TW201022260A - Heterocyclic compounds as pesticides - Google Patents
Heterocyclic compounds as pesticides Download PDFInfo
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- TW201022260A TW201022260A TW098124024A TW98124024A TW201022260A TW 201022260 A TW201022260 A TW 201022260A TW 098124024 A TW098124024 A TW 098124024A TW 98124024 A TW98124024 A TW 98124024A TW 201022260 A TW201022260 A TW 201022260A
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- Prior art keywords
- group
- alkyl
- alkoxy
- substituted
- base
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- 150000002391 heterocyclic compounds Chemical class 0.000 title abstract description 5
- 239000000575 pesticide Substances 0.000 title 1
- 238000000034 method Methods 0.000 claims abstract description 25
- 241000607479 Yersinia pestis Species 0.000 claims abstract description 13
- -1 imidazolyl 1,2,3-triazolyl Chemical group 0.000 claims description 493
- 125000000217 alkyl group Chemical group 0.000 claims description 441
- 150000001875 compounds Chemical class 0.000 claims description 200
- 125000003545 alkoxy group Chemical group 0.000 claims description 184
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 148
- 229910052736 halogen Inorganic materials 0.000 claims description 133
- 125000001188 haloalkyl group Chemical group 0.000 claims description 100
- 125000004076 pyridyl group Chemical group 0.000 claims description 100
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 87
- 239000000203 mixture Substances 0.000 claims description 85
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 81
- 125000002971 oxazolyl group Chemical group 0.000 claims description 81
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 81
- 150000002367 halogens Chemical group 0.000 claims description 79
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 79
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 73
- 229910052739 hydrogen Inorganic materials 0.000 claims description 73
- 239000001257 hydrogen Substances 0.000 claims description 73
- KVGZZAHHUNAVKZ-UHFFFAOYSA-N 1,4-Dioxin Chemical compound O1C=COC=C1 KVGZZAHHUNAVKZ-UHFFFAOYSA-N 0.000 claims description 70
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 68
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 64
- 125000002883 imidazolyl group Chemical group 0.000 claims description 64
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 57
- 238000003971 tillage Methods 0.000 claims description 57
- 239000011593 sulfur Chemical group 0.000 claims description 55
- 229910052717 sulfur Chemical group 0.000 claims description 55
- 125000000335 thiazolyl group Chemical group 0.000 claims description 54
- 125000001072 heteroaryl group Chemical group 0.000 claims description 53
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 53
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 53
- 125000004414 alkyl thio group Chemical group 0.000 claims description 52
- 239000001301 oxygen Substances 0.000 claims description 52
- 229910052760 oxygen Inorganic materials 0.000 claims description 52
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 50
- 125000000623 heterocyclic group Chemical group 0.000 claims description 50
- 125000001424 substituent group Chemical group 0.000 claims description 50
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 46
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 40
- 125000003282 alkyl amino group Chemical group 0.000 claims description 39
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 38
- 239000000126 substance Substances 0.000 claims description 38
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 35
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 35
- 125000001544 thienyl group Chemical group 0.000 claims description 35
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 33
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 31
- 125000002541 furyl group Chemical group 0.000 claims description 31
- SFDJOSRHYKHMOK-UHFFFAOYSA-N nitramide Chemical compound N[N+]([O-])=O SFDJOSRHYKHMOK-UHFFFAOYSA-N 0.000 claims description 28
- 125000003118 aryl group Chemical group 0.000 claims description 26
- 125000005956 isoquinolyl group Chemical group 0.000 claims description 26
- 125000006350 alkyl thio alkyl group Chemical group 0.000 claims description 25
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 25
- 125000000304 alkynyl group Chemical group 0.000 claims description 24
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims description 24
- 150000001412 amines Chemical class 0.000 claims description 23
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 23
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 22
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims description 21
- 150000002576 ketones Chemical class 0.000 claims description 21
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 claims description 21
- 125000000168 pyrrolyl group Chemical group 0.000 claims description 21
- 229910052786 argon Inorganic materials 0.000 claims description 20
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims description 20
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims description 20
- 229910052757 nitrogen Inorganic materials 0.000 claims description 20
- 125000004504 1,2,4-oxadiazolyl group Chemical group 0.000 claims description 19
- 125000004604 benzisothiazolyl group Chemical group S1N=C(C2=C1C=CC=C2)* 0.000 claims description 19
- 125000004966 cyanoalkyl group Chemical group 0.000 claims description 19
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 19
- 125000004511 1,2,3-thiadiazolyl group Chemical group 0.000 claims description 18
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 claims description 18
- 125000001786 isothiazolyl group Chemical group 0.000 claims description 18
- XUWHAWMETYGRKB-UHFFFAOYSA-N piperidin-2-one Chemical compound O=C1CCCCN1 XUWHAWMETYGRKB-UHFFFAOYSA-N 0.000 claims description 17
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 16
- 125000004514 1,2,4-thiadiazolyl group Chemical group 0.000 claims description 15
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 15
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 claims description 15
- 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 claims description 14
- 150000002923 oximes Chemical class 0.000 claims description 14
- 125000001399 1,2,3-triazolyl group Chemical group N1N=NC(=C1)* 0.000 claims description 13
- 125000004520 1,3,4-thiadiazolyl group Chemical group 0.000 claims description 13
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 13
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 13
- 125000001781 1,3,4-oxadiazolyl group Chemical group 0.000 claims description 12
- 125000004506 1,2,5-oxadiazolyl group Chemical group 0.000 claims description 11
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 11
- 125000004593 naphthyridinyl group Chemical group N1=C(C=CC2=CC=CN=C12)* 0.000 claims description 11
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 claims description 11
