Theoretical study on the deoxyribose radicals formed by hydrogen abstraction
Citations Over TimeTop 10% of 1994 papers
Abstract
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTTheoretical study on the deoxyribose radicals formed by hydrogen abstractionKarol Miaskiewicz and Roman OsmanCite this: J. Am. Chem. Soc. 1994, 116, 1, 232–238Publication Date (Print):January 1, 1994Publication History Published online1 May 2002Published inissue 1 January 1994https://doi.org/10.1021/ja00080a027Request reuse permissionsArticle Views308Altmetric-Citations113LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InReddit PDF (1 MB) Get e-Alertsclose Get e-Alerts
Related Papers
- → Electron elastic scattering from biomolecular targets: 1,3-dihydroxytetrahydrofuran, deoxyribose, THFA monophosphate and deoxyribose monophosphate(2023)2 cited
- → Deoxyribose breakdown by the adriamycin semiquinone and H2O2: evidence for hydroxyl radical participation(1982)90 cited
- → Protection of deoxyribose and DNA from degradation by using aqueous extracts of several wild plants(2007)26 cited
- → Modification of the deoxyribose test to detect strong iron binding(2016)10 cited
- Mechanism Underlying Protective Effect of 6-Hydroxykaempferol-3-O-β-glucoside Deoxyribose against Oxidative Damage to Deoxyribose(2013)