Abstract
Procedures have been developed for the
determination of the type and location of sugar units present in anthocyanins
and other flavonoid glycosides. These procedures are based on standard chemical
reactions and have been adapted to a microscale using paper chromatography.
Individual flavonoids were found to
respond variably to enzymic and chemical hydrolyses, which therefore yield
information of limited use only. On the other hand, controlled oxidation has
been shown to provide information on the type and position of sugar units
attached to the flavonoid nucleus. Degradation using peroxide releases the
sugars at the 3-position ; permanganate treatment releases sugars attached to
readily ruptured cyclic systems ; and ozonolysis releases sugars attached to
phenolic and enolic hydroxyl groups. These three techniques, when used
together, can result in the absolute identification of anthocyanins and most
other flavonoid glycosides.
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