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Volumn 6, Issue 22, 2000, Pages 4163-4169

The 7-nitroindole nucleoside as a photochemical precursor of 2′-deoxyribonolactone: Access to DNA fragments containing this oxidative abasic lesion

Author keywords

Abasic lesions; DNA oxidation; Molecular modeling; Oligonucleotides; Photochemistry

Indexed keywords

NUCLEOSIDE DERIVATIVE; OLIGONUCLEOTIDE;

EID: 0034680509     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/1521-3765(20001117)6:22<4163::AID-CHEM4163>3.0.CO;2-K     Document Type: Article
Times cited : (47)

References (96)
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    • The incorporation of the 5-and 6-nitroindole nucleosides into oligonucleootides was previously described. They are used as universal base analogues: D. Loakes, D. M. Brown, Nucleic Acid Res. 1994, 22, 4039-4043.
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    • Loakes, D.1    Brown, D.M.2
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    • The photochemistry of nitro and nitroso groups
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    • Biosym Technologies, 9685 Scranton Road, San Diego, CA 92121-2777 (USA)
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    • 13C NMR and MS data in accordance with the described data; see F. Fariña, M. V. Martin, M. C. Paredes, Synthesis, 1973, 167-168. The mechanism of formation of 9 is currently under study. Presumably this reaction occurs by intermediate formation of 5-methylenefuranone.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.