EP1706377A1 - Derives d'acide tetramique substitue par un cis-alcoxyspiro - Google Patents

Derives d'acide tetramique substitue par un cis-alcoxyspiro

Info

Publication number
EP1706377A1
EP1706377A1 EP04804377A EP04804377A EP1706377A1 EP 1706377 A1 EP1706377 A1 EP 1706377A1 EP 04804377 A EP04804377 A EP 04804377A EP 04804377 A EP04804377 A EP 04804377A EP 1706377 A1 EP1706377 A1 EP 1706377A1
Authority
EP
European Patent Office
Prior art keywords
alkyl
alkoxy
compounds
formula
phenyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP04804377A
Other languages
German (de)
English (en)
Inventor
Reiner Fischer
Stefan Lehr
Dieter Feucht
Peter Lösel
Olga Malsam
Guido Bojack
Thomas Auler
Martin Jeffrey Hills
Heinz Kehne
Christopher Hugh Rosinger
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer CropScience AG
Original Assignee
Bayer CropScience AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bayer CropScience AG filed Critical Bayer CropScience AG
Publication of EP1706377A1 publication Critical patent/EP1706377A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/45—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
    • C07C233/52—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a ring other than a six-membered aromatic ring
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
    • A01N43/38—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings condensed with carbocyclic rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
    • A01N47/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom containing —O—CO—O— groups; Thio analogues thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/54—Spiro-condensed
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14—The ring being saturated

Definitions

  • EP-A-582198 4-carboxy-chroman-4-yl-acetic acid (AC -304415, see EP-A-613618), 4-chlorophenoxyacetic acid, 3,3'-dimeth yl-4-methoxy-benzophenone, l-bromo-4-chloromethylsulfonyl-benzene, l- [4- (N-2-methoxybenzoylsulfamoyl) phenyl] -3-methyl-urea (aka N- (2-methoxy-benzoyl) -4 - [(methylamino-carbonyl) -amino] -benzenesulfonamide), l- [4- (N-2-methoxybenzoyl-sulfamoyl) -phenyl] -3,3-dimethyl-urea, l- [4- (N- 4,5-dimethylbenzoylsulfamoyl) phenyl]
  • R 20 represents hydrogen or -CC 4 - alkyl
  • Acetonitrile, ethyl acetate, dimethyl sulfoxide, tetrahydrofuran, dimethylformamide, methylene chloride are preferably used.
  • Otiorrhynchus sulcatus Otiorrhynchus sulcatus, Cosmopolites sordidus, Ceuthorrhynchus assimilis, Hypera postica, Dermestes spp., Trogoderma spp., Anthrenus spp., Attagenus spp., Lyctus spp., Meligethes aeneus, Ptinus spp., Giptusibbium psol. Tenebrio molitor, Agriotes spp., Conoderus spp., Melolontha melolontha, Amphimallon solstitialis, Costelytra zealandica, Lissorhoptrus oryzophilus.
  • the preferred transgenic (genetically engineered) plants or plant cultivars to be treated according to the invention include all plants which, through the genetic engineering modification, have received genetic material which gives these plants particularly advantageous, valuable properties (“traits”). Examples of such properties are better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or to water or soil salt content, increased flowering performance, easier harvesting, accelerated ripening, higher crop yields, higher quality and / or higher nutritional value of the harvested products, higher shelf life and / or workability of the harvested products.
  • Nematocerina and Brachycerina e.g. Aedes spp., Anopheles spp., Culex spp., Simulium spp., Eusimulium spp., Phlebotomus spp., Lutzomyia spp., Culicoides spp., Chrysops spp., Hybomitra spp., Atylotus spp., Tabanus spp., Haematopota ., Philipomyia spp., Braula spp., Musca spp., Hydrotaea spp., Stomoxys spp., Haematobia spp., Morellia spp., Fannia spp., Glossina spp., Calliphora spp., Glossina spp., Calliphora spp., Glossina spp.,
  • Siphonaptrida e.g. Pulex spp., Ctenocephalides spp., Xenopsylla spp., Ceratophyllus spp ..
  • Insecticides such as Chlo ⁇ yriphos, Phoxim, Silafluofin, Alphamethrin, Cyfluthrin, Cypermethrin, Deltamethrin, Permethrin, Imidacloprid, NI-25, Flufenoxuron, Hexaflumuron, Transfluthrin, Methoxyphenuroprid, Thiacloxiduron as well as fungicides such as epoxyconazole, hexaconazole, azaconazole, propiconazole, tebuconazole, cyproconazole, metconazole, imazalil, dichlorofluoride, tolylfluanid, 3-iodo-2-propynylbutylcarbamate, N-octyl-isothiazolin-3-one and 4,5 -N-octylisothiazolin-3-one.
  • the active compound combinations according to the invention can be applied before and after emergence of the plants, that is to say in the pre-emergence and post-emergence process.
  • Solvent 78 parts by weight of acetone 1.5 parts by weight of dimethylformamide emulsifier: 0.5 part by weight of alkylaryl polyglycol ether
  • Chinese cabbage leaf slices (Brassica pekinensis) are sprayed with an active ingredient preparation of the desired concentration and, after drying, are populated with larvae of the horseradish leaf beetle (Phaedon cochleariae).
  • Bean leaf slices Phaseolus vulgaris
  • Triticae Tricholine dexase
  • Bean leaf slices Phaseolus vulgaris
  • which are affected by all stages of the common spider mite Tetranychus urticae
  • an active ingredient preparation of the desired concentration is sprayed with an active ingredient preparation of the desired concentration.
  • active compound 1 part by weight of active compound is mixed with the stated amount of solvent and the stated amount of emulsifier, and the concentrate is diluted with water to the desired concentration.

