About: Synthesis of Tricyclic Heterocycles via a Tandem ArylAlkylation/Heck Coupling Sequence

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_3/w
Subject	Article
Title	Synthesis of Tricyclic Heterocycles via a Tandem ArylAlkylation/Heck Coupling Sequence
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_3/101021jo0617868/m/print http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_3/101021jo0617868/m/web
related by	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_3/101021jo0617868/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_3/101021jo0617868/authorship/2 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_3/101021jo0617868/authorship/3
Author	Lautens Mark Alberico Dino Rudolph Alena
Abstract	A norbornene-mediated palladium-catalyzed sequence is described in which two alkyl−aryl bonds andone alkenyl−aryl bond are formed in one pot with use of microwave irradiation. A variety of symmetricaland unsymmetrical oxygen-, nitrogen-, silicon-, and sulfur-containing tricyclic heterocycles weresynthesized from a Heck acceptor and an aryl iodide containing two tethered alkyl halides. This approachwas further applied to the synthesis of a tricyclic mescaline analogue.
article type	research-article
is part of this journal	The Journal of Organic Chemistry

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