Academic literature on the topic '3-hydroxy-2(1H)-pyridinone'

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Journal articles on the topic "3-hydroxy-2(1H)-pyridinone"

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Nelson, William O., Timothy B. Karpishin, Steven J. Rettig, and Chris Orvig. "Physical and structural studies of N-substituted-3-hydroxy-2-methyl-4(1H)-pyridinones." Canadian Journal of Chemistry 66, no. 1 (1988): 123–31. http://dx.doi.org/10.1139/v88-019.

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A series of 3-hydroxy-2-methyl-4(1H)-pyridinones has been prepared with the substituents H, CH3, n-C6H11, and CH2CH2NH2 at the ring N. The dipyridinone 1,6-bis(3-hydroxy-2-methyl-4(1H)-pyridinon-1-yl)hexane has also been synthesized. The products with H and CH3 substituents have been studied by single crystal X-ray diffraction. Crystals of 3-hydroxy-2-methyl-4-pyridinone are monoclinic, a = 6.8351(4), b = 10.2249(4), c = 8.6525(4) Å, β = 105.215(4)°, Z = 4, space group P21/n and those of 3-hydroxy-1,2-dimethyl-4-pyridinone are orthorhombic, a = 7.3036(4), b = 13.0490(6), c = 13.7681(7) Å, Z =
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Orvig, C., S. J. Rettig, and Z. Zhang. "1-Carboxymethyl-3-hydroxy-2-methyl-4(1H)-pyridinone (monoclinic form 2)." Acta Crystallographica Section C Crystal Structure Communications 50, no. 9 (1994): 1511–14. http://dx.doi.org/10.1107/s0108270194000508.

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Stoyanov, Edmont, and Ivo Ivanov. "4-Hydroxy-6-methyl-3-nitroso-1-phenethyl-2(1H)-pyridinone." Molecules 5, no. 12 (2000): M132. http://dx.doi.org/10.3390/m132.

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Di Marco, Valerio B., G. Giorgio Bombi, Andrea Tapparo, Annie K. Powell, and Christopher E. Anson. "Complexation of aluminium(III) with 3-hydroxy-2(1H )-pyridinone. Solution state study and crystal structure of tris(3-hydroxy-2(1H )-pyridinonato)aluminium(III)." Journal of the Chemical Society, Dalton Transactions, no. 15 (1999): 2427–32. http://dx.doi.org/10.1039/a902997d.

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Simpson, Linda, Steven J. Rettig, James Trotter, and Chris Orvig. "1-n-Propyl- and 1-n-butyl-3-hydroxy-2-methyl-4-pyridinone complexes of group 13 (IIIA) metal ions." Canadian Journal of Chemistry 69, no. 5 (1991): 893–900. http://dx.doi.org/10.1139/v91-131.

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The aluminum, gallium, and indium tris(ligand) complexes of 3-hydroxy-2-methyl-1-n-propyl-4-pyridinone and 1-n-butyl-3-hydroxy-2-methyl-4-pyridinone have been prepared and characterized. All six compounds were prepared in a one-pot synthesis from maltol, n-propyl-, or n-butylamine and an appropriate metal(III) salt, and were completely characterized (IR, FAB-MS, 1H NMR, 27Al NMR, elemental analysis). Three of the six complexes were studied by single-crystal X-ray diffraction and were found to form trihydrates, unlike their 1-methyl and 1-ethyl analogues, which formed dodecahydrates. The n-buty
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Nagy, Sándor, András Ozsváth, Attila Cs Bényei, Etelka Farkas, and Péter Buglyó. "Donor Atom Preference of Organoruthenium and Organorhodium Cations on the Interaction with Novel Ambidentate (N,N) and (O,O) Chelating Ligands in Aqueous Solution." Molecules 26, no. 12 (2021): 3586. http://dx.doi.org/10.3390/molecules26123586.

