Relevant bibliographies by topics / 6-dimethylpyridine

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Academic literature on the topic '6-dimethylpyridine'

Author: Grafiati
Published: 2 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "6-dimethylpyridine"

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Hensena, Karl, Markus Kettner, Thorsten Stumpf, and Michael Bolte. "Synthese und Kristallstrukturbestimmung von Silicium-Komplexen der Koordinationszahl sechs mit Dimethylpyridinen/ Syntheses and Crystal Structure Determination of Hexacoordinated Silicon-Complexes with Dimethylpyridines." Zeitschrift für Naturforschung B 55, no. 10 (2000): 901–6. http://dx.doi.org/10.1515/znb-2000-1003.

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Abstract Trichlorosilane, HSiCl3, forms with 3,4-dimethylpyridine in aprotic solvents a crystalline l:2-compound which is stable at room temperature and readily soluble in CHCl3. Colourless crystals of the dicationic complex, [H2Si(3,4-dimethylpyridine)4]2+ 2Cl- · 6 CHCl3 (verified by X-ray structure analysis) are obtained by dismutation of HSiCl3(3,4-dimethylpyridine)2 in CHCl3 within one week at room temperature.29Si NM R indicates that SiCl4 is generated as a second product. H2SiCl2 with 2,4-dimethylpyridine as well as MeHSiBr2 with 3,5-dimethylpyridine in aprotic solvents form 1:2-compound
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2

Döring, Cindy, and Peter G. Jones. "Crystal structures of seven gold(III) complexes of the form LAuX 3 (L = substituted pyridine, X = Cl or Br)." Acta Crystallographica Section E Crystallographic Communications 80, no. 8 (2024): 894–909. http://dx.doi.org/10.1107/s2056989024007266.

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The structures of seven gold(III) halide derivatives of general formula LAuX 3 (L = methylpyridines or dimethylpyridines, X = Cl or Br) are presented: trichlorido(2-methylpyridine)gold(III), [AuCl3(C6H7N)], 1 (as two polymorphs 1a and 1b); tribromido(2-methylpyridine)gold(III), [AuBr3(C6H7N)], 2; tribromido(3-methylpyridine)gold(III), [AuBr3(C6H7N)], 3; tribromido(2,4-dimethylpyridine)gold(III), [AuBr3(C7H9N)], 4; trichlorido(3,5-dimethylpyridine)gold(III), [AuCl3(C7H9N)], 5; tribromido(3,5-dimethylpyridine)gold(III), [AuBr3(C7H9N)], 6, and trichlorido(2,6-dimethylpyridine)gold(III), [AuCl3(C7
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3

Khasaeva, Fatima M. "Utilisation of 2,6-dimethylpyridine by Arthrobacter sp." International Journal of Nanobiotechnology and Pharmacy, no. 1 (July 30, 2015): 19–22. https://doi.org/10.5281/zenodo.29598.

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Igor, A. Parshikov, I. Zaraisky Evgeny, and M. Khasaeva Fatima. "Degradation of 2,6-dimethylpyridine by Arthrobacter crystallopoietes." Ecology, Environment and Conservation 22, no. 4 (2017): 1673–76. https://doi.org/10.5281/zenodo.1157087.

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Degradation of pyridines in waste water is an important issue for chemical and pharmaceutical industries. The biodegradation of 2,6-dimethylpyridine was investigated by the bacterium Arthrobacter crystallopoietes KM-4, which resulted in the formation of three metabolites: 2,6-dimethylpyridin-3-ol, 2,6-dimethylpyridin-3,4-diol, and 2,4-dioxopentanoic acid.
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Abdel-Hafez, Shams H., Ragaa A. Ahmed, Mohamed A. Abdel-Azim, and Khairy M. Hassan. "Selenium containing Heterocycles: Part 1. Synthesis of Some New Substituted Pyrido[3′,2′:4,5]selenolo[3,2-d]pyrimidines and Related Fused Tetracyclic Systems." Journal of Chemical Research 2007, no. 10 (2007): 580–84. http://dx.doi.org/10.3184/030823407x25506.

