
Nucleosides and Nucleotides p. 2499 - 2510 (1999)
Update date:2022-08-05
Topics:
Saladino, Raffaele
Mezzetti, Maurizio
Mincione, Enrico
Palamara, Anna Teresa
Savini, Patrizia
Marini, Stefano
A convenient and mild synthesis of 5-bromo-N4-substituted-1-(β-D- arabinofuranosyl)cytosine and 5-bromo-O4-methyl-1-(β-D- arabinofuranosyl)pyrimidin-2(1H)-one derivatives by selective oxyfunctionalization of the corresponding 4-thionucleosides with 3,3- dimethyldioxirane is reported. The cytotoxicity and the antiviral activity against parainfluenza 1 (Sendai virus) of all new synthesized products are also reported.
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Doi:10.1246/bcsj.55.2299
(1982)Doi:10.1021/ja00386a027
(1982)Doi:10.1021/ja00342a037
(1983)Doi:10.1002/(SICI)1099-0690(199901)1999:1<231::AID-EJOC231>3.0.CO;2-U
(1999)Doi:10.1007/BF00568943
(1982)Doi:10.1021/jo00145a047
(1982)