About: Functionalized Chiral Ionic Liquid CatalyzedEnantioselective Desymmetrizations of ProchiralKetones via Asymmetric Michael AdditionReaction

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_24/w
Subject	Note
Title	Functionalized Chiral Ionic Liquid CatalyzedEnantioselective Desymmetrizations of ProchiralKetones via Asymmetric Michael AdditionReaction
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_24/101021jo7020357/m/web http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_24/101021jo7020357/m/print
related by	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_24/101021jo7020357/authorship/4 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_24/101021jo7020357/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_24/101021jo7020357/authorship/2 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_24/101021jo7020357/authorship/5 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_24/101021jo7020357/authorship/3
Author	Cheng Jin-Pei Luo Sanzhong Qiao Yupu Zhang Long Mi Xueling
Abstract	Functionalized chiral ionic liquids were found to be highlyeffective and reusable organocatalysts for asymmetric Michaeladditions of 4-substituted cyclohexanones. The desymmetrization reaction afforded the desired Michael adductsbearing three carbon stereocenters with up to 99% ee.
article type	brief-report
is part of this journal	The Journal of Organic Chemistry

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