| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10564870 | Current Opinion in Chemical Biology | 2013 | 9 Pages |
Abstract
- Chemical synthesis provided access to O-linked and S-linked oligosialic acids.
- Oxazolidinone-protected sialyl donors enable α-selective sialylation.
- Enzymatic synthesis has been applied to prepare sialic acid-containing saccharides.
Related Topics
Physical Sciences and Engineering
Chemistry
Chemistry (General)
Authors
Avijit K Adak, Ching-Ching Yu, Chien-Fu Liang, Chun-Cheng Lin,