Zeitschriftenartikel zum Thema „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, Nr. 03 (Juni 2011): 279–95. http://dx.doi.org/10.1142/s021963361100644x.
Scrypynets, Yu V., G. O. Fedosenko, G. V. Maltsev, I. I. Chebotars'ka, D. I. Aleksandrova, S. N. Kashutskуy und A. V. Yegorova. „DETERMINATION OF THE IONIZATION CONSTANT OF FAVIPIRAVIR API“. Odesa National University Herald. Chemistry 28, Nr. 2(85) (12.09.2023): 52–61. http://dx.doi.org/10.18524/2304-0947.2023.2(85).286603.
Babu, Numbury Surendra, und 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, Nr. 2 (22.01.2015): 3485–97. http://dx.doi.org/10.24297/jac.v11i2.6691.
Hallé, Jean-Claude, Jacques Lelievre und François Terrier. „Solvent effect on preferred protonation sites in nicotinate and isonicotinate anions“. Canadian Journal of Chemistry 74, Nr. 4 (01.04.1996): 613–20. http://dx.doi.org/10.1139/v96-065.
Mchedlov-Petrossyan, Nikolay O., und 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, Nr. 1 (20.02.2021): 1–24. http://dx.doi.org/10.3390/liquids1010001.
Nishimura, N., K. Danjo, Y. Sueishi und S. Yamamoto. „Solvent and Pressure Effects on the Tautomeric Equilibrium of 4-Phenylazo-1-naphthol“. Australian Journal of Chemistry 41, Nr. 6 (1988): 863. http://dx.doi.org/10.1071/ch9880863.
Lopez, Concepcion, Rosa Ma Claramunt, Swiatoslaw Trofimenko und José Elguero. „A 13C NMR spectroscopy study of the structure of N-H pyrazoles and indazoles“. Canadian Journal of Chemistry 71, Nr. 5 (01.05.1993): 678–84. http://dx.doi.org/10.1139/v93-092.
Němcová, Irena, Oldřich Valcl und Jiří Makovička. „The interactions of tensides with calconalide I“. Collection of Czechoslovak Chemical Communications 56, Nr. 10 (1991): 2100–2106. http://dx.doi.org/10.1135/cccc19912100.
Acree, William E., und Sheryl A. Tucker. „Thermochemical Investigations of Tautomeric Equilibrium. Variation of the Calculated Equilibrium Constant with Binary Solvent Composition“. Physics and Chemistry of Liquids 20, Nr. 2-3 (September 1989): 135–45. http://dx.doi.org/10.1080/00319108908036400.
Moskaeva, Elena, Ahina Mosharenkova, Sergey Shekhovtsov und Nikolay Mchedlov-Petrossyan. „PROTOLYTIC EQUILIBRIUM OF TETRA- AND PENTANITROFLUORESCEINS IN A BINARY SOLVENT ACETONITRILE – DIMETHYL SULFOXIDE (MASS RATIO 96 : 4)“. Ukrainian Chemistry Journal 87, Nr. 5 (25.06.2021): 25–37. http://dx.doi.org/10.33609/2708-129x.87.05.2021.25-37.
Harris, Victoria H., Clifford L. Smith, W. Jonathan Cummins, Alan L. Hamilton, Harry Adams, Mark Dickman, David P. Hornby und 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, Nr. 5 (März 2003): 1389–401. http://dx.doi.org/10.1016/s0022-2836(03)00051-2.
Raczyńska, Ewa D. „Influence of Substituent on Tautomeric Equilibrium Constant in 5(6)-Substituted Benzimidazoles in the Gas Phase“. Journal of Chemical Research, Nr. 11 (1998): 704–5. http://dx.doi.org/10.1039/a802613k.
CHARIF, I. E., S. M. MEKELLECHE und 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, Nr. 06 (Dezember 2010): 1021–32. http://dx.doi.org/10.1142/s0219633610006171.
Ramírez-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, Nr. 1-3 (15.06.2001): 1–6. http://dx.doi.org/10.1016/s0166-1280(00)00649-7.
Obukhova, Olena M., Nikolay O. Mchedlov-Petrossyan, Natalya A. Vodolazkaya, Leonid D. Patsenker und Andrey O. Doroshenko. „Stability of Rhodamine Lactone Cycle in Solutions: Chain–Ring Tautomerism, Acid–Base Equilibria, Interaction with Lewis Acids, and Fluorescence“. Colorants 1, Nr. 1 (24.02.2022): 58–90. http://dx.doi.org/10.3390/colorants1010006.