Abstract

L'invention concerne de nouveaux dérivés d'acide tétramique substitué par un cis-alcoxyspiro, de la formule (I) où A, G, X, Y et Z ont la signification susmentionnée. L'invention concerne plusieurs procédés et produits intermédiaires destinés à leur production, et leur utilisation comme pesticides et/ou herbicides, ainsi que des produits herbicides sélectifs contenant, d'une part, des dérivés d'acide tétramique substitué par un cis-alcoxyspiro et, d'autre part, au moins un composé améliorant la la compatibilité avec des plantes cultivées.
EP04804377A 2004-01-09 2004-12-29 Derives d'acide tetramique substitue par un cis-alcoxyspiro Withdrawn EP1706377A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102004001433A DE102004001433A1 (de) 2004-01-09 2004-01-09 cis-Alkoxyspiro-substituierte Tetramsäure-Derivate
PCT/EP2004/014791 WO2005066125A1 (fr) 2004-01-09 2004-12-29 Derives d'acide tetramique substitue par un cis-alcoxyspiro

Publications (1)

Publication Number Publication Date
EP1706377A1 true EP1706377A1 (fr) 2006-10-04

Family

ID=34744645

Family Applications (1)

Application Number Title Priority Date Filing Date
EP04804377A Withdrawn EP1706377A1 (fr) 2004-01-09 2004-12-29 Derives d'acide tetramique substitue par un cis-alcoxyspiro

Country Status (10)

Country Link
US (1) US20070244007A1 (fr)
EP (1) EP1706377A1 (fr)
JP (1) JP2007520476A (fr)
KR (1) KR20060110355A (fr)
CN (1) CN1902174A (fr)
AR (1) AR048058A1 (fr)
BR (1) BRPI0417758A (fr)
CA (1) CA2552737A1 (fr)
DE (1) DE102004001433A1 (fr)
WO (1) WO2005066125A1 (fr)

