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Enantioselective Aldol Reaction of <i>tert</i>‐Butyl Acetate using Titanium‐Carbohydrate Complexes
128
Citations
18
References
1989
Year
EngineeringTemperature DependentOrganic ChemistryTitanium Reagent 1CatalysisSynthetic ChemistryChemistryStereoselective SynthesisAsymmetric CatalysisTitanium‐carbohydrate ComplexesAldol ReactionEnantioselective SynthesisBiomolecular Engineering
The enantioselective transformation of many aldehydes to tert-butyl esters of 3-hydroxycarboxylic acids is possible with the titanium reagent 1 (R*, see preceding communication). Acetate enolates could not be directly used previously. Surprisingly, this aldol reaction is hardly temperature dependent, so that a high induction may also be achieved at room temperature. The reagents (CPTiC13 and R*OH) can be recovered.
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