Publication | Closed Access
Asymmetric, Catalytic, and Direct Self-Aldol Reaction of Acetaldehyde Catalyzed by Diarylprolinol
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Citations
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References
2008
Year
Novel OrganocatalystsDirect Self-aldol ReactionEngineeringEnantioselective SynthesisBiochemistryAcetaldehyde CatalyzedNatural SciencesOrganic ChemistryCatalysisStereoselective SynthesisChemistryTrimer AcetalNatural Product SynthesisAsymmetric CatalysisAcetaldehyde Molecule
An asymmetric, catalytic, and direct self-aldol reaction of acetaldehyde was catalyzed by diarylprolinol in NMP, affording the trimer acetal, which was generated by the reaction of the self-aldol product with another acetaldehyde molecule in a moderate yield with good enantioselectivity. Acetal is the synthetic equivalent of the self-aldol product, which can be converted into other synthetically useful compounds in one pot without compromising the enantioselectivity.
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