Статті в журналах з теми "Autoxidative reactions"
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Wolff, S. P., and R. T. Dean. "Glucose autoxidation and protein modification. The potential role of ‘autoxidative glycosylation’ in diabetes." Biochemical Journal 245, no. 1 (July 1, 1987): 243–50. http://dx.doi.org/10.1042/bj2450243.
Повний текст джерелаCilliers, Johannes J. L., and Vernon L. Singleton. "Nonenzymic Autoxidative Reactions of Caffeic Acid in Wine." American Journal of Enology and Viticulture 41, no. 1 (1990): 84–86. http://dx.doi.org/10.5344/ajev.1990.41.1.84.
Повний текст джерелаCilliers, Johannes J. L., and Vernon L. Singleton. "Nonenzymic autoxidative phenolic browning reactions in a caffeic acid model system." Journal of Agricultural and Food Chemistry 37, no. 4 (July 1989): 890–96. http://dx.doi.org/10.1021/jf00088a013.
Повний текст джерелаCilliers, Johannes J. L., and Vernon L. Singleton. "Characterization of the products of nonenzymic autoxidative phenolic reactions in a caffeic acid model system." Journal of Agricultural and Food Chemistry 39, no. 7 (July 1991): 1298–303. http://dx.doi.org/10.1021/jf00007a021.
Повний текст джерелаField, J. A., and G. Lettinga. "Treatment and Detoxification of Aqueous Spruce Bark Extracts by Aspergillus niger." Water Science and Technology 24, no. 3-4 (August 1, 1991): 127–37. http://dx.doi.org/10.2166/wst.1991.0469.
Повний текст джерелаBallesteros, Daniel, Hugh W. Pritchard, and Christina Walters. "Dry architecture: towards the understanding of the variation of longevity in desiccation-tolerant germplasm." Seed Science Research 30, no. 2 (June 2020): 142–55. http://dx.doi.org/10.1017/s0960258520000239.
Повний текст джерелаZeng, Meirong, Nadja Heine, and Kevin R. Wilson. "Evidence that Criegee intermediates drive autoxidation in unsaturated lipids." Proceedings of the National Academy of Sciences 117, no. 9 (February 18, 2020): 4486–90. http://dx.doi.org/10.1073/pnas.1920765117.
Повний текст джерелаVeselinović, Aleksandar, Ružica Nikolić, and Goran Nikolić. "Application of multivariate curve resolution-alternating least squares (MCR-ALS) for resolving pyrogallol autoxidation in weakly alkaline aqueous solutions." Open Chemistry 10, no. 6 (December 1, 2012): 1942–48. http://dx.doi.org/10.2478/s11532-012-0125-z.
Повний текст джерелаGriesser, Markus, Jean-Philippe R. Chauvin, and Derek A. Pratt. "The hydrogen atom transfer reactivity of sulfinic acids." Chemical Science 9, no. 36 (2018): 7218–29. http://dx.doi.org/10.1039/c8sc02400f.
Повний текст джерелаXu, Ruochong, Joel A. Thornton, Ben H. Lee, Yanxu Zhang, Lyatt Jaeglé, Felipe D. Lopez-Hilfiker, Pekka Rantala, and Tuukka Petäjä. "Global simulations of monoterpene-derived peroxy radical fates and the distributions of highly oxygenated organic molecules (HOMs) and accretion products." Atmospheric Chemistry and Physics 22, no. 8 (April 26, 2022): 5477–94. http://dx.doi.org/10.5194/acp-22-5477-2022.
Повний текст джерелаXu, Ruochong, Joel A. Thornton, Ben H. Lee, Yanxu Zhang, Lyatt Jaeglé, Felipe D. Lopez-Hilfiker, Pekka Rantala, and Tuukka Petäjä. "Global simulations of monoterpene-derived peroxy radical fates and the distributions of highly oxygenated organic molecules (HOMs) and accretion products." Atmospheric Chemistry and Physics 22, no. 8 (April 26, 2022): 5477–94. http://dx.doi.org/10.5194/acp-22-5477-2022.
Повний текст джерелаGuillén, Francisco, Carmen Muñoz, Víctor Gómez-Toribio, Angel T. Martínez, and María Jesús Martínez. "Oxygen Activation during Oxidation of Methoxyhydroquinones by Laccase from Pleurotus eryngii." Applied and Environmental Microbiology 66, no. 1 (January 1, 2000): 170–75. http://dx.doi.org/10.1128/aem.66.1.170-175.2000.
Повний текст джерелаSchervish, Meredith, and Neil M. Donahue. "Peroxy radical chemistry and the volatility basis set." Atmospheric Chemistry and Physics 20, no. 2 (January 31, 2020): 1183–99. http://dx.doi.org/10.5194/acp-20-1183-2020.
