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Journal articles on the topic 'P-nitroacetophenone'

Author: Grafiati
Published: 4 June 2021
Last updated: 12 February 2022

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1

Murali Krishna, C., S. Basu, and A. K. Roy. "Studies on p-nitroacetophenone triplet state." Journal of Photochemistry and Photobiology A: Chemistry 95, no. 2 (1996): 111–13. http://dx.doi.org/10.1016/1010-6030(95)04249-0.

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2

Erofeev, Yu V., P. M. Kochergin, U. M. Azizov, and K. Kh Razikov. "Methods of preparation of p-nitroacetophenone (review)." Pharmaceutical Chemistry Journal 19, no. 1 (1985): 47–59. http://dx.doi.org/10.1007/bf00767105.

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3

Murali Krishna, C., and A. K. Roy. "Studies on p-nitroacetophenone-sensitized lipid peroxidation." Journal of Photochemistry and Photobiology B: Biology 34, no. 1 (1996): 47–50. http://dx.doi.org/10.1016/1011-1344(95)07273-x.

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4

Zhu, Yanqing, Guangxuan Ding, Xinbao Li, and Hongkun Zhao. "Solid–Liquid Phase Equilibrium for Ternary Systems of p-Nitroacetophenone plus m-Nitroacetophenone plus Methanol/Toluene/Ethyl Acetate." Journal of Chemical & Engineering Data 64, no. 9 (2019): 4066–76. http://dx.doi.org/10.1021/acs.jced.9b00416.

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5

Liu, Miaomiao, Weiqiang Tang, Yisheng Xu, et al. "Pd-SnO2/Al2O3 heteroaggregate nanocatalysts for selective hydrogenations of p-nitroacetophenone and p-nitrobenzaldehyde." Applied Catalysis A: General 549 (January 2018): 273–79. http://dx.doi.org/10.1016/j.apcata.2017.10.004.

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6

Laszakovits, Juliana R., Stephanie M. Berg, Brady G. Anderson, Jessie E. O’Brien, Kristine H. Wammer, and Charles M. Sharpless. "p-Nitroanisole/Pyridine and p-Nitroacetophenone/Pyridine Actinometers Revisited: Quantum Yield in Comparison to Ferrioxalate." Environmental Science & Technology Letters 4, no. 1 (2016): 11–14. http://dx.doi.org/10.1021/acs.estlett.6b00422.

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7

Pei, Kemei, Yufang Ma, Xuming Zheng, and Haiyang Li. "Resonance Raman spectroscopic and density functional theory study of p-nitroacetophenone (PNAP)." Chemical Physics Letters 437, no. 1-3 (2007): 153–58. http://dx.doi.org/10.1016/j.cplett.2007.02.013.

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8

Zakharova, G. V., and A. K. Chibisov. "Primary processes in the thiacyanine dimer-photosensitized reduction of p-nitroacetophenone in water by." High Energy Chemistry 47, no. 6 (2013): 322–26. http://dx.doi.org/10.1134/s001814391306012x.

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9

Qiu, Xiao Yang, Su Zhi Li, and An Ran Shi. "Synthesis and Biological Activities of Chalcones Derived from Nitroacetophenone." Advanced Materials Research 518-523 (May 2012): 255–60. http://dx.doi.org/10.4028/www.scientific.net/amr.518-523.255.

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A series of nitrochalcones (compounds 1-10) were synthesized by reacting appropriate nitroacetophenones and suitable benzaldehydes. The synthesized products were evaluated for their cytotoxic, antibacterial (Bacillus subtilis, Escherichia coli, Pseudomonas fluorescence and Staphylococcus aureus) and antifungal (Aspergillus niger, Candida albicans and Trichophyton rubrum) activities in vitro. Among the compounds tested, (E)-3-(4-fluorophenyl)-1-(3-nitrophenyl)- prop-2-en-1-one (10) showed the favorable in vitro cytotoxic activity against human nasopharyngeal epidermoid tumor cell line KB, and (
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10

Parkinson, A., P. E. Thomas, D. E. Ryan, et al. "Mechanism of inactivation of rat liver microsomal cytochrome P-450c by 2-bromo-4'-nitroacetophenone." Journal of Biological Chemistry 261, no. 25 (1986): 11487–95. http://dx.doi.org/10.1016/s0021-9258(18)67270-9.

