Abstract
The glycone part of the flavonoid triglycoside, kaempferol 3-O-β-d-glucopyranosyl-(1→4)-α-l-rhamnopyranosyl-(1→6)-β-d-galactopyranoside, has been synthesized in good yield and stereoselectivity using N-iodosuccinimide and HClO4-silica promoted glycosylations of thioglycoside donors.
Original language | English |
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Pages (from-to) | 1697-1701 |
Number of pages | 5 |
Journal | Carbohydrate Research |
Volume | 341 |
Issue number | 10 |
DOIs | |
Publication status | Published - 24 Jul 2006 |
Keywords
- Antidiabetic
- Flavonoids
- HClO-silica