SK439090A3 - Isoxazoles herbicides, process for their preparation, intermediates for their preparation, herbicidal composition them containing, and their use - Google Patents
Isoxazoles herbicides, process for their preparation, intermediates for their preparation, herbicidal composition them containing, and their use Download PDFInfo
- Publication number
- SK439090A3 SK439090A3 SK4390-90A SK439090A SK439090A3 SK 439090 A3 SK439090 A3 SK 439090A3 SK 439090 A SK439090 A SK 439090A SK 439090 A3 SK439090 A3 SK 439090A3
- Authority
- SK
- Slovakia
- Prior art keywords
- isoxazole
- group
- nitro
- formula
- compounds
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 117
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 35
- 238000002360 preparation method Methods 0.000 title claims description 21
- 238000000034 method Methods 0.000 title claims description 16
- 239000000543 intermediate Substances 0.000 title claims description 9
- 150000002545 isoxazoles Chemical class 0.000 title claims description 8
- 239000004009 herbicide Substances 0.000 title description 10
- 150000001875 compounds Chemical class 0.000 claims abstract description 148
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 26
- 125000005843 halogen group Chemical group 0.000 claims abstract description 23
- 150000003839 salts Chemical class 0.000 claims abstract description 22
- 125000003118 aryl group Chemical group 0.000 claims abstract description 7
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 6
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 4
- 125000000304 alkynyl group Chemical group 0.000 claims abstract description 4
- 125000000392 cycloalkenyl group Chemical group 0.000 claims abstract description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 133
- -1 cyano, nitro, amino Chemical group 0.000 claims description 117
- 239000007787 solid Substances 0.000 claims description 82
- 241000196324 Embryophyta Species 0.000 claims description 61
- 239000000243 solution Substances 0.000 claims description 59
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 51
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 48
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- 230000012010 growth Effects 0.000 claims description 26
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- 125000004432 carbon atom Chemical group C* 0.000 claims description 21
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- WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 claims description 14
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 14
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
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- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 claims description 3
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- UWNMGKQAIFQHDD-UHFFFAOYSA-N [5-(4-methoxyphenyl)-1,2-oxazol-4-yl]-[2-nitro-4-(trifluoromethyl)phenyl]methanone Chemical compound C1=CC(OC)=CC=C1C1=C(C(=O)C=2C(=CC(=CC=2)C(F)(F)F)[N+]([O-])=O)C=NO1 UWNMGKQAIFQHDD-UHFFFAOYSA-N 0.000 claims description 2
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- VSERVYAFXWKHEP-UHFFFAOYSA-N tert-butyl 2-(cyclobutanecarbonyl)-3-[2-nitro-4-(trifluoromethyl)phenyl]-3-oxopropanoate Chemical compound C=1C=C(C(F)(F)F)C=C([N+]([O-])=O)C=1C(=O)C(C(=O)OC(C)(C)C)C(=O)C1CCC1 VSERVYAFXWKHEP-UHFFFAOYSA-N 0.000 description 1
- QERBADQEIVXPTO-UHFFFAOYSA-N tert-butyl 2-(cyclopentanecarbonyl)-3-[2-nitro-4-(trifluoromethyl)phenyl]-3-oxopropanoate Chemical compound C=1C=C(C(F)(F)F)C=C([N+]([O-])=O)C=1C(=O)C(C(=O)OC(C)(C)C)C(=O)C1CCCC1 QERBADQEIVXPTO-UHFFFAOYSA-N 0.000 description 1
