Academic literature on the topic '4-Bromoacetophenone'

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Journal articles on the topic "4-Bromoacetophenone"

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Galstyan, A., A. Bushuyev, A. Krasilnikova, and M. Zhurba. "The oxidation of 4-bromacetophenone by ozone in acetic acid." Voprosy Khimii i Khimicheskoi Tekhnologii, no. 5 (October 2021): 37–42. http://dx.doi.org/10.32434/0321-4095-2021-138-5-37-42.

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The kinetics and mechanism of oxidation of 4-bromoacetophenone by ozone in acetic acid solution have been studied. It was shown that 77% of the starting material is oxidized by the benzene ring; 8% of 4-bromobenzoic acid and small amounts of carbon (IV) oxide were identified among the side chain ozonation products. The main reaction products are aliphatic peroxide compounds, which have in their structure one hydroperoxide group. Manganese (II) acetate was shown to be the most effective catalyst for the side chain reaction of 4-bromoacetophenone in acetic acid. High selectivity for the side cha
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2

Wender, Paul A., and Raok Jeon. "Bromoacetophenone-Based Photonucleases: Photoinduced Cleavage of DNA by 4‘-Bromoacetophenone−Pyrrolecarboxamide Conjugates." Organic Letters 1, no. 13 (1999): 2117–20. http://dx.doi.org/10.1021/ol9903279.

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Lopes, Raquel de Oliveira, Joyce Benzaquem Ribeiro, Aline de Souza Ramos, et al. "Highly enantioselective bioreduction of 4-bromoacetophenone." Tetrahedron: Asymmetry 22, no. 18-19 (2011): 1763–66. http://dx.doi.org/10.1016/j.tetasy.2011.10.014.

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4

Trivedi, Mahendra Kumar, Alice Branton, Dahryn Trivedi, Gopal Nayak, Gunin Saikia, and Snehasis Jana. "Characterization of Physico-Chemical and Spectroscopic Properties of Biofield Energy Treated 4-Bromoacetophenone." American Journal of Physical Chemistry 4, no. 4 (2015): 30–37. https://doi.org/10.11648/j.ajpc.20150404.11.

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4-Bromoacetophenone is an acetophenone derivative known for its usefulness in organic coupling reactions and various biological applications. The aim of the study was to evaluate the impact of biofield energy treatment on 4-bromoacetophenone using various analytical methods. The material is divided into two groups for this study i.e. control and treated. The control group remained as untreated and the treated group was subjected to Mr. Trivedi’s biofield energy treatment. Then, both the samples were characterized using X-ray diffraction (XRD), differential scanning calorimetry (DSC), the
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Trivedi, Mahendra Kumar, Alice Branton, Dahryn Trivedi, Gopal Nayak, Gunin Saikia, and Snehasis Jana. "Characterization of Physico-Chemical and Spectroscopic Properties of Biofield Energy Treated 4-Bromoacetophenone." American Journal of Physical Chemistry 4, no. 4 (2015): 30–37. https://doi.org/10.5281/zenodo.168163.

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4-Bromoacetophenone is an acetophenone derivative known for its usefulness in organic coupling reactions and various biological applications. The aim of the study was to evaluate the impact of biofield energy treatment on 4-bromoacetophenone using various analytical methods. The material is divided into two groups for this study i.e. control and treated. The control group remained as untreated and the treated group was subjected to Mr. Trivedi’s biofield energy treatment. Then, both the samples were characterized using X-ray diffraction (XRD), differential scanning calorimetry (DSC), the
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6

Skorokhod, K. S., and A. G. Galstyan. "Kinetics of catalytic oxidation 4-bromethylbenzene by ozone in acetic acid." Catalysis and petrochemistry, no. 30 (2020): 83–89. http://dx.doi.org/10.15407/kataliz2020.30.083.

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The kinetic regularities of catalytic oxidation of 4-bromoethylbenzene by ozone to create an eco-logical, low-temperature technology for the synthesis of 4-bromoacetophenone have been studied. The experiment was performed in a glass reactor with a porous membrane under conditions of kinetic regime at a temperature of 293-333 K. The concentration of ozone in the gas phase was determined by spectrophotometric method. Analysis of 4-bromoacetophenone and its oxidation products was performed by gas-liquid chromatography. Oxidation of 4-bromoethylbenzene by ozone in a solution of acetic acid at a te
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7

Jeon, Raok, and Paul A. Wender. "Photocleavage of DNA by 4′-bromoacetophenone analogs." Archives of Pharmacal Research 24, no. 1 (2001): 39–43. http://dx.doi.org/10.1007/bf02976491.

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8

Fischer, Andreas, H. S. Yathirajan, B. V. Ashalatha, B. Narayana, and B. K. Sarojini. "(2E)-3-(Biphenyl-4-yl)-1-(4-bromophenyl)prop-2-en-1-one." Acta Crystallographica Section E Structure Reports Online 63, no. 3 (2007): o1355—o1356. http://dx.doi.org/10.1107/s1600536807006915.

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The title compound, C21H15BrO, was obtained from 4-bromoacetophenone and biphenyl-4-carbaldehyde. The geometry of the molecule is unexceptional. The compound crystallizes isostructurally with the corresponding chloro compound.
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Bahrin, Lucian Gabriel, Catalin Neculai Lungu, Iuliean Vasile Asaftei, and Ion Sandu. "Synthesis of 4-(4-Hydroxyaryl)-1,3-Dithiolium Perchlorates." Revista de Chimie 70, no. 2 (2019): 527–31. http://dx.doi.org/10.37358/rc.19.2.6949.

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4-(3,5-Dibromo-4-hydroxyphenyl)-2-(N,N-dialkylamino)-1,3-dithiol-2-ylium perchlorates have been synthesized by acid catalyzed cyclocondensation of 1-(3,5-dibromo-4-hydroxyphenyl)-1-oxaethan-2-yl dithiocarbamates. The latter compounds have been obtained from the reaction of the corresponding substituted w-bromoacetophenone with various salts of dithiocarbamic acids.
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Chanysheva, A. R., N. V. Privalov, and V. V. Zorin. "Stereodirected Biocatalyzed Reduction of 4-Bromoacetophenone in (R)-(+)-1-(4-Bromophenyl)ethanol." Russian Journal of General Chemistry 94, no. 13 (2024): 3639–42. https://doi.org/10.1134/s1070363224130255.

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Conference papers on the topic "4-Bromoacetophenone"

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Редькин, Н. А., and Д. А. Корсиков. "DI(4-METHOXYPHENYL)TELLUROXIDE AS A CATALYST IN THE ALDOLS CONDENSATION REACTION." In Инновации и «зелёные» технологии : IV Всероссийская научно-практическая конференция. Crossref, 2024. http://dx.doi.org/10.34830/sounb-conf.2023.14.11.027.

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Работа посвящена изучению реакции альдольной конденсации в присутствии теллурорганического катализатора. Было исследовано протекание реакции между 3,4-диметоксибензальдегидом с п-бромацетофеноном в присутствии гидроксида натрия и ди(4-метоксифенил)теллуроксида. Показано, что на протекание химических реакций конденсации влияют концентрация катализатора, природа растворителя, температура. The work is devoted to the study of the aldol condensation reaction in the presence of an organotellurium catalyst. The reaction between 3,4-dimethoxybenzaldehyde and p-bromoacetophenone in the presence of sodi
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