RU2003101389A - Фенилзамещенные производные 5,6-дигидро-пирона в качестве пестицидов и гербицидов - Google Patents
Фенилзамещенные производные 5,6-дигидро-пирона в качестве пестицидов и гербицидов Download PDFInfo
- Publication number
- RU2003101389A RU2003101389A RU2003101389/04A RU2003101389A RU2003101389A RU 2003101389 A RU2003101389 A RU 2003101389A RU 2003101389/04 A RU2003101389/04 A RU 2003101389/04A RU 2003101389 A RU2003101389 A RU 2003101389A RU 2003101389 A RU2003101389 A RU 2003101389A
- Authority
- RU
- Russia
- Prior art keywords
- carbon atoms
- alkyl
- necessary
- alkoxy
- substituted
- Prior art date
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- 239000004009 herbicide Substances 0.000 title claims abstract 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 title claims 37
- 239000000575 pesticide Substances 0.000 title abstract 2
- QBDAFARLDLCWAT-UHFFFAOYSA-N 2,3-dihydropyran-6-one Chemical class O=C1OCCC=C1 QBDAFARLDLCWAT-UHFFFAOYSA-N 0.000 title 1
- -1 phenyl-substituted 5,6-dihydro-pyrone Chemical class 0.000 claims abstract 12
- 238000000034 method Methods 0.000 claims abstract 4
- 238000002360 preparation method Methods 0.000 claims abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 265
- 125000000217 alkyl group Chemical group 0.000 claims 119
- 125000003545 alkoxy group Chemical group 0.000 claims 72
- 229910052739 hydrogen Inorganic materials 0.000 claims 51
- 239000001257 hydrogen Substances 0.000 claims 51
- 229910052801 chlorine Inorganic materials 0.000 claims 44
- 239000000460 chlorine Substances 0.000 claims 44
- 150000001875 compounds Chemical class 0.000 claims 42
- 150000002431 hydrogen Chemical group 0.000 claims 40
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 39
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 39
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 39
- 229910052794 bromium Inorganic materials 0.000 claims 39
- 229910052736 halogen Inorganic materials 0.000 claims 38
- 150000002367 halogens Chemical group 0.000 claims 38
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 35
- 229910052731 fluorine Inorganic materials 0.000 claims 34
- 239000011737 fluorine Substances 0.000 claims 34
- 125000003342 alkenyl group Chemical group 0.000 claims 28
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 26
- 229910052760 oxygen Inorganic materials 0.000 claims 26
- 239000001301 oxygen Substances 0.000 claims 26
- 125000004093 cyano group Chemical group *C#N 0.000 claims 25
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 24
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 21
- 229910052717 sulfur Chemical group 0.000 claims 21
- 239000011593 sulfur Chemical group 0.000 claims 21
- 229910052799 carbon Inorganic materials 0.000 claims 20
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 20
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 19
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 18
- 125000000753 cycloalkyl group Chemical group 0.000 claims 18
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 18
- 125000001153 fluoro group Chemical group F* 0.000 claims 15
- 125000004414 alkyl thio group Chemical group 0.000 claims 13
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 13
- 150000001721 carbon Chemical group 0.000 claims 12
- 239000003085 diluting agent Substances 0.000 claims 12
- 125000001188 haloalkyl group Chemical group 0.000 claims 12
- 125000004438 haloalkoxy group Chemical group 0.000 claims 11
- 239000003795 chemical substances by application Substances 0.000 claims 10
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 10
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 9
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 8
- 239000002253 acid Substances 0.000 claims 7
- 125000004429 atom Chemical group 0.000 claims 7
- 125000001072 heteroaryl group Chemical group 0.000 claims 7
- 241000607479 Yersinia pestis Species 0.000 claims 6
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims 6
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 6
- 239000003054 catalyst Substances 0.000 claims 5
