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Journal articles on the topic '2-ethylpyridine'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Neumann, Tristan, Inke Jess, Cesar dos Santos Cunha, Huayna Terraschke, and Christian Näther. "Cd(II) and Zn(II) thiocyanate coordination compounds with 3-ethylpyridine: synthesis, crystal structures and properties." Zeitschrift für Naturforschung B 73, no. 2 (2018): 115–23. http://dx.doi.org/10.1515/znb-2017-0186.

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AbstractReaction of Cd(NCS)2 and Zn(NCS)2 with 3-ethylpyridine leads to the formation of compounds of compositions M(NCS)2(3-ethylpyridine)4 (M=Cd, 1-Cd; Zn, 1-Zn) and M(NCS)2(3-ethylpyridine)2 (M=Cd, 2-Cd; Zn, 2-Zn). 1-Cd and 1-Zn are isotypic and form discrete complexes in which the metal cations are octahedrally coordinated by two trans-coordinating N-bonded thiocyanate anions and four 3-ethylpyridine co-ligands. In 2-Cd the cations are also octahedrally coordinated but linked into chains by pairs of μ-1,3-bridging anionic ligands. 2-Zn is built up of discrete complexes, in which the Zn cat

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2

Lee, Jay J., Sung-Keun Rhee, and Sung-Taik Lee. "Degradation of 3-Methylpyridine and 3-Ethylpyridine by Gordonia nitida LE31." Applied and Environmental Microbiology 67, no. 9 (2001): 4342–45. http://dx.doi.org/10.1128/aem.67.9.4342-4345.2001.

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ABSTRACT Cells of Gordonia nitida LE31 grown on 3-methylpyridine degraded 3-ethylpyridine without a lag time and vice versa. Cyclic intermediates were not detected, but formic acid was identified as a metabolite. Degradation of levulinic acid was induced in cells grown on 3-methylpyridine and 3-ethylpyridine. Levulinic aldehyde dehydrogenase and formamidase activities were higher in cells grown on 3-methylpyridine and 3-ethylpyridine than in cells grown on acetate. These data indicate that 3-methylpyridine and 3-ethylpyridine were degraded via a new pathway involving C-2–C-3 ring cleavage.

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3

Moscotti, D., and L. Forni. "Catalytic oxydehydrogenation of 2-ethylpyridine." Applied Catalysis A: General 134, no. 2 (1996): 263–74. http://dx.doi.org/10.1016/0926-860x(95)00204-9.

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4

M., Bhoopal, Pradeep Kumar D., and Satyanarayana S. "Equilibrium constants for the pH-dependent axial ligation of alkyl(aquo)cobaloximes by pyridine and substituted pyridines." Journal of Indian Chemical Society Vol. 80, July 2003 (2003): 683–86. https://doi.org/10.5281/zenodo.5835386.

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Department of Chemistry, Osmania University, Hyderabad-500 007, India <em>E-mail</em> : ssnsirsani@yahoo.com <em>Manuscript received 23 September 2002, accepted 13 February 2003</em> Equilibria for the reaction of alkyl(aquo)cobaloximes (R = CH<sub>3</sub>, C<sub>2</sub>H<sub>5</sub>) with pyridine and substituted pyridines (4- methylpyridine, 4-ethylpyridine, 4-aminopyridine, 2-ethylpyridine and 2-aminopyridine) were studied as a function of pH at 25°, 1.0 <em>M</em> ionic strength (KCl) by spectrophotometric technique. Affinity of binding was interpreted based on the basicity of incoming

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5

Chung, J., G. Melkonian, L. Ji, and P. Talbot. "THE CIGARETTE SMOKE COMPONENTS 2-ETHYLPYRIDINE AND 3-ETHYLPYRIDINE DISRUPT CHICK CHORIOALLANTOIC MEMBRANE ULTRASTRUCTURE." Journal of Investigative Medicine 52 (January 2004): S90—S91. http://dx.doi.org/10.1097/00042871-200401001-00069.

