WO2001015533A1 - Selektive herbizide auf basis eines substituierten phenylsulfonylaminocarbonyltriazolinons und safenern - Google Patents

Selektive herbizide auf basis eines substituierten phenylsulfonylaminocarbonyltriazolinons und safenern Download PDF

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Publication number
WO2001015533A1
WO2001015533A1 PCT/EP2000/007982 EP0007982W WO0115533A1 WO 2001015533 A1 WO2001015533 A1 WO 2001015533A1 EP 0007982 W EP0007982 W EP 0007982W WO 0115533 A1 WO0115533 A1 WO 0115533A1
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WO
WIPO (PCT)
Prior art keywords
alkyl
hydrogen
halogen
substituted
methyl
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.)
Ceased
Application number
PCT/EP2000/007982
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German (de)
English (en)
French (fr)
Inventor
Dieter Feucht
Peter Dahmen
Mark Wilhelm Drewes
Birgit Krauskopf
Mathias Kremer
Rolf Pontzen
Hans-Joachim Santel
Arndt Wellmann
Joachim Kluth
Klaus-Helmut Müller
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 AG
Original Assignee
Bayer 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 AG filed Critical Bayer AG
Priority to CA002382305A priority Critical patent/CA2382305A1/en
Priority to US10/069,350 priority patent/US6649565B1/en
Priority to BR0013646-8A priority patent/BR0013646A/pt
Priority to AU74094/00A priority patent/AU771120B2/en
Priority to UA2002032396A priority patent/UA73142C2/uk
Priority to EP00962323A priority patent/EP1211941B1/de
Priority to DK00962323T priority patent/DK1211941T3/da
Priority to HU0301992A priority patent/HU230217B1/hu
Priority to DE50004584T priority patent/DE50004584D1/de
Priority to JP2001519762A priority patent/JP2003508413A/ja
Priority to PL362853A priority patent/PL200541B1/pl
Priority to MXPA02002039A priority patent/MXPA02002039A/es
Priority to AT00962323T priority patent/ATE254849T1/de
Publication of WO2001015533A1 publication Critical patent/WO2001015533A1/de
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • 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
    • A01N47/08—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 one or more single bonds to nitrogen atoms
    • A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof

