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Diastereoselective aldol condensations of tin enolates with aldehydes
Authors:Sharada Shenvi  JK Stille
Institution:Department of Chemistry Colorado State University Fort Collins, Colorado 80523 USA
Abstract:The reaction of tin enolates of cyclohexanone or propiophenone with benzaldehyde at ?78°C gives predominately the threo aldol diastereomer.
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