- 150000003839 salts Chemical class 0.000 claims description 11
- 125000004502 1,2,3-oxadiazolyl group Chemical group 0.000 claims description 10
- 125000003342 alkenyl group Chemical group 0.000 claims description 10
- CPNGPNLZQNNVQM-UHFFFAOYSA-N pteridine Chemical compound N1=CN=CC2=NC=CN=C21 CPNGPNLZQNNVQM-UHFFFAOYSA-N 0.000 claims description 10
- 150000001204 N-oxides Chemical class 0.000 claims description 9
- 125000004517 1,2,5-thiadiazolyl group Chemical group 0.000 claims description 8
- 125000004995 haloalkylthio group Chemical group 0.000 claims description 8
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 claims description 8
- BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 claims description 8
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 8
- 125000003107 substituted aryl group Chemical group 0.000 claims description 8
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 claims description 7
- 125000000532 dioxanyl group Chemical group 0.000 claims description 7
- 150000004032 porphyrins Chemical class 0.000 claims description 7
- 125000001042 pteridinyl group Chemical group N1=C(N=CC2=NC=CN=C12)* 0.000 claims description 7
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 6
- 125000005605 benzo group Chemical group 0.000 claims description 6
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims description 5
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 claims description 4
- 229960005181 morphine Drugs 0.000 claims description 4
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims description 3
- 125000000033 alkoxyamino group Chemical group 0.000 claims description 2
- 125000001769 aryl amino group Chemical group 0.000 claims description 2
- 125000005879 dioxolanyl group Chemical group 0.000 claims description 2
- 125000005358 mercaptoalkyl group Chemical group 0.000 claims description 2
- 125000004001 thioalkyl group Chemical group 0.000 claims description 2
- KTZQTRPPVKQPFO-UHFFFAOYSA-N 1,2-benzoxazole Chemical compound C1=CC=C2C=NOC2=C1 KTZQTRPPVKQPFO-UHFFFAOYSA-N 0.000 claims 1
- WLXYHLHNIRJAIG-UHFFFAOYSA-N 2h-benzo[e]isoindole Chemical compound C1=CC=C2C3=CNC=C3C=CC2=C1 WLXYHLHNIRJAIG-UHFFFAOYSA-N 0.000 claims 1
- 241000722949 Apocynum Species 0.000 claims 1
- 235000018185 Betula X alpestris Nutrition 0.000 claims 1
- 235000018212 Betula X uliginosa Nutrition 0.000 claims 1
- 125000000732 arylene group Chemical group 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
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 230000003211 malignant effect Effects 0.000 claims 1
- 229910044991 metal oxide Inorganic materials 0.000 claims 1
- 150000004706 metal oxides Chemical class 0.000 claims 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 238000002360 preparation method Methods 0.000 abstract description 36
- 241001465754 Metazoa Species 0.000 abstract description 13
- 241000238631 Hexapoda Species 0.000 abstract description 12
- 241000238421 Arthropoda Species 0.000 abstract description 4
- 239000002585 base Substances 0.000 description 295
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 99
- 125000001715 oxadiazolyl group Chemical group 0.000 description 68
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 54
- 241000196324 Embryophyta Species 0.000 description 52
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 50
- 125000005843 halogen group Chemical group 0.000 description 47
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 40
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 39
- 235000019439 ethyl acetate Nutrition 0.000 description 38
- 125000003277 amino group Chemical group 0.000 description 37
- 238000001704 evaporation Methods 0.000 description 37
- 125000001113 thiadiazolyl group Chemical group 0.000 description 37
- 230000008020 evaporation Effects 0.000 description 36
- 239000000243 solution Substances 0.000 description 36
- 125000001425 triazolyl group Chemical group 0.000 description 36
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 32
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 32
- 238000005160 1H NMR spectroscopy Methods 0.000 description 31
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 30
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 29
- 239000011651 chromium Substances 0.000 description 28
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 27
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 27
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 description 26
- 235000019253 formic acid Nutrition 0.000 description 24
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 23
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 description 23
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 21
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 description 21
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 21
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 20
- 235000019441 ethanol Nutrition 0.000 description 20
- 239000007789 gas Substances 0.000 description 20
- 125000000468 ketone group Chemical group 0.000 description 20
- BVTJGGGYKAMDBN-UHFFFAOYSA-N Dioxetane Chemical group C1COO1 BVTJGGGYKAMDBN-UHFFFAOYSA-N 0.000 description 19
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 19
- 239000002253 acid Substances 0.000 description 19
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 18
- 238000009472 formulation Methods 0.000 description 18
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 17
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 16
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 16
- 239000005864 Sulphur Substances 0.000 description 16
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 16
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 16
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- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 14
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- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 description 8
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- 229920002994 synthetic fiber Polymers 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- HOWHQWFXSLOJEF-MGZLOUMQSA-N systemin Chemical compound NCCCC[C@H](N)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(O)=O)C(=O)OC(=O)[C@@H]1CCCN1C(=O)[C@H]1N(C(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H]2N(CCC2)C(=O)[C@H]2N(CCC2)C(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](C)N)C(C)C)CCC1 HOWHQWFXSLOJEF-MGZLOUMQSA-N 0.000 description 1
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- 235000018553 tannin Nutrition 0.000 description 1
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- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
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- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- 239000003451 thiazide diuretic agent Substances 0.000 description 1
- 150000003557 thiazoles Chemical class 0.000 description 1
