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Journal articles on the topic 'Oxamic acid'

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Author: Grafiati

Published: 19 October 2024

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1

Yang, L., L. Liu, B. A. Olsen, and 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, no. 3 (April 2000): 487–93. http://dx.doi.org/10.1016/s0731-7085(00)00230-2.

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2

Nuñez, L., L. Barral, and G. Pilcher. "Enthalpies of combustion of oxamic acid, oxamide, and dithiooxamide." Journal of Chemical Thermodynamics 20, no. 10 (October 1988): 1211–16. http://dx.doi.org/10.1016/0021-9614(88)90105-x.

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3

Veltsistas, P. G., C. D. Papadimitriou, A. M. Z. Slawin, and 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, no. 3 (March 1999): 222–23. http://dx.doi.org/10.1177/174751989902300326.

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The reaction of NdIII with oxamic acid yields [Nd(Hoxm)3(H2oxm)·2.5H2O] n 1 (H2oxm = oxamic acid) which contains nine-coordinate Nd centres linked into chains via four-coordinate Hoxm- ligands; the chains are connected via an array of H-bonds.

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4

Lin, Shu-Kun. "N-(3,4-Dichlorophenyl)methyl Oxamic Acid." Molecules 2, no. 12 (April 15, 1997): M4. http://dx.doi.org/10.3390/m4.

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5

PETYUNIN, G. P., A. V. CHUBENKO, and KH M. AL'RAKHAVI. "ChemInform Abstract: Reaction of 2-Aminopyridine with Oxalic and Oxamic Acid Esters." ChemInform 27, no. 47 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199647149.

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6

Orge, C. A., J. L. Faria, and M. F. R. Pereira. "Removal of oxalic acid, oxamic acid and aniline by a combined photolysis and ozonation process." Environmental Technology 36, no. 9 (November 13, 2014): 1075–83. http://dx.doi.org/10.1080/09593330.2014.974682.

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7

Zarzyka, 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, no. 1 (January 1, 2015): 1–10. http://dx.doi.org/10.1515/polyeng-2013-0318.

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Abstract Hydroxyalkyl derivatives containing oxamidoester and oxamide fragments have been separately obtained using oxamic acid, oxamide and alkylene carbonates. It has been proven that the presence of oxamidoester and oxamide structural fragments in oligomer structures is responsible for the thermal stability of these products. Rigid, thermally stable polyurethane foams were obtained with the use of oligomers with oxamidoestercarbamidoimide, carbamide, oxamidoester and oxamide groups as polyols components. The properties of these foamed materials were compared with each other and with the properties of reference foams. It was found that the polyurethane foams characterized by the best properties were obtained from hydroxypropyl derivatives of oxamide.

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8

Lan, Yixiang, Chao Wang, Fan Yuan, Tadesse Haile Fereja, Baohua Lou, Shuang Han, Jianping Li, and Guobao Xu. "Electrochemiluminescence of 3,4,9,10-perylenetetracarboxylic acid/oxamic hydrazide and its application in the detection of tannic acid." Analyst 144, no. 15 (2019): 4493–98. http://dx.doi.org/10.1039/c9an00615j.

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9

DELGADO, G. E., L. M. BELANDRIA, M. GUILLEN, A. J. MORA, and L. E. SEIJAS. "STRUCTURAL CHARACTERIZATION OF 2-AMINO-2-OXOACETIC ACID BY X-RAY POWDER DIFFRACTION AND QUANTUM CHEMISTRY." Periódico Tchê Química 16, no. 33 (March 20, 2019): 516–23. http://dx.doi.org/10.52571/ptq.v16.n33.2019.531_periodico33_pgs_516_523.pdf.

