AR103843A1 - Combinaciones de compuestos activos - Google Patents
Combinaciones de compuestos activosInfo
- Publication number
- AR103843A1 AR103843A1 ARP160100563A ARP160100563A AR103843A1 AR 103843 A1 AR103843 A1 AR 103843A1 AR P160100563 A ARP160100563 A AR P160100563A AR P160100563 A ARP160100563 A AR P160100563A AR 103843 A1 AR103843 A1 AR 103843A1
- Authority
- AR
- Argentina
- Prior art keywords
- methyl
- phenyl
- pyrazol
- dihydro
- triazol
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 6
- -1 2,4-dichlorophenoxy Chemical group 0.000 abstract 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 12
- 125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 abstract 10
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 abstract 10
- 239000003112 inhibitor Substances 0.000 abstract 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 10
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 abstract 9
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 abstract 9
- RWTNPBWLLIMQHL-UHFFFAOYSA-N fexofenadine Chemical compound C1=CC(C(C)(C(O)=O)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 RWTNPBWLLIMQHL-UHFFFAOYSA-N 0.000 abstract 7
- 239000000203 mixture Substances 0.000 abstract 6
- 241000233866 Fungi Species 0.000 abstract 4
- 230000003032 phytopathogenic effect Effects 0.000 abstract 4
- 150000003839 salts Chemical class 0.000 abstract 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 3
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 abstract 3
- JLIDBLDQVAYHNE-YKALOCIXSA-N (+)-Abscisic acid Chemical compound OC(=O)/C=C(/C)\C=C\[C@@]1(O)C(C)=CC(=O)CC1(C)C JLIDBLDQVAYHNE-YKALOCIXSA-N 0.000 abstract 2
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 abstract 2
- WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical compound C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 abstract 2
- LGDSHSYDSCRFAB-UHFFFAOYSA-N Methyl isothiocyanate Chemical compound CN=C=S LGDSHSYDSCRFAB-UHFFFAOYSA-N 0.000 abstract 2
- LKJPYSCBVHEWIU-UHFFFAOYSA-N N-[4-cyano-3-(trifluoromethyl)phenyl]-3-[(4-fluorophenyl)sulfonyl]-2-hydroxy-2-methylpropanamide Chemical compound C=1C=C(C#N)C(C(F)(F)F)=CC=1NC(=O)C(O)(C)CS(=O)(=O)C1=CC=C(F)C=C1 LKJPYSCBVHEWIU-UHFFFAOYSA-N 0.000 abstract 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 2
- 229930182764 Polyoxin Natural products 0.000 abstract 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 2
- 235000010290 biphenyl Nutrition 0.000 abstract 2
- 239000004305 biphenyl Substances 0.000 abstract 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 abstract 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 abstract 2
- 239000011575 calcium Substances 0.000 abstract 2
- 229910052791 calcium Inorganic materials 0.000 abstract 2
- ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Chemical compound CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- XRECTZIEBJDKEO-UHFFFAOYSA-N flucytosine Chemical compound NC1=NC(=O)NC=C1F XRECTZIEBJDKEO-UHFFFAOYSA-N 0.000 abstract 2
- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- HQUIFHINFGFWLJ-UHFFFAOYSA-N n-[(cyclopropylmethoxyamino)-[6-(difluoromethoxy)-2,3-difluorophenyl]methylidene]-2-phenylacetamide Chemical compound FC(F)OC1=CC=C(F)C(F)=C1C(NOCC1CC1)=NC(=O)CC1=CC=CC=C1 HQUIFHINFGFWLJ-UHFFFAOYSA-N 0.000 abstract 2
- 125000004269 oxiran-2-yl group Chemical group [H]C1([H])OC1([H])* 0.000 abstract 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 abstract 2
- JGCSKOVQDXEQHI-UHFFFAOYSA-N phenazine-1-carboxylic acid Chemical compound C1=CC=C2N=C3C(C(=O)O)=CC=CC3=NC2=C1 JGCSKOVQDXEQHI-UHFFFAOYSA-N 0.000 abstract 2
- QJBZDBLBQWFTPZ-UHFFFAOYSA-N pyrrolnitrin Chemical compound [O-][N+](=O)C1=C(Cl)C=CC=C1C1=CNC=C1Cl QJBZDBLBQWFTPZ-UHFFFAOYSA-N 0.000 abstract 2
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 abstract 2
- 239000011734 sodium Substances 0.000 abstract 2
- 229910052708 sodium Inorganic materials 0.000 abstract 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 239000011593 sulfur Substances 0.000 abstract 2
- 238000003786 synthesis reaction Methods 0.000 abstract 2
- 230000009261 transgenic effect Effects 0.000 abstract 2
- SPXBEYPYQKZKGX-USXIJHARSA-N (1R,2S,5S)-2-(chloromethyl)-5-[(4-chlorophenyl)methyl]-2-methyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentan-1-ol Chemical compound C[C@]1(CCl)CC[C@@H](Cc2ccc(Cl)cc2)[C@]1(O)Cn1cncn1 SPXBEYPYQKZKGX-USXIJHARSA-N 0.000 abstract 1
- SPXBEYPYQKZKGX-PVAVHDDUSA-N (1s,2r,5r)-2-(chloromethyl)-5-[(4-chlorophenyl)methyl]-2-methyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentan-1-ol Chemical compound C([C@H]1CC[C@]([C@]1(O)CN1N=CN=C1)(CCl)C)C1=CC=C(Cl)C=C1 SPXBEYPYQKZKGX-PVAVHDDUSA-N 0.000 abstract 1
- HPMOLIHDZUCPIZ-GXSJLCMTSA-N (2R)-2-(1-chlorocyclopropyl)-4-[(1S)-2,2-dichlorocyclopropyl]-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound O[C@](CC[C@H]1CC1(Cl)Cl)(Cn1cncn1)C1(Cl)CC1 HPMOLIHDZUCPIZ-GXSJLCMTSA-N 0.000 abstract 1
- HPMOLIHDZUCPIZ-KOLCDFICSA-N (2S)-2-(1-chlorocyclopropyl)-4-[(1R)-2,2-dichlorocyclopropyl]-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound O[C@@](CC[C@@H]1CC1(Cl)Cl)(Cn1cncn1)C1(Cl)CC1 HPMOLIHDZUCPIZ-KOLCDFICSA-N 0.000 abstract 1
- HPMOLIHDZUCPIZ-ONGXEEELSA-N (2S)-2-(1-chlorocyclopropyl)-4-[(1S)-2,2-dichlorocyclopropyl]-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound O[C@@](CC[C@H]1CC1(Cl)Cl)(Cn1cncn1)C1(Cl)CC1 HPMOLIHDZUCPIZ-ONGXEEELSA-N 0.000 abstract 1
- XDEHMKQLKPZERH-BYPYZUCNSA-N (2s)-2-amino-3-methylbutanamide Chemical compound CC(C)[C@H](N)C(N)=O XDEHMKQLKPZERH-BYPYZUCNSA-N 0.000 abstract 1
- DBTMGCOVALSLOR-DEVYUCJPSA-N (2s,3r,4s,5r,6r)-4-[(2s,3r,4s,5r,6r)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-(hydroxymethyl)oxane-2,3,5-triol Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](CO)O[C@H](O)[C@@H]2O)O)O[C@H](CO)[C@H]1O DBTMGCOVALSLOR-DEVYUCJPSA-N 0.000 abstract 1
