Linked from

The 12 pages that link to Aldol reaction, each with the reason it gives.

• AldehydeRelated: Many aldehydes with alpha hydrogens form new carbon–carbon bonds through this reaction.

• Nucleophilic additionRelated: Its bond-forming step is nucleophilic addition of an enolate to a carbonyl.

• AcetoneRelated: Acetone can form an enolate and undergo aldol addition or condensation.

• EnolateRelated: The enolate adds to another carbonyl, producing a beta-hydroxy carbonyl compound.

• EnolRelated: Enol nucleophiles are the carbon-bond-forming partners in this reaction.

• Keto–enol tautomerismRelated: Enol formation provides the nucleophilic partner that initiates aldol bond formation.

• GlyceraldehydeRelated: Glyceraldehyde can participate as a small carbonyl-containing aldose.

• PentaerythritolRelated: Repeated aldol additions are part of the reaction sequence used to build pentaerythritol’s carbon skeleton.

• ButyraldehydeRelated: Butyraldehyde can form an enolate and participate in aldol addition and condensation reactions.

• Titanium tetrachlorideRelated: TiCl₄ can activate carbonyl compounds and promote stereoselective aldol variants.

• PropionaldehydeRelated: Propionaldehyde can form an enolate and couple with another aldehyde molecule.