo da fonteSaraswat, Apoorv, e Rana Krishna Pal Singh. "Utilization of Dissociation Constant (pKa) Value Perspective of -CH Acid in Electrochemical Synthesis of 4H-Chromene and its Derivatives". Asian Journal of Chemistry 32, n.º 7 (2020): 1697–702. http://dx.doi.org/10.14233/ajchem.2020.22663.
Texto completo da fonteChebotarev, Alexandr N., Denys V. Snigur e Kateryna V. Bevziuk. "STUDY OF PROTOLYTIC EQUILIBRIA IN SOLUTIONS OF HYDROXYANTHRAQUINONE DYES BY CHEMICAL CHROMATICITY METHOD". IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 60, n.º 3 (13 de abril de 2017): 22. http://dx.doi.org/10.6060/tcct.2017603.5418.
Texto completo da fonteRak, Janusz, Piotr Skurski, Ludwika Jozwiak e Jerzy Blazejowski. "Theoretical Studies on the Effect of the Medium on Tautomeric Phenomena in Neutral and Protonated Acridin-9-amine. Mechanism of Tautomerization in Neutral Entities". Australian Journal of Chemistry 50, n.º 2 (1997): 97. http://dx.doi.org/10.1071/c96184.
Texto completo da fonteAnderson, John C., e A. Douglas Broadbent. "The influence of pH in the tautomerism of 9,10-anthracenediols and 1,3-diketones". Canadian Journal of Chemistry 64, n.º 1 (1 de janeiro de 1986): 127–32. http://dx.doi.org/10.1139/v86-022.
Texto completo da fonteSargolzaei, M., M. Afshar e H. Nikoofard. "Solvent Effect on The Equilibrium and Rate Constant of the Tautomeric Reaction in Nexium, Skelaxin, Aldara and Efavirenz Drugs: A Dft Study". Journal of Structural Chemistry 59, n.º 2 (março de 2018): 297–305. http://dx.doi.org/10.1134/s0022476618020063.
Texto completo da fonteOu, Zhongping, Xueyan Chen, Lina Ye, Songlin Xue, Yuanyuan Fang, Xiaoqin Jiang e Karl M. Kadish. "N-confusedmeso-tetraaryl-substituted free-base porphyrins: determination of protonation and deprotonation constants in nonaqueous media". Journal of Porphyrins and Phthalocyanines 19, n.º 01-03 (janeiro de 2015): 251–60. http://dx.doi.org/10.1142/s1088424614501132.
Texto completo da fonteAlbayrak Kaştaş, Çiğdem, e Gökhan Kaştaş. "Dependence of tautomerism on substituent type in o-hydroxy Schiff bases". Macedonian Journal of Chemistry and Chemical Engineering 38, n.º 1 (16 de maio de 2019): 85. http://dx.doi.org/10.20450/mjcce.2019.1531.
Texto completo da fonteAlmdal, Kristoffer, Hanne Eggert, Ole Hammerich, Lars Skattebøl, Povl Krogsgaard-Larsen, Ragnar Ryhage e Roland Isaksson. "Determination of the Equilibrium Constant for the Tautomeric 9-Hydroxyanthracene/9-Anthrone System in Aprotic Solvents by a Novel Application of Cyclic Voltammetry." Acta Chemica Scandinavica 40b (1986): 230–32. http://dx.doi.org/10.3891/acta.chem.scand.40b-0230.
Texto completo da fonteKunyima, Anaclet B., Joseph C. Kuburhanwa, Heritier M. Kaseya, Benoît M. Mukendi e Michel B. Kunyima. "Kinetic and Thermodynamic Study of Extraction of Oleoresin Containing Curcuminoids from Turmeric (Curcuma Longa L.)". European Journal of Advanced Chemistry Research 3, n.º 2 (24 de julho de 2022): 15–26. http://dx.doi.org/10.24018/ejchem.2022.3.2.107.
Texto completo da fonteDemukhamedova, S. "THEORETICAL QUANTUM-CHEMICAL SIMULATION OF THE STRUCTURE AND PROPERTIES OF CARNOSINE DIPEPTIDE BY THE DFT METHOD". Russian Journal of Biological Physics and Chemisrty 7, n.º 2 (15 de novembro de 2022): 241–50. http://dx.doi.org/10.29039/rusjbpc.2022.0509.
Texto completo da fonteHush, NS, MK Livett, JB Peel e GD Willett. "Variable-Temperature Ultraviolet Photoelectron-Spectroscopy of the Keto-Enol Tautomers of Pentane-2,4-Dione". Australian Journal of Chemistry 40, n.º 3 (1987): 599. http://dx.doi.org/10.1071/ch9870599.
