About: Alkenes from Terminal Epoxides Using Lithium 2,2,6,6-Tetramethylpiperidideand Organolithiums or Grignard Reagents

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/jacsat/2004/volume_126/issue_39/w
Subject	Communication
Title	Alkenes from Terminal Epoxides Using Lithium 2,2,6,6-Tetramethylpiperidideand Organolithiums or Grignard Reagents
has manifestation of work	http://hub.abes.fr/acs/periodical/jacsat/2004/volume_126/issue_39/101021ja045513a/m/print http://hub.abes.fr/acs/periodical/jacsat/2004/volume_126/issue_39/101021ja045513a/m/web
related by	http://hub.abes.fr/acs/periodical/jacsat/2004/volume_126/issue_39/101021ja045513a/authorship/1 http://hub.abes.fr/acs/periodical/jacsat/2004/volume_126/issue_39/101021ja045513a/authorship/2 http://hub.abes.fr/acs/periodical/jacsat/2004/volume_126/issue_39/101021ja045513a/authorship/3
Author	Fleming Matthew J. Stanway Steven J. Hodgson David M.
Abstract	E-Alkenes (including arylated alkenes, dienes, and allylsilanes) are efficiently prepared by α-deprotonation of terminal epoxides using lithium 2,2,6,6-tetramethylpiperidide, followed by in situ trapping with organolithiums or Grignard reagents.
article type	rapid-communication
is part of this journal	Journal of the American Chemical Society

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