A Fundamental Assumption about OH- Attack in Phosphate Ester Hydrolysis Is Not Fully Justified
- 1 June 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 119 (23) , 5473-5474
- https://doi.org/10.1021/ja964270m
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- Mechanistic Analysis of the Observed Linear Free Energy Relationships in p21ras and Related SystemsBiochemistry, 1996
- Linear Free Energy Relationships in the Intrinsic and GTPase Activating Protein-Stimulated Guanosine 5‘-Triphosphate Hydrolysis of p21rasBiochemistry, 1996
- Structure-Energy Analysis of the Role of Metal Ions in Phosphodiester Bond Hydrolysis by DNA Polymerase IJournal of the American Chemical Society, 1995
- Hydrolysis rate difference between cyclic and acyclic phosphate esters: solvation versus strainJournal of the American Chemical Society, 1993
- Do pentacoordinate oxyphosphorane intermediates always exist?Journal of the American Chemical Society, 1993
- Nonexistence of dianionic pentacovalent intermediates in an ab initio study of the base-catalyzed hydrolysis of ethylene phosphateJournal of the American Chemical Society, 1990
- Stereoelectronic effects in the reactions of phosphate diesters. Ab initio molecular orbital calculations of reaction surfaces. 2Journal of the American Chemical Society, 1979
- Theoretical calculations of the hydrolysis energies of some "high-energy" molecules. 2. A survey of some biologically important hydrolytic reactionsJournal of the American Chemical Society, 1978
- Theoretical studies of enzymic reactions: Dielectric, electrostatic and steric stabilization of the carbonium ion in the reaction of lysozymeJournal of Molecular Biology, 1976
- Formulation of the reaction coordinateThe Journal of Physical Chemistry, 1970