| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1390987 | Carbohydrate Research | 2006 | 5 Pages |
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.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Balaram Mukhopadhyay, Robert A. Field,