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Knorr, Rudolf, Ruf, Friedrich, Högerl, Johann, Hilpert, Monika, Hassel, Petra (1985) (1-Alkoxyalkyl)malonaldehyd-dianile. aus Formylmalonaldehyd-dianil durch Aldimin-Reduktion und 1,3-Anilin-Verschiebung. Chemische Berichte, 118. 4743-4753 doi:10.1002/cber.19851181209

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Reference TypeJournal (article/letter/editorial)
Title(1-Alkoxyalkyl)malonaldehyd-dianile. aus Formylmalonaldehyd-dianil durch Aldimin-Reduktion und 1,3-Anilin-Verschiebung
JournalChemische Berichte
AuthorsKnorr, RudolfAuthor
Ruf, FriedrichAuthor
Högerl, JohannAuthor
Hilpert, MonikaAuthor
Hassel, PetraAuthor
Year1985 (December)Volume118
PublisherWiley
DOIdoi:10.1002/cber.19851181209Search in ResearchGate
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Mindat Ref. ID4329461Long-form Identifiermindat:1:5:4329461:9
GUID0
Full ReferenceKnorr, Rudolf, Ruf, Friedrich, Högerl, Johann, Hilpert, Monika, Hassel, Petra (1985) (1-Alkoxyalkyl)malonaldehyd-dianile. aus Formylmalonaldehyd-dianil durch Aldimin-Reduktion und 1,3-Anilin-Verschiebung. Chemische Berichte, 118. 4743-4753 doi:10.1002/cber.19851181209
Plain TextKnorr, Rudolf, Ruf, Friedrich, Högerl, Johann, Hilpert, Monika, Hassel, Petra (1985) (1-Alkoxyalkyl)malonaldehyd-dianile. aus Formylmalonaldehyd-dianil durch Aldimin-Reduktion und 1,3-Anilin-Verschiebung. Chemische Berichte, 118. 4743-4753 doi:10.1002/cber.19851181209
In(1985) Chemische Berichte Vol. 118. Wiley

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Ruf, Friedrich, Högerl, Johann, Knorr, Rudolf, Bronberger, Hildegard (1985) (1-Alkenyl)malonaldehyd-dianile aus Formylmalonaldehyd-dianil. Chemische Berichte, 118. 4754-4759 doi:10.1002/cber.19851181210
Knorr, Rudolf, Ruf, Friedrich (1985) Synthesen und Tautomerieverhältnisse von β-Keto-enaminen und Vinamidin-Derivaten mit Bornengerüst. Chemische Berichte, 118. 4486-4495 doi:10.1002/cber.19851181119
KNORR, R., RUF, F., HOEGERL, J., HILPERT, M., HASSEL, P. (1986) ChemInform Abstract: Paramagnetically Induced NMR Shifts. Part 12. (1-Alkoxyalkyl)malonaldehyde Dianils by Aldimine Reduction of Formylmalonaldehyde Dianil and 1,3-Migration of the Anilino Group. Chemischer Informationsdienst, 17 (11) doi:10.1002/chin.198611174
Knorr, Rudolf, Hintermeyer-;Hilpert, Monika, Mehlstäubl, Johann, Hoang, Thi Phung, Neuner, Brigitte, Bührer, Petra (1993) (E/Z) Equilibria, 16. Lone Electron Pair Donor Quality of the Imino Function: Synthesis and Reactivity of Sterically Strongly Congested Iminocyclopentanes. Chemische Berichte, 126. 211-215 doi:10.1002/cber.19931260129
Knorr, Rudolf, Hintermeyer-Hilpert, Monika, Böhrer, Petra (1990) (E,Z) Equilibria, 12. Differential NMR Shielding by Phenyl, Assigned from Chemical Labelling and (Z,E) Equilibration. Chemische Berichte, 123. 1137-1141 doi:10.1002/cber.19901230529
Knorr, Rudolf, Mehlstäubl, Johann, Böhrer, Petra (1989) Erschöpfende α-Alkylierung von Fünfring-Ketonen mit Natriumhydrid und Dimethylsulfat oder Ethyliodid. Chemische Berichte, 122. 1791-1793 doi:10.1002/cber.19891220927
Stahl, Ingfried (1985) 1,3-Dithienium- und 1,3-Dithioleniumsalze, II. Synthese monocyclothioacetalisierter 1,3-Diketone aus Silylenolethern. Chemische Berichte, 118. 1798-1808 doi:10.1002/cber.19851180507
Böhrer, Gerald, Böhrer, Petra, Knorr, Rudolf (1990) Cyclopropan-Derivate, 3. (1-Alkylcyclopropyl)ketone durch Acylierung von α-substituierten γ-Lactonen. Chemische Berichte, 123. 2167-2172 doi:10.1002/cber.19901231113
Knorr, Rudolf, Lattke, Ernst, Ruf, Friedrich, Reißig, Hans-Ulrich (1981) Vinyl-to-Benzyl Isomerization and Electrocyclizations in Lithio Derivatives ofo-Tolylstilbenes. Chemische Berichte, 114. 1592-1599 doi:10.1002/cber.19811140503
Knorr, Rudolf, Hoang, Thi Phung, Mehlstäubl, Johann, Hintermeyer-;Hilpert, Monika, Lüdemann, Hans-;Dietrich, Lang, Elmar, Sextl, Gerhard, Rattay, Wilfried, Bührer, Petra (1993) Sterically Congested Molecules, 6. Lone Electron Pair Donor Quality of the Imino Function: Increased Front Strain and Electronic Substituent Effects on Sterically Accelerated Nitrogen Inversion in Iminocyclopentanes. Chemische Berichte, 126. 217-224 doi:10.1002/cber.19931260130
Stahl, Ingfried (1985) 1,3-Dithienium- und 1,3-Dithioleniumsalze, III. Synthese cyclischer Dithioacetale von β-Ketoestern aus Keten-silylacetalen. Chemische Berichte, 118. 3159-3165 doi:10.1002/cber.19851180815
 
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