- HNKJADCVZUBCPG-UHFFFAOYSA-N thioanisole Chemical compound CSC1=CC=CC=C1 HNKJADCVZUBCPG-UHFFFAOYSA-N 0.000 description 1
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- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 108700012359 toxins Proteins 0.000 description 1
- 238000012549 training Methods 0.000 description 1
- FFSJPOPLSWBGQY-UHFFFAOYSA-N triazol-4-one Chemical group O=C1C=NN=N1 FFSJPOPLSWBGQY-UHFFFAOYSA-N 0.000 description 1
- 125000005881 triazolinyl group Chemical group 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229930191535 trisporin Natural products 0.000 description 1
- 238000000870 ultraviolet spectroscopy Methods 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- 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
- A01N43/74—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 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- 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
- A01N43/82—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 three ring hetero atoms
-
- 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
- A01N43/84—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 six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
-
- 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
- A01N43/88—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 six-membered rings with three ring hetero atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (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)
- Agronomy & Crop Science (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08012898 | 2008-07-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW201022260A true TW201022260A (en) | 2010-06-16 |
Family
ID=40084204
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW098124024A TW201022260A (en) | 2008-07-17 | 2009-07-16 | Heterocyclic compounds as pesticides |
Country Status (15)
| Country | Link |
|---|---|
| US (2) | US8809547B2 (OSRAM) |
| EP (6) | EP2591674B1 (OSRAM) |
| JP (2) | JP5681105B2 (OSRAM) |
| KR (1) | KR20110030700A (OSRAM) |
| CN (2) | CN102159079B (OSRAM) |
| AR (1) | AR072572A1 (OSRAM) |
| AU (1) | AU2009270520A1 (OSRAM) |
| BR (2) | BRPI0916218B1 (OSRAM) |
| CA (1) | CA2730844A1 (OSRAM) |
| CO (1) | CO6341525A2 (OSRAM) |
| ES (6) | ES2426953T3 (OSRAM) |
| MX (1) | MX2011000477A (OSRAM) |
| TW (1) | TW201022260A (OSRAM) |
| WO (1) | WO2010006713A2 (OSRAM) |
| ZA (1) | ZA201100371B (OSRAM) |
Families Citing this family (264)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2010013705A (es) * | 2008-06-13 | 2011-02-25 | Bayer Cropscience Ag | Nuevas amidas y tioamidas heteroaromaticas como plaguicidas. |
| BRPI0916218B1 (pt) | 2008-07-17 | 2018-11-27 | Bayer Cropscience Ag | compostos heterocíclicos como composições praguicidas |
| UA107791C2 (en) | 2009-05-05 | 2015-02-25 | Dow Agrosciences Llc | Pesticidal compositions |
| CN102573478B (zh) * | 2009-10-12 | 2015-12-16 | 拜尔农作物科学股份公司 | 作为杀虫剂的1-(吡啶-3-基)-吡唑和1-(嘧啶-5-基)-吡唑 |
| WO2011128304A2 (de) | 2010-04-16 | 2011-10-20 | Bayer Cropscience Ag | Neue heterocyclische verbindungen als schädlingsbekämpfungsmittel |
| EP2382865A1 (de) | 2010-04-28 | 2011-11-02 | Bayer CropScience AG | Synergistische Wirkstoffkombinationen |
| JP5868957B2 (ja) | 2010-05-05 | 2016-02-24 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングＢａｙｅｒ Ｉｎｔｅｌｌｅｃｔｕａｌ Ｐｒｏｐｅｒｔｙ ＧｍｂＨ | 殺虫剤としてのチアゾール誘導体 |
| MX341267B (es) | 2010-06-18 | 2016-08-09 | Bayer Ip Gmbh | Combinaciones de principios activos con propiedades insecticidas y acaricidas. |
| ES2626601T3 (es) * | 2010-06-28 | 2017-07-25 | Bayer Intellectual Property Gmbh | Compuestos heterocíclicos como pesticidas |
| WO2012004293A2 (de) | 2010-07-08 | 2012-01-12 | Bayer Cropscience Ag | Insektizide und fungizide wirkstoffkombinationen |
| JP2012017289A (ja) | 2010-07-08 | 2012-01-26 | Bayer Cropscience Ag | 殺虫性ピロリン誘導体 |
| NZ606849A (en) * | 2010-08-31 | 2014-08-29 | Dow Agrosciences Llc | Substituted amino thiadiazole pesticidal compositions |
| JP2012082186A (ja) | 2010-09-15 | 2012-04-26 | Bayer Cropscience Ag | 殺虫性アリールピロリジン類 |
| JP2012062267A (ja) | 2010-09-15 | 2012-03-29 | Bayer Cropscience Ag | 殺虫性ピロリンｎ−オキサイド誘導体 |
| WO2012045680A2 (de) | 2010-10-04 | 2012-04-12 | Bayer Cropscience Ag | Insektizide und fungizide wirkstoffkombinationen |
| US9084424B2 (en) | 2010-10-21 | 2015-07-21 | Bayer Intellectual Property Gmbh | N-benzyl heterocyclic carboxamides |
| WO2012052412A1 (de) | 2010-10-22 | 2012-04-26 | Bayer Cropscience Ag | Neue heterocylische verbindungen als schädlingsbekämpfungsmittel |
| CA2815117A1 (en) | 2010-11-02 | 2012-05-10 | Bayer Intellectual Property Gmbh | N-hetarylmethyl pyrazolylcarboxamides |
| US8815271B2 (en) | 2010-11-03 | 2014-08-26 | Dow Agrosciences, Llc. | Pesticidal compositions and processes related thereto |
| EP2640706B1 (en) | 2010-11-15 | 2017-03-01 | Bayer Intellectual Property GmbH | N-aryl pyrazole(thio)carboxamides |
| SG190295A1 (en) | 2010-11-29 | 2013-06-28 | Bayer Ip Gmbh | Alpha,beta-unsaturated imines |
| EP2648518A2 (en) * | 2010-12-10 | 2013-10-16 | Basf Se | Pyrazole compounds for controlling invertebrate pests |
| EP2675789A1 (de) | 2011-02-17 | 2013-12-25 | Bayer Intellectual Property GmbH | Substituierte 3-(biphenyl-3-yl)-8,8-difluor-4-hydroxy-1-azaspiro[4.5]dec-3-en-2-one zur therapie und halogensubstituierte spirocyclische ketoenole |
| CN103476256B (zh) | 2011-02-17 | 2016-01-20 | 拜耳知识产权有限责任公司 | Sdhi杀真菌剂用于常规育种的asr耐受性的茎溃疡抗性和／或蛙眼叶斑病抗性大豆品种的用途 |
| BR112013021019A2 (pt) | 2011-02-17 | 2019-02-26 | Bayer Ip Gmbh | uso de fungicidas sdhi em variedades de soja cultivadas de forma convencional com tolerância à ferrugem asiática da soja (asr), resistentes ao cancro da haste e/ou à mancha foliar olho-de-rã |
| CA2828639C (en) | 2011-03-01 | 2019-02-12 | Bayer Intellectual Property Gmbh | 2-acyloxypyrrolin-4-ones |
| AR085509A1 (es) | 2011-03-09 | 2013-10-09 | Bayer Cropscience Ag | Indol- y bencimidazolcarboxamidas como insecticidas y acaricidas |
| WO2012120105A1 (en) | 2011-03-10 | 2012-09-13 | Bayer Cropscience Ag | Use of lipochito-oligosaccharide compounds for safeguarding seed safety of treated seeds |
| AU2012230503B2 (en) | 2011-03-18 | 2016-07-07 | Bayer Intellectual Property Gmbh | N-(3-carbamoylphenyl)-1H-pyrazole-5-carboxamide derivatives and the use thereof for controlling animal pests |
| EP2532661A1 (en) | 2011-06-10 | 2012-12-12 | Syngenta Participations AG | Novel insecticides |
| EP2535334A1 (de) | 2011-06-17 | 2012-12-19 | Bayer CropScience AG | Kristalline Modifikationen von Penflufen |
| EP2540718A1 (en) | 2011-06-29 | 2013-01-02 | Syngenta Participations AG. | Novel insecticides |
| EP2540163A1 (en) | 2011-06-30 | 2013-01-02 | Bayer CropScience AG | Nematocide N-cyclopropyl-sulfonylamide derivatives |
| KR20140048257A (ko) | 2011-07-15 | 2014-04-23 | 바스프 에스이 | 동물 해충을 퇴치하기 위해 치환된 3-피리딜 티아졸 화합물 및 유도체 i을 사용하는 살충 방법 |
| DK2736327T3 (en) | 2011-07-26 | 2018-04-23 | Clariant Int Ltd | Etherized lactate esters, processes for their preparation and their use in improving the action of plant protection products |
