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Enantioselective Acylation of 1,2- and 1,3-Diols Catalyzed by Aminophosphinite Derivatives of (1<i>S</i>,2<i>R</i>)-1-Amino-2-indanol
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Citations
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References
2012
Year
Aminophosphinite DerivativesNovel OrganocatalystsEngineeringEffective CatalystOrganic ChemistryEnantioselective AcylationCatalysisAvailable AminoindanolChemistrySynthetic ChemistryStereoselective SynthesisAsymmetric CatalysisPhosphinite DerivativeEnantioselective SynthesisBiomolecular Engineering1,3-Diols Catalyzed
A phosphinite derivative that can be easily prepared in two steps from commercially available aminoindanol was found to be an effective catalyst for enantioselective acylation of diols. For the asymmetric desymmetrization of meso-1,2-diols, the corresponding monoester was obtained in up to 95% ee from the reaction in the presence of 5 mol % catalyst.
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