Abstract
Thioglycosides are among the most common glycosyl donors that find broad application in the synthesis of glycans and glycoconjugates. However, the requirement for toxic and/or large access of activators needed for common glycosylations with thioglycosides remains a notable drawback. Due to the increased awareness of the chemical waste impact on the environment, synthetic studies have been driven by the goal of finding non-toxic reagents. The main focus of this review is to highlight recent methods for thioglycoside activation that rely on transition metal catalysis.
| Original language | American English |
|---|---|
| Journal | Chemistry - A European Journal |
| Volume | 28 |
| DOIs | |
| State | Published - Mar 7 2022 |
Disciplines
- Biochemistry, Biophysics, and Structural Biology