Independent Generation and Study of 5,6-Dihydro-2‘-deoxyuridin-6-yl, a Member of the Major Family of Reactive Intermediates Formed in DNA from the Effects of γ-Radiolysis
- 1 May 2003
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 68 (11) , 4275-4280
- https://doi.org/10.1021/jo034038g
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- The effect of the base in the fragmentation of nucleotide C4′ radicalsTetrahedron, 2002
- Dynamics of Alkene Radical Cation/Phosphate Anion Pair Formation from Nucleotide C4‘ Radicals. The DNA/RNA Paradox RevisitedJournal of the American Chemical Society, 2001
- Models of DNA C1‘ Radicals. Structural, Spectral, and Chemical Properties of the Thyminylmethyl Radical and the 2‘-Deoxyuridin-1‘-yl RadicalJournal of the American Chemical Society, 2000
- Kinetics of 2‘-Deoxyuridin-1‘-yl Radical ReactionsJournal of the American Chemical Society, 1999
- Chemistry of DNA DamagePublished by Elsevier ,1999
- Investigating Nucleic Acid Damage Processes via Independent Generation of Reactive IntermediatesChemical Research in Toxicology, 1998
- Oxidative Strand Scission of Nucleic Acids: Routes Initiated by Hydrogen Abstraction from the Sugar MoietyChemical Reviews, 1998
- The chemistry of single-stranded 4′-DNA radicals: influence of the radical precursor on anaerobic and aerobic strand cleavageChemistry & Biology, 1995
- Cleavage of Single-Stranded 4'-Oligonucleotide Radicals in the Presence of O2Journal of the American Chemical Society, 1995
- Carbon—Hydrogen Bonds of DNA Sugar Units as Targets for Chemical Nucleases and DrugsAngewandte Chemie International Edition in English, 1995