Повний текст джерелаOrdoñez, I. D., and E. Cadenas. "Thiol oxidation coupled to DT-diaphorase-catalysed reduction of diaziquone. Reductive and oxidative pathways of diaziquone semiquinone modulated by glutathione and superoxide dismutase." Biochemical Journal 286, no. 2 (September 1, 1992): 481–90. http://dx.doi.org/10.1042/bj2860481.
Повний текст джерелаPraske, Eric, Rasmus V. Otkjær, John D. Crounse, J. Caleb Hethcox, Brian M. Stoltz, Henrik G. Kjaergaard, and Paul O. Wennberg. "Atmospheric autoxidation is increasingly important in urban and suburban North America." Proceedings of the National Academy of Sciences 115, no. 1 (December 18, 2017): 64–69. http://dx.doi.org/10.1073/pnas.1715540115.
Повний текст джерелаFábián, István, and Gábor Lente. "Light-induced multistep redox reactions: The diode-array spectrophotometer as a photoreactor." Pure and Applied Chemistry 82, no. 10 (June 23, 2010): 1957–73. http://dx.doi.org/10.1351/pac-con-09-11-16.
Повний текст джерелаLimpanuparb, Taweetham, Pakpong Roongruangsree, and Cherprang Areekul. "A DFT investigation of the blue bottle experiment: E ∘ half-cell analysis of autoxidation catalysed by redox indicators." Royal Society Open Science 4, no. 11 (November 2017): 170708. http://dx.doi.org/10.1098/rsos.170708.
Повний текст джерелаMilano, Francesco, Marco Lopresti, Danilo Vona, Gabrielle Buscemi, Mariangela Cantore, Gianluca M. Farinola, and Massimo Trotta. "Activity of photosynthetic Reaction Centers coated with polydopamine." MRS Advances 5, no. 45 (2020): 2299–307. http://dx.doi.org/10.1557/adv.2020.275.
Повний текст джерелаEndalew, Abebe K., and Yohannes Kiros. "Catalytic Autoxidation of Fatty Acid Methyl Esters from Jatropha Oil." Journal of Fuels 2014 (October 16, 2014): 1–6. http://dx.doi.org/10.1155/2014/470790.
Повний текст джерелаRichters, Stefanie, Hartmut Herrmann та Torsten Berndt. "Different pathways of the formation of highly oxidized multifunctional organic compounds (HOMs) from the gas-phase ozonolysis of <i>β</i>-caryophyllene". Atmospheric Chemistry and Physics 16, № 15 (4 серпня 2016): 9831–45. http://dx.doi.org/10.5194/acp-16-9831-2016.
Повний текст джерелаMillington, Keith R., Michael J. Jones, Siti Farhana Zakaria, and George Maurdev. "Using Chemiluminescence to Study the Photodegradation of Materials." Materials Science Forum 654-656 (June 2010): 2414–17. http://dx.doi.org/10.4028/www.scientific.net/msf.654-656.2414.
Повний текст джерелаHassanein, Mahmoud T., Shady S. Gerges, Mohamed A. Abdo, and Sahar H. El-Khalafy. "Studies on the oxidation of 2,6-di-tert-butylphenol by molecular oxygen catalyzed by cobalt(II) tetraarylporphyrins bound to cationic latex." Journal of Porphyrins and Phthalocyanines 09, no. 09 (September 2005): 621–25. http://dx.doi.org/10.1142/s1088424605000721.
Повний текст джерелаRissanen, Matti P., Jyri Mikkilä, Siddharth Iyer, and Jani Hakala. "Multi-scheme chemical ionization inlet (MION) for fast switching of reagent ion chemistry in atmospheric pressure chemical ionization mass spectrometry (CIMS) applications." Atmospheric Measurement Techniques 12, no. 12 (December 17, 2019): 6635–46. http://dx.doi.org/10.5194/amt-12-6635-2019.
Повний текст джерелаJankovic, Ivana, and Ljubica Josimovic. "Autoxidation of tryptophan in aqueous solutions." Journal of the Serbian Chemical Society 66, no. 9 (2001): 571–80. http://dx.doi.org/10.2298/jsc0109571j.
Повний текст джерелаSiddiquee, Muhammad N., and Arno de Klerk. "Heterocyclic Addition Reactions during Low Temperature Autoxidation." Energy & Fuels 29, no. 7 (June 22, 2015): 4236–44. http://dx.doi.org/10.1021/acs.energyfuels.5b00767.
