ZW12181A1 - Derivatives of cyclopropane carboxylic acid their preparation their use in the control of parasites of plants and of animals the compositions containing them and the intermediates obtained - Google Patents
Derivatives of cyclopropane carboxylic acid their preparation their use in the control of parasites of plants and of animals the compositions containing them and the intermediates obtainedInfo
- Publication number
- ZW12181A1 ZW12181A1 ZW121/81A ZW12181A ZW12181A1 ZW 12181 A1 ZW12181 A1 ZW 12181A1 ZW 121/81 A ZW121/81 A ZW 121/81A ZW 12181 A ZW12181 A ZW 12181A ZW 12181 A1 ZW12181 A1 ZW 12181A1
- Authority
- ZW
- Zimbabwe
- Prior art keywords
- group
- radical
- carbon atoms
- see diagramm
- atom
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/74—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C69/743—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring of acids with a three-membered ring and with unsaturation outside the ring
- C07C69/747—Chrysanthemumic acid esters
-
- 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
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
-
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/74—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C69/743—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring of acids with a three-membered ring and with unsaturation outside the ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
- C07D213/647—One oxygen atom attached in position 2 or 6 and having in the molecule an acyl radical containing a saturated three-membered ring, e.g. chrysanthemumic acid esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/72—Two oxygen atoms, e.g. hydantoin
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/40—Radicals substituted by oxygen atoms
- C07D307/42—Singly bound oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Emergency Medicine (AREA)
- Environmental Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Furan Compounds (AREA)
- Indole Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Pyrane Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Catalysts (AREA)
- Peptides Or Proteins (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
1. Claims (for the contracting States : BE, CH, DE, FR, GB, IT, LI, LU, NL, SE) In all the possible isomer forms, the compounds with the formula (I') : see diagramm : EP0041021,P51,F1 in which the double bond has Z geometry, the cyclopropane copula is of 1R cis structure and A' represents : either an alkyl radical containing 1-18 carbon atoms, or a benzyl radical possibly substituted by one or more radicals chosen from the group constituted by alkyl radicals containing 1-4 carbon atoms, alkenyl radicals containing 2-6 carbon atoms, alkenyloxy radicals containing 2-6 carbon atoms, alkadienyl radicals containing 4-8 carbon atoms, the methylenedioxy residue, and the halogen atoms, or a see diagramm : EP0041021,P51,F2 group, in which the substituent R1 represents a hydrogen atom or a methyl radical and the substituent R2 represents a monocyclic aryl or a -CH2 -C -= CH group and notably a 5-benzyl-3-furylmethyl group, or a see diagramm : EP0041021,P51,F3 group in which R3 represents an aliphatic organic radical containing 2-6 carbon atoms and one or more carbon-carbon unsaturations and notably the radicals -CH2 -CH=CH2 , -CH2 -CH=CH-CH3 , -CH2 -CH=CH-C2 H5 , -CH2 -CH=CH-CH=CH2 , or a see diagramm : EP0041021,P51,F4 group, in which R3 retains the same significance as previously, each of R'1 and R'2 , identical or different, represents a hydrogen atom, a halogen atom, an alkyl radical containing 1-6 carbon atoms, an aryl radical containing 6-10 carbon atoms, an alkyloxycarbonyl group containing 2-5 carbon atoms, or a cyano group, or a see diagramm : EP0041021,P51,F5 