Durch Ammoniumylsalze initiierte Diels‐Alder‐Reaktion von Ketenen‐Steuerung der [2 + 2]‐ vs. [4 + 2]‐Selektivität
- 1 August 1991
- journal article
- zuschrift
- Published by Wiley in Angewandte Chemie
- Vol. 103 (8) , 981-983
- https://doi.org/10.1002/ange.19911030815
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Competing hole catalyzed Diels-Alder and cyclobutanation/vinylcyclobutane rearrangement paths. A mechanistic dichotomyJournal of the American Chemical Society, 1990
- Cation radical cycloadditions and related sigmatropic reactionsTetrahedron, 1989
- A theoretical study of the reaction of ketene radical cation with ethylene: nucleophilic addition or concerted [2 + 1] cycloaddition?Journal of the American Chemical Society, 1988
- Mechanistic diagnosis of aminium salt initiated Diels-Alder cycloadditions in the diene/diene formatJournal of the American Chemical Society, 1987
- Organic syntheses with electrochemically regenerable redox systemsPublished by Springer Nature ,1987
- Electrochemically induced [4+2]-cycloadditions - a mechanistic interpretation of the cation radical Diels-Alder reaction based on preparative resultsTetrahedron Letters, 1987
- Distinction between aminium cation radical and protic acid catalyzed Diels-Alder reactionsJournal of the American Chemical Society, 1984
- Die Erhaltung der OrbitalsymmetrieAngewandte Chemie, 1969
- The Conservation of Orbital SymmetryAngewandte Chemie International Edition in English, 1969
- Cycloadditionen der Ketene, VI. Zur Anlagerung des Diphenylketens an 1.3‐DieneEuropean Journal of Inorganic Chemistry, 1969