- AESOVJYUXGEHCV-UHFFFAOYSA-N (5-bromo-2-methoxy-4-methylpyridin-3-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(C)C(Br)=CN=C1OC AESOVJYUXGEHCV-UHFFFAOYSA-N 0.000 abstract 1
- JERZEQUMJNCPRJ-KRWDZBQOSA-N (R)-mefentrifluconazole Chemical compound C([C@@](O)(C)C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)C(F)(F)F)N1C=NC=N1 JERZEQUMJNCPRJ-KRWDZBQOSA-N 0.000 abstract 1
- ZEXXEODAXHSRDJ-FQEVSTJZSA-N (S)-fluoxapiprolin Chemical compound CS(=O)(=O)Oc1cccc(Cl)c1[C@@H]1CC(=NO1)c1csc(n1)C1CCN(CC1)C(=O)Cn1nc(cc1C(F)F)C(F)F ZEXXEODAXHSRDJ-FQEVSTJZSA-N 0.000 abstract 1
- PDPWCKVFIFAQIQ-SFHVURJKSA-N (S)-mandestrobin Chemical compound CNC(=O)[C@@H](OC)C1=CC=CC=C1COC1=CC(C)=CC=C1C PDPWCKVFIFAQIQ-SFHVURJKSA-N 0.000 abstract 1
- JERZEQUMJNCPRJ-QGZVFWFLSA-N (S)-mefentrifluconazole Chemical compound C([C@](O)(C)C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)C(F)(F)F)N1C=NC=N1 JERZEQUMJNCPRJ-QGZVFWFLSA-N 0.000 abstract 1
- IAQLCKZJGNTRDO-IBGZPJMESA-N (S)-oxathiapiprolin Chemical compound CC1=CC(C(F)(F)F)=NN1CC(=O)N1CCC(C=2SC=C(N=2)C=2C[C@H](ON=2)C=2C(=CC=CC=2F)F)CC1 IAQLCKZJGNTRDO-IBGZPJMESA-N 0.000 abstract 1
- YDHZUCLRCLIJRL-HXUWFJFHSA-N (r)-[3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl]-pyridin-3-ylmethanol Chemical compound C=1([C@H](O)C=2C=NC=CC=2)C(C=2C(=CC(Cl)=CC=2)F)=NOC=1C1=CC=C(F)C=C1F YDHZUCLRCLIJRL-HXUWFJFHSA-N 0.000 abstract 1
- YDHZUCLRCLIJRL-FQEVSTJZSA-N (s)-[3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl]-pyridin-3-ylmethanol Chemical compound C=1([C@@H](O)C=2C=NC=CC=2)C(C=2C(=CC(Cl)=CC=2)F)=NOC=1C1=CC=C(F)C=C1F YDHZUCLRCLIJRL-FQEVSTJZSA-N 0.000 abstract 1
- QEUOHPLVFSQWME-CYVLTUHYSA-N (z)-3-(4-tert-butylphenyl)-3-(2-chloropyridin-4-yl)-1-morpholin-4-ylprop-2-en-1-one Chemical compound C1=CC(C(C)(C)C)=CC=C1C(\C=1C=C(Cl)N=CC=1)=C\C(=O)N1CCOCC1 QEUOHPLVFSQWME-CYVLTUHYSA-N 0.000 abstract 1
- XBCKTJDKWPZLJH-ZUPCBTBPSA-N (z,2e)-5-[1-(4-chlorophenyl)pyrazol-3-yl]oxy-2-methoxyimino-n,3-dimethylpent-3-enamide Chemical compound N1=C(OC\C=C(\C)/C(=N\OC)/C(=O)NC)C=CN1C1=CC=C(Cl)C=C1 XBCKTJDKWPZLJH-ZUPCBTBPSA-N 0.000 abstract 1
- 125000003626 1,2,4-triazol-1-yl group Chemical group [*]N1N=C([H])N=C1[H] 0.000 abstract 1
- DGWHDIYEULVUTH-UHFFFAOYSA-N 1-(1,2,4-triazol-1-yl)propan-2-ol Chemical compound CC(O)CN1C=NC=N1 DGWHDIYEULVUTH-UHFFFAOYSA-N 0.000 abstract 1
- BQYJATMQXGBDHF-DJJJIMSYSA-N 1-[[(2r,4s)-2-[2-chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-1,3-dioxolan-2-yl]methyl]-1,2,4-triazole Chemical compound O1[C@@H](C)CO[C@@]1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-DJJJIMSYSA-N 0.000 abstract 1
- BQYJATMQXGBDHF-ORAYPTAESA-N 1-[[(2s,4s)-2-[2-chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-1,3-dioxolan-2-yl]methyl]-1,2,4-triazole Chemical compound O1[C@@H](C)CO[C@]1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-ORAYPTAESA-N 0.000 abstract 1
- 125000006426 1-chlorocyclopropyl group Chemical group [H]C1([H])C([H])([H])C1(Cl)* 0.000 abstract 1
- HILAYQUKKYWPJW-UHFFFAOYSA-N 1-dodecylguanidine Chemical compound CCCCCCCCCCCCN=C(N)N HILAYQUKKYWPJW-UHFFFAOYSA-N 0.000 abstract 1
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 abstract 1
- OKRROXQXGNEUSS-UHFFFAOYSA-N 1h-imidazol-1-ium-1-carboxylate Chemical compound OC(=O)N1C=CN=C1 OKRROXQXGNEUSS-UHFFFAOYSA-N 0.000 abstract 1
- OILIYWFQRJOPAI-UHFFFAOYSA-N 2-(2-chlorophenyl)-1h-benzimidazole Chemical compound ClC1=CC=CC=C1C1=NC2=CC=CC=C2N1 OILIYWFQRJOPAI-UHFFFAOYSA-N 0.000 abstract 1
- DNBMPXLFKQCOBV-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OCCOCCOCC)=NC2=C1 DNBMPXLFKQCOBV-UHFFFAOYSA-N 0.000 abstract 1
- KWLVWJPJKJMCSH-UHFFFAOYSA-N 2-(4-chlorophenyl)-N-{2-[3-methoxy-4-(prop-2-yn-1-yloxy)phenyl]ethyl}-2-(prop-2-yn-1-yloxy)acetamide Chemical compound C1=C(OCC#C)C(OC)=CC(CCNC(=O)C(OCC#C)C=2C=CC(Cl)=CC=2)=C1 KWLVWJPJKJMCSH-UHFFFAOYSA-N 0.000 abstract 1
- AGVACZYQCJRDQE-UHFFFAOYSA-N 2-(6-benzylpyridin-2-yl)quinazoline Chemical compound C=1C=CC(C=2N=C3C=CC=CC3=CN=2)=NC=1CC1=CC=CC=C1 AGVACZYQCJRDQE-UHFFFAOYSA-N 0.000 abstract 1
- SPXBEYPYQKZKGX-UHFFFAOYSA-N 2-(chloromethyl)-5-[(4-chlorophenyl)methyl]-2-methyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentan-1-ol Chemical compound C1=NC=NN1CC1(O)C(C)(CCl)CCC1CC1=CC=C(Cl)C=C1 SPXBEYPYQKZKGX-UHFFFAOYSA-N 0.000 abstract 1
- IYRCSBXNZXXLHZ-LYRGGWFBSA-N 2-[(2r,4r,5r)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-1h-1,2,4-triazole-3-thione Chemical compound N1([C@@H]([C@H](O)C(C)(C)C)C[C@H](C)CC=2C(=CC(Cl)=CC=2)Cl)NC=NC1=S IYRCSBXNZXXLHZ-LYRGGWFBSA-N 0.000 abstract 1
- IYRCSBXNZXXLHZ-HFBAOOFYSA-N 2-[(2r,4r,5s)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-1h-1,2,4-triazole-3-thione Chemical compound N1([C@@H]([C@@H](O)C(C)(C)C)C[C@H](C)CC=2C(=CC(Cl)=CC=2)Cl)NC=NC1=S IYRCSBXNZXXLHZ-HFBAOOFYSA-N 0.000 abstract 1
- IYRCSBXNZXXLHZ-XFBWCDHKSA-N 2-[(2r,4s,5s)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-1h-1,2,4-triazole-3-thione Chemical compound N1([C@H]([C@@H](O)C(C)(C)C)C[C@H](C)CC=2C(=CC(Cl)=CC=2)Cl)NC=NC1=S IYRCSBXNZXXLHZ-XFBWCDHKSA-N 0.000 abstract 1
- QKJJCZYFXJCKRX-HZHKWBLPSA-N 2-[(2s,3s,6r)-6-[4-amino-5-(hydroxymethyl)-2-oxopyrimidin-1-yl]-3-[[(2s)-2-amino-3-hydroxypropanoyl]amino]-3,6-dihydro-2h-pyran-2-yl]-5-(diaminomethylideneamino)-2,4-dihydroxypentanoic acid Chemical compound O1[C@H](C(O)(CC(O)CN=C(N)N)C(O)=O)[C@@H](NC(=O)[C@H](CO)N)C=C[C@@H]1N1C(=O)N=C(N)C(CO)=C1 QKJJCZYFXJCKRX-HZHKWBLPSA-N 0.000 abstract 1
- IYRCSBXNZXXLHZ-XZJROXQQSA-N 2-[(2s,4r,5r)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-1h-1,2,4-triazole-3-thione Chemical compound N1([C@@H]([C@H](O)C(C)(C)C)C[C@@H](C)CC=2C(=CC(Cl)=CC=2)Cl)NC=NC1=S IYRCSBXNZXXLHZ-XZJROXQQSA-N 0.000 abstract 1
