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International Journal of Molecular Sciences|May 27, 2015
Calculated third order rate constants for interpreting the mechanisms of hydrolyses of chloroformates, carboxylic Acid halides, sulfonyl chlorides and phosphorochloridatesT William Bentley
The Journal of Organic Chemistry|February 28, 2004
Secondary alpha-deuterium kinetic isotope effects: assumptions simplifying interpretations of mechanisms of solvolyses of secondary alkyl sulfonatesT William Bentley
Chemistry (Weinheim an Der Bergstrasse, Germany)|July 5, 2006
Additivity rules using similarity models for chemical reactivity: calculation and interpretation of electrofugality and nucleofugalityT William Bentley
Organic & Biomolecular Chemistry|August 3, 2011
Nucleophilicity parameters for amines, amino acids and peptides in water. Variations in selectivities for quinone methidesT William Bentley
The Journal of Organic Chemistry|July 18, 2008
Structural effects on the solvolytic reactivity of carboxylic and sulfonic acid chlorides. Comparisons with gas-phase data for cation formationT William Bentley
Organic & Biomolecular Chemistry|August 30, 2003
Reinterpretation of the kinetic data and the non-steady state hypothesis (two-step mechanism) for the S(N)2 reaction between p-nitrophenoxide and methyl iodide in aprotic solvents containing waterEduardo Humeres, T William Bentley
Organic & Biomolecular Chemistry|August 12, 2004
Role of hydroxyl concentrations in solvatochromic measures of solvent polarity of alcohols and alcohol-water mixtures-evidence that preferential solvation effects may be overestimatedT William Bentley, In Sun Koo
The Journal of Organic Chemistry|November 1, 1996
S(N)2 Mechanism for Alcoholysis, Aminolysis, and Hydrolysis of Acetyl ChlorideT. William Bentley, Gareth Llewellyn, J. Anthony McAlister
The Journal of Organic Chemistry|January 28, 2006
Unsubstituted bicyclo[1.1.0]but-2-ylcarbinyl cationsT William Bentley, Bernd Engels, Thomas Hupp, et al.
Analytical and Bioanalytical Chemistry|March 23, 2015
Revised sample preparation for the analysis of oxysterols by enzyme-assisted derivatisation for sterol analysis (EADSA)Peter J Crick, T William Bentley, Yuqin Wang, et al.
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