Literature DB >> 15122630

The unique role of fluorine in the design of active ingredients for modern crop protection.

Peter Jeschke1.   

Abstract

The task of inventing and developing active ingredients with useful biological activities requires a search for novel chemical substructures. This process may trigger the discovery of whole classes of chemicals of potential commercial interest. Similar biological effects can often be achieved by completely different compounds. However, compounds within a given structural family may exhibit quite different biological activities depending on their interactions with different intracellular proteins like enzymes or receptors. By varying the functional groups and structural elements of a lead compound, its interaction with the active site of the target protein, as well as its physicochemical, pharmacokinetic, and dynamic properties can be improved. In this context, the introduction of fluorine into active ingredients has become an important concept in the quest for a modern crop protection product with optimal efficacy, environmental safety, user friendliness, and economic viability. Fluorinated organic compounds represent an important and growing family of commercial agrochemicals. A number of recently developed agrochemical candidates represent novel classes of chemical compounds with new modes of action; several of these compounds contain new fluorinated substituents. However, the complex structure-activity relationships associated with biologically active molecules mean that the introduction of fluorine can lead to either an increase or a decrease in the efficacy of a compound depending on its changed mode of action, physicochemical properties, target interaction, or metabolic susceptibility and transformation. Therefore, it is still difficult to predict the sites in a molecule at which fluorine substitution will result in optimal desired effects.

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Year:  2004        PMID: 15122630     DOI: 10.1002/cbic.200300833

Source DB:  PubMed          Journal:  Chembiochem        ISSN: 1439-4227            Impact factor:   3.164


  60 in total

1.  Synthesis and Characterization of New Fluorinated Tetrazines Displaying a High Fluorescence Yield.

Authors:  Refka Guermazi; Lorna Royer; Laurent Galmiche; Gilles Clavier; Pierre Audebert; Ahmed Hedhli
Journal:  J Fluoresc       Date:  2016-05-30       Impact factor: 2.217

Review 2.  Catalysis for fluorination and trifluoromethylation.

Authors:  Takeru Furuya; Adam S Kamlet; Tobias Ritter
Journal:  Nature       Date:  2011-05-26       Impact factor: 49.962

3.  Entropy drives selective fluorine recognition in the fluoroacetyl-CoA thioesterase from Streptomyces cattleya.

Authors:  Amy M Weeks; Ningkun Wang; Jeffrey G Pelton; Michelle C Y Chang
Journal:  Proc Natl Acad Sci U S A       Date:  2018-02-16       Impact factor: 11.205

4.  Asymmetric silver-catalysed intermolecular bromotrifluoromethoxylation of alkenes with a new trifluoromethoxylation reagent.

Authors:  Shuo Guo; Fei Cong; Rui Guo; Liang Wang; Pingping Tang
Journal:  Nat Chem       Date:  2017-01-23       Impact factor: 24.427

5.  Photochemical Perfluoroalkylation with Pyridine N-Oxides: Mechanistic Insights and Performance on a Kilogram Scale.

Authors:  Joel W Beatty; James J Douglas; Richard Miller; Rory C McAtee; Kevin P Cole; Corey R J Stephenson
Journal:  Chem       Date:  2016-09-08       Impact factor: 22.804

6.  Metal-free 18F-labeling of aryl-CF2H via nucleophilic radiofluorination and oxidative C-H activation.

Authors:  Gengyang Yuan; Feng Wang; Nickeisha A Stephenson; Lu Wang; Benjamin H Rotstein; Neil Vasdev; Pingping Tang; Steven H Liang
Journal:  Chem Commun (Camb)       Date:  2016-12-20       Impact factor: 6.222

7.  The toxicity of the N-hydroxy and 6-hydroxy metabolites of 3,4-dichloropropionanilide does not depend on calcium release-activated calcium channel inhibition.

Authors:  Tricia L Lewis; Ida Holásková; John B Barnett
Journal:  Toxicol Sci       Date:  2012-10-12       Impact factor: 4.849

8.  Themed series in organo-fluorine chemistry.

Authors:  David O'Hagan
Journal:  Beilstein J Org Chem       Date:  2008-04-25       Impact factor: 2.883

9.  Fluorinated photoremovable protecting groups: the influence of fluoro substituents on the photo-Favorskii rearrangement.

Authors:  Kenneth F Stensrud; Dominik Heger; Peter Sebej; Jakob Wirz; Richard S Givens
Journal:  Photochem Photobiol Sci       Date:  2008-04-03       Impact factor: 3.982

Review 10.  Modern Approaches for Asymmetric Construction of Carbon-Fluorine Quaternary Stereogenic Centers: Synthetic Challenges and Pharmaceutical Needs.

Authors:  Yi Zhu; Jianlin Han; Jiandong Wang; Norio Shibata; Mikiko Sodeoka; Vadim A Soloshonok; Jaime A S Coelho; F Dean Toste
Journal:  Chem Rev       Date:  2018-04-02       Impact factor: 60.622

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