Radical Route for the Alkylation of Purine Nucleosides at C6 via Minisci Reaction
2014
Xia, Ran | Xie, Ming-Sheng | Niu, Hong-Ying | Qu, Gui-Rong | Guo, Hai-Ming
A highly regioselective Minisci reaction with the decarboxylative alkylation of purine nucleosides under mild conditions was developed. With 5 mol % AgNO₃ as a catalyst and (NH₄)₂S₂O₈ as an oxidant, a series of purine nucleosides including ribosyl, deoxyribosyl, arabinosyl purine nucleosides worked well with primary, secondary, and tertiary aliphatic carboxylic acids.
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