Повний текст джерелаMiller, D. "Transition metals as catalysts of “autoxidation” reactions." Free Radical Biology and Medicine 8, no. 1 (1990): 95–108. http://dx.doi.org/10.1016/0891-5849(90)90148-c.
Повний текст джерелаRudziński, Krzysztof J., and Rafał Szmigielski. "Aqueous Reactions of Sulfate Radical-Anions with Nitrophenols in Atmospheric Context." Atmosphere 10, no. 12 (December 9, 2019): 795. http://dx.doi.org/10.3390/atmos10120795.
Повний текст джерелаZhang, Shi-Nan, Zhong-Hua Xue, Xiu Lin, Yun-Xiao Lin, Hui Su, Shin-Ichi Hirano, Xin-Hao Li, and Jie-Sheng Chen. "Autoxidation of polythiophene tethered to carbon cloth boosts its electrocatalytic activity towards durable water oxidation." Journal of Materials Chemistry A 8, no. 38 (2020): 19793–98. http://dx.doi.org/10.1039/d0ta06368a.
Повний текст джерелаRudziński, K. J., L. Gmachowski, and I. Kuznietsova. "Isoprene, sulphoxy radical-anions and acidity." Atmospheric Chemistry and Physics Discussions 8, no. 6 (December 12, 2008): 20869–900. http://dx.doi.org/10.5194/acpd-8-20869-2008.
Повний текст джерелаZhang, Qing-An, Xi Wang, Yun Song, Xue-Hui Fan, and Juan Francisco García Martín. "Optimization of Pyrogallol Autoxidation Conditions and Its Application in Evaluation of Superoxide Anion Radical Scavenging Capacity for Four Antioxidants." Journal of AOAC INTERNATIONAL 99, no. 2 (March 1, 2016): 504–11. http://dx.doi.org/10.5740/jaoacint.15-0223.
Повний текст джерелаKazin, Vyacheslav N., Evgenii A. Guzov, Valentina A. Moshareva, and Evgenii M. Pliss. "Influence of a Constant Magnetic Field on the Mechanism of Adrenaline Oxidation." Magnetochemistry 8, no. 7 (July 1, 2022): 70. http://dx.doi.org/10.3390/magnetochemistry8070070.
Повний текст джерелаNohl, H., L. Gille, and K. Staniek. "The Exogenous NADH Dehydrogenase of Heart Mitochondria Is the Key Enzyme Responsible for Selective Cardiotoxicity of Anthracyclines." Zeitschrift für Naturforschung C 53, no. 3-4 (April 1, 1998): 279–85. http://dx.doi.org/10.1515/znc-1998-3-419.
Повний текст джерелаWolff, S. P., and M. J. C. Crabbe. "Low apparent aldose reductase activity produced by monosaccharide autoxidation." Biochemical Journal 226, no. 3 (March 15, 1985): 625–30. http://dx.doi.org/10.1042/bj2260625.
Повний текст джерелаWang, Yuwei, Archit Mehra, Jordan E. Krechmer, Gan Yang, Xiaoyu Hu, Yiqun Lu, Andrew Lambe, et al. "Oxygenated products formed from OH-initiated reactions of trimethylbenzene: autoxidation and accretion." Atmospheric Chemistry and Physics 20, no. 15 (August 14, 2020): 9563–79. http://dx.doi.org/10.5194/acp-20-9563-2020.
Повний текст джерелаMorishita, Y., S. Murata, and S. Sunada. "Studies On An Aerobic Oxidation Of Dibenzothiophene And Related Compounds Using Ruthenium Catalyst." Archives of Metallurgy and Materials 60, no. 2 (June 1, 2015): 1015–16. http://dx.doi.org/10.1515/amm-2015-0252.
Повний текст джерелаIyer, Jayant, Isha Saraf, Andrew Ray, Michael Brunsteiner, and Amrit Paudel. "Assessment of Diverse Solid−State Accelerated Autoxidation Methods for Droperidol." Pharmaceutics 14, no. 6 (May 24, 2022): 1114. http://dx.doi.org/10.3390/pharmaceutics14061114.
Повний текст джерелаKamińska, Adrianna, Nikola Maciejewska, Piotr Miądlicki, Karolina Kiełbasa, Joanna Sreńscek-Nazzal та Beata Michalkiewicz. "Fe-modified activated carbon obtained from biomass as a catalyst for α-pinene autoxidation". Polish Journal of Chemical Technology 23, № 2 (1 червня 2021): 73–80. http://dx.doi.org/10.2478/pjct-2021-0020.
