Enantioselective Aldol Reaction using Recyclable Montmorillonite-Entrapped N-(2-Thiophenesulfonyl)prolinamide

N‐(2‐Thiophenesulfonyl)prolinamide could be easily introduced into Montmorillonite by a simple ion‐exchange reaction. The asymmetric aldol reactions between various isatins with acetone or acetaldehyde using a heterogeneous Montmorillonite‐entrapped organocatalyst afforded products with high enantio...

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Veröffentlicht in:Advanced synthesis & catalysis 2010-07, Vol.352 (10), p.1621-1624
Hauptverfasser: Hara, Noriyuki, Nakamura, Shuichi, Shibata, Norio, Toru, Takeshi
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Sprache:eng
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Zusammenfassung:N‐(2‐Thiophenesulfonyl)prolinamide could be easily introduced into Montmorillonite by a simple ion‐exchange reaction. The asymmetric aldol reactions between various isatins with acetone or acetaldehyde using a heterogeneous Montmorillonite‐entrapped organocatalyst afforded products with high enantioselectivity. The catalyst was readily reusable without significant loss of catalytic activity or enantioselectivity.
ISSN:1615-4150
1615-4169
1615-4169
DOI:10.1002/adsc.201000214