About: Diastereoselective Formal Synthesis of a Monoterpene Alkaloid,(−)-Incarvilline

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_17/w
Subject	Article
Title	Diastereoselective Formal Synthesis of a Monoterpene Alkaloid,(−)-Incarvilline
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_17/101021jo0709091/m/print http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_17/101021jo0709091/m/web
related by	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_17/101021jo0709091/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_17/101021jo0709091/authorship/2
Author	Kaneda Kyosuke Honda Toshio
Abstract	Diastereoselective formal synthesis of a monoterpene alkaloid, (−)-incarvilline, the key intermediate forthe synthesis of (−)-incarvillateine, was achieved by using an intramolecular Pauson−Khand reaction of(S)-N-[(E)-2-butenyl]-N-(3-butynyl-2-methoxymethoxy)-p-toluenesulfonamide as a key step.
article type	research-article
is part of this journal	The Journal of Organic Chemistry

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