| UA115128C2 (uk) | 2011-07-27 | 2017-09-25 | Байєр Інтеллектуал Проперті Гмбх | Протравлювання насіння для боротьби з фітопатогенними грибами |
| JP2013082632A (ja) | 2011-10-05 | 2013-05-09 | Bayer Cropscience Ag | 農薬製剤及びその製造方法 |
| US8937083B2 (en) * | 2011-10-26 | 2015-01-20 | DowAgroSciences, LLC | Pesticidal compositions and processes related thereto |
| CA2852776A1 (en) * | 2011-10-26 | 2013-05-02 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
| EP2604118A1 (en) | 2011-12-15 | 2013-06-19 | Bayer CropScience AG | Active ingredient combinations having insecticidal and acaricidal properties |
| IN2014CN04325A (OSRAM) | 2011-12-19 | 2015-09-04 | Bayer Cropscience Ag | |
| BR112014014972A2 (pt) | 2011-12-20 | 2017-06-13 | Bayer Ip Gmbh | novas amidas aromáticas inseticidas |
| EP2606726A1 (de) | 2011-12-21 | 2013-06-26 | Bayer CropScience AG | N-Arylamidine-substituierte trifluoroethylsulfid-Derivate als Akarizide und Insektizide |
| JP5970811B2 (ja) | 2011-12-28 | 2016-08-17 | セイコーエプソン株式会社 | 発光素子、発光装置および電子機器 |
| US20150011394A1 (en) | 2012-01-21 | 2015-01-08 | Bayer Intellectual Property Gmbh | Use of host defense inducers for controlling bacterial harmful organisms in useful plants |
| CN104321317B (zh) | 2012-03-14 | 2016-09-21 | 拜耳知识产权有限责任公司 | 杀虫的芳基吡咯烷 |
| WO2013156433A1 (en) | 2012-04-17 | 2013-10-24 | Syngenta Participations Ag | Insecticidally active thiazole derivatives |
| WO2013156431A1 (en) | 2012-04-17 | 2013-10-24 | Syngenta Participations Ag | Pesticidally active pyridyl- and pyrimidyl- substituted thiazole and thiadiazole derivatives |
| US9282739B2 (en) | 2012-04-27 | 2016-03-15 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
| US9708288B2 (en) | 2012-04-27 | 2017-07-18 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
| RU2627654C2 (ru) | 2012-04-27 | 2017-08-09 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | Пестицидные композиции и относящиеся к ним способы |
| CN104302173B (zh) | 2012-05-16 | 2019-10-15 | 拜尔农作物科学股份公司 | 水包油(o/w)杀虫制剂 |
| AP2014008101A0 (en) | 2012-05-16 | 2014-12-31 | Bayer Cropscience Ag | Insecticidal water-in-oil (W/O) formulation |
| CN104302637A (zh) * | 2012-05-16 | 2015-01-21 | 纳幕尔杜邦公司 | 1,3-二芳基取代的杂环杀虫剂 |
| AR091104A1 (es) | 2012-05-22 | 2015-01-14 | Bayer Cropscience Ag | Combinaciones de compuestos activos que comprenden un derivado lipo-quitooligosacarido y un compuesto nematicida, insecticida o fungicida |
| CN104540494B (zh) | 2012-05-30 | 2017-10-24 | 科莱恩金融(Bvi)有限公司 | N‑甲基‑n‑酰基葡糖胺作为增溶剂的用途 |
| NZ701724A (en) | 2012-05-30 | 2016-11-25 | Bayer Cropscience Ag | Compositions comprising a biological control agent and an insecticide |
| US10864275B2 (en) | 2012-05-30 | 2020-12-15 | Clariant International Ltd. | N-methyl-N-acylglucamine-containing composition |
| WO2013178658A1 (en) | 2012-05-30 | 2013-12-05 | Bayer Cropscience Ag | Compositions comprising a biological control agent and an insecticide |
| EP2671881A1 (en) * | 2012-06-07 | 2013-12-11 | Syngenta Participations AG. | Pesticidally active pyridyl- and pyrimidyl- substituted thiazole derivatives |
| MX2014015265A (es) | 2012-06-14 | 2015-08-12 | Basf Se | Metodos plaguicidas que utilizan compuestos de 3-piridiltiazol sustituido y derivados para combatir plagas de animales. |
| WO2014007395A1 (ja) * | 2012-07-06 | 2014-01-09 | 日産化学工業株式会社 | ピラゾール若しくはチアゾール誘導体又はその塩及び有害生物防除剤 |
| EP2879493B1 (en) | 2012-07-31 | 2018-09-19 | Bayer CropScience AG | Pesticidal compositions comprising a terpene mixture and flupyradifurone |
| US9345247B2 (en) | 2012-08-17 | 2016-05-24 | Bayer Cropscience Ag | Azaindole carboxylic acid amides and azaindole thiocarboxylic acid amides for use as insecticides and acaricides |
| ES2651074T3 (es) | 2012-10-02 | 2018-01-24 | Bayer Cropscience Ag | Compuestos heterocíclicos como plaguicidas |
| CN103772416B (zh) * | 2012-10-18 | 2018-01-19 | 精工爱普生株式会社 | 噻二唑系化合物、发光元件用化合物、发光元件、发光装置、认证装置以及电子设备 |
| WO2014060381A1 (de) | 2012-10-18 | 2014-04-24 | Bayer Cropscience Ag | Heterocyclische verbindungen als schädlingsbekämpfungsmittel |
| CN104884449A (zh) * | 2012-10-31 | 2015-09-02 | 拜尔农作物科学股份公司 | 作为害虫防治剂的新的杂环化合物 |
| DE102012021647A1 (de) | 2012-11-03 | 2014-05-08 | Clariant International Ltd. | Wässrige Adjuvant-Zusammensetzungen |
| WO2014079766A1 (en) | 2012-11-22 | 2014-05-30 | Basf Se | Pesticidal mixtures |
| CN104902756B (zh) | 2012-11-22 | 2018-11-27 | 巴斯夫公司 | 农药混合物 |
| WO2014079772A1 (en) | 2012-11-22 | 2014-05-30 | Basf Se | Pesticidal mixtures |
| WO2014079774A1 (en) | 2012-11-22 | 2014-05-30 | Basf Se | Pesticidal mixtures |
| WO2014079841A1 (en) | 2012-11-22 | 2014-05-30 | Basf Se | Pesticidal mixtures |
| CA2889775A1 (en) | 2012-11-22 | 2014-05-30 | Basf Corporation | Pesticidal mixtures |
| WO2014079804A1 (en) | 2012-11-22 | 2014-05-30 | Basf Se | Pesticidal mixtures |
| WO2014079773A1 (en) | 2012-11-22 | 2014-05-30 | Basf Se | Pesticidal mixtures |
| WO2014079770A1 (en) | 2012-11-22 | 2014-05-30 | Basf Se | Pesticidal mixtures |
| WO2014079813A1 (en) | 2012-11-23 | 2014-05-30 | Basf Se | Pesticidal mixtures |
| WO2014079752A1 (en) | 2012-11-23 | 2014-05-30 | Basf Se | Pesticidal mixtures |
| EP2738171A1 (en) | 2012-11-30 | 2014-06-04 | Syngenta Participations AG. | Pesticidally active tricyclic pyridyl derivatives |
| CN104837351A (zh) | 2012-11-30 | 2015-08-12 | 拜耳作物科学股份公司 | 二元杀真菌或杀虫混合物 |
| WO2014083088A2 (en) | 2012-11-30 | 2014-06-05 | Bayer Cropscience Ag | Binary fungicidal mixtures |
| BR112015012781A2 (pt) | 2012-12-03 | 2018-06-26 | Bayer Cropscience Ag | composição compreendendo agentes de controle biológico |
| WO2014086753A2 (en) | 2012-12-03 | 2014-06-12 | Bayer Cropscience Ag | Composition comprising biological control agents |
| WO2014086749A2 (en) | 2012-12-03 | 2014-06-12 | Bayer Cropscience Ag | Composition comprising a biological control agent and an insecticide |
| MX2015006631A (es) | 2012-12-03 | 2015-08-05 | Bayer Cropscience Ag | Composicion que comprende un agente de control biologico y un insecticida. |
| US9867377B2 (en) | 2012-12-03 | 2018-01-16 | Bayer Cropscience Ag | Composition comprising a biological control agent and an insecticide |
| AR093909A1 (es) | 2012-12-12 | 2015-06-24 | Bayer Cropscience Ag | Uso de ingredientes activos para controlar nematodos en cultivos resistentes a nematodos |
| AR093996A1 (es) | 2012-12-18 | 2015-07-01 | Bayer Cropscience Ag | Combinaciones bactericidas y fungicidas binarias |
| WO2014102245A1 (en) * | 2012-12-27 | 2014-07-03 | Basf Se | Cyano-substituted 2-(pyridin-3-yl)-5-hetaryl-thiazole compounds for combating invertebrate pests |
| CN105189489A (zh) | 2012-12-27 | 2015-12-23 | 巴斯夫欧洲公司 | 用于防除无脊椎动物害虫的带有亚胺或亚胺衍生取代基的2-(吡啶-3-基)-5-杂芳基噻唑化合物 |
| JP6321042B2 (ja) | 2013-02-06 | 2018-05-09 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 新規なハロゲン置換された化合物 |
| BR112015018676A2 (pt) | 2013-02-11 | 2017-07-18 | Bayer Cropscience Lp | composições que compreendem gougerotina e um agente de controle biológico |
| CA2898725A1 (en) | 2013-02-11 | 2014-08-14 | Bayer Cropscience Lp | Compositions comprising a streptomyces-based biological control agent and an insecticide |
