Journal article
Oxidative damage of proline residues by nitrate radicals (NO3): A kinetic and product study
JG Nathanael, JM White, A Richter, MR Nuske, U Wille
Organic and Biomolecular Chemistry | ROYAL SOC CHEMISTRY | Published : 2020
DOI: 10.1039/d0ob01337d
Abstract
Tertiary amides, such as in N-acylated proline or N-methyl glycine residues, react rapidly with nitrate radicals (NO3) with absolute rate coefficients in the range of 4-7 × 108 M-1 s-1 in acetonitrile. The major pathway proceeds through oxidative electron transfer (ET) at nitrogen, whereas hydrogen abstraction is only a minor contributor under these conditions. However, steric hindrance at the amide, for example by alkyl side chains at the α-carbon, lowers the rate coefficient by up to 75%, indicating that NO3-induced oxidation of amide bonds proceeds through initial formation of a charge transfer complex. Furthermore, the rate of oxidative damage of proline and N-methyl glycine is significa..
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Awarded by University of Melbourne
Funding Acknowledgements
This work was supported by the Australian Research Council through the Linkage, Infrastructure, Equipment and Facilities (LIEF) Grant Scheme and The University of Melbourne through the High-Performance Computing facility.<SUP>31</SUP>