- 125000001309 chloro group Chemical group Cl* 0.000 claims 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 5
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 5
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 5
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 4
- 125000003282 alkyl amino group Chemical group 0.000 claims 4
- 125000006350 alkyl thio alkyl group Chemical group 0.000 claims 4
- 239000002585 base Substances 0.000 claims 4
- 125000004663 dialkyl amino group Chemical group 0.000 claims 4
- 125000005842 heteroatom Chemical group 0.000 claims 4
- 229910021645 metal ion Inorganic materials 0.000 claims 4
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 4
- 125000000304 alkynyl group Chemical group 0.000 claims 3
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 3
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 3
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 3
- 125000005359 phenoxyalkyl group Chemical group 0.000 claims 3
- 125000004076 pyridyl group Chemical group 0.000 claims 3
- 125000006413 ring segment Chemical group 0.000 claims 3
- 239000002904 solvent Substances 0.000 claims 3
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims 2
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 claims 2
- 125000005108 alkenylthio group Chemical group 0.000 claims 2
- 125000005366 cycloalkylthio group Chemical group 0.000 claims 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 2
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims 2
- 125000005326 heteroaryloxy alkyl group Chemical group 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 125000002071 phenylalkoxy group Chemical group 0.000 claims 2
- 125000003884 phenylalkyl group Chemical group 0.000 claims 2
- 125000004660 phenylalkylthio group Chemical group 0.000 claims 2
- 125000001544 thienyl group Chemical group 0.000 claims 2
- SQQWBSBBCSFQGC-JLHYYAGUSA-N ubiquinone-2 Chemical compound COC1=C(OC)C(=O)C(C\C=C(/C)CCC=C(C)C)=C(C)C1=O SQQWBSBBCSFQGC-JLHYYAGUSA-N 0.000 claims 2
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 125000003710 aryl alkyl group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims 1
- 125000005620 boronic acid group Chemical class 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 238000009833 condensation Methods 0.000 claims 1
- 230000005494 condensation Effects 0.000 claims 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
- 125000004705 ethylthio group Chemical group C(C)S* 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 239000011630 iodine Substances 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 150000002736 metal compounds Chemical class 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 150000003254 radicals Chemical class 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 0 CC(C)C1(C2)C(CCCC3)C3C2(C(C)N)C(C)*CCC1 Chemical compound CC(C)C1(C2)C(CCCC3)C3C2(C(C)N)C(C)*CCC1 0.000 description 3
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
- A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom
-
- 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
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered 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
- 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
- C07C69/67—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 saturated acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/32—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/96—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings spiro-condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/655—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms
- C07F9/6552—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a six-membered ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrane Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10030094.4 | 2000-06-19 | ||
| DE10030094A DE10030094A1 (de) | 2000-06-19 | 2000-06-19 | Phenylsubstituierte 5,6-Dihydro-pyron-Derivate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2003101389A true RU2003101389A (ru) | 2004-06-27 |
Family
