Enhanced reactivity of the pyrimidine peroxyl radical towards the C–H bond in duplex DNA – a theoretical study
Author:
Affiliation:
1. School of Chemistry and Chemical Engineering
2. Beijing Institute of Technology
3. Beijing
4. China
5. Département de Médecine Nucléaire et Radiobiologie
6. Faculté de Médecine
7. Université de Sherbrooke
8. Sherbrooke
9. Canada JIH 5N4
Abstract
The peroxyl radical exhibits a much stronger reactivity towards C1′–H1′ in duplex DNA with respect to single-stranded DNA.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB00302F
Reference46 articles.
1. C–H functionalization logic in total synthesis
2. Undirected, Homogeneous C–H Bond Functionalization: Challenges and Opportunities
3. Recent developments in natural product synthesis using metal-catalysed C–H bond functionalisation
4. The Essential Role of Bond Energetics in C–H Activation/Functionalization
5. Oxygenation via C–H/C–C Bond Activation with Molecular Oxygen
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Oxidatively generated tandem DNA modifications by pyrimidinyl and 2-deoxyribosyl peroxyl radicals;Free Radical Biology and Medicine;2023-02
2. Dynamics of 5R-Tg Base Flipping in DNA Duplexes Based on Simulations─Agreement with Experiments and Beyond;Journal of Chemical Information and Modeling;2022-01-07
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