Publication detail

Immobilized chiral acylthiourea organocatalyst for Michael reactions

Authors: Androvič Ladislav | Drabina Pavel | Sedlák Miloš

Year: 2015

Type of publication: ostatní - přednáška nebo poster

Page from-to: nestránkováno

Titles:

Language	Name	Abstract	Keywords
eng	Immobilized chiral acylthiourea organocatalyst for Michael reactions	Swellable pearl styrene copolymer was used for anchoring optically pure chiral acylthiourea as the catalyst for the enantioselective Michael reaction of cyclohexanone with nitrostyrene. The catalyst gave the product in high conversions (77-99%) and excellent enantioselectivity (60-99% ee).

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