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- W2100064163 endingPage "2853" @default.
- W2100064163 startingPage "2849" @default.
- W2100064163 abstract "Abstract A novel category of diarylprolinol silyl ether catalysts which contain different lengths of alkylamine tags, was designed and synthesized. These catalysts were used, along with benzoic acid as the co‐catalyst, to catalyze the asymmetric Michael reaction of the highly reactive acetaldehyde with nitroolefins. For the reactions studied, this catalytic system exhibited high reactivity in brine without any organic solvents; good yields (30–61%) and high enantioselectivities (80–97% ee ) for a wide variety of nitrostyrenes were obtained." @default.
- W2100064163 created "2016-06-24" @default.
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- W2100064163 creator A5058940439 @default.
- W2100064163 creator A5073372121 @default.
- W2100064163 date "2012-09-28" @default.
- W2100064163 modified "2023-10-09" @default.
- W2100064163 title "Asymmetric Michael Reaction of Acetaldehyde with Nitroolefins Catalyzed by Highly Water‐Compatible Organocatalysts in Aqueous Media" @default.
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