group, in which B represents a CH2 group, or a C=O group, or a hetero element chosen from oxygen and sulphur, R4 represents a hydrogen atom, a methyl radical, a -CONH2 radical, a -CSNH2 radical or a -C -= CH radical R5 represents a halogen atom or a methyl radical and n represents a numeral 0, 1 or 2, and notably the 3-phenoxybenzyl, alpha-ethynyl-3-phenoxybenzyl, 3-benzoylbenzyl, 1-(3-phenoxyphenyl) ethyl or alpha-thioamido-3-phenoxybenzyl groups, or a see diagramm : EP0041021,P52,F1 group, or a see diagramm : EP0041021,P52,F2 group, in which each of the substituents R6 , R7 , R8 , R9 represents a hydrogen atom, a chlorine atom, or a methyl radical and in which S/I signifies an aromatic ring or a similar dihydro or tetrahydro ring, or a see diagramm : EP0041021,P52,F3 group, or a see diagramm : EP0041021,P52,F4 group, in which R10 represents a hydrogen atom or a CN radical, R12 represents a -CH2 - radical or an oxygen atom, R11 represents a thiazolyl or thiadiazolyl radical of which the bond with see diagramm : EP0041021,P52,F5 may be found at any one of the available positions, R12 being linked to R11 by the carbon atom situated between the sulphur atom and a nitrogen atom, or a see diagramm : EP0041021,P52,F6 group, or a see diagramm : EP0041021,P53,F1 group in which R13 represents a hydrogen atom or a CN radical, or a see diagramm : EP0041021,P53,F2 group, in which R13 is defined as above and the benzoyl radical is in position 3 or 4, or a see diagramm : EP0041021,P53,F3 group, in which R14 represents a hydrogen atom, a methyl, ethynyl or cyano radical and R15 and R16 , which are different from one another, represents a hydrogen, fluorine or bromine atom, or a see diagramm : EP0041021,P53,F4 group in which R14 is defined as above, each of the R17 's represents, independently, an alkyl group containing 1-4 carbon atoms, an alkoxy group containing 1-4 carbon atoms, an alkylthio group containing 1-4 carbon atoms, an alkylsulphonyl group containing 1-4 carbon atoms, or a trifluoromethyl, 3,4-methylenedioxy, chloro, fluoro, or bromo group, p represents a numeral 0, 1 or 2 and B' represents an oxygen atom or a sulphur atom, and R represents an alkyl radical, linear, branched or cyclic, saturated or unsaturated, containing 1-18 carbon atoms, as well as the mixtures of these isomers. 1. Claims (for the contracting State AT) Preparation process for all the possible isomer forms, of compounds with the formula (I') : see diagramm : EP0041021,P57,F2 in which the double bond has Z geometry, A' represents : either an alkyl radical containing 1-18 carbon atoms, or a benzyl radical possibly substituted by one or more radicals chosen from the group constituted by the alkyl radicals containing 1-4 carbon atoms, the alkenyl radicals containing 2-6 carbon atoms, the alkenyloxy radicals containing 2-6 carbon atoms, the alkadienyl radicals containing 4-8 carbon atoms, the methylene dioxy residue, and the halogen atoms, or a see diagramm : EP0041021,P58,F1 group, in which the substituent R1 represents a hydrogen atom or a methyl radical and the substituent R2 represents a monocyclic aryl or a -CH2 -C -= CH group and notably a 5-benzyl-3-furylmethyl group, or a see diagramm : EP0041021,P58,F2 group, in which R3 represents an aliphatic organic radical containing 2-6 carbon atoms and or more carbon-carbon unsaturations and notably the -CH2 -CH=CH2 , -CH2 CH=CH-CH3 , -CH2 CH=CH-C2 H5 , -CH2 -CH=CH-CH=CH2 radicals, or a see diagramm : EP0041021,P58,F3 group, in which R3 retains the same significance as previously, R'1 and R'2 identical or different, each represent a hydrogen atom, a halogen atom, an alkyl radical containing 1-6 carbons atoms, an aryl radical containing 6-10 carbon atoms, an alkyloxycarbonyl group containing 2-5 