Stereoelectronic control in the cleavage of tetrahedral intermediates in the hydrolysis of esters and amides
- 1 January 1975
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 31 (20) , 2463-2490
- https://doi.org/10.1016/0040-4020(75)80257-2
Abstract
No abstract availableThis publication has 60 references indexed in Scilit:
- The Oxidation of Acetals by OzoneCanadian Journal of Chemistry, 1974
- Hydrotrioxides. Formation and kinetics of decompositionJournal of the American Chemical Society, 1974
- The Importance of Conformation of the Tetrahedral Intermediate in the Hydrolysis of Amides. Selective Cleavage of the Tetrahedral Intermediate Controlled by Orbital OrientationCanadian Journal of Chemistry, 1973
- The Importance of Conformation in the Ozonolysis of AcetalsCanadian Journal of Chemistry, 1972
- The Importance of Conformation of the Tetrahedral Intermediate in the Hydrolysis of Esters. Selective Cleavage of the Tetrahedral Intermediate Controlled by Orbital OrientationCanadian Journal of Chemistry, 1972
- Ozonolysis of Acetals. (1) Ester Synthesis, (2) THP Ether Cleavage, (3) Selective Oxidation of β-Glycoside, (4) Oxidative Removal of Benzylidene and Ethylidene Protecting GroupsCanadian Journal of Chemistry, 1971
- The Anomeric Effect: The Conformational Equilibria of Tetrahydro-1,3-oxazines and 1-Methyl-1,3-diazaneCanadian Journal of Chemistry, 1971
- Effects of unshared pairs of electrons and their solvation on conformational equilibriaPure and Applied Chemistry, 1971
- Dipole moments and conformation of acetalsCollection of Czechoslovak Chemical Communications, 1968
- Mechanisms of Catalysis of Nucleophilic Reactions of Carboxylic Acid Derivatives.Chemical Reviews, 1960