Artículos de revistas sobre el tema "Oxamic acid"
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Yang, L., L. Liu, B. A. Olsen y M. A. Nussbaum. "The determination of oxalic acid, oxamic acid, and oxamide in a drug substance by ion-exclusion chromatography". Journal of Pharmaceutical and Biomedical Analysis 22, n.º 3 (abril de 2000): 487–93. http://dx.doi.org/10.1016/s0731-7085(00)00230-2.
Texto completoNuñez, L., L. Barral y G. Pilcher. "Enthalpies of combustion of oxamic acid, oxamide, and dithiooxamide". Journal of Chemical Thermodynamics 20, n.º 10 (octubre de 1988): 1211–16. http://dx.doi.org/10.1016/0021-9614(88)90105-x.
Texto completoVeltsistas, P. G., C. D. Papadimitriou, A. M. Z. Slawin y J. D. Woollins. "Synthesis, Characterization and X-Ray Structural Determination of the Nine-coordinate Tris-aqua Tetra-oxamato Neodymium(III) Complex [Nd(Hoxm)3(H2oxm)·2.5H2O]n". Journal of Chemical Research 23, n.º 3 (marzo de 1999): 222–23. http://dx.doi.org/10.1177/174751989902300326.
Texto completoLin, Shu-Kun. "N-(3,4-Dichlorophenyl)methyl Oxamic Acid". Molecules 2, n.º 12 (15 de abril de 1997): M4. http://dx.doi.org/10.3390/m4.
Texto completoPETYUNIN, G. P., A. V. CHUBENKO y KH M. AL'RAKHAVI. "ChemInform Abstract: Reaction of 2-Aminopyridine with Oxalic and Oxamic Acid Esters." ChemInform 27, n.º 47 (4 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199647149.
Texto completoOrge, C. A., J. L. Faria y M. F. R. Pereira. "Removal of oxalic acid, oxamic acid and aniline by a combined photolysis and ozonation process". Environmental Technology 36, n.º 9 (13 de noviembre de 2014): 1075–83. http://dx.doi.org/10.1080/09593330.2014.974682.
Texto completoZarzyka, Iwona. "Oligomers with structural elements of imidazolidinetrione obtained from oxamic acid and oxamide: polyurethane foams modified by structural elements of imidazolidinetrione". Journal of Polymer Engineering 35, n.º 1 (1 de enero de 2015): 1–10. http://dx.doi.org/10.1515/polyeng-2013-0318.
Texto completoLan, Yixiang, Chao Wang, Fan Yuan, Tadesse Haile Fereja, Baohua Lou, Shuang Han, Jianping Li y Guobao Xu. "Electrochemiluminescence of 3,4,9,10-perylenetetracarboxylic acid/oxamic hydrazide and its application in the detection of tannic acid". Analyst 144, n.º 15 (2019): 4493–98. http://dx.doi.org/10.1039/c9an00615j.
Texto completoDELGADO, G. E., L. M. BELANDRIA, M. GUILLEN, A. J. MORA y L. E. SEIJAS. "STRUCTURAL CHARACTERIZATION OF 2-AMINO-2-OXOACETIC ACID BY X-RAY POWDER DIFFRACTION AND QUANTUM CHEMISTRY". Periódico Tchê Química 16, n.º 33 (20 de marzo de 2019): 516–23. http://dx.doi.org/10.52571/ptq.v16.n33.2019.531_periodico33_pgs_516_523.pdf.
Texto completoVolkova, Yulia A., Elena I. Chernoburova, Albina S. Petrova, Alexander A. Shtil y Igor V. Zavarzin. "Reactions of hydrazones derived from oxamic acid thiohydrazides". Phosphorus, Sulfur, and Silicon and the Related Elements 192, n.º 2 (21 de octubre de 2016): 237–40. http://dx.doi.org/10.1080/10426507.2016.1250759.
