Basicite de benzophénones et methyl-2 benzophénones polysubstituées: Rôle de la torsion moléculaire et des interactions électroniques dans la transmission des effets de substituants
Author:
Publisher
Elsevier BV
Subject
General Engineering
Reference27 articles.
1. PROTONATION OF THE CARBONYL GROUP: II. THE BASICITIES OF SUBSTITUTED BENZALDEHYDES
2. The Protonation of the Carbonyl Group. I. The Basicity of Substituted Acetophenones1
3. The Position of Protonation of the Carboxyl Group1
4. Carbonyl Reactions. XIX. The Basicities of Substituted Chalcones
5. Weak bases in strong acids. V. Substituent effects in the formation of some protonated ketones and the corresponding carbonium ions
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2. A novel synthesis of 1-substituted 2H-isoquinolin-3-ones;Journal of Heterocyclic Chemistry;2004-11
3. A Dipole Moment Study of 2-Methyl- and 2,6-Dimethylacetophenones;Zeitschrift für Physikalische Chemie;1983-02-01
4. Carbon-13 nuclear magnetic resonance spectra of ortho-substituted acetophenones: enhanced substituent effects on the carbonyl group;Journal of the Chemical Society, Perkin Transactions 2;1982
5. Infrared study of polysubstitution effects in benzophenones and acetophenones: contribution of inter and intracycle interaction mechanism;Spectrochimica Acta Part A: Molecular Spectroscopy;1981-01
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