JP2011506369A5 - - Google Patents
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- Publication number
- JP2011506369A5 JP2011506369A5 JP2010537312A JP2010537312A JP2011506369A5 JP 2011506369 A5 JP2011506369 A5 JP 2011506369A5 JP 2010537312 A JP2010537312 A JP 2010537312A JP 2010537312 A JP2010537312 A JP 2010537312A JP 2011506369 A5 JP2011506369 A5 JP 2011506369A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- substituted
- haloalkyl
- alkoxy
- halogen
- 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.)
- Granted
Links
- 125000000217 alkyl group Chemical group 0.000 claims 208
- 229910052736 halogen Inorganic materials 0.000 claims 65
- 150000002367 halogens Chemical class 0.000 claims 65
- -1 C1-C6Alkoxy Chemical group 0.000 claims 60
- 125000001188 haloalkyl group Chemical group 0.000 claims 56
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 54
- 125000003545 alkoxy group Chemical group 0.000 claims 52
- 125000004093 cyano group Chemical group *C#N 0.000 claims 51
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 32
- 150000001875 compounds Chemical class 0.000 claims 30
- 125000004438 haloalkoxy group Chemical group 0.000 claims 29
- 125000001072 heteroaryl group Chemical group 0.000 claims 27
- 229910052739 hydrogen Inorganic materials 0.000 claims 19
- 239000001257 hydrogen Substances 0.000 claims 19
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 18
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 claims 17
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 17
- 125000004455 (C1-C3) alkylthio group Chemical group 0.000 claims 16
- 229910052760 oxygen Inorganic materials 0.000 claims 14
- 229910052717 sulfur Inorganic materials 0.000 claims 12
- 239000001301 oxygen Substances 0.000 claims 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 9
- 125000000753 cycloalkyl group Chemical group 0.000 claims 9
- 150000002431 hydrogen Chemical class 0.000 claims 9
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 9
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 8
- 125000003342 alkenyl group Chemical group 0.000 claims 8
- 125000000304 alkynyl group Chemical group 0.000 claims 8
- 125000000262 haloalkenyl group Chemical group 0.000 claims 8
- 125000004434 sulfur atom Chemical group 0.000 claims 8
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 7
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 6
- 125000004103 aminoalkyl group Chemical group 0.000 claims 6
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 6
- 125000004966 cyanoalkyl group Chemical group 0.000 claims 6
- 125000005240 diheteroarylamino group Chemical group 0.000 claims 6
- 125000005241 heteroarylamino group Chemical group 0.000 claims 6
- 238000000034 method Methods 0.000 claims 6
- 125000004971 nitroalkyl group Chemical group 0.000 claims 6
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims 6
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 6
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 5
- 239000000203 mixture Substances 0.000 claims 5
- 229920006395 saturated elastomer Polymers 0.000 claims 5
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 4
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 4
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 4
- 125000004076 pyridyl group Chemical group 0.000 claims 4
- 241000196324 Embryophyta Species 0.000 claims 3
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 3
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 3
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims 2
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims 2
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 2
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims 2