Texto completoFleischer, Sandra, Stefan C. Weiss, Thomas Lucke, Wolfram Seitz, Wolfgang Schulz y Walter H. Weber. "Formation of Oxamic Acid During Drinking Water Treatment". Ozone: Science & Engineering 37, n.º 5 (26 de junio de 2015): 441–49. http://dx.doi.org/10.1080/01919512.2015.1040911.
Texto completoKomendantova, Anna S., Konstantin A. Lyssenko, Igor V. Zavarzin y Yulia A. Volkova. "Iodine-promoted synthesis of pyrazoles from 1,3-dicarbonyl compounds and oxamic acid thiohydrazides". Organic Chemistry Frontiers 7, n.º 13 (2020): 1640–46. http://dx.doi.org/10.1039/d0qo00476f.
Texto completoRodríguez-Páez, Lorena, Miguel Angel Chena-Taboada, Arturo Cabrera-Hernández, Joaquín Cordero-Martínez y Carlos Wong. "Oxamic acid analogues as LDH-C4-specific competitive inhibitors". Journal of Enzyme Inhibition and Medicinal Chemistry 26, n.º 4 (25 de marzo de 2011): 579–86. http://dx.doi.org/10.3109/14756366.2011.566221.
Texto completoZarzyka-Niemiec, Iwona. "Hydroxyalkoxy derivatives of oxamic acid: polyol substrates for polyurethane foams". Polymer International 58, n.º 4 (abril de 2009): 388–95. http://dx.doi.org/10.1002/pi.2543.
Texto completoPelster, B. "Mechanisms of acid release in isolated gas gland cells of the European eel Anguilla anguilla". American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 269, n.º 4 (1 de octubre de 1995): R793—R799. http://dx.doi.org/10.1152/ajpregu.1995.269.4.r793.
Texto completoChoi, Seoung-ryoung, Aaron B. Beeler, Anupam Pradhan, E. Blake Watkins, John M. Rimoldi, Babu Tekwani y Mitchell A. Avery. "Generation of Oxamic Acid Libraries: Antimalarials and Inhibitors ofPlasmodium falciparumLactate Dehydrogenase". Journal of Combinatorial Chemistry 9, n.º 2 (marzo de 2007): 292–300. http://dx.doi.org/10.1021/cc060110n.
Texto completoKrayushkin, M. M., V. N. Yarovenko y I. V. Zavarzin. "Synthesis of heterocyclic compounds based on oxamic acid monothiooxamides and thiohydrazides". Russian Chemical Bulletin 68, n.º 6 (junio de 2019): 1143–63. http://dx.doi.org/10.1007/s11172-019-2533-0.
Texto completovan Alphen, J. "Esters of ethylene-1:2-di-oxamic acid and its derivatives". Recueil des Travaux Chimiques des Pays-Bas 53, n.º 12 (3 de septiembre de 2010): 1159–66. http://dx.doi.org/10.1002/recl.19340531217.
Texto completoMatsumoto, K. "Antitumor activities of platinum blues containing α-pyrrolidone, 3,3-dimethylglutarimide, orotic acid, succinamic acid and oxamic acid". Inorganica Chimica Acta 151, n.º 1 (enero de 1988): 9–10. http://dx.doi.org/10.1016/s0020-1693(00)83475-1.
Texto completoBie, Chao, Yun Gao, Jia Su, Yamin Dong, Xiangguang Guo y Xiaoqi Sun. "The efficient separation of thorium from rare earth using oxamic acid in hydrochloric acid medium". Separation and Purification Technology 251 (noviembre de 2020): 117358. http://dx.doi.org/10.1016/j.seppur.2020.117358.
Texto completoCowell, A. J. y M. Tremayne. "The co-crystallisation and thermal behaviour of oxamic acid, nicotinamide and isonicotinamide". Acta Crystallographica Section A Foundations of Crystallography 64, a1 (23 de agosto de 2008): C209. http://dx.doi.org/10.1107/s010876730809329x.
