TBD facilitates the enolization of the ketoaldehyde by abstracting a proton from the α-carbonyl position, leading to the formation of an enolate intermediate. The enolate is a nucleophilic species and can attack the carbonyl carbon of another ketoaldehyde.
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1-(4-bromo-phenyl)-heptane-1,7-diol
Propanoic acid, 3,3,3-trifluoro-, phenylmethyl ester
7-oxoandrostane-3,17-diyl diacetate