| US20160024108A1 (en) | 2013-03-12 | 2016-01-28 | Bayer Cropscience Aktiengesellschaft | Use of dithiine-tetracarboximides for controlling bacterial harmful organisms in useful plants |
| US9554573B2 (en) | 2013-04-19 | 2017-01-31 | Bayer Cropscience Aktiengesellschaft | Binary insecticidal or pesticidal mixture |
| WO2014170300A1 (en) | 2013-04-19 | 2014-10-23 | Basf Se | N-substituted acyl-imino-pyridine compounds and derivatives for combating animal pests |
| BR112015026113A2 (pt) | 2013-04-19 | 2017-07-25 | Bayer Cropscience Ag | combinações de compostos ativos que apresentam propriedades inseticidas |
| EP3010889B1 (de) | 2013-06-20 | 2018-10-03 | Bayer CropScience Aktiengesellschaft | Arylsulfid- und arylsulfoxid-derivate als akarizide und insektizide |
| BR112015031291A2 (pt) | 2013-06-20 | 2017-07-25 | Bayer Cropscience Ag | derivados de sulfureto de arila e derivados de arilalquil sulfóxido como acaricidas e inseticidas |
| EP3019481B1 (de) | 2013-07-08 | 2019-03-06 | Bayer CropScience Aktiengesellschaft | Sechsgliedrige c-n-verknüpfte arylsulfid- und arylsulfoxid- derivate als schädlingsbekämpfungsmittel |
| EP3057430A4 (en) | 2013-10-17 | 2017-09-13 | Dow AgroSciences LLC | Processes for the preparation of pesticidal compounds |
| KR20160075565A (ko) | 2013-10-17 | 2016-06-29 | 다우 아그로사이언시즈 엘엘씨 | 살충성 화합물의 제조 방법 |
| BR112016008070B8 (pt) | 2013-10-17 | 2022-08-23 | Dow Agrosciences Llc | Compostos pesticidas, e seus processos de preparação |
| CN105636446B (zh) | 2013-10-17 | 2018-07-13 | 美国陶氏益农公司 | 制备杀虫化合物的方法 |
| EP3057426A4 (en) | 2013-10-17 | 2017-03-29 | Dow AgroSciences LLC | Processes for the preparation of pesticidal compounds |
| JP2016535010A (ja) | 2013-10-17 | 2016-11-10 | ダウ アグロサイエンシィズ エルエルシー | 有害生物防除性化合物の製造方法 |
| CN105636440A (zh) | 2013-10-17 | 2016-06-01 | 美国陶氏益农公司 | 制备杀虫化合物的方法 |
| MX386864B (es) | 2013-10-18 | 2025-03-19 | Basf Agrochemical Products Bv | Uso de derivado de carboxamida activo como plaguicida en métodos de aplicación y tratamiento de suelo y semillas. |
| CN105792652A (zh) | 2013-10-22 | 2016-07-20 | 美国陶氏益农公司 | 协同杀虫组合物和相关方法 |
| AR098091A1 (es) | 2013-10-22 | 2016-05-04 | Dow Agrosciences Llc | Composiciones pesticidas sinérgicas y métodos relacionados |
| EP3060044A4 (en) | 2013-10-22 | 2017-04-05 | Dow AgroSciences LLC | Synergistic pesticidal compositions and related methods |
| US9155304B2 (en) | 2013-10-22 | 2015-10-13 | Dow Agrosciences Llc | Synergistic pesticidal compositions and related methods |
| CA2927226A1 (en) | 2013-10-22 | 2015-04-30 | Dow Agrosciences Llc | Synergistic pesticidal compositions and related methods |
| US9497966B2 (en) | 2013-10-22 | 2016-11-22 | Dow Agrosciences Llc | Pesticidal compositions and related methods |
| AR098094A1 (es) | 2013-10-22 | 2016-05-04 | Dow Agrosciences Llc | Composiciones plaguicidas sinérgicas y métodos relacionados |
| US9137998B2 (en) | 2013-10-22 | 2015-09-22 | Dow Agrosciences Llc | Pesticidal compositions and related methods |
| AR098101A1 (es) | 2013-10-22 | 2016-05-04 | Dow Agrosciences Llc | Composiciones plaguicidas y métodos relacionados |
| MX2016005319A (es) | 2013-10-22 | 2016-08-12 | Dow Agrosciences Llc | Composiciones pesticidas y metodos relacionados. |
| CN105828608A (zh) | 2013-10-22 | 2016-08-03 | 美国陶氏益农公司 | 杀虫组合物和与其相关的方法 |
| JP2016538265A (ja) | 2013-10-22 | 2016-12-08 | ダウ アグロサイエンシィズ エルエルシー | 相乗的有害生物防除組成物および関連する方法 |
| RU2658995C2 (ru) | 2013-10-22 | 2018-06-26 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | Пестицидные композиции и связанные с ними способы |
| CA2927206A1 (en) | 2013-10-22 | 2015-04-30 | Dow Agrosciences Llc | Synergistic pesticidal compositions and related methods |
| WO2015061140A1 (en) | 2013-10-22 | 2015-04-30 | Dow Agrosciences Llc | Synergistic pesticidal compositions and related methods |
| EP3060054A4 (en) | 2013-10-22 | 2017-04-05 | Dow AgroSciences LLC | Synergistic pesticidal compositions and related methods |
| CN105792650A (zh) | 2013-10-22 | 2016-07-20 | 美国陶氏益农公司 | 协同杀虫组合物和相关方法 |
| CN103588768B (zh) * | 2013-11-29 | 2016-03-30 | 华南农业大学 | 含呋喃环2,5-二取代-1,3,4-噻二唑类化合物在制备致病疫霉菌抑菌剂中的应用 |
| DE202014008415U1 (de) | 2014-02-19 | 2014-11-25 | Clariant International Ltd. | Wässrige Adjuvant-Zusammensetzung zur Wirkungssteigerung von Elektrolyt-Wirkstoffen |
| DE202014008418U1 (de) | 2014-02-19 | 2014-11-14 | Clariant International Ltd. | Schaumarme agrochemische Zusammensetzungen |
| AR101816A1 (es) * | 2014-04-02 | 2017-01-18 | Bayer Cropscience Ag | Derivados de 3-[(pirazol-5-il)-heteroaril]-benzamidas como agentes pesticidas |
| WO2015160618A1 (en) | 2014-04-16 | 2015-10-22 | Bayer Cropscience Lp | Compositions comprising ningnanmycin and a biological control agent |
| WO2015160620A1 (en) | 2014-04-16 | 2015-10-22 | Bayer Cropscience Lp | Compositions comprising ningnanmycin and an insecticide |
| DE102014005771A1 (de) | 2014-04-23 | 2015-10-29 | Clariant International Ltd. | Verwendung von wässrigen driftreduzierenden Zusammensetzungen |
| JP6493394B2 (ja) * | 2014-04-24 | 2019-04-03 | 住友化学株式会社 | ジアリール−アゾール化合物 |
| EP3186229A4 (en) | 2014-07-31 | 2018-01-10 | Dow AgroSciences LLC | Process for the preparation of 3-(3-chloro-1h-pyrazol-1-yl)pyridine |
| EP3174856A4 (en) | 2014-07-31 | 2018-01-10 | Dow AgroSciences LLC | Process for the preparation of 3-(3-chloro-1h-pyrazol-1-yl)pyridine |
| US9249122B1 (en) | 2014-07-31 | 2016-02-02 | Dow Agrosciences Llc | Process for the preparation of 3-(3-chloro-1H-pyrazol-1-yl)pyridine |
| DE102014012022A1 (de) | 2014-08-13 | 2016-02-18 | Clariant International Ltd. | Organische Ammoniumsalze von anionischen Pestiziden |
| WO2016028328A1 (en) | 2014-08-19 | 2016-02-25 | Dow Agrosciences Llc | Process for the preparation of 3-(3-chloro-1h-pyrazol-1-yl)pyridine |
| JP2017528469A (ja) | 2014-09-12 | 2017-09-28 | ダウ アグロサイエンシィズ エルエルシー | ３−（３−クロロ−１ｈ−ピラゾール−１−イル）ピリジンの調製方法 |
| BR112017005140A2 (pt) | 2014-10-06 | 2018-01-23 | Basf Se | compostos, mistura, composição, métodos para a proteção de culturas e para o combate ou controle de praga de invertebrados, método não terapêutico para o tratamento de animais infestados ou infectados por parasitas e semente |
| TWI667230B (zh) | 2014-10-30 | 2019-08-01 | 比利時商健生藥品公司 | 用作ＲＯＲγｔ調節劑之三氟甲基醇 |
| EP3212642B1 (en) | 2014-10-30 | 2019-10-30 | Janssen Pharmaceutica NV | Amide substituted thiazoles as modulators of rorgammat |
| LT3212641T (lt) * | 2014-10-30 | 2019-02-11 | Janssen Pharmaceutica Nv | Tiazolai, kaip roryt moduliatoriai |
| BR112017009513A2 (pt) | 2014-11-06 | 2018-02-06 | Basf Se | utilização de um composto heterobicíclico, utilização dos compostos i, compostos, composição agrícola ou veterinária, método para o combate ou controle de pragas, método para a proteção de culturas e sementes |
| BR112017011791A2 (pt) * | 2014-12-02 | 2018-02-27 | Bayer Cropscience Aktiengesellschaft | compostos bicíclicos como agentes de controle de pragas |
| US20170265474A1 (en) * | 2014-12-02 | 2017-09-21 | Bayer Cropscience Aktiengesellschaft | Bicyclic compounds as pest control agents |