carbon atoms, or a cyano group, or a see diagramm : EP0041021,P58,F4 group, in which B represents a CH2 or C=O group, or a hetero element chosen from oxygen and sulphur, R4 represents a hydrogen atom, a methyl radical, a -CONH2 radical, a -CSNH2 radical or a -C -= CH radical, R5 represents a halogen atom or a methyl radical and n represents a numerical 0, 1 or 2, and notably the 3-phenoxybenzyl, alpha-ethynyl-3-phenoxybenzyl, 3-benzoylbenzyl, 1-(3-phenoxyphenyl)ethyl or alpha-thiomado-3-phenoxybenzyl group, or a see diagramm : EP0041021,P58,F5 group or a see diagramm : EP0041021,P59,F1 group, in which each of the substituents R6 , R7 , R8 , R9 , represents a hydrogen atom, a chlorine atom or a methyl radical and in which S/I signifies an aromatic ring or a similar dihydro or tetrahydro ring, or a see diagramm : EP0041021,P59,F2 group, or a see diagramm : EP0041021,P59,F3 group in which R10 represents a hydrogen atom or a CN radical, R12 represents a -CH2 - radical or an oxygen atom, R11 represents a thiazolyl or thiadiazolyl radical of which the bond with see diagramm : EP0041021,P59,F4 may be found in any of the available positions, R12 being linked to R11 by the carbon atom situated between the sulphur atom and a nitrogen atom, or a see diagramm : EP0041021,P59,F5 group, or a see diagramm : EP0041021,P59,F6 group, in which R13 represents a hydrogen atom or a CN radical, or a see diagramm : EP0041021,P60,F1 group, in which R13 is defined as above and the benzoyl radical is in position 3 or 4, or a see diagramm : EP0041021,P60,F2 group, in which R14 represents a hydrogen atom, a methyl, ethynyl or cyano radical, and each of R15 and R16 , which are different, represents a hydrogen, fluorine or bromine atom, or a see diagramm : EP0041021,P60,F3 group, in which R14 is defined as above, each of the R17 's represents, independently, an alkyl group containing 1-4 carbon atoms, an alkoxy group containing 1-4 carbon atoms, an alkylthio group containing 1-4 carbon atoms, an alkylsulphonyl group containing 1-4 carbon atoms, or a trifluoromethyl, 3,4-methylenedioxy, chloro, fluoro or bromo group, p represents a numeral 0, 1 or 2 and B' represents an oxygen atom or a sulphur atom, and R represents an alkyl radical, linear branched or cyclic, saturated or unsaturated, containing 1-18 carbon atoms, as well as the mixtures of these isomers, characterized in that an acid with the formula (II) : see diagramm : EP0041021,P60,F4 in which the double bond has Z geometry, R being defined as previously, or a functional derivative of this acid, is submitted to the action of an alcohol with the formula (III) : A'OH in which A' retains the same significance as previously, and in this way the corresponding compound with the formula (I') is obtained.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8011569A FR2482955A1 (en) | 1980-05-23 | 1980-05-23 | NOVEL DERIVATIVES OF CYCLOPROPANE CARBOXYLIC ACID, PROCESS FOR PREPARING THEM AND THEIR APPLICATION TO THE FIGHT AGAINST PARASITES |
Publications (1)
Publication Number | Publication Date |
---|---|
ZW12181A1 true ZW12181A1 (en) | 1981-10-14 |
Family
ID=9242299
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZW121/81A ZW12181A1 (en) | 1980-05-23 | 1981-05-26 | Derivatives of cyclopropane carboxylic acid their preparation their use in the control of parasites of plants and of animals the compositions containing them and the intermediates obtained |
Country Status (25)
Country | Link |
---|---|
EP (1) | EP0041021B1 (en) |
JP (3) | JPS5711943A (en) |
KR (1) | KR840001341B1 (en) |
AT (1) | ATE8616T1 (en) |
BR (1) | BR8103240A (en) |
CA (2) | CA1242647A (en) |
DD (2) | DD206731A5 (en) |
DE (1) | DE3165037D1 (en) |
DK (1) | DK163918C (en) |
EG (1) | EG15439A (en) |
ES (2) | ES8300080A1 (en) |
