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Additional recommended knowledge
The first step in this procedure is an acid catalyzed aldol condensation between benzaldehyde and a 3-oxypentanone to a o-hydroxychalcone. Bromination of the alkene group gives a dibromo-adduct which rearranges to the flavonol by reaction with potassium hydroxide.
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Auwers_synthesis". A list of authors is available in Wikipedia.|