Ionic-liquid-supported organocatalyst: Efficient and recyclable ionic-liquid-anchored proline for asymmetric aldol reaction

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Abstract

Ionic-liquid-anchored (2S,4R)-4-hydroxyproline 12 catalyzes direct asymmetric aldol reactions with comparable enantioselectivities in DMSO, and with superior enantioselectivities in neat acetone or 2-butanone, than (S)-proline (8) (up to 28% ee difference) itself. Furthermore, the supported catalyst 12 can be easily recycled and reused for at least four times without significant loss of yields and enantioselectivity. © 2006 Wiley-VCH Verlag GmbH & Co. KGaA.

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Miao, W., & Chan, T. H. (2006). Ionic-liquid-supported organocatalyst: Efficient and recyclable ionic-liquid-anchored proline for asymmetric aldol reaction. Advanced Synthesis and Catalysis, 348(12–13), 1711–1718. https://doi.org/10.1002/adsc.200606059

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