- IYRCSBXNZXXLHZ-IUIKQTSFSA-N 2-[(2s,4r,5s)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-1h-1,2,4-triazole-3-thione Chemical compound N1([C@@H]([C@@H](O)C(C)(C)C)C[C@@H](C)CC=2C(=CC(Cl)=CC=2)Cl)NC=NC1=S IYRCSBXNZXXLHZ-IUIKQTSFSA-N 0.000 abstract 1
- IYRCSBXNZXXLHZ-UVBJJODRSA-N 2-[(2s,4s,5r)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-1h-1,2,4-triazole-3-thione Chemical compound N1([C@H]([C@H](O)C(C)(C)C)C[C@@H](C)CC=2C(=CC(Cl)=CC=2)Cl)NC=NC1=S IYRCSBXNZXXLHZ-UVBJJODRSA-N 0.000 abstract 1
- ZEXXEODAXHSRDJ-UHFFFAOYSA-N 2-[(ethanesulfonyl)amino]-5-fluoro-4-[4-methyl-5-oxo-3-(trifluoromethyl)-4,5-dihydro-1H-1,2,4-triazol-1-yl]benzene-1-carbothioamide Chemical compound CS(=O)(=O)OC1=CC=CC(Cl)=C1C1ON=C(C=2N=C(SC=2)C2CCN(CC2)C(=O)CN2C(=CC(=N2)C(F)F)C(F)F)C1 ZEXXEODAXHSRDJ-UHFFFAOYSA-N 0.000 abstract 1
- IYRCSBXNZXXLHZ-UHFFFAOYSA-N 2-[1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-1h-1,2,4-triazole-3-thione Chemical compound C=1C=C(Cl)C=C(Cl)C=1CC(C)CC(C(O)C(C)(C)C)N1N=CNC1=S IYRCSBXNZXXLHZ-UHFFFAOYSA-N 0.000 abstract 1
- APQLZYDMZKPQFH-HXUWFJFHSA-N 2-[1-[2-[5-methyl-3-(trifluoromethyl)pyrazol-1-yl]acetyl]piperidin-4-yl]-n-[(1r)-1,2,3,4-tetrahydronaphthalen-1-yl]-1,3-thiazole-4-carboxamide Chemical compound CC1=CC(C(F)(F)F)=NN1CC(=O)N1CCC(C=2SC=C(N=2)C(=O)N[C@H]2C3=CC=CC=C3CCC2)CC1 APQLZYDMZKPQFH-HXUWFJFHSA-N 0.000 abstract 1
- GSSLIXUCWSWMKG-UHFFFAOYSA-N 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C=1C=C(OC=2C=CC(Cl)=CC=2)C=C(Cl)C=1C(O)(CC)CN1C=NC=N1 GSSLIXUCWSWMKG-UHFFFAOYSA-N 0.000 abstract 1
- GYATVWZBWGYBFH-UHFFFAOYSA-N 2-[2-fluoro-6-(8-fluoro-2-methylquinolin-3-yl)oxyphenyl]propan-2-ol Chemical compound CC1=NC2=C(F)C=CC=C2C=C1OC1=CC=CC(F)=C1C(C)(C)O GYATVWZBWGYBFH-UHFFFAOYSA-N 0.000 abstract 1
- HSUIUGJIZSLSPE-UHFFFAOYSA-N 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C=1C=C(OC=2C=CC(Cl)=CC=2)C=C(C(F)(F)F)C=1C(O)(CC)CN1C=NC=N1 HSUIUGJIZSLSPE-UHFFFAOYSA-N 0.000 abstract 1
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- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 abstract 1
- JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 abstract 1
- DBXFMOWZRXXBRN-LWKPJOBUSA-N valifenalate Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)NC(CC(=O)OC)C1=CC=C(Cl)C=C1 DBXFMOWZRXXBRN-LWKPJOBUSA-N 0.000 abstract 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 abstract 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 abstract 1
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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- 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
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- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/34—Nitriles
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- 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
- A01N43/42—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 condensed with carbocyclic rings
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- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
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- 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
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
- A01N47/14—Di-thio analogues thereof
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- 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
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/18—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pretreatment Of Seeds And Plants (AREA)
Abstract
Reivindicación 1: Combinaciones que comprenden: (A) al menos una de fórmula (1) donde X¹, X² independientemente representa H, halógeno, alquilo-C₁₋₈, haloalquilo-C₁₋₈, alquiloxi-C₁₋₈, alquilsulfanilo-C₁₋₈, ciano; R¹ representa H, alquilo-C₁₋₈, haloalquilo-C₁₋₈, cicloalquilo-C₃₋₈, halocicloalquilo-C₃₋₈, alquilo-C₁₋₄-cicloalquilo-C₃₋₈; alquilo-C₁₋₄-halocicloalquilo-C₃₋₈; R², R³ independientemente representan H, alquilo-C₁₋₈, haloalquilo-C₁₋₈, cicloalquilo-C₃₋₈, halocicloalquilo-C₃₋₈, alquilo-C₁₋₄-cicloalquilo-C₃₋₈, alquilo-C₁₋₄-halocicloalquilo-C₃₋₈; o una sal agroquímicamente aceptable de estos, y (B) al menos un compuesto activo adicional que se selecciona de los siguientes grupos: 1) Inhibidores de la biosíntesis de ergosterol, por ejemplo (1.065) Pirisoxazol, (1.066) 2-{[3-(2-clorofenil)-2-(2,4-difluorofenil)oxiran-2-il]metil}-2,4-dihidro-3H-1,2,4-triazol-3-tiona, (1.067) 1-{[3-(2-clorofenil)-2-(2,4-difluorofenil)oxiran-2-il]metil}-1H-1,2,4-triazol-5-il tiocianato, (1.068) 5-(alilsulfanil)-1-{[3-(2-clorofenil)-2-(2,4-difluorofenil)oxiran-2-il]metil}-1H-1,2,4-triazol, (1.069) 2-[1-(2,4-diclorofenil)-5-hidroxi-2,6,6-trimetilheptan-4-il]-2,4-dihidro-3H-1,2,4-triazol-3-tiona, (1.070) 2-{[rel(2R,3S)-3-(2-clorofenil)-2-(2,4-difluorofenil)oxiran-2-il]metil}-2,4-dihidro-3H-1,2,4-triazol-3-tiona, (1.071) 2-{[rel(2R,3R)-3-(2-clorofenil)-2-(2,4-difluorofenil)oxiran-2-il]metil}-2,4-dihidro-3H-1,2,4-triazol-3-tiona, (1.072) 1-{[rel(2R,3S)-3-(2-clorofenil)-2-(2,4-difluorofenil)oxiran-2-il]metil}-1H-1,2,4-triazol-5-il tiocianato, (1.073) 1-{[rel(2R,3R)-3-(2-clorofenil)-2-(2,4-difluorofenil)oxiran-2-il]metil}-1H-1,2,4-triazol-5-il tiocianato, (1.074) 5-(alilsulfanil)-1-{[rel(2R,3S)-3-(2-clorofenil)-2-(2,4-difluorofenil)oxiran-2-il]metil}-1H-1,2,4-triazol, (1.075) 5-(alilsulfanil)-1-{[rel(2R,3R)-3-(2-clorofenil)-2-(2,4-difluorofenil)oxiran-2-il]metil}-1H-1,2,4-triazol, (1.076) 2-[(2S,4S,5S)-1-(2,4-diclorofenil)-5-hidroxi-2,6,6-trimetilheptan-4-il]-2,4-dihidro-3H-1,2,4-triazol-3-tiona, (1.077) 2-[(2R,4S,5S)-1-(2,4-diclorofenil)-5-hidroxi-2,6,6-trimetilheptan-4-il]-2,4-dihidro-3H-1,2,4-triazol-3-tiona, (1.078) 2-[(2R,4R,5R)-1-(2,4-diclorofenil)-5-hidroxi-2,6,6-trimetilheptan-4-il]-2,4-dihidro-3H-1,2,4-triazol-3-tiona, (1.079) 