Abstract
The reagent system based on the combined use of Et3SiH/I2 acts as an efficient N-glycosidation promoter for the synthesis of natural and sugar-modified nucleosides. An analysis of reaction stereoselectivity in the absence of C2-positioned stereodirecting groups revealed high selectivity with six-membered substrates, depending on the nucleophilic character of the nucleobase or based on anomerization reactions. The synthetic utility of the Et3SiH/I2-mediated N-glycosidation reaction was highlighted by its use in the synthesis of the investigational drug apricitabine.
| Original language | English |
|---|---|
| Article number | 9030 |
| Journal | International Journal of Molecular Sciences |
| Volume | 25 |
| Issue number | 16 |
| DOIs | |
| Publication status | Published - Aug 2024 |
| Externally published | Yes |
Keywords
- anomerization
- apricitabine
- glycosyl iodide
- iodine/triethylsilane
- N-glycosidation
- nucleosides
- stereoselectivity
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