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- W2006028638 endingPage "4169" @default.
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- W2006028638 abstract "On the basis of molecular modeling studies, the 7-nitroindole nucleoside 1 was selected as a suitable photochemical precursor for photochemical generation of the C1' deoxyribosyl radical under irradiation, which led to 2'-deoxyribonolactone. The nitro-indole nucleoside derivatives 1a and 1b were prepared and their conformation was determined by X-ray crystallography and NMR spectroscopy. The photoreaction of these nucleosides gave the corresponding deoxyribonolactone derivatives efficiently, with release of 7-nitrosoindole. This reaction was successfully applied to synthesis of oligonucleotides containing the deoxyribonolactone lesion." @default.
- W2006028638 created "2016-06-24" @default.
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- W2006028638 creator A5075602639 @default.
- W2006028638 creator A5089116898 @default.
- W2006028638 date "2000-11-17" @default.
- W2006028638 modified "2023-10-14" @default.
- W2006028638 title "The 7-Nitroindole Nucleoside as a Photochemical Precursor of 2′-Deoxyribonolactone: Access to DNA Fragments Containing This Oxidative Abasic Lesion" @default.
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- W2006028638 doi "https://doi.org/10.1002/1521-3765(20001117)6:22<4163::aid-chem4163>3.0.co;2-k" @default.
- W2006028638 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/11128280" @default.
- W2006028638 hasPublicationYear "2000" @default.
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