Texto completo da fonteSigel, H. "Acid-base properties of purine residues and the effect of metal ions: Quantification of rare nucleobase tautomers". Pure and Applied Chemistry 76, n.º 10 (1 de janeiro de 2004): 1869–86. http://dx.doi.org/10.1351/pac200476101869.
Texto completo da fonteOuali, M., C. Laboulais, H. Leh, D. Gill, E. Xhuvani, F. Zouhiri, D. Desmaele et al. "Tautomers of styrylquinoline derivatives containing a methoxy substituent: computation of their population in aqueous solution and their interaction with RSV integrase catalytic core." Acta Biochimica Polonica 47, n.º 1 (31 de março de 2000): 11–22. http://dx.doi.org/10.18388/abp.2000_4058.
Texto completo da fonteZdanovskaia, Maria A., Brian J. Esselman, Samuel M. Kougias, Brent K. Amberger, John F. Stanton, R. Claude Woods e Robert J. McMahon. "Precise equilibrium structures of 1H- and 2H-1,2,3-triazoles (C2H3N3) by millimeter-wave spectroscopy". Journal of Chemical Physics 157, n.º 8 (28 de agosto de 2022): 084305. http://dx.doi.org/10.1063/5.0097750.
Texto completo da fonteBuncel, Erwin. "1999 R.U. Lemieux Award Lecture Adventures with azo-, azoxy-, and hydrazoarenes: from the Wallach to the benzidine rearrangement. Molecular electronics". Canadian Journal of Chemistry 78, n.º 10 (1 de outubro de 2000): 1251–71. http://dx.doi.org/10.1139/v00-126.
Texto completo da fonteNguyen, Nguyen Tran, Vo Viet Dai, Nguyen Ngoc Tri, Luc Van Meervelt, Nguyen Tien Trung e Wim Dehaen. "Experimental and theoretical studies on the synthesis of 1,4,5-trisubstituted pyrrolidine-2,3-diones". Beilstein Journal of Organic Chemistry 18 (31 de agosto de 2022): 1140–53. http://dx.doi.org/10.3762/bjoc.18.118.
Texto completo da fonteMari, Matteo, Debora Carrozza, Gianluca Malavasi, Ettore Venturi, Giulia Avino, Pier Cesare Capponi, Michele Iori et al. "Curcumin-Based β-Diketo Ligands for Ga3+: Thermodynamic Investigation of Potential Metal-Based Drugs". Pharmaceuticals 15, n.º 7 (12 de julho de 2022): 854. http://dx.doi.org/10.3390/ph15070854.
Texto completo da fonteHerrenknecht, Christine, Elisabeth Guernet-Nivaud, Olivier Lafont, Michel Guernet e Claire Gueutin. "Chemical electrochemical mechanism. Electrochemical reduction of some pyrazolidine-3,5-diones in DMSO. Relation between voltammetric behavior and 1H nuclear magnetic resonance spectra". Canadian Journal of Chemistry 66, n.º 5 (1 de maio de 1988): 1199–202. http://dx.doi.org/10.1139/v88-196.
Texto completo da fonteWierzchowski, Jacek, Agnieszka Bzowska, Katarzyna Stępniak e David Shugar. "Interactions of Calf Spleen Purine Nucleoside Phosphorylase with 8-Azaguanine, and a Bisubstrate Analogue Inhibitor: Implications for the Reaction Mechanism". Zeitschrift für Naturforschung C 59, n.º 9-10 (1 de outubro de 2004): 713–25. http://dx.doi.org/10.1515/znc-2004-9-1017.
Texto completo da fonteLeškovskis, Kristaps, Anatoly Mishnev, Irina Novosjolova e Māris Turks. "SNAr Reactions of 2,4-Diazidopyrido[3,2-d]pyrimidine and Azide-Tetrazole Equilibrium Studies of the Obtained 5-Substituted Tetrazolo[1,5-a]pyrido[2,3-e]pyrimidines". Molecules 27, n.º 22 (8 de novembro de 2022): 7675. http://dx.doi.org/10.3390/molecules27227675.
Texto completo da fonteBunting, John W., James P. Kanter, Raymond Nelander e Zhennan Wu. "The acidity and tautomerism of β-diketones in aqueous solution". Canadian Journal of Chemistry 73, n.º 8 (1 de agosto de 1995): 1305–11. http://dx.doi.org/10.1139/v95-161.
Texto completo da fonteBlanco, Carlos A., e Michael J. Hynes. "Catalysis of the deprotonation of β-diketones during formation of the 1:1 metal complexes". Canadian Journal of Chemistry 70, n.º 8 (1 de agosto de 1992): 2285–89. http://dx.doi.org/10.1139/v92-287.
