About: An Intramolecular aza-[3 + 3] Annulation Approach toAzaphenalene Alkaloids. Total Synthesis of Myrrhine

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_7/w
Subject	Article
Title	An Intramolecular aza-[3 + 3] Annulation Approach toAzaphenalene Alkaloids. Total Synthesis of Myrrhine
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_7/101021jo062533h/m/print http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_7/101021jo062533h/m/web
related by	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_7/101021jo062533h/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_7/101021jo062533h/authorship/2
Author	Gerasyuto Aleksey I. Hsung Richard P.
Abstract	A detailed account on the stereoselective total syntheses of azaphenalene alkaloids via an intramolecularaza-[3 + 3] annulation strategy is described here. All five members of the Coccinellidae family of defensivealkaloids were prepared from the same common intermediate, which was derived from a stereoselectiveaza-[3 + 3] annulation reaction.
article type	research-article
is part of this journal	The Journal of Organic Chemistry

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