Site-specific insertion of the (5R*) and (5S*) diastereoisomers of 1-[2-deoxy-β-D-erythro-pentofuranosyl]-5-hydroxyhydantoin into oligodeoxyribonucleotides

European Journal of Organic Chemistry

Volumn , Issue 11, 2001, Pages 2091-2099

  Muller, Evelyne ^a   Gasparutto, Didier ^a   Lebrun, Colette ^a   Cadet, Jean ^a  

^a CEA GRENOBLE   (France)

Author keywords

5 Hydroxyhydantoin nucleoside; DNA damage; Oligonucleotides synthesis; Ozonolysis; Protecting groups

Indexed keywords

1 (2 DEOXY BETA DEXTRO ERYTHRO PENTOFURANOSYL) 5 HYDROXYHYDANTOIN; ENDONUCLEASE; HYDANTOIN DERIVATIVE; LEVULINIC ACID; NUCLEOSIDE; OLIGODEOXYNUCLEOTIDE; PHOSPHORAMIDIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; DIASTEREOISOMER; HYDROLYSIS; MASS SPECTROMETRY; PHOTOSENSITIZATION; REACTION ANALYSIS;

EID: 0034990220     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200106)2001:11<2091::AID-EJOC2091>3.0.CO;2-2     Document Type: Article

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