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Journal articles on the topic 'Oxy-radicals'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 February 2022

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1

CERUTTI, P. "Oxy-radicals and cancer." Lancet 344, no. 8926 (1994): 862–63. http://dx.doi.org/10.1016/s0140-6736(94)92832-0.

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2

von Ahsen, Stefan, Helge Willner, and Gustavo A. Argüello. "Fluorocarbon oxy and peroxy radicals." Journal of Fluorine Chemistry 125, no. 7 (2004): 1057–70. http://dx.doi.org/10.1016/j.jfluchem.2004.02.008.

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3

Turovskii, A. A., N. A. Turovskii, R. V. Kucher, V. V. Petrenko, A. A. Andrianov, and V. G. Kaloerova. "Reactivity of unstable oxy-radicals." Theoretical and Experimental Chemistry 22, no. 2 (1986): 212–14. http://dx.doi.org/10.1007/bf00519197.

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4

Brough, Peter, Serge Gambarelli, Jean-François Jacquot, André Grand, Jacques Pécaut, and Paul Rey. "1,2-Dihydrotriazinyl-N-oxy Free Radicals." Chemistry - A European Journal 17, no. 40 (2011): 11250–57. http://dx.doi.org/10.1002/chem.201100433.

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5

Simic, Michael G., David S. Bergtold, and Lisa R. Karam. "Generation of oxy radicals in biosystems." Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 214, no. 1 (1989): 3–12. http://dx.doi.org/10.1016/0027-5107(89)90192-9.

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6

Marnett, Lawrence J. "Oxy radicals, lipid peroxidation and DNA damage." Toxicology 181-182 (December 2002): 219–22. http://dx.doi.org/10.1016/s0300-483x(02)00448-1.

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7

Ewing, David. "Oxy-radicals in Molecular Biology and Pathology." American Journal of Clinical Oncology 12, no. 5 (1989): 457. http://dx.doi.org/10.1097/00000421-198910000-00022.

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8

Halliwell, Barry. "Oxy-radicals in molecular biology and pathology." FEBS Letters 244, no. 2 (1989): 501–2. http://dx.doi.org/10.1016/0014-5793(89)80599-x.

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9

Pryor, William A. "Oxy-radicals in molecular biology and pathology." Free Radical Biology and Medicine 8, no. 3 (1990): 305. http://dx.doi.org/10.1016/0891-5849(90)90078-w.

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10

MINOTTI, GIORGIO. "Metals and Membrane Lipid Damage by Oxy-Radicals." Annals of the New York Academy of Sciences 551, no. 1 Membrane in C (1988): 34–44. http://dx.doi.org/10.1111/j.1749-6632.1988.tb22318.x.

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11

Chandra, Mahesh, Vivek Gupta, Anil Kumar Rath, et al. "Effect of Oral Vitamin E on Oxy-Free Radical Status in Acute Myocardial Infarction." Asian Cardiovascular and Thoracic Annals 3, no. 3-4 (1995): 117–22. http://dx.doi.org/10.1177/021849239500300406.

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The present work was conducted to study the status of oxidative stress (oxy-free radicals) in 24 patients with acute myocardial infarction and 12 matched healthy control patients and furthermore evaluate the effect of oral vitamin E on altered oxyfree radicals in these patients. The parameters assessed for oxy-free radical status were superoxide anion and malonyldialdehyde. These were found to be increased during acute myocardial infarction and this increment had a normalizing trend with the passage of time. It was found that the administration of vitamin E accelerated the normalizing trend of

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12

Yoshii, Tomomi, Saori Tsuzuki, Shunya Sakurai, et al. "N-Hydroxybenzimidazole as a structurally modifiable platform for N-oxyl radicals for direct C–H functionalization reactions." Chemical Science 11, no. 22 (2020): 5772–78. http://dx.doi.org/10.1039/d0sc02134b.

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13

Ames, James R., Michael D. Ryan, and Peter Kovacic. "Mechanism of antibacterial action: Electron transfer and oxy radicals." Journal of Free Radicals in Biology & Medicine 2, no. 5-6 (1986): 377–91. http://dx.doi.org/10.1016/s0748-5514(86)80040-x.

