[1] Yin H, Xu L, Porter N A. Free radical lipid peroxidation: Mechanisms and analysis[J].Chem Rev, 2011,111: 5944-5972
[2] Niki E. Lipid peroxidation: physiological levels and dual biological effects[J].Free Radic Biol Med, 2009, 47: 469-484
[3] Halliwell B, Gutteridge J. Free Radicals in Biology and Medicine[M]. Oxford University Press, 2007
[4] Blair I A. DNA adducts with lipid peroxidation products[J].J Biol Chem, 2008, 283: 15545-15549
[5] Lee S H, Oe T, Blair I A. Vitamin C-induced decomposition of lipid hydroperoxides to endogenous genotoxins[J].Science, 2001, 292: 2083-2086
[6] Qian S Y, Yue G H, Tomer K B, et al. Identification of all classes of spin-trapped carbon-centered radicals in soybean lipoxygenase-dependent lipid peroxidations of omega-6 polyunsaturated fatty acids via LC/ESR, LC/MS, and tandem MS[J].Free Radic Biol Med, 2003, 34: 1017-1028
[7] Iwahashi H, Hirai T, Kumamoto K. High performance liquid chromatography/electron spin resonance/mass spectrometry analyses of radicals formed in an anaerobic reaction of 9- (or 13-) hydroperoxide octadecadienoic acids with ferrous ions[J].J Chromatogr A, 2006, 1132: 67-75
[8] Spiteller P, Kern W, Reiner J, et al. Aldehydic lipid peroxidation products derived from linoleic acid[J].Biochimica. et. Biophysica. Acta. (BBA)-Mol. Cell Biol Lipids, 2001, 1531: 188-208
[9] Schneider C, Porter N A, Brash A R. Routes to 4-hydroxynonenal: Fundamental issues in the mechanisms of lipid peroxidation[J].J Biol Chem, 2008, 283: 15539-15543
[10] Bolton J L, Trush M A, Penning T M, et al. Role of quinones in toxicology[J].Chem Res Toxicol, 2000, 13: 135-160
[11] Song Y, Wagner B A, Witmer J R, et al. Nonenzymatic displacement of chlorine and formation of free radicals upon the reaction of glutathione with PCB quinones[J].Proc Natl Acad Sci USA, 2009, 106: 9725-9730
[12] Zhu B Z, Shan G Q. Potential mechanism for pentachlorophenol-induced carcinogenicity: A novel mechanism for metal-independent production of hydroxyl radicals[J].Chem Res Toxicol, 2009, 22: 969-977
[13] Meunier B. Chemistry. Catalytic degradation of chlorinated phenols[J].Science, 2002, 296: 270-271
[14] Gupta S S, Stadler M, Noser C A, et al. Rapid total destruction of chlorophenols by activated hydrogen peroxide[J].Science, 2002, 296: 326-328
[15] Sorokin A, Meunier B, Seris J L. Efficient oxidative dechlorination and aromatic ring cleavage of chlorinated phenols catalyzed by iron sulfophthalocyanine[J].Science, 1995, 268: 1163-1166
[16] Zhao Y, Qin F, Boyd J M, et al. Characterization and determination of chloro- and bromo-benzoquinones as new chlorination disinfection byproducts in drinking water[J].Anal Chem, 2010, 82: 4599-4605
[17] Qin F, Zhao Y Y, Zhao Y, et al. A toxic disinfection by-product, 2,6-dichloro-1,4-benzoquinone, identified in drinking water[J].Angew Chem Int Ed, 2010, 49: 790-792
[18] Zhu B Z, Zhao H T, Kalyanaraman B, et al. Mechanism of metal-independent decomposition of organic hydroperoxides and formation of alkoxyl radicals by halogenated quinones[J].Proc Natl Acad Sci USA, 2007, 104: 3698-3702
[19] Zhu B Z, Shan G Q, Huang C H, et al. Metal-independent decomposition of hydroperoxides by halogenated quinones: Detection and identification of a quinone ketoxy radical[J].Proc Natl Acad Sci USA, 2009, 106: 11466-11471
[20] Zhu B Z, Zhao H T, Kalyanaraman B, et al. Metal-independent production of hydroxyl radicals by halogenated quinones and hydrogen peroxide: an ESR spin trapping study[J].Free Radic Biol Med, 2002, 32: 465-473
[21] Zhu B Z, Kalyanaraman B, Jiang G B. Molecular mechanism for metal-independent production of hydroxyl radicals by hydrogen peroxide and halogenated quinones[J].Proc Natl Acad Sci USA, 2007, 104: 17575-17578
[22] Zhu B Z, Zhu J G, Mao L, et al. Detoxifying carcinogenic polyhalogenated quinones by hydroxamic acids via an unusual double Lossen rearrangement mechanism[J].Proc Natl Acad Sci USA, 2010, 107: 20686-20690
[23] Zhu B Z, Mao L, Huang C H, et al. Unprecedented hydroxyl radical-dependent two-step chemiluminescence production by polyhalogenated quinoid carcinogens and H2O2[J].Proc Natl Acad Sci USA, 2012, 109: 16046-16051
[24] Qin H, Huang C H, Shan G Q, et al. Molecular mechanism of metal-independent decomposition of lipid hydroperoxide 13-HPODE by halogenated quinoid carcinogens[J].Free Radic Biol Med, 2013, 63: 459-466
[25] Petersen D R, Doorn J A. Reactions of 4-hydroxynonenal with proteins and cellular targets[J].Free Radic Biol Med, 2004, 37: 937-945
[26] Awasthi Y C, Sharma R, Sharma A, et al. Self-regulatory role of 4-hydroxynonenal in signaling for stress-induced programmed cell death[J].Free Radic Biol Med, 2008, 45: 111-118