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6

Chung, J., G. Melkonian, L. Ji, and P. Talbot. "THE CIGARETTE SMOKE COMPONENTS 2-ETHYLPYRIDINE AND 3-ETHYLPYRIDINE DISRUPT CHICK CHORIOALLANTOIC MEMBRANE ULTRASTRUCTURE." Journal of Investigative Medicine 52 (January 2004): S171. http://dx.doi.org/10.1097/00042871-200401001-00525.

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7

Chung, J., G. Melkonian, L. Ji, and P. Talbot. "The Cigarette Smoke Components 2-Ethylpyridine and 3-Ethylpyridine Disrupt Chick Chorioallantoic Membrane Ultrastructure." Journal of Investigative Medicine 52, no. 1_suppl_part_3 (2001): 171. http://dx.doi.org/10.1177/108155890105201s532.

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8

Chung, J., G. Melkonian, L. Ji, and P. Talbot. "The Cigarette Smoke Components 2-Ethylpyridine and 3-Ethylpyridine Disrupt Chick Chorioallantoic Membrane Ultrastructure." Journal of Investigative Medicine 52, no. 1_suppl_part_1 (2001): 90–91. http://dx.doi.org/10.1177/108155890105201s69.

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9

Gleich, E., Z. Warnke, and D. Wyrzykowski. "REACTIONS OF ELEMENTAL SELENIUM WITH 2-ETHYLPYRIDINE." Phosphorus, Sulfur, and Silicon and the Related Elements 179, no. 3 (2004): 615–26. http://dx.doi.org/10.1080/10426500490422281.

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10

Gubareva, A. I., P. A. Gerasimov, N. A. Tarbeeva, and V. M. Kunderenko. "Physicochemical properties of 2-methyl-5-ethylpyridine." Pharmaceutical Chemistry Journal 26, no. 3 (1992): 233–34. http://dx.doi.org/10.1007/bf00772936.

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11

Chung, J., G. Melkonian, L. Ji, and P. Talbot. "525 THE CIGARETTE SMOKE COMPONENTS 2-ETHYLPYRIDINE AND 3-ETHYLPYRIDINE DISRUPT CHICK CHORIOALLANTOIC MEMBRANE ULTRASTRUCTURE." Journal of Investigative Medicine 52, Suppl 1 (2004): S171.2—S171. http://dx.doi.org/10.1136/jim-52-suppl1-525.

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12

Chung, J., G. Melkonian, L. Ji, and P. Talbot. "69 THE CIGARETTE SMOKE COMPONENTS 2-ETHYLPYRIDINE AND 3-ETHYLPYRIDINE DISRUPT CHICK CHORIOALLANTOIC MEMBRANE ULTRASTRUCTURE." Journal of Investigative Medicine 52, Suppl 1 (2004): S90.6—S91. http://dx.doi.org/10.1136/jim-52-suppl1-69.

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13

Moioli, Emanuele, Leo Schmid, Peter Wasserscheid, and Hannsjörg Freund. "A new reaction route for the synthesis of 2-methyl-5-ethylpyridine." Reaction Chemistry & Engineering 2, no. 5 (2017): 754–62. http://dx.doi.org/10.1039/c7re00100b.

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14

Sembaev, D. Kh, O. K. Yugay, and S. G. Klepikova. "About the Routes of Oxidative Conversion of 2-methyl-5-ethylpyridine on Vanadium Oxide Modified Catalyst." Eurasian Chemico-Technological Journal 6, no. 2 (2017): 127. http://dx.doi.org/10.18321/ectj601.

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<p>The vapor phase oxidation of 2-methyl-5-ethylpyridine (MEP) on modified vanadium oxide catalyst has been investigated. Di(5-ethyl)-2-pyridil, 2-methyl-5-acethylpyridine and 3-acethylpyridine have been identified as intermediates of MEP oxidation by NMR <sup>13</sup>C spectroscopic and gas chromatography mass spectrometry methods. It has been shown that the interaction between the pyridine base and acidic proton donating sites on the catalyst surface causes an increase of substituents reactivity in 2-position in all stages of 2-methyl-5-ethylpyridine transformation inducing

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15

Miyazawa, Satoru, Reina Hosono, Ryota Osuga, Junko Nomura Kondo, and Sayaka Uchida. "Effect of the ammonium ion on proton conduction in porous ionic crystals based on Keggin-type silicododecatungstate." Acta Crystallographica Section C Structural Chemistry 74, no. 11 (2018): 1289–94. http://dx.doi.org/10.1107/s2053229618008227.

