Unusual ring-chain tautomerism in some cyclic nitronic esters
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference4 articles.
1. The Reaction between 2-Nitro-1-phenylpropene and Cyclohexanone
2. 6-Hydroxy-5,6-dihydro-4H-1,2-oxazine 2-oxide system. Absence of ring-chain tautomerism in 5,5-dinitro-2-pentanone
3. Cyclic nitronic esters
4. Vinylamines. Part IX. Reaction of cyclohexanone enamines with αβ-unsaturated ketones
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2. Uncatalyzed reactions of α-(trihaloethylidene)nitroalkanes with push–pull enamines: a new type of ring–ring tautomerism in cyclobutane derivatives and the dramatic effect of the trihalomethyl group on the reaction pathway;Tetrahedron Letters;2011-11
3. Unusual ring-chain tautomerism in bicyclo[4.2.0]octane derivatives;Tetrahedron Letters;2011-06
4. Are Oxazolidinones Really Unproductive, Parasitic Species in Proline Catalysis? – Thoughts and Experiments Pointing to an Alternative View;Helvetica Chimica Acta;2007-03
5. Diels-Alder cycloaddittion reactions of enaminothions with nitroalkenes;Tetrahedron;1990-01
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