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Ionic-liquid-supported organocatalyst for the enantioselective Michael addition of ketones to nitroolefins

Journal

TETRAHEDRON-ASYMMETRY
Volume 18, Issue 17, Pages 2086-2090

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2007.08.029

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Ionic-liquid-supported triazole-pyrrolidine 2, for the direct asymmetric Michael reaction was successfully synthesized. The supported catalyst demonstrated good activity and high enantioselectivity in the addition of cyclohexanone to nitroolefins. Furthermore, the supported catalyst can be readily recovered and reused four times without significant loss of catalytic activity. (C) 2007 Published by Elsevier Ltd.

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