Classical and three-dimensional QSAR in agrochemistry : developed from a symposium sponsored by the Division of Agrochemicals at the 208th National Meeting of the American Chemical Society, Washington, DC, August 21-25, 1994

Status of QSAR at the End of the Twentieth Century Quantitative Structure-Activity and Database-Aided Bioisosteric Structural Transformation Procedure as Methodologies of Agrochemical Design Hydrophobicity Parameter of Heteroaromatic Compounds Derived from Various Partitioning Systems Theoretical Estimation of Octanol-Water Partition Coefficient for Organophosphorus Pesticides The Calculation of Pesticide Hydrophobicity by Computer Transport Parameter Dependence on Intermolecular Forces QSARs from Mathematical Models: Systemic Behavior of Pesticides Hydrophobicity and Systemic Activities of Fungicidal Triazoles and Bleaching Herbicidal Compounds The Incidence of Delayed-Type Contact Dermatitis in Modern Pesticides QSARs in Environmental Toxicology and Chemistry: Recent Developments Noncongeneric Structure-Toxicity Correlation Using Fuzzy Adaptive Least-Squares Computer-Aided Molecular Modeling and Structure-Activity Analyses of New Antifungal Tertiary Amines QSARs and Three-Dimensional Shape Studies of Fungicidal Azolylmethylcyclopentanols: Molecular Design of Novel Fungicides Metconazole and Ipconazole Structure-Activity Relationships of Quinone and Acridone Photosystem II Inhibitors The QSAR of Insecticidal Uncouplers Quantitative Structure-Activity and Molecular Modeling Studies of Novel Fungicides and Herbicides Having 1,2,4-Thiadiazoline Structures Applications of a New Hydrophobicity Parameter of Amino Acid Side Chains to Quantitative Structure-Activity Analyses of Oligopeptides Successful Application of the QSAR Paradigm in Discovery Programs Comparative QSAR: Understanding Hydrophobic Interactions Applications of Scaled Rank-Sum Statistics in Herbicide QSAR Novel Structure-Activity Insights from Neural Network Models Three-Dimensional Quantitative Structure-Activity Analysis of Steroidal and Dibenzoylhydrazine-Type Ecdysone Agonists Comparison of Classical QSAR and Comparative Molecular Field Analysis: Toward Lateral Validations Distance Comparisons: A New Strategy for Examining Three-Dimensional Structure-Activity Relationships