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Proton conduction in crystalline porous materials has received much attention from basic scientific research through to practical applications. Polyoxometalates (POMs) can efficiently transport protons because of their small superficial negative charge density. A simple method for enhancing proton conductivity is to introduce NH4 + into the crystal structure, because NH4 + can form hydrogen bonds and function as a proton carrier. According to these considerations, NH4 + was introduced into the porous structure of A 2[Cr3O(OOCH)6(etpy)3]2[α-SiW12O40]·nH2O (A = Li, Na, K and Cs; etpy = 4-ethylpy

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16

Sekine, A., Y. Ohashi, E. Shimizu та K. Hori. "Structures of (β-cyanoethyl)(3-ethylpyridine)bis(dimethylglyoximato)cobalt(III) (1) and (β-cyanoethyl)(4-ethylpyridine)bis(dimethylglyoximato)cobalt(III) (2)". Acta Crystallographica Section C Crystal Structure Communications 47, № 1 (1991): 53–56. http://dx.doi.org/10.1107/s0108270190006667.

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17

Poletaeva, D. A., I. I. Faingold, Yu V. Soldatova, et al. "Membranotropic and Antiradical Properties of 2-Nitroxysuccinate 3-Hydroxy-6-Methyl-2-Ethylpyridine." Bulletin of Experimental Biology and Medicine 167, no. 6 (2019): 744–46. http://dx.doi.org/10.1007/s10517-019-04613-x.

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18

Edema, Jilles J. H., Rob Libbers, Arwin Ridder, Richard M. Kellogg, and Anthony L. Spek. "Novel silicon bisalkoxy complexes with a pseudo-atrane structure. Synthesis and molecular structures of 2,6-di(2-hydroxy(2-adamantyl)) ethylpyridine and 2,6-di(2-oxy(2-adamantylidine))ethylpyridine dimethylsilicon." Journal of Organometallic Chemistry 464, no. 2 (1994): 127–31. http://dx.doi.org/10.1016/0022-328x(94)87265-1.

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19

Anjani, Solankee, Kapadia Kishor, Solankee Sejal, and Patel Ghanshyam. "Synthesis and antibacterial evaluation of s-triazine based chalcones and their derivatives." Journal of Indian Chemical Society Vol. 86, Aug 2009 (2009): 837–40. https://doi.org/10.5281/zenodo.5815010.

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Department of Chemistry, B. K. M. Science College, Valsad-396 001, Gujarat, India (Affiliated to The Veer Narmad South Gujarat University, Surat-395 007, Gujarat, India) <em>E-mail </em>: dranjani_solankee@yahoo.com <em>Manuscript received 3 April 2008, revised 19 March 2009 .. accepted 31 March 2009</em> Various 2-(phenylamino/4<em>'</em> -substituted phenylamino)-4-(phenylamino/4<em>' </em>-substituted phenylamino)-6-[4<em>'</em> -{3<em>"</em> -(4<em>"'</em>- {2<em>'</em> -(5<em>' </em>-ethylpyridin-2<em>' </em>-yl)-ethoxy }-phenyl)-2<em>"</em>-prop

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20

Pokidova, O. V., E. V. Batova, A. P. Sadkov, A. B. Eremeev, B. S. Fedorov, and A. I. Kotelnikov. "Reactivity of 2-nitroxysuccinate 3-hydroxy-6-methyl-2-ethylpyridine and reference drugs in model NO-generating systems." Доклады Академии наук 486, no. 4 (2019): 437–40. http://dx.doi.org/10.31857/s0869-56524864437-440.

