
Journal of Medicinal Chemistry p. 3850 - 3854 (1994)
Update date:2022-08-03
Topics:
Okruszek
Olesiak
Balzarini
Appropriately protected nucleoside 5'-O-(2-thio-1,3,2-dithiaphospholanes) react with inorganic pyrophosphate in the presence of a strong base catalyst (DBU) to give nucleoside 5'-O-(1,1-dithiotriphosphates) 1a-g. The latter compounds, including an AZT analogue, show modest antivirial activity against HIV-1 and HIV-2 replication in CEM cells. The AZT and deoxyadenosine derivatives were found to be inhibitors of HIV reverse transcriptase.
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Doi:10.1016/0040-4039(94)88434-X
(1994)Doi:10.1007/s10895-013-1303-x
(2014)Doi:10.1002/anie.201402661
(2014)Doi:10.3762/bjoc.10.124
(2014)Doi:10.2298/JSC130706115P
(2014)Doi:10.1016/0008-6215(94)00326-B
(1995)