Aryldiones incorporating a [1,4,5]oxadiazepane ring. Part 2: Chemistry and biology of the cereal herbicide pinoxaden
BACKGROUND: Pinoxaden is a new cereal herbicide that provides outstanding levels of post‐emergence activity against a broad spectrum of grass weed species for worldwide selective use in both wheat and barley. RESULTS: Factors influencing activity and tolerance to pinoxaden were in part linked to dis...
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creator | Muehlebach, Michel Cederbaum, Fredrik Cornes, Derek Friedmann, Adrian A Glock, Jutta Hall, Gavin Indolese, Adriano F Kloer, Daniel P Le Goupil, Gael Maetzke, Thomas Meier, Hans Schneider, Rudolf Stoller, André Szczepanski, Henry Wendeborn, Sebastian Widmer, Hansjuerg |
description | BACKGROUND: Pinoxaden is a new cereal herbicide that provides outstanding levels of post‐emergence activity against a broad spectrum of grass weed species for worldwide selective use in both wheat and barley.
RESULTS: Factors influencing activity and tolerance to pinoxaden were in part linked to distinct structural parts of the active ingredient. Three complementary contributions that decisively impact upon the herbicidal potency against grasses were identified: a preferred 2,6‐diethyl‐4‐methyl aromatic substitution pattern, a dione area suitable for proherbicide formation and beneficial adjuvant effects. The uptake and translocation pattern of pinoxaden when coapplied with its tailored adjuvant were analysed by autoradiography, indicating extensive and rapid penetration, followed by effective distribution throughout the plant. Crop injury reduction on incorporation of the [1,4,5]oxadiazepane ring into the aryldione template was reinforced with safener technology. Comparative studies on the behaviour of pinoxaden applied either alone or in combination with the safener cloquintocet‐mexyl demonstrated that addition of the safener resulted in significant enhancement of metabolic degradation in wheat and barley, providing excellent crop tolerance and a substantial selectivity margin without adverse effects on weed control.
CONCLUSION: The biological potential of pinoxaden and its active principle pinoxaden dione in terms of grass weed control and tolerance in cereals was fully exploited by inclusion of the safener cloquintocet‐mexyl in the formulation in combination with a specific and tailor‐made tank‐mix adjuvant based on methylated rape seed oil. Copyright © 2011 Society of Chemical Industry |
doi_str_mv | 10.1002/ps.2204 |
format | Article |
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RESULTS: Factors influencing activity and tolerance to pinoxaden were in part linked to distinct structural parts of the active ingredient. Three complementary contributions that decisively impact upon the herbicidal potency against grasses were identified: a preferred 2,6‐diethyl‐4‐methyl aromatic substitution pattern, a dione area suitable for proherbicide formation and beneficial adjuvant effects. The uptake and translocation pattern of pinoxaden when coapplied with its tailored adjuvant were analysed by autoradiography, indicating extensive and rapid penetration, followed by effective distribution throughout the plant. Crop injury reduction on incorporation of the [1,4,5]oxadiazepane ring into the aryldione template was reinforced with safener technology. Comparative studies on the behaviour of pinoxaden applied either alone or in combination with the safener cloquintocet‐mexyl demonstrated that addition of the safener resulted in significant enhancement of metabolic degradation in wheat and barley, providing excellent crop tolerance and a substantial selectivity margin without adverse effects on weed control.
