2022
DOI: 10.1039/d2cp02095e
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The complete mechanism of an aldol condensation in water

Abstract: The base-catalyzed aldol condensation between benzaldehyde and p-acetylbenzoic acid in water shows an inverse solvent kinetic isotope effect, k3,D2O/k3,H2O, of 1.33±0.03. The reaction is definitely faster in D2O. This is...

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“…2,6-Diacetylpyridine underwent Claisen–Schmidt condensation 26 with the required substituted aromatic aldehyde to afford the chalcone precursors 1–3 in acceptable yield (34–73%). After extensive investigation, it was discovered that a 2 : 1 ratio of ketone to aldehyde with catalytic amount of NaOH promoted formation of the required mono-chalcone and minimal formation of the bis-chalcone side product (ESI S3†).…”
Section: Resultsmentioning
confidence: 99%
“…2,6-Diacetylpyridine underwent Claisen–Schmidt condensation 26 with the required substituted aromatic aldehyde to afford the chalcone precursors 1–3 in acceptable yield (34–73%). After extensive investigation, it was discovered that a 2 : 1 ratio of ketone to aldehyde with catalytic amount of NaOH promoted formation of the required mono-chalcone and minimal formation of the bis-chalcone side product (ESI S3†).…”
Section: Resultsmentioning
confidence: 99%