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Two novel, pyridinone-based chelating ligands containing separated (O,O) and (Namino,Nhet) chelating sets (Namino = secondary amine; Nhet = pyrrole N for H(L3) (1-(3-(((1H-pyrrole-2-yl)methyl)-amino)propyl)-3-hydroxy-2-methylpyridin-4(1H)-one) or pyridine N for H(L5) (3-hydroxy-2-methyl-1-(3-((pyridin-2-ylmethyl)amino)propyl)pyridin-4(1H)-one)) were synthesized via reduction of the appropriate imines. Their proton dissociation processes were explored, and the molecular structures of two synthons were assessed by X-ray crystallography. These ambidentate chelating ligands are intended to develop
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Rai, Bijaya L., Hicham Khodr, and Robert C. Hider. "Synthesis, physico-chemical and iron(III)-chelating properties of novel hexadentate 3-hydroxy-2(1H)pyridinone ligands." Tetrahedron 55, no. 4 (1999): 1129–42. http://dx.doi.org/10.1016/s0040-4020(98)01091-6.

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Xu, Jide, Patricia W. Durbin, Birgitta Kullgren, Shirley N. Ebbe, Linda C. Uhlir, and Kenneth N. Raymond. "Synthesis and Initial Evaluation for In Vivo Chelation of Pu(IV) of a Mixed Octadentate Spermine-Based Ligand Containing 4-Carbamoyl-3-hydroxy-1-methyl-2(1H)-pyridinone and 6-Carbamoyl-1-hydroxy-2(1H)-pyridinone." Journal of Medicinal Chemistry 45, no. 18 (2002): 3963–71. http://dx.doi.org/10.1021/jm010564t.

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Rai, Bijaya L., Hicham Khodr, and Robert C. Hider. "ChemInform Abstract: Synthesis, Physico-Chemical and Iron(III)-Chelating Properties of Novel Hexadentate 3-Hydroxy-2(1H)pyridinone Ligands." ChemInform 30, no. 22 (2010): no. http://dx.doi.org/10.1002/chin.199922141.

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Buglyó, Péter, Eszter Márta Nagy, and Imre Sóvágó. "Vanadium(III) binding strengths of small biomolecules." Pure and Applied Chemistry 77, no. 9 (2005): 1583–94. http://dx.doi.org/10.1351/pac200577091583.

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The hydrolysis of vanadium(III) and the complex formation reactions between V(III) and weakly coordinating [glycine (GLY), DL-aspartic acid (ASP), D-penicillamine (PEN), DL-histidine (HIS)] or strongly coordinating [N,O] donor [picolinic (PIC) or 6-methylpicolinic acid (MePIC)] and [O,O] donor [maltol (MALT), 1,2-dimethyl-3-hydroxy-4-(1H)-pyridinone (DHP), tiron (TIR)] ligands were studied at 25.0 °C and an ionic strength of 0.20 M (KCl) in aqueous solution using combined pH-potentiometric and UV-vis spectroscopic techniques. Although some interaction between the amino acids and V(III) was fou
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Dissertations / Theses on the topic "3-hydroxy-2(1H)-pyridinone"

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Di, Marco Valerio B. "Studio della formazione di complessi tra alluminio e molecole di interesse ambientale, biologico e farmaceutico." Doctoral thesis, Università degli studi di Padova, 2014. http://hdl.handle.net/11577/3424177.

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In this thesis work, the coordination properties of several ligands with pharmaceutical, biological and toxicological properties towards Al3+ have been studied. The investigated molecules are 3-hydroxy-2-(1H)-pyridinone (HPyr), 2-hydroxyphenylethanone (HPE), 2-hydroxybenzeneacetic acid (HBA), 2-hydroxynicotinic acid (HNic), 3-hydroxypicolinic acid (HPic), and glutamic acid (Glu). The reliability of the speciation data has been considered as one of the primary goals. For this reason, each metal-ligand system has been studied by means of a combination of more analytical techniques, so that inde
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Book chapters on the topic "3-hydroxy-2(1H)-pyridinone"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(III) complex with 3-hydroxy-2(1H)-pyridinone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_216.

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