2-[(2S,4R,5R)-1-(2,4-diclorofenil)-5-hidroxi-2,6,6-trimetilheptan-4-il]-2,4-dihidro-3H-1,2,4-triazol-3-tiona, (1.080) 2-[(2S,4S,5R)-1-(2,4-diclorofenil)-5-hidroxi-2,6,6-trimetilheptan-4-il]-2,4-dihidro-3H-1,2,4-triazol-3-tiona, (1.081) 2-[(2R,4S,5R)-1-(2,4-diclorofenil)-5-hidroxi-2,6,6-trimetilheptan-4-il]-2,4-dihidro-3H-1,2,4-triazol-3-tiona, (1.082) 2-[(2R,4R,5S)-1-(2,4-diclorofenil)-5-hidroxi-2,6,6-trimetilheptan-4-il]-2,4-dihidro-3H-1,2,4-triazol-3-tiona, (1.083) 2-[(2S,4R,5S)-1-(2,4-diclorofenil)-5-hidroxi-2,6,6-trimetilheptan-4-il]-2,4-dihidro-3H-1,2,4-triazol-3-tiona, (1.084) 2-[4-(4-clorofenoxi)-2-(trifluorometil)fenil]-1-(1H-1,2,4-triazol-1-il)propan-2-ol, (1.085) 2-[4-(4-clorofenoxi)-2-(trifluorometil)fenil]-1-(1H-1,2,4-triazol-1-il)butan-2-ol, (1.086) 2-[4-(4-clorofenoxi)-2-(trifluorometil)fenil]-1-(1H-1,2,4-triazol-1-il)pentan-2-ol, (1.087) 2-[2-cloro-4-(4-clorofenoxi)fenil]-1-(1H-1,2,4-triazol-1-il)butan-2-ol, (1.088) 2-[2-cloro-4-(2,4-diclorofenoxi)fenil]-1-(1H-1,2,4-triazol-1-il)propan-2-ol, (1.089) (2R)-2-(1-clorociclopropil)-4-[(1R)-2,2-diclorociclopropil]-1-(1H-1,2,4-triazol-1-il)butan-2-ol, (1.090) (2R)-2-(1-clorociclopropil)-4-[(1S)-2,2-diclorociclopropil]-1-(1H-1,2,4-triazol-1-il)butan-2-ol, (1.091) (2S)-2-(1-clorociclopropil)-4-[(1S)-2,2-diclorociclopropil]-1-(1H-1,2,4-triazol-1-il)butan-2-ol, (1.092) (2S)-2-(1-clorociclopropil)-4-[(1R)-2,2-diclorociclopropil]-1-(1H-1,2,4-triazol-1-il)butan-2-ol, (1.093) (1S,2R,5R)-5-(4-clorobenzil)-2-(clorometil)-2-metil-1-(1H-1,2,4-triazol-1-ilmetil)ciclopentanol, (1.094) (1R,2S,5S)-5-(4-clorobenzil)-2-(clorometil)-2-metil-1-(1H-1,2,4-triazol-1-ilmetil)ciclopentanol, (1.095) 5-(4-clorobenzil)-2-(clorometil)-2-metil-1-(1H-1,2,4-triazol-1-ilmetil)ciclopentanol, (1.096) (2R)-2-[4-(4-clorofenoxi)-2-(trifluorometil)fenil]-1-(1H-1,2,4-triazol-1-il)propan-2-ol, (1.097) (2S)-2-[4-(4-clorofenoxi)-2-(trifluorometil)fenil]-1-(1H-1,2,4-triazol-1-il)propan-2-ol, (1.098) 1-({(2R,4S)-2-[2-cloro-4-(4-clorofenoxi)fenil]-4-metil-1,3-dioxolan-2-il}metil)-1H-1,2,4-triazol, (1.099) 1-({(2S,4S)-2-[2-cloro-4-(4-clorofenoxi)fenil]-4-metil-1,3-dioxolan-2-il}metil)-1H-1,2,4-triazol, (1.100) fenpirazamina, (1.101) N-(4-{[3-(4-clorobenzil)-1,2,4-tiadiazol-5-il]oxi}-2,5-dimetilfenil)-N-etil-N-metilimidoformamida, (1.102) N-{4-[(3-tert-butil-4-ciano-1,2-tiazol-5-il)oxi]-2-cloro-5-metilfenil}-N-etil-N-metilimidoformamida, (1.103) [3-(4-cloro-2-fluorofenil)-5-(2,4-difluorofenil)-1,2-oxazol-4-il](piridin-3-il)metanol, (1.104) (S)-[3-(4-cloro-2-fluorofenil)-5-(2,4-difluorofenil)-1,2-oxazol-4-il](piridin-3-il)metanol, (1.105) (R)-[3-(4-cloro-2-fluorofenil)-5-(2,4-difluorofenil)-1,2-oxazol-4-il](piridin-3-il)metanol, (1.106) N-[5-bromo-6-(2,3-dihidro-1H-inden-2-iloxi)-2-metilpiridin-3-il]-N-etil-N-metilimidoformamida, (1.107) N-{5-bromo-6-[1-(3,5-difluorofenil)etoxi]-2-metilpiridin-3-il}-N-etil-N-metilimidoformamida, (1.108) N-{5-bromo-6-[(1R)-1-(3,5-difluorofenil)etoxi]-2-metilpiridin-3-il}-N-etil-N-metilimidoformamida, (1.109) N-{5-bromo-6-[(1S)-1-(3,5-difluorofenil)etoxi]-2-metilpiridin-3-il}-N-etil-N-metilimidoformamida, (1.110) N-{5-bromo-6-[(cis-4-isopropilciclohexil)oxi]-2-metilpiridin-3-il}-N-etil-N-metilimidoformamida, (1.111) N-{5-bromo-6-[(trans-4-isopropiciclohexil)oxi]-2-metilpiridin-3-il}-N-etil-N-metilimidoformamida, (1.112) N-(2,5-dimetil-4-fenoxifenil)-N-etil-N-metilimidoformamida, (1.113) N-{4-[(4,5-dicloro-1,3-tiazol-2-il)oxi]-2,5-dimetilfenil}-N-etil-N-metilimidoformamida, (1.114) N-(4-{3-[(difluorometil)sulfanil]fenoxi}-2,5-dimetilfenil)-N-etil-N-metilimidoformamida, (1.115) N-(2,5-dimetil-4-{3-[(1,1,2,2-tetrafluoroetil)sulfanil]fenoxi}fenil)-N-etil-N-metilimidoformamida, (1.116) N-(2,5-dimetil-4-{3-[(2,2,2-trifluoroetil)sulfanil]fenoxi}fenil)-N-etil-N-metilimidoformamida, (1.117) N-(2,5-dimetil-4-{3-[(2,2,3,3-tetrafluoropropil)sulfanil]fenoxi}fenil)-N-etil-N-metilimidoformamida, (1.118) N-(2,5-dimetil-4-{3-[(pentafluoroetil)sulfanil]fenoxi}fenil)-N-etil-N-metilimidoformamida, (1.119) N-(4-{[3-(difluorometoxi)fenil]sulfanil}-2,5-dimetilfenil)-N-etil-N-metilimidoformamida, (1.120) N-(2,5-dimetil-4-{[3-(1,1,2,2-tetrafluoroetoxi)fenil]sulfanil}fenil)-N-etil-N-metilimidoformamida, (1.121) N-(2,5-dimetil-4-{[3-(2,2,2-trifluoroetoxi)fenil]sulfanil}fenil)-N-etil-N-metilimidoformamida, (1.122) N-(2,5-dimetil-4-{[3-(2,2,3,3-tetrafluoropropoxi)fenil]sulfanil}fenil)-N-etil-N-metilimidoformamida, (1.123) N-(2,5-dimetil-4-{[3-(pentafluoroetoxi)fenil]sulfanil}fenil)-N-etil-N-metilimidoformamida; 3) Inhibidores de la cadena respiratoria en el complejo III, por ejemplo (3.027) Fenaminostrobina, (3.033) (2E,3Z)-5-{[1-(4-clorofenil)-1H-pirazol-3-il]oxi}-2-(metoxiimino)-N,3-dimetilpent-3-enamida, (3.034) (2S)-2-{2-[(2,5-dimetilfenoxi)metil]fenil}-2-metoxi-N-metilacetamida, (3.035) (3S,6S,7R,8R)-8-bencil-3-[({3-[(isobutiriloxi)metoxi]-4-metoxipiridin-2-il}carbonil)amino]-6-metil-4,9-dioxo-1,5-dioxonan-7-il 2-metilpropanoato; 4) Inhibidores de la mitosis y división celular, por ejemplo (4.001) benomilo, (4.002) carbendazim, (4.003) clorfenazol, (4.004) dietofencarb, (4.005) etaboxam, (4.006) fluopicolida, (4.007) fuberidazol, (4.008) pencicuron, (4.009) tiabendazol, (4.010) tiofanato-metilo, (4.011) tiofanato, (4.012) zoxamida, (4.013) 5-cloro-7-(4-metilpiperidin-1-il)-6-(2,4,6-trifluorofenil)[1,2,4]triazolo[1,5-a]pirimidina, (4.014) 3-cloro-5-(6-cloropiridin-3-il)-6-metil-4-(2,4,6-trifluorofenil)piridazina, (4.015) 3-cloro-5-(4-clorofenil)-4-(2,6-difluorofenil)-6-metilpiridazina, (4.016) 4-(4-clorofenil)-5-(2,6-difluorofenil)-3,6-dimetilpiridazina, (4.017) N-[(5-bromo-3-cloropiridin-2-il)metil]-2,4-dicloronicotinamida, (4.018) N-[1-(5-bromo-3-cloropiridin-2-il)etil]-2,4-dicloronicotinamida, (4.019) N-[1-(5-bromo-3-cloropiridin-2-il)etil]-2-fluoro-4-yodonicotinamida, (4.020) N-(4-cloro-2,6-difluorofenil)-4-(2-cloro-4-fluorofenil)-1,3-dimetil-1H-pirazol-5-amina, (4.021) 