Literature DB >> 19701961

The unique role of halogen substituents in the design of modern agrochemicals.

Peter Jeschke1.   

Abstract

The past 30 years have witnessed a period of significant expansion in the use of halogenated compounds in the field of agrochemical research and development. The introduction of halogens into active ingredients has become an important concept in the quest for a modern agrochemical with optimal efficacy, environmental safety, user friendliness and economic viability. Outstanding progress has been made, especially in synthetic methods for particular halogen-substituted key intermediates that were previously prohibitively expensive. Interestingly, there has been a rise in the number of commercial products containing 'mixed' halogens, e.g. one or more fluorine, chlorine, bromine or iodine atoms in addition to one or more further halogen atoms. Extrapolation of the current trend indicates that a definite growth is to be expected in fluorine-substituted agrochemicals throughout the twenty-first century. A number of these recently developed agrochemical candidates containing halogen substituents represent novel classes of chemical compounds with new modes of action. However, the complex structure-activity relationships associated with biologically active molecules mean that the introduction of halogens 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. In spite of modern design concepts, it is still difficult to predict the sites in a molecule at which halogen substitution will result in optimal desired effects. This review describes comprehensively the successful utilisation of halogens and their unique role in the design of modern agrochemicals, exemplified by various commercial products from Bayer CropScience coming from different agrochemical areas.

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Year:  2010        PMID: 19701961     DOI: 10.1002/ps.1829

Source DB:  PubMed          Journal:  Pest Manag Sci        ISSN: 1526-498X            Impact factor:   4.845


  55 in total

1.  Rapid, one-pot synthesis of β-siloxy-α-haloaldehydes.

Authors:  Jakub Saadi; Matsujiro Akakura; Hisashi Yamamoto
Journal:  J Am Chem Soc       Date:  2011-08-18       Impact factor: 15.419

2.  Synthesis of β-hydroxy-α-haloesters through super silyl ester directed syn-selective aldol reaction.

Authors:  Susumu Oda; Hisashi Yamamoto
Journal:  Org Lett       Date:  2013-11-08       Impact factor: 6.005

3.  Improving the stability and catalyst lifetime of the halogenase RebH by directed evolution.

Authors:  Catherine B Poor; Mary C Andorfer; Jared C Lewis
Journal:  Chembiochem       Date:  2014-05-21       Impact factor: 3.164

4.  Enantioselective Desymmetrization of Methylenedianilines via Enzyme-Catalyzed Remote Halogenation.

Authors:  James T Payne; Paul H Butkovich; Yifan Gu; Kyle N Kunze; Hyun June Park; Duo-Sheng Wang; Jared C Lewis
Journal:  J Am Chem Soc       Date:  2018-01-08       Impact factor: 15.419

5.  Aromatic Halogenation by Using Bifunctional Flavin Reductase-Halogenase Fusion Enzymes.

Authors:  Mary C Andorfer; Ketaki D Belsare; Anna M Girlich; Jared C Lewis
Journal:  Chembiochem       Date:  2017-09-22       Impact factor: 3.164

6.  Synthesis of Alkyl Halides from Aldehydes via Deformylative Halogenation.

Authors:  Shengzong Liang; Tatsuya Kumon; Ricardo A Angnes; Melissa Sanchez; Bo Xu; Gerald B Hammond
Journal:  Org Lett       Date:  2019-05-03       Impact factor: 6.005

7.  Selective Halogenation of Pyridines Using Designed Phosphine Reagents.

Authors:  Jeffrey N Levy; Juan V Alegre-Requena; Renrong Liu; Robert S Paton; Andrew McNally
Journal:  J Am Chem Soc       Date:  2020-06-10       Impact factor: 15.419

8.  β-Siloxy-α-haloketones through highly diastereoselective single and double mukaiyama aldol reactions.

Authors:  Jakub Saadi; Hisashi Yamamoto
Journal:  Chemistry       Date:  2013-02-19       Impact factor: 5.236

9.  Pd-catalyzed C-H fluorination with nucleophilic fluoride.

Authors:  Kate B McMurtrey; Joy M Racowski; Melanie S Sanford
Journal:  Org Lett       Date:  2012-07-30       Impact factor: 6.005

10.  Regioselective arene halogenation using the FAD-dependent halogenase RebH.

Authors:  James T Payne; Mary C Andorfer; Jared C Lewis
Journal:  Angew Chem Int Ed Engl       Date:  2013-04-16       Impact factor: 15.336

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