The mechanism of the base-catalysed alcoholysis of triorganosilanes
- 9 April 1974
- journal article
- Published by Elsevier in Journal of Organometallic Chemistry
- Vol. 69 (2), 185-192
- https://doi.org/10.1016/s0022-328x(00)90236-5
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Stereochemistry of asymmetric silicon. XIX. Nucleophilic substitutions involving hydrogen and carbon as leaving groups and further demonstration of stereochemistry crossoverJournal of the American Chemical Society, 1972
- Catalysis in organosilicon chemistry. III. Catalytic mode, solvent isotope effets, and transition-state structure in hydride expulsion from siliconJournal of the American Chemical Society, 1972
- Evidence for proton transfer concomitant with hydride expulsion from silanesTetrahedron Letters, 1970
- Catalysis in ester cleavage. III. Solvent isotope effects and transition-state solvation in the basic methanolysis of estersJournal of the American Chemical Society, 1969
- The fractionation of hydrogen and deuterium isotopes in solutions of sodium methoxideJournal of the Chemical Society D: Chemical Communications, 1969
- Theoretical studies of proton-transfer reactions. II. Reaction of water wih hydride ionJournal of the American Chemical Society, 1968
- The Mechanism of Hydride Transfer. II. Details of Isotope Effects in Pyridine-Diphenylborane HydrolysisJournal of the American Chemical Society, 1962
- Amine Boranes. III. Hydrolysis of Pyridine Diphenylborane and the Mechanism of Hydride Transfer ReactionsJournal of the American Chemical Society, 1958
- Mechanisms for carbon–hydrogen bond breakageQuarterly Reviews, Chemical Society, 1958
- Hydrogen Isotope Effects in the Alkaline Cleavage of Triorganosilanes1Journal of the American Chemical Society, 1955