133931-97-2Relevant academic research and scientific papers
Deamination and dimroth rearrangement of deoxyadenosine - Styrene oxide adducts in DNA
Barlow, Thomas,Takeshita, Junko,Dipple, Anthony
, p. 838 - 845 (1998)
In reactions between styrene oxide and the ring nitrogen at the 1- position of deoxyadenosine, the epoxide is opened at both the α- (benzylic) and β-carbons. The 1-substituted nucleosides formed are unstable and subsequently undergo either Dimroth rearran
Studies of the mechanisms of adduction of 2'-deoxyadenosine with styrene oxide and polycyclic aromatic hydrocarbon dihydrodiol epoxides
Kim, Hye-Young H.,Finneman, Jari I.,Harris, Constance M.,Harris, Thomas M.
, p. 625 - 637 (2000)
The mechanism of adduction of 2'-deoxyadenosine by styrene oxide and polycyclic aromatic hydrocarbon dihydrodiol epoxides has been explored using 15N6-labeled adenine nucleosides. The extent of reaction at N1 versus N6 was
