Journal of Medicinal Chemistry p. 2131 - 2137 (1987)
Update date:2022-08-03
Topics:
Herdewijn
Pauwels
Baba
Balzarini
De Clercq
A systematic synthesis was undertaken of 2',3'-dideoxyadenosine analogues with either an azido, fluorine, or hydroxyl group substituted in the 'up' or 'down' position of C-2 or C-3 of the sugar moiety. The compounds were evaluated against the cytopathogen
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Doi:10.1016/S0022-328X(00)83008-9
(1981)Doi:10.1021/ja01864a601
(1940)Doi:10.1016/S0040-4039(00)71463-8
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(1982)
