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 HClO 4–silica promoted glycosylations of thioglycoside donors.
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