
Bioorganic and Medicinal Chemistry Letters p. 373 - 378 (1996)
Update date:2022-08-03
Topics:
Matulic-Adamic
Gonzalez
Usman
Beigelman
Protected pyridin-2- and pyridin-4-one ribonucleosides 3 and 9 were synthesized using a one-pot reaction of silylated bases with 1-O-acetyl-tri-O-benzoyl-β-D-ribofuranose (2) in the presence of CF3SO3SiMe3. The nucleosides were converted in 4 steps into 3'-O-phosphoramidites 7 and 11 which were incorporated into hammerhead ribozyme substrates using solid-phase phosphoramidite chemistry.
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Doi:10.1021/ja01617a052
(1955)Doi:10.1016/0040-4020(68)88079-2
(1968)Doi:10.1016/0040-4039(96)00139-6
(1996)Doi:10.1055/s-1996-4199
(1996)Doi:10.1021/om950905z
(1996)Doi:10.1016/0040-4039(96)00140-2
(1996)