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Relevant bibliographies by topics / 6-dicarboxamide

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Journal articles

Academic literature on the topic '6-dicarboxamide'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "6-dicarboxamide"

1

Puckowska, Anna, Magdalena Gawel, Marlena Komorowska, et al. "Synthesis and Structural Characterization of Pyridine-2,6-dicarboxamide and Furan-2,5-dicarboxamide Derivatives." Molecules 27, no. 6 (2022): 1819. http://dx.doi.org/10.3390/molecules27061819.

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Derivatives based on pyridine-2-6- and furan-2,5-dicarboxamide scaffolds reveal numerous chemical properties and biological activities. This fact makes them an exciting research topic in supramolecular and coordination chemistry and in discovering new pharmacologically-active compounds. This work aimed to obtain a series of symmetrical pyridine-2-6- and furan-2,5-dicarboxamides through a condensation reaction of the appropriate acyl chlorides and aromatic amides. Successful syntheses were confirmed with NMR spectroscopy. We solved their crystal structures for seven compounds; two pyridine and

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2

Witt, Matthias, Dirk Kreft, and Hans-Friedrich Grützmacher. "Effects of Internal Hydrogen Bonds between Amide Groups: Protonation of Alicyclic Diamides." European Journal of Mass Spectrometry 9, no. 2 (2003): 81–95. http://dx.doi.org/10.1255/ejms.535.

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The proton affinity ( PA) of cyclopentane carboxamide 1, cyclohexane carboxamide 2 and their secondary and tertiary amide derivatives S1, S2, T1 and T2, was determined by the thermokinetic method and the kinetic method [ PA(1) = 888 ± 5 kJ mol−1; PA(2) = 892 ± 5 kJ mol−1; PA(S1) = 920 ± 6 kJ mol−1; PA(S2) = 920 ± 6 kJ mol−1; PA(T1) = 938 ± 6 kJ mol−1; PA(T2) = 938 ± 6 kJ mol−1]. Special entropy effects are not observed. Additionally, the effects of protonation have been studied using an advanced kinetic method for all isomers 3–7 of cyclopentane dicarboxamides and cyclohexane dicarboxamides (w

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3

Talaei, Bahareh, Majid Heravi, Hossein Oskooie, and Atieh Rezvanian. "An Approach to the Diastereoselective Synthesis of Cyclohexane-1,3-dicarboxamide Derivatives via a Pseudo Five-Component Reaction Based on Diketene." Synlett 29, no. 02 (2017): 225–29. http://dx.doi.org/10.1055/s-0036-1590980.

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A one-pot pseudo five-component reaction for the synthesis of 2-aryl-4-hydroxy-4-methyl-6-oxo-N 1,N 3-dialkylcyclohexane-1,3-dicarboxamide derivatives involving different primary amines, various aromatic aldehydes, and diketene in the presence of triethylamine with high yields is achieved.

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4

M, Heravi; Majid, B. Talaei, H.A. Oskooie, and A. Rezvanian. "An Approach to the Diastereoselective Synthesis of Cyclohexane-1,3-dicarboxamide Derivatives via a Pseudo Five-Component Reaction Based on Diketene." Synlett 29, no. 2 (2018): 225–29. https://doi.org/10.1055/s-0036-1590980.

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A one-pot pseudo five-component reaction for the synthesis of 2-aryl-4-hydroxy-4-methyl-6-oxo- N <sup>1</sup>, N <sup>3</sup> -dialkylcyclohexane-1,3-dicarboxamide derivatives involving different primary amines, various aromatic aldehydes, and diketene in the presence of triethylamine with high yields is achieved.

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5

Molnar, Maja, Mario Komar, and Igor Jerković. "N2,N6-Bis(6-iodo-2-methyl-4-oxoquinazolin-3(4H)-yl)pyridine-2,6-dicarboxamide." Molbank 2022, no. 4 (2022): M1500. http://dx.doi.org/10.3390/m1500.

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A green chemistry method was applied in the synthesis of N2,N6-bis(6-iodo-2-methyl-4-oxoquinazolin-3(4H)-yl)pyridine-2,6-dicarboxamide. The desired compound was synthesized mechanochemically, using a choline chloride-based deep eutectic solvent as a catalyst. The synthesis took 20 min and the new compound was characterized using different spectral methods.

