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- W2000439789 abstract "Enantiomerenüberschüsse bis zu 77% ee konnten bei der Michael‐Addition von Diisopropylmalonat an Enone und Enale in Gegenwart von 5 Mol‐ % des wasserhaltigen Rb‐Salzes von L‐Prolin als Katalysator erreicht werden. Die absolute Konfiguration der Produkte deutet an, daß der nucleophile Angriff ‐ unabhängig von der Konfiguration der CC‐Bindung ‐ immer von derselben Seite der CO‐Ebene erfolgt. magnified image" @default.
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- W2000439789 date "1993-08-01" @default.
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- W2000439789 title "Eine katalytische enantioselektive Michael-Addition eines Malonats an prochirale α,β-ungesättigte Aldehyde und Ketone" @default.
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- W2000439789 doi "https://doi.org/10.1002/ange.19931050832" @default.
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