- ICPBEPIECKKPKM-UHFFFAOYSA-N tert-butyl 2-(cyclopentanecarbonyl)-3-[2-nitro-4-(trifluoromethyl)phenyl]-3-oxopropanoate tert-butyl 3-cyclopentyl-3-oxopropanoate Chemical compound C1(CCCC1)C(C(C(=O)OC(C)(C)C)C(C1=C(C=C(C=C1)C(F)(F)F)[N+](=O)[O-])=O)=O.C1(CCCC1)C(CC(=O)OC(C)(C)C)=O ICPBEPIECKKPKM-UHFFFAOYSA-N 0.000 description 1
- HKQZNBUHSMZTRS-UHFFFAOYSA-N tert-butyl 2-(cyclopropanecarbonyl)-3-(2,3-dichloro-4-methylsulfonylphenyl)-3-oxopropanoate Chemical compound C=1C=C(S(C)(=O)=O)C(Cl)=C(Cl)C=1C(=O)C(C(=O)OC(C)(C)C)C(=O)C1CC1 HKQZNBUHSMZTRS-UHFFFAOYSA-N 0.000 description 1
- SAHSSSWHHKGGRL-UHFFFAOYSA-N tert-butyl 2-(cyclopropanecarbonyl)-3-(2,4-dichlorophenyl)-3-oxopropanoate Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)C(C(=O)OC(C)(C)C)C(=O)C1CC1 SAHSSSWHHKGGRL-UHFFFAOYSA-N 0.000 description 1
- ASWYGFOMZKXBFC-UHFFFAOYSA-N tert-butyl 2-(cyclopropanecarbonyl)-3-(4-fluoro-2-nitrophenyl)-3-oxopropanoate Chemical compound C=1C=C(F)C=C([N+]([O-])=O)C=1C(=O)C(C(=O)OC(C)(C)C)C(=O)C1CC1 ASWYGFOMZKXBFC-UHFFFAOYSA-N 0.000 description 1
- DLKPUROZACWDGA-UHFFFAOYSA-N tert-butyl 2-(cyclopropanecarbonyl)-3-[2-nitro-4-(1,1,2,2,2-pentafluoroethyl)phenyl]-3-oxopropanoate Chemical compound C=1C=C(C(F)(F)C(F)(F)F)C=C([N+]([O-])=O)C=1C(=O)C(C(=O)OC(C)(C)C)C(=O)C1CC1 DLKPUROZACWDGA-UHFFFAOYSA-N 0.000 description 1
- OLEMYBLIHBBIFR-UHFFFAOYSA-N tert-butyl 2-(cyclopropanecarbonyl)-3-[2-nitro-4-(1,1,2,2,2-pentafluoroethyl)phenyl]-3-oxopropanoate 2-nitro-4-(1,1,2,2,2-pentafluoroethyl)benzoyl chloride Chemical compound C1(CC1)C(C(C(=O)OC(C)(C)C)C(C1=C(C=C(C=C1)C(C(F)(F)F)(F)F)[N+](=O)[O-])=O)=O.[N+](=O)([O-])C1=C(C(=O)Cl)C=CC(=C1)C(C(F)(F)F)(F)F OLEMYBLIHBBIFR-UHFFFAOYSA-N 0.000 description 1
- POZSEDYRLFHJST-UHFFFAOYSA-N tert-butyl 2-(cyclopropanecarbonyl)-3-[2-nitro-4-(trifluoromethyl)phenyl]-3-oxopropanoate Chemical compound C=1C=C(C(F)(F)F)C=C([N+]([O-])=O)C=1C(=O)C(C(=O)OC(C)(C)C)C(=O)C1CC1 POZSEDYRLFHJST-UHFFFAOYSA-N 0.000 description 1
- UGHRDHIMVQGZIS-UHFFFAOYSA-N tert-butyl 2-(cyclopropanecarbonyl)-3-[4-methylsulfonyl-2-(trifluoromethyl)phenyl]-3-oxopropanoate Chemical compound C=1C=C(S(C)(=O)=O)C=C(C(F)(F)F)C=1C(=O)C(C(=O)OC(C)(C)C)C(=O)C1CC1 UGHRDHIMVQGZIS-UHFFFAOYSA-N 0.000 description 1
- MWYWRRDQSMZEEK-UHFFFAOYSA-N tert-butyl 2-[2,4-bis(trifluoromethyl)benzoyl]-3-cyclopropyl-3-oxopropanoate Chemical compound C=1C=C(C(F)(F)F)C=C(C(F)(F)F)C=1C(=O)C(C(=O)OC(C)(C)C)C(=O)C1CC1 MWYWRRDQSMZEEK-UHFFFAOYSA-N 0.000 description 1
- XNFLHXFZVSIQFK-UHFFFAOYSA-N tert-butyl 2-[2-chloro-4-(trifluoromethyl)benzoyl]-3-cyclopropyl-3-oxopropanoate Chemical compound C=1C=C(C(F)(F)F)C=C(Cl)C=1C(=O)C(C(=O)OC(C)(C)C)C(=O)C1CC1 XNFLHXFZVSIQFK-UHFFFAOYSA-N 0.000 description 1
- LYHZRVARDWVOJO-UHFFFAOYSA-N tert-butyl 2-[2-nitro-4-(1,1,2,2,2-pentafluoroethyl)benzoyl]-3-oxobutanoate Chemical compound CC(C)(C)OC(=O)C(C(=O)C)C(=O)C1=CC=C(C(F)(F)C(F)(F)F)C=C1[N+]([O-])=O LYHZRVARDWVOJO-UHFFFAOYSA-N 0.000 description 1
- NPLPUIYTRIKYMS-UHFFFAOYSA-N tert-butyl 2-[2-nitro-4-(trifluoromethyl)benzoyl]-3-oxopentanoate Chemical compound CC(C)(C)OC(=O)C(C(=O)CC)C(=O)C1=CC=C(C(F)(F)F)C=C1[N+]([O-])=O NPLPUIYTRIKYMS-UHFFFAOYSA-N 0.000 description 1
- WERFPONBGKTAIU-UHFFFAOYSA-N tert-butyl 2-[2-nitro-4-(trifluoromethyl)benzoyl]-3-oxopentanoate tert-butyl 3-oxopentanoate Chemical compound [N+](=O)([O-])C1=C(C(=O)C(C(=O)OC(C)(C)C)C(CC)=O)C=CC(=C1)C(F)(F)F.O=C(CC(=O)OC(C)(C)C)CC WERFPONBGKTAIU-UHFFFAOYSA-N 0.000 description 1
- ZEBZTOWJHQOBHG-UHFFFAOYSA-N tert-butyl 2-[4-chloro-2-(trifluoromethyl)benzoyl]-3-oxobutanoate 1-[4-chloro-2-(trifluoromethyl)phenyl]butane-1,3-dione Chemical compound ClC1=CC(=C(C(=O)C(C(=O)OC(C)(C)C)C(C)=O)C=C1)C(F)(F)F.ClC1=CC(=C(C=C1)C(CC(C)=O)=O)C(F)(F)F ZEBZTOWJHQOBHG-UHFFFAOYSA-N 0.000 description 1
- HOHBQWITMXOSOW-UHFFFAOYSA-N tert-butyl 2-trimethylsilylacetate Chemical compound CC(C)(C)OC(=O)C[Si](C)(C)C HOHBQWITMXOSOW-UHFFFAOYSA-N 0.000 description 1