CONCLUSION: The biological potential of pinoxaden and its active principle pinoxaden dione in terms of grass weed control and tolerance in cereals was fully exploited by inclusion of the safener cloquintocet‐mexyl in the formulation in combination with a specific and tailor‐made tank‐mix adjuvant based on methylated rape seed oil. Copyright © 2011 Society of Chemical Industry</description><identifier>ISSN: 1526-498X</identifier><identifier>EISSN: 1526-4998</identifier><identifier>DOI: 10.1002/ps.2204</identifier><identifier>PMID: 21656896</identifier><identifier>CODEN: PMSCFC</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>5]oxadiazepane ; [1,4,5]oxadiazepane ; Adigor ; adjuvant ; Adjuvants, Pharmaceutic - chemistry ; Adjuvants, Pharmaceutic - pharmacology ; Autoradiography ; Axial ; Barley ; Biology ; Cereal crops ; cereals ; Chemistry ; cloquintocet-mexyl ; Comparative studies ; Crystallography, X-Ray ; cyclic hydrazine ; graminicide ; grass weed control ; Grasses ; herbicide ; Herbicide Resistance ; Herbicides ; Herbicides - chemistry ; Herbicides - pharmacology ; Heterocyclic Compounds, 2-Ring - chemistry ; Heterocyclic Compounds, 2-Ring - pharmacology ; keto-enol tautomerism ; pinoxaden ; Plant Weeds - drug effects ; Poaceae - drug effects ; post-emergence ; Quinolines - pharmacology ; Rapeseed oil ; safener ; Structure-Activity Relationship ; Translocation ; uptake and translocation ; Weed Control ; Weeds ; Wheat</subject><ispartof>Pest management science, 2011-12, Vol.67 (12), p.1499-1521</ispartof><rights>Copyright © 2011 Society of Chemical Industry</rights><rights>Copyright © 2011 Society of Chemical Industry.</rights><rights>Copyright John Wiley and Sons, Limited Dec 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3814-687740ef93865b5b33e9d7cb6f921db54784a84edb80480b13eb772d9f5dc0f13</citedby><cites>FETCH-LOGICAL-c3814-687740ef93865b5b33e9d7cb6f921db54784a84edb80480b13eb772d9f5dc0f13</cites></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.2204$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fps.2204$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21656896$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Muehlebach, Michel</creatorcontrib><creatorcontrib>Cederbaum, Fredrik</creatorcontrib><creatorcontrib>Cornes, Derek</creatorcontrib><creatorcontrib>Friedmann, Adrian A</creatorcontrib><creatorcontrib>Glock, Jutta</creatorcontrib><creatorcontrib>Hall, Gavin</creatorcontrib><creatorcontrib>Indolese, Adriano F</creatorcontrib><creatorcontrib>Kloer, Daniel P</creatorcontrib><creatorcontrib>Le Goupil, Gael</creatorcontrib><creatorcontrib>Maetzke, Thomas</creatorcontrib><creatorcontrib>Meier, Hans</creatorcontrib><creatorcontrib>Schneider, Rudolf</creatorcontrib><creatorcontrib>Stoller, André</creatorcontrib><creatorcontrib>Szczepanski, Henry</creatorcontrib><creatorcontrib>Wendeborn, Sebastian</creatorcontrib><creatorcontrib>Widmer, Hansjuerg</creatorcontrib><title>Aryldiones incorporating a [1,4,5]oxadiazepane ring. Part 2: Chemistry and biology of the cereal herbicide pinoxaden</title><title>Pest management science</title><addtitle>Pest. Manag. Sci</addtitle><description>BACKGROUND: Pinoxaden is a new cereal herbicide that provides outstanding levels of post‐emergence activity against a broad spectrum of grass weed species for worldwide selective use in both wheat and barley.
RESULTS: Factors influencing activity and tolerance to pinoxaden were in part linked to distinct structural parts of the active ingredient. Three complementary contributions that decisively impact upon the herbicidal potency against grasses were identified: a preferred 2,6‐diethyl‐4‐methyl aromatic substitution pattern, a dione area suitable for proherbicide formation and beneficial adjuvant effects. The uptake and translocation pattern of pinoxaden when coapplied with its tailored adjuvant were analysed by autoradiography, indicating extensive and rapid penetration, followed by effective distribution throughout the plant. Crop injury reduction on incorporation of the [1,4,5]oxadiazepane ring into the aryldione template was reinforced with safener technology. Comparative studies on the behaviour of pinoxaden applied either alone or in combination with the safener cloquintocet‐mexyl demonstrated that addition of the safener resulted in significant enhancement of metabolic degradation in wheat and barley, providing excellent crop tolerance and a substantial selectivity margin without adverse effects on weed control.
