Organocatalytic Asymmetric syn-Selective Direct Aldol Reaction in Ionic Liquid
A practical and recyclable organocatalytic strategy is developed to provide syn-selective aldol products in ionic liquid. The siloxy serine organocatalyst mediates the direct aldol reaction of TBSO-protected hydroxyacetone with a variety of aldehyde to provide the β-hydroxycarbonyl scaffolds in good...
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Veröffentlicht in: | Chemistry letters 2010-05, Vol.39 (5), p.490-492 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | A practical and recyclable organocatalytic strategy is developed to provide syn-selective aldol products in ionic liquid. The siloxy serine organocatalyst mediates the direct aldol reaction of TBSO-protected hydroxyacetone with a variety of aldehyde to provide the β-hydroxycarbonyl scaffolds in good yields and enantioselectivities up to 94%. |
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ISSN: | 0366-7022 1348-0715 |
DOI: | 10.1246/cl.2010.490 |