Abstract
A general protocol for functionalization of glycosyl thiols has been reported. This protocol is based on a single-electron Ni/photoredox dual-catalyzed cross coupling between 1-thiosugars and a broad range of aryl bromides and iodides as well as alkenyl and alkynyl halides. This base-free method gives access to a series of functionalized thioglycosides in moderate to excellent yields with a perfect control of the anomeric configuration. Moreover, it has been shown that this methodology may be transposed successfully to the continuous-flow photoredox chemistry.
| Original language | English |
|---|---|
| Pages (from-to) | 5132-5137 |
| Number of pages | 6 |
| Journal | Organic Letters |
| Volume | 21 |
| Issue number | 13 |
| DOIs | |
| Publication status | Published - 18 Jun 2019 |
| Externally published | Yes |