Relevant bibliographies by topics / Acetophenone oxime

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  2. Dissertations / Theses

Academic literature on the topic 'Acetophenone oxime'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 July 2025

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Journal articles on the topic "Acetophenone oxime"

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Singh, Surinderjit, M. PS Ishar, Gajendra Singh, and Rajinder Singh. "Efficient, microwave-assisted intramolecular 1,3-dipolar cycloadditions of oximes and N-methylnitrones derived from o-alkenylmethoxy-acetophenones." Canadian Journal of Chemistry 83, no. 3 (2005): 260–65. http://dx.doi.org/10.1139/v05-049.

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Contrary to literature reports, the o-allyloxy- and crotyloxy-acetophenone-oximes (2a, 2b) are transformed to nitrones, which undergo regio- and stereoselective intramolecular 1,3-dipolar cycloadditions, both on microwave heating under solvent free conditions and refluxing in toluene, to afford novel cycloadducts (5a, 5b); the oxazepine-N-oxide (3a) reported to be formed in 98% yield was obtained only as a minor product (~10%). However, o-cinnamyloxy-acetophenone-oxime (2c) under similar conditions undergoes intramolecular N-alkylation to afford nitrone (3c). The reactions carried out under mi
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2

Ali Bawa, Ramadan, and Hana Mansoure Elmajdoub. "Synthesis of Some Bridged Unsymmetrical Terphthaloyl Oxime Esters." Academic Journal of Chemistry, no. 56 (June 10, 2020): 55–57. http://dx.doi.org/10.32861/ajc.56.55.57.

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Three unsymmetrical bridged terphthaloyl acetophenone oxime esters have been synthesized throughout an esterification process between three acetophenone oximes and the terphthaloyl chloride under mild basic conditions. Spectroscopic techniques, such as IR, HNMR and mass spectrometer, were used to confirm the structures of the desired oxime esters. The yields of the resulting oxime esters ranged from 50% to 73%.
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Ali Bawa, Ramadan, and Hana Mansoure Elmajdoub. "Synthesis of a Number of Unsymmetrical Bridged Terphthaloyl Acetophenone Oxime Esters." Academic Journal of Chemistry, no. 57 (August 8, 2020): 98–100. http://dx.doi.org/10.32861/ajc.57.98.100.

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A number of unsymmetrical bridged terphthaloyl acetophenone oxime esters has been synthesized throughout an esterification reaction between four different acetophenone oximes and the terphthaloyl chloride in a molar ratio of (2:1) under mild basic conditions. Spectroscopic techniques, such as IR, HNMR and mass spectrometer, were used to confirm the structures of the targeted oxime esters. The yields of the obtained oxime esters ranged from 80% to 95%.
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Ali Bawa, Ramadan, and Mona Mohammed Friwan. "Synthesis of Some Acetophenone Oximes and Their Corresponding Bridged Terphthaloyl Oxime Esters." Academic Journal of Life Sciences, no. 511 (November 2, 2019): 87–92. http://dx.doi.org/10.32861/ajls.511.87.92.

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The objective of this study is to synthesize a number of oximes along with their terphthaloyl oxime esters derived from acetophenone, 4-methylacetophenone, 4-hydroxyacetophenone, 4-aminoacetophenone and 4-nitroacetophenone as a part of ongoing research. Five acetophenone oximes have been synthesized by refluxing the acetophenone derivative with a solution of hydroxylamine hydrochloride in the presence of potassium hydroxide. The corresponding acetophenone oximes were obtained as solid materials in moderate to good yields. The structures of the resulting oximes were confirmed using IR, NMR and
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5

Song, J. H., S. M. Bae, E. J. Lee, J. H. Cho, and D. I. Jung. "Formation of Benzodiazepines and Pyrazinylquinoxalines from Aromatic and Heteroaromatic Ketones via Deoximation." Asian Journal of Chemistry 32, no. 7 (2020): 1676–80. http://dx.doi.org/10.14233/ajchem.2020.22639.

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The report stated that the treatment of o-phenylenediamine with acetone dicarboxylic acid, acetone and acetophenone afforded 2,4,4-trimethyl-3H-5-hydro-1,5-benzodiazepine. However, direct reactions of o-phenylenediamine with oximes (acetone oxime, acetophenone oxime, and benzophenone oxime) as ketone equivalents did not occur. In the course of present investigations, it is found that dichloroamine-T can be an efficient reagent for the conversion of oximes into the corresponding carbonyl compounds. As a part of a research program related to the synthetic study of pharmacologically interesting b
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Beirakhov, A. G., I. M. Orlova, E. G. Il’in, Yu E. Gorbunova, and Yu N. Mikhailov. "Uranyl complexes with acetophenone oxime." Russian Journal of Inorganic Chemistry 52, no. 1 (2007): 34–41. http://dx.doi.org/10.1134/s003602360701007x.