Definitions

  • the invention relates to new selective herbicidal combinations of active ingredients, the 2- (2-methoxycarbonyl-phenylsulfonylaminocarbonyl) -4-methyl-5-propoxy-2,4-dihydro-3H-l, 2,4-triazol-3-one and / or its salts, in particular its sodium salt, on the one hand and at least one compound which improves the ultimate plant tolerance on the other hand and can be used with particularly good results for selective weed control in various crops.
  • Substituted phenylsulfonylaminocarbonyl-triazolinones are known to be effective herbicides (see e.g. EP-A 507 171). However, the action of these compounds and / or their compatibility with crop plants are not entirely satisfactory under all conditions.
  • R 3 is hydrogen, C Cg-alkyl or C Cg-alkyl substituted by C Cö-alkoxy or C3-C 6 - alkenyloxy and
  • X j represents hydrogen or chlorine
  • R 40 and R 41 are independently hydrogen or halogen
  • R2 7 and R 2 g independently of one another are hydrogen or halogen and
  • R 2 9, R30 and R31 independently of one another are C 1 -C 4 -alkyl
  • R3 5 and R36 are independently hydrogen, C j -CG alkyl, C3-Cg cycloalkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl,
  • R35 and R36 together form a -Cß-alkylene bridge, which can be interrupted by oxygen, sulfur, SO, SO 2 , NH or -N (C r C 4 alkyl) -;
  • R 37 represents hydrogen or -CC 4 alkyl
  • R33 for hydrogen, halogen, cyano, trifluoromethyl, nitro, C 1 -C 4 -alkyl, C, -C 4 -alkoxy, C r C 4 -alkylthio, C r C 4 -alkylsulf ⁇ nyl, C r C 4 - Alkylsulfonyl, -COOR j , -CONR k R m , -COR n , -SO 2 -NR k R m or -OSO 2 -C ⁇ -C 4 alkyl;
  • R g for hydrogen, halogen, cyano, nitro, C r C 4 alkyl, C r C 4 haloalkyl, C r C 4 alkylthio, C r C 4 alkylsulfmyl, C r C 4 alkylsulfonyl, -COOR j , -CONR k R m , -COR n , -SO 2 NR k R m , -OSO 2 -C r C 4 alkyl, C r C 6 alkoxy or C r C 6 alkoxy substituted by C j -0 4 -alkoxy or halogen, C 3 -C 5 -alkenyloxy, or C3-Cg-alkenyloxy substituted by halogen, or C3-Cg-alkynyloxy, or
  • R33 and R3 4 together form a C 3 -C 4 alkylene bridge which may be substituted by halogen or C ⁇ -C4 alkyl, or C3-C4 alkenylene group which may be substituted by halogen or C ⁇ -C4-alkyl, or Form C3-C 4 alkadienylene bridge, which may be substituted by halogen or C j -C 4 alkyl;
  • R 34 and R n are independently hydrogen, halogen, Cj-C 4 alkyl, trifluoromethyl, C r C 6 alkoxy, C r C 6 alkylthio or -COOR j ;
  • Rc represents hydrogen, halogen, nitro, C 1 -C 4 -alkyl or methoxy
  • R d for hydrogen, halogen, nitro, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, CC 4 alkylthio, C r C 4 alkylsulfonyl, C r C 4 alkylsulfonyl, -COOR j or CONR k R m stands;
  • R e represents hydrogen, halogen, C r C 4 alkyl, -COOR j , trifluoromethyl or methoxy, or
  • R d and R e together form a C 3 -C 4 alkylene bridge;
  • R represents hydrogen, halogen or -CC 4 alkyl;
  • R x and R y independently of one another represent hydrogen, halogen, C 1 -C 4 -alkyl, C r C 4 -alkoxy, C r C 4 -alkylthio, -COOR 38 , trifluoromethyl, nitro or cyano;
  • R j , R k and R m are independently hydrogen or -CC 4 alkyl; or
  • R and R m together form a C 4 -C 6 alkylene bridge, which can be interrupted by oxygen, NH or -N (Cj-C 4 alkyl) -;
  • R n is -C-alkyl, phenyl, or phenyl substituted by halogen, CC-alkyl, methoxy, nitro or trifluoromethyl;
  • Phenylaminocarbonyl which is unsubstituted or the same as or phenyl - 9
  • R 60 and R 6j independently of one another for C 1 -C 4 -alkyl, or Rg 0 and R ß ⁇ together for - (CH 2 ) 5 -; stand; R 62 for hydrogen, Cj-C 4 alkyl
  • R 56 and R 57 independently of one another are C Cg-alkyl or C 2 -Cg-alkenyl; or
  • R 58 and R 59 are independently hydrogen or C Cg alkyl; or wherein
  • R79 is hydrogen or chlorine
  • Rg Q means cyano or trifluoromethyl
  • Rg j represents hydrogen or methyl
  • Rg 2 is hydrogen, C ] -C -alkyl, C ] -C 4 -alkyl substituted by CC - alkyl-X 2 - or C r C 4 -haloalkyl-X 2 -, C r C 4 -haloalkyl, nitro,
  • R 8 hydrogen, halogen, C ] -C 4 alkyl, trifluoromethyl, -C-C 4 alkoxy or C ] -C 4 haloalkoxy;
  • R 8 is hydrogen, halogen or C 1 -C 4 alkyl;
  • U, V, Wj and Z 4 independently of one another oxygen, sulfur, C (R 92 ) R93, carbonyl, NR9 4 , one group
  • R 95 and R 96 are independently hydrogen or C] -Cg alkyl; or R95 and R 96 together form a C 2 -C 6 alkylene group;
  • X 2 is oxygen or -S (O) s ;
  • R 99 is hydrogen, C r C 8 alkyl, C r C 8 haloalkyl, C r C 4 alkoxy C r C 8 alkyl, C 3 -C 6 alkenyloxy C r C 8 alkyl or phenyl C r C 8 - alkyl, where the phenyl ring by halogen, C j -C 4 alkyl, trifluoromethyl, methoxy or methyl-S (O) s - may be substituted, C3-C6 alkenyl, C3-C6-haloalkenyl, phenyl ⁇ - -alkenyl, C3-C 6 - alkynyl, phenyl ⁇ -Cg-alkynyl, oxetanyl, furyl or tetrahydrofuryl;