- CHBUAVKFDIVTMW-UHFFFAOYSA-N tert-butyl 3-(1-methylcyclopropyl)-3-oxopropanoate Chemical compound CC(C)(C)OC(=O)CC(=O)C1(C)CC1 CHBUAVKFDIVTMW-UHFFFAOYSA-N 0.000 description 1
- MBOJKHRJJWTMOB-UHFFFAOYSA-N tert-butyl 4,4-dimethyl-2-[2-nitro-4-(trifluoromethyl)benzoyl]-3-oxopentanoate Chemical compound CC(C)(C)OC(=O)C(C(=O)C(C)(C)C)C(=O)C1=CC=C(C(F)(F)F)C=C1[N+]([O-])=O MBOJKHRJJWTMOB-UHFFFAOYSA-N 0.000 description 1
- RZGHQHORDHWMRA-UHFFFAOYSA-N tert-butyl 4-methyl-2-[2-nitro-4-(1,1,2,2,2-pentafluoroethyl)benzoyl]-3-oxopentanoate Chemical compound CC(C)(C)OC(=O)C(C(=O)C(C)C)C(=O)C1=CC=C(C(F)(F)C(F)(F)F)C=C1[N+]([O-])=O RZGHQHORDHWMRA-UHFFFAOYSA-N 0.000 description 1
- WMOVHXAZOJBABW-UHFFFAOYSA-N tert-butyl acetate Chemical compound CC(=O)OC(C)(C)C WMOVHXAZOJBABW-UHFFFAOYSA-N 0.000 description 1
- IOGXOCVLYRDXLW-UHFFFAOYSA-N tert-butyl nitrite Chemical compound CC(C)(C)ON=O IOGXOCVLYRDXLW-UHFFFAOYSA-N 0.000 description 1
- 239000012414 tert-butyl nitrite Substances 0.000 description 1
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 238000000844 transformation Methods 0.000 description 1
- 229940047183 tribulus Drugs 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/45—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by at least one doubly—bound oxygen atom, not being part of a —CHO group
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/07—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms
- C07C205/11—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms having nitro groups bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/49—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
- C07C205/55—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups or carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/49—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
- C07C205/56—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups bound to carbon atoms of six-membered aromatic rings and carboxyl groups bound to acyclic carbon atoms of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/49—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
- C07C205/57—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C205/58—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton the carbon skeleton being further substituted by halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/32—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring
- C07C255/40—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by doubly-bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C255/56—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and doubly-bound oxygen atoms bound to the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C255/57—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and carboxyl groups, other than cyano groups, bound to the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/16—Sulfones; Sulfoxides having sulfone or sulfoxide groups and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C317/22—Sulfones; Sulfoxides having sulfone or sulfoxide groups and singly-bound oxygen atoms bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/80—Ketones containing a keto group bound to a six-membered aromatic ring containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/80—Ketones containing a keto group bound to a six-membered aromatic ring containing halogen
- C07C49/813—Ketones containing a keto group bound to a six-membered aromatic ring containing halogen polycyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/84—Ketones containing a keto group bound to a six-membered aromatic ring containing ether groups, groups, groups, or groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/738—Esters of keto-carboxylic acids or aldehydo-carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more 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