CONCLUSION: The biological potential of pinoxaden and its active principle pinoxaden dione in terms of grass weed control and tolerance in cereals was fully exploited by inclusion of the safener cloquintocet‐mexyl in the formulation in combination with a specific and tailor‐made tank‐mix adjuvant based on methylated rape seed oil. Copyright © 2011 Society of Chemical Industry</description><subject>5]oxadiazepane</subject><subject>[1,4,5]oxadiazepane</subject><subject>Adigor</subject><subject>adjuvant</subject><subject>Adjuvants, Pharmaceutic - chemistry</subject><subject>Adjuvants, Pharmaceutic - pharmacology</subject><subject>Autoradiography</subject><subject>Axial</subject><subject>Barley</subject><subject>Biology</subject><subject>Cereal crops</subject><subject>cereals</subject><subject>Chemistry</subject><subject>cloquintocet-mexyl</subject><subject>Comparative studies</subject><subject>Crystallography, X-Ray</subject><subject>cyclic hydrazine</subject><subject>graminicide</subject><subject>grass weed control</subject><subject>Grasses</subject><subject>herbicide</subject><subject>Herbicide Resistance</subject><subject>Herbicides</subject><subject>Herbicides - chemistry</subject><subject>Herbicides - pharmacology</subject><subject>Heterocyclic Compounds, 2-Ring - chemistry</subject><subject>Heterocyclic Compounds, 2-Ring - pharmacology</subject><subject>keto-enol tautomerism</subject><subject>pinoxaden</subject><subject>Plant Weeds - drug effects</subject><subject>Poaceae - drug effects</subject><subject>post-emergence</subject><subject>Quinolines - pharmacology</subject><subject>Rapeseed oil</subject><subject>safener</subject><subject>Structure-Activity Relationship</subject><subject>Translocation</subject><subject>uptake and translocation</subject><subject>Weed Control</subject><subject>Weeds</subject><subject>Wheat</subject><issn>1526-498X</issn><issn>1526-4998</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kVtrFDEUgIMo9qL4DyT40gc7azJJZhLfymKrWLRQtYJISCZnuqmzk2kyi53--mbZdQXBp3PgfHznhtALSmaUkPLNkGZlSfgjtE9FWRVcKfl4l8vve-ggpRtCiFKqfIr2SlqJSqpqH40nceqcDz0k7PsmxCFEM_r-Ghv8gx7zY_Ez3BnnzT0Mpgccc2mGL0wccfkWzxew9GmMEza9w9aHLlxPOLR4XABuIILp8AKi9Y13gAffr13QP0NPWtMleL6Nh-jr6bsv8_fF-eezD_OT86JhkvKiknXNCbSKyUpYYRkD5erGVq0qqbOC15IbycFZSbgkljKwdV061QrXkJayQ3S08Q4x3K4gjTpP20DX5U3CKmlFGOWCSpLJV_-QN2EV-zxchjhhuSH_q2tiSClCq4folyZOmhK9foMekl6_IZMvt7qVXYLbcX_unoHXG-C372D6n0dfXG51xYbOt4a7HW3iL13VrBb66tOZvvrGq49MzvUlewAUoZ5F</recordid><startdate>201112</startdate><enddate>201112</enddate><creator>Muehlebach, Michel</creator><creator>Cederbaum, Fredrik</creator><creator>Cornes, Derek</creator><creator>Friedmann, Adrian A</creator><creator>Glock, Jutta</creator><creator>Hall, Gavin</creator><creator>Indolese, Adriano F</creator><creator>Kloer, Daniel P</creator><creator>Le Goupil, Gael</creator><creator>Maetzke, Thomas</creator><creator>Meier, Hans</creator><creator>Schneider, Rudolf</creator><creator>Stoller, André</creator><creator>Szczepanski, Henry</creator><creator>Wendeborn, Sebastian</creator><creator>Widmer, Hansjuerg</creator><general>John Wiley & Sons, Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</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>201112</creationdate><title>Aryldiones incorporating a [1,4,5]oxadiazepane ring. Part 2: Chemistry and biology of the cereal herbicide pinoxaden</title><author>Muehlebach, Michel ; Cederbaum, Fredrik ; Cornes, Derek ; Friedmann, Adrian A ; Glock, Jutta ; Hall, Gavin ; Indolese, Adriano F ; Kloer, Daniel P ; Le Goupil, Gael ; Maetzke, Thomas ; Meier, Hans ; Schneider, Rudolf ; Stoller, André ; Szczepanski, Henry ; Wendeborn, Sebastian ; Widmer, Hansjuerg</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3814-687740ef93865b5b33e9d7cb6f921db54784a84edb80480b13eb772d9f5dc0f13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>5]oxadiazepane</topic><topic>[1,4,5]oxadiazepane</topic><topic>Adigor</topic><topic>adjuvant</topic><topic>Adjuvants, Pharmaceutic - chemistry</topic><topic>Adjuvants, Pharmaceutic - pharmacology</topic><topic>Autoradiography</topic><topic>Axial</topic><topic>Barley</topic><topic>Biology</topic><topic>Cereal crops</topic><topic>cereals</topic><topic>Chemistry</topic><topic>cloquintocet-mexyl</topic><topic>Comparative studies</topic><topic>Crystallography, X-Ray</topic><topic>cyclic hydrazine</topic><topic>graminicide</topic><topic>grass weed control</topic><topic>Grasses</topic><topic>herbicide</topic><topic>Herbicide Resistance</topic><topic>Herbicides</topic><topic>Herbicides - chemistry</topic><topic>Herbicides - pharmacology</topic><topic>Heterocyclic Compounds, 2-Ring - chemistry</topic><topic>Heterocyclic Compounds, 2-Ring - pharmacology</topic><topic>keto-enol tautomerism</topic><topic>pinoxaden</topic><topic>Plant Weeds - drug effects</topic><topic>Poaceae - drug effects</topic><topic>post-emergence</topic><topic>Quinolines - pharmacology</topic><topic>Rapeseed oil</topic><topic>safener</topic><topic>Structure-Activity