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 2
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 2
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- XPDWGBQVDMORPB-UHFFFAOYSA-N Fluoroform Chemical compound FC(F)F XPDWGBQVDMORPB-UHFFFAOYSA-N 0.000 claims 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims 2
- 125000000278 alkyl amino alkyl group Chemical group 0.000 claims 2
- 125000003282 alkyl amino group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 2
- 229910052794 bromium Inorganic materials 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 239000000460 chlorine Substances 0.000 claims 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
- 125000002541 furyl group Chemical group 0.000 claims 2
- 230000002363 herbicidal effect Effects 0.000 claims 2
- 239000004009 herbicide Substances 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 125000002883 imidazolyl group Chemical group 0.000 claims 2
- 125000001786 isothiazolyl group Chemical group 0.000 claims 2
- 125000000842 isoxazolyl group Chemical group 0.000 claims 2
- 125000001715 oxadiazolyl group Chemical group 0.000 claims 2
- 125000002971 oxazolyl group Chemical group 0.000 claims 2
- 125000003566 oxetanyl group Chemical group 0.000 claims 2
- 239000000575 pesticide Substances 0.000 claims 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 2
- 125000003373 pyrazinyl group Chemical group 0.000 claims 2
- 125000003226 pyrazolyl group Chemical group 0.000 claims 2
- 125000002098 pyridazinyl group Chemical group 0.000 claims 2
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 2
- 125000000168 pyrrolyl group Chemical group 0.000 claims 2
- 239000002904 solvent Substances 0.000 claims 2
- 125000003831 tetrazolyl group Chemical group 0.000 claims 2
- 125000001113 thiadiazolyl group Chemical group 0.000 claims 2
- 125000000335 thiazolyl group Chemical group 0.000 claims 2
- 125000001544 thienyl group Chemical group 0.000 claims 2
- 125000004306 triazinyl group Chemical group 0.000 claims 2
- 125000001425 triazolyl group Chemical group 0.000 claims 2
- 125000006559 (C1-C3) alkylamino group Chemical group 0.000 claims 1
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 1
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims 1
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 1
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 1
- SQAINHDHICKHLX-UHFFFAOYSA-N 1-naphthaldehyde Chemical compound C1=CC=C2C(C=O)=CC=CC2=C1 SQAINHDHICKHLX-UHFFFAOYSA-N 0.000 claims 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 claims 1
- 240000002791 Brassica napus Species 0.000 claims 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 claims 1
- 239000007848 Bronsted acid Substances 0.000 claims 1
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims 1
- 244000025254 Cannabis sativa Species 0.000 claims 1
- 229920000742 Cotton Polymers 0.000 claims 1
- 244000068988 Glycine max Species 0.000 claims 1
- 235000010469 Glycine max Nutrition 0.000 claims 1
- 244000299507 Gossypium hirsutum Species 0.000 claims 1
- 239000002841 Lewis acid Substances 0.000 claims 1
- 150000001204 N-oxides Chemical class 0.000 claims 1
- 240000007594 Oryza sativa Species 0.000 claims 1
- 235000007164 Oryza sativa Nutrition 0.000 claims 1
- 240000000111 Saccharum officinarum Species 0.000 claims 1
- 235000007201 Saccharum officinarum Nutrition 0.000 claims 1
- 235000021536 Sugar beet Nutrition 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 240000008042 Zea mays Species 0.000 claims 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- 125000005418 aryl aryl group Chemical group 0.000 claims 1
- 239000002585 base Substances 0.000 claims 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 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