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The ability of the 2-nitroxysuccinate 3-hydroxy-6-methyl-2-ethylpyridine (I) compound to generate nitrite ions (NO2) and nitrogen monoxide (NO) in model systems with cysteine (Cys) and deoxyhemoglobin (Hb) has been studied. It has been established that there is a more efficient release NO2 and NO from compound I than from Nicorandil. The accumulation rate is 1.5 times higher in the system of Cys with I than with Nitroglycerin. It is shown that, unlike Nitroglycerin, compound I is not reduced by Hb.

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21

Warda, S. A. "Aqua(2-ethylpyridine-N)(N-salicylideneglycinato-O,N,O')copper(II)." Acta Crystallographica Section C Crystal Structure Communications 54, no. 9 (1998): 1236–38. http://dx.doi.org/10.1107/s0108270198004673.

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22

Pladzyk, Agnieszka, та Katarzyna Baranowska. "Ammine(2-ethylpyridine-κN)bis(tri-tert-butoxysilanethiolato-κS)cobalt(II)". Acta Crystallographica Section E Structure Reports Online 63, № 6 (2007): m1594. http://dx.doi.org/10.1107/s1600536807025421.

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23

Muthu, S., G. Ramachandran, and J. Uma maheswari. "Vibrational spectroscopic investigation on the structure of 2-ethylpyridine-4-carbothioamide." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 93 (July 2012): 214–22. http://dx.doi.org/10.1016/j.saa.2012.02.107.

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24

Wibaut, J. P., and E. C. Kooyman. "Syntheses of 3,4-dimethylpyridine, 2,3-dimethylpyridine and 2-methyl-3-ethylpyridine." Recueil des Travaux Chimiques des Pays-Bas 63, no. 12 (2010): 231–38. http://dx.doi.org/10.1002/recl.19440631202.

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25

Goher, Mohamed A. S., Albert Escuer, Morsy A. M. Abu-Youssef, and Franz A. Mautner. "Syntheses, X-ray structures, spectroscopic and magnetic studies of two new polymeric copper (II) azide complexes; [Cu (3-ethylpyridine)2 (N3)2]n and [Cu (4-ethylpyridine)2 (N3)2]n." Polyhedron 17, no. 23-24 (1998): 4265–73. http://dx.doi.org/10.1016/s0277-5387(98)00237-x.

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26

Klahn, Marcus, Anke Spannenberg, and Uwe Rosenthal. "2-Vinylpyridine–tris(pentafluorophenyl)borane hexane monosolvate." Acta Crystallographica Section E Structure Reports Online 68, no. 4 (2012): o1261. http://dx.doi.org/10.1107/s1600536812013153.

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The title compound, C7H7N·B(C6F5)3·C6H14, was obtained by the stoichiometric reaction of 2-vinylpyridine and tris(pentafluorophenyl)borane in toluene. The formed adduct exhibits a restricted rotation along the B—N bond resulting in an asymmetry, which can be also observed in the19F NMR spectra. The B—N distance is equivalent to the distances found for 2-methylpyridine and 2-ethylpyridine B(C6F5)3adducts. For the final refinement, the contributions of disordered solvent molecules were removed from the diffraction data with SQUEEZE inPLATON[van der Sluis & Spek (1990).Acta Cryst.A46, 194–201

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27

Bender, Tobias, and Paultheo von Zezschwitz. "Total Synthesis of 4-Acetyl-1,3-Dihydroimidazo[4,5-c]Pyridin-2-One, a New Microbial Metabolite from a Streptomyces Species." Natural Product Communications 4, no. 7 (2009): 1934578X0900400. http://dx.doi.org/10.1177/1934578x0900400719.

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The structure of a new secondary metabolite from Streptomyces sp. was determined as 4-acetyl-1,3-dihydroimidazo[4,5-c]pyridin-2-one by synthesis of the natural product itself and of the regioisomeric 7-acetylimidazo[4,5-b]pyridine derivative. The former compound was prepared, in 28% overall yield, in a sequence of nitration, reduction, condensation, and Stille reaction of 4-aminopyridine, while the regioisomer was obtained in 5% overall yield by amination, nitration, reduction, condensation, and oxidation of 4-ethylpyridine.