  • R 85 is hydrogen or -CC 4 alkyl
  • R 86 is hydrogen, C j -C alkyl or -CC 4 alkylcarbonyl
  • Rg 7 is hydrogen or -CC 4 alkyl
  • Rg 6 and R 87 together form a C 4 or C 5 alkylene group
  • Rgg, Rgg, R90 and R 91 are independently hydrogen or C 1 -C 4 alkyl; or R 88 together with R 89 or R 90 together with R 91 are independently C 4 or C 5 alkylene, where one carbon atom can be replaced by oxygen, sulfur or one or two carbon atoms by -NR j oo ";
  • R 92 , RJOO and R 9 are independently hydrogen or C r C 8 alkyl; or R 92 and R93 together are C -Cg alkylene;
  • R 94 is hydrogen or C ] -Cg alkyl
  • R 97 hydrogen; C r C 8 alkyl, phenyl, phenyl-C r C 8 alkyl, where the phenyl rings can be substituted by fluorine, chlorine, bromine, nitro, cyano, -OCH3, C 1 -C 4 -alkyl or CH 3 SO 2 - , C J -C 4 alkoxy-C r C 8 alkyl, C 3 -C 6 alkenyl or C 3 -C 6 alkynyl;
  • R 98 is hydrogen, C r C 8 alkyl, C 3 -C 6 alkenyl or C 3 -C 6 alkynyl, or
  • R9 7 and R 98 together are C 4 - or C5-alkylene, it being possible for one carbon atom to be replaced by oxygen or sulfur, or one or two carbon atoms to be replaced by -NR 1 01-;
  • R 101 hydrogen or -CC 4 alkyl
  • R 103 is hydrogen, C r C 6 alkyl, C 3 -C 6 cycloalkyl, C 3 -C 6 alkenyl or C 3 -C6 alkynyl; and R 1 04, 105 un ( 106 independently of one another are hydrogen, Cj-Cg-alkyl, C3-Cg-cycloalkyl or Ci-Cg-alkoxy, with the proviso that one of the substituents R 1 0 4 , R10 5 and d R 10 6 is different from hydrogen,
  • compositions which are characterized by comprising an active compound combination
  • a preferred embodiment is therefore also a mixture containing the compound of formula (I) and / or its salts on the one hand and 2,4-D and / or its derivatives on the other hand.
  • Typical derivatives of 2,4-D are, for example, their esters.
  • the compound is diethyl-1- (2,4-dichlorophenyl) -4,5-dihydro-5-methyl-1H-pyrazole-3,5-dicarboxylate (mefenpyr-diethyl), most preferred.
  • the salts of the compound of formula (I) are preferably the sodium, potassium, ammonium, methylammonium, ethylammonium, n- or i-propylammonium, n-, i-, s- or t-butylammonium, dimethylammonium -, Diethylammonium-, Di-n-propylammonium-, Di-i-propylammonium-, Di-n-butyl-ammonium-, Di-i-butyl- ammonium-, Di-s-butylammonium-, Trimethylammonium-, Triethylammonium-,
  • Tripropylammonium, Tributylammonium, Trimethylsulfonium and Triethylsulfonium salts Tripropylammonium, Tributylammonium, Trimethylsulfonium and Triethylsulfonium salts.
  • Salts of compounds of the formulas (II) or (III) are particularly preferably the sodium, potassium, ammonium, methylammonium, ethylammonium, n- or i-
  • Group (b) are suitable, the damaging effect of 2- (2-methoxycarbonylphenylsulfonylaminocarbonyl) -4-methyl-5-propoxy-2,4-dihydro-3H-l, 2,4-triazol-3-one and its Salts, in particular its sodium salt, are almost completely removed from the cultivated plants without impairing the herbicidal activity against the weeds.
  • the active substance combinations according to the invention can e.g. can be used in the following plants:
  • Galinsoga Chenopodium, Urtica, Senecio, Amaranthus, Portulaca, Xanthium, Convolvulus, Ipomoea, Polygonum, Sesbania, Ambrosia, Cirsium, Carduus, Sonchus, Solanum, Rorippa, Rotala, Lindernia, Lamium, Veronica, Dutilon, Emo Viola, galeopsis, papaver, centaurea, trifolium, ranunculus, taraxacum.
  • the cultivated plants are all plants and plant cultivars including transgenic plants and plant cultivars.
  • the advantageous effect of the compatibility of cultivated plants of the active compound combinations according to the invention is particularly pronounced at certain concentration ratios.
  • the weight ratios of the active ingredients in the active ingredient combinations can be varied within relatively large ranges. In general, 1 part by weight of active ingredient of the formula (I) or its salts is from 0.001 to 1000
  • Parts by weight preferably 0.01 to 100 parts by weight and particularly preferably 0.1 to 10 parts by weight of one of the compounds mentioned above under (b) which improves the tolerance of the crop plants (antidots / safener).
  • the active ingredients or combinations of active ingredients can be converted into the customary formulations, such as solutions, emulsions, wettable powders, suspensions, powders, Dusts, pastes, soluble powders, granules, suspension emulsion concentrates, active ingredient-impregnated natural and synthetic substances as well as fine encapsulation in polymeric substances.