4-(2-cloro-4-fluorofenil)-N-(2-fluorofenil)-1,3-dimetil-1H-pirazol-5-amina, (4.022) 4-(2-cloro-4-fluorofenil)-N-(2,6-difluorofenil)-1,3-dimetil-1H-pirazol-5-amina, (4.023) 4-(2-cloro-4-fluorofenil)-N-(2-cloro-6-fluorofenil)-1,3-dimetil-1H-pirazol-5-amina, (4.024) 4-(2-bromo-4-fluorofenil)-N-(2-cloro-6-fluorofenil)-1,3-dimetil-1H-pirazol-5-amina, (4.025) N-(2-bromo-6-fluorofenil)-4-(2-cloro-4-fluorofenil)-1,3-dimetil-1H-pirazol-5-amina, (4.026) 4-(2-bromo-4-fluorofenil)-N-(2-bromofenil)-1,3-dimetil-1H-pirazol-5-amina, (4.027) 4-(2-bromo-4-fluorofenil)-N-(2-bromo-6-fluorofenil)-1,3-dimetil-1H-pirazol-5-amina, (4.028) 4-(2-bromo-4-fluorofenil)-N-(2-clorofenil)-1,3-dimetil-1H-pirazol-5-amina, (4.029) N-(2-bromofenil)-4-(2-cloro-4-fluorofenil)-1,3-dimetil-1H-pirazol-5-amina, (4.030) 4-(2-cloro-4-fluorofenil)-N-(2-clorofenil)-1,3-dimetil-1H-pirazol-5-amina, (4.031) 4-(2-bromo-4-fluorofenil)-N-(2,6-difluorofenil)-1,3-dimetil-1H-pirazol-5-amina, (4.032) 4-(2-bromo-4-fluorofenil)-N-(2-fluorofenil)-1,3-dimetil-1H-pirazol-5-amina, (4.033) 3-cloro-4-(2,6-difluorofenil)-6-metil-5-fenilpiridazina; 5) Los compuestos capaces de tener una acción multisitio, por ejemplo (5.001) mezcla bordeaux, (5.002) captafol, (5.003) captan, (5.004) clorotalonil, (5.005) hidróxido de cobre, (5.006) naftenato de cobre, (5.007) óxido de cobre, (5.008) oxicloruro de cobre, (5.009) sulfato de cobre(2+), (5.010) diclofluanid, (5.011) ditianon, (5.012) dodina, (5.013) dodina base libre, (5.014) ferbam, (5.015) fluorofolpet, (5.016) folpet, (5.017) guazatina, (5.018) guazatina acetato, (5.019) iminoctadina, (5.020) iminoctadina albesilato, (5.021) iminoctadina triacetato, (5.022) mancobre, (5.023) mancozeb, (5.024) maneb, (5.025) metiram, (5.026) metiram zinc, (5.027) oxina-cobre, (5.028) propamidina, (5.029) propineb, (5.030) azufre y preparaciones de azufre que incluyen polisulfuro de calcio, (5.031) tiram, (5.032) tolilfluanid, (5.033) zineb, (5.034) ziram, (5.035) anilazina; 6) Los compuestos capaces de inducir una defensa al hospedador, por ejemplo (6.001) acibenzolar-S-metilo, (6.002) isotianil, (6.003) probenazol, (6.004) tiadinil, (6.005) laminarin; 7) Los inhibidores de la biosíntesis de aminoácido y/o proteína, por ejemplo (7.001) andoprim, (7.002) blasticidina-S, (7.003) ciprodinil, (7.004) kasugamicina, (7.005) kasugamicina clorhidrato hidrato, (7.006) mepanipirim, (7.007) pirimetanil, (7.008) 3-(5-fluoro-3,3,4,4-tetrametil-3,4-dihidroisoquinolin-1-il)quinolina, (7.009) oxitetraciclina, (7.010) streptomicina; 8) Inhibidores de la producción de ATP, por ejemplo (8.001) fentin acetato, (8.002) fentin cloruro, (8.003) fentin hidróxido, (8.004) siltiofam; 9) Inhibidores de la síntesis de la pared celular, por ejemplo (9.001) bentiavalicarb, (9.002) dimetomorf, (9.003) flumorf, (9.004) iprovalicarb, (9.005) mandipropamid, (9.006) polioxinas, (9.007) polioxorim, (9.008) validamicina A, (9.009) valifenalato, (9.010) polioxina B, (9.011) (2E)-3-(4-terc-butilfenil)-3-(2-cloropiridin-4-il)-1-(morfolin-4-il)prop-2-en-1-ona, (9.012) (2Z)-3-(4-terc-butilfenil)-3-(2-cloropiridin-4-il)-1-(morfolin-4-il)prop-2-en-1-ona, (9.013) pirimorf; 10) Inhibidores de la síntesis de membranas y lípidos, por ejemplo (10.001) bifenilo, (10.002) cloroneb, (10.003) dicloran, (10.004) edifenfos, (10.005) eiridiazol, (10.006) yodocarb, (10.007) iprobenfos, (10.008) isoprotiolano, (10.009) propamocarb, (10.010) propamocarb clorhidrato, (10.011) protiocarb, (10.012) pirazofos, (10.013) quintozeno, (10.014) tecnazeno, (10.015) tolclofos-metilo; 11) Inhibidores de la biosíntesis de melanina, por ejemplo (11.001) carpropamid, (11.002) diclocimet, (11.003) fenoxanil, (11.004) ftalida, (11.005) piroquilon, (11.006) triciclazol, (11.007) 2,2,2-trifluoroetil{3-metil-1-[(4-metilbenzoil)amino]butan-2-il}carbamato; 12) Inhibidores de la síntesis de ácido nucleico, por ejemplo (12.001) benalaxilo, (12.002) benalaxil-M (kiralaxilo), (12.003) bupirimato, (12.004) clozilacon, (12.005) dimetirimol, (12.006) etirimol, (12.007) furalaxilo, (12.008) himexazol, (12.009) metalaxilo, (12.010) metalaxil-M (mefenoxam), (12.011) ofurace, (12.012) oxadixilo, (12.013) ácido oxolínico, (12.01.4)octilinona; 13) Inhibidores de la transducción de señal, por ejemplo (13.001) clozolinato, (13.002) fenpiclonil, (13.003) fludioxonil, (13.004) iprodiona, (13.005) procimidona, (13.006) quinoxifen, (13.007) vinclozolin, (13.008) proquinazid; 14) Los compuestos capaces de actuar como desacoplador, por ejemplo (14.001) binapacrilo, (14.002) dinocap, (14.003) ferimzona, (14.004) fluazinam, (14.005) meptildinocap; 15) Otros compuestos, por ejemplo (15.001) bentiazol, (15.002) betoxazin, (15.003) capsimicina, (15.004) carvona, (15.005) chinometionat, (15.006) piriofenona (clazafenona), (15.007) cufraneb, (15.008) ciflufenamid, (15.009) cimoxanil, (15.010) ciprosulfamida, (15.011) dazomet, (15.012) debacarb, (15.013) diclorofeno, (15.014) diclomezina, (15.015) difenzoquat, (15.016) difenzoquat metilsulfato, (15.017) difenilamina, (15.018) ecomato, (15.019) flumetover, (15.020) fluoroimida, (15.021) flusulfamida, (15.022) flutianil, (15.023) fosetil-aluminio, (15.024) fosetil-calcio, (15.025) fosetil-sodio, (15.026) hexaclorobenceno, (15.027) irumamicina, (15.028) metasulfocarb, (15.029) metil isotiocianato, (15.030) metrafenona, (15.031) mildiomicina, (15.032) natamicina, (15.033) níquel dimetilditiocarbamato, (15.034) nitrotal-isopropilo, (15.035) oxamocarb, (15.036) oxifentiin, (15.037) pentaclorofenol y sales, (15.038) fenotrina, (15.039) ácido fosfórico y sus