Cristiani, Franco, Francesco A. Devillanova, Angelo Diaz, Francesco Isaia, Gaetano Verani, Francesco Demartin und Giuseppe Saba. „2-S-Methyl-5,5-dimethylimidazolin-4-one: chemical behaviour and crystal structure of its Δ1 tautomer“. Canadian Journal of Chemistry 69, Nr. 3 (01.03.1991): 383–90. http://dx.doi.org/10.1139/v91-059.
Saraswat, Apoorv, und 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, Nr. 7 (2020): 1697–702. http://dx.doi.org/10.14233/ajchem.2020.22663.
Chebotarev, Alexandr N., Denys V. Snigur und Kateryna V. Bevziuk. „STUDY OF PROTOLYTIC EQUILIBRIA IN SOLUTIONS OF HYDROXYANTHRAQUINONE DYES BY CHEMICAL CHROMATICITY METHOD“. IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 60, Nr. 3 (13.04.2017): 22. http://dx.doi.org/10.6060/tcct.2017603.5418.
Rak, Janusz, Piotr Skurski, Ludwika Jozwiak und 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, Nr. 2 (1997): 97. http://dx.doi.org/10.1071/c96184.
Anderson, John C., und A. Douglas Broadbent. „The influence of pH in the tautomerism of 9,10-anthracenediols and 1,3-diketones“. Canadian Journal of Chemistry 64, Nr. 1 (01.01.1986): 127–32. http://dx.doi.org/10.1139/v86-022.
Sargolzaei, M., M. Afshar und 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, Nr. 2 (März 2018): 297–305. http://dx.doi.org/10.1134/s0022476618020063.
Ou, Zhongping, Xueyan Chen, Lina Ye, Songlin Xue, Yuanyuan Fang, Xiaoqin Jiang und 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, Nr. 01-03 (Januar 2015): 251–60. http://dx.doi.org/10.1142/s1088424614501132.
Albayrak Kaştaş, Çiğdem, und Gökhan Kaştaş. „Dependence of tautomerism on substituent type in o-hydroxy Schiff bases“. Macedonian Journal of Chemistry and Chemical Engineering 38, Nr. 1 (16.05.2019): 85. http://dx.doi.org/10.20450/mjcce.2019.1531.
Almdal, Kristoffer, Hanne Eggert, Ole Hammerich, Lars Skattebøl, Povl Krogsgaard-Larsen, Ragnar Ryhage und 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.
Kunyima, Anaclet B., Joseph C. Kuburhanwa, Heritier M. Kaseya, Benoît M. Mukendi und 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, Nr. 2 (24.07.2022): 15–26. http://dx.doi.org/10.24018/ejchem.2022.3.2.107.
Demukhamedova, 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, Nr. 2 (15.11.2022): 241–50. http://dx.doi.org/10.29039/rusjbpc.2022.0509.
Hush, NS, MK Livett, JB Peel und GD Willett. „Variable-Temperature Ultraviolet Photoelectron-Spectroscopy of the Keto-Enol Tautomers of Pentane-2,4-Dione“. Australian Journal of Chemistry 40, Nr. 3 (1987): 599. http://dx.doi.org/10.1071/ch9870599.
Sigel, H. „Acid-base properties of purine residues and the effect of metal ions: Quantification of rare nucleobase tautomers“. Pure and Applied Chemistry 76, Nr. 10 (01.01.2004): 1869–86. http://dx.doi.org/10.1351/pac200476101869.
Ouali, 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, Nr. 1 (31.03.2000): 11–22. http://dx.doi.org/10.18388/abp.2000_4058.
Zdanovskaia, Maria A., Brian J. Esselman, Samuel M. Kougias, Brent K. Amberger, John F. Stanton, R. Claude Woods und Robert J. McMahon. „Precise equilibrium structures of 1H- and 2H-1,2,3-triazoles (C2H3N3) by millimeter-wave spectroscopy“. Journal of Chemical Physics 157, Nr. 8 (28.08.2022): 084305. http://dx.doi.org/10.1063/5.0097750.
Buncel, 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, Nr. 10 (01.10.2000): 1251–71. http://dx.doi.org/10.1139/v00-126.
Nguyen, Nguyen Tran, Vo Viet Dai, Nguyen Ngoc Tri, Luc Van Meervelt, Nguyen Tien Trung und Wim Dehaen. „Experimental and theoretical studies on the synthesis of 1,4,5-trisubstituted pyrrolidine-2,3-diones“. Beilstein Journal of Organic Chemistry 18 (31.08.2022): 1140–53. http://dx.doi.org/10.3762/bjoc.18.118.
Mari, 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, Nr. 7 (12.07.2022): 854. http://dx.doi.org/10.3390/ph15070854.
