About: Syntheses of S-Enantiomers of Hanishin,Longamide B, and Longamide B MethylEster from l-Aspartic Acid β-Methyl Ester:Establishment of Absolute Stereochemistry

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2005/volume_70/issue_22/w
Subject	Note
Title	Syntheses of S-Enantiomers of Hanishin,Longamide B, and Longamide B MethylEster from l-Aspartic Acid β-Methyl Ester:Establishment of Absolute Stereochemistry
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2005/volume_70/issue_22/101021jo051555l/m/print http://hub.abes.fr/acs/periodical/joceah/2005/volume_70/issue_22/101021jo051555l/m/web
related by	http://hub.abes.fr/acs/periodical/joceah/2005/volume_70/issue_22/101021jo051555l/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2005/volume_70/issue_22/101021jo051555l/authorship/2 http://hub.abes.fr/acs/periodical/joceah/2005/volume_70/issue_22/101021jo051555l/authorship/3 http://hub.abes.fr/acs/periodical/joceah/2005/volume_70/issue_22/101021jo051555l/authorship/4
Author	Minassian Frédéric Pelloux-Léon Nadia Vallée Yannick Patel Jignesh
Abstract	Total syntheses of enantiopure hanishin, longamide B, andlongamide B methyl ester are described. Absolute configurations of these natural products have been established.
article type	brief-report
is part of this journal	The Journal of Organic Chemistry

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