Fluorinated alcohol mediated displacement of the C10 acetoxy group of benzo[a]pyrene-7,8,9,10-tetrahydrotetraol tetraacetates: A new route to diol epoxide-deoxyguanosine adducts

Journal of Organic Chemistry

Volumn 72, Issue 26, 2007, Pages 9983-9990

  Yagi, Haruhiko ^a   Jerina, Donald M ^a  

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

Author keywords

[No Author keywords available]

Indexed keywords

CONFORMATIONS; FLUORINATION; ISOMERS; SUBSTITUTION REACTIONS;

ACETOXY GROUP; PURINE NUCLEOPHILES; TETRAACETATES;

ALCOHOLS;

ACETIC ACID DERIVATIVE; ALCOHOL; DEOXYGUANOSINE; EPOXIDE; PYRENE DERIVATIVE; TRIFLUOROETHANOL;

ACETYLATION; ARTICLE; HYDROLYSIS; STEREOCHEMISTRY; STEREOISOMERISM; SUBSTITUTION REACTION;

7,8-DIHYDRO-7,8-DIHYDROXYBENZO(A)PYRENE 9,10-OXIDE; DEOXYGUANOSINE; DNA ADDUCTS; HYDROLYSIS; MOLECULAR CONFORMATION; ORGANOSILICON COMPOUNDS; PROPANOLS; STEREOISOMERISM; TRIFLUOROETHANOL;

EID: 37549036745     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo701705c     Document Type: Article

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