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28

MEI, LUO, XU JIA, and ZHANG JING CHENG. "Synthesis and catalytic activity of metallo-organic complexes bearing 5-amino 2-ethylpyridine -2-carboximidate." Journal of Chemical Sciences 128, no. 6 (2016): 855–60. http://dx.doi.org/10.1007/s12039-016-1095-z.

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29

Wöhlert, Susanne, Inke Jess, and Christian Näther. "New Coordination Compounds Based on Cd(NCS)2(4-Ethylpyridine)x(x= 4, 2, 1)." Zeitschrift für anorganische und allgemeine Chemie 639, no. 2 (2013): 385–91. http://dx.doi.org/10.1002/zaac.201200479.

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30

Gimadieva, Alfiya Raisovna, Yuliya Zulkifovna Khazimullina, Aigiza Aidarovna Gilimkhanova, and Akhat Gaziz:anovich Mustafin. "Efficient modification of peroxydisulfate oxidation reactions of nitrogen-containing heterocycles 6-methyluracil and pyridine." Beilstein Journal of Organic Chemistry 20 (October 16, 2024): 2599–607. http://dx.doi.org/10.3762/bjoc.20.219.

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Nitrogen-containing heterocyclic compounds are widely used in pharmacology due to their pronounced biological activities and low toxicities. The introduction of a hydroxy function into uracil and pyridine molecules has led to compounds with antioxidant, anti-inflammatory, and immunomodulatory activity (3-hydroxy-6-methyl-2-ethylpyridine, 5-hydroxy-6-methyluracil, etc.). One of the successful methods for hydroxylation is peroxydisulfate oxidation. By modifying the Elbs reaction through catalysis and the introduction of additional oxidants, we have been able to significantly increase the yields

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31

M., Bhoopal, and Satyanarayana S. "Synthesis, isolation and characterization of alkyl(aquo) and alkyl(ligand)cobaloximes." Journal of Indian Chemical Society Vol. 81, Oct 2004 (2004): 837–41. https://doi.org/10.5281/zenodo.5832456.

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Department of Chemistry, Osmania University, Hyderabad-500 007, India <em>E-mail</em>: ssnsirasani@yahoo.com <em>Manuscript received 6 May 2003, revised 10 February 2004, accepted 11 May 2004</em> Alkyl(aquo)cobaloximes, [RCo(DH)<sub>2</sub>(H<sub>2</sub>O)](R<strong> = </strong>CH<sub>3</sub> and C<sub>2</sub>H<sub>5</sub>) have been prepared. These aquo complexes upon reacting with pyridine and substituted pyridincs give alkyl(ligand)cobaloximes [RCo(DH)<sub>2</sub>L], where L = pyridine, 4-methylpyridine, 4-ethylpyridine and 4-aminopyridine. These cobaloximes are characterized by electronic

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32

Ascenso, José R., Cristina G. de Azevedo, Alberto R. Dias, et al. "Amido- and imido-ethylpyridine titanium complexes. Crystal structure of {Ti[NCH2CH2py]Cl2(THF)}2." Journal of Organometallic Chemistry 632, no. 1-2 (2001): 17–26. http://dx.doi.org/10.1016/s0022-328x(01)00837-3.

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33

Kvachakhiya, Lekso L., Vladimir K. Shormanov, and Elena V. Maksina. "Determination of Mexidol in tablets by the method of derivative spectrophotometry." Человек и его здоровье 26, no. 2 (2023): 80–85. http://dx.doi.org/10.21626/vestnik/2023-2/10.

