About: Oxidative Rearrangement of Tertiary Allylic Alcohols Employing Oxoammonium Salts

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_12/w
Subject	Note
Title	Oxidative Rearrangement of Tertiary Allylic Alcohols Employing Oxoammonium Salts
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_12/101021jo800634r/m/print http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_12/101021jo800634r/m/web
related by	http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_12/101021jo800634r/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_12/101021jo800634r/authorship/2 http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_12/101021jo800634r/authorship/3
Author	http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_12/101021jo800634r/shibuyamasatoshi Iwabuchi Yoshiharu Tomizawa Masaki
Abstract	Practical and highly efficient methods for oxidative rearrangement of tertiary allylic alcohols to β-substituted α,β-unsaturated carbonyl compounds employing oxoammonium salts are described. The methods developed are applicable to acyclic substrates as well as medium membered ring substrates and macrocyclic substrates. The counteranion of the oxoammonium salt plays crucial roles on this oxidative rearrangement.
is part of this journal	The Journal of Organic Chemistry

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