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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Veröffentlicht in:Pest management science 2011-12, Vol.67 (12), p.1499-1521
Hauptverfasser: 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
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container_issue 12
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container_title Pest management science
container_volume 67
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
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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. 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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. 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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 &amp; 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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