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New series of selenolo[2,3- b]pyridine, pyrido[3′,2′:4,5]selenolo[3,2- d]pyrimidine, 7,8-dihydro-2,4-dimethylpyrrolo [1,2- a]pyrido[3′,2′:4,5]selenolo[3,2- d]pyrimidin-10(6 H)-one and 7,9-dimethylpyrido[3′,2′:4,5]selenolo[3,2- d][1,2,4] triazolo[4,3- c]pyrimidine derivatives were synthesised from 3-cyano-4,6-dimethylpyridine-2(1 H)-selenone (1). Spectroscopic (IR, 1H, MS) of the newly synthesised compounds are reported.
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Su, Biyun, Jianshe Zhao, Yong Cui, Yongqing Liang, and Wenhua Sun. "Controlled Synthesis of 2‐Acetyl‐6‐carbethoxypyridine and 2,6‐Diacetylpyridine from 2,6‐Dimethylpyridine." Synthetic Communications 35, no. 17 (2005): 2317–24. http://dx.doi.org/10.1080/00397910500186995.

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7

Tsygankova, VA, YaV Andrusevich, NM Vasylenko, et al. "The Use of Thioxopyrimidine Derivatives as New Regulators of Growth and Photosynthesis of Barley." Journal of Plant Science and Phytopathology 8, no. 2 (2024): 090–99. http://dx.doi.org/10.29328/journal.jpsp.1001139.

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New synthetic compounds - thioxopyrimidine derivatives as regulators of vegetative growth and photosynthesis of spring barley (Hordeum vulgare L.) variety Acordine were studied. The growth-regulatory effect of new synthetic compounds, thioxopyrimidine derivatives, used in a concentration of 10-6M, was compared with the growth-regulatory effect of a plant hormone auxin IAA (1H-indol-3-yl)acetic acid) or synthetic plant growth regulators, derivatives of sodium and potassium salts of 6-methyl-2-mercapto-4-hydroxypyrimidine (Methyur, Kamethur), N-oxide-2,6-dimethylpyridine (Ivin), used in a simila
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8

Dakhno, P. G., V. K. Kindop, K. V. Gordeev, et al. "Oxidation of 4,6-dimethyl-2-thioxo-1,2-dihydropyridine3-carbonitriles with potassium hexacyanoferrate(III): synthesis and molecular docking of bis(pyrid-2-yl)disulfides." Журнал общей химии 93, no. 12 (2023): 1833–45. http://dx.doi.org/10.31857/s0044460x2312003x.

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The reaction of 4,6-dimethyl-2-thioxo-1,2-dihydropyridin-3-carbonitriles with K3[Fe(CN)6] in an alkaline medium led to the formation of a mixture of oxidation products: bis(3-cyanopyridin-2-yl)disulfides and potassium 3-cyano-4,6-dimethylpyridine-2-sulfonates. Structure of the compounds was confirmed by NMR, IR spectroscopy and high-resolution mass spectrometry data. According to the results of molecular docking, 2,2′-dithiobis(5-butyl-4,6-dimethylnicotinonitrile) exhibits affinity for the zinc finger binding site of the HIV-1 p7 nucleocapsid protein.
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Lyczko, Krzysztof, Monika Lyczko, Sylwia Meczynska-Wielgosz, Marcin Kruszewski, and Józef Mieczkowski. "Tricarbonylrhenium(I) complexes with the N,6-dimethylpyridine-2-carbothioamide ligand: combined experimental and calculation studies." Journal of Coordination Chemistry 71, no. 14 (2018): 2146–64. http://dx.doi.org/10.1080/00958972.2018.1476686.

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10

Wucherer, Edward J., and Earl L. Muetterties. "Synthesis of bis(.eta.6-2,6-dimethylpyridine)metal complexes of titanium, molybdenum, and vanadium by metal vapor deposition. Spectral properties of bis(.eta.6-2,6-dimethylpyridine)metal complexes of chromium, titanium, vanadium, molybdenum, and chromium(1+)." Organometallics 6, no. 8 (1987): 1691–95. http://dx.doi.org/10.1021/om00151a014.

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Book chapters on the topic "6-dimethylpyridine"

1

Wohlfarth, Ch. "Dielectric constant of 2,6-dimethylpyridine." In Supplement to IV/6. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_231.

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Wohlfarth, Ch. "Dielectric constant of the mixture (1) acetonitrile; (2) 2,6-dimethylpyridine." In Supplement to IV/6. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_505.

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Al-Ahmary, Khairia M., Fatimah A. Alshehri, Faten M. Atlam, and Mohamed K. Awad. "Investigating the Novel Hydrogen-Bonded Charge Transfer Complex between Chloranilic Acid and 2-Amino-4, 6-Dimethylpyridine: Spectroscopic Characterization, Molecular Modeling and DFT/TD-DFT/PCM Calculations." In Recent Developments in Chemistry and Biochemistry Research Vol. 1. B P International, 2024. http://dx.doi.org/10.9734/bpi/rdcbr/v1/7636c.

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