Revised assignment of absolute configuration of the cis- and trans-N 6-deoxyadenosine adducts at C14 of (±)-11β, 12α-dihydroxy-13α,14α-epoxy-11,12,13,14-tetrahydrodibenzo[a,l] pyrene by stereoselective synthesis

Chemical Research in Toxicology

Volumn 21, Issue 12, 2008, Pages 2379-2392

  Yagi, Haruhiko ^a   Frank, Heinrich ^b   Seidel, Albrecht ^b   Jerina, Donald M ^a  

^a NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

^b Prof Dr Gernot Grimmer Foundation   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

PYRENE DERIVATIVE;

AMINOHYDROXYLATION; AMMONOLYSIS; ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; SYNTHESIS;

CARCINOGENS; DEOXYADENOSINES; DIHYDROXYDIHYDROBENZOPYRENES; DNA ADDUCTS; EPOXY COMPOUNDS; MOLECULAR CONFORMATION; STEREOISOMERISM;

EID: 58149098747     PISSN: 0893228X     EISSN: None     Source Type: Journal    
DOI: 10.1021/tx800268f     Document Type: Article

References (34)

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