About: Synthesis of 3-Substituted Quinolines viaTransition-Metal-Catalyzed ReductiveCyclization of o-Nitro Baylis−HillmanAcetates

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_16/w
Subject	Note
Title	Synthesis of 3-Substituted Quinolines viaTransition-Metal-Catalyzed ReductiveCyclization of o-Nitro Baylis−HillmanAcetates
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_16/101021jo034447c/m/web http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_16/101021jo034447c/m/print
related by	http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_16/101021jo034447c/authorship/2 http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_16/101021jo034447c/authorship/1
Author	Nicholas Kenneth M. O'Del David K.
Abstract	Reductive cyclization of o-nitro-substituted Baylis−Hillman acetates by carbon monoxide, catalyzed by[Cp*Fe(CO)2]2, gives moderate to good yields of 3-substitutedquinolines.
article type	brief-report
is part of this journal	The Journal of Organic Chemistry

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