FI (1) | FI78902C (en) |
FR (1) | FR2482955A1 (en) |
GR (1) | GR81534B (en) |
HU (1) | HU191031B (en) |
IE (1) | IE52150B1 (en) |
IL (1) | IL62914A (en) |
MA (1) | MA19150A1 (en) |
NZ (1) | NZ197175A (en) |
OA (1) | OA06818A (en) |
PH (1) | PH20786A (en) |
PT (1) | PT73078B (en) |
SU (1) | SU1342408A3 (en) |
ZA (1) | ZA813384B (en) |
ZW (1) | ZW12181A1 (en) |
Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
OA06786A (en) * | 1980-04-16 | 1982-12-31 | Roussel Uclaf | New derivatives of cyclopropane acid, their preparation, their application to the fight against parasites of plants and animals, the compositions containing them and the new intermediates obtained. |
FR2491060A1 (en) * | 1980-10-01 | 1982-04-02 | Roussel Uclaf | PYRETHRIC ACID-RELATED CARBOXYLIC CYCLOPROPANIC ACID ESTERS, METHOD FOR THE PREPARATION THEREOF AND THEIR USE IN THE FIGHT AGAINST PESTS |
FR2536389B2 (en) * | 1982-11-22 | 1986-06-27 | Roussel Uclaf | ESTERS OF CYCLOPROPANE CARBOXYLIC ACIDS RELATED TO PYRETRIC ACID, THEIR PREPARATION PROCESS AND THEIR APPLICATION TO PEST CONTROL |
FR2500451B1 (en) * | 1981-02-26 | 1986-09-26 | Roussel Uclaf | ESTERS OF HETEROCYCLIC ALCOHOLS DERIVED FROM THIAZOLE OR THIADIAZOLE, PROCESS FOR THEIR PREPARATION AND PESTICIDE COMPOSITIONS CONTAINING THEM |
FR2517677B1 (en) * | 1981-12-09 | 1986-05-16 | Roussel Uclaf | NOVEL ETHERS WITH ORGANIC REMAINS CONTAINING CHIRAL ATOMS, THEIR PREPARATION PROCESS AND THEIR APPLICATION TO THE SPLITTING OF ALCOHOLS OR CERTAIN HEMIACETAL STRUCTURE COMPOUNDS. |
FR2526018A1 (en) * | 1982-04-30 | 1983-11-04 | Roussel Uclaf | Alpha cyano phenoxy cyclopropane carboxylate(s) - are low toxicity insecticides and acaricides for plants, animals, and buildings |
FR2526017B1 (en) * | 1982-04-30 | 1985-10-11 | Roussel Uclaf | ESTER OF CYCLOPROPANE CARBOXYLIC ACID AND CYANO (4-FLUORO 3-PHENOXYPHENYL) METHYLIC ALCOHOL (S), PREPARATION METHOD THEREOF AND PESTICIDE COMPOSITIONS CONTAINING THE SAME |
ATE20888T1 (en) * | 1982-05-10 | 1986-08-15 | Ciba Geigy Ag | CYCLOPROPANECARBONIC ACID DERIVATIVES. |
FR2533416B1 (en) * | 1982-09-29 | 1988-09-02 | Roussel Uclaf | NOVEL PESTICIDE COMPOSITIONS CONTAINING A PHOTOSTABILIZER |
FR2539411B2 (en) * | 1983-01-17 | 1986-04-25 | Roussel Uclaf | NOVEL DERIVATIVES OF CYCLOPROPANE CARBOXYLIC ACID, THEIR PREPARATION METHOD, THEIR APPLICATION TO THE CONTROL OF PESTS |
FR2574403B1 (en) * | 1984-12-06 | 1987-01-30 | Roussel Uclaf | NOVEL ESTERS DERIVED FROM CYCLOPROPANE CARBOXYLIC ACID AND (R) 2- (6-PHENOXY PYRIDYL) ETHANOL, THEIR PREPARATION PROCESS AND THEIR APPLICATION TO PEST CONTROL |
FR2586675B1 (en) * | 1985-08-27 | 1987-12-11 | Roussel Uclaf | NOVEL ESTERS OF CYCLOPROPANE CARBOXYLIC ACID AND 2,3 DIHYDRO-4-PHENYL-IH-INDEN-2-OL, THEIR PREPARATION PROCESS AND THEIR APPLICATION TO PEST CONTROL |
FR2610624B1 (en) * | 1987-02-06 | 1989-06-09 | Roussel Uclaf | NOVEL ESTERS OF PYRETHRIC ACID-LIKE CYCLOPROPANECARBOXYLIC ACIDS, THEIR PREPARATION PROCESS AND THEIR APPLICATION TO PEST CONTROL |
JP2570388B2 (en) * | 1988-06-10 | 1997-01-08 | 住友化学工業株式会社 | Carboxylic acid esters and their use as insecticides |
US5055491A (en) * | 1989-04-10 | 1991-10-08 | Sumitomo Chemical Company, Limited | Carboxylic acid esters, methods for producing them and insecticides and/or acaricides containing them as an active ingredient |
FR2678611B1 (en) * | 1991-07-04 | 1995-01-20 | Roussel Uclaf | NOVEL PYRETHRINOUID ESTERS OF ALCOHOL 1,3,4,5,6,7-HEXAHYDRO 1,3-DIOXO-2H-ISOINDOL-2-YL-METHYLIQUE, THEIR PREPARATION PROCESS AND THEIR APPLICATION AS PESTICIDES. |
FR2678609B1 (en) * | 1991-07-04 | 1994-08-26 | Roussel Uclaf | NOVEL PYRETHRINOUID ESTERS OF THE ALCOHOL 4-AMINO 2,3,5,6-TETRAFLUOROPHENYL METHYLIQUE, THEIR PREPARATION PROCESS AND THEIR APPLICATION AS PESTICIDES. |