Families Citing this family (56)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102004011006A1 (de) * 2004-03-06 2005-09-22 Bayer Cropscience Ag Suspensionskonzentrate auf Ölbasis
DE102004030753A1 (de) 2004-06-25 2006-01-19 Bayer Cropscience Ag 3'-Alkoxy spirocyclische Tetram- und Tretronsäuren
DE102004044827A1 (de) * 2004-09-16 2006-03-23 Bayer Cropscience Ag Jod-phenylsubstituierte cyclische Ketoenole
DE102004053192A1 (de) 2004-11-04 2006-05-11 Bayer Cropscience Ag 2-Alkoxy-6-alkyl-phenyl substituierte spirocyclische Tetramsäure-Derivate
DE102004053191A1 (de) * 2004-11-04 2006-05-11 Bayer Cropscience Ag 2,6-Diethyl-4-methyl-phenyl substituierte Tetramsäure-Derivate
DE102005008021A1 (de) 2005-02-22 2006-08-24 Bayer Cropscience Ag Spiroketal-substituierte cyclische Ketoenole
DE102005051325A1 (de) 2005-10-27 2007-05-03 Bayer Cropscience Ag Alkoxyalkyl spirocyclische Tetram- und Tetronsäuren
DE102005059469A1 (de) 2005-12-13 2007-06-14 Bayer Cropscience Ag Insektizide Zusammensetzungen mit verbesserter Wirkung
DE102005059471A1 (de) * 2005-12-13 2007-07-12 Bayer Cropscience Ag Herbizide Zusammensetzungen mit verbesserter Wirkung
DE102005059891A1 (de) 2005-12-15 2007-06-28 Bayer Cropscience Ag 3'-Alkoxy-spirocyclopentyl substituierte Tetram- und Tetronsäuren
DE102006007882A1 (de) 2006-02-21 2007-08-30 Bayer Cropscience Ag Cycloalkyl-phenylsubstituierte cyclische Ketoenole
DE102006018828A1 (de) 2006-04-22 2007-10-25 Bayer Cropscience Ag Alkoxyalkyl-substituierte cyclische Ketoenole
DE102006022821A1 (de) 2006-05-12 2007-11-15 Bayer Cropscience Ag Verwendung von Tetramsäurederivaten zur Bekämpfung von Insekten aus der Ordnung der Käfer (Coleoptera), Thrips (Tysanoptera), Wanzen (Hemiptera), Fliegen (Diptera) und Zikaden (Auchenorrhynchae)
DE102006025874A1 (de) 2006-06-02 2007-12-06 Bayer Cropscience Ag Alkoxyalkyl-substituierte cyclische Ketoenole
DE102006027731A1 (de) 2006-06-16 2007-12-20 Bayer Cropscience Ag Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
DE102006033154A1 (de) 2006-07-18 2008-01-24 Bayer Cropscience Ag Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
CA2658225C (fr) * 2006-07-26 2014-02-11 Dow Agrosciences Llc Compositions herbicides
DE102006050148A1 (de) 2006-10-25 2008-04-30 Bayer Cropscience Ag Trifluormethoxy-phenylsubstituierte Tetramsäure-Derivate
DE102006057036A1 (de) 2006-12-04 2008-06-05 Bayer Cropscience Ag Biphenylsubstituierte spirocyclische Ketoenole
DE102006057037A1 (de) 2006-12-04 2008-06-05 Bayer Cropscience Ag cis-Alkoxyspirocyclische biphenylsubstituierte Tetramsäure-Derivate
DE102007009957A1 (de) 2006-12-27 2008-07-03 Bayer Cropscience Ag Verfahren zur verbesserten Nutzung des Produktionsptentials transgener Pflanzen
EP2011394A1 (fr) * 2007-07-03 2009-01-07 Bayer CropScience AG Utilisation de dérivés d'acide tétramique pour combattre les vecteurs transmettant des virus
EP2014169A1 (fr) 2007-07-09 2009-01-14 Bayer CropScience AG Concentré soluble de tétramères 3-(2-alkoxy-4-chlor-6-alkyl-phenyl)-substitués et leurs énols correspondants
EP2020413A1 (fr) 2007-08-02 2009-02-04 Bayer CropScience AG Dérivé de tétrame et d'acide tétramique oxaspirocyclique et spiro substitué
EP2039248A1 (fr) * 2007-09-21 2009-03-25 Bayer CropScience AG Combinaisons d'agents actifs à propriétés insecticides et acaricides
EP2045240A1 (fr) 2007-09-25 2009-04-08 Bayer CropScience AG Dérivé de tétrame et d'acide tétramique halogénalkoxyspirocyclique
EP2103615A1 (fr) 2008-03-19 2009-09-23 Bayer CropScience AG Tétramate de 4'4'-dioxaspiro-spirocyclique substitué
EP2127522A1 (fr) 2008-05-29 2009-12-02 Bayer CropScience AG Combinaisons de principes actifs presentant des propriétés insecticides et acaricides
TW201031327A (en) 2008-11-14 2010-09-01 Bayer Cropscience Ag Active compound combinations having insecticidal and acaricidal properties
