Abstract
Stereocontrolled efficient syntheses of β-d-(1→6)-linked di-, tetra- and octa-galactans as model compounds of arabino-3,6-galactans isolated from Astragalus mongholicus are described. The syntheses consisted of simple glycosylation cycles: an acceptor and a donor prepared from a common compound were coupled, and the glycosylation product was converted to the acceptor and donor of the next glycosylation.
Original language | English |
---|---|
Pages (from-to) | 563-578 |
Number of pages | 16 |
Journal | Heterocycles |
Volume | 90 |
Issue number | 1 |
DOIs | |
Publication status | Published - 2015 |
ASJC Scopus subject areas
- Analytical Chemistry
- Pharmacology
- Organic Chemistry