About: Total Synthesis of Anhydrolycorinone Utilizing SequentialIntramolecular Diels−Alder Reactions of a 1,3,4-Oxadiazole

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_21/w
Subject	Article
Title	Total Synthesis of Anhydrolycorinone Utilizing SequentialIntramolecular Diels−Alder Reactions of a 1,3,4-Oxadiazole
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_21/101021jo020437k/m/web http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_21/101021jo020437k/m/print
related by	http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_21/101021jo020437k/authorship/2 http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_21/101021jo020437k/authorship/1
Author	Boger Dale L. Wolkenberg Scott E.
Abstract	A convergent total synthesis of anhydrolycorinone is detailed, enlisting sequential intramolecularDiels−Alder reactions of a suitably substituted 2-amino-1,3,4-oxadiazole defining a novel oxadiazole→ furan → benzene Diels−Alder strategy.
article type	research-article
is part of this journal	The Journal of Organic Chemistry

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