Herrenknecht, Christine, Elisabeth Guernet-Nivaud, Olivier Lafont, Michel Guernet und 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, Nr. 5 (01.05.1988): 1199–202. http://dx.doi.org/10.1139/v88-196.
Wierzchowski, Jacek, Agnieszka Bzowska, Katarzyna Stępniak und 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, Nr. 9-10 (01.10.2004): 713–25. http://dx.doi.org/10.1515/znc-2004-9-1017.
Leškovskis, Kristaps, Anatoly Mishnev, Irina Novosjolova und 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, Nr. 22 (08.11.2022): 7675. http://dx.doi.org/10.3390/molecules27227675.
Bunting, John W., James P. Kanter, Raymond Nelander und Zhennan Wu. „The acidity and tautomerism of β-diketones in aqueous solution“. Canadian Journal of Chemistry 73, Nr. 8 (01.08.1995): 1305–11. http://dx.doi.org/10.1139/v95-161.
Blanco, Carlos A., und Michael J. Hynes. „Catalysis of the deprotonation of β-diketones during formation of the 1:1 metal complexes“. Canadian Journal of Chemistry 70, Nr. 8 (01.08.1992): 2285–89. http://dx.doi.org/10.1139/v92-287.
Sadutto, Daniele, Paolo Guglielmi, Simone Carradori, Daniela Secci und 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, Nr. 18 (08.09.2023): 6518. http://dx.doi.org/10.3390/molecules28186518.
Al-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, Nr. 10-11 (01.11.2008): 693–702. http://dx.doi.org/10.1515/zna-2008-10-1113.
Rojas, Antonio, Alfonso Perez-Encabo, Ignacio Herraiz-Sierra und 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, Nr. 4 (01.04.2001): 448–54. http://dx.doi.org/10.1139/v01-061.
Capponi, Marco, Ivo G. Gut, Bruno Hellrung, Gaby Persy und Jakob Wirz. „Ketonization equilibria of phenol in aqueous solution“. Canadian Journal of Chemistry 77, Nr. 5-6 (01.06.1999): 605–13. http://dx.doi.org/10.1139/v99-048.
Saad, Gamal R., Magdi M. Naoum und Hanna A. Rizk. „Dielectric polarization and molecular interaction. Part II. Acetylacetone, benzoylacetone, and dibenzoylmethane – triethyl amine – cyclohexane systems“. Canadian Journal of Chemistry 67, Nr. 2 (01.02.1989): 284–88. http://dx.doi.org/10.1139/v89-047.
Khandogin, Jana, und Charles L. Brooks. „Constant pH Molecular Dynamics with Proton Tautomerism“. Biophysical Journal 89, Nr. 1 (Juli 2005): 141–57. http://dx.doi.org/10.1529/biophysj.105.061341.
Rzepiela, Kacper, Aneta Buczek, Teobald Kupka und Małgorzata A. Broda. „Factors Governing the Chemical Stability and NMR Parameters of Uracil Tautomers and Its 5-Halogen Derivatives“. Molecules 25, Nr. 17 (28.08.2020): 3931. http://dx.doi.org/10.3390/molecules25173931.
Baron, Marie-Hélène, Sabine Halut-Desportes, Hai-Fen Ye, Jack Huet und Edith Favre. „Spectroscopic conformational study of PMS 952, a specific imidazoline ligand. Experimental results“. Canadian Journal of Chemistry 77, Nr. 12 (05.12.1999): 2015–24. http://dx.doi.org/10.1139/v99-191.
Pachulia, Z., und J. Kereselidze. „Calculation of tautomeric equilibrium constants in complementary DNA pairs“. Journal of Biological Physics and Chemistry 16, Nr. 4 (30.12.2016): 177–80. http://dx.doi.org/10.4024/20pa16a.jbpc.16.04.
Shawali, Ahmad S., Mosselhi A. N. Mosselhi und Thoraya A. Farghaly. „Synthesis and Tautomeric Structure of 2-arylazo-4H-imidazo[2,1-b][1,3,4]thiadiazines“. Journal of Chemical Research 2007, Nr. 8 (August 2007): 479–83. http://dx.doi.org/10.3184/030823407x237885.
Costantino, Luca, Giulio Rastelli, Maria C. Rossi und Albano Albasini. „Quantitative measurement of proton dissociation and tautomeric constants of apigeninidin“. Journal of the Chemical Society, Perkin Transactions 2, Nr. 2 (1995): 227. http://dx.doi.org/10.1039/p29950000227.
Lyčka, Antonín, Libuše Havlíčková, Alois Koloničný und 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, Nr. 3 (1987): 736–41. http://dx.doi.org/10.1135/cccc19870736.