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2-amino-2-oxoacetic acid, carbamoyl formic acid, or oxamic acid is an active pharmaceutical ingredient (API) of great importance mainly because is an inhibitor of lactic dehydrogenase (LDH). It acts as an inhibitor to the metabolic pathways of the tumor cells and exhibited significant anticancer activity against nasopharyngeal carcinoma (NPC) cells in vitro and can be considered as a potential drug for the treatment of type 2 diabetes. Also, this compound could be used as a building block in the design of supramolecular architectures based on hydrogen bonds through the complimentary hydrogen-bond functionalities of the carbonyl and amide functional groups present. Single-crystal X-ray diffraction is the most powerful technique for crystal structure determination of small molecules. However, for several materials, including oxamic acid, it could be complicated to grow single crystals of suitable size and quality that make them appropriated to structure analysis. For this reason, the structural study was conducted with powder X-ray diffraction which is a process significantly more challenging than structure determination from single-crystal data. Oxamic acid has been characterized by FT-IR and NMR spectroscopic techniques, thermal TGA-DSC analysis, semi-empirical PM7 calculations, and X-ray powder diffraction. The title compound crystallizes in the monoclinic system with space group Cc, Z=4, and unit cell parameters a= 9.4994(4) Å, b= 5.4380(2) Å, c= 6.8636(3) Å, b= 107.149(2)°, V= 338.79(2) Å3. The molecule has a trans conformation. The molecular structure and crystal packing are stabilized mainly by intra- and intermolecular O--H···O and N--H···O hydrogen bonds. The structural characterization of this type of API compound is important to understand its mechanisms of action due to its considerable biological effects. In particular, for oxamic acid, this structural study would allow subsequent examination of its medicinal properties as an antitumor and antidiabetic agent.

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10

Volkova, Yulia A., Elena I. Chernoburova, Albina S. Petrova, Alexander A. Shtil, and Igor V. Zavarzin. "Reactions of hydrazones derived from oxamic acid thiohydrazides." Phosphorus, Sulfur, and Silicon and the Related Elements 192, no. 2 (October 21, 2016): 237–40. http://dx.doi.org/10.1080/10426507.2016.1250759.

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11

Fleischer, Sandra, Stefan C. Weiss, Thomas Lucke, Wolfram Seitz, Wolfgang Schulz, and Walter H. Weber. "Formation of Oxamic Acid During Drinking Water Treatment." Ozone: Science & Engineering 37, no. 5 (June 26, 2015): 441–49. http://dx.doi.org/10.1080/01919512.2015.1040911.

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12

Komendantova, Anna S., Konstantin A. Lyssenko, Igor V. Zavarzin, and Yulia A. Volkova. "Iodine-promoted synthesis of pyrazoles from 1,3-dicarbonyl compounds and oxamic acid thiohydrazides." Organic Chemistry Frontiers 7, no. 13 (2020): 1640–46. http://dx.doi.org/10.1039/d0qo00476f.

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A novel approach to 3,4-dicarbonyl-substituted pyrazoles from 1,3-dicarbonyl compounds and oxamic acid thiohydrazides was developed via iodine-promoted cascade imination/halogenation/cyclization/ring contraction reaction.

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13

Rodríguez-Páez, Lorena, Miguel Angel Chena-Taboada, Arturo Cabrera-Hernández, Joaquín Cordero-Martínez, and Carlos Wong. "Oxamic acid analogues as LDH-C4-specific competitive inhibitors." Journal of Enzyme Inhibition and Medicinal Chemistry 26, no. 4 (March 25, 2011): 579–86. http://dx.doi.org/10.3109/14756366.2011.566221.

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14

Zarzyka-Niemiec, Iwona. "Hydroxyalkoxy derivatives of oxamic acid: polyol substrates for polyurethane foams." Polymer International 58, no. 4 (April 2009): 388–95. http://dx.doi.org/10.1002/pi.2543.

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15

Pelster, 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, no. 4 (October 1, 1995): R793—R799. http://dx.doi.org/10.1152/ajpregu.1995.269.4.r793.