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 claims 1
- ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 235000013339 cereals Nutrition 0.000 claims 1
- 235000005822 corn Nutrition 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 claims 1
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 239000011630 iodine Substances 0.000 claims 1
- 150000007517 lewis acids Chemical class 0.000 claims 1
- 239000003446 ligand Substances 0.000 claims 1
- 229910052763 palladium Inorganic materials 0.000 claims 1
- 125000006678 phenoxycarbonyl group Chemical group 0.000 claims 1
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 claims 1
- 125000006239 protecting group Chemical group 0.000 claims 1
- 125000005400 pyridylcarbonyl group Chemical group N1=C(C=CC=C1)C(=O)* 0.000 claims 1
- 235000009566 rice Nutrition 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 244000045561 useful plants Species 0.000 claims 1
- 0 CC(C(C(C(C(*)(*)*C1(*)*)=O)=C1O*)=CC=**)=CC* Chemical compound CC(C(C(C(C(*)(*)*C1(*)*)=O)=C1O*)=CC=**)=CC* 0.000 description 5
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN2616/DEL/2007 | 2007-12-13 | ||
| IN2616DE2007 | 2007-12-13 | ||
| PCT/EP2008/010513 WO2009074314A1 (en) | 2007-12-13 | 2008-12-11 | 4-phenylpyrane-3,5-diones, 4-phenylthiopyrane-3,5-diones and 2-phenylcyclohexane-1,3,5-triones as herbicides |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011506369A JP2011506369A (ja) | 2011-03-03 |
| JP2011506369A5 true JP2011506369A5 (https=) | 2012-03-01 |
| JP5607537B2 JP5607537B2 (ja) | 2014-10-15 |
Family
ID=40395408
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010537312A Expired - Fee Related JP5607537B2 (ja) | 2007-12-13 | 2008-12-11 | 除草剤としての４−フェニルピラン−３，５−ジオン類、４−フェニルチオピラン−３，５−ジオン類、及び２−フェニルシクロヘキサン−１，３，５−トリオン類 |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US8895761B2 (https=) |
| EP (1) | EP2222657B1 (https=) |
| JP (1) | JP5607537B2 (https=) |
| KR (1) | KR20100100965A (https=) |
| CN (1) | CN101918386B (https=) |
| AP (1) | AP2010005287A0 (https=) |
| AR (1) | AR069678A1 (https=) |
| AU (1) | AU2008334887B2 (https=) |
| CA (1) | CA2707598A1 (https=) |
| CO (1) | CO6170061A1 (https=) |
| CR (1) | CR11488A (https=) |
| CU (1) | CU20100122A7 (https=) |
| EA (1) | EA020918B1 (https=) |
| EC (1) | ECSP088961A (https=) |
| ES (1) | ES2395595T3 (https=) |
| HR (1) | HRP20121012T1 (https=) |
| IL (1) | IL206162A0 (https=) |
| MA (1) | MA31907B1 (https=) |
| MX (1) | MX2010006279A (https=) |
| NI (1) | NI201000098A (https=) |
| NZ (1) | NZ585790A (https=) |
| PL (1) | PL2222657T3 (https=) |
| SV (1) | SV2010003593A (https=) |
| TN (1) | TN2010000269A1 (https=) |
| TW (1) | TW200942173A (https=) |
| UA (1) | UA101346C2 (https=) |
| WO (1) | WO2009074314A1 (https=) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0712653D0 (en) | 2007-06-28 | 2007-08-08 | Syngenta Ltd | Novel herbicides |
| GB0900641D0 (en) | 2009-01-15 | 2009-02-25 | Syngenta Ltd | Novel herbicides |
| GB0901086D0 (en) | 2009-01-22 | 2009-03-11 | Syngenta Ltd | Novel herbicides |
| GB0901834D0 (en) | 2009-02-04 | 2009-03-11 | Syngenta Ltd | Novel herbicides |
| GB0901835D0 (en) | 2009-02-04 | 2009-03-11 | Syngenta Ltd | Novel herbicides |
| BRPI1008949B1 (pt) | 2009-03-11 | 2018-07-10 | Bayer Intellectual Property Gmbh | Cetoenóis haloalquilmetilenóxi-fenil-substituídos e seu uso, composição, seu uso e seu método de produção, métodos para combate de pestes animais e/ou crescimento de plantas indesejadas |
| WO2010136431A1 (en) | 2009-05-29 | 2010-12-02 | Syngenta Limited | Spiro epoxides as intermediates |
| DE102010008644A1 (de) | 2010-02-15 | 2011-08-18 | Bayer Schering Pharma Aktiengesellschaft, 13353 | Zyklische Ketoenole zur Therapie |