Texto completoBazureau, J. P. y M. Le Corre. "New synthesis of protected α-dehydro α-aminoacids from substituted oxamic acid". Tetrahedron Letters 29, n.º 16 (enero de 1988): 1919–20. http://dx.doi.org/10.1016/s0040-4039(00)82078-x.
Texto completoZARZYKA-NIEMIEC, IWONA. "Synthesis and application of oligomers obtained from oxamic acid and ethylene carbonate". Polimery 54, n.º 02 (febrero de 2009): 099–105. http://dx.doi.org/10.14314/polimery.2009.099.
Texto completoNok, Andrew J., Humphrey C. Nzelibe y Sarah K. Yako. "Trypanosoma evansi Sialidase: Surface Localization, Properties and Hydrolysis of Ghost Red Blood Cells and Brain Cells-Implications in Trypanosomiasis". Zeitschrift für Naturforschung C 58, n.º 7-8 (1 de agosto de 2003): 594–601. http://dx.doi.org/10.1515/znc-2003-7-825.
Texto completoYokoyama, Naokata, Gordon N. Walker, Alan J. Main, James L. Stanton, Michael M. Morrissey, Charles Boehm, Allan Engle, Alan D. Neubert y Jong M. Wasvary. "Synthesis and Structure-Activity Relationships of Oxamic Acid and Acetic Acid Derivatives Related to L-Thyronine". Journal of Medicinal Chemistry 38, n.º 4 (febrero de 1995): 695–707. http://dx.doi.org/10.1021/jm00004a015.
Texto completoStanton, James L., Edna Cahill, Ronald Dotson, Jenny Tan, Hollis C. Tomaselli, Jong M. Wasvary, Zouhair F. Stephan y Ronald E. Steele. "Synthesis and biological activity of phenoxyphenyl oxamic acid derivatives related to l-thyronine". Bioorganic & Medicinal Chemistry Letters 10, n.º 15 (agosto de 2000): 1661–63. http://dx.doi.org/10.1016/s0960-894x(00)00309-7.
Texto completoSosio, A., I. Caramazza, D. Morelli y A. Carenzi. "Pharmacological evaluation of Z 1819, a new oxamic acid derivative, as antianaphylactic agent". Pharmacological Research Communications 20 (septiembre de 1988): 365. http://dx.doi.org/10.1016/s0031-6989(88)80495-8.
Texto completoMartinez Belmonte, Marta y Daniel J. Price. "Strong asymmetric hydrogen bonding in 2-(oxamoylamino)ethylammonium oxamate–oxamic acid (1/1)". Acta Crystallographica Section C Crystal Structure Communications 66, n.º 3 (24 de febrero de 2010): o147—o150. http://dx.doi.org/10.1107/s0108270110004233.
Texto completoDesseyn, Herman y Georges Schoeters. "The Vibrational Analysis of the Copper Complexes with Planar Oxamides and Oxamic Acid". Bulletin des Sociétés Chimiques Belges 95, n.º 1 (1 de septiembre de 2010): 13–27. http://dx.doi.org/10.1002/bscb.19860950102.
Texto completoZarzyka-Niemiec, Iwona. "Hydroxyalkylation of oxamic acid with propylene carbonate: Synthesis, composition, and properties of products". Journal of Applied Polymer Science 110, n.º 1 (5 de octubre de 2008): 66–75. http://dx.doi.org/10.1002/app.28609.
Texto completoZhang, Jie, Qing-Xia Liu, A.-Hui Li, Bao-Lin Liu y Ruo-Jie Tao. "Synthesis, Crystal Structures and Properties of Two Heterometallic Complexes [Cu2M] (M = Cd, Mn) with a Novel Oxamato-bridged Ligand". Zeitschrift für Naturforschung B 69, n.º 1 (1 de enero de 2014): 49–54. http://dx.doi.org/10.5560/znb.2014-3127.
