Abstract:
Ionic liquid-supported (1S,2S)- and (1R,2R)-1,2-bis[(S)-prolinamido]-1,2-diphenylethanes act as organocatalysts in asymmetric aldol reactions of acetone with α-keto esters or trifluoroacetophenone providing high yields and from moderate to high enantioselectivity. Recycling of the catalyst with a gradual decrease in conversion and ee values is possible.
Citation:
S. V. Kochetkov, A. S. Kucherenko, S. G. Zlotin, “Asymmetric aldol reactions in ketone/ketone systems catalyzed by ionic liquid-supported C2-symmetrical organocatalyst”, Mendeleev Commun., 25:3 (2015), 168–170
Linking options:
https://www.mathnet.ru/eng/mendc2338
https://www.mathnet.ru/eng/mendc/v25/i3/p168
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