Chiral 2-(?-Aminoalkyl)-oxazolines by ring transformation of lactam derivatives
Author:
Publisher
Wiley
Subject
Environmental Engineering
Reference7 articles.
1. Synthesis of enantiomerically pure ω-amino acids by asymmetric α-alkylation of chiral ω-aminoalkyloxazolines
2. Ringöffnende Aminolyse von Lactamen. Ein einfacher Zugang zu 2-(ω-aminoalkyl)substituierten, fünf-und sechsgliedrigen Heterocyclen
3. US-Pat. 3 399 197 (1968);
4. Novel Derivatives of Biogenic ?-Aminoacids by ring transformations with lactam derivatives
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1. ChemInform Abstract: Chiral 2-(ω-Aminoalkyl)oxazolines by Ring Transformation of Lactam Derivatives.;ChemInform;2010-08-04
2. Five-, Six-, and Seven-membered Lactim Ethers. Methods of Synthesis and Chemical Properties. (Review);Chemistry of Heterocyclic Compounds;2005-05
3. Recent Advances in Ring Transformations of Five-Membered Heterocycles and Their Fused Derivatives;European Journal of Organic Chemistry;2001-09
4. Enantioselective synthesis of S-substituted ω-amino-α-thiohydroxycarboxylic acids via sulfenylation of 2-(ω-aminoalkyl)-oxazolines;Tetrahedron: Asymmetry;1997-07
5. 4-(1-Methyl-2-sulfamoylvinyl)pyrazoles by Ring Transformation of 1,1-dioxo-2H-1,2-thiazine-4-carbaldehydes with hydrazines;Journal für Praktische Chemie/Chemiker-Zeitung;1997
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