  • formulations are prepared in a known manner, e.g. B. by mixing the active ingredients with extenders, ie liquid solvents and / or solid carriers, optionally using surface-active agents, ie emulsifiers and / or dispersants and / or foam-generating agents.
  • organic solvents can also be used as auxiliary solvents.
  • auxiliary solvents e.g. organic solvents
  • aromatics such as xylene, toluene, or alkylnaphthalenes
  • chlorinated aromatics and chlorinated aliphatic hydrocarbons such as chlorobenzenes, chlorethylenes or methylene chloride
  • aliphatic hydrocarbons such as cyclohexane or paraffins, e.g. Petroleum fractions, mineral and vegetable oils, alcohols, such as
  • ammonium salts and natural rock powders such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth and synthetic rock powders, such as highly disperse silica, aluminum oxide and silicates, as solid carriers for granules are possible: eg broken and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite and synthetic granules from inorganic and organic flours as well as granules from organic material such as sawdust, coconut shells, corn cobs and tobacco stems; suitable emulsifying and / or foam-generating agents are: for example nonionic and anionic emulsifiers, such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, for example alkylaryl polyglycol ethers, alkyl sulfonates, alkyl sulfates, aryl
  • Adhesives such as carboxymethyl cellulose, natural and synthetic powdery, granular or latex-shaped polymers can be used in the formulations, such as
  • Gum arabic polyvinyl alcohol, polyvinyl acetate, as well as natural phospholipids such as cephalins and lecithins and synthetic phospholipids.
  • Other additives can be mineral and vegetable oils.
  • Dyes such as inorganic pigments, e.g. Iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo and metal phthalocyanine dyes and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc can be used.
  • the formulations generally contain between 0.1 and 95 percent by weight of active ingredients, including the safing active ingredients, preferably between 0.5 and 90%.
  • the active compound combinations according to the invention are generally used in the form of finished formulations.
  • the active ingredients contained in the active ingredient combinations can also be mixed in individual formulations during use, i.e. be used in the form of tank mixes.
  • the new combinations of active ingredients can also be used in a mixture with other known herbicides, ready-to-use formulations or tank mixes being possible.
  • a mixture with other known active compounds such as fungicides, insecticides, acaricides, nematicides, bird repellants, growth agents, plant nutrients and agents which improve soil structure, is also possible.
  • active compounds such as fungicides, insecticides, acaricides, nematicides, bird repellants, growth agents, plant nutrients and agents which improve soil structure
  • Formulations as additional additives plant-compatible mineral or Vegetable oils (eg the commercial preparation "Oleo® DuPont 11E") or ammonium salts such as ammonium sulfate or ammonium rhodanide.
  • plant-compatible mineral or Vegetable oils eg the commercial preparation "Oleo® DuPont 11E”
  • ammonium salts such as ammonium sulfate or ammonium rhodanide.
  • the new active substance combinations can be used as such, in the form of their formulations or in the use forms prepared therefrom by further dilution, such as ready-to-use solutions, suspensions, emulsions, powders, pastes and granules. They are used in the usual way, e.g. by pouring, spraying, spraying, dusting or scattering.
  • the application rates of the active compound combinations according to the invention can be varied within a certain range; they hang among other things depending on the weather and soil factors.
  • the application rates are between 0.05 and 5 kg per ha, preferably between 0.05 and 2 kg per ha, particularly preferably between 0.1 and 1.0 kg per ha.
  • 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.
  • the sodium salt of the compound of formula (I) was applied as 70 WG or 70 WP, the mefenpyr-diethyl as 100 EC and the fenchlorazole-ethyl and the cloquintocet-mexyl as self-made active ingredient laboratory formulation.
  • An aqueous spray mixture containing 0.1% of the Renex-36 additive was prepared from the active ingredients and, if appropriate, the safeners.
  • Test plants which were grown in 10 ⁇ 10 cm pots (growing medium: soil or vermiculte) are sprayed with the active compound preparation in such a way that the desired amounts of active compound are applied per unit area.
  • the concentration of the spray liquor is chosen so that the particular amounts of active compound desired are applied in 500 l of water / ha.

