Asymmetric aza-Claisen rearrangement of glycolamide and glycinamide enolates. Synthesis of optically active α-hydroxy and α-amino acids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 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. Stereocontrolled synthesis of highly oxygenated acyclic systems via the enolate Claisen rearrangement of O-protected allylic glycolates
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