| US9485989B2 (en) | 2010-05-31 | 2016-11-08 | Syngenta Participations Ag | Method of controlling neonicotinoid resistant hemiptera |
| BR112012030408A2 (pt) | 2010-05-31 | 2015-09-29 | Syngenta Participations Ag | método de melhoramento de culturas |
| CA2798253A1 (en) | 2010-05-31 | 2011-12-08 | Syngenta Participations Ag | Pesticidal compositions |
| CN103002740B (zh) | 2010-05-31 | 2016-11-09 | 先正达参股股份有限公司 | 杀虫组合物 |
| TWI572282B (zh) | 2011-11-30 | 2017-03-01 | 先正達合夥公司 | 含有螺雜環吡咯啶二酮的殺有害生物混合物 |
| EA026738B1 (ru) | 2012-01-17 | 2017-05-31 | Зингента Партисипейшнс Аг | Пестицидные смеси, содержащие спирогетероциклические пирролидиндионы |
| EP2804481A2 (en) | 2012-01-17 | 2014-11-26 | Syngenta Participations AG | Pesticidal mixtures including spiroheterocyclic pyrrolidine diones |
| BR112014017562B1 (pt) | 2012-01-17 | 2020-11-03 | Syngenta Participations Ag. | mistura pesticida, método de controle de insetos, ácaros, nematódeos ou moluscos e método de proteção de uma semente contra o ataque de pragas |
| WO2013107794A2 (en) | 2012-01-17 | 2013-07-25 | Syngenta Participations Ag | Pesticidal mixtures including spiroheterocyclic pyrrolidine diones |
| UA113753C2 (xx) | 2012-01-26 | 2017-03-10 | Фенілзаміщені кетоеноли для боротьби з паразитами риб | |
| CN102643213B (zh) * | 2012-04-11 | 2014-04-09 | 暨明医药科技（苏州）有限公司 | 3,5-二甲基-4-溴甲基苯基腈的制备方法 |
| WO2014096289A2 (en) * | 2012-12-21 | 2014-06-26 | Syngenta Limited | Herbicidally active cyclic dione compounds, or derivatives thereof, substituted by a phenyl which has an alkynyl-containing substituent |
| WO2014187846A1 (en) | 2013-05-23 | 2014-11-27 | Syngenta Participations Ag | Tank-mix formulations |
| GB201310047D0 (en) | 2013-06-05 | 2013-07-17 | Syngenta Ltd | Compounds |
| EP4706730A3 (en) | 2013-08-20 | 2026-04-08 | Boston Scientific Scimed, Inc. | Braided hemostasis shaft for improved torsional response |
| GB201507497D0 (en) * | 2015-04-30 | 2015-06-17 | Syngenta Participations Ag | Herbicidal compounds |
| CN106106568A (zh) * | 2016-06-20 | 2016-11-16 | 河南中天恒信生物化学科技有限公司 | 一种微生物农药及其制备方法 |
| CN106818827A (zh) * | 2016-12-15 | 2017-06-13 | 新昌县奥而特农业科技有限公司 | 一种除草剂组合物及其应用 |
| CN110776410B (zh) * | 2019-11-28 | 2020-08-21 | 东北农业大学 | 一种含肉桂酰基的三酮类化合物、制备方法及其应用 |
| CN118530144A (zh) * | 2023-02-21 | 2024-08-23 | 中国医学科学院药物研究所 | 一种派恩加滨的制备方法 |
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| US4659372A (en) | 1977-03-28 | 1987-04-21 | Union Carbide Corporation | Biocidal 2-aryl-1,3-cyclohexanedione enol ester compounds |
| US4209532A (en) | 1977-03-28 | 1980-06-24 | Union Carbide Corporation | Biocidal 2-aryl-1,3-cyclohexane dione compounds and alkali metal and ammonium salts thereof |
| PT67818A (en) | 1977-03-28 | 1978-04-01 | Union Carbide Corp | Process for the synthesis of biocidal 2-aryl-1,3-cycloalkanedionas and their enol esters |
| US4175135A (en) | 1978-07-18 | 1979-11-20 | Union Carbide Corporation | Method of controlling acarina ectoparasites on warmblooded animals by orally administering to the animal an ectoparasitically effective amount of a 2-aryl-1,3-cyclohexanedione compound, and alkali metal salts, ammonium salts and enol esters thereof |
| US4526723A (en) | 1978-09-27 | 1985-07-02 | Union Carbide Corporation | Biocidal enol esters of non-ortho substituted 2-aryl-1-3-cycloalkanedione compounds |
| US4409153A (en) | 1980-03-28 | 1983-10-11 | Union Carbide Corporation | O-(2-Aryl-3-oxo-1-cyclohexenyl) phosphates |
| US4489012A (en) | 1982-02-23 | 1984-12-18 | Union Carbide Corporation | Enol-phosphorous esters of 2-aryl-1,3-cycloalkanediones compounds |
| CN1038093A (zh) | 1988-04-18 | 1989-12-20 | 山道士有限公司 | 对有机化合物和关于有机化合物的改进 |
