Academic literature on the topic 'Ethoxy derivatives'

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Journal articles on the topic "Ethoxy derivatives"

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Hoai, N. T., Tran Thi Yen Ngoc, Nguyen Dang Nam та ін. "Effect oF β-Alanine on The Preparation of 4-Ethoxy-Cinnamic Acid". Open Materials Science Journal 12, № 1 (2018): 58–67. http://dx.doi.org/10.2174/1874088x01812010058.

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Objective:Cinnamic acid and its derivatives have a numerous potential applications in many different fields such as pharmacy, organic “building blocks”, and corrosion inhibitors.Method:It is well-known that Verley-Doebner modification is a high efficient method for the preparation of cinnamic acid derivaties, especially with the compounds containing electron-donating subtituents at para position in aromatic ring. In this paper, 4-ethoxy-cinnamic acid was synthesized according to Verley-Doebner reaction with the use of pyrine acting as catalyst and solvent. The effect of the β-alanine concentra
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Göksel, Meltem, Mahmut Durmuş, and Devrim Atilla. "A comparative study on photophysical and photochemical properties of zinc phthalocyanines with different molecular symmetries." Journal of Porphyrins and Phthalocyanines 16, no. 07n08 (2012): 895–906. http://dx.doi.org/10.1142/s1088424612500964.

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The five possible non-peripherally substituted zinc(II) phthalocyanines with different molecular symmetries (Pc1–Pc5) were synthesized from statistical condensation of the phthalonitrile derivatives (A and B). 2-[2-(2-ethoxyethoxy)ethoxy]-1-[2-((2-ethoxyethoxy)-ethoxy)ethoxymethyl]ethyloxy and 2′-[(tert-butoxycarbonyl)amino]ethoxy groups were used as substituents. The structures of the new compounds were characterized using elemental analysis and spectroscopic data including IR, 1H and 13C NMR, electronic absorption and mass spectra. The photophysical and photochemical properties of these new
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Kang, Hyo Sim, Sun Wha Oh, and Young Soo Kang. "Comparison of Optical Properties of Pyrazoline Derivative Nanoparticles." Solid State Phenomena 119 (January 2007): 39–42. http://dx.doi.org/10.4028/www.scientific.net/ssp.119.39.

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We prepared various pyrazoline derivatives which possess dimethylamino-, ethoxy-, isopropyl-phenyl ring at the 5-position of pyrazoline. The nanoparticles of pyrazoline derivative ranging from tens to hundreds of nanometers by the reprecipitation method have been successfully prepared and their optical size-dependent properties have been investigated with UV-vis, fluorescence spectroscopy, DLS (Dynamic Light Scattering) and SEM. The size-dependent optical properties of pyrazoline organic nanoparticles have been observed in the order of dimethylamino- > ethoxy- > isopropyl- in electro-don
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Yu-Xiu, Liu, Cui Ming-Bo, Zhao Qi-Qi, Wang Qing-Min, Liu Ying, and Huang Run-Qiu. "Reduction of Pyrimidine Derivatives by LiAlH4." Journal of Chemical Research 2007, no. 8 (2007): 490–93. http://dx.doi.org/10.3184/030823407x240872.

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The reduction of ethyl 2-methylthio-(or 2-ethoxy)pyrimidine-5-carboxylate by LiAlH4 afforded ethyl 2-methylthio-(or 2-ethoxy)-1,6-dihydropyrimidine-5-carboxylate as the main product. Similarly, the reduction of 2-methylthio-(or 2-methoxy)pyrimidine-5-carboxamide by LiAlH4 gave 2-methylthio-(or 2-methoxy)-1,6-dihydropyrimidine-5-carbonitrile as main product.
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Xiao, Pan-Lei, Xiu-Ying Song, Xin-Ting Xiong, Da-Yong Peng, and Xu-Liang Nie. "Synthesis, Crystal Structure, Spectral Characterization and Antifungal Activity of Novel Phenolic Acid Triazole Derivatives." Molecules 28, no. 19 (2023): 6970. http://dx.doi.org/10.3390/molecules28196970.

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At present, phenolic acid derivatives and triazole derivatives have a good antifungal effect, which has attracted widespread attention. A series of novel phenolic acid triazole derivatives were synthesized, and their structures were characterized by IR, MS, NMR, and X-ray crystal diffraction. Compound methyl 4-(2-bromoethoxy)benzoate, methyl 4-(2-(1H-1,2,4-triazol-1-yl) ethoxy)benzoate, 4-(2-(1H-1,2,4-triazol-1-yl)ethoxy)benzoic acid and 4-(2-(1H-1,2,4-triazol-1-yl) ethoxy)-3-methoxybenzoic acid crystallize in the monoclinic system with space group P21/n, the monoclinic system with space group
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Gürsoy Kol, Özlem, Sevda Manap, Murat Beytur, Fevzi Aytemiz, Muzaffer Alkan, and Haydar Yüksek. "Antibacterial and antioxidant activities of novel 2-ethoxy- 4-[(4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl)azomethine]- phenyl 3-methoxybenzoate derivatives." Journal of Research in Pharmacy 29, no. 2 (2024): 692–704. https://doi.org/10.12991/jrespharm.1664907.