| DE102014018274A1 (de) | 2014-12-12 | 2015-07-30 | Clariant International Ltd. | Zuckertenside und deren Verwendung in agrochemischen Zusammensetzungen |
| EP3232780B1 (de) | 2014-12-19 | 2021-08-04 | Clariant International Ltd | Wässrige elektrolyt enthaltende adjuvant-zusammensetzungen, wirkstoff enthaltende zusammensetzungen und deren verwendung |
| MX383651B (es) | 2014-12-22 | 2025-03-14 | Bayer Cropscience Lp | Método para utilizar una cepa de bacillus subtilis o bacillus pumilus para tratar o prevenir la enfermedad de la piña. |
| EP3253209A1 (en) | 2015-02-06 | 2017-12-13 | Basf Se | Pyrazole compounds as nitrification inhibitors |
| WO2016128261A2 (en) | 2015-02-11 | 2016-08-18 | Basf Se | Pesticidal mixture comprising a pyrazole compound, an insecticide and a fungicide |
| CN104860927A (zh) * | 2015-04-02 | 2015-08-26 | 宁波大学 | 一种1h-3,5-二(3-吡啶基)-4-氯吡唑化合物及其制备方法和应用 |
| BR112017021450B1 (pt) | 2015-04-07 | 2021-12-28 | Basf Agrochemical Products B.V. | Métodos de controle de pragas, método de melhoria da saúde vegetal e semente revestida |
| WO2016170130A1 (en) | 2015-04-22 | 2016-10-27 | Basf Se | Molluscicide and bait composition comprising a molluscicide |
| MX2017014459A (es) | 2015-05-12 | 2018-03-16 | Basf Se | Compuestos de tioeter como inhibidores de la nitrificacion. |
| WO2016198613A1 (en) | 2015-06-11 | 2016-12-15 | Basf Se | N-(thio)acylimino compounds |
| WO2016198611A1 (en) | 2015-06-11 | 2016-12-15 | Basf Se | N-(thio)acylimino heterocyclic compounds |
| WO2017016883A1 (en) | 2015-07-24 | 2017-02-02 | Basf Se | Process for preparation of cyclopentene compounds |
| WO2017050685A1 (en) * | 2015-09-25 | 2017-03-30 | Syngenta Participations Ag | Pesticidally active polycyclic derivatives with 5-membered sulfur containing heterocyclic ring systems |
| WO2017055386A1 (en) | 2015-10-02 | 2017-04-06 | Basf Se | Imino compounds with a 2-chloropyrimidin-5-yl substituent as pest-control agents |
| DE102015219651A1 (de) | 2015-10-09 | 2017-04-13 | Clariant International Ltd. | Zusammensetzungen enthaltend Zuckeramin und Fettsäure |
| DE202015008045U1 (de) | 2015-10-09 | 2015-12-09 | Clariant International Ltd. | Universelle Pigmentdispersionen auf Basis von N-Alkylglukaminen |
| PL3383183T3 (pl) | 2015-11-30 | 2020-11-16 | Basf Se | Kompozycje zawierające cis-jasmon i bacillus amyloliquefaciens |
| WO2017153217A1 (en) | 2016-03-09 | 2017-09-14 | Basf Se | Spirocyclic derivatives |
| BR112018068042A2 (pt) | 2016-03-11 | 2019-01-08 | Basf Se | métodos para controlar pragas de plantas, material de propagação de planta e uso de um ou mais compostos de fórmula i |
| CA3015934A1 (en) | 2016-04-01 | 2017-10-05 | Basf Se | Bicyclic compounds |
| BR122021026787B1 (pt) | 2016-04-24 | 2023-05-16 | Bayer Cropscience Aktiengesellschaft | Uso de cepa qst 713 de bacillus subtilis, e método para controle de murcha de fusarium em plantas da família musaceae |
| TW201803869A (zh) | 2016-04-27 | 2018-02-01 | 健生藥品公司 | 作為ＲＯＲγＴ調節劑之６－胺基吡啶－３－基噻唑 |
| DE202016003070U1 (de) | 2016-05-09 | 2016-06-07 | Clariant International Ltd. | Stabilisatoren für Silikatfarben |
| AU2017267129A1 (en) | 2016-05-18 | 2018-11-22 | Basf Se | Capsules comprising benzylpropargylethers for use as nitrification inhibitors |
| US20190159451A1 (en) | 2016-07-29 | 2019-05-30 | Bayer Cropscience Aktiengesellschaft | Active compound combinations and methods to protect the propagation material of plants |
| US20200077658A1 (en) | 2016-12-16 | 2020-03-12 | Basf Se | Pesticidal Compounds |
| US10100033B2 (en) | 2016-12-29 | 2018-10-16 | Dow Agrosciences Llc | Processes for the preparation of pesticidal compounds |
| WO2018125817A1 (en) | 2016-12-29 | 2018-07-05 | Dow Agrosciences Llc | Processes for the preparation of pesticidal compounds |
| WO2018162312A1 (en) | 2017-03-10 | 2018-09-13 | Basf Se | Spirocyclic derivatives |
| WO2018166855A1 (en) | 2017-03-16 | 2018-09-20 | Basf Se | Heterobicyclic substituted dihydroisoxazoles |
| BR112019020277B1 (pt) | 2017-03-28 | 2023-02-14 | Basf Se | Compostos, composição, método para combater ou controlar pragas de invertebrados, método para proteger plantas em crescimento, semente tratada, usos de um composto da fórmula i |
| MX2019011785A (es) | 2017-03-31 | 2019-11-18 | Basf Se | Proceso para preparar compuestos de 2,3-dihidrotiazolo[3,2-a]pirim idin-4-io quirales. |
| WO2018192793A1 (en) | 2017-04-20 | 2018-10-25 | Basf Se | Substituted rhodanine derivatives |
| MX2019012813A (es) | 2017-04-26 | 2020-01-14 | Basf Se | Derivados de succinimida sustituida como plaguicidas. |
| ES2910854T3 (es) | 2017-05-10 | 2022-05-13 | Basf Se | Compuestos pesticidas bicíclicos |
| WO2018224455A1 (en) | 2017-06-07 | 2018-12-13 | Basf Se | Substituted cyclopropyl derivatives |
| BR112019025331A2 (pt) | 2017-06-16 | 2020-06-23 | Basf Se | Compostos da fórmula (i), composição, métodos de proteção de safras e de combate, método não terapêutico de tratamento, semente, uso dos compostos e uso de composto |
| BR112019025191B1 (pt) | 2017-06-19 | 2023-11-28 | Basf Se | Compostos de pirimidínio substituídos, composição, método para proteger culturas, semente revestida, uso dos compostos e uso de um composto |
| WO2018234488A1 (en) | 2017-06-23 | 2018-12-27 | Basf Se | Substituted cyclopropyl derivatives |
| WO2019042932A1 (en) | 2017-08-31 | 2019-03-07 | Basf Se | METHOD FOR CONTROLLING RICE PARASITES IN RICE |
| EP3453706A1 (en) | 2017-09-08 | 2019-03-13 | Basf Se | Pesticidal imidazole compounds |
| US11399543B2 (en) | 2017-10-13 | 2022-08-02 | Basf Se | Substituted 1,2,3,5-tetrahydroimidazo[1,2-a]pyrimidiniumolates for combating animal pests |
| WO2019121143A1 (en) | 2017-12-20 | 2019-06-27 | Basf Se | Substituted cyclopropyl derivatives |
| MX2020006566A (es) | 2017-12-21 | 2020-09-25 | Basf Se | Compuestos plaguicidas. |
| IL275726B2 (en) | 2018-01-09 | 2024-06-01 | Basf Se | Silylethynyl hetaryl compounds as nitrification inhibitors |
| WO2019137995A1 (en) | 2018-01-11 | 2019-07-18 | Basf Se | Novel pyridazine compounds for controlling invertebrate pests |
| PE20211754A1 (es) | 2018-02-28 | 2021-09-06 | Basf Se | Uso de compuestos de alcoxi pirazol funcionalizados con n como inhibidores de la nitrificacion |
| WO2019166558A1 (en) | 2018-02-28 | 2019-09-06 | Basf Se | Use of pyrazole propargyl ethers as nitrification inhibitors |
| BR112020016425A2 (pt) | 2018-02-28 | 2020-12-15 | Basf Se | Uso de composto de alcoxipirazol, composição para uso na redução da nitrificação, mistura agroquímica e métodos de redução da nitrificação e de tratamento de fertilizante ou composição |
| WO2019175713A1 (en) | 2018-03-14 | 2019-09-19 | Basf Corporation | New catechol molecules and their use as inhibitors to p450 related metabolic pathways |
| WO2019175712A1 (en) | 2018-03-14 | 2019-09-19 | Basf Corporation | New uses for catechol molecules as inhibitors to glutathione s-transferase metabolic pathways |
| WO2019185413A1 (en) | 2018-03-27 | 2019-10-03 | Basf Se | Pesticidal substituted cyclopropyl derivatives |
