Specific reciprocal methyl/hydrogen transfer reactions and hydrogen exchange processes between aryl rings in crowded ketone cation radicals
- 25 February 1985
- journal article
- Published by Elsevier in International Journal of Mass Spectrometry and Ion Processes
- Vol. 63 (2-3) , 289-304
- https://doi.org/10.1016/0168-1176(85)80031-8
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Mechanism of keto Å enol tautomerism of ionized vinyl alcohol versus acetaldehyde and their dissociation to C2H3O+ and H·. An ab initio molecular orbital studyInternational Journal of Mass Spectrometry and Ion Processes, 1984
- Stable simple enols. 3. Static and dynamic NMR behavior of crowded triarylethenols and related compounds. Three-ring flip as the threshold mechanism for enantiomerization of crowded triarylvinyl propellersJournal of the American Chemical Society, 1984
- Highly specific reciprocal methyl/hydrogen transfer reactions preceding some unimolecular dissociations of crowded enol cation radicals in the gas phase as examples for conformationally controlled processesJournal of the American Chemical Society, 1984
- Barrier to 1,3‐sigmatropic shift in odd electron ions. A MINDO/3 study of H, OH, CH3 and C6H5 migrationJournal of Mass Spectrometry, 1982
- Thermochemistry and unimolecular reactions of ionized 1,2-dimesityl-2-phenylethanone and 2,2-dimesityl-1-phenylethanone and their enols and enol acetates in the gas phaseJournal of the American Chemical Society, 1981
- Simple enols: How rare are they?Journal of Chemical Education, 1980
- Simple enolsChemical Reviews, 1979
- Chemie isolierter KationenAngewandte Chemie, 1979
- Vinyl Alcohols. XVIII.1 Increased HindranceJournal of the American Chemical Society, 1946
- Vinyl Alcohols. XIII.1 1,2-Dimesityl-2-phenylvinyl AlcoholJournal of the American Chemical Society, 1944