1, 3-Dipolar cycloaddition between ethyl trifluoroacetoacetate and N-(benzylidene)methylamine N-oxide
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1991/P1/P19910002888
Reference19 articles.
1. Novel Ring Transformation of 3-Benzoylisoxazolidines into 2-Hydroxydihydrofurans. N–O Cleavage vs. 1,3-Dipolar Cycloreversion
2. Alkylation of ethyl 4,4,4-trifluoroacetoacetate. First example of a reversible O-alkylation process leading to C-alkylation
3. Methods generale d'acess aux trifluoromethylcetones. 1ère partie: Alkylation directe du trifluoroacetylacetate d'ethyle
4. Alkylation du trifluoroacetylacetate d'ethyle methode generale d'acces aux trifluoromethylcetones. 2ème Partie: alkylations indirects du TFAAE
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2. ChemInform Abstract: 1,3-Dipolar Cycloaddition Between Ethyl Trifluoroacetoacetate and N-( Benzylidene)methylamine N-Oxide.;ChemInform;2010-08-22
3. Ethyl 4,4,4-trifluorocrotonate;Encyclopedia of Reagents for Organic Synthesis;2003-04-15
4. Cycloaddition reactions of β-trifluoroacetylvinyl ethers;Tetrahedron;2003-04
5. No. 1 - 2902;Landolt-Börnstein - Group III Condensed Matter;2003
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