About: Synthesis of Chiral 3-Substituted Indanones via an EnantioselectiveReductive-Heck Reaction

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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	Article
Title	Synthesis of Chiral 3-Substituted Indanones via an EnantioselectiveReductive-Heck Reaction
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_24/101021jo701741y/m/web http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_24/101021jo701741y/m/print
related by	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_24/101021jo701741y/authorship/3 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_24/101021jo701741y/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_24/101021jo701741y/authorship/2
Author	Minatti Ana Buchwald Stephen L. Zheng Xiaolai
Abstract	An efficient intramolecular palladium-catalyzed, asymmetric reductive-Heck reaction has been developed,which allowed for the synthesis of either enantiomerically enriched 3-substituted indanones or α-exo-methylene indanones depending on the base used.
article type	research-article
is part of this journal	The Journal of Organic Chemistry

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