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

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

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Veröffentlicht in:Journal of organic chemistry 2005-10, Vol.70 (22), p.9081-9084
Hauptverfasser: Patel, Jignesh, Pelloux-Léon, Nadia, Minassian, Frédéric, Vallée, Yannick
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container_end_page 9084
container_issue 22
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container_title Journal of organic chemistry
container_volume 70
creator Patel, Jignesh
Pelloux-Léon, Nadia
Minassian, Frédéric
Vallée, Yannick
description Total syntheses of enantiopure hanishin, longamide B, and longamide B methyl ester are described. Absolute configurations of these natural products have been established.
doi_str_mv 10.1021/jo051555l
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subjects Aspartic Acid - chemistry
Chemical Sciences
Chemistry
Esters - chemical synthesis
Esters - chemistry
Exact sciences and technology
Heterocyclic compounds
Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings
Molecular Structure
Organic chemistry
Preparations and properties
Pyrroles - chemical synthesis
Pyrroles - chemistry
Stereoisomerism
title Syntheses of S-Enantiomers of Hanishin, Longamide B, and Longamide B Methyl Ester from l-Aspartic Acid β-Methyl Ester: Establishment of Absolute Stereochemistry
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