Synthesis and application of trifluoromethylpyridines as a key structural motif in active agrochemical and pharmaceutical ingredients
Author:
Affiliation:
1. Bioscience Business Headquarters, Ishihara Sangyo Kaisha, Ltd.
2. Central Research Institute, Ishihara Sangyo Kaisha, Ltd.
3. Healthcare Business Development Headquarters, Ishihara Sangyo Kaisha, Ltd.
Publisher
Pesticide Science Society of Japan
Subject
Health, Toxicology and Mutagenesis,Insect Science
Link
https://www.jstage.jst.go.jp/article/jpestics/46/2/46_D21-012/_pdf
Reference140 articles.
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2. 2) A. Bondi: van der Waals Volumes and Radii. J. Phys. Chem. 68, 441–451 (1964).
3. 3) A. L. Allred: ELECTRONEGATIVITY VALUES FROM THERMOCHEMICAL DATA. J. Inorg. Nucl. Chem. 17, 215–221 (1961).
4. 4) C. Hansch, A. Leo and R. W. Taft: A Survey of Hammett Substituent Constants and Resonance and Field Parameters. Chem. Rev. 91, 165–195 (1991).
5. 5) J. E. Huheey: The Electronegativity of Groups. J. Phys. Chem. 69, 3284–3291 (1965).
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