| DE19808261A1 (de) | 1998-02-27 | 1999-10-28 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| RO120911B1 (ro) | 1998-03-13 | 2006-09-29 | Novartis Ag | Derivaţi de 3-hidroxi-4-aril-5-oxopirazolină, activi ca erbicide |
| DE19813354A1 (de) | 1998-03-26 | 1999-09-30 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| CN100386313C (zh) | 1998-12-21 | 2008-05-07 | 辛根塔参与股份公司 | 新的除草剂 |
| CN1272324C (zh) | 1999-09-07 | 2006-08-30 | 辛根塔参与股份公司 | 新颖的除草剂 |
| PL356456A1 (en) * | 1999-09-07 | 2004-06-28 | Syngenta Participations Ag | Novel herbicides |
| DE10016544A1 (de) | 2000-04-03 | 2001-10-11 | Bayer Ag | C2-phenylsubstituierte Ketoenole |
| DE10019145A1 (de) | 2000-04-18 | 2001-10-25 | Bayer Ag | Phenylsubstituierte 4-Hydroxy-tetrahydropyridone |
| DE10030094A1 (de) * | 2000-06-19 | 2001-12-20 | Bayer Ag | Phenylsubstituierte 5,6-Dihydro-pyron-Derivate |
| DE10139465A1 (de) | 2001-08-10 | 2003-02-20 | Bayer Cropscience Ag | Selektive Herbizide auf Basis von substituierten, cayclischen Ketoenolen und Safenern |
| DE10160007A1 (de) | 2001-12-06 | 2003-06-18 | Bayer Cropscience Ag | [1.2]-Oxazin-3,5-dione |
| DE10326386A1 (de) | 2003-06-12 | 2004-12-30 | Bayer Cropscience Ag | N-Heterocyclyl-phenylsubstituierte cyclische Ketoenole |
| WO2005123667A1 (en) | 2004-06-22 | 2005-12-29 | Syngenta Participations Ag | Substituted bicyclooctenes and their use as herbicides |
| EP1827438B2 (en) | 2004-09-20 | 2014-12-10 | Xenon Pharmaceuticals Inc. | Piperazin derivatives for inhibiting human stearoyl-coa-desaturase |
| MX2007003318A (es) | 2004-09-20 | 2007-05-18 | Xenon Pharmaceuticals Inc | Derivados heterociclicos y su uso como agentes terapeuticos. |
| KR101490723B1 (ko) * | 2006-12-14 | 2015-02-06 | 신젠타 파티서페이션즈 아게 | 신규한 제초제로서의 4-페닐-피란-3,5-디온, 4-페닐-티오피란-3,5-디온 및 사이클로헥산트리온 |
| GB0704653D0 (en) | 2007-03-09 | 2007-04-18 | Syngenta Participations Ag | Novel herbicides |
| GB0704652D0 (en) | 2007-03-09 | 2007-04-18 | Syngenta Participations Ag | Novel herbicides |
| GB0714981D0 (en) | 2007-08-01 | 2007-09-12 | Syngenta Ltd | Novel herbicides |
| GB0810728D0 (en) | 2008-06-11 | 2008-07-16 | Syngenta Ltd | Novel herbicides |
| WO2010136431A1 (en) * | 2009-05-29 | 2010-12-02 | Syngenta Limited | Spiro epoxides as intermediates |
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2008
- 2008-12-11 US US12/747,395 patent/US8895761B2/en not_active Expired - Fee Related
- 2008-12-11 ES ES08859463T patent/ES2395595T3/es active Active
- 2008-12-11 AU AU2008334887A patent/AU2008334887B2/en not_active Ceased
- 2008-12-11 MX MX2010006279A patent/MX2010006279A/es active IP Right Grant
- 2008-12-11 KR KR1020107015428A patent/KR20100100965A/ko not_active Withdrawn
- 2008-12-11 AP AP2010005287A patent/AP2010005287A0/en unknown
- 2008-12-11 UA UAA201008389A patent/UA101346C2/ru unknown
- 2008-12-11 EC EC2008008961A patent/ECSP088961A/es unknown
- 2008-12-11 PL PL08859463T patent/PL2222657T3/pl unknown
- 2008-12-11 CO CO08131444A patent/CO6170061A1/es active IP Right Grant
- 2008-12-11 CU CU20100122A patent/CU20100122A7/es unknown
- 2008-12-11 CA CA2707598A patent/CA2707598A1/en not_active Abandoned
- 2008-12-11 JP JP2010537312A patent/JP5607537B2/ja not_active Expired - Fee Related
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- 2008-12-11 NZ NZ585790A patent/NZ585790A/en not_active IP Right Cessation
- 2008-12-11 WO PCT/EP2008/010513 patent/WO2009074314A1/en not_active Ceased
- 2008-12-11 EP EP08859463A patent/EP2222657B1/en not_active Not-in-force
- 2008-12-11 EA EA201000888A patent/EA020918B1/ru not_active IP Right Cessation
- 2008-12-12 TW TW097148351A patent/TW200942173A/zh unknown
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2010
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- 2010-06-10 MA MA32902A patent/MA31907B1/fr unknown
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