| CN112423590B (zh) | 2018-05-15 | 2022-07-08 | 巴斯夫欧洲公司 | 包含benzpyrimoxan和oxazosulfyl的混合物和用途以及它们的施用方法 |
| WO2019224092A1 (en) | 2018-05-22 | 2019-11-28 | Basf Se | Pesticidally active c15-derivatives of ginkgolides |
| CA3103929A1 (en) | 2018-06-18 | 2019-12-26 | Janssen Pharmaceutica Nv | Phenyl substituted pyrazoles as modulators of roryt |
| CN112334450A (zh) | 2018-06-18 | 2021-02-05 | 詹森药业有限公司 | 作为RORγt的调节剂的苯基和吡啶基取代的咪唑 |
| EP3806958B1 (en) | 2018-06-18 | 2022-09-07 | Janssen Pharmaceutica NV | 6-aminopyridin-3-yl pyrazoles as modulators of roryt |
| ES2925473T3 (es) | 2018-06-18 | 2022-10-18 | Janssen Pharmaceutica Nv | Pirazoles de piridinilo como moduladores de RORyt |
| WO2020002472A1 (en) | 2018-06-28 | 2020-01-02 | Basf Se | Use of alkynylthiophenes as nitrification inhibitors |
| DK3826983T3 (da) | 2018-07-23 | 2024-08-05 | Basf Se | Anvendelse af substituerede 2-thiazoliner som nitrificeringshæmmere |
| US12151991B2 (en) | 2018-07-23 | 2024-11-26 | Basf Se | Use of a substituted thiazolidine compound as nitrification inhibitor |
| EP3613736A1 (en) | 2018-08-22 | 2020-02-26 | Basf Se | Substituted glutarimide derivatives |
| US12534440B2 (en) | 2018-09-20 | 2026-01-27 | Kansas State University Research Foundation | Compounds with copper- or zinc-activated toxicity against microbial infection |
| EP3628158A1 (en) | 2018-09-28 | 2020-04-01 | Basf Se | Pesticidal mixture comprising a mesoionic compound and a biopesticide |
| EP3628156A1 (en) | 2018-09-28 | 2020-04-01 | Basf Se | Method for controlling pests of sugarcane, citrus, rapeseed, and potato plants |
| US20220046925A1 (en) | 2018-09-28 | 2022-02-17 | Basf Se | Method of controlling pests by seed treatment application of a mesoionic compound or mixture thereof |
| EP3628157A1 (en) | 2018-09-28 | 2020-04-01 | Basf Se | Method of controlling insecticide resistant insects and virus transmission to plants |
| EP3643705A1 (en) | 2018-10-24 | 2020-04-29 | Basf Se | Pesticidal compounds |
| WO2020109039A1 (en) | 2018-11-28 | 2020-06-04 | Basf Se | Pesticidal compounds |
| US20230031024A1 (en) | 2018-12-18 | 2023-02-02 | Basf Se | Substituted pyrimidinium compounds for combating animal pests |
| EP3696177A1 (en) | 2019-02-12 | 2020-08-19 | Basf Se | Heterocyclic compounds for the control of invertebrate pests |
| EP3975718A1 (en) | 2019-05-29 | 2022-04-06 | Basf Se | Mesoionic imidazolium compounds and derivatives for combating animal pests |
| EP3769623A1 (en) | 2019-07-22 | 2021-01-27 | Basf Se | Mesoionic imidazolium compounds and derivatives for combating animal pests |
| EP3766879A1 (en) | 2019-07-19 | 2021-01-20 | Basf Se | Pesticidal pyrazole derivatives |
| PH12022550166A1 (en) * | 2019-07-23 | 2022-11-14 | Bayer Ag | Novel heteroaryl-triazole compounds as pesticides |
| CN112314611B (zh) * | 2019-08-04 | 2021-07-30 | 河北谷之润科技有限公司 | 噁线酚用于防治跳甲的用途 |
| CN114845551B (zh) | 2019-12-23 | 2025-04-29 | 巴斯夫欧洲公司 | 酶增强农业化学活性化合物的根吸收 |
| US20230106291A1 (en) | 2020-02-28 | 2023-04-06 | BASF Agro B.V. | Methods and uses of a mixture comprising alpha-cypermethrin and dinotefuran for controlling invertebrate pests in t |
| CN115443267B (zh) | 2020-04-28 | 2025-09-05 | 巴斯夫欧洲公司 | 杀害虫化合物 |
| EP3909950A1 (en) | 2020-05-13 | 2021-11-17 | Basf Se | Heterocyclic compounds for the control of invertebrate pests |
| CN116829521A (zh) | 2021-02-02 | 2023-09-29 | 巴斯夫欧洲公司 | Dcd和烷氧基吡唑作为硝化抑制剂的协同增效作用 |
| EP4043444A1 (en) | 2021-02-11 | 2022-08-17 | Basf Se | Substituted isoxazoline derivatives |
| EP4341248A1 (en) | 2021-05-21 | 2024-03-27 | Basf Se | Use of an n-functionalized alkoxy pyrazole compound as nitrification inhibitor |
| EP4341245A1 (en) | 2021-05-21 | 2024-03-27 | Basf Se | Use of ethynylpyridine compounds as nitrification inhibitors |
| BR112023027004A2 (pt) | 2021-06-21 | 2024-03-12 | Basf Se | Estrutura de metal-orgânica, uso da estrutura de metal-orgânica, composição para uso na redução da nitrificação, mistura agroquímica e métodos de redução da nitrificação, de tratamento de fertilizante ou composição de fertilizante e de preparação de uma estrutura de metal-orgânica |
| EP4119547A1 (en) | 2021-07-12 | 2023-01-18 | Basf Se | Triazole compounds for the control of invertebrate pests |
| EP4140986A1 (en) | 2021-08-23 | 2023-03-01 | Basf Se | Pyrazine compounds for the control of invertebrate pests |
| EP4140995A1 (en) | 2021-08-27 | 2023-03-01 | Basf Se | Pyrazine compounds for the control of invertebrate pests |
| EP4151631A1 (en) | 2021-09-20 | 2023-03-22 | Basf Se | Heterocyclic compounds for the control of invertebrate pests |
| EP4194453A1 (en) | 2021-12-08 | 2023-06-14 | Basf Se | Pyrazine compounds for the control of invertebrate pests |
| EP4198033A1 (en) | 2021-12-14 | 2023-06-21 | Basf Se | Heterocyclic compounds for the control of invertebrate pests |
| EP4198023A1 (en) | 2021-12-16 | 2023-06-21 | Basf Se | Pesticidally active thiosemicarbazone compounds |
| EP4238971A1 (en) | 2022-03-02 | 2023-09-06 | Basf Se | Substituted isoxazoline derivatives |
| WO2023203066A1 (en) | 2022-04-21 | 2023-10-26 | Basf Se | Synergistic action as nitrification inhibitors of dcd oligomers with alkoxypyrazole and its oligomers |
| WO2023208447A1 (en) | 2022-04-25 | 2023-11-02 | Basf Se | An emulsifiable concentrate having a (substituted) benzaldehyde-based solvent system |
| CN119212989A (zh) * | 2022-05-18 | 2024-12-27 | 豪夫迈·罗氏有限公司 | 作为sting激动剂的吡唑衍生物 |
| CA3263381A1 (en) | 2022-08-02 | 2024-02-08 | Basf Se | PYRAZOLO PESTICIDE COMPOUNDS |
| EP4342885A1 (en) | 2022-09-20 | 2024-03-27 | Basf Se | N-(3-(aminomethyl)-phenyl)-5-(4-phenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-amine derivatives and similar compounds as pesticides |
| TW202434579A (zh) | 2022-11-16 | 2024-09-01 | 瑞士商先正達農作物保護股份公司 | 殺微生物的四氫異喹啉衍生物 |
| WO2024115512A1 (en) | 2022-11-30 | 2024-06-06 | Syngenta Crop Protection Ag | Microbiocidal tetrahydroisoquinoline derivatives |
| TW202439972A (zh) | 2022-11-30 | 2024-10-16 | 瑞士商先正達農作物保護股份公司 | 殺真菌組成物 |
| EP4389210A1 (en) | 2022-12-21 | 2024-06-26 | Basf Se | Heteroaryl compounds for the control of invertebrate pests |
| PY2403614A (es) | 2023-01-27 | 2025-09-11 | Syngenta Crop Protection Ag | Derivados de pirazol microbiocidas |
| PY2404467A (es) | 2023-02-01 | 2025-03-31 | Syngenta Crop Protection Ag | Composiciones fungicidas |
| EP4455137A1 (en) | 2023-04-24 | 2024-10-30 | Basf Se | Pyrimidine compounds for the control of invertebrate pests |
| EP4467535A1 (en) | 2023-05-25 | 2024-11-27 | Basf Se | Lactam pesticidal compounds |
| EP4488273A1 (en) | 2023-07-06 | 2025-01-08 | Basf Se | Triazole compounds for the control of invertebrate pests |
| EP4488270A1 (en) | 2023-07-06 | 2025-01-08 | Basf Se | Triazole compounds for the control of invertebrate pests |
| EP4488269A1 (en) | 2023-07-06 | 2025-01-08 | Basf Se | Triazole compounds for the control of invertebrate pests |
| WO2025117659A1 (en) | 2023-11-29 | 2025-06-05 | Basf Corporation | Insecticide delivery by nanocarriers |
| EP4574819A1 (en) | 2023-12-22 | 2025-06-25 | Basf Se | Diazinone compounds for the control of invertebrate pests |