sales, (15.040) propamocarb-fosetilato, (15.041) propanosina-sodio, (15.042) pirrolnitrina, (15.043) tebufloquin, (15.044) tecloftalam, (15.045) tolnifanida, (15.046) triazoxida, (15.047) triclamida, (15.048) zarilamid, (15.049) 1-(4-{4-[(5R)-5-(2,6-difluorofenil)-4,5-dihidro-1,2-oxazol-3-il]-1,3-tiazol-2-il}piperidin-1-il)-2-[5-metil-3-(trifluorometil)-1H-pirazol-1-il]etanona, (15.050) 1-(4-{4-[(5S)-5-(2,6-difluorofenil)-4,5-dihidro-1,2-oxazol-3-il]-1,3-tiazol-2-il}piperidin-1-il)-2-[5-metil-3-(trifluorometil)-1H-pirazol-1-il]etanona, (15.051) Oxatiapiprolina, (15.052) 1-(4-inetoxifenoxi)-3,3-dimetilbutan-2-il 1H-imidazol-1-carboxilato, (15.053) 2,3,5,6-tetracloro-4-(metilsulfonil)piridina, (15.054) 2,3-dibutil-6,-clorotieno[2,3-d]pirimidin-4(3H)-ona, (15.055) 2,6-dimetil-1H,5H-[1,4]ditiino[2,3-c:5,6-c]dipirrolo-1,3,5,7(2H,6H)-tetrona, (15.056) 2-[5-metil-3-(trifluorometil)-1H-pirazol-1-il]-1-(4-{4-[(5R)-5-fenil-4,5-dihidro-1,2-oxazol-3-il]-1,3-tiazol-2-il}piperidin-1-il)etanona, (15.057) 2-[5-metil-3-(trifluorometil)-1H-pirazol-1-il]-1-(4-{4-[(5S)-5-fenil-4,5-dihidro-1,2-oxazol-3-il]-1,3-tiazol-2-il}piperidin-1-il)etanona, (15.058) 2-[5-metil-3-(trifluorometil)-1H-pirazol-1-il]-1-{4-[4-(5-fenil-4,5-dihidro-1,2-oxazol-3-il)-1,3-tiazol-2-il]piperidin-1-il}etanona, (15.059) 2-butoxi-6-yodo-3-propil-4H-cromen-4-ona, (15.060) 2-cloro-5-[2-cloro-1-(2,6-difluoro-4-metoxifenil)-4-metil-1H-imidazol-5-il]piridina, (15.061) 2-fenilfenol y sales, (15.062) 3-(4,4,5-trifluoro-3,3-dimetil-3,4-dihidroisoquinolin-1-il)quinolina, (15.063) 3,4,5-triocloropiridina-2,6-dicarbonitrilo, (15.064) 5-amino-1,3,4-tiadiazol-2-tiol, (15.065) 5-cloro-N-fenil-N-(prop-2-in-1-il)tiofeno-2-sulfonohidrazida, (15.066) 5-fluoro-2-[(4-fluorobencil)oxi]pirimidin-4-amina, (15.067) 5-fluoro-2-[(4-metilbencil)oxi]pirimidin-4-amina, (15.068) 5-metil-6-octil[1,2,4]triazolo[1,5-a]pirimidin-7-amina, (15.069) etil (2Z)-3-amino-2-ciano-3-fenilacrilato, (15.070) N-(4-clorobencil)-3-[3-metoxi-4-(prop-2-in-1-iloxi)fenil]propanamida, (15.071) N-[(4-clorofenil)(ciano)metil]-3-[3-metoxi-4-(prop-2-in-1-iloxi)fenil]propanamida, (15.072) N-{(E)-[(ciclopropilmetoxi)imino][6-(difluorometoxi)-2,3-difluorofenil]metil}-2-fenilacetamida, (15.073) N-{(Z)-[(ciclopropilmetoxi)imino][6-(difluorometoxi)-2,3-difluorofenil]metil}-2-fenilacetamida, (15.074) N-metil-2-(1-{[5-metil-3-(trifluorometil)-1H-pirazol-1-il]acetil}piperidin-4-il)-N-(1,2,3,4-tetrahidronaftalen-1-il)-1,3-tiazol-4-carboxamida, (15.075) N-metil-2-(1-{[5-metil-3-(trifluorometil)-1H-pirazol-1-il]acetil}piperidin-4-il)-N-[(1R)-1,2,3,4-tetrahidronaftalen-1-il]-1,3-tiazol-4-carboxamida, (15.076) N-metil-2-(1-{[5-metil-3-(trifluorometil)-1H-pirazol-1-il]acetil}piperidin-4-il)-N-[(1S)-1,2,3,4-tetrahidronaftalen-1-il]-1,3-tiazol-4-carboxamida, (15.077) pentil{6-[({[(1-metil-1H-tetrazol-5-il)(fenil)metileno]amino}oxi)metil]piridin-2-il}carbamato, (15.078) ácido fenazina-1-carboxílico, (15.079) quinolin-8-ol, (15.080) quinolin-8-ol sulfato (2:1), (15.081) terc-butil {6-[({[(1-metil-1H-tetrazol-5-il)(fenil)metileno]amino}oxi)metil]piridin-2-il}carbamato, (15.082) (5-bromo-2-metoxi-4-metilpiridin-3-il)(2,3,4-trimetoxi-6-metilfenil)metanona, (15.083) N-[2-(4-{[3-(4-clorofenil)prop-2-in-1-il]oxi}-3-metoxifenil)etil]-N2-(metilsulfonil)valinamida, (15.084) ácido 4-oxo-4-[(2-feniletil)amino]butanoico, (15.085) but-3-in-1-il{6-[({[(Z)-(1-metil-1H-tetrazol-5-il)(fenil)metileno]amino}oxi)metil]piridin-2-il}carbamato, (15.086) 4-amino-5-fluoropirimidin-2-ol (forma tautomérica: 4-amino-5-fluoropirimidin-2(1H)-ona), (15.087) propil 3,4,5-trihidroxibenzoato, (15.088) 2-(6-bencilpiridin-2-il)quinazolina, (15.089) 2-[6-(3-fluoro-4-metoxifenil)-5-metilpiridin-2-il]quinazolina, (15.090) 3-(4,4-difluoro-3,3-dimetil-3,4-dihidroisoquinolin-1-il)quinolina, (15.091) ácido abscísico, (15.092) 9-fluoro-2,2-dimetil-5-(quinolin-3-il)-2,3-dihidro-1,4-benzoxazepina, (15.093) 2-{2-fluoro-6-[(8-fluoro-2-metilquinolin-3-il)oxi]fenil}propan-2-ol, (15.094) 2-{2-[(7,8-difluoro-2-metilquinolin-3-il)oxi]-6-fluorofenil}propan-2-ol, (15.095) 2-[3,5-bis(difluorometil)-1H-pirazol-1-il]-1-[4-(4-{5-[2-(prop-2-in-1-iloxi)fenil]-4,5-dihidro-1,2-oxazol-3-il}-1,3-tiazol-2-il)piperidin-1-il]etanona, (15.096) 2-[3,5-bis(difluorometil)-1H-pirazol-1-il]-1-[4-(4-{5-[2-fluoro-6-(prop-2-in-1-iloxi)fenil]-4,5-dihidro-1,2-oxazol-3-il}-1,3-tiazol-2-il)piperidin-1-il]etanona, (15.097) 2-[3,5-bis(difluorometil)-1H-pirazol-1-il]-1-[4-(4-{S-[2-cloro-6-(prop-2-in-1-iloxi)fenil]-4,5-dihidro-1,2-oxazol-3-il}-1,3-tiazol-2-il)piperidin-1-il]etanona, (15.098) 2-{3-[2-(1-{[3,5-bis(difluorometil)-1H-pirazol-1-il]acetil}piperidin-4-il)-1,3-tiazol-4-il]-4,5-dihidro-1,2-oxazol-5-il}fenil metanosulfonato, (15.099) 2-{3-[2-(1-{[3,5-bis(difluorometil)-1H-pirazol-1-il]acetil}piperidin-4-il)-1,3-tiazol-4-il]-4,5-dihidro-1,2-oxazol-5-il}-3-clorofenil metanosulfonato, (15.100) 2-[3,5-bis(difluorometil)-1H-pirazol-1-il]-1-[4-(4-{(5S)-5-[2-(prop-2-in-1-iloxi)fenil]-4,5-dihidro-1,2-oxazol-3-il}-1,3-tiazol-2-il)piperidin-1-i]]etanona, (15.101) 2-[3,5-bis(difluorometil)-1H-pirazol-1-il]-1-[4-(4-{(5R)-5-[2-(prop-2-in-1-iloxi)fenil]-4,5-dihidro-1,2-oxazol-3-il}-1,3-tiazol-2-il)piperidin-1-il]etanona, (15.102) 2-[3,5-bis(difluorometil)-1H-pirazol-1-il]-1-[4-(4-{(5S)-5-[2-fluoro-6-(prop-2-in-1-iloxi)fenil]-4,5-dihidro-1,2-oxazol-3-il}-1,3-tiazol-2-il)piperidin-1-il]etanona, (15.103) 2-[3,5-bis(difluorometil)-1H-pirazol-1-il]-1-[4-(4-{(5R)-5-[2-flúor-6-(prop-2-in-1-iloxi)fenil]-4,5-dihidro-1,2-oxazol-3-il}-1,3-tiazol-2-il)piperidin-1-il]etanona, (15.104) 2-[3,5-bis(difluorometil)-1H-pirazol-1-il]-1-[4-(4-{(5S)-5-[2-cloro-6-(prop-2-in-1-iloxi)fenil]-4,5-dihidro-1,2-oxazol-3-il}-1,3-tiazol-2-il)piperidin-1-il]etanona, (15.105) 