US8389443B2 (en) * 2008-12-02 2013-03-05 Bayer Cropscience Ag Geminal alkoxy/alkylspirocyclic substituted tetramate derivatives
US8846946B2 (en) 2008-12-02 2014-09-30 Bayer Cropscience Ag Germinal alkoxy/alkylspirocyclic substituted tetramate derivatives
AR075126A1 (es) 2009-01-29 2011-03-09 Bayer Cropscience Ag Metodo para el mejor uso del potencial de produccion de plantas transgenicas
HUE035166T2 (en) 2009-03-11 2018-05-02 Bayer Ip Gmbh Halogenalkylmethyleneoxyphenyl substituted ketoenols
DE102009028001A1 (de) 2009-07-24 2011-01-27 Bayer Cropscience Ag Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
WO2011098440A2 (fr) 2010-02-10 2011-08-18 Bayer Cropscience Ag Cétoénols cyliques à substitution biphényle
EP2534147B1 (fr) * 2010-02-10 2015-06-17 Bayer Intellectual Property GmbH Dérivés d'acides tétramiques substitués de manière spirohétérocyclique
DE102010008644A1 (de) 2010-02-15 2011-08-18 Bayer Schering Pharma Aktiengesellschaft, 13353 Zyklische Ketoenole zur Therapie
DE102010008643A1 (de) 2010-02-15 2011-08-18 Bayer Schering Pharma Aktiengesellschaft, 13353 Zyklische Ketoenole zur Therapie
DE102010008642A1 (de) 2010-02-15 2011-08-18 Bayer Schering Pharma Aktiengesellschaft, 13353 Zyklische Ketoenole zur Therapie
WO2011131623A1 (fr) 2010-04-20 2011-10-27 Bayer Cropscience Ag Composition insecticide et/ou herbicide à action améliorée, à base de dérivés d'acide tétramique à substituants spirohétérocycliques
TWI545112B (zh) 2011-01-25 2016-08-11 拜耳作物科學股份有限公司 １－ｈ－吡咯啶－２，４－二酮衍生物之製備方法
DE102011011040A1 (de) 2011-02-08 2012-08-09 Bayer Pharma Aktiengesellschaft (5s,8s)-3-(4'-Chlor-3'-fluor-4-methylbiphenyl-3-yl)-4-hydroxy-8-methoxy-1-azaspiro[4.5]dec-3-en-2-on (Verbindung A) zur Therapie
US8946124B2 (en) 2011-02-17 2015-02-03 Bayer Intellectual Property Gmbh Substituted 3-(biphenyl-3-yl)-8,8-difluoro-4-hydroxy-1-azaspiro[4.5]dec-3-en-2-ones for therapy and halogen-substituted spirocyclic ketoenols
DE102011080405A1 (de) 2011-08-04 2013-02-07 Bayer Pharma AG Substituierte 3-(Biphenyl-3-yl)-8,8-difluor-4-hydroxy-1-azaspiro[4.5]dec-3-en-2-one zur Therapie
KR101789527B1 (ko) 2011-03-01 2017-10-25 바이엘 인텔렉쳐 프로퍼티 게엠베하 2-아실옥시피롤린-4-온
ES2549061T3 (es) 2011-03-11 2015-10-22 Bayer Intellectual Property Gmbh Derivados de 1H-pirrolidina-2,4-diona espirocíclicos cis-alcoxi-sustituidos
DE102011080406A1 (de) 2011-08-04 2013-02-07 Bayer Pharma AG Substituierte 3-(Biphenyl-3-yl)-4-hydroxy-8-methoxy-1-azaspiro8[4.5]dec-3-en-2-one
AU2013211636B2 (en) 2012-01-26 2016-09-29 Bayer Intellectual Property Gmbh Phenyl-substituted ketoenols for controlling fish parasites
US10519085B2 (en) 2016-01-15 2019-12-31 Bayer Cropscience Aktiengesellschaft Process for preparing substituted 2-arylethanols
CN108976215B (zh) * 2017-05-31 2022-02-11 河北兰升生物科技有限公司 苯基酮烯醇衍生物的晶体及其制备方法、以及包含该晶体的农药组合物
US10743535B2 (en) 2017-08-18 2020-08-18 H&K Solutions Llc Insecticide for flight-capable pests
WO2019197652A1 (fr) 2018-04-13 2019-10-17 Bayer Aktiengesellschaft Formulation solide de mélanges insecticides
WO2019197617A1 (fr) 2018-04-13 2019-10-17 Bayer Cropscience Aktiengesellschaft Utilisation de dérivés d'acide tétramique pour lutter contre des bioagresseurs animaux par arrosage, pulvérisation, traitement de trou de plantation ou application sur raie.
WO2019197612A1 (fr) 2018-04-13 2019-10-17 Bayer Cropscience Aktiengesellschaft Utilisation de dérivés d'acide tétramique pour lutter contre les bioagresseurs animaux par arrosage ou pulvérisation
WO2019197620A1 (fr) 2018-04-13 2019-10-17 Bayer Cropscience Aktiengesellschaft Utilisation de dérivés d'acide tétramique pour lutter contre des insectes spéciaux
JP2021521151A (ja) 2018-04-13 2021-08-26 バイエル・クロップサイエンス・アクチェンゲゼルシャフト 特定の昆虫を防除するためのテトラミン酸誘導体の使用

