About: Domino Coupling Relay Approach to Polycyclic Pyrrole-2-carboxylates

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_31/w
Subject	Communication
Title	Domino Coupling Relay Approach to Polycyclic Pyrrole-2-carboxylates
has manifestation of work	http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_31/101021ja053408a/m/print http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_31/101021ja053408a/m/web
related by	http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_31/101021ja053408a/authorship/1 http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_31/101021ja053408a/authorship/4 http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_31/101021ja053408a/authorship/2 http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_31/101021ja053408a/authorship/3
Author	Hayashi Hiroki Saigoku Tomoaki Nishiyama Hisao Yamamoto Yoshihiko
Abstract	CuBr2-catalyzed three-component coupling of N-benzylallylamine, ethyl glyoxalate, and terminal alkynes afforded glycine-tethered 1,6-enynes, which were further transformed into polycyclic pyrrole-2-carboxylates via novel cycloisomerization/Diels−Alder cycloaddition/dehydrogenation sequence under iridium-catalyzed conditions.
article type	rapid-communication
is part of this journal	Journal of the American Chemical Society

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