ID=7646216
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2003101389/04A RU2003101389A (ru) | 2000-06-19 | 2001-06-08 | Фенилзамещенные производные 5,6-дигидро-пирона в качестве пестицидов и гербицидов |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US6906007B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP1303505B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP4898070B2 (cg-RX-API-DMAC7.html) |
| KR (1) | KR100798733B1 (cg-RX-API-DMAC7.html) |
| CN (1) | CN1229368C (cg-RX-API-DMAC7.html) |
| AT (1) | ATE407128T1 (cg-RX-API-DMAC7.html) |
| AU (3) | AU2001270560B2 (cg-RX-API-DMAC7.html) |
| BR (1) | BR0112063B1 (cg-RX-API-DMAC7.html) |
| CA (1) | CA2412152C (cg-RX-API-DMAC7.html) |
| DE (2) | DE10030094A1 (cg-RX-API-DMAC7.html) |
| ES (1) | ES2312453T3 (cg-RX-API-DMAC7.html) |
| MX (1) | MXPA02012604A (cg-RX-API-DMAC7.html) |
| PL (1) | PL359216A1 (cg-RX-API-DMAC7.html) |
| RU (1) | RU2003101389A (cg-RX-API-DMAC7.html) |
| UA (1) | UA74835C2 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2001098288A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10311300A1 (de) * | 2003-03-14 | 2004-09-23 | Bayer Cropscience Ag | 2,4,6-Phenylsubstituierte cyclische Ketoenole |
| DE10337497A1 (de) | 2003-08-14 | 2005-03-10 | Bayer Cropscience Ag | 4-Biphenylsubstituierte-Pyrazolidin-3,5-dion-Derivate |
| CN1310899C (zh) * | 2003-11-11 | 2007-04-18 | 沈阳化工研究院 | 具有杀虫、杀菌活性的苯并吡喃酮类化合物及制备与应用 |
| DE102004032421A1 (de) * | 2004-07-05 | 2006-01-26 | Bayer Cropscience Ag | Phenylsubstituierte [1.2]-Oxazin-3,5-dion-und Dihydropyron-Derivate |
| DE102004035133A1 (de) * | 2004-07-20 | 2006-02-16 | Bayer Cropscience Ag | Selektive Insektizide auf Basis von substituierten, cyclischen Ketoenolen und Safenern |
| DE102005059469A1 (de) * | 2005-12-13 | 2007-06-14 | Bayer Cropscience Ag | Insektizide Zusammensetzungen mit verbesserter Wirkung |
| DE102006007882A1 (de) | 2006-02-21 | 2007-08-30 | Bayer Cropscience Ag | Cycloalkyl-phenylsubstituierte cyclische Ketoenole |
| MY152503A (en) * | 2006-12-14 | 2014-10-15 | Syngenta Participations Ag | 4-phenyl-pyrane-3, 5-diones, 4-phenyl-thiopyrane-3, 5-diones and cyclohexanetriones as novel herbicides |
| GB0704652D0 (en) * | 2007-03-09 | 2007-04-18 | Syngenta Participations Ag | Novel herbicides |
| US7901701B2 (en) * | 2007-10-29 | 2011-03-08 | Lignotech Usa, Inc. | Methods for producing dried pesticide compositions |
| EP2222657B1 (en) | 2007-12-13 | 2012-09-12 | Syngenta Limited | Pyrandiones, thiopyrandiones and cyclohexantriones having herbicidal properties |
| EP2300449A1 (en) * | 2008-06-12 | 2011-03-30 | Syngenta Participations AG | Pesticidal compositions containing a pyrandione or a thiopyrandione or a cyclohexanetrione derivative |
| GB0810815D0 (en) * | 2008-06-12 | 2008-07-23 | Syngenta Ltd | Novel herbicides |
| GB0900864D0 (en) | 2009-01-19 | 2009-03-04 | Syngenta Ltd | Novel Herbicides |
| MX2011009188A (es) | 2009-03-11 | 2011-09-26 | Bayer Cropscience Ag | Cetoenoles sustituidos con haloalquilmetilenoxi-fenilo. |
| WO2010127142A2 (en) * | 2009-04-29 | 2010-11-04 | Lignotech Usa, Inc. | Use of lignosulfonates in suspo-emulsions for producing pesticide compositions |
| CN102471206B (zh) * | 2009-07-17 | 2014-08-20 | 辛根塔有限公司 | 除草剂 |
| DE102010008644A1 (de) | 2010-02-15 | 2011-08-18 | Bayer Schering Pharma Aktiengesellschaft, 13353 | Zyklische Ketoenole zur Therapie |
| WO2013021044A1 (de) | 2011-08-11 | 2013-02-14 | Bayer Intellectual Property Gmbh | 1,2,4-triazolyl-substituierte ketoenole |
| WO2013110612A1 (en) | 2012-01-26 | 2013-08-01 | Bayer Intellectual Property Gmbh | Phenyl-substituted ketoenols for controlling fish parasites |
| BR112015010873A2 (pt) * | 2012-11-28 | 2017-07-11 | Sumitomo Chemical Co | compostos à base de di-hidropirona e herbicidas compreendendo os mesmos |
| CN104430351A (zh) * | 2014-12-31 | 2015-03-25 | 江阴苏利化学股份有限公司 | 一种含有吡喃酮的防治甘蓝蚜虫的农药组合物 |
| CN108164072A (zh) * | 2018-01-15 | 2018-06-15 | 昆明理工大学 | 一种微波-超重力联合处理稀土生产氨氮废水的装置和应用方法 |
| CN112850985B (zh) * | 2021-01-11 | 2023-05-26 | 广东腾昊建设工程有限公司 | 一种用于水处理的微滤净化处理设备 |
