Comments on “Solvation Parameters. 2. A Simplified Molecular Topology To Generate Easily Optimized Values”
- 1 September 2006
- journal article
- Published by American Chemical Society (ACS) in Journal of Chemical Information and Modeling
- Vol. 46 (5), 1879-1881
- https://doi.org/10.1021/ci600254x
Abstract
A polemic is presented in regards to a recent paper by Laffort and Héricourt [J. Chem. Inf. Model. 2006, 46, 1723−1734].This publication has 11 references indexed in Scilit:
- Solvation Parameters. 2. A Simplified Molecular Topology to Generate Easily Optimized ValuesJournal of Chemical Information and Modeling, 2006
- Solvation parameters: Part 1. Mutual improvements of several approaches and determination of two first sets of optimized valuesJournal of Chromatography A, 2005
- Chemical Toxicity Correlations for Several Fish Species Based on the Abraham Solvation Parameter ModelChemical Research in Toxicology, 2005
- SOLUBILITY BEHAVIOR OF CRYSTALLINE POLYCYCLIC AROMATIC HYDROCARBONS (PAHs): PREDICTION OF FLUORENE SOLUBILITIES IN ORGANIC SOLVENTS WITH THE ABRAHAM SOLVATION PARAMETER MODELPolycyclic Aromatic Compounds, 2005
- Solubility of 9-fluorenone, thianthrene and xanthene in organic solventsFluid Phase Equilibria, 2005
- Air to Blood Distribution of Volatile Organic Compounds: A Linear Free Energy AnalysisChemical Research in Toxicology, 2005
- Determination of sets of solute descriptors from chromatographic measurementsJournal of Chromatography A, 2004
- Solubility predictions for crystalline nonelectrolyte solutes dissolved in organic solvents based upon the Abraham general solvation modelCanadian Journal of Chemistry, 2001
- Characterization of lipophilicity scales using vectors from solvation energy descriptorsJournal of Pharmaceutical Sciences, 1999
- Scales of solute hydrogen-bonding: their construction and application to physicochemical and biochemical processesChemical Society Reviews, 1993