FR2687149B1 (en) * | 1992-02-12 | 1995-11-03 | Roussel Uclaf | NOVEL PYRETHRINOUID ESTERS DERIVED FROM THIAZOLIC ALCOHOLS, THEIR PREPARATION PROCESS AND THEIR APPLICATION AS PESTICIDES. |
EP0754674B1 (en) * | 1995-02-07 | 2001-12-19 | Dainihon Jochugiku Co., Ltd. | Novel carboxylic ester derivatives, process for producing the same, and insecticide or insectifuge containing the same |
US5852048A (en) * | 1995-03-01 | 1998-12-22 | Sumitomo Chemical Company, Limited | Ester compound and a pesticidal agent containing the same as an active ingredient |
JP4488765B2 (en) * | 2004-02-26 | 2010-06-23 | 大日本除蟲菊株式会社 | Aerosol insecticide |
WO2006118955A2 (en) | 2005-04-29 | 2006-11-09 | Wyeth | Process for preparing 3,3-disubstituted oxindoles and thio-oxindoles |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS515450B1 (en) * | 1971-06-29 | 1976-02-20 | ||
DE2326077C2 (en) * | 1972-05-25 | 1985-12-12 | National Research Development Corp., London | Unsaturated cyclopropanecarboxylic acids and their derivatives, their preparation and insecticides containing them |
CH589408A5 (en) * | 1973-04-18 | 1977-07-15 | Ciba Geigy Ag | |
DE2706222A1 (en) * | 1976-02-16 | 1977-08-18 | Ciba Geigy Ag | CYCLOPROPANCARBONIC ACID ESTERS, METHOD OF MANUFACTURING AND USING them |
US4242357A (en) * | 1976-04-09 | 1980-12-30 | Bayer Aktiengesellschaft | Carboxylic acid esters for combating pests |
CA1117673A (en) * | 1977-12-29 | 1982-02-02 | Hajime Shichijo | Tuning apparatus |
HU176938B (en) * | 1978-02-23 | 1981-06-28 | Chinoin Gyogyszer Es Vegyeszet | Process for preparing new chrysanthemic acid ester derivatives |
HU176939B (en) * | 1978-02-23 | 1981-06-28 | Chinoin Gyogyszer Es Vegyeszet | Process for pproducing derivatives of esters of chrisanthemic acid |
-
1980
- 1980-05-23 FR FR8011569A patent/FR2482955A1/en active Granted
-
1981
- 1981-05-15 SU SU813284396A patent/SU1342408A3/en active
- 1981-05-20 IL IL62914A patent/IL62914A/en unknown
- 1981-05-20 MA MA19359A patent/MA19150A1/en unknown
- 1981-05-20 GR GR65014A patent/GR81534B/el unknown
- 1981-05-20 EG EG81281A patent/EG15439A/en active
- 1981-05-20 ZA ZA00813384A patent/ZA813384B/en unknown
- 1981-05-21 HU HU811483A patent/HU191031B/en unknown
- 1981-05-21 FI FI811566A patent/FI78902C/en not_active IP Right Cessation
- 1981-05-22 DD DD81245453A patent/DD206731A5/en not_active IP Right Cessation
- 1981-05-22 KR KR1019810001819A patent/KR840001341B1/en active
- 1981-05-22 DD DD81230196A patent/DD159068A5/en not_active IP Right Cessation
- 1981-05-22 DK DK225881A patent/DK163918C/en not_active IP Right Cessation
- 1981-05-22 ES ES502428A patent/ES8300080A1/en not_active Expired
- 1981-05-22 DE DE8181400816T patent/DE3165037D1/en not_active Expired
- 1981-05-22 CA CA000378114A patent/CA1242647A/en not_active Expired
- 1981-05-22 PT PT73078A patent/PT73078B/en not_active IP Right Cessation
- 1981-05-22 IE IE1151/81A patent/IE52150B1/en not_active IP Right Cessation
- 1981-05-22 AT AT81400816T patent/ATE8616T1/en not_active IP Right Cessation
- 1981-05-22 JP JP7682481A patent/JPS5711943A/en active Granted
- 1981-05-22 CA CA000378108A patent/CA1237433A/en not_active Expired
- 1981-05-22 EP EP81400816A patent/EP0041021B1/en not_active Expired
- 1981-05-22 NZ NZ197175A patent/NZ197175A/en unknown
- 1981-05-23 OA OA57411A patent/OA06818A/en unknown
- 1981-05-25 BR BR8103240A patent/BR8103240A/en unknown
- 1981-05-25 PH PH25671A patent/PH20786A/en unknown
- 1981-05-26 ZW ZW121/81A patent/ZW12181A1/en unknown
-
1982
- 1982-05-18 ES ES512286A patent/ES8304914A1/en not_active Expired
-
1984
- 1984-07-06 JP JP59139236A patent/JPS60214761A/en active Granted
-
1990
- 1990-12-19 JP JP41176890A patent/JPH0699354B2/en not_active Expired - Lifetime
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