Texto completoBuduru, Prasad y Sundara Raja Reddy B.C. "Oxamic acid and p-aminobenzoic acid functionalized gold nanoparticles as a probe for colorimetric detection of Fe3+ ion". Sensors and Actuators B: Chemical 237 (diciembre de 2016): 935–43. http://dx.doi.org/10.1016/j.snb.2016.06.167.
Texto completoKryzhna, S. I., O. M. Litvinova, M. E. Bereznyakova y G. P. Fomina. "Screening of the diuretic activity from the series of new derivatives of oxamic acid". Klìnìčna farmacìâ 19, n.º 1 (10 de marzo de 2015): 42–45. http://dx.doi.org/10.24959/cphj.15.1318.
Texto completoYuan, Ming, Li Chen, Junwei Wang, Shenjie Chen, Kongchao Wang, Yongbo Xue, Guangmin Yao, Zengwei Luo y Yonghui Zhang. "Transition-Metal-Free Synthesis of Phenanthridinones from Biaryl-2-oxamic Acid under Radical Conditions". Organic Letters 17, n.º 2 (8 de enero de 2015): 346–49. http://dx.doi.org/10.1021/ol503459s.
Texto completoRaczyńska, Ewa D., Małgorzata Hallmann y Kinga Duczmal. "Quantum-chemical studies of amide–iminol tautomerism for inhibitor of lactate dehydrogenase: Oxamic acid". Computational and Theoretical Chemistry 964, n.º 1-3 (marzo de 2011): 310–17. http://dx.doi.org/10.1016/j.comptc.2011.01.017.
Texto completoChiarino, Dario, Giancarlo Grancini, Viviana Frigeni, Ivano Biasini y Angelo Carenzi. "N-(4-Isoxazolylthiazol-2-yl)oxamic acid derivatives as potent orally active antianaphylactic agents". Journal of Medicinal Chemistry 34, n.º 2 (febrero de 1991): 600–605. http://dx.doi.org/10.1021/jm00106a020.
Texto completoMolina, P., Ma J. Vilaplana, P. L. Andreu y J. Møller. "Oxamic acid derivaties in heterocyclic synthesis: Preparation of 1,2,4-triazolo[1,5-a]pyrazine derivatives". Journal of Heterocyclic Chemistry 24, n.º 5 (septiembre de 1987): 1281–84. http://dx.doi.org/10.1002/jhet.5570240509.
Texto completoVansant, Christoffel, Herman O. Desseyn y Spyros P. Perlepes. "The synthesis, spectroscopic and thermal study of oxamic acid compounds of some metal(II) ions". Transition Metal Chemistry 20, n.º 5 (octubre de 1995): 454–59. http://dx.doi.org/10.1007/bf00141516.
Texto completoStanton, James L., Edna Cahill, Ronald Dotson, Jenny Tan, Hollis C. Tomaselli, Jong M. Wasvary, Zouhair F. Stephan y Ronald E. Steele. "ChemInform Abstract: Synthesis and Biological Activity of Phenoxyphenyl Oxamic Acid Derivatives Related to L-Thyronine." ChemInform 31, n.º 44 (31 de octubre de 2000): no. http://dx.doi.org/10.1002/chin.200044207.
Texto completoMichaelides, A. y S. Skoulika. "Gel growth of single crystals of complexes of oxamic acid with divalent metals (Pb2+, Ca2+, Cd2+". Journal of Crystal Growth 94, n.º 1 (enero de 1989): 208–12. http://dx.doi.org/10.1016/0022-0248(89)90620-9.
Texto completoHalasa, Anna, Leszek Lapinski, Hanna Rostkowska, Igor Reva y Maciej J. Nowak. "Tunable Diode Lasers as a Tool for Conformational Control: The Case of Matrix-Isolated Oxamic Acid". Journal of Physical Chemistry A 119, n.º 11 (21 de marzo de 2014): 2203–10. http://dx.doi.org/10.1021/jp501448m.
