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Relevant bibliographies by topics / Pyridine-4-carboxylic acid

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Academic literature on the topic 'Pyridine-4-carboxylic acid'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Pyridine-4-carboxylic acid"

1

Gillis, RG, and QN Porter. "5-Methoxyphenanthrene-4-carboxylic Acid." Australian Journal of Chemistry 42, no. 6 (1989): 1007. http://dx.doi.org/10.1071/ch9891007.

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Lead tetraacetate oxidation of phenanthrene-4,5-dicarboxylic acid in acetonitrile with pyridine affords 5-hydroxyphenanthrene-4-carboxylic acid as its lactone , which can be methylated as the sodium salt, giving 5-methoxyphenanthrene-4-carboxylic acid, albeit in poor yield. New spectroscopic evidence (particularly 13C n.m.r.) confirms that 5-formylphenanthrene-4-carboxylic acid, which is an intermediate in the synthesis, exists as the lactol , 4-hydroxyphenanthro[4,5-cdeloxepin-G(4H)-one.

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Saeed, Atif, Lubna Shakir, Mahtab A. Khan, Arsalan Ali, and Awais Ali Zaidi. "Haloperidol induced Parkinson’s disease mice model and motor-function modulation with Pyridine-3-carboxylic acid." Biomedical Research and Therapy 4, no. 05 (2017): 1305. http://dx.doi.org/10.15419/bmrat.v4i05.169.

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Introduction: Motor-function modulation through Pyridine-3-carboxylic acid was assessed against. Haloperidol induced Parkinson’s disease (PD) in albino-mice. The objectives of this study were to test the effect of Haloperidol in development of PD, effectiveness of Pyridine-3-carboxylic acid in mice and evaluation of the motor-function changes in mice before and after treatment. Methods: The study was divided into 3 phases: During Phase-I (randomization), all the subjects were randomly divided into 4 groups and trained for wire-hanging, grip strength, vertical rod and swim tests for 1 wee

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3

Ye, Naike, and Joseph M. Tanski. "The crystal structure of 5-(trifluoromethyl)picolinic acid monohydrate reveals a water-bridged hydrogen-bonding network." Acta Crystallographica Section E Crystallographic Communications 76, no. 11 (2020): 1752–56. http://dx.doi.org/10.1107/s2056989020013523.

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The title compound [systematic name: 5-(trifluoromethyl)pyridine-2-carboxylic acid monohydrate], C7H4F3NO2·H2O, is the acid hydrate of a pyridine with a carboxylic acid group and a trifluoromethyl substituent situated para to one another on the aromatic ring. The molecule forms a centrosymmetric water-bridged hydrogen-bonding dimer with graph-set notation R 4 4 (12). Hydrogen-bonding distances of 2.5219 (11) and 2.8213 (11) Å are observed between the donor carboxylic acid and the bridging water acceptor, and the donor water and carbonyl oxygen acceptor, respectively. The dimers are further lin

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Ifeanacho, Ezetonu Abireh, Christian Ejuiwa Mba, and Chiadikobi Lawrence Ozoemena. "ACUTE NICOTINE & PYRIDINE-3-CARBOXYLIC ACID SYNERGY PROTECTS NICOTINE INDUCED TESTICULAR DEGENERATION AND MODERATES MALONDIALDEHYDE LEVELS." International Journal of Novel Research in Healthcare and Nursing 11, no. 1 (2024): 125–30. https://doi.org/10.5281/zenodo.10612811.

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<strong>Abstract:</strong><em> </em>Nicotine is a naturally produced alkaloid in the Solanaceae family of plants, widely used as a recreational substance or an anxiolytic and acts as a receptor agonist at most nicotinic acetylcholine receptors (nAChRs). Pyridine 3-carboxylic acid is a monocarboxylic derivative of pyridine. Also known as niacin, it is a water-soluble vitamin that is indispensable in the diet of humans and animals and has a variety of important applications, such as in matrices for matrix-assisted laser desorption ionization (MALDI) mass spectrometr

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5

Wibaut, J. P. "The preparation of pyridine-4-carboxylic acid and of piperidine-4-carboxylic acid by catalytic reduction of 2,6-dichloropyridine-4-carboxylic acid." Recueil des Travaux Chimiques des Pays-Bas 63, no. 7 (2010): 141–46. http://dx.doi.org/10.1002/recl.19440630704.

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6

Qin, Zengquan, Hilary A. Jenkins, Simon J. Coles, Kenneth W. Muir, and Richard J. Puddephatt. "Self-assembly of one-dimensional polymers by coordination and hydrogen bonding in palladium(II) complexes." Canadian Journal of Chemistry 77, no. 1 (1999): 155–57. http://dx.doi.org/10.1139/v99-027.

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The ligands L = pyridine- or quinoline-carboxylic acid easily give complexes trans-[PdCl2L2], which self-assemble through hydrogen bonding between carboxylic acid groups to give one-dimensional polymers, as proved by structure determinations when L = NC5H4COOH-4, NC5H4COOH-3, and 2-Ph-NC9H5COOH-4.Key words: polymer, hydrogen-bonding, palladium, coordination.

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7

Smith, Graham, and Urs D. Wermuth. "4-(4-Nitrobenzyl)pyridinium 3-carboxy-4-hydroxybenzenesulfonate." Acta Crystallographica Section E Structure Reports Online 69, no. 2 (2013): o206. http://dx.doi.org/10.1107/s1600536813000093.

