نتایج جستجو برای: radical trapping

تعداد نتایج: 111787  

Journal: :The Journal of biological chemistry 1987
B G Taffe N Takahashi T W Kensler R P Mason

The organic hydroperoxides tert-butyl hydroperoxide and cumene hydroperoxide are tumor promoters in the skin of SENCAR mice, and this activity is presumed to be mediated through the activation of the hydroperoxides to free radical species. In this study we have assessed the generation of free radicals from organic hydroperoxides in the target cell (the murine basal keratinocyte) using electron ...

Journal: :Beilstein Journal of Organic Chemistry 2008
Hélio A Stefani Rafael C Guadagnin Artur F Keppler Giancarlo V Botteselle João V Comasseto Carlos A Suganuma

Through direct transmetalation reaction of Z-vinylic tellurides with nBuLi was observed the unexpected isomerization of double bonds leading to potassium E-vinyltrifluoroborates salts in low to moderate yields. Using EPR spin trapping experiments the radical species that promoted the stereoinversion of Z-vinylic organometallic species during the preparation of potassium vinyltrifluoroborate sal...

Journal: :Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 2013
Seiko Nakagawa

The reaction of the hydroxy radical with thymidine and poly-hydroxy benzenes; i.e., catechol, resorcinol, hydroquinone, and pyrogallol, was studied by ESR spin trapping combined with the UV-A photolysis of hydrogen peroxide. The obtained relative reaction rates reasonably agreed with those previously obtained by pulse radiolysis. Electron distribution in the HOMO obtained by DFT calculations al...

2014
Nicholas A. White Tomislav Rovis

A novel oxidative N-heterocyclic carbene-catalyzed reaction pathway has been discovered. Alkyl and aryl enals undergo β-hydroxylation via oxygen atom transfer from electron-deficient nitrobenzenes, followed by trapping of the resultant acyl azolium by the solvent. The proposed mechanism involves a single electron transfer event to initiate the reaction followed by radical recombination. This re...

2017
Guo-Xing Li Cristian A. Morales-Rivera Fang Gao Yaxin Wang Gang He Peng Liu Gong Chen

We report a unified photoredox-catalysis strategy for both hydroxylation and amidation of tertiary and benzylic C–H bonds. Use of hydroxyl perfluorobenziodoxole (PFBl–OH) oxidant is critical for efficient tertiary C–H functionalization, likely due to the enhanced electrophilicity of the benziodoxole radical. Benzylic methylene C–H bonds can be hydroxylated or amidated using unmodified hydroxyl ...

Journal: :The Journal of biological chemistry 2005
Dario C Ramirez Sandra E Gomez Mejiba Ronald P Mason

It is well known that hydrogen peroxide (H2O2)-induced copper-catalyzed fragmentation of proteins follows a site-specific oxidative mechanism mediated by hydroxyl radical-like species (i.e. Cu(I)O, Cu(II)/*OH or Cu(III)) that ends in increased carbonyl formation and protein fragmentation. We have found that the nitrone spin trap DMPO (5,5-dimethyl-1-pyrroline N-oxide) prevented such processes b...

2010
Kalina Ranguelova Marcelo G. Bonini Ronald P. Mason

BACKGROUND Sulfur dioxide, formed during the combustion of fossil fuels, is a major air pollutant near large cities. Its two ionized forms in aqueous solution, sulfite and (bi)sulfite, are widely used as preservatives and antioxidants to prevent food and beverage spoilage. (Bi)sulfite can be oxidized by peroxidases to form the very reactive sulfur trioxide anion radical (*SO(3)-). This free rad...

Journal: :Journal of the American Chemical Society 2004
Melanie A O'Neill Chikara Dohno Jacqueline K Barton

Photoexcited 2-aminopurine (Ap*) is extensively exploited as a fluorescent base analogue in the study of DNA structure and dynamics. Quenching of Ap* in DNA is often attributed to stacking interactions between Ap* and DNA bases, despite compelling evidence indicating that charge transfer (CT) between Ap* and DNA bases contributes to quenching. Here we present direct chemical evidence that Ap* u...

Journal: :Angewandte Chemie 2021

Efforts to generate organomanganese reagents under ball-milling conditions have led the serendipitous discovery that manganese metal can mediate reductive dimerization of arylidene malonates. The newly uncovered process has been optimized and its mechanism explored using CV measurements, radical trapping experiments, EPR spectroscopy, solution control reactions. This unique reactivity also be t...

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