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Zalewski, R. I., Dunn, G. E. (1968) Protonation of conjugated carbonyl groups in sulfuric acid solution. I. Adaptation of the amide acidity function HA for protonation of the carbonyl group in non-Hammett bases. Canadian Journal of Chemistry, 46 (14). 2469-2470 doi:10.1139/v68-403

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Reference TypeJournal (article/letter/editorial)
TitleProtonation of conjugated carbonyl groups in sulfuric acid solution. I. Adaptation of the amide acidity function HA for protonation of the carbonyl group in non-Hammett bases
JournalCanadian Journal of Chemistry
AuthorsZalewski, R. I.Author
Dunn, G. E.Author
Year1968 (July 15)Volume46
Issue14
PublisherCanadian Science Publishing
DOIdoi:10.1139/v68-403Search in ResearchGate
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Mindat Ref. ID8291261Long-form Identifiermindat:1:5:8291261:7
GUID0
Full ReferenceZalewski, R. I., Dunn, G. E. (1968) Protonation of conjugated carbonyl groups in sulfuric acid solution. I. Adaptation of the amide acidity function HA for protonation of the carbonyl group in non-Hammett bases. Canadian Journal of Chemistry, 46 (14). 2469-2470 doi:10.1139/v68-403
Plain TextZalewski, R. I., Dunn, G. E. (1968) Protonation of conjugated carbonyl groups in sulfuric acid solution. I. Adaptation of the amide acidity function HA for protonation of the carbonyl group in non-Hammett bases. Canadian Journal of Chemistry, 46 (14). 2469-2470 doi:10.1139/v68-403
In(1968, July) Canadian Journal of Chemistry Vol. 46 (14) Canadian Science Publishing

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Zalewski, R. I., Dunn, G. E. (1969) Protonation of conjugated carbonyl groups in sulfuric acid solutions. II. Protonation and basicity of α,β-unsaturated alicyclic ketones. Canadian Journal of Chemistry, 47 (12). 2263-2270 doi:10.1139/v69-366
Zalewski, R. I., Dunn, G. E. (1970) Protonation of conjugated carbonyl groups in sulfuric acid solutions. III. α,β-Unsaturated ketosteroids. Canadian Journal of Chemistry, 48 (16). 2538-2541 doi:10.1139/v70-429
Vetešník, P., Bielavský, J., Večeřa, M. (1968) Protonation of polyacid organic bases. III. Hammett acidity function H+ for aqueous sulfuric acid. Collection of Czechoslovak Chemical Communications, 33. 1687-1692 doi:10.1135/cccc19681687
Dolman, Douglas, Stewart, Ross (1967) An acidity function in ethanol – sulfuric acid based on the protonation of diphenylamines. Canadian Journal of Chemistry, 45 (9). 903-910 doi:10.1139/v67-154
Dunn, G. E., Janzen, E. G., Rodewald, W. (1968) Mechanism of decarboxylation of substituted salicylic acids. I. Kinetics in quinoline solution. Canadian Journal of Chemistry, 46 (18). 2905-2909 doi:10.1139/v68-483
Hopkinson, A. C., Csizmadia, I. G. (1974) An Ab Initio Study of the Effect of Substituents on Protonation of the Carbonyl Group. Canadian Journal of Chemistry, 52 (4). 546-554 doi:10.1139/v74-085
Allen., A. D., Barrett, P. F. (1968) Kinetics of some substitution reactions of the Group VI metal carbonyl halides. Canadian Journal of Chemistry, 46 (10). 1655-1661 doi:10.1139/v68-277
Yates, K., Stewart, Ross (1959) PROTONATION OF THE CARBONYL GROUP: II. THE BASICITIES OF SUBSTITUTED BENZALDEHYDES. Canadian Journal of Chemistry, 37 (4). 664-671 doi:10.1139/v59-092
Stewart, Ross, Granger, M. R., Moodie, R. B., Muenster, L. J. (1963) THE PROTONATION OF THE CARBONYL GROUP: III. DIARYL KETONES. Canadian Journal of Chemistry, 41 (5). 1065-1070 doi:10.1139/v63-152
Dunn, G. E., Buccini, John (1968) Effect of changing pH upon the kinetic 13C-isotope effect in the decarboxylation of 4-methoxyanthranilic acid. Canadian Journal of Chemistry, 46 (4). 563-566 doi:10.1139/v68-092
Robinson, E. A., Zaidi, S. A. A. (1968) On sulfenium ions in 100% sulfuric acid. Canadian Journal of Chemistry, 46 (24). 3927-3928 doi:10.1139/v68-651
 
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