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14

Vogl, Georg, and Erich F. Elstner. "Diesel soot particles catalyze the production of oxy-radicals." Toxicology Letters 47, no. 1 (1989): 17–23. http://dx.doi.org/10.1016/0378-4274(89)90082-9.

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15

Zhang, Yong-Kang, and De-Kang Shen. "Synthesis of a Dihydroxy-Substituted Aminoxyl Spin Label and its Crown Ether and Cyclic Diester Derivatives." Zeitschrift für Naturforschung B 48, no. 4 (1993): 505–10. http://dx.doi.org/10.1515/znb-1993-0417.

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A novel dihydroxy-substituted aminoxyl spin label, 4-hydroxy-3-(3'-hydroxypropyl)-2,2,6,6-tetramethylpiperidine-1-oxy (5), has been prepared. From this aminoxyl radical, a spin-labeled crown ether, 16,16,18,18-tetramethyl-2,5,8,11-tetraoxa-17-azabicyclo[ 13,4,0]-nonadecane-17-oxy (12), and a spin-labeled cyclic diester, 16,16,18,18-tetramethyl-3,10-dioxo-2,5,8,11-tetraoxa-17-azabicyclo[13,4,o]nonadecane-17-oxy (13), have been acquired. Other four new stable aminoxyl radicals 8,9,10, and 11 have also been obtained within the synthetic approach. It has been demonstrated that the cyclic ether com

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16

Kosobutskii, V. S. "Structure and reactions of carbon-centered α-oxy(Oxo)Radicals". High Energy Chemistry 40, № 5 (2006): 277–95. http://dx.doi.org/10.1134/s0018143906050018.

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17

Pryor, W. A. "Oxy-Radicals and Related Species: Their Formation, Lifetimes, and Reactions." Annual Review of Physiology 48, no. 1 (1986): 657–67. http://dx.doi.org/10.1146/annurev.ph.48.030186.003301.

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18

Matthews, Donald P., and James R. McCarthy. "Addition of .alpha.-oxy radicals to 1-fluoro-1-phenylsulfonylethylene." Journal of Organic Chemistry 55, no. 9 (1990): 2973–75. http://dx.doi.org/10.1021/jo00296a081.

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19

BOLLI, R. "Role of oxy-radicals in postischemic myocardial dysfunction (?myocardial stunning?)." Journal of Molecular and Cellular Cardiology 20 (August 1988): S15. http://dx.doi.org/10.1016/0022-2828(88)91566-0.

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20

Li, Xiaoqing, Xiangsheng Xu, Zhi Wang, Xiaoyu Yan, Xiaoxue He та Xinhuan Yan. "Iminyl-Radical-Mediated Cyanoalkylarylation of Activated Alkenes Enabled by Silver-Catalyzed Decarboxylation of α-Imino Oxy Acids". Synlett 31, № 08 (2020): 809–12. http://dx.doi.org/10.1055/s-0039-1691595.

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An iminyl-radical-mediated cyanoalkylarylation of α,β-unsaturated imides with cyclic α-imino oxy acids leading to isoquinoline-1,3(2H,4H)-dione derivatives has been developed. The procedure involves the generation of iminyl radicals through silver-catalyzed oxidative decarboxylation, followed by a C–C bond cleavage, cyanoalkylation, and C–H-functionalization cascade.

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21

Ames, James R., Ulrich Hollstein, Anré R. Gagneux, Michael D. Ryan, and Peter Kovacic. "An integrated concept of amebicidal action: Electron transfer and oxy radicals." Free Radical Biology and Medicine 3, no. 2 (1987): 85–96. http://dx.doi.org/10.1016/s0891-5849(87)80002-3.

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22

Hinojosa, O., and T. J. Jacks. "Interference by Desferrioxamine of Spin Trapping Oxy-Radicals For ESR Analysis." Analytical Letters 19, no. 7-8 (1986): 725–33. http://dx.doi.org/10.1080/00032718608066258.

