Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 6334-6342 |
| Number of pages | 9 |
| Journal | ACS Catalysis |
| Volume | 11 |
| Issue number | 10 |
| DOIs | |
| Publication status | Published - 21 May 2021 |
| Externally published | Yes |
Keywords
- alkynyl C-nucleosides
- anomeric radicals
- copper
- dual photoredox catalysis
- glycosyl carboxylic acids
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