S. Bellon et al., 5-(Phenylthiomethyl)-2 '-deoxyuridine as an efficient photoreactive precursor to generate single and multiple lesions within DNA fragments, NUCLEOS NUC, 20(4-7), 2001, pp. 967-971
5-(Phenylthiomethyl)-2'-deoxyuridine was successfully incorporated into DNA
oligomers by automated DNA synthesis using phosphoramidite chemistry. UV e
xposure of the latter thionucleoside containing oligonucleotides under anae
robic and aerobic conditions gives rise to specific base lesions. The photo
products have been isolated and further characterized on the basis of NMR a
nd mass spectrometric analyses.