Fungicidal activity and chemical constitution
- 1 August 1969
- journal article
- Published by Wiley in Annals of Applied Biology
- Vol. 64 (1) , 131-137
- https://doi.org/10.1111/j.1744-7348.1969.tb02863.x
Abstract
SUMMARY: Structure/activity relationships for members of five homologous 4‐(1‐substituted alkyl)‐2,6‐dinitrophenols and apple mildew are discussed with special reference to their hydrophobic bonding constants π. It is suggested that π values may be of use in predicting potential anti‐mildew fungicides with similar modes of action to those of the substances studied.Keywords
This publication has 11 references indexed in Scilit:
- Chromatography of dinitrophenolsJournal of Chromatography A, 1969
- Fungicidal activity and chemical constitutionAnnals of Applied Biology, 1969
- Structures and pesticidal activities of derivatives of dinitrophenols. IX.—Effects of substitution of dinitrophenols with C4 to C13 α-branched alkyl groups and of esterification on the eradication of apple mildewJournal of the Science of Food and Agriculture, 1968
- Fungicidal activity and chemical constitution. XIV.—Preparation of 4-substituted 2,6-dinitrophenolsJournal of the Science of Food and Agriculture, 1968
- Fungicidal activity and chemical constitution: XIII.* Active components of commercial formulations containing dinocapAnnals of Applied Biology, 1966
- Greenhouse evaluation of chemicals for control of powdery mildewsAnnals of Applied Biology, 1966
- A Simple Assessment of Partition Data for Correlating Structure and Biological Activity Using Thin-Layer ChromatographyNature, 1965
- A New Substituent Constant, π, Derived from Partition CoefficientsJournal of the American Chemical Society, 1964
- p-σ-π Analysis. A Method for the Correlation of Biological Activity and Chemical StructureJournal of the American Chemical Society, 1964
- The Permeability of Nitella Cells to Non‐EleetrolytesPhysiologia Plantarum, 1954