| WO2025172368A1 (en) | 2024-02-13 | 2025-08-21 | Syngenta Crop Protection Ag | (5-isoxazol-3-yl)-[4-(pyrazol-4-yl)-3,4-dihydro-1h-isoquinolin-2-yl]methanone derivatives for use as fungicides |
| WO2025242699A1 (en) | 2024-05-22 | 2025-11-27 | Basf Se | Method for improving rainfastness of an agrochemical active ingredient |
| WO2026037853A1 (en) | 2024-08-14 | 2026-02-19 | Basf Se | Benzoxazole derivatives as pesticidal compounds |
| WO2026041702A1 (en) | 2024-08-21 | 2026-02-26 | Basf Se | Benzoxazole derivatives as pesticidal compounds |
| WO2026093251A1 (en) | 2024-10-28 | 2026-05-07 | Basf Se | Pesticidal compounds and uses thereof |
Family Cites Families (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL261797A (OSRAM) | 1960-03-01 | |||
| CH411906A (de) | 1960-03-01 | 1966-04-30 | Ciba Geigy | Verfahren zur Herstellung neuer 1,3,4-Thiadiazole |
| BE626467A (OSRAM) * | 1961-12-28 | |||
| DE1287997B (OSRAM) * | 1964-04-05 | 1969-01-23 | ||
| CA962269A (en) | 1971-05-05 | 1975-02-04 | Uniroyal Ltd. | Thiazoles, and their use as insecticides |
| FR2531711A1 (fr) * | 1982-08-13 | 1984-02-17 | Rhone Poulenc Sante | Nouveaux derives de la cephalosporine, leur preparation et les medicaments qui les contiennent |
| DE3641184A1 (de) * | 1985-12-04 | 1987-06-11 | Ciba Geigy Ag | Schaedlingsbekaempfungsmittel |
| EP0288432A1 (de) * | 1987-04-09 | 1988-10-26 | Ciba-Geigy Ag | Schädlingsbekämpfungsmittel |
| US5668148A (en) | 1995-04-20 | 1997-09-16 | Merck & Co., Inc. | Alpha1a adrenergic receptor antagonists |
| GB9603226D0 (en) * | 1996-02-15 | 1996-04-17 | Pharmacia Spa | Heterocyclyl-ergoline derivatives |
| DE19721031A1 (de) | 1997-05-20 | 1998-11-26 | Bayer Ag | Substituierte Pyridylpyrazole |
| WO1998056785A1 (en) | 1997-06-12 | 1998-12-17 | Sumitomo Pharmaceuticals Co., Ltd. | Pyrazole derivatives |
| WO2003015776A1 (en) | 2001-08-13 | 2003-02-27 | Janssen Pharmaceutica N.V. | 2,4,5-trisubstituted thiazolyl derivatives and their antiinflammatory activity |
| PL376925A1 (pl) | 2002-11-27 | 2006-01-09 | Incyte Corporation | Pochodne 3-aminopirolidyny jako modulatory receptorów chemokiny |
| BRPI0412382A (pt) * | 2003-07-08 | 2006-09-19 | Astrazeneca Ab | composto , método para a verificação de novos compostos medicinais que se ligam a e modulam a atividade, por agonismo , agonismo parcial, ou antagonismo, do receptor de acetilcolina nicotìnico alfa7, método de tratamento ou profilaxia de uma doença ou condição humana, método para tratamento de jetlag, induzindo interrupção de fumar, vìcio em nicotina, abstinência, dor, e para colite ulcerativa, composição farmacêutica, e, método de tratamento ou prevenção de uma condição ou distúrbio que surge da disfunção de neurotransmissão do receptor de acetilcolina nicotìnico em um mamìfero, e, uso de um composto |
| US7763609B2 (en) * | 2003-12-15 | 2010-07-27 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| GB0412019D0 (en) * | 2004-05-28 | 2004-06-30 | Novartis Ag | Organic compounds |
| JP4932735B2 (ja) * | 2004-12-17 | 2012-05-16 | アムジエン・インコーポレーテツド | アミノピリミジン化合物および使用方法 |
| AU2006258124B8 (en) | 2005-06-10 | 2010-01-07 | Merck Sharp & Dohme Corp. | Inhibitors of Akt activity |
| US20070197532A1 (en) * | 2005-11-18 | 2007-08-23 | Cao Sheldon X | Glucokinase activators |
| PE20080401A1 (es) * | 2006-07-07 | 2008-06-23 | Boehringer Ingelheim Int | DERIVADOS DE HETEROARIL-FENIL SUSTITUIDOS COMO INHIBIDORES DE B-Raf-QUINASAS |
| WO2008049864A1 (en) * | 2006-10-25 | 2008-05-02 | Neurosearch A/S | Oxadiazole and thiadiazole compounds and their use as nicotinic acetylcholine receptor modulators |
| WO2009003998A2 (en) * | 2007-07-02 | 2009-01-08 | Boehringer Ingelheim International Gmbh | Antiproliferative compounds based on 5-membered heterocycles |
| MX2010013705A (es) | 2008-06-13 | 2011-02-25 | Bayer Cropscience Ag | Nuevas amidas y tioamidas heteroaromaticas como plaguicidas. |
| BRPI0916218B1 (pt) | 2008-07-17 | 2018-11-27 | Bayer Cropscience Ag | compostos heterocíclicos como composições praguicidas |
| UA107791C2 (en) * | 2009-05-05 | 2015-02-25 | Dow Agrosciences Llc | Pesticidal compositions |
| CN102573478B (zh) | 2009-10-12 | 2015-12-16 | 拜尔农作物科学股份公司 | 作为杀虫剂的1-(吡啶-3-基)-吡唑和1-(嘧啶-5-基)-吡唑 |
| WO2011128304A2 (de) | 2010-04-16 | 2011-10-20 | Bayer Cropscience Ag | Neue heterocyclische verbindungen als schädlingsbekämpfungsmittel |
| ES2626601T3 (es) | 2010-06-28 | 2017-07-25 | Bayer Intellectual Property Gmbh | Compuestos heterocíclicos como pesticidas |
| BR112013000925A2 (pt) | 2010-07-15 | 2020-12-01 | Bayer Intellectual Property Gmbh | compostos heterocíclicos como pesticidas |
-
2009
- 2009-07-04 BR BRPI0916218A patent/BRPI0916218B1/pt not_active IP Right Cessation
- 2009-07-04 EP EP12191540.9A patent/EP2591674B1/de not_active Not-in-force
- 2009-07-04 MX MX2011000477A patent/MX2011000477A/es not_active Application Discontinuation
- 2009-07-04 EP EP12191542.5A patent/EP2583556B1/de not_active Not-in-force
- 2009-07-04 KR KR1020117003579A patent/KR20110030700A/ko not_active Ceased
- 2009-07-04 ES ES09776952T patent/ES2426953T3/es active Active
- 2009-07-04 CN CN200980136317.5A patent/CN102159079B/zh not_active Expired - Fee Related
- 2009-07-04 EP EP12191544.1A patent/EP2586311B1/de not_active Not-in-force
- 2009-07-04 CN CN201510050896.9A patent/CN104642337B/zh not_active Expired - Fee Related
- 2009-07-04 EP EP12191543.3A patent/EP2583557B1/de not_active Not-in-force
- 2009-07-04 EP EP09776952.5A patent/EP2309857B1/de not_active Not-in-force
- 2009-07-04 EP EP12191545.8A patent/EP2586312B1/de not_active Not-in-force
- 2009-07-04 JP JP2011517777A patent/JP5681105B2/ja not_active Expired - Fee Related
- 2009-07-04 ES ES12191544.1T patent/ES2618022T3/es active Active
- 2009-07-04 BR BR122018010510A patent/BR122018010510B1/pt not_active IP Right Cessation
- 2009-07-04 AU AU2009270520A patent/AU2009270520A1/en not_active Abandoned
- 2009-07-04 WO PCT/EP2009/004832 patent/WO2010006713A2/de not_active Ceased
- 2009-07-04 ES ES12191542.5T patent/ES2567183T3/es active Active
- 2009-07-04 ES ES12191540.9T patent/ES2573149T3/es active Active
- 2009-07-04 US US13/054,401 patent/US8809547B2/en not_active Expired - Fee Related
- 2009-07-04 CA CA2730844A patent/CA2730844A1/en not_active Abandoned
- 2009-07-04 ES ES12191543.3T patent/ES2567786T3/es active Active
- 2009-07-04 ES ES12191545.8T patent/ES2579085T3/es active Active
- 2009-07-16 TW TW098124024A patent/TW201022260A/zh unknown
- 2009-07-17 AR ARP090102737A patent/AR072572A1/es not_active Application Discontinuation
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2011
- 2011-01-14 ZA ZA2011/00371A patent/ZA201100371B/en unknown
- 2011-01-17 CO CO11004295A patent/CO6341525A2/es not_active Application Discontinuation
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2014
- 2014-04-28 JP JP2014092763A patent/JP6026461B2/ja not_active Expired - Fee Related
- 2014-07-09 US US14/327,144 patent/US9451775B2/en not_active Expired - Fee Related
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