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Mexidol (3-hydroxy-6-methyl-2-ethylpyridine succinate) is a drug that exhibits neuroprotective, antihypoxic, anti-ischemic, nootropic, anti-stress and geroprotective effects and can suppress or slow down oxidation reactions. Оbjective: to develop a selective and simple method for assessing the content of mexidol in tablets. Materials and methods. The objects of the study were mexidol (3-hydroxy-6-methyl-2-ethylpyridine succinate) and Mexidol tablets 0.125 g. Derivative spectrophotometry was used as an analysis method. Results. The ability of mexidol to intensively absorb electromagnetic radiat

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34

SARI, Musa, Orhan ATAKOL, Nazife YILMAZ, and Dinçer ÜLKÜ. "Crystal Structure of {2-((2-Hydroxyphenyl)iminomethyll-4,6-dinitrophenolato-O,N,O'}tris(3-ethylpyridine-N)nickel. (II)." Analytical Sciences 15, no. 4 (1999): 401–2. http://dx.doi.org/10.2116/analsci.15.401.

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35

Grigor’eva, N. G., N. A. Filippova, S. V. Bubennov, A. N. Khazipova, B. I. Kutepov, and V. A. Dyakonov. "Microporous and Micro-meso-macroporous Y Zeolites in the Synthesis of 2-Methyl-5-ethylpyridine." Petroleum Chemistry 61, no. 3 (2021): 364–69. http://dx.doi.org/10.1134/s0965544121030075.

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36

Dyachenko, V. D., S. G. Krivokolysko, and V. P. Litvinov. "Synthesis and alkylation of 6-methyl-5-phenylcarbamoyl-3-cyano-4-ethylpyridine-2(1H)thione." Chemistry of Heterocyclic Compounds 32, no. 9 (1996): 1055–57. http://dx.doi.org/10.1007/bf01164712.

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37

DYACHENKO, V. D., S. G. KRIVOKOLYSKO, and V. P. LITVINOV. "ChemInform Abstract: Synthesis and Reactions of 6-Amino-3,5-dicyano-4-ethylpyridine-2(1H)- thione." ChemInform 28, no. 4 (2010): no. http://dx.doi.org/10.1002/chin.199704160.

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38

Liu, Min, Wak-Kim Poo, and Yu-ling Lin. "Pyrazine, 2-ethylpyridine, and 3-ethylpyridine are cigarette smoke components that alter the growth of normal and malignant human lung cells, and play a role in multidrug resistance development." Experimental and Molecular Pathology 98, no. 1 (2015): 18–26. http://dx.doi.org/10.1016/j.yexmp.2014.11.008.

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39

Pokidova, O. V., E. V. Batova, A. P. Sadkov, A. B. Eremeev, B. S. Fedorov, and A. I. Kotelnikov. "The Reactivity of 3-Hydroxy-6-methyl-2-ethylpyridine 2-Nitroxysuccinate and Reference Drugs in Model NO-Generating Systems." Doklady Chemistry 486, no. 2 (2019): 152–55. http://dx.doi.org/10.1134/s0012500819060016.

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40

Pochtennaya, V. M., and D. Kh Sembaev. "Effect of Reaction Medium on V-Ti Oxide Catalyst Composition in 2-Methyl-5-Ethylpyridine Ammoxidation." Eurasian Chemico-Technological Journal 4, no. 3 (2017): 183. http://dx.doi.org/10.18321/ectj532.

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<p>A chemical composition of V-Ti oxide catalyst changes in accordance with the reaction medium composition in a process of 2-methyl-5-ethylpyrydine ammoxidation into nicotinonitrile in an integral reactor. The presence of alkylpyridine concentration gradient along the catalyst bed leads to the appearance of V<sub>2</sub>O<sub>5</sub> content gradient in the catalyst. V<sub>2</sub>O<sub>5</sub> concentration increases in the conditions of alkylpyridine completed conversion in consequence of oxidative decomposition of VO<sub>2</sub&

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41

AlQaradawi, Siham Y., Adel Mostafa та A. A. Bengali. "Charge-transfer complexes formed in the reaction of 2-amino-4-ethylpyridine with π-electron acceptors". Journal of Molecular Structure 1106 (лютий 2016): 10–18. http://dx.doi.org/10.1016/j.molstruc.2015.10.100.

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42

Majerz, I., and W. Sawka-Dobrowolska. "Structure and spectroscopic properties of the solid complex of 2-ethylpyridine with 2,6-dichloro-4-nitrophenol." Journal of Chemical Crystallography 26, no. 2 (1996): 147–52. http://dx.doi.org/10.1007/bf01669732.

