A Stereoselective Synthesis of (−)-Isoiridomyrmecin. Application of the Asymmetric Aza-Claisen Rearrangement
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/23/3/23_3_543/_pdf
Reference18 articles.
1. Aza-claisen rearrangement of amide enolates. Stereoselective synthesis of 2,3-disubstituted carboxamides
2. A few new methods for asymmetric synthesis
3. A Few New Methods Toward Asymmetric Synthesis
4. Asymmetric Induction in Aza-Claisen Rearrangement of Carboxamide Enolates. Effect of Chiral Auxiliary on Nitrogen.
5. Asymmetric aza-Claisen rearrangement of glycolamide and glycinamide enolates. Synthesis of optically active α-hydroxy and α-amino acids
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3. Construction of an asymmetric quaternary carbon via an asymmetric aza-Claisen rearrangement and its application in the total synthesis of (+)-α-cuparenone;Tetrahedron: Asymmetry;2012-05
4. 2nd Generation Palladium-Catalyzed Cycloalkenylation in Iridoid Synthesis: Diastereoselective Total Synthesis of Isoiridomyrmecin and Isodihydronepetalactone;HETEROCYCLES;2012
5. Scope and applications of second generation palladium-catalyzed cycloalkenylation. Stereoselective total syntheses of isoiridomyrmecin, isodihydronepetalactone, and α-skytanthine;Tetrahedron;2011-12
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