Abstract
(Matrix Presented) Thioglycosides protected as trans-2,3-cyclic carbonates have significantly lower anomeric reactivities than fully acylated and N-acyl-protected thioglycosides and can be used as acceptors in chemoselective glycosylations with a wide range of thioglycosyl donors. The resulting thioglycosides can be further activated to give 1.2-cis-linked glycosides.
| Original language | English |
|---|---|
| Pages (from-to) | 4201-4203 |
| Number of pages | 3 |
| Journal | Organic Letters |
| Volume | 3 |
| Issue number | 26 |
| DOIs | |
| Publication status | Published - 27 Dec 2001 |
| Externally published | Yes |