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In the present study, 3-alkyl/aryl-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones (1) reacted with 3-ethoxy-4- (3-methoxybenzoxy)-benzaldehyde (2) to obtain the corresponding nine new 2-ethoxy-4-[(3-alkyl/aryl-4,5-dihydro-1H- 1,2,4-triazol-5-one-4-yl)azomethine]-phenyl 3-methoxybenzoates (3). The compounds 3 were also treated with 4- piperidinecarboxamide in the presence of formaldehyde according to the Mannich reaction to synthesize 2-ethoxy-4-{[3- alkyl/aryl-1-(4-piperidinecarboxamide-1-yl-methyl)-4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl]-azomethine}-phenyl 3- methoxy-benzoates (4). The structur
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Çiçek, Baki, Merve Çağlı, Remziye Tülek, and Ali Teke. "Synthesis and optical characterization of bipod carbazole derivatives." Heterocyclic Communications 26, no. 1 (2020): 148–56. http://dx.doi.org/10.1515/hc-2020-0111.

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AbstractIn this study, some new biscarbazole derivatives were synthesized for the purpose of being used in OLED technologies and related areas. The following compounds: {1,2-bis(2-(3,6-diphenyl-9H-carbazole-9-yl) ethoxy)ethane (C-1), bis[2-(2-(3,6- diphenyl-9H-carbazole-9-yl) ethoxy)etyl]ether (C-2), bis[2-(2-(3,6-di(naphthalene-1-yl)-9H-carbazol-9-yl)ethoxy)etyl]ether (C-3) and bis [2-(2-(3,6-di(naphthalene-2-yl)-9H-carbazol-9-yl)ethoxy) ethyl]ether (C-4) were synthesized by Suzuki-Miyaura Cross Coupling reactions. The structural properties of the synthesized compounds were characterized by F
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Cai, Xiao-hua, and Bing Xie. "Synthesis and insulin-sensitizing activity of (S)-2-ethoxy-3-phenylpropanoic acid derivatives." Canadian Journal of Chemistry 84, no. 9 (2006): 1106–9. http://dx.doi.org/10.1139/v06-145.

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A series of (S)-2-ethoxy-3-phenylpropanoic acid derivatives were synthesized and their insulin-sensitizing activities were evaluated in 3T3-L1 cells. Compounds 1b (EC30 = 9.43 × 10–3 µmol/L), 1d (EC30 = 7.45 × 10–3 µmol/L), 1e (EC30 = 6.22 × 10–3 µmol/L), and 1f (EC30 = 7.76 × 10–3 µmol/L) exhibited more potent insulin-sensitizing activity than rosiglitazone (EC30 = 2.06 × 10–2 µmol/L).Key words: (S)-2-ethoxy-3-phenylpropanoic acid derivatives, type 2 diabetes, insulin-sensitizing agents.
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Raad, H. Turkey, A. Razzak Mahmood kubba Ammar, A. Fadhil Ammar, and N. AlShawi 3. Nada. "Synthesis and Anti-Inflammatory Activity of Some -5-Ethoxy-2- Mercapto Benzimidazole Derivatives." International Journal of Current Pharmaceutical Review and Research 8, no. 1 (2017): 24–27. https://doi.org/10.5281/zenodo.12678320.

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This article includes a description of new series of 5-ethoxy-2-mercapto benzimidazole derivatives, synthesized andevaluated for the anti-inflammatory activity; the synthesis involved the reaction of the parent nucleus (5-ethoxy-2-mercapto benzimidazole) with different p-phenacyl bromide substituents. All the newly synthesized compounds werescreened for their anti-inflammatory activity by egg albumin-induced rat hind paw edema method.
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Al-Rashdi, Kamelah S., Bandar A. Babgi, Ehab M. M. Ali, et al. "Tuning the anticancer properties of Pt(ii) complexes via structurally flexible N-(2-picolyl)salicylimine ligands." RSC Advances 12, no. 42 (2022): 27582–95. http://dx.doi.org/10.1039/d2ra04992a.

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Book chapters on the topic "Ethoxy derivatives"

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"Chapter 7 The Speculative Ethos." In The Social Life of Financial Derivatives. Duke University Press, 2020. http://dx.doi.org/10.1515/9780822372837-009.