Повний текст джерелаPostlethwait, Edward M., Rafael Cueto, Leonard W. Velsor, and William A. Pryor. "O3-induced formation of bioactive lipids: estimated surface concentrations and lining layer effects." American Journal of Physiology-Lung Cellular and Molecular Physiology 274, no. 6 (June 1, 1998): L1006—L1016. http://dx.doi.org/10.1152/ajplung.1998.274.6.l1006.
Повний текст джерелаDEAN, Roger T., Shanlin FU, Roland STOCKER, and Michael J. DAVIES. "Biochemistry and pathology of radical-mediated protein oxidation." Biochemical Journal 324, no. 1 (May 15, 1997): 1–18. http://dx.doi.org/10.1042/bj3240001.
Повний текст джерелаPeres, Matheus R., Vanessa R. Miranda, Aguinaldo R. Robinson De Souza, Nelson H. Morgon, and Valdecir F. Ximenes. "Autoxidation of melatonin at excited state: mechanism proposal for formation of N1-acetyl-N2-formyl-5-methoxykynuramine." Melatonin Research 5, no. 3 (September 30, 2022): 325–34. http://dx.doi.org/10.32794/mr112500135.
Повний текст джерелаStrader, Michael Brad, Rachel Bangle, Claire J. Parker Siburt, Cornelius L. Varnado, Jayashree Soman, Andres S. Benitez Cardenas, Premila P. Samuel та ін. "Engineering oxidative stability in human hemoglobin based on the Hb providence (βK82D) mutation and genetic cross-linking". Biochemical Journal 474, № 24 (11 грудня 2017): 4171–92. http://dx.doi.org/10.1042/bcj20170491.
Повний текст джерелаSlavíková, Barbora, Alexander Kasal та Miloš Buděšínský. "Autoxidation vs Hydrolysis in 16α-Acyloxy Steroids". Collection of Czechoslovak Chemical Communications 64, № 7 (1999): 1125–34. http://dx.doi.org/10.1135/cccc19991125.
Повний текст джерелаKrazinski, J. L., S. P. Vanka, J. A. Pearce, and W. M. Roquemore. "A Computational Fluid Dynamics and Chemistry Model for Jet Fuel Thermal Stability." Journal of Engineering for Gas Turbines and Power 114, no. 1 (January 1, 1992): 104–10. http://dx.doi.org/10.1115/1.2906291.
Повний текст джерелаBarclay, Lawrence Ross Coates, Steven Jeffrey Locke, and Joseph Mark MacNeil. "Autoxidation in micelles. Synergism of vitamin C with lipid-soluble vitamin E and water-soluble Trolox." Canadian Journal of Chemistry 63, no. 2 (February 1, 1985): 366–74. http://dx.doi.org/10.1139/v85-062.
Повний текст джерелаShahidi, Fereidoon, and Abul Hossain. "Role of Lipids in Food Flavor Generation." Molecules 27, no. 15 (August 6, 2022): 5014. http://dx.doi.org/10.3390/molecules27155014.
Повний текст джерелаNivinskas, H., R. L. Koder, Z. Anusevicius, J. Sarlauskas, A. F. Miller, and N. Cenas. "Two-electron reduction of nitroaromatic compounds by Enterobacter cloacae NAD(P)H nitroreductase: description of quantitative structure-activity relationships." Acta Biochimica Polonica 47, no. 4 (December 31, 2000): 941–49. http://dx.doi.org/10.18388/abp.2000_3949.
Повний текст джерелаLissel, Manfred. "Reaktionen mit Kaliumsuperoxid 3 [1] Über den Mechanismus der Ketonspaltung durch KO2 / Reactions with Potassium Superoxide 3 [1] On the Mechanism of the Cleavage of Ketones by KO2." Zeitschrift für Naturforschung B 42, no. 1 (January 1, 1987): 12–14. http://dx.doi.org/10.1515/znb-1987-0104.
Повний текст джерелаChen, Hauh-Jyun Candy, and Fung-Lung Chung. "Formation of Etheno Adducts in Reactions of Enals via Autoxidation." Chemical Research in Toxicology 7, no. 6 (November 1994): 857–60. http://dx.doi.org/10.1021/tx00042a021.
Повний текст джерелаSiddiquee, Muhammad N., and Arno de Klerk. "Hydrocarbon Addition Reactions during Low-Temperature Autoxidation of Oilsands Bitumen." Energy & Fuels 28, no. 11 (October 16, 2014): 6848–59. http://dx.doi.org/10.1021/ef501694s.
Повний текст джерелаTajima, G., and K. Shikama. "Autoxidation of oxymyoglobin. An overall stoichiometry including subsequent side reactions." Journal of Biological Chemistry 262, no. 26 (September 1987): 12603–6. http://dx.doi.org/10.1016/s0021-9258(18)45248-9.
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