2-[3,5-bis(difluorometil)-1H-pirazol-1-il]-1-[4-(4-{(5R)-5-[2-cloro-6-(prop-2-in-1-iloxi)fenil]-4,5-dihidro-1,2-oxazol-3-il}-1,3-tiazol-2-il)piperidin-1-il]etanona, (15.106) 2-{(5S)-3-[2-(1-{[3,5-bis(difluorometil)-1H-pirazol-1-il]acetil}piperidin-4-il)-1,3-tiazol-4-il]-4,5-dihidro-1,2-oxazol-5-il}fenil metanosulfonato, (15.107) 2-{(5R)-3-[2-(1-{[3,5-bis(difluorometil)-1H-pirazol-1-il]acetil}piperidin-4-il)-1,3-tiazol-4-il]-4,5-dihidro-1,2-oxazol-5-il}fenil metanosulfonato, (15.108) 2-{(5S)-3-[2-(1-{[3,5-bis(difluorometil)-1H-pirazol-1-il]acetil}piperidin-4-il)-1,3-tiazol-4-il]-4,5-dihidro-1,2-oxazol-5-il}-3-clorofenil metanosulfonato, (15.109) 2-{(5R)-3-[2-(1-{[3,5-bis(difluorometil)-1H-pirazol-1-il]acetil}piperidin-4-il)-1,3-tiazol-4-il]-4,5-dihidro-1,2-oxazol-5-il}-3-clorofenil metanosulfonato. Reivindicación 5: Un método para controlar hongos fitopatogénicos dañinos, caracterizado por que las mezclas de acuerdo con la reivindicación 1 a 4 se aplican al hongo fitopatogénico dañino y/o su hábitat. Reivindicación 7: El uso de las mezclas de acuerdo con las reivindicaciones 1 a 4 para el control de hongos fitopatogénicos dañinos. Reivindicación 8: Un proceso para producir composiciones para controlar hongos fitopatogénicos dañinos, caracterizado por que las mezclas de acuerdo con las reivindicaciones 1 a 4 se mezclan con extensores y/o tensioactivos. Reivindicación 9: El uso de las mezclas de acuerdo con las reivindicaciones 1 a 4 para el tratamiento de plantas transgénicas. Reivindicación 10: El uso de mezclas de acuerdo con las reivindicaciones 1 a 4 para el tratamiento de semillas y de semillas de plantas transgénicas.
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| WO2017063973A1 (en) | 2015-10-14 | 2017-04-20 | Syngenta Participations Ag | Fungicidal compositions |
| WO2017178549A1 (en) | 2016-04-12 | 2017-10-19 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
| BR112018074943B1 (pt) | 2016-06-03 | 2022-07-26 | Syngenta Participations Ag | Compostos derivados de oxadiazol microbiocidas, composição agroquímica, método para controlar ou prevenir a infestação de plantas úteis por microrganismos fitopatogênicos e uso dos referidos compostos |
| AR108745A1 (es) | 2016-06-21 | 2018-09-19 | Syngenta Participations Ag | Derivados de oxadiazol microbiocidas |
| WO2018015447A1 (en) | 2016-07-22 | 2018-01-25 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
| US20190284148A1 (en) | 2016-07-22 | 2019-09-19 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
| WO2018015458A1 (en) | 2016-07-22 | 2018-01-25 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
| WO2018029242A1 (en) | 2016-08-11 | 2018-02-15 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
| WO2018055133A1 (en) | 2016-09-23 | 2018-03-29 | Syngenta Participations Ag | Microbiocidal tetrazolone derivatives |
| CN109923112A (zh) | 2016-09-23 | 2019-06-21 | 先正达参股股份有限公司 | 杀微生物的噁二唑衍生物 |
| WO2018065414A1 (en) | 2016-10-06 | 2018-04-12 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
| UY37623A (es) | 2017-03-03 | 2018-09-28 | Syngenta Participations Ag | Derivados de oxadiazol tiofeno fungicidas |
| US20200187502A1 (en) | 2017-03-10 | 2020-06-18 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
| BR112019020253B1 (pt) | 2017-03-31 | 2023-04-25 | Syngenta Participations Ag | Composições fungicidas, método de controle ou prevenção de fungos fitopatogênicos e processo para a preparação de um composto de fórmula (i) |
| BR112019020134B1 (pt) | 2017-03-31 | 2023-05-09 | Syngenta Participations Ag | Composições fungicidas |
| WO2018185013A1 (en) | 2017-04-03 | 2018-10-11 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
| BR112019020735B1 (pt) | 2017-04-05 | 2023-12-05 | Syngenta Participations Ag | Compostos derivados de oxadiazol microbiocidas e seu uso, composição agroquímica e método para controlar ou prevenir a infestação de plantas úteis por microrganismos fitopatogênicos |
| BR112019020756B1 (pt) | 2017-04-05 | 2023-11-28 | Syngenta Participations Ag | Compostos derivados de oxadiazol microbicidas, composição agroquímica compreendendo os mesmos, método para controlar ou prevenir a infestação de plantas úteis por microrganismos fitopatogênicos e uso desses compostos |
| WO2018184986A1 (en) | 2017-04-05 | 2018-10-11 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
| WO2018184985A1 (en) | 2017-04-05 | 2018-10-11 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
| BR112019020819B1 (pt) | 2017-04-05 | 2023-12-05 | Syngenta Participations Ag | Composto de fórmula (i), composição agroquímica, método para controlar ou prevenir a infestação de plantas úteis por micro-organismos fitopatogênicos e uso de um composto de fórmula (i) |
| BR112019021019B1 (pt) | 2017-04-05 | 2023-12-05 | Syngenta Participations Ag | Compostos derivados de oxadiazol microbiocidas, composição agrícola, método para controlar ou prevenir a infestação de plantas úteis por microrganismos fitopatogênicos e uso de um composto derivado de oxadiazol |
| WO2018185211A1 (en) | 2017-04-06 | 2018-10-11 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
| WO2018219773A1 (en) | 2017-06-02 | 2018-12-06 | Syngenta Participations Ag | Fungicidal compositions |
| US11447481B2 (en) | 2017-06-02 | 2022-09-20 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
| WO2018228896A1 (en) | 2017-06-14 | 2018-12-20 | Syngenta Participations Ag | Fungicidal compositions |
| WO2019002151A1 (en) | 2017-06-28 | 2019-01-03 | Syngenta Participations Ag | FUNGICIDE COMPOSITIONS |
| CN110537204A (zh) | 2017-06-28 | 2019-12-03 | 渊慧科技有限公司 | 使用分割和分类神经网络的可泛化医学图像分析 |
| WO2019007719A1 (en) | 2017-07-07 | 2019-01-10 | Basf Se | PESTICIDE MIXTURES |
| WO2019011929A1 (en) | 2017-07-11 | 2019-01-17 | Syngenta Participations Ag | MICROBIOCIDE OXADIAZOLE DERIVATIVES |