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Mechanisms of acid production and of acid release have been analyzed in isolated gas gland cells of the eel swimbladder using a cytosensor microphysiometer. Incubation of isolated cells with oxamic acid caused a dose-dependent decrease in the rate of proton release. At the highest oxamic acid concentration used (20 mmol/l), proton release was reduced by approximately 40%; incubation with sodium fluoride (10 mmol/l) or removal of glucose from the extracellular medium caused 60 and 80% reduction, respectively. NaCN had little effect on proton secretion. Proton release of isolated gas gland cells was largely dependent on the extracellular sodium concentration, and this sodium effect was in part inhibitable by amiloride. A 15-20% reduction in the rate of proton secretion was observed in the presence of 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid, an inhibitor of anion exchange. Inhibition of mammalian H(+)-K(+)-adenosinetriphosphatase with omeprazole had no effect, whereas bafilomycin, an inhibitor of vesicular H(+)-adenosinetriphosphatase, induced a 25% reduction in proton secretion. Ethoxzolamide, a membrane-permeable inhibitor of carbonic anhydrase, caused a 60% reduction in proton secretion (inhibition constant = 54.4 nmol/l). Prontosil-dextran, a membrane-impermeable sulfonamide, also reduced the proton release, thus indicating the presence of a membrane-bound carbonic anhydrase facing the extracellular space.

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16

Choi, Seoung-ryoung, Aaron B. Beeler, Anupam Pradhan, E. Blake Watkins, John M. Rimoldi, Babu Tekwani, and Mitchell A. Avery. "Generation of Oxamic Acid Libraries: Antimalarials and Inhibitors ofPlasmodium falciparumLactate Dehydrogenase." Journal of Combinatorial Chemistry 9, no. 2 (March 2007): 292–300. http://dx.doi.org/10.1021/cc060110n.

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17

Krayushkin, M. M., V. N. Yarovenko, and I. V. Zavarzin. "Synthesis of heterocyclic compounds based on oxamic acid monothiooxamides and thiohydrazides." Russian Chemical Bulletin 68, no. 6 (June 2019): 1143–63. http://dx.doi.org/10.1007/s11172-019-2533-0.

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18

van Alphen, J. "Esters of ethylene-1:2-di-oxamic acid and its derivatives." Recueil des Travaux Chimiques des Pays-Bas 53, no. 12 (September 3, 2010): 1159–66. http://dx.doi.org/10.1002/recl.19340531217.

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19

Matsumoto, K. "Antitumor activities of platinum blues containing α-pyrrolidone, 3,3-dimethylglutarimide, orotic acid, succinamic acid and oxamic acid." Inorganica Chimica Acta 151, no. 1 (January 1988): 9–10. http://dx.doi.org/10.1016/s0020-1693(00)83475-1.

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20

Bie, Chao, Yun Gao, Jia Su, Yamin Dong, Xiangguang Guo, and Xiaoqi Sun. "The efficient separation of thorium from rare earth using oxamic acid in hydrochloric acid medium." Separation and Purification Technology 251 (November 2020): 117358. http://dx.doi.org/10.1016/j.seppur.2020.117358.

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21

Cowell, A. J., and M. Tremayne. "The co-crystallisation and thermal behaviour of oxamic acid, nicotinamide and isonicotinamide." Acta Crystallographica Section A Foundations of Crystallography 64, a1 (August 23, 2008): C209. http://dx.doi.org/10.1107/s010876730809329x.

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22

Bazureau, J. P., and M. Le Corre. "New synthesis of protected α-dehydro α-aminoacids from substituted oxamic acid." Tetrahedron Letters 29, no. 16 (January 1988): 1919–20. http://dx.doi.org/10.1016/s0040-4039(00)82078-x.

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23

ZARZYKA-NIEMIEC, IWONA. "Synthesis and application of oligomers obtained from oxamic acid and ethylene carbonate." Polimery 54, no. 02 (February 2009): 099–105. http://dx.doi.org/10.14314/polimery.2009.099.

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24

Nok, Andrew J., Humphrey C. Nzelibe, and 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, no. 7-8 (August 1, 2003): 594–601. http://dx.doi.org/10.1515/znc-2003-7-825.

