About: Indirect Trapping of the RetroconjugateAddition Reaction Intermediate Involvedin the Epimerization of Lobeline: Application to the Synthesis of(−)-Sedamine

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2004/volume_69/issue_24/w
Subject	Note
Title	Indirect Trapping of the RetroconjugateAddition Reaction Intermediate Involvedin the Epimerization of Lobeline: Application to the Synthesis of(−)-Sedamine
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2004/volume_69/issue_24/101021jo048848j/m/print http://hub.abes.fr/acs/periodical/joceah/2004/volume_69/issue_24/101021jo048848j/m/web
related by	http://hub.abes.fr/acs/periodical/joceah/2004/volume_69/issue_24/101021jo048848j/authorship/2 http://hub.abes.fr/acs/periodical/joceah/2004/volume_69/issue_24/101021jo048848j/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2004/volume_69/issue_24/101021jo048848j/authorship/3
Author	Crooks Peter A. Dwoskin Linda P. Zheng Guangrong
Abstract	Alkyl chloroformates induced indirect trappingof the retroconjugate addition reaction intermediate involvedin the epimerization of lobeline is described. This strategywas applied to the conversion of (−)-lobeline to (−)-sedaminein high overall yield.
article type	brief-report
is part of this journal	The Journal of Organic Chemistry

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