One-Pot Synthesis of Chiral α-Substituted β,γ-Epoxy Aldehyde Derivatives through an Asymmetric Aldol Reaction of Chloroacetaldehyde
Water is welcome! Chiral α‐substituted β,γ‐epoxides have been prepared in good yields and with excellent enantioselectivities in a one‐pot synthetic procedure. The key reaction of this process, which involves a series of uninterrupted sequential reactions, is an asymmetric aldol reaction of aqueous...
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Veröffentlicht in: | Angewandte Chemie (International ed.) 2011-03, Vol.50 (12), p.2804-2807 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Water is welcome! Chiral α‐substituted β,γ‐epoxides have been prepared in good yields and with excellent enantioselectivities in a one‐pot synthetic procedure. The key reaction of this process, which involves a series of uninterrupted sequential reactions, is an asymmetric aldol reaction of aqueous chloroacetaldehyde mediated by a diarylprolinol derivative (see scheme). |
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ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.201005577 |