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Abstract A membrane-bound sialidase was isolated from blood stream (BS) Trypanosoma evansi partially purified and characterized. The enzyme is a glycosyl phosphatidyl inositol (GPI) membrane anchored protein. It was solubilized from T.evansi cells recovered from infected camel blood by detergent treatment with Triton CF 54 and partially purified by a series of chromatography steps. The enzyme was optimally active at pH 5.5 and 37 °C. It had a Kᴍ and Vmax values of 4.8 x 10-6ᴍ and 3.75 x 10-6 mol/min.mg protein with Neu5Acα2, 3lac as substrate respectively. The Kᴍ and Vmax values with fetuin (4-nitrophenyl-oxamic acid) as substrate were 2.9 x 10-2ᴍ and 4.2 \ 10-3 mol/min.mg protein in the same respect. Kinetic analysis with methly umbelliferyl sialate (MU-Neu5Ac) gave Kᴍ and Vmax values of 0.17 mᴍ and 0.84 mmol/min.mg protein respectively. The T. evansi SD could hydrolyse internally linked sialic acid residues of the ganglioside GM2 , but was inactive towards colomic acid, and Neu5Ac2, 6. lac. When ghost red blood cell (RBC) was used as substrate, it desialylated the RBC in the following order of efficiency; mouse, rat, camel, goat, and dog. Similarly, cerebral cells isolated from BalbC mouse was desialylated by the T. evansi SD. Inhibition studies using 2-deoxy-2, 3 didehydro-N-acetyl neuraminic acid (NeuAc2, 3en) against MU-Neu5Ac revealed a competitive inhibition pattern with Ki of 5.8 μm. The enzyme was also inhibited non-competitively by parahydroxy oxamic acid (pHOA), and competitively by N-ethylmaleimide and N-bromosuccinate with Ki values of 25, 42, and 53 μm, respectively. It was activated by Mg2+ ion and inhibited by Cu2+ and Zn2+.

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25

Yokoyama, Naokata, Gordon N. Walker, Alan J. Main, James L. Stanton, Michael M. Morrissey, Charles Boehm, Allan Engle, Alan D. Neubert, and Jong M. Wasvary. "Synthesis and Structure-Activity Relationships of Oxamic Acid and Acetic Acid Derivatives Related to L-Thyronine." Journal of Medicinal Chemistry 38, no. 4 (February 1995): 695–707. http://dx.doi.org/10.1021/jm00004a015.

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26

Stanton, James L., Edna Cahill, Ronald Dotson, Jenny Tan, Hollis C. Tomaselli, Jong M. Wasvary, Zouhair F. Stephan, and Ronald E. Steele. "Synthesis and biological activity of phenoxyphenyl oxamic acid derivatives related to l-thyronine." Bioorganic & Medicinal Chemistry Letters 10, no. 15 (August 2000): 1661–63. http://dx.doi.org/10.1016/s0960-894x(00)00309-7.

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27

Sosio, A., I. Caramazza, D. Morelli, and A. Carenzi. "Pharmacological evaluation of Z 1819, a new oxamic acid derivative, as antianaphylactic agent." Pharmacological Research Communications 20 (September 1988): 365. http://dx.doi.org/10.1016/s0031-6989(88)80495-8.

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28

Martinez Belmonte, Marta, and Daniel J. Price. "Strong asymmetric hydrogen bonding in 2-(oxamoylamino)ethylammonium oxamate–oxamic acid (1/1)." Acta Crystallographica Section C Crystal Structure Communications 66, no. 3 (February 24, 2010): o147—o150. http://dx.doi.org/10.1107/s0108270110004233.

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29

Desseyn, Herman, and Georges Schoeters. "The Vibrational Analysis of the Copper Complexes with Planar Oxamides and Oxamic Acid." Bulletin des Sociétés Chimiques Belges 95, no. 1 (September 1, 2010): 13–27. http://dx.doi.org/10.1002/bscb.19860950102.

