Fungicide mixtures based on amide compounds and pyridine derivatives
Fungicidal mixture comprises: (1) an amide compound of formula (I) and (2) a dicarboxamide fungicide and/or one or more compounds (III), (IV), (V), (VI), (VII), (VIII) and/or (IX). Fungicidal mixture comprises: (1) an amide compound of formula (I); and (2) a synegistically effective amount of a seco...
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creator | M. SCHERER K. SCHELBERGER K. EICKEN |
description | Fungicidal mixture comprises: (1) an amide compound of formula (I) and (2) a dicarboxamide fungicide and/or one or more compounds (III), (IV), (V), (VI), (VII), (VIII) and/or (IX). Fungicidal mixture comprises: (1) an amide compound of formula (I); and (2) a synegistically effective amount of a second component comprising: (i) a dicarboxamide fungicide; (ii) a pyrimidine derivative of formula (III); (iii) fludioxinil (IV) and/or fenpiclonil (V); (iv) a phthalimide derivative selected from captan (VIa), captafol (VIb) and folpet (VII); (v) fluazinam (VIII); and/or (vi) dichlofluanid (IXa) or tolylfluanid (IXb). [Image] A : Ar or Het (both optionally substituted by 1-3 alkyl, halo, CHF 2, CF 3, (halo)alkoxy, alkylthio, alkylsulfinyl or alkylsulfonyl; R 1>H; R 2>phenyl (optionally substituted by 1-3 Q and optionally fused to a group M); or cycloalkyl (optionally substituted by 1-3 Q); M : a saturated 5-membered ring which may contain an O or S atom and is optionally substituted by one or more alkyl; Ar : an aryl group; Het : an aromatic or non-aromatic, 5-6 membered heterocycle which contains 1-3 N, O or S atoms; Q : alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkenyl, cycloalkyloxy, cycloalkenyloxy, phenyl or halo; in Q, the (cyclo)aliphatic residues are optionally halogenated, the cycloaliphatic residues are optionally substituted by 1-3 alkyl, and the phenyl is optionally substituted by 1-5 halo and/or 1-3 (halo)alkyl, (halo)alkoxy or (halo)alkylthio; R : methyl, propyn-1-yl or cyclopropyl ACTIVITY : Fungicidal. MECHANISM OF ACTION : None given. |
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EICKEN</creatorcontrib><description>Fungicidal mixture comprises: (1) an amide compound of formula (I) and (2) a dicarboxamide fungicide and/or one or more compounds (III), (IV), (V), (VI), (VII), (VIII) and/or (IX). Fungicidal mixture comprises: (1) an amide compound of formula (I); and (2) a synegistically effective amount of a second component comprising: (i) a dicarboxamide fungicide; (ii) a pyrimidine derivative of formula (III); (iii) fludioxinil (IV) and/or fenpiclonil (V); (iv) a phthalimide derivative selected from captan (VIa), captafol (VIb) and folpet (VII); (v) fluazinam (VIII); and/or (vi) dichlofluanid (IXa) or tolylfluanid (IXb). [Image] A : Ar or Het (both optionally substituted by 1-3 alkyl, halo, CHF 2, CF 3, (halo)alkoxy, alkylthio, alkylsulfinyl or alkylsulfonyl; R 1>H; R 2>phenyl (optionally substituted by 1-3 Q and optionally fused to a group M); or cycloalkyl (optionally substituted by 1-3 Q); M : a saturated 5-membered ring which may contain an O or S atom and is optionally substituted by one or more alkyl; Ar : an aryl group; Het : an aromatic or non-aromatic, 5-6 membered heterocycle which contains 1-3 N, O or S atoms; Q : alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkenyl, cycloalkyloxy, cycloalkenyloxy, phenyl or halo; in Q, the (cyclo)aliphatic residues are optionally halogenated, the cycloaliphatic residues are optionally substituted by 1-3 alkyl, and the phenyl is optionally substituted by 1-5 halo and/or 1-3 (halo)alkyl, (halo)alkoxy or (halo)alkylthio; R : methyl, propyn-1-yl or cyclopropyl ACTIVITY : Fungicidal. MECHANISM OF ACTION : None given.</description><edition>7</edition><language>eng</language><subject>AGRICULTURE ; ANIMAL HUSBANDRY ; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES, AS HERBICIDES ; FISHING ; FORESTRY ; HUMAN NECESSITIES ; HUNTING ; PEST REPELLANTS OR ATTRACTANTS ; PLANT GROWTH REGULATORS ; PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTSTHEREOF ; TRAPPING</subject><creationdate>2001</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20010131&DB=EPODOC&CC=CN&NR=1282208A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25543,76294</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20010131&DB=EPODOC&CC=CN&NR=1282208A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>M. SCHERER</creatorcontrib><creatorcontrib>K. SCHELBERGER</creatorcontrib><creatorcontrib>K. EICKEN</creatorcontrib><title>Fungicide mixtures based on amide compounds and pyridine derivatives</title><description>Fungicidal mixture comprises: (1) an amide compound of formula (I) and (2) a dicarboxamide fungicide and/or one or more compounds (III), (IV), (V), (VI), (VII), (VIII) and/or (IX). Fungicidal mixture comprises: (1) an amide compound of formula (I); and (2) a synegistically effective amount of a second component comprising: (i) a dicarboxamide fungicide; (ii) a pyrimidine derivative of formula (III); (iii) fludioxinil (IV) and/or fenpiclonil (V); (iv) a phthalimide derivative selected from captan (VIa), captafol (VIb) and folpet (VII); (v) fluazinam (VIII); and/or (vi) dichlofluanid (IXa) or tolylfluanid (IXb). [Image] A : Ar or Het (both optionally substituted by 1-3 alkyl, halo, CHF 2, CF 3, (halo)alkoxy, alkylthio, alkylsulfinyl or alkylsulfonyl; R 1>H; R 2>phenyl (optionally substituted by 1-3 Q and optionally fused to a group M); or cycloalkyl (optionally substituted by 1-3 Q); M : a saturated 5-membered ring which may contain an O or S atom and is optionally substituted by one or more alkyl; Ar : an aryl group; Het : an aromatic or non-aromatic, 5-6 membered heterocycle which contains 1-3 N, O or S atoms; Q : alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkenyl, cycloalkyloxy, cycloalkenyloxy, phenyl or halo; in Q, the (cyclo)aliphatic residues are optionally halogenated, the cycloaliphatic residues are optionally substituted by 1-3 alkyl, and the phenyl is optionally substituted by 1-5 halo and/or 1-3 (halo)alkyl, (halo)alkoxy or (halo)alkylthio; R : methyl, propyn-1-yl or cyclopropyl ACTIVITY : Fungicidal. MECHANISM OF ACTION : None given.</description><subject>AGRICULTURE</subject><subject>ANIMAL HUSBANDRY</subject><subject>BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES, AS HERBICIDES</subject><subject>FISHING</subject><subject>FORESTRY</subject><subject>HUMAN NECESSITIES</subject><subject>HUNTING</subject><subject>PEST REPELLANTS OR ATTRACTANTS</subject><subject>PLANT GROWTH REGULATORS</subject><subject>PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTSTHEREOF</subject><subject>TRAPPING</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2001</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZHBxK81Lz0zOTElVyM2sKCktSi1WSEosTk1RyM9TSMwFiSfn5xbkl-alFCsk5qUoFFQWZaZk5qUqpKQWZZYllmSWpRbzMLCmJeYUp_JCaW4GeTfXEGcP3dSC_PjU4oLE5NS81JJ4Zz9DIwsjIwMLR2PCKgAUozJV</recordid><startdate>20010131</startdate><enddate>20010131</enddate><creator>M. SCHERER</creator><creator>K. SCHELBERGER</creator><creator>K. EICKEN</creator><scope>EVB</scope></search><sort><creationdate>20010131</creationdate><title>Fungicide mixtures based on amide compounds and pyridine derivatives</title><author>M. SCHERER ; K. SCHELBERGER ; K. EICKEN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CN1282208A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>2001</creationdate><topic>AGRICULTURE</topic><topic>ANIMAL HUSBANDRY</topic><topic>BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES, AS HERBICIDES</topic><topic>FISHING</topic><topic>FORESTRY</topic><topic>HUMAN NECESSITIES</topic><topic>HUNTING</topic><topic>PEST REPELLANTS OR ATTRACTANTS</topic><topic>PLANT GROWTH REGULATORS</topic><topic>PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTSTHEREOF</topic><topic>TRAPPING</topic><toplevel>online_resources</toplevel><creatorcontrib>M. SCHERER</creatorcontrib><creatorcontrib>K. SCHELBERGER</creatorcontrib><creatorcontrib>K. EICKEN</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>M. SCHERER</au><au>K. SCHELBERGER</au><au>K. EICKEN</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Fungicide mixtures based on amide compounds and pyridine derivatives</title><date>2001-01-31</date><risdate>2001</risdate><abstract>Fungicidal mixture comprises: (1) an amide compound of formula (I) and (2) a dicarboxamide fungicide and/or one or more compounds (III), (IV), (V), (VI), (VII), (VIII) and/or (IX). Fungicidal mixture comprises: (1) an amide compound of formula (I); and (2) a synegistically effective amount of a second component comprising: (i) a dicarboxamide fungicide; (ii) a pyrimidine derivative of formula (III); (iii) fludioxinil (IV) and/or fenpiclonil (V); (iv) a phthalimide derivative selected from captan (VIa), captafol (VIb) and folpet (VII); (v) fluazinam (VIII); and/or (vi) dichlofluanid (IXa) or tolylfluanid (IXb). [Image] A : Ar or Het (both optionally substituted by 1-3 alkyl, halo, CHF 2, CF 3, (halo)alkoxy, alkylthio, alkylsulfinyl or alkylsulfonyl; R 1>H; R 2>phenyl (optionally substituted by 1-3 Q and optionally fused to a group M); or cycloalkyl (optionally substituted by 1-3 Q); M : a saturated 5-membered ring which may contain an O or S atom and is optionally substituted by one or more alkyl; Ar : an aryl group; Het : an aromatic or non-aromatic, 5-6 membered heterocycle which contains 1-3 N, O or S atoms; Q : alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkenyl, cycloalkyloxy, cycloalkenyloxy, phenyl or halo; in Q, the (cyclo)aliphatic residues are optionally halogenated, the cycloaliphatic residues are optionally substituted by 1-3 alkyl, and the phenyl is optionally substituted by 1-5 halo and/or 1-3 (halo)alkyl, (halo)alkoxy or (halo)alkylthio; R : methyl, propyn-1-yl or cyclopropyl ACTIVITY : Fungicidal. MECHANISM OF ACTION : None given.</abstract><edition>7</edition><oa>free_for_read</oa></addata></record> |
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subjects | AGRICULTURE ANIMAL HUSBANDRY BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES, AS HERBICIDES FISHING FORESTRY HUMAN NECESSITIES HUNTING PEST REPELLANTS OR ATTRACTANTS PLANT GROWTH REGULATORS PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTSTHEREOF TRAPPING |
title | Fungicide mixtures based on amide compounds and pyridine derivatives |
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