Copper/H2O2-Mediated oxidation of 2′-deoxyguanosine in the presence of 2-naphthol leads to the formation of two distinct isomeric adducts

Journal of Organic Chemistry

Volumn 76, Issue 19, 2011, Pages 7953-7963

  Fleming, Aaron M ^a   Kannan, Arunkumar ^a   Muller, James G ^a   Liao, Yi ^a   Burrows, Cynthia J ^a  

^a UNIVERSITY OF UTAH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

2-NAPHTHOLS; ATROPISOMERS; CANONICAL BASIS; DELETERIOUS EFFECTS; DEOXYGUANOSINE (DG); DIASTEREOMERIC; DIFFERENT STRUCTURE; ELECTRON-RICH; GENOMIC DNA; IRON SALTS; ISOMERIC PRODUCTS; MUTAGENIC EFFECT; NUCLEOBASES; OXIDATION PROCESS; OXIDATIVE CONDITIONS; PHENOLIC COMPOUNDS; REACTIVE OXYGEN SPECIES;

BIOMOLECULES; LEAD COMPOUNDS; OXIDATION; SPECTROSCOPIC ANALYSIS;

PHENOLS;

2 NAPHTHOL; ALKYL GROUP; COPPER; DEOXYGUANOSINE; GENOMIC DNA; HYDROGEN PEROXIDE; NAPHTHALENE DERIVATIVE; NUCLEOSIDE; REACTIVE OXYGEN METABOLITE; 2-NAPHTHOL; NAPHTHOL DERIVATIVE; OXIDIZING AGENT; PHENOL;

ALKYLATION; ARTICLE; CHEMICAL STRUCTURE; CONTROLLED STUDY; DIASTEREOISOMER; ISOMER; ISOMERIZATION; MUTAGENIC ACTIVITY; OXIDATION; OXIDATIVE STRESS; REACTION ANALYSIS; SPECTROSCOPY; STEREOCHEMISTRY; CHEMISTRY; ELECTRON; ISOMERISM; OXIDATION REDUCTION REACTION; PH;

COPPER; DEOXYGUANOSINE; ELECTRONS; HYDROGEN PEROXIDE; HYDROGEN-ION CONCENTRATION; ISOMERISM; NAPHTHOLS; OXIDANTS; OXIDATION-REDUCTION; PHENOL;

EID: 80054092826     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo201423n     Document Type: Article

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