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30

Zarzyka-Niemiec, Iwona. "Hydroxyalkylation of oxamic acid with propylene carbonate: Synthesis, composition, and properties of products." Journal of Applied Polymer Science 110, no. 1 (October 5, 2008): 66–75. http://dx.doi.org/10.1002/app.28609.

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31

Zhang, Jie, Qing-Xia Liu, A.-Hui Li, Bao-Lin Liu, and 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, no. 1 (January 1, 2014): 49–54. http://dx.doi.org/10.5560/znb.2014-3127.

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Two novel trinuclear oxamato-bridged thiosemicarbazone complexes, [Cu(obte)]2Cd(DMF)2 (2) and [Cu(obte)]2Mn(DMF)2 (3) (H2obte = N-(2-benzaldehyde) oxamic acid ethyl ester thiosemicarbazone (1); DMF=dimethylformamide), have been synthesized and characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis (TGA) and single-crystal X-ray diffraction. Complexes 2 and 3 are isostructural, displaying a trinuclear structure. The luminescence properties of complexes 2 and 3 were investigated in the solid state at room temperature. The ligand 1 and its complex 2 have been evaluated for their antitumor activities against K562 cells.

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32

Buduru, Prasad, and 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 (December 2016): 935–43. http://dx.doi.org/10.1016/j.snb.2016.06.167.

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33

Kryzhna, S. I., O. M. Litvinova, M. E. Bereznyakova, and G. P. Fomina. "Screening of the diuretic activity from the series of new derivatives of oxamic acid." Klìnìčna farmacìâ 19, no. 1 (March 10, 2015): 42–45. http://dx.doi.org/10.24959/cphj.15.1318.

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34

Yuan, Ming, Li Chen, Junwei Wang, Shenjie Chen, Kongchao Wang, Yongbo Xue, Guangmin Yao, Zengwei Luo, and Yonghui Zhang. "Transition-Metal-Free Synthesis of Phenanthridinones from Biaryl-2-oxamic Acid under Radical Conditions." Organic Letters 17, no. 2 (January 8, 2015): 346–49. http://dx.doi.org/10.1021/ol503459s.

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35

Raczyńska, Ewa D., Małgorzata Hallmann, and Kinga Duczmal. "Quantum-chemical studies of amide–iminol tautomerism for inhibitor of lactate dehydrogenase: Oxamic acid." Computational and Theoretical Chemistry 964, no. 1-3 (March 2011): 310–17. http://dx.doi.org/10.1016/j.comptc.2011.01.017.

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36

Chiarino, Dario, Giancarlo Grancini, Viviana Frigeni, Ivano Biasini, and Angelo Carenzi. "N-(4-Isoxazolylthiazol-2-yl)oxamic acid derivatives as potent orally active antianaphylactic agents." Journal of Medicinal Chemistry 34, no. 2 (February 1991): 600–605. http://dx.doi.org/10.1021/jm00106a020.

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37

Molina, P., Ma J. Vilaplana, P. L. Andreu, and J. Møller. "Oxamic acid derivaties in heterocyclic synthesis: Preparation of 1,2,4-triazolo[1,5-a]pyrazine derivatives." Journal of Heterocyclic Chemistry 24, no. 5 (September 1987): 1281–84. http://dx.doi.org/10.1002/jhet.5570240509.

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38

Vansant, Christoffel, Herman O. Desseyn, and Spyros P. Perlepes. "The synthesis, spectroscopic and thermal study of oxamic acid compounds of some metal(II) ions." Transition Metal Chemistry 20, no. 5 (October 1995): 454–59. http://dx.doi.org/10.1007/bf00141516.

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39

Stanton, James L., Edna Cahill, Ronald Dotson, Jenny Tan, Hollis C. Tomaselli, Jong M. Wasvary, Zouhair F. Stephan, and Ronald E. Steele. "ChemInform Abstract: Synthesis and Biological Activity of Phenoxyphenyl Oxamic Acid Derivatives Related to L-Thyronine." ChemInform 31, no. 44 (October 31, 2000): no. http://dx.doi.org/10.1002/chin.200044207.