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  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
PCT/EP2000/007982 1999-08-27 2000-08-16 Selektive herbizide auf basis eines substituierten phenylsulfonylaminocarbonyltriazolinons und safenern Ceased WO2001015533A1 (de)

Priority Applications (13)

Application Number Priority Date Filing Date Title
CA002382305A CA2382305A1 (en) 1999-08-27 2000-08-16 Selective herbicides on the basis of a substituted phenylsulfonylaminocarbonyltriazolinone and safeners
US10/069,350 US6649565B1 (en) 1999-08-27 2000-08-16 Selective herbicides on the basis of a substituted phenylsulfonylaminocarbonyltriazolinone and safeners
BR0013646-8A BR0013646A (pt) 1999-08-27 2000-08-16 Herbicidas seletivos à base de uma fenilsulfonilaminocarboniltriazolinona substituìda e protetores
AU74094/00A AU771120B2 (en) 1999-08-27 2000-08-16 Selective herbicides on the basis of a substituted phenylsulfonylaminocarbonyltriazolinone and safeners
UA2002032396A UA73142C2 (uk) 1999-08-27 2000-08-16 Гербіцидний засіб на основі заміщеного фенілсульфоніламінокарбонілтриазолінону
EP00962323A EP1211941B1 (de) 1999-08-27 2000-08-16 Selektive herbizide auf basis eines substituierten phenylsulfonylaminocarbonyltriazolinons und safenern
DK00962323T DK1211941T3 (da) 1999-08-27 2000-08-16 Selektive herbicider på grundlag af en substitueret phenylsulfonylaminocarbonyltriazolinon og modgifte
HU0301992A HU230217B1 (hu) 1999-08-27 2000-08-16 Szubsztituált fenilszulfonilaminokarbonil-triazolinon-származékot és széfenert tartalmazó szelektív herbicid készítmények
DE50004584T DE50004584D1 (de) 1999-08-27 2000-08-16 Selektive herbizide auf basis eines substituierten phenylsulfonylaminocarbonyltriazolinons und safenern
JP2001519762A JP2003508413A (ja) 1999-08-27 2000-08-16 置換されたフェニルスルホニルアミノカルボニルトリアゾリノンおよび毒性緩和剤を基礎とした選択的除草剤
PL362853A PL200541B1 (pl) 1999-08-27 2000-08-16 Selektywny środek chwastobójczy, zastosowanie selektywnego środka, sposób zwalczania chwastów i sposób wytwarzania środka chwastobójczego
MXPA02002039A MXPA02002039A (es) 1999-08-27 2000-08-16 Herbicidas selectivos a base de una fenilsulfonilaminocarboniltriazolinona substituida y protectores.
AT00962323T ATE254849T1 (de) 1999-08-27 2000-08-16 Selektive herbizide auf basis eines substituierten phenylsulfonylaminocarbonyltriazolinons und safenern