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In the title salt, C12H11N2O2+·C7H5O6S−, the dihedral angle between the benzene and pyridine rings in the 4-(4-nitrobenzyl)pyridinium cation is 82.7 (2)°. Within the anion there is an intramolecular hydroxy-O—H...O(carboxylic acid) bond. In the crystal, the cation forms a single N+—H...Osulfonatehydrogen bond with the anion. These cation–anion pairs interact through duplex anion carboxylic acid O—H...Osulfonatehydrogen bonds, giving a centrosymmetric cyclic association [graph setR22(16)]. The crystals studied were non-merohedrally twinned.

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8

Sinaga, Cinthia Uly Hotnami, and Asep Wahyu Nugraha. "Determining the Most Stable Structure of Benzamided Derivatives Using Density Functional Theory (DFT)." Indonesian Journal of Chemical Science and Technology (IJCST) 4, no. 2 (2021): 49. http://dx.doi.org/10.24114/ijcst.v4i2.27594.

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This study aims to determine the energy change ∆E and determine the most stable compound based on computation results using the Density Functional Theory (DFT) method. In determining the energy change ∆E and determining the most stable compound, computational chemical calculations were used using NWChem version 6.6 software with the DFT method with the B3LYP / 3-21G base set hybrid function, the results of the calculations were visualized using the Jmol software. The results of computational calculations on the compound Benzamide is 57467.3632844735 kJ / mol, (4 - chlorocarbonyl - benzial) - p

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Shiga, Takuya, Mao Noguchi, Takuto Matsumoto, et al. "A series of tetranuclear [2 × 2] grid complexes derived from an asymmetric ligand: Structural differences based on metal ion affinities." Pure and Applied Chemistry 83, no. 9 (2011): 1721–29. http://dx.doi.org/10.1351/pac-con-10-12-01.

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A series of tetranuclear grid-type complexes were prepared by the reaction of the asymmetric multidentate ligand HL (HL = 2-[3-(2-hydroxyphenyl)-1H-pyrazol-5-yl]-6-pyridine carboxylic acid ethylester) with different metal sources. The tetranuclear copper complex, [Cu4(L1)4(NO3)4(H2O)4]·Et2O·2MeOH (1, HL1 = 2-[3-(2-hydroxyphenyl)-1H-pyrazol-5-yl]-6-pyridine carboxylic acid methyl ester) consists of four ligands, four copper ions, four nitrate ions and four water molecules, forming a [2 × 2] grid structure, in which all four copper ions have the same coordination environment. On the other hand,

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Pinheiro, Luiz C. S., Alice M. R. Bernardino, Solange M. S. V. Wardell, James L. Wardell, and Edward R. T. Tiekink. "4-(3-Fluoroanilino)thieno[2,3-b]pyridine-6-carboxylic acid." Acta Crystallographica Section E Structure Reports Online 68, no. 7 (2012): o2217—o2218. http://dx.doi.org/10.1107/s1600536812027195.

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Book chapters on the topic "Pyridine-4-carboxylic acid"

1

Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed-ligand copper(II) with pyridine and α-H-(tetradecachlorotriphenyl)methane-4-carboxylic acid." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_125.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of β-octamolybdate supported copper(II) complex with mixed ligands (2,2-bipyridine and pyridine-4-carboxylic acid)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_416.

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Panunzio, Mauro, Maria Antonietta Lentini, Eileen Campana, Giorgio Martelli, and Paola Vicennati. "Multistep Microwave-Assisted Solvent-Free Organic Reactions: Synthesis of 1,6-Disubstituted-4-Oxo-1,4-Dihydro-Pyridine-3-Carboxylic Acid Benzyl Esters." In Advances in Microwave and Radio Frequency Processing. Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/978-3-540-32944-2_41.

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4

Ji, Yaozhen, Changwei An, and Tong Liu. "Photocatalytic Activity of Two MOFs Materials for Degradation of Dye Wastewater." In Advances in Transdisciplinary Engineering. IOS Press, 2023. http://dx.doi.org/10.3233/atde230407.

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Two MOFs materials, [Ni (3,4-PBC)2(H2O)] (1) and [Co (3,4-PBC)2(H2O)] (2), [fuchsin acid and Methyl orange acid] (2), were synthesized by using pyridine carboxylic acid ligand 3-pyridin-4-benzoic acid (3,4-HPBC) as building block and transition metal Ni (II) and Co (II) as central ions. The results indicate that two types of MOFs materials and sensitized TiO2 composite materials have good photodegradation activity against two pollutants.

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Taber, Douglass F. "Heteroaromatics: The Mal Synthesis of Clausevatine D." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0066.

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Huanfeng Jiang of the South China University of Technology showed (J. Org. Chem. 2010, 75, 966) that an alkynoate 1 could be condensed with a 1,3-dicarbonyl compound 2 to give, under oxidizing conditions, the furan 3. Phil Ho Lee of Kangwon National University found (Tetrahedron Lett. 2010, 51, 1899) that the enyne 4 cyclized smoothly to the furan 5. Yahong Li of Suzhou University and Vladimir Gevorgyan of the University of Illinois, Chicago, demonstrated (J. Am. Chem. Soc. 2010, 132, 7645) that the cyclization of 6 proceeded with silyl migration, to give 7. François Bilodeau and Pat Forgione

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6

Wu, Y. J. "Cyclization of 3-Nitrogen-Functionalized Pyridine-4-carboxylic Acids with Nitrogen-Containing Compounds." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-116-00670.

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