Formation of Three-electron Bonds in One-electron Oxidized Methionine Dipeptides: A Pulse Radiolytic Study
Author:
Publisher
Informa UK Limited
Subject
General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1080/09553008714551561
Reference13 articles.
1. S∴N and S∴O three-electron-bonded radicals and radical cations in aqueous solutions
2. Electron spin resonance studies. Part 64. The hydroxyl radical-induced decarboxylation of methionine and some related compounds
3. Reactivity of the hydroxyl radical in aqueous solutions
4. Pulse radiolysis generation of sulfur radical cations stabilized by neighboring carboxylate and alcohol groups
5. Formation and reduction reactions of .alpha.-amino radicals derived from methionine and its derivatives in aqueous solutions
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2. Oxidation studies of a novel peptide model N-acetyl-3-(methylthio)propylamine;Journal of Photochemistry and Photobiology A: Chemistry;2017-03
3. Formation of a Three-Electron Sulfur–Sulfur Bond as a Probe for Interaction between Side Chains of Methionine Residues;The Journal of Physical Chemistry B;2016-08-30
4. Photosensitized Oxidation of Methionine-Containing Dipeptides. From the Transients to the Final Products;The Journal of Physical Chemistry B;2014-07-02
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