| CN115414900B (zh) * | 2022-08-25 | 2025-07-22 | 格林美（江苏）钴业股份有限公司 | 一种带沉降器的循环式溶镍装置 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3542809A (en) | 1968-10-23 | 1970-11-24 | Pfizer | Synthesis of arylchlorocarbonyl ketenes |
| FR2368952A1 (fr) * | 1976-02-25 | 1978-05-26 | Lipha | Nouveaux aminoalcoxy-4 (2 h) pyranone-2,3 substitues-5,6 condenses |
| JPH0625210A (ja) * | 1991-05-10 | 1994-02-01 | Dainippon Ink & Chem Inc | 光学活性５，６−ジヒドロ−２−ピロン誘導体、及びその製造方法、その誘導体を含む液晶組成物及び液晶表示素子 |
| AU6845094A (en) | 1993-06-07 | 1995-01-03 | Bayer Aktiengesellschaft | Iodopropargyl carbamates and their use as biocides in the protection of plants and materials |
| SI0729463T1 (en) | 1993-11-19 | 2002-08-31 | Parke Davis & Company | 5,6-dihydropyrone derivatives as protease inhibitors and antiviral agents |
| HUT77668A (hu) * | 1993-11-19 | 1998-07-28 | Parke, Davis & Company | Vírusellenes hatású 5,6-dihidropiron-származékok és hatóanyagként azokat tartalmazó gyógyszerkészítmények |
| US5789440A (en) | 1993-11-19 | 1998-08-04 | Warner-Lambert Company | 5,6-dihydropyrone derivatives as protease inhibitors and antiviral agents |
| 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 |
| DE19708607A1 (de) * | 1997-03-03 | 1998-09-10 | Bayer Ag | 2-Arylcyclopentan-1,3-dione |
| DE19808261A1 (de) | 1998-02-27 | 1999-10-28 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
-
2000
- 2000-06-19 DE DE10030094A patent/DE10030094A1/de not_active Withdrawn
-
2001
- 2001-06-08 AT AT01949391T patent/ATE407128T1/de not_active IP Right Cessation
- 2001-06-08 ES ES01949391T patent/ES2312453T3/es not_active Expired - Lifetime
- 2001-06-08 RU RU2003101389/04A patent/RU2003101389A/ru not_active Application Discontinuation
- 2001-06-08 BR BRPI0112063-8A patent/BR0112063B1/pt not_active IP Right Cessation
- 2001-06-08 DE DE50114285T patent/DE50114285D1/de not_active Expired - Lifetime
- 2001-06-08 AU AU2001270560A patent/AU2001270560B2/en not_active Ceased
- 2001-06-08 JP JP2002504244A patent/JP4898070B2/ja not_active Expired - Fee Related
- 2001-06-08 PL PL01359216A patent/PL359216A1/xx not_active Application Discontinuation
- 2001-06-08 CN CNB018129773A patent/CN1229368C/zh not_active Expired - Fee Related
- 2001-06-08 AU AU7056001A patent/AU7056001A/xx active Pending
- 2001-06-08 WO PCT/EP2001/006522 patent/WO2001098288A1/de not_active Ceased
- 2001-06-08 MX MXPA02012604A patent/MXPA02012604A/es active IP Right Grant
- 2001-06-08 KR KR1020027016812A patent/KR100798733B1/ko not_active Expired - Fee Related
- 2001-06-08 US US10/311,009 patent/US6906007B2/en not_active Expired - Fee Related
- 2001-06-08 CA CA002412152A patent/CA2412152C/en not_active Expired - Fee Related
- 2001-06-08 EP EP01949391A patent/EP1303505B1/de not_active Expired - Lifetime
- 2001-08-06 UA UA2003010460A patent/UA74835C2/uk unknown
-
2006
- 2006-10-11 AU AU2006228042A patent/AU2006228042A1/en not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| US20040102516A1 (en) | 2004-05-27 |
| BR0112063B1 (pt) | 2012-01-10 |
| MXPA02012604A (es) | 2004-05-17 |
| CA2412152C (en) | 2007-08-28 |
| KR20030031494A (ko) | 2003-04-21 |
| ES2312453T3 (es) | 2009-03-01 |
| PL359216A1 (en) | 2004-08-23 |
| EP1303505A1 (de) | 2003-04-23 |
| DE10030094A1 (de) | 2001-12-20 |
| WO2001098288A1 (de) | 2001-12-27 |
| EP1303505B1 (de) | 2008-09-03 |
| US6906007B2 (en) | 2005-06-14 |
| AU2006228042A1 (en) | 2006-11-09 |
| CA2412152A1 (en) | 2001-12-27 |
| KR100798733B1 (ko) | 2008-01-29 |
| JP2004501144A (ja) | 2004-01-15 |
| ATE407128T1 (de) | 2008-09-15 |
| AU2001270560B2 (en) | 2006-03-09 |
| AU2001270560C1 (en) | 2002-01-02 |
| CN1229368C (zh) | 2005-11-30 |
| AU7056001A (en) | 2002-01-02 |
| JP4898070B2 (ja) | 2012-03-14 |
| DE50114285D1 (de) | 2008-10-16 |
| BR0112063A (pt) | 2003-05-13 |
| CN1443181A (zh) | 2003-09-17 |
| UA74835C2 (en) | 2006-02-15 |
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| Date | Code | Title | Description |
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| FA92 | Acknowledgement of application withdrawn (lack of supplementary materials submitted) |
Effective date: 20060718 |