Abstract
The diphenylketone Shiff-base appeared to be a very good protection from amino groups of serine and threonine for glycosylation reaction. O-Glycosides of these amino acids with different monosaccharides, aminosugars and deoxysugars were obtained with excellent yield and very high stereoselectivity. Products of glycosylation reactions were used as building blocks for solid phase glycopeptide synthesis.
| Translated title of the contribution | New chemical method for synthesis of O-linked glycopeptides |
|---|---|
| Original language | Polish |
| Pages (from-to) | 493-503 |
| Number of pages | 11 |
| Journal | Postpy higieny i medycyny doświadczalnej |
| Volume | 50 |
| Issue number | 5 |
| State | Published - 1996 |
ASJC Scopus subject areas
- Microbiology (medical)
- Infectious Diseases