- C07D261/14—Nitrogen atoms
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Environmental Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Health & Medical Sciences (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB898920519A GB8920519D0 (en) | 1989-09-11 | 1989-09-11 | New compositions of matter |
Publications (2)
Publication Number | Publication Date |
---|---|
SK280820B6 SK280820B6 (sk) | 2000-08-14 |
SK439090A3 true SK439090A3 (en) | 2000-08-14 |
Family
ID=10662884
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SK4390-90A SK439090A3 (en) | 1989-09-11 | 1990-09-10 | Isoxazoles herbicides, process for their preparation, intermediates for their preparation, herbicidal composition them containing, and their use |
Country Status (32)
Country | Link |
---|---|
EP (1) | EP0418175B1 (fr) |
JP (1) | JP3100054B2 (fr) |
KR (1) | KR0161979B1 (fr) |
CN (2) | CN1037058C (fr) |
AT (1) | ATE140453T1 (fr) |
AU (1) | AU635316B2 (fr) |
BA (1) | BA97208A (fr) |
BG (1) | BG60562B1 (fr) |
BR (1) | BR9004698A (fr) |
CA (1) | CA2024956C (fr) |
CZ (1) | CZ285582B6 (fr) |
DE (1) | DE69027823T2 (fr) |
DK (1) | DK0418175T3 (fr) |
EG (1) | EG19315A (fr) |
ES (1) | ES2089003T3 (fr) |
FI (1) | FI104172B (fr) |
GB (1) | GB8920519D0 (fr) |
GR (1) | GR3020573T3 (fr) |
HU (3) | HU9600452D0 (fr) |
IE (1) | IE76313B1 (fr) |
IL (3) | IL110703A (fr) |
MA (1) | MA21947A1 (fr) |
MY (1) | MY108540A (fr) |
NZ (1) | NZ235251A (fr) |
OA (1) | OA09311A (fr) |
PT (1) | PT95281B (fr) |
RU (1) | RU2060663C1 (fr) |
SK (1) | SK439090A3 (fr) |
TR (1) | TR25897A (fr) |
UA (1) | UA26972A1 (fr) |
YU (1) | YU48133B (fr) |
ZA (1) | ZA907217B (fr) |
Families Citing this family (85)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5650533A (en) * | 1989-09-11 | 1997-07-22 | Rhone-Poulenc Agriculture Ltd. | Intermediates to herbicidal 4-substituted isoxazoles |
US5747424A (en) * | 1989-09-11 | 1998-05-05 | Rhone-Poulenc Agriculture Ltd. | Herbicidal 4-substituted isoxazol |
GB9025469D0 (en) * | 1990-11-22 | 1991-01-09 | Rhone Poulenc Agriculture | New compositions of matter |
US5656573A (en) * | 1989-09-11 | 1997-08-12 | Rhone-Poulenc Agriculture Ltd. | Herbicidal 4-substituted isoxazoles |
GB9115377D0 (en) * | 1991-07-17 | 1991-09-04 | Rhone Poulenc Agriculture | New compositions of matter |
IL102674A (en) * | 1991-08-05 | 1996-11-14 | Rhone Poulenc Agriculture | History of 4-benzoyl isoxazole, the process for their preparation and herbicides containing the same |
GB9116834D0 (en) * | 1991-08-05 | 1991-09-18 | Rhone Poulenc Agriculture | Compositions of new matter |
JPH0570407A (ja) * | 1991-09-17 | 1993-03-23 | Fuji Photo Film Co Ltd | シクロプロパンカルボニル酢酸エステル |
US5334753A (en) * | 1992-03-12 | 1994-08-02 | Rhone-Poulenc Agriculture Ltd | Processes for preparing ortho-substituted benzoic acids |
TR27434A (tr) * | 1992-03-12 | 1995-05-23 | Rhone Poulenc Agrochimie | Yeni 4-benzoilisoksazol türevleri, bunlari ihtiva eden terkipler ve bunlarin herbisidler olarak kullanilmalari. |
GB9215551D0 (en) * | 1992-07-22 | 1992-09-02 | Rhone Poulenc Agriculture | New compositions of matter |
GB9219779D0 (en) * | 1992-09-18 | 1992-10-28 | Rhone Poulenc Agriculture | Compositions of new matter |
JPH08504781A (ja) * | 1992-12-18 | 1996-05-21 | ローヌ−プーラン・アグリカルチヤー・リミテツド | 4−ベンゾイルイソオキサゾール誘導体及び除草剤としてのその使用 |
GB9302049D0 (en) * | 1993-02-03 | 1993-03-24 | Rhone Poulenc Agriculture | Compositions of new matter |
GB9302072D0 (en) * | 1993-02-03 | 1993-03-24 | Rhone Poulenc Agriculture | New compositions of matter |
GB9302071D0 (en) * | 1993-02-03 | 1993-03-24 | Rhone Poulenc Agriculture | Compositions of matter |
CA2117413C (fr) * | 1993-07-30 | 2006-11-21 | Neil Geach | Derives herbicides isoxazole-4-yl-methanone |
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