Ammoniumyl Salt‐Induced Diels‐Alder Reaction of Ketenes—Control of [2 + 2] vs. [4 + 2] Selectivity
- 1 August 1991
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 30 (8) , 999-1001
- https://doi.org/10.1002/anie.199109991
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
- Mechanistic diagnosis of aminium salt initiated Diels-Alder cycloadditions in the diene/diene formatJournal of the American Chemical Society, 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
- [2 + 1] Cycloaddition of ketene radical cation and ethyleneJournal of the American Chemical Society, 1984
- Acid-catalyzed rearrangement of cyclobutanones. VI. Syntheses of chrysenes and steroid-like substancesCanadian Journal of Chemistry, 1981
- Acid-catalyzed reactions of cyclobutanones. III. Formation of substituted 2-tetralones from α-phenylcyclobutanonesCanadian Journal of Chemistry, 1978
- 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