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Santos, Josana Pereira dos, Rafael César Gonçalves Pereira, Victor Hugo dos Santos, et al. "Attempts to synthesize a trimeric derivative of pristimerin with potential activity against cancer cells." In Themes focused on interdisciplinarity and sustainable development worldwide V. 02. Seven Editora, 2024. http://dx.doi.org/10.56238/sevened2024.003-056.

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Pristimerin exhibits significant potential as a therapeutic agent, demonstrating activity against various human cancer cells. The assumption is that the trimer of pristimerin enhances the strength and selectivity of pristimerin-DNA interactions through a multivalent effect. Therefore, to synthesize the trimer of pristimerin, a multi-step route was adopted. The initial step involved the synthesis of 2-(2-(2-azidoetoxy)ethoxy)ethan-1-ol (R1) through an SN2 reaction, with a yield of 52%. The compound N-(tert-butoxyl-carbonyl)-tris-(hydroxymethyl)aminomethane (R2), with the amino group protected b
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Malhotra, Geeta Verma. "HARMONIZING TRADITIONS AND INNOVATION: EXPLORING THE SYNERGY OF AYURVEDA AND MODERN BIOTECHNOLOGY THROUGH FERMENTATION TECHNOLOGY." In Futuristic Trends in Biotechnology Volume 3 Book 21. Iterative International Publishers, Selfypage Developers Pvt Ltd, 2024. http://dx.doi.org/10.58532/v3bkbt21p1ch6.

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Biotechnology, a dynamic field harnessing biological systems, organisms, and derivatives, drives transformative solutions across sectors. This article explores its historical evolution, tracing origins to ancient practices that laid its foundation. Biotechnology's phases encompass ancient fermentation, selective breeding, microbiological discoveries, genetic engineering, and personalized medicine. Central to biotechnology, fermentation optimizes microorganism-driven biochemical reactions for diverse industries, yielding pharmaceuticals, biofuels, and more. Ayurveda intersects with biotechnolog
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Donaldson, Ian. "Gathering and Losing the Self Jonson and Biography." In Jonson’s Magic Houses. Oxford University PressOxford, 1997. http://dx.doi.org/10.1093/oso/9780198183945.003.0003.

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Abstract IN 1919 Gregory Smith began his study of Ben Jonson in the English Men of Letters series with these confident words: We know more of Jonson than any of the great writers of his age. There are no mysteries, or at least great mysteries, in his literary career, and the bio grapher is not driven, with the Shakespearians, to conjectural reconstruction from the shards of record and anecdote. Even his personality stands forth fresh and convincing beside the blurred portrait of Marlowe, or Shake speare, or Fletcher. For this fuller knowledge we are indebted to Jonson himself. Half a dozen yea
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Conference papers on the topic "Ethoxy derivatives"

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Marliyana, Soerya Dewi, Maulidan Firdaus, Muhamad Widyo Wartono, Diana Inas Utami, and Uly Wulan Apriani. "Evaluation of the Antibacterial Activity of Pinostrobin Derivative Compounds from Ethylation and Allylation Reactions." In 8th International Conference on Advanced Material for Better Future. Trans Tech Publications Ltd, 2025. https://doi.org/10.4028/p-s3ucax.

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Temu Kunci (Kaempferia pandurata Roxb.) is one of the plants from the Zingiberaceae family that contains secondary metabolites derived from flavonoids. Studies on the bioactivity of flavonoid compounds from this species have shown various biological activities such as antibacterial, antioxidant, antiviral, antitumor, antipyretic, anti-inflammatory, analgesic, and insecticidal properties. Pinostrobin (5-hydroxy-7-methoxy flavanone) (1) is the major flavonoid found in the rhizomes of this plant and has been successfully derivatized through ethylation and allylation reactions. Two compounds were
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Breviario, F., F. Bertocchi, M. Prosdocimi, and E. Deiena. "INHIBITION BY AD6 (8-MONOCHLORO -3-BETA-DIETHYLAMINOETHYL -4- METHYL -7- ETHOXY CARBONYL METHOXY COUMARIN) OF POLYMORPHONUCLEAR LEUKOCYTES ADHESION TO ENDOTHELIAL CELLS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643163.

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Increased leukocyte adhesion to the endothelial lining of blood vessels is an essential event in inf laaaation and the pathogenesis of certain vascular deseases. The aonocyte product interleukin-1 (IL-1) has been shown to enhance the adherence of huaan periferal blood polyaorphonuclear leukocytes (PMN) to huaan uabilical vein endothelial cells (EC). In this study AD6, a couaarin derivative which inhibits platelet aggregation and coronary throabus foraation in experimental aniaals, was found .to inhibit PMN adhesion to control and IL-i-treated EC. Suspensions of washed 51Cr labeled PMN were add
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