Synthesis and UV photolysis of oligodeoxynucleotides that contain 5-(phenylthiomethyl)-2'-deoxyuridine: a specific photolabile precursor of 5-(2'-deoxyuridilyl)methyl radical
- PMID: 10804560
- DOI: "V体育官网入口" 10.1021/ol005643y
Synthesis and UV photolysis of oligodeoxynucleotides that contain 5-(phenylthiomethyl)-2'-deoxyuridine: a specific photolabile precursor of 5-(2'-deoxyuridilyl)methyl radical
Abstract (V体育官网入口)
[formula: see text] The title exocyclic radical (2) is generated via photochemical cleavage of 5-(phenylthiomethyl)-2'-deoxyuridine (8). The latter thionucleoside (8) was successfully incorporated into DNA oligomers by automated DNA synthesis using phosphoramidite chemistry. UV exposure of 8 containing oligonucleotides under (an)aerobic conditions gives rise to specific base lesions VSports手机版. The photoproducts have been isolated and further characterized on the basis of detailed NMR and mass spectrometric analyses. .
Publication types
- "V体育平台登录" Actions
MeSH terms
- "V体育平台登录" Actions
- V体育官网 - Actions
Substances (V体育安卓版)
- "V体育官网入口" Actions
LinkOut - more resources
Other Literature Sources (V体育ios版)