| WO2019011923A1 (en) | 2017-07-11 | 2019-01-17 | Syngenta Participations Ag | MICROBIOCIDE OXADIAZOLE DERIVATIVES |
| WO2019011926A1 (en) | 2017-07-11 | 2019-01-17 | Syngenta Participations Ag | MICROBIOCIDE OXADIAZOLE DERIVATIVES |
| WO2019011928A1 (en) | 2017-07-11 | 2019-01-17 | Syngenta Participations Ag | MICROBIOCIDE OXADIAZOLE DERIVATIVES |
| BR112020000371A2 (pt) | 2017-07-12 | 2020-07-14 | Syngenta Participations Ag | derivados de oxadiazol microbiocidas |
| WO2019012001A1 (en) | 2017-07-12 | 2019-01-17 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
| WO2019012003A1 (en) | 2017-07-13 | 2019-01-17 | Syngenta Participations Ag | MICROBIOCIDE OXADIAZOLE DERIVATIVES |
| ES2906980T3 (es) | 2017-09-13 | 2022-04-21 | Syngenta Participations Ag | Derivados de quinolina (tio)carboxamida microbiocidas |
| US11178869B2 (en) | 2017-09-13 | 2021-11-23 | Syngenta Participations Ag | Microbiocidal quinoline (thio)carboxamide derivatives |
| EP3681286B1 (en) | 2017-09-13 | 2021-12-15 | Syngenta Participations AG | Microbiocidal quinoline (thio)carboxamide derivatives |
| WO2019053019A1 (en) | 2017-09-13 | 2019-03-21 | Syngenta Participations Ag | MICROBIOCIDE DERIVATIVES OF QUINOLINE (THIO) CARBOXAMIDE |
| EP3681285B1 (en) | 2017-09-13 | 2021-11-17 | Syngenta Participations AG | Microbiocidal quinoline (thio)carboxamide derivatives |
| ES2894763T3 (es) | 2017-09-13 | 2022-02-15 | Syngenta Participations Ag | Derivados de quinolina (tio)carboxamida microbiocidas |
| ES2896598T3 (es) | 2017-09-13 | 2022-02-24 | Syngenta Participations Ag | Derivados de quinolina (tio)carboxamida microbiocidas |
| UY37912A (es) | 2017-10-05 | 2019-05-31 | Syngenta Participations Ag | Derivados de picolinamida fungicidas que portan grupos terminales heteroarilo o heteroariloxi |
| UY37913A (es) | 2017-10-05 | 2019-05-31 | Syngenta Participations Ag | Derivados de picolinamida fungicidas que portan un grupo terminal cuaternario |
| EP3710429B1 (en) | 2017-11-15 | 2023-04-05 | Syngenta Participations AG | Microbiocidal picolinamide derivatives |
| CN111356679A (zh) | 2017-11-20 | 2020-06-30 | 先正达参股股份有限公司 | 杀微生物的噁二唑衍生物 |
| CN111406055B (zh) | 2017-11-29 | 2023-09-22 | 先正达参股股份有限公司 | 杀微生物的噻唑衍生物 |
| WO2019121149A1 (en) | 2017-12-19 | 2019-06-27 | Syngenta Participations Ag | Microbiocidal picolinamide derivatives |
| WO2019207062A1 (en) | 2018-04-26 | 2019-10-31 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
| CN112351981A (zh) | 2018-06-29 | 2021-02-09 | 先正达农作物保护股份公司 | 杀微生物的噁二唑衍生物 |
| WO2020007658A1 (en) | 2018-07-02 | 2020-01-09 | Syngenta Crop Protection Ag | 3-(2-thienyl)-5-(trifluoromethyl)-1,2,4-oxadiazole derivatives as agrochemical fungicides |
| CN112689631A (zh) | 2018-07-16 | 2021-04-20 | 先正达农作物保护股份公司 | 杀微生物的噁二唑衍生物 |
| EP3853207B1 (en) | 2018-09-19 | 2022-10-19 | Syngenta Crop Protection AG | Microbiocidal quinoline carboxamide derivatives |
| US20220030867A1 (en) | 2018-09-26 | 2022-02-03 | Syngenta Crop Protection Ag | Fungicidal compositions |
| WO2020070131A1 (en) | 2018-10-06 | 2020-04-09 | Syngenta Participations Ag | Microbiocidal quinoline dihydro-(thiazine)oxazine derivatives |
| WO2020070132A1 (en) | 2018-10-06 | 2020-04-09 | Syngenta Participations Ag | Microbiocidal quinoline dihydro-(thiazine)oxazine derivatives |
| TW202035404A (zh) | 2018-10-24 | 2020-10-01 | 瑞士商先正達農作物保護公司 | 具有含亞碸亞胺的取代基之殺有害生物活性雜環衍生物 |
| CN113348169A (zh) | 2018-12-31 | 2021-09-03 | 先正达农作物保护股份公司 | 具有含硫取代基的杀有害生物活性的杂环衍生物 |
| WO2020141135A1 (en) | 2018-12-31 | 2020-07-09 | Syngenta Crop Protection Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| KR20210131350A (ko) | 2019-02-20 | 2021-11-02 | 바스프 에스이 | 피라졸 화합물을 포함하는 살충 혼합물 |
| WO2020207870A1 (en) | 2019-04-12 | 2020-10-15 | Basf Se | Pesticidal mixtures |
| AR120376A1 (es) * | 2019-11-11 | 2022-02-09 | Pi Industries Ltd | Heteroaril piperidiniletanonas sustituidas con actividad fungicida |
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| DE256503T1 (de) * | 1986-08-12 | 1990-02-08 | Mitsubishi Kasei Corp., Tokio/Tokyo | Pyridincarboxamid-derivate und ihre verwendung als fungizides mittel. |
| DE10349501A1 (de) * | 2003-10-23 | 2005-05-25 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| WO2011135835A1 (en) * | 2010-04-28 | 2011-11-03 | Sumitomo Chemical Company, Limited | Plant disease control composition and its use |
| CN102858172A (zh) * | 2010-04-28 | 2013-01-02 | 住友化学株式会社 | 植物病害组合物及其用途 |
| ITMI20121045A1 (it) * | 2012-06-15 | 2013-12-16 | Isagro Ricerca Srl | Composizioni sinergiche per la protezione di colture agrarie e relativo uso |
| JP6393273B2 (ja) | 2012-12-19 | 2018-09-19 | 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 | 殺菌剤としてのジフルオロメチル−ニコチン酸−インダニルカルボキサミド類 |
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- 2016-03-01 CR CR20170401A patent/CR20170401A/es unknown
- 2016-03-01 AU AU2016227796A patent/AU2016227796A1/en not_active Abandoned
- 2016-03-01 CA CA2978515A patent/CA2978515A1/en not_active Abandoned
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- 2017-09-01 CO CONC2017/0009023A patent/CO2017009023A2/es unknown
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111225921A (zh) * | 2017-10-24 | 2020-06-02 | 拜耳股份公司 | 被取代的三唑衍生物的前药及其用途 |
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| AU2016227796A1 (en) | 2017-08-17 |
| CO2017009023A2 (es) | 2017-11-21 |
| UY36571A (es) | 2016-09-30 |
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| GT201700192A (es) | 2018-12-19 |
| EP3264897A1 (en) | 2018-01-10 |
| EA201791959A1 (ru) | 2018-03-30 |
| BR112017018843A2 (pt) | 2018-07-24 |
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| MX2017011264A (es) | 2018-02-19 |
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