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23

Bhuyan, Durga K., and Kailash C. Bhuyan. "Oxy Radicals in the Eye Tissues of Rabbits After DiquatIn Vivo." Free Radical Research Communications 13, no. 1 (1991): 621–27. http://dx.doi.org/10.3109/10715769109145838.

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24

Ames, James R., Michael D. Ryan, and Peter Kovacic. "Mode of action of antiprotozoan agents. Electron transfer and oxy radicals." Life Sciences 41, no. 16 (1987): 1895–902. http://dx.doi.org/10.1016/0024-3205(87)90740-5.

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25

Lidon, Fernando Cebola, and Miguel Gouveia Teixeira. "Oxy radicals production and control in the chloroplast of Mn-treated rice." Plant Science 152, no. 1 (2000): 7–15. http://dx.doi.org/10.1016/s0168-9452(99)00179-x.

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26

UKAI, Mitsuko, Hiromi KAMEYA, Hideo NAKAMURA, and Yuhei SHIMOYAMA. "Radical Scavenging Activities of Plant Food of Alkyl-oxy and Superoxide Radicals." Food Science and Technology Research 15, no. 6 (2009): 619–24. http://dx.doi.org/10.3136/fstr.15.619.

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27

Giese, Bernd, Michel Bulliard, Joachim Dickhaut та ін. "1,2-Stereoinduction in β-Oxy-Radicals: The Influence of the α-Substituent". Synlett 1995, № 01 (1995): 116–18. http://dx.doi.org/10.1055/s-1995-4867.

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28

Das, U. N., K. V. Kumar, P. S. Prabha, B. V. R. Murthy, and P. Neela. "Oxy-radicals, lipid peroxides and essential fatty acids in patients with glomerular disorders." Prostaglandins, Leukotrienes and Essential Fatty Acids 49, no. 2 (1993): 603–7. http://dx.doi.org/10.1016/0952-3278(93)90167-u.

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29

El-Agamey, Ali, Ann Cantrell, Edward J. Land, David J. McGarvey, and T. George Truscott. "Are dietary carotenoids beneficial? Reactions of carotenoids with oxy-radicals and singlet oxygen." Photochemical & Photobiological Sciences 3, no. 8 (2004): 802. http://dx.doi.org/10.1039/b315651f.

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30

Mutsuda, Mitsuteru, and Hajime Komada. "Direct bonding between poly(oxy-2,6-dimethyl-1,4-phenylene) and rubber with radicals." Journal of Applied Polymer Science 95, no. 1 (2004): 53–59. http://dx.doi.org/10.1002/app.20803.

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31

Shimizu, Daiki, Juwon Oh, Ko Furukawa, Dongho Kim та Atsuhiro Osuka. "Triarylporphyrin meso-Oxy Radicals: Remarkable Chemical Stabilities and Oxidation to Oxophlorin π-Cations". Journal of the American Chemical Society 137, № 49 (2015): 15584–94. http://dx.doi.org/10.1021/jacs.5b11223.

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32

Rontani, J. F., and C. Aubert. "Effect of oxy-free radicals upon the phytyl chain during chlorophyll a photodegradation." Journal of Photochemistry and Photobiology A: Chemistry 79, no. 3 (1994): 167–72. http://dx.doi.org/10.1016/1010-6030(93)03762-6.

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33

Schönheit, Katrin, Ingolf E. Blasig, Bernd Ebert, Arpad Tosaki, and Hans Löwe. "Correlation between spin trapping of oxy-radicals and functional failure during myocardial reperfusion." Journal of Molecular and Cellular Cardiology 22 (May 1990): S47. http://dx.doi.org/10.1016/0022-2828(90)91670-3.

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34

Moufid, Nadira, Philippe Renaud, Carla Hassler, and Bernd Giese. "Efficient Control of the Stereoselectivity in Reactions of 2-Oxy-Substituted Benzylic Radicals." Helvetica Chimica Acta 78, no. 4 (1995): 1006–12. http://dx.doi.org/10.1002/hlca.19950780422.

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35

Zalma, Roger, Lionel Bonneau, Joëlle Guignard, Henri Pezerat, and Marie-Claude Jaurand. "Formation of oxy radicals by oxygen reduction arising from the surface activity of asbestos." Canadian Journal of Chemistry 65, no. 10 (1987): 2338–41. http://dx.doi.org/10.1139/v87-390.

