Calculated energies for proton abstraction from substituted benzenes, and their significance for base cleavage of aryltrimethylsilanes
- 2 May 1978
- journal article
- research article
- Published by Elsevier in Journal of Organometallic Chemistry
- Vol. 150 (2) , C23-C24
- https://doi.org/10.1016/s0022-328x(00)84735-x
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Aromatic reactivity. Part LXI. Reactivities and solvent isotope effects in the base cleavage of triorgano-silicon, -germanium, and -tin groups from furan, thiophen, benzofuran, and benzothiophen ringsJournal of the Chemical Society, Perkin Transactions 2, 1976
- Alkaline cleavage of substituted phenyltrimethylsilanes in aqueous dimethylsulphoxideJournal of Organometallic Chemistry, 1971
- Aromatic reactivity. Part XLVI. Interpretation of the substituent effects in base-catalysed cleavage of aryltrimethyl-silanes and -stannanesJournal of the Chemical Society B: Physical Organic, 1971
- Molecular orbital theory of the electronic structure of organic compounds. I. Substituent effects and dipole momentsJournal of the American Chemical Society, 1967
- Aromatic reactivity. Part XXXV. Alkali cleavage of aryltrimethylstannanes: an unusual electrophilic aromatic substitutionJournal of the Chemical Society B: Physical Organic, 1967
- Acidity of Hydrocarbons. XX. Comparison of Relative Proton Exchange Rates of Hydrocarbons with Lithium Cyclohexylamide and Cesium Cyclohexylamide1Journal of the American Chemical Society, 1965
- Mechanism study of the protophilic substitution of hydrogen in aromatic compounds by means of hydrogen isotope exchange with liquid ammoniaTetrahedron, 1962
- Exchange Reactions of Deuterated Benzene Derivatives with Potassium Amide in Liquid Ammonia1aJournal of the American Chemical Society, 1955