Relevant bibliographies by topics / Oxy-radicals

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Oxy-radicals'

Author: Grafiati
Published: 4 June 2021
Last updated: 9 February 2022

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Journal articles on the topic "Oxy-radicals"

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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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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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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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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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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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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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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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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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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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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Dissertations / Theses on the topic "Oxy-radicals"

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Tinkler, Jane Heather. "The excited states and radical ions of the carotenoids." Thesis, Keele University, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.295804.

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Lescic, Sergiu. "Etude théorique du mécanisme de décomposition d'adduits de spin issus du piégeage de radicaux alkylperoxyle par des N-oxy-pyrrolines." Thesis, Aix-Marseille, 2015. http://www.theses.fr/2015AIXM4752.

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A l'aide de la spectroscopie par Résonance Paramagnétique Électronique (RPE), la détection des certaines espèces radicalaires à très faible durée de vie se fait par la méthode du spin-trapping. Cette technique permet de caractériser ces radicaux “libres” en les piégeant à l'aide d'une molécule diamagnétique (nitrone) pour donner naissance à une espèce paramagnétique persistante (adduit de spin), ayant un spectre RPE caractéristique du radical piégé. Le temps de demi-vie d'un adduit du spin est fortement corrélé à la nature de la nitrone et du radical piégé (alkyle, alc
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3

Moreno, Ruben Gregorio Moreno. "Estudos de lesão ao DNA promovida pela autoxidação de S(IV) na presença de complexos de Cu(III)/tetraglicina. Efeito sinérgico de Ni(II), Co(II) e Mn(II)." Universidade de São Paulo, 2005. http://www.teses.usp.br/teses/disponiveis/46/46133/tde-04062007-032229/.

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O presente trabalho apresenta estudos de lesão em biomoléculas (DNA e 2\'-deoxiguanosina) induzida por Cu(III)/tetraglicina (Cu(III)/G4), radicais de óxidos de enxofre (SO3·-, SO4·-, SO5·-), HO· e HSO5-, espécies estas geradas durante a autoxidação de S(IV) na presença de Cu(II)/G4 ou Cu(II) (ausência de tetraglicina) e traços de um segundo íon metálico (Ni(II), Co(II) ou Mn(II)). A formação dos radicais SO3·- e HO· foi detectada pela técnica de ressonância paramagnética eletrônica (EPR). As técnicas de espectrofotometria e dicroísmo circular foram emp
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Books on the topic "Oxy-radicals"

1

Thomas, Barry C. The role of oxy-radicals in polysaccharide degradation. University of Salford, 1987.

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2

Cerutti. Oxy-radicals Molecular Bio & Path (Ucla Symposia on Molecular and Cellular Biology, Vol 82). WILEY-LISS, 1988.

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3

A, Cerutti Peter, Fridovich Irwin, McCord Joe M, Upjohn Company, University of California, Los Angeles., and Upjohn-UCLA Symposium on Oxy-Radicals in Molecular Biology and Pathology (1988 : Park City, Utah), eds. Oxy-radicals in molecular biology and pathology: Proceedings of an Upjohn-UCLA symposium, held at Park City, Utah, January 24-30, 1988. A.R. Liss, 1988.

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Book chapters on the topic "Oxy-radicals"

1

Jovanovic, Slobodan V., and Michael G. Simic. "Redox Properties of Oxy and Antioxidant Radicals." In Oxygen Radicals in Biology and Medicine. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-5568-7_16.

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Bolli, Roberto, and Robert Roberts. "Role of Oxy-Radicals in Postischemic Myocardial Dysfunction." In Oxygen Radicals in the Pathophysiology of Heart Disease. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-1743-2_14.

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3

Galeotti, T., S. Borrello, M. E. De Leo, and L. Masotti. "The Involvement of Oxy-Radicals in Cancer Cell Killing and Growth." In Free Radicals: from Basic Science to Medicine. Birkhäuser Basel, 1993. http://dx.doi.org/10.1007/978-3-0348-9116-5_19.

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Witz, G., B. Czerniecki, S. C. Gad, and Bernard D. Goldstein. "In Vivo Stimulation of Oxy Radicals by Mouse Skin Tumor Promoters." In Anticarcinogenesis and Radiation Protection. Springer US, 1987. http://dx.doi.org/10.1007/978-1-4615-6462-1_31.

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Thomas, James A., and Eun-Mi Park. "Oxy Radical-Initiated Protein S-Thiolation and Enzymic Dethiolation." In Oxygen Radicals in Biology and Medicine. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-5568-7_56.

