unique role of halogen substituents in the design of modern agrochemicals
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 effic...
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description | 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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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.</description><identifier>ISSN: 1526-498X</identifier><identifier>ISSN: 1526-4998</identifier><identifier>EISSN: 1526-4998</identifier><identifier>DOI: 10.1002/ps.1829</identifier><identifier>PMID: 19701961</identifier><identifier>CODEN: PMSCFC</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Agriculture ; agrochemicals ; bioavailability ; Biological and medical sciences ; Chemical compounds ; Chlorine ; Control ; Effects ; Fundamental and applied biological sciences. Psychology ; Fungal plant pathogens ; fungicides ; Fungicides, Industrial - chemistry ; halogen effects ; halogenated agrochemicals ; halogens ; Halogens - chemistry ; herbicides ; Herbicides - chemistry ; insecticides ; Insecticides - chemistry ; literature reviews ; mechanism of action ; mode of action ; Molecules ; Parasitic plants. Weeds ; Pesticides ; physicochemical properties ; physicochemistry ; Phytopathology. Animal pests. Plant and forest protection ; Protozoa. Invertebrates ; R&D ; Research & development ; resistance ; selectivity ; structure-activity relationship ; structure-activity relationships ; Weeds</subject><ispartof>Pest management science, 2010, Vol.66 (1), p.10-27</ispartof><rights>Copyright © 2009 Society of Chemical Industry</rights><rights>2015 INIST-CNRS</rights><rights>Copyright John Wiley and Sons, Limited Jan 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4369-18a3854bf22eda65802f2cb82a53543e09f6d8a8da18f43acdd7a2fa19de12203</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fps.1829$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fps.1829$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,4010,27900,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22245462$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19701961$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jeschke, Peter</creatorcontrib><title>unique role of halogen substituents in the design of modern agrochemicals</title><title>Pest management science</title><addtitle>Pest. Manag. Sci</addtitle><description>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.</description><subject>Agriculture</subject><subject>agrochemicals</subject><subject>bioavailability</subject><subject>Biological and medical sciences</subject><subject>Chemical compounds</subject><subject>Chlorine</subject><subject>Control</subject><subject>Effects</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fungal plant pathogens</subject><subject>fungicides</subject><subject>Fungicides, Industrial - chemistry</subject><subject>halogen effects</subject><subject>halogenated agrochemicals</subject><subject>halogens</subject><subject>Halogens - chemistry</subject><subject>herbicides</subject><subject>Herbicides - chemistry</subject><subject>insecticides</subject><subject>Insecticides - chemistry</subject><subject>literature reviews</subject><subject>mechanism of action</subject><subject>mode of action</subject><subject>Molecules</subject><subject>Parasitic plants. Weeds</subject><subject>Pesticides</subject><subject>physicochemical properties</subject><subject>physicochemistry</subject><subject>Phytopathology. Animal pests. Plant and forest protection</subject><subject>Protozoa. Invertebrates</subject><subject>R&D</subject><subject>Research & development</subject><subject>resistance</subject><subject>selectivity</subject><subject>structure-activity relationship</subject><subject>structure-activity relationships</subject><subject>Weeds</subject><issn>1526-498X</issn><issn>1526-4998</issn><issn>1526-4998</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90d9PFDEQB_DGYPil8T-AjQnRhCy2091u-6hEkUDQiBy-Nb1te1fYbc92N8p_b887zoQHn6YPn8x8O4PQK4JPCMbwbpFOCAfxDO2SGlhZCcG3Nm_-YwftpXSHMRZCwDbaIaLBRDCyi85H736OpoihM0WwxVx1YWZ8kcZpGtwwGj-kwvlimJtCm-Rmfqn6oE30hZrF0M5N71rVpRfouc3FvFzXfXTz6eP308_l5Zez89P3l2VbUSZKwhXldTW1AEYrVnMMFtopB1XTuqIGC8s0V1wrwm1FVat1o8AqIrQhAJjuozervosYcvI0yN6l1nSd8iaMSTaUNoJRzrN8-19JMGBeU8og09dP6F0Yo8__kADAMKMNy-hgjcZpb7RcRNer-CAft5nB0RqolFdio_KtSxuXO1V19Xfa8cr9cp15-NcHy-Ux5SJHy8eUX6-XJetypV0azO-NVvFesoY2tby9OpPs6sPk9tvFRE6yP1x5q4LMJ8oJbq4BE4pJQxjknH8AXBenDg</recordid><startdate>2010</startdate><enddate>2010</enddate><creator>Jeschke, Peter</creator><general>John Wiley & Sons, Ltd</general><general>Wiley</general><general>Wiley Subscription Services, Inc</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QR</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>SOI</scope><scope>7X8</scope></search><sort><creationdate>2010</creationdate><title>unique role of halogen substituents in the design of modern agrochemicals</title><author>Jeschke, Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4369-18a3854bf22eda65802f2cb82a53543e09f6d8a8da18f43acdd7a2fa19de12203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Agriculture</topic><topic>agrochemicals</topic><topic>bioavailability</topic><topic>Biological and medical sciences</topic><topic>Chemical compounds</topic><topic>Chlorine</topic><topic>Control</topic><topic>Effects</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fungal plant pathogens</topic><topic>fungicides</topic><topic>Fungicides, Industrial - chemistry</topic><topic>halogen effects</topic><topic>halogenated agrochemicals</topic><topic>halogens</topic><topic>Halogens - chemistry</topic><topic>herbicides</topic><topic>Herbicides - chemistry</topic><topic>insecticides</topic><topic>Insecticides - chemistry</topic><topic>literature reviews</topic><topic>mechanism of action</topic><topic>mode of action</topic><topic>Molecules</topic><topic>Parasitic plants. Weeds</topic><topic>Pesticides</topic><topic>physicochemical properties</topic><topic>physicochemistry</topic><topic>Phytopathology. Animal pests. Plant and forest protection</topic><topic>Protozoa. Invertebrates</topic><topic>R&D</topic><topic>Research & development</topic><topic>resistance</topic><topic>selectivity</topic><topic>structure-activity relationship</topic><topic>structure-activity relationships</topic><topic>Weeds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jeschke, Peter</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Chemoreception Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Pest management science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jeschke, Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>unique role of halogen substituents in the design of modern agrochemicals</atitle><jtitle>Pest management science</jtitle><addtitle>Pest. Manag. Sci</addtitle><date>2010</date><risdate>2010</risdate><volume>66</volume><issue>1</issue><spage>10</spage><epage>27</epage><pages>10-27</pages><issn>1526-498X</issn><issn>1526-4998</issn><eissn>1526-4998</eissn><coden>PMSCFC</coden><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. 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subjects | Agriculture agrochemicals bioavailability Biological and medical sciences Chemical compounds Chlorine Control Effects Fundamental and applied biological sciences. Psychology Fungal plant pathogens fungicides Fungicides, Industrial - chemistry halogen effects halogenated agrochemicals halogens Halogens - chemistry herbicides Herbicides - chemistry insecticides Insecticides - chemistry literature reviews mechanism of action mode of action Molecules Parasitic plants. Weeds Pesticides physicochemical properties physicochemistry Phytopathology. Animal pests. Plant and forest protection Protozoa. Invertebrates R&D Research & development resistance selectivity structure-activity relationship structure-activity relationships Weeds |
title | unique role of halogen substituents in the design of modern agrochemicals |
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