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40

Michaelides, A., and S. Skoulika. "Gel growth of single crystals of complexes of oxamic acid with divalent metals (Pb2+, Ca2+, Cd2+." Journal of Crystal Growth 94, no. 1 (January 1989): 208–12. http://dx.doi.org/10.1016/0022-0248(89)90620-9.

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41

Halasa, Anna, Leszek Lapinski, Hanna Rostkowska, Igor Reva, and 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, no. 11 (March 21, 2014): 2203–10. http://dx.doi.org/10.1021/jp501448m.

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42

CHIARINO, D., G. GRANCINI, V. FRIGENI, I. BIASINI, and A. CARENZI. "ChemInform Abstract: N-(4-Isoxazolylthiazol-2-yl)oxamic Acid Derivatives as Potent Orally Active Antianaphylactic Agents." ChemInform 22, no. 38 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199138157.

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43

Ruddraraju, Kasi Viswanatharaju, Devesh Aggarwal, Congwei Niu, Erica Anne Baker, Ruo-yu Zhang, Li Wu, and 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, no. 17 (August 5, 2020): 9212–27. http://dx.doi.org/10.1021/acs.jmedchem.0c00302.

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44

Orge, Carla A., O. Salomé G. P. Soares, Patrícia S. F. Ramalho, M. Fernando R. Pereira, and Joaquim L. Faria. "Magnetic Nanoparticles for Photocatalytic Ozonation of Organic Pollutants." Catalysts 9, no. 9 (August 22, 2019): 703. http://dx.doi.org/10.3390/catal9090703.

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Magnetic nanoparticles (MNP) composed of iron oxide (or other metal–FeO cores) coated with carbon produced by chemical vapour decomposition (CVD) were used in the photocatalytic ozonation of oxamic acid (OMA) which we selected as a model pollutant. The incorporation of Ag and Cu on FeO enhanced the efficiency of the process. The carbon phase significantly increased the photocatalytic activity towards the conversion of OMA. As for the synthesis process, raising the temperature of CVD improved the performance of the produced photocatalysts. The obtained results suggested that the carbon phase is directly related to high catalytic activity. The most active photocatalyst (C@FeO_CVD850) was used in the removal of other compounds (dyes, industrial pollutants and herbicides) from water and high mineralization levels were attained. This material was also revealed to be stable during reutilisation.

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45

Wolfs, Ilse, and 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, no. 10 (September 1995): 1601–15. http://dx.doi.org/10.1016/0584-8539(95)01527-2.

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46

Molina, P., A. Tárraga, A. Espinosa, and 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, no. 02 (1987): 128–34. http://dx.doi.org/10.1055/s-1987-27860.

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47

Dugarte-Dugarte, Analio J., Jacco van de Streek, Antonio M. dos Santos, Luke L. Daemen, Alexander A. Puretzky, Graciela Díaz de Delgado, and 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 (February 2019): 310–16. http://dx.doi.org/10.1016/j.molstruc.2018.09.089.

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48

Orge, Carla A., Maria J. Sampaio, Joaquim L. Faria, M. Fernando R. Pereira, and 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, no. 5 (October 2020): 104172. http://dx.doi.org/10.1016/j.jece.2020.104172.

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49

Orge, Carla A., O. Salomé G. P. Soares, Joaquim L. Faria, and 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, no. 6 (December 2017): 5599–607. http://dx.doi.org/10.1016/j.jece.2017.10.030.

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Espinoza, L. Carolina, Pamela Sepúlveda, Alejandra García, Denis Martins de Godoi, and Ricardo Salazar. "Degradation of oxamic acid using dimensionally stable anodes (DSA) based on a mixture of RuO2 and IrO2 nanoparticles." Chemosphere 251 (July 2020): 126674. http://dx.doi.org/10.1016/j.chemosphere.2020.126674.

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