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1152860C (zh) * 1995-06-30 2004-06-09 拜尔公司 二烷基-卤代苯基取代的酮-烯醇
DE19621522A1 (de) * 1996-05-29 1997-12-04 Hoechst Schering Agrevo Gmbh Neue N-Acylsulfonamide, neue Mischungen aus Herbiziden und Antidots und deren Verwendung
DE19742951A1 (de) * 1997-09-29 1999-04-15 Hoechst Schering Agrevo Gmbh Acylsulfamoylbenzoesäureamide, diese enthaltende nutzpflanzenschützende Mittel und Verfahren zu ihrer Herstellung
DE10139465A1 (de) * 2001-08-10 2003-02-20 Bayer Cropscience Ag Selektive Herbizide auf Basis von substituierten, cayclischen Ketoenolen und Safenern
DE10146910A1 (de) * 2001-09-24 2003-04-10 Bayer Cropscience Ag Spirocyclische 3-Phenyl-3-substituierte-4-ketolaktame und -laktone
DE10326386A1 (de) * 2003-06-12 2004-12-30 Bayer Cropscience Ag N-Heterocyclyl-phenylsubstituierte cyclische Ketoenole

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2005066125A1 *

Also Published As

Publication number Publication date
KR20060110355A (ko) 2006-10-24
US20070244007A1 (en) 2007-10-18
BRPI0417758A (pt) 2007-04-10
AR048058A1 (es) 2006-03-29
CA2552737A1 (fr) 2005-07-21
WO2005066125A1 (fr) 2005-07-21
CN1902174A (zh) 2007-01-24
JP2007520476A (ja) 2007-07-26
DE102004001433A1 (de) 2005-08-18

Similar Documents

Publication Publication Date Title
AU2004290516B2 (en) 2-ethyl-4,6-dimethyl-phenyl-substituted tetramic acid derivatives as pest control agents and/or herbicides
EP1220841B1 (fr) Cetoenols spirocycliques substitues par trifluoromethyle
WO2005066125A1 (fr) Derives d'acide tetramique substitue par un cis-alcoxyspiro
EP1682501A2 (fr) Derives d'acide tetramique spirocycliques substitues par 2-halogeno-6-alkylphenyle
EP1687272A1 (fr) Derives d'acide tetramique spirocycliques a substitution 2-ethyl-4,6-dimethyl-phenyle
WO2004065366A1 (fr) Derives d'acide tetramique substitues par 2,4-dihalogeno-6-(c2-c3-alkyl)-phenyle
EP1697321A1 (fr) Derives d'acide tetramique spirocycliques substitues par 2-halogeno-6-alkylphenyle
EP1280770A1 (fr) Cetoenols cycliques substitues par phenyle c 2? utilises comme agents de lutte contre les parasites et comme herbicides
WO2004024688A1 (fr) Kétoénoles spirocycliques substitués
DE102004044827A1 (de) Jod-phenylsubstituierte cyclische Ketoenole
DE10311300A1 (de) 2,4,6-Phenylsubstituierte cyclische Ketoenole
DE10331675A1 (de) Hetarylsubstituierte Pyrazolidindion-Derivate
WO2001098288A1 (fr) Derives de 5,6-dihydro-pyrone substitues par phenyle utilises comme pesticides et herbicides
WO2001079204A1 (fr) 4-hydroxytetrahydropyridone a substitution phenyle et leur utilisation en tant que pesticides et herbicides
EP1296979B1 (fr) HETEROCYCLES A SUBSTITUTION HETEROARYLE et leur utilisation comme pesticides
WO2002088098A1 (fr) 1,3-diones carbocycliques a substitution thiazolyl en tant que pesticides
WO2003010145A1 (fr) 4-hydroxy-quinolones substituees par biphenyle et leur utilisation comme pesticides et herbicides
EP1349854B1 (fr) Acides homotetramiques et homotetroniques a substitution hetaryle et utilisation en tant que pesticides

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20060809

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU MC NL PL PT RO SE SI SK TR

DAX Request for extension of the european patent (deleted)
17Q First examination report despatched

Effective date: 20081201

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20110701