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Formation of hydroxyl radicals, in relatively large quantities, by oxygen reduction due to the surface activity of asbestos in a cell-free system is demonstrated, using electron spin resonance and a spin trapping agent. The quantity of OH• produced (in general, above 1014 mg−1 for a Canadian chrysotile) is a function of activation or passivation of the electron donor surface sites of the minerals. The role of these radicals in oxidative stress in relation to the toxic properties of these minerals is discussed.

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36

Dorion, D., A. Zhong, C. Chiu, C. R. Forrest, B. Boyd, and C. Y. Pang. "Role of xanthine oxidase in reperfusion injury of ischemic skeletal muscles in the pig and human." Journal of Applied Physiology 75, no. 1 (1993): 246–55. http://dx.doi.org/10.1152/jappl.1993.75.1.246.

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We investigated whether xanthine oxidase (XO) is a major source of oxygen-derived free radicals (oxy-radicals) in the pig and human skeletal muscles. It was observed that xanthine dehydrogenase and XO activities in nonischemic pig latissimus dorsi (LD) and gracilis muscles and human LD and rectus abdominis (RA) muscles were < 0.5 mU/g wet wt. The pig LD muscle hypoxanthine content increased significantly from 0.33 +/- 0.02 to 2.33 +/- 0.44 mumol/g dry wt after 5 h of warm ischemia, but the muscle uric acid content remained unchanged up to 2 h of reperfusion. Similarly, the hypoxanthine cont

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37

Fontecave, Marc, Maryse Jaouen, Daniel Mansuy, Dominique Costa, Roger Zalma, and Henri Pezerat. "Microsomal lipid peroxidation and oxy-radicals formation are induced by insoluble iron-containing minerals." Biochemical and Biophysical Research Communications 173, no. 3 (1990): 912–18. http://dx.doi.org/10.1016/s0006-291x(05)80872-1.

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38

Deltch, Edwin A., William Bridges, Li Ma, Rodnay Berg, Robert Specian, and Nail Granger. "ROLE OF XANTHINE OXIDASE AND NEUTROPHIL GENERATED OXY-RADICALS IN SHOCK-INDUCED BACTERIAL TRANSLOCATION." Journal of Trauma: Injury, Infection, and Critical Care 29, no. 7 (1989): 1027. http://dx.doi.org/10.1097/00005373-198907000-00028.

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39

GIESE, B., M. BULLIARD, J. DICKHAUT та ін. "ChemInform Abstract: 1,2-Stereoinduction in β-Oxy-Radicals: The Influence of the . alpha.-Substituent." ChemInform 26, № 33 (2010): no. http://dx.doi.org/10.1002/chin.199533032.

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40

Tong Mak, I., Patricia Boeheme, and William B. Weglicki. "Ca-blockers reverse impaired enddothelial cell (EC) growth/survival due to OXY-radicals(R·)." Free Radical Biology and Medicine 15, no. 5 (1993): 514. http://dx.doi.org/10.1016/0891-5849(93)90349-y.

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41

Dong, Jianyang, Zhen Wang, Xiaochen Wang, Hongjian Song, Yuxiu Liu, and Qingmin Wang. "Ketones and aldehydes as alkyl radical equivalents for C─H functionalization of heteroarenes." Science Advances 5, no. 10 (2019): eaax9955. http://dx.doi.org/10.1126/sciadv.aax9955.

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The polar nature of the C═O bond commonly allows it to undergo direct attack by nucleophiles at the electrophilic carbon atom in which ketones and aldehydes act as alkyl carbocation equivalents. In contrast, transformations in which ketones and aldehydes act as alkyl radical equivalents (generated in carbonyl carbon) are unknown. Here, we describe a new catalytic activation mode that combines proton-coupled electron transfer (PCET) with spin-center shift (SCS) and enables C─H alkylation of heteroarenes using ketones and aldehydes as alkyl radical equivalents. This transformation proceeded via

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42

Wang, Xuebin, Gaofeng Dai, Gregory Yablonsk, Milan Vujanovic, and Richard Axelbaum. "A kinetic evaluation on no2 formation in the post-flame region of pressurized oxy-combustion process." Thermal Science, no. 00 (2020): 236. http://dx.doi.org/10.2298/tsci200415236w.