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Yoshikawa, Toshikazu. "[71] Oxy radicals in endotoxin shock." In Oxygen Radicals in Biological Systems Part B: Oxygen Radicals and Antioxidants. Elsevier, 1990. http://dx.doi.org/10.1016/0076-6879(90)86163-p.

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Yoshikawa, Toshikazu. "[70] Oxy radicals in disseminated intravascular coagulation." In Oxygen Radicals in Biological Systems Part B: Oxygen Radicals and Antioxidants. Elsevier, 1990. http://dx.doi.org/10.1016/0076-6879(90)86162-o.

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8

Taber, Douglass F. "Oxidation of Organic Functional Groups." In Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0008.

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Cancheng Guo of Hunan University devised (J. Org. Chem. 2014, 79, 2709) con­ditions for the oxidative cleavage of an alkyne 1 to the esters 2 and 3. Hirokazu Arimoto of Tohoku University found (Chem. Commun. 2014, 50, 2758) that IBX oxidized a primary alcohol 4 to the acid 5 one carbon shorter. David Milstein of the Weizmann Institute of Science uncovered (J. Am. Chem. Soc. 2014, 136, 2998) condi­tions for the direct oxidation of the cyclic amine 6 to the lactam 7, with concomitant evolution of H₂. Cyclic ene sulfonamides such as 9 are versatile synthetic intermediates. Henri Doucet of the Université de Rennes reported (Adv. Synth. Catal. 2014, 356, 119) the regioselective conversion of 8 to 9. In this case, the oxidizing agent was the organo-PdBr intermediate. There have been many reports of the functionalization of the oxygenated carbons of cyclic ethers, as exemplified by the conversion of 10 to 11, observed (J. Org. Chem. 2014, 79, 3847) by Jianlin Han of Nanjing University. If these methods were regiose­lective with an acyclic benzyl ether, this could be a new method for the removal of that common protecting group. Jianliang Xiao of the University of Liverpool described (J. Am. Chem. Soc. 2014, 136, 8350) a selective benzylic ether oxidation that converted 12 to 13. Baris Temelli of Hacettepe University effected (Synthesis 2014, 46, 1407) the conversion of a primary nitro compound 14 into the corresponding nitrile 15. Jean- Michel Vatèle of Université Lyon 1 oxidized (Synlett 2014, 25, 1275) the primary alcohol 16 to the nitrile 17. Many methods have been put forward for the oxidation of primary alcohols to alde­hydes and secondary alcohols to ketones. Piperidinium oxy radicals such as TEMPO are widely used to catalyze this transformation. Yoshikazu Kimura of Iharanikkei Chemical Industry Co. Ltd. established (Synlett 2014, 25, 596) a manufacturing proc­ess for crystalline NaOCl•5H₂O that served as the bulk oxidant for the conversion of 18 to 19. Neither a ketone nor an aldehyde was chlorinated under the reaction condi­tions. Yoshiharu Iwabuchi of Tohoku University showed (Angew. Chem. Int. Ed. 2014, 53, 3236) that with his piperidinium oxy radical AZADO and Cu catalysis, air could be the bulk oxidant for the otherwise difficult conversion of the amino alcohol 20 to the amino ketone 21.
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Wagner, J. R., J. E. Van Lier, C. Decarroz, M. Berger, and J. Cadet. "[52] Photodynarnic methods for oxy radical-induced DNA damage." In Oxygen Radicals in Biological Systems Part B: Oxygen Radicals and Antioxidants. Elsevier, 1990. http://dx.doi.org/10.1016/0076-6879(90)86144-k.

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Conference papers on the topic "Oxy-radicals"

1

Karra, Shashank K., and Sourabh V. Apte. "Numerical Investigation of High-Speed Oxy-Fuel Pulsed Detonation for Direct Power Extraction." In ASME 2020 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2020. http://dx.doi.org/10.1115/imece2020-23989.

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Abstract Oxy-fuel based pulse detonation system can be used for direct power extraction when combined with magnetohydrodynamics (MHD). A space-time conservation element solution element (CE/SE) method is used to investigate the operational envelope of oxy-coal detonations with gaseous methane as a surrogate fuel. The CE/SE method results in a consistent multidimensional formulation for structured/unstructured meshes by providing flux conservation in space and time without the need for complex Riemann solvers to capture solution discontinuities. A modified revised Jones-Lindstedt (JL-R) reactio
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