Syntheses of S-Enantiomers of Hanishin, Longamide B, and Longamide B Methyl Ester from L-Aspartic Acid β-Methyl Ester: Establishment of Absolute Stereochemistry - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Journal of Organic Chemistry Année : 2005

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

Résumé

Total syntheses of enantiopure Hanishin, Longamide B, and Longamide B methyl ester are described. Absolute configurations of these natural products have been established.

Domaines

Chimie

Dates et versions

hal-04331287 , version 1 (11-12-2023)

Licence

Copyright (Tous droits réservés)

Identifiants

Citer

Jignesh Patel, Nadia Pelloux-Léon, Frédéric Minassian, Yannick Vallée. Syntheses of S-Enantiomers of Hanishin, Longamide B, and Longamide B Methyl Ester from L-Aspartic Acid β-Methyl Ester: Establishment of Absolute Stereochemistry. Journal of Organic Chemistry, 2005, 70 (22), pp.9081-9084. ⟨10.1021/jo051555l⟩. ⟨hal-04331287⟩

Collections

UGA CNRS DCM
5 Consultations
1 Téléchargements

Altmetric

Partager

Gmail Facebook X LinkedIn More