Abstract
The nonhydrolyzable glycosidic linkage to sialic acid in the C-glycoside analogue of sTn, 1, is the key feature of the redesigned glycoconjugate. This potential antitumor and anti-HIV agent was prepared in one enzymatic and seventeen chemical steps starting from diisopropylidene galactopyranose.
Original language | English |
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Pages (from-to) | 2073-2075 |
Number of pages | 3 |
Journal | Angewandte Chemie - International Edition |
Volume | 42 |
Issue number | 18 |
DOIs | |
State | Published - 9 May 2003 |
Externally published | Yes |
Keywords
- Anti-HIV agents
- Antitumor agents
- C-glycosides
- Glycopeptides
- Sialic acid