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19940860A DE19940860A1 (de) 1999-08-27 1999-08-27 Selektive Herbizide auf Basis eines substituierten Phenylsulfonyl aminocarbonyltriazolinons und Safenern II
DE19940860.2 1999-08-27

Publications (1)

Publication Number Publication Date
WO2001015533A1 true WO2001015533A1 (de) 2001-03-08

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PCT/EP2000/007982 Ceased WO2001015533A1 (de) 1999-08-27 2000-08-16 Selektive herbizide auf basis eines substituierten phenylsulfonylaminocarbonyltriazolinons und safenern

Country Status (20)

Country Link
US (1) US6649565B1 (enExample)
EP (1) EP1211941B1 (enExample)
JP (1) JP2003508413A (enExample)
CN (1) CN1198507C (enExample)
AR (1) AR025397A1 (enExample)
AT (1) ATE254849T1 (enExample)
AU (1) AU771120B2 (enExample)
BR (1) BR0013646A (enExample)
CA (1) CA2382305A1 (enExample)
CZ (1) CZ303831B6 (enExample)
DE (2) DE19940860A1 (enExample)
DK (1) DK1211941T3 (enExample)
ES (1) ES2208423T3 (enExample)
HU (1) HU230217B1 (enExample)
MX (1) MXPA02002039A (enExample)
PL (1) PL200541B1 (enExample)
RU (1) RU2266648C2 (enExample)
UA (1) UA73142C2 (enExample)
WO (1) WO2001015533A1 (enExample)
ZA (1) ZA200200593B (enExample)

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JP2004537570A (ja) * 2001-08-10 2004-12-16 バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト 置換環状ケト−エノール系選択的除草剤および毒性緩和剤
JP2005501900A (ja) * 2001-09-03 2005-01-20 バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト 置換アリールスルホニルアミノカルボニル−トリアゾリノン及び薬害軽減剤に基づく選択的除草剤
WO2007028504A3 (de) * 2005-09-08 2007-09-13 Bayer Cropscience Ag Neue sulfonamid-haltige feste formulierungen
US7781374B2 (en) * 2001-09-21 2010-08-24 Bayer Cropscience Ag Herbicides containing substituted Thien-3-yl-Sulphonylamino(thio)carbonyl-triazolin(thi)ones
US8530384B2 (en) 2004-03-05 2013-09-10 Bayer Cropscience Ag Herbicides based on substituted thien-3-yl-sulphonylamino(thio) carbonyl-triazolin(thi)ones and 4-HPPD-inhibitors
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DE19940860A1 (de) * 1999-08-27 2001-03-01 Bayer Ag Selektive Herbizide auf Basis eines substituierten Phenylsulfonyl aminocarbonyltriazolinons und Safenern II
DE10146590A1 (de) * 2001-09-21 2003-04-10 Bayer Cropscience Ag Selektive Herbizide auf Basis von substituierten Thien-3-yl-sulfonylamino(thio)carbonyl-triazolin(thi)onen und Safenern
DE102004035136A1 (de) * 2004-07-20 2006-02-16 Bayer Cropscience Gmbh Safening-Methode
US8940742B2 (en) 2012-04-10 2015-01-27 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
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EP1211941B1 (de) 2003-11-26
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DE19940860A1 (de) 2001-03-01
AR025397A1 (es) 2002-11-27
AU7409400A (en) 2001-03-26
EP1211941A1 (de) 2002-06-12
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HUP0301992A2 (en) 2003-09-29
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AU771120B2 (en) 2004-03-11
CN1198507C (zh) 2005-04-27
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ZA200200593B (en) 2003-03-26
ATE254849T1 (de) 2003-12-15
HU230217B1 (hu) 2015-10-28
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