Résumé
Alkynyl C-nucleosides are of high value for various applications; however, their synthesis remains underexplored. Here we report a simple route toward the synthesis of alkynyl C-nucleosides from simple and stable furanosyl carboxylic acids and terminal alkynes under low-cost and nontoxic copper catalysis. The approach that we report here demonstrates the power of Cu/photoredox dual catalysis to access highly complex glycosides under mild conditions.
| langue originale | Anglais |
|---|---|
| Pages (de - à) | 6334-6342 |
| Nombre de pages | 9 |
| journal | ACS Catalysis |
| Volume | 11 |
| Numéro de publication | 10 |
| Les DOIs | |
| état | Publié - 21 mai 2021 |
| Modification externe | Oui |
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