Formation cinetique d'invertomeres stables de l'azote lors de l'addition des esters nitroniques aux olefines α,β-diactivees
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. Esters nitroniques isomeres geometriques: configuration, activite dipolaire-1,3 comparee et stereochimie de leur addition a diverses olefines activees
2. Langsame Inversion am pyramidal gebundenen Stickstoff: Isolierung und Epimerisierung diastereomerer N-Methoxy-3,3-di-methoxycarbonyl-5-cyan-1, 2-oxazolidine. Vorläufige Mitteilung
3. Langsame Inversion am pyramidal gebundenen Stickstoff: Konfiguration und Konformation beim Strukturtyp der N, N-Dialkoxy-alkylamine aus der Sicht eines semiempirischen MO-Modells
4. Langsame Inversion am pyramidal gebundenen Stickstoff: Kristallstrukturanalyse destrans-N-Methoxy-3, 3-di-methoxycarbonyl-5-cyan-1, 2-oxazolidins
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1. Reduction of chromano–piperidine-fused isoxazolidines: Tandem intramolecular rearrangements leading to 2-(methylamino)-4-oxo- N -phenyl- N -propyl-4 H -chromene-3-carboxamide;Tetrahedron Letters;2017-06
2. Partially Saturated Polynuclear Isoxazoles;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02
3. References;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02
4. Intramolecular low-temperature 1,3-dipolar cycloadditions of nitrones: synthesis of chromano-heterocycles;Tetrahedron;2007-05
5. Regio- and stereoselective thermal cycloaddition of α-aryl-N-phenylnitrones to 16-dehydropregnenolone acetate: π-facial selective addition of the minor rotamers of the nitrones;Tetrahedron Letters;2000-09
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