Texto completoCHIARINO, D., G. GRANCINI, V. FRIGENI, I. BIASINI y A. CARENZI. "ChemInform Abstract: N-(4-Isoxazolylthiazol-2-yl)oxamic Acid Derivatives as Potent Orally Active Antianaphylactic Agents." ChemInform 22, n.º 38 (22 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199138157.
Texto completoRuddraraju, Kasi Viswanatharaju, Devesh Aggarwal, Congwei Niu, Erica Anne Baker, Ruo-yu Zhang, Li Wu y Zhong-Yin Zhang. "Highly Potent and Selective N-Aryl Oxamic Acid-Based Inhibitors for Mycobacterium tuberculosis Protein Tyrosine Phosphatase B". Journal of Medicinal Chemistry 63, n.º 17 (5 de agosto de 2020): 9212–27. http://dx.doi.org/10.1021/acs.jmedchem.0c00302.
Texto completoOrge, Carla A., O. Salomé G. P. Soares, Patrícia S. F. Ramalho, M. Fernando R. Pereira y Joaquim L. Faria. "Magnetic Nanoparticles for Photocatalytic Ozonation of Organic Pollutants". Catalysts 9, n.º 9 (22 de agosto de 2019): 703. http://dx.doi.org/10.3390/catal9090703.
Texto completoWolfs, Ilse y Herman O. Desseyn. "Hydrogen bond patterns in solid state carboxylic acids. Vibrational study of the hydrogen bond patterns in oxamic, malonamic and succinamic acid". Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 51, n.º 10 (septiembre de 1995): 1601–15. http://dx.doi.org/10.1016/0584-8539(95)01527-2.
Texto completoMolina, P., A. Tárraga, A. Espinosa y M. J. Lidón. "Oxamic Acid Derivatives in Heterocyclic Synthesis: Preparation of 1,4-Oxazine and 1,2,4-Triazino[5,6-e][1,3,4]oxadiazine Derivatives". Synthesis 1987, n.º 02 (1987): 128–34. http://dx.doi.org/10.1055/s-1987-27860.
Texto completoDugarte-Dugarte, Analio J., Jacco van de Streek, Antonio M. dos Santos, Luke L. Daemen, Alexander A. Puretzky, Graciela Díaz de Delgado y José Miguel Delgado. "Structure determination of oxamic acid from laboratory powder X-Ray diffraction data and energy minimization by DFT-D". Journal of Molecular Structure 1177 (febrero de 2019): 310–16. http://dx.doi.org/10.1016/j.molstruc.2018.09.089.
Texto completoOrge, Carla A., Maria J. Sampaio, Joaquim L. Faria, M. Fernando R. Pereira y Cláudia G. Silva. "Efficiency and stability of metal-free carbon nitride in the photocatalytic ozonation of oxamic acid under visible light". Journal of Environmental Chemical Engineering 8, n.º 5 (octubre de 2020): 104172. http://dx.doi.org/10.1016/j.jece.2020.104172.
Texto completoOrge, Carla A., O. Salomé G. P. Soares, Joaquim L. Faria y M. Fernando R. Pereira. "Synthesis of TiO2-Carbon Nanotubes through ball-milling method for mineralization of oxamic acid (OMA) by photocatalytic ozonation". Journal of Environmental Chemical Engineering 5, n.º 6 (diciembre de 2017): 5599–607. http://dx.doi.org/10.1016/j.jece.2017.10.030.
Texto completoEspinoza, L. Carolina, Pamela Sepúlveda, Alejandra García, Denis Martins de Godoi y Ricardo Salazar. "Degradation of oxamic acid using dimensionally stable anodes (DSA) based on a mixture of RuO2 and IrO2 nanoparticles". Chemosphere 251 (julio de 2020): 126674. http://dx.doi.org/10.1016/j.chemosphere.2020.126674.
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