Publication | Closed Access
Chiral Ytterbium Complex‐Catalyzed Direct Asymmetric Aldol‐Tishchenko Reaction: Synthesis of <i>anti</i>‐1,3‐Diols
43
Citations
59
References
2006
Year
Asymmetric CatalysisAsymmetric Aldol-tishchenko ReactionEngineeringBiochemistryAromatic KetonesOrganic ChemistryOrganometallic CatalysisStereoselective SynthesisEvans-tishchenko ReductionSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
The asymmetric aldol-Tishchenko reaction of aromatic aldehydes with aliphatic and aromatic ketones has been developed as an efficient strategy for the synthesis of anti-1,3-diols in good yield with high diastereocontrol and good levels of enantioselectivity. This domino-type reaction is catalyzed by a chiral ytterbium complex that promotes both the aldol reaction through enolization of the carbonyl compound and the Evans-Tishchenko reduction of the aldol intermediate. The stereochemistry of the resulting diols is also investigated and finally proved by using CD techniques.
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