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43

Suvorov, B. V., S. B. Bakirova, V. A. Serazetdinova, and D. T. Ishaeva. "A method for the preparation of nicotinic acid and its amide from 2-methyl-5-ethylpyridine." Pharmaceutical Chemistry Journal 26, no. 11-12 (1993): 894–96. http://dx.doi.org/10.1007/bf00767669.

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44

Arata, Shinobu, Haruna Torigoe, Tomotaka Iihoshi, Naohide Matsumoto, Françoise Dahan та Jean-Pierre Tuchagues. "NH/π Interaction in a Spin-Crossover Complex [FeII(HLMe)2](BPh4)2·2CH3CN (BPh4-= Tetraphenylborate; HLMe= 2-Methylimidazol-4-yl-methylideneamino-2-ethylpyridine)". Inorganic Chemistry 44, № 25 (2005): 9288–92. http://dx.doi.org/10.1021/ic051215i.

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45

Gupta, Tarkeshwar, Ashis K. Patra, Shanta Dhar, Munirathinam Nethaji, and Akhil R. Chakravarty. "Effect of copper-sulphur bond on the DNA photo-cleavage activity of 2-(methylthio)ethylpyridine-2-carbaldimine copper(II) complexes." Journal of Chemical Sciences 117, no. 2 (2005): 123–32. http://dx.doi.org/10.1007/bf03356106.

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46

Kenney, MC, S. Mansoor, N. Gupta, P. Falatoonzadeh, and BD Kuppermann. "2-ethylpyridine, a cigarette smoke component, causes mitochondrial damage in human retinal pigment epithelial cells in vitro." Indian Journal of Ophthalmology 62, no. 1 (2014): 16. http://dx.doi.org/10.4103/0301-4738.126168.

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47

Sekioka, Ryuichi, Shugo Honda, Eriko Honjo та ін. "Discovery of N-ethylpyridine-2-carboxamide derivatives as a novel scaffold for orally active γ-secretase modulators". Bioorganic & Medicinal Chemistry 28, № 1 (2020): 115132. http://dx.doi.org/10.1016/j.bmc.2019.115132.

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DYACHENKO, V. D., S. G. KRIVOKOLYSKO, and V. P. LITVINOV. "ChemInform Abstract: Synthesis and Alkylation of 6-Methyl-5-phenylcarbamoyl-3-cyano-4- ethylpyridine-2(1H)thione." ChemInform 28, no. 13 (2010): no. http://dx.doi.org/10.1002/chin.199713110.

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Brunelli, Claudio, Yining Zhao, Melissa-Hanna Brown, and Pat Sandra. "Pharmaceutical analysis by supercritical fluid chromatography: Optimization of the mobile phase composition on a 2-ethylpyridine column." Journal of Separation Science 31, no. 8 (2008): 1299–306. http://dx.doi.org/10.1002/jssc.200700555.

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Gu, Sai Qi, Na Wu, Xi Chang Wang, Jing Jing Zhang, and Si Ru Ji. "Analysis of Key Odor Compounds in Steamed Chinese Mitten Crab (Eriocheir sinensis)." Advanced Materials Research 941-944 (June 2014): 1026–35. http://dx.doi.org/10.4028/www.scientific.net/amr.941-944.1026.

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Abstract:

Key odor compounds in different edible parts (abdomen, claw, leg meat and gonad) of steamed female Chinese mitten crab (Eriocheir sinensis) were extracted by a new type of adsorbent (MonoTrap), identified by gas chromatography-mass spectrometry (GC-MS) and determined by gas chromatography-olfactometry (GC-O). Ninteen key odor compounds (odor intensity value≥3) were obtained in Chinese mitten crab, among which trimethylamine (fishy), (Z)-4-heptenal (fishy) and 2-ethylpyridine (roasted potato) were found in all four edible parts of Eriocheir sinensis. In addition, 8 KOCs (2-ethylfuran, benzaldeh

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