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11

Chow, Yuan L., Josette Michon, Pierre Michon, claude Morat та A. Rassat. "Photochemical reaction between β-cyclodextrin and p-nitroacetophenone in an inclusion complex in water solution". Tetrahedron Letters 33, № 23 (1992): 3315–18. http://dx.doi.org/10.1016/s0040-4039(00)92076-8.

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12

Mitra, Anita, Tapati Banerjee, P. Roychowdhury, Nityananda Saha, and Satima Das. "X-Ray crystal structure of bis-(p-nitroacetophenone-4,6-dimethyl-2-pyrimidyl hydrazone) copper(i) perchlorate." Polyhedron 15, no. 19 (1996): 3371–75. http://dx.doi.org/10.1016/0277-5387(96)00027-7.

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13

Parkinson, A., D. E. Ryan, P. E. Thomas, et al. "Chemical modification and inactivation of rat liver microsomal cytochrome P-450c by 2-bromo-4'-nitroacetophenone." Journal of Biological Chemistry 261, no. 25 (1986): 11478–86. http://dx.doi.org/10.1016/s0021-9258(18)67269-2.

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14

CAFFERATA, L. F. R., and J. C. AUTINO. "ChemInform Abstract: A Convenient Preparation of 1-Hydroperoxy-(1-p-Nitrophenyl)ethanol by the Acid-Catalyzed Oxidation of p-Nitroacetophenone with Hydrogen Peroxide." ChemInform 26, no. 44 (2010): no. http://dx.doi.org/10.1002/chin.199544097.

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15

Cafferata, Lázaro F. R., and Juan C. Autino. "A CONVENIENT PREPARATION OF 1-HYDROPEROXY-(1-p-NITROPHENYL)ETHANOL BY THE ACID-CATALYZED OXIDATION OFp-NITROACETOPHENONE WITH HYDROGEN PEROXIDE." Organic Preparations and Procedures International 27, no. 4 (1995): 483–87. http://dx.doi.org/10.1080/00304949509458482.

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16

Pandeya, Surendra N., and Neha Rajput. "Synthesis and Anticonvulsant Activity of Various Mannich and Schiff Bases of 1,5-Benzodiazepines." International Journal of Medicinal Chemistry 2012 (November 28, 2012): 1–10. http://dx.doi.org/10.1155/2012/237965.

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Benzodiazepines have a various behavioral effects in addition to their anxiolytic action. There is every reason to believe that the BZ/GABA receptor complex is involved in these effects, since GABAmimetic manipulations modify the effect of BZ in tests of convulsive activity, motor function, and appetitive behavior. 1,5-Benzodiazepines are biologically important molecules and are extensively used clinically as analgesic, hypnotic, sedative, and antidepressive agents. Hence, 1,5-Benzodiazepines were synthesized by condensation of o-phenylenediamine and ketones, for example, cyclohexanone and ace
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17

Das, Suresh, and Clemens von Sonntag. "The Oxidation of Trimethylamine by OH Radicals in Aqueous Solution, as Studied by Pulse Radiolysis, ESR, and Product Analysis. The Reactions of the Alkylamine Radical Cation, the Aminoalkyl Radical, and the Protonated Aminoalkyl Radical." Zeitschrift für Naturforschung B 41, no. 4 (1986): 505–13. http://dx.doi.org/10.1515/znb-1986-0418.

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Hydroxyl radical reactions with trimethylamine in aqueous solution lead to the formation of the aminoalkyl radical (CH3)2NCH2 (A) and its conjugated acid (CH3)2HN+CH2 (AH+) as well as to the alkylamine radical cation (CH3)3N+(N+). These radicals are transform ed into each other by hydrolytic reactions, e.g.[xxx]Radicals AH+ are more acidic (pKa ≈ 3.6) than the radicals N+(pKa ≈ 8.0). Consequently, N+ predom inate over AH+ under quasi equilibrium conditions (e.g. in the presence of phosphate buffer) and are the only species observed by ESR in acid solutions. Reacting with the protonated amine.
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18

EROFEEV, YU V., P. M. KOCHERGIN, U. M. AZIZOV, and K. KH RAZIKOV. "ChemInform Abstract: METHODS FOR THE SYNTHESIS OF P-NITROACETOPHENONE. REVIEW." Chemischer Informationsdienst 16, no. 24 (1985). http://dx.doi.org/10.1002/chin.198524392.

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