Synthesis, reaction, and structure of chiral N-methyl-2-oxazolidinones from 3-ethoxy-6-(N-methyl-N-tert-butoxycarbonyl)amino-2,4-hexadienoates
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Synthesis and Reactions of Ethyl 6-Aryl-3-ethoxy-6-oxo-2,4-hexadienoates.
2. Novel Annulation of 6-Aryl-3-ethoxy-6-hydroxy-2,4-hexadienoates to 5-Benzoyl-3-ethoxycyclopent-2-en-1-ones under Basic Conditions
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2. ChemInform Abstract: Synthesis, Reaction, and Structure of Chiral N-Methyl-2-oxazolidinones from 3-Ethoxy-6-(N-methyl-N-tert-butoxycarbonyl)amino-2,4-hexadienoates.;ChemInform;2010-06-23
3. One-Pot Cyclizations of (2,4-Dioxobutylidene)phosphoranes and (2-Alkoxy-4-oxobut-2-enylidene)phosphoranes;Synthesis;2008-12
4. Highly Stereoselective Intramolecular SN2′ Cyclization Yielding Chiral Oxazolidin-2-ones: General Route to α-Hydroxy-β-amino Acids;Synlett;2005
5. Condensations of Ethyl 3-Ethoxy-4-(triphenylphosphoranylidene)-2-butenoate with α,β-Unsaturated Carbonyl Compounds;Monatshefte f�r Chemie / Chemical Monthly;2002-12-01
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