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7

Ali Bawa, Ramadan, and Mona Mohammed Friwan. "Synthesis and Antifungal Study of Some Acetophenone Oximes and Their Terphthaloyl Oxime Esters." Academic Journal of Chemistry, no. 410 (October 25, 2018): 96–101. http://dx.doi.org/10.32861/ajc.510.96.101.

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Acetophenone oximes 1 – 5 along with their terphthaloyl oxime esters 6 – 10 have been synthesized in moderate to good yields. Only one oxime was formed in as E/Z two isomers in a ratio of (8:1). These resulting oxime derivatives were involved in an antifungal screening against the Aspergillus niger at concentration of 30 ppm. Two commercially available antifungal agents, clorotimazole and daktarin, were employed as references at the same concentration, 30 ppm. The antifungal results for the oxime derivatives 1 – 10 showed inhibitory levels ranging from 38% to 100%, whereas the antifungal poten
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8

Pham, Phuc H., Khang X. Nguyen, Hoai T. B. Pham, Thien T. Tran, Tung T. Nguyen, and Nam T. S. Phan. "Functionalization of C–H bonds in acetophenone oximes with arylacetic acids and elemental sulfur." RSC Advances 10, no. 19 (2020): 11024–32. http://dx.doi.org/10.1039/d0ra00808g.

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9

de Lijser, HJ Peter, Jason S. Kim, Suzanne M. McGrorty, and Erin M. Ulloa. "Substituent effects in oxime radical cations. 1. Photosensitized reactions of acetophenone oximes." Canadian Journal of Chemistry 81, no. 6 (2003): 575–85. http://dx.doi.org/10.1139/v03-052.

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A variety of ortho-, meta-, and para-substituted (-H, -F, -Cl, -CF3, -CN (meta and para only), -CH3, -OCH3, and -NO2) acetophenone oximes were synthesized and studied using laser flash photolysis (LFP) and steady-state photolysis experiments in acetonitrile with chloranil as the photosensitizer. In addition, semi-empirical (AM1) calculations were performed on the neutral species, the radical cations, and the corresponding iminoxyl radicals. The data was analyzed in terms of the electrochemical peak potentials of the oximes, the quenching rates of triplet chloranil (LFP), the calculated ionizat
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10

Perekalin, Dmitry S., Evgeniya A. Trifonova, Alina A. Komarova, and Denis Chusov. "Variability of Rhodium(III)-Catalyzed Reactions of Aromatic Oximes with Alkenes." Synlett 31, no. 11 (2020): 1117–20. http://dx.doi.org/10.1055/s-0040-1707961.

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Acetophenone oxime reacts with various alkenes in the presence of the rhodium catalyst [Cp*RhCl2]2 (2.5 mol%; Cp* = pentamethylcyclopentadienyl) and 1,1,1,3,3,3-hexafluoropropan-2-ol as an important cosolvent. Styrene, aliphatic terminal alkenes, and strained cyclic alkenes gave the corresponding substituted dihydroisoquinolines in yields of 50–99%. On the other hand, alkenes containing functional groups close to the double bond gave a variety of different products. The reactions of acetophenone oxime with styrene or dec-1-ene in the presence of the chiral catalyst [(C5H2 t Bu2CH2 t Bu)RhI2]2
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Dissertations / Theses on the topic "Acetophenone oxime"

1

Wang, Shao-Chien, and 王韶謙. "1.Palladium-Catalyzed ortho-C-H Bond Activation of Acetophenone Oxime Ethers2.Investigation of Blue LEDs Promoted Synthesis of Dithioacetals." Thesis, 2017. http://ndltd.ncl.edu.tw/handle/97404562666650034342.

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碩士<br>國立中興大學<br>化學系所<br>105<br>In the first part of this thesis, we report an efficient palladium-catalyzed ortho-C-H arylation of acetophenone oxime Ethers with aryl pinacol boronic esters, leading to the biaryl derivatives in good yields. The sequential process of iridium-catalyzed C-H borylation and palladium-catalyzed ortho-C-H arylation makes the present protocol access functionalized biaryl arenes. In the second part of this thesis, we achieve a simple and elegant method for dithioacetalization of aldehyde using blue LEDs irradiation under photochemical reaction. The salient feature
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