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Pressurized oxy-combustion is a promising technology that can significantly reduce the energy penalty associated with first generation oxy-combustion for CO2 capture in coal-fired power plants. However, higher pressure enhances the production of strong acid gases, including NO2 and SO3, aggravating the corrosion threat during flue gas recirculation. In the flame region, high temperature NOx exists mainly as NO, while conversion from NO to NO2 happened in post-flame region. In this study, the conversion of NO ? NO2 has been kinetically evaluated under representative post-flame conditions of pre

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43

Qu, Jinqing, Toru Katsumata, Masaharu Satoh, Jun Wada, and Toshio Masuda. "Poly(7-oxanorbornenes) carrying 2,2,6,6-tetramethylpiperidine-1-oxy (TEMPO) radicals: Synthesis and charge/discharge properties." Polymer 50, no. 2 (2009): 391–96. http://dx.doi.org/10.1016/j.polymer.2008.11.028.

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44

MOUFID, N., P. RENAUD, C. HASSLER, and B. GIESE. "ChemInform Abstract: Efficient Control of the Stereoselectivity in Reactions of 2-Oxy- Substituted Benzylic Radicals." ChemInform 26, no. 38 (2010): no. http://dx.doi.org/10.1002/chin.199538035.

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45

Janssen, Michiel H. A., Juan F. Chesa Castellana, Hayley Jackman, Peter J. Dunn, and Roger A. Sheldon. "Towards greener solvents for the bleach oxidation of alcohols catalysed by stable N-oxy radicals." Green Chemistry 13, no. 4 (2011): 905. http://dx.doi.org/10.1039/c0gc00684j.

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46

Rusvai, Erzsébet, Miklos Végh, Mihály Kramer, and István Horváth. "Hydroxylation of aniline mediated by heme-bound oxy-radicals in a heme peptide model system." Biochemical Pharmacology 37, no. 23 (1988): 4574–77. http://dx.doi.org/10.1016/0006-2952(88)90675-2.

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47

Vichnevetskaia, Klara D., and D. N. Roy. "Oxidative stress and antioxidative defense with an emphasis on plants antioxidants." Environmental Reviews 7, no. 1 (1999): 31–51. http://dx.doi.org/10.1139/a99-004.

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Increased levels of active oxygen species or free radicals can create an oxidative stress. Concentration of free radicals in living cells increases as a result of exposure to environmental stresses that lead to aging, carcinogenesis, and immunodeficiencies in animals, and membrane leakage, senescence, chlorophyll destruction, and decreased photosynthesis in plants. The antioxidative system of higher plants consists of enzymes, low molecular weight compounds (among them peptides, vitamins, flavonoids, phenolic acids, alkaloids, etc.), and integrated detoxification chains. Enzymatic defense in p

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48

Jiang, Heng, та Armido Studer. "Amidyl Radicals by Oxidation of α‐Amido‐oxy Acids: Transition‐Metal‐Free Amidofluorination of Unactivated Alkenes". Angewandte Chemie 130, № 33 (2018): 10867–71. http://dx.doi.org/10.1002/ange.201804966.

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49

Jiang, Heng, та Armido Studer. "Amidyl Radicals by Oxidation of α‐Amido‐oxy Acids: Transition‐Metal‐Free Amidofluorination of Unactivated Alkenes". Angewandte Chemie International Edition 57, № 33 (2018): 10707–11. http://dx.doi.org/10.1002/anie.201804966.

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50

Zhang, Yang, Bo Yang, Jie Gan, Changgeng Liu, Xi Shu, and Jinian Shu. "Nitration of particle-associated PAHs and their derivatives (nitro-, oxy-, and hydroxy-PAHs) with NO3 radicals." Atmospheric Environment 45, no. 15 (2011): 2515–21. http://dx.doi.org/10.1016/j.atmosenv.2011.02.034.

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