Relationship</topic><topic>Translocation</topic><topic>uptake and translocation</topic><topic>Weed Control</topic><topic>Weeds</topic><topic>Wheat</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Muehlebach, Michel</creatorcontrib><creatorcontrib>Cederbaum, Fredrik</creatorcontrib><creatorcontrib>Cornes, Derek</creatorcontrib><creatorcontrib>Friedmann, Adrian A</creatorcontrib><creatorcontrib>Glock, Jutta</creatorcontrib><creatorcontrib>Hall, Gavin</creatorcontrib><creatorcontrib>Indolese, Adriano F</creatorcontrib><creatorcontrib>Kloer, Daniel P</creatorcontrib><creatorcontrib>Le Goupil, Gael</creatorcontrib><creatorcontrib>Maetzke, Thomas</creatorcontrib><creatorcontrib>Meier, Hans</creatorcontrib><creatorcontrib>Schneider, Rudolf</creatorcontrib><creatorcontrib>Stoller, André</creatorcontrib><creatorcontrib>Szczepanski, Henry</creatorcontrib><creatorcontrib>Wendeborn, Sebastian</creatorcontrib><creatorcontrib>Widmer, Hansjuerg</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</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>Muehlebach, Michel</au><au>Cederbaum, Fredrik</au><au>Cornes, Derek</au><au>Friedmann, Adrian A</au><au>Glock, Jutta</au><au>Hall, Gavin</au><au>Indolese, Adriano F</au><au>Kloer, Daniel P</au><au>Le Goupil, Gael</au><au>Maetzke, Thomas</au><au>Meier, Hans</au><au>Schneider, Rudolf</au><au>Stoller, André</au><au>Szczepanski, Henry</au><au>Wendeborn, Sebastian</au><au>Widmer, Hansjuerg</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aryldiones incorporating a [1,4,5]oxadiazepane ring. Part 2: Chemistry and biology of the cereal herbicide pinoxaden</atitle><jtitle>Pest management science</jtitle><addtitle>Pest. Manag. Sci</addtitle><date>2011-12</date><risdate>2011</risdate><volume>67</volume><issue>12</issue><spage>1499</spage><epage>1521</epage><pages>1499-1521</pages><issn>1526-498X</issn><eissn>1526-4998</eissn><coden>PMSCFC</coden><abstract>BACKGROUND: Pinoxaden is a new cereal herbicide that provides outstanding levels of post‐emergence activity against a broad spectrum of grass weed species for worldwide selective use in both wheat and barley.
RESULTS: Factors influencing activity and tolerance to pinoxaden were in part linked to distinct structural parts of the active ingredient. Three complementary contributions that decisively impact upon the herbicidal potency against grasses were identified: a preferred 2,6‐diethyl‐4‐methyl aromatic substitution pattern, a dione area suitable for proherbicide formation and beneficial adjuvant effects. The uptake and translocation pattern of pinoxaden when coapplied with its tailored adjuvant were analysed by autoradiography, indicating extensive and rapid penetration, followed by effective distribution throughout the plant. Crop injury reduction on incorporation of the [1,4,5]oxadiazepane ring into the aryldione template was reinforced with safener technology. Comparative studies on the behaviour of pinoxaden applied either alone or in combination with the safener cloquintocet‐mexyl demonstrated that addition of the safener resulted in significant enhancement of metabolic degradation in wheat and barley, providing excellent crop tolerance and a substantial selectivity margin without adverse effects on weed control.
CONCLUSION: The biological potential of pinoxaden and its active principle pinoxaden dione in terms of grass weed control and tolerance in cereals was fully exploited by inclusion of the safener cloquintocet‐mexyl in the formulation in combination with a specific and tailor‐made tank‐mix adjuvant based on methylated rape seed oil. Copyright © 2011 Society of Chemical Industry</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>21656896</pmid><doi>10.1002/ps.2204</doi><tpages>23</tpages></addata></record> |
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subjects | 5]oxadiazepane [1,4,5]oxadiazepane Adigor adjuvant Adjuvants, Pharmaceutic - chemistry Adjuvants, Pharmaceutic - pharmacology Autoradiography Axial Barley Biology Cereal crops cereals Chemistry cloquintocet-mexyl Comparative studies Crystallography, X-Ray cyclic hydrazine graminicide grass weed control Grasses herbicide Herbicide Resistance Herbicides Herbicides - chemistry Herbicides - pharmacology Heterocyclic Compounds, 2-Ring - chemistry Heterocyclic Compounds, 2-Ring - pharmacology keto-enol tautomerism pinoxaden Plant Weeds - drug effects Poaceae - drug effects post-emergence Quinolines - pharmacology Rapeseed oil safener Structure-Activity Relationship Translocation uptake and translocation Weed Control Weeds Wheat |
title | Aryldiones incorporating a [1,4,5]oxadiazepane ring. Part 2: Chemistry and biology of the cereal herbicide pinoxaden |
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