About: Facially Selective and Regioselective Carbometalation ofCyclopropenes by Aryl Grignard Reagents

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_2/w
Subject	Article
Title	Facially Selective and Regioselective Carbometalation ofCyclopropenes by Aryl Grignard Reagents
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_2/101021jo702176x/m/print http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_2/101021jo702176x/m/web
related by	http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_2/101021jo702176x/authorship/2 http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_2/101021jo702176x/authorship/3 http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_2/101021jo702176x/authorship/1
Author	Liu Xiaozhong Yan Ni Fox Joseph M.
Abstract	Described is a Cu-catalyzed methodology for adding aryl Grignard reagents to 3-hydroxymethylcyclopropene derivatives with high regio- and diastereoselectivity. The cyclopropylmetals can be trapped witha variety of electrophiles to generate highly substituted cyclopropanes.
article type	research-article
is part of this journal	The Journal of Organic Chemistry

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