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6

Yurchenko, A., Y. Matveichuk, and E. Bartashevich. "The Response of the Nickel Chemical Bonds to the Tensile Deformation in the Nickel Pyridindi-carboxamide." Bulletin of the South Ural State University series "Chemistry" 16, no. 2 (2024): 127–35. http://dx.doi.org/10.14529/chem240215.

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We have carried out a theoretic research of plasticity for the coordination and noncovalent bonds modelling uniaxial mechanical deformation of the crystal cell of bis(2-N,6-N-dibutylpyridin-2,6-dicarboxamide)-nickel (II) dichloride. For this purpose, we have modeled stretching deformation of the crystal structure along its crystallographic axes using the 3-corrected Hartree-Fock method with the following semi-empirical corrections for the weak interactions (the Grimme correction of dispersion interactions, D3, basis set superposition error removal by the atom-pair wise geomet-rical counterpois

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7

Cati, Dilovan S., and Helen Stoeckli-Evans. "The crystal structures of three pyrazine-2,5-dicarboxamides: three-dimensional supramolecular structures." Acta Crystallographica Section E Crystallographic Communications 73, no. 5 (2017): 729–34. http://dx.doi.org/10.1107/s2056989017005898.

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The complete molecules of the title compounds,N2,N5-bis(pyridin-2-ylmethyl)pyrazine-2,5-dicarboxamide, C18H16N6O2(I), 3,6-dimethyl-N2,N5-bis(pyridin-2-ylmethyl)pyrazine-2,5-dicarboxamide, C20H20N6O2(II), andN2,N5-bis(pyridin-4-ylmethyl)pyrazine-2,5-dicarboxamide, C18H16N6O2(III), are generated by inversion symmetry, with the pyrazine rings being located about centres of inversion. Each molecule has an extended conformation with the pyridine rings inclined to the pyrazine ring by 89.17 (7)° in (I), 75.83 (8)° in (II) and by 82.71 (6)° in (III). In the crystal of (I), molecules are linked by N—H

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8

Jan, Chin Yee, Norzianah Binti Haji Shamsudin, Ai Ling Tan, David J. Young, Seik Weng Ng, and Edward R. T. Tiekink. "4-Nitrophthalamide." Acta Crystallographica Section E Structure Reports Online 70, no. 3 (2014): o293. http://dx.doi.org/10.1107/s1600536814002955.

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In the title compound, C8H7N3O4(systematic name: 4-nitrobenzene-1,2-dicarboxamide), each of the substituents is twisted out of the plane of the benzene ring to which it is attached [dihedral angles of 11.36 (2)° for the nitro group, and 60.89 (6) and 34.39 (6)° for the amide groups]. The amide groups are orientated to either side of the least-squares plane through the benzene ring with the amine groups being directed furthest apart. In the crystal, a three-dimensional architecture is established by a network of N—H...O hydrogen bonds.

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9

Papanikolaou, Michael G., Alexander Elliott, James McAllister, et al. "Electrocatalytic hydrogen production by dinuclear cobalt(ii) compounds containing redox-active diamidate ligands: a combined experimental and theoretical study." Dalton Transactions 49, no. 44 (2020): 15718–30. http://dx.doi.org/10.1039/d0dt02617d.

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The chiral dicobalt(ii) complex [Co<sup>II</sup><sub>2</sub>(μ<sub>2</sub>-L)<sub>2</sub>] (1) (H<sub>2</sub>L = N<sup>2</sup>,N<sup>6</sup>-di(quinolin-8-yl)pyridine-2,6-dicarboxamide) and its tert-butyl analogue [Co<sup>II</sup><sub>2</sub>(μ<sub>2</sub>-LBu)<sub>2</sub>] (2) were structurally characterized and their catalytic evolution of H<sub>2</sub> was investigated.

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10

Lu, Hai-bin, Shi-han Wang, Qing-min Li, and Yong-sheng Wang. "Design, synthesis and evaluation of 6-oxo-1, 6-dihydropyrimidine-2,5-dicarboxamide derivatives as MMP 13 inhibitors." Chemical Research in Chinese Universities 29, no. 1 (2012): 67–70. http://dx.doi.org/10.1007/s40242-012-2131-2.

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