Texto completo da fonteSadutto, Daniele, Paolo Guglielmi, Simone Carradori, Daniela Secci e Roberto Cirilli. "Kinetic Study on the Base-Catalyzed Imine-Enamine Tautomerism of a Chiral Biologically Active Isoxazoline Derivative by HPLC on Amylose Tris(3,5-dimethylphenylcarbamate) Chiral Stationary Phase". Molecules 28, n.º 18 (8 de setembro de 2023): 6518. http://dx.doi.org/10.3390/molecules28186518.
Texto completo da fonteAl-Omari, Hamzeh S. M. "Effect of Different Substituents on Uracil and its 2-Hydroxy-4-oxo Enol Tautomer – A Theoretical Study". Zeitschrift für Naturforschung A 63, n.º 10-11 (1 de novembro de 2008): 693–702. http://dx.doi.org/10.1515/zna-2008-10-1113.
Texto completo da fonteRojas, Antonio, Alfonso Perez-Encabo, Ignacio Herraiz-Sierra e Carlos A. Blanco. "Tautomerization tendencies of 2-acetylcycloalkanones, 2-acetyl-1,3-cycloalkanediones, and cyclic β-keto esters of five- and six-membered rings". Canadian Journal of Chemistry 79, n.º 4 (1 de abril de 2001): 448–54. http://dx.doi.org/10.1139/v01-061.
Texto completo da fonteCapponi, Marco, Ivo G. Gut, Bruno Hellrung, Gaby Persy e Jakob Wirz. "Ketonization equilibria of phenol in aqueous solution". Canadian Journal of Chemistry 77, n.º 5-6 (1 de junho de 1999): 605–13. http://dx.doi.org/10.1139/v99-048.
Texto completo da fonteSaad, Gamal R., Magdi M. Naoum e Hanna A. Rizk. "Dielectric polarization and molecular interaction. Part II. Acetylacetone, benzoylacetone, and dibenzoylmethane – triethyl amine – cyclohexane systems". Canadian Journal of Chemistry 67, n.º 2 (1 de fevereiro de 1989): 284–88. http://dx.doi.org/10.1139/v89-047.
Texto completo da fonteKhandogin, Jana, e Charles L. Brooks. "Constant pH Molecular Dynamics with Proton Tautomerism". Biophysical Journal 89, n.º 1 (julho de 2005): 141–57. http://dx.doi.org/10.1529/biophysj.105.061341.
Texto completo da fonteRzepiela, Kacper, Aneta Buczek, Teobald Kupka e Małgorzata A. Broda. "Factors Governing the Chemical Stability and NMR Parameters of Uracil Tautomers and Its 5-Halogen Derivatives". Molecules 25, n.º 17 (28 de agosto de 2020): 3931. http://dx.doi.org/10.3390/molecules25173931.
Texto completo da fonteBaron, Marie-Hélène, Sabine Halut-Desportes, Hai-Fen Ye, Jack Huet e Edith Favre. "Spectroscopic conformational study of PMS 952, a specific imidazoline ligand. Experimental results". Canadian Journal of Chemistry 77, n.º 12 (5 de dezembro de 1999): 2015–24. http://dx.doi.org/10.1139/v99-191.
Texto completo da fontePachulia, Z., e J. Kereselidze. "Calculation of tautomeric equilibrium constants in complementary DNA pairs". Journal of Biological Physics and Chemistry 16, n.º 4 (30 de dezembro de 2016): 177–80. http://dx.doi.org/10.4024/20pa16a.jbpc.16.04.
Texto completo da fonteShawali, Ahmad S., Mosselhi A. N. Mosselhi e Thoraya A. Farghaly. "Synthesis and Tautomeric Structure of 2-arylazo-4H-imidazo[2,1-b][1,3,4]thiadiazines". Journal of Chemical Research 2007, n.º 8 (agosto de 2007): 479–83. http://dx.doi.org/10.3184/030823407x237885.
Texto completo da fonteCostantino, Luca, Giulio Rastelli, Maria C. Rossi e Albano Albasini. "Quantitative measurement of proton dissociation and tautomeric constants of apigeninidin". Journal of the Chemical Society, Perkin Transactions 2, n.º 2 (1995): 227. http://dx.doi.org/10.1039/p29950000227.
Texto completo da fonteLyčka, Antonín, Libuše Havlíčková, Alois Koloničný e Josef Jirman. "15N NMR study of amino-imino tautomerism in derivatives of 1,4-bis(substituted amino)-9,10-anthraquinones and 1,4-bis(substituted amino)-2,3-dihydro-9,10-anthraquinones". Collection of Czechoslovak Chemical Communications 52, n.º 3 (1987): 736–41. http://dx.doi.org/10.1135/cccc19870736.
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