LV11684B - Pesticides - Google Patents
Pesticides Download PDFInfo
- Publication number
- LV11684B LV11684B LVP-96-314A LV960314A LV11684B LV 11684 B LV11684 B LV 11684B LV 960314 A LV960314 A LV 960314A LV 11684 B LV11684 B LV 11684B
- Authority
- LV
- Latvia
- Prior art keywords
- alkyl
- formula
- methyl
- compound
- phenyl
- Prior art date
Links
- 239000000575 pesticide Substances 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims description 222
- 125000005843 halogen group Chemical group 0.000 claims description 189
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 170
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 163
- 229910052736 halogen Inorganic materials 0.000 claims description 146
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 137
- 150000002367 halogens Chemical class 0.000 claims description 124
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 116
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 101
- 125000000217 alkyl group Chemical group 0.000 claims description 88
- 229910052739 hydrogen Inorganic materials 0.000 claims description 84
- 239000001257 hydrogen Substances 0.000 claims description 84
- 239000000203 mixture Substances 0.000 claims description 84
- 239000004480 active ingredient Substances 0.000 claims description 74
- -1 p -phenylene Chemical group 0.000 claims description 64
- 125000001424 substituent group Chemical group 0.000 claims description 52
- 229910052757 nitrogen Inorganic materials 0.000 claims description 51
- 125000004970 halomethyl group Chemical group 0.000 claims description 46
- 150000002431 hydrogen Chemical class 0.000 claims description 43
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 40
- 229910052760 oxygen Inorganic materials 0.000 claims description 38
- 238000000034 method Methods 0.000 claims description 37
- 241000233866 Fungi Species 0.000 claims description 35
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 32
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 32
- 125000004076 pyridyl group Chemical group 0.000 claims description 32
- 125000001544 thienyl group Chemical group 0.000 claims description 25
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims description 23
- 238000002360 preparation method Methods 0.000 claims description 23
- 125000005842 heteroatom Chemical group 0.000 claims description 22
- 241000607479 Yersinia pestis Species 0.000 claims description 21
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 21
- 229910052717 sulfur Inorganic materials 0.000 claims description 20
- 229920006395 saturated elastomer Polymers 0.000 claims description 19
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 17
- 125000003118 aryl group Chemical group 0.000 claims description 16
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims description 16
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 15
- 239000001301 oxygen Substances 0.000 claims description 15
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 claims description 15
- 125000001188 haloalkyl group Chemical group 0.000 claims description 14
- 239000002904 solvent Substances 0.000 claims description 11
- 244000005700 microbiome Species 0.000 claims description 10
- 241000238876 Acari Species 0.000 claims description 9
- 230000003032 phytopathogenic effect Effects 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 9
- 241000238631 Hexapoda Species 0.000 claims description 8
- ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 claims description 7
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 7
- 125000000623 heterocyclic group Chemical group 0.000 claims description 7
- 150000002576 ketones Chemical class 0.000 claims description 7
- 150000002923 oximes Chemical class 0.000 claims description 7
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 5
- 125000003342 alkenyl group Chemical group 0.000 claims description 5
- 125000000304 alkynyl group Chemical group 0.000 claims description 5
- 125000002757 morpholinyl group Chemical group 0.000 claims description 5
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 5
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 5
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical class OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 claims description 4
- YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical compound C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 claims description 3
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims description 3
- 125000002785 azepinyl group Chemical group 0.000 claims description 3
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 claims description 3
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 claims description 3
- DYROHZMICXBUMX-UHFFFAOYSA-N methoxymethylidene(triphenyl)-$l^{5}-phosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=COC)C1=CC=CC=C1 DYROHZMICXBUMX-UHFFFAOYSA-N 0.000 claims description 3
- 125000001425 triazolyl group Chemical group 0.000 claims description 3
- 150000002085 enols Chemical class 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims 27
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 16
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 11
- 125000005530 alkylenedioxy group Chemical group 0.000 claims 10
- 125000003302 alkenyloxy group Chemical group 0.000 claims 8
- 125000005133 alkynyloxy group Chemical group 0.000 claims 7
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 4
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 3
- 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 claims 3
- 125000003386 piperidinyl group Chemical group 0.000 claims 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
- 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 claims 2
- 125000004966 cyanoalkyl group Chemical group 0.000 claims 2
- 125000002883 imidazolyl group Chemical group 0.000 claims 2
- 125000003226 pyrazolyl group Chemical group 0.000 claims 2
- 125000000168 pyrrolyl group Chemical group 0.000 claims 2
- 125000004568 thiomorpholinyl group Chemical group 0.000 claims 2
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000001399 1,2,3-triazolyl group Chemical group N1N=NC(=C1)* 0.000 claims 1
- GMPKIPWJBDOURN-UHFFFAOYSA-N Methoxyamine Chemical compound CON GMPKIPWJBDOURN-UHFFFAOYSA-N 0.000 claims 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 125000004981 cycloalkylmethyl group Chemical group 0.000 claims 1
- 239000012022 methylating agents Substances 0.000 claims 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 claims 1
- 229910017604 nitric acid Inorganic materials 0.000 claims 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 737
- 239000000460 chlorine Substances 0.000 description 75
- 241000196324 Embryophyta Species 0.000 description 69
- 239000003921 oil Substances 0.000 description 61
- 235000019198 oils Nutrition 0.000 description 61
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 description 40
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 27
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 27
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 25
- 239000000725 suspension Substances 0.000 description 25
- 239000007921 spray Substances 0.000 description 22
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 21
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 19
- 239000002689 soil Substances 0.000 description 19
- 206010061217 Infestation Diseases 0.000 description 18
- 239000011347 resin Substances 0.000 description 18
- 229920005989 resin Polymers 0.000 description 18
- 239000000126 substance Substances 0.000 description 17
- 125000004430 oxygen atom Chemical group O* 0.000 description 16
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 15
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- 240000007594 Oryza sativa Species 0.000 description 15
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 14
- 239000000243 solution Substances 0.000 description 13
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 11
- 238000011081 inoculation Methods 0.000 description 11
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 10
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 10
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 10
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 10
- 239000000654 additive Substances 0.000 description 10
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- 239000002585 base Substances 0.000 description 9
- 201000010099 disease Diseases 0.000 description 9
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 8
- 235000007164 Oryza sativa Nutrition 0.000 description 8
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
- 241000209140 Triticum Species 0.000 description 8
- 235000013339 cereals Nutrition 0.000 description 8
- 229910052801 chlorine Inorganic materials 0.000 description 8
- 235000013399 edible fruits Nutrition 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 239000000839 emulsion Substances 0.000 description 8
- 229910052731 fluorine Inorganic materials 0.000 description 8
- 239000011737 fluorine Substances 0.000 description 8
- 235000009566 rice Nutrition 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- 238000005507 spraying Methods 0.000 description 8
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 7
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 7
- 229910052794 bromium Inorganic materials 0.000 description 7
- 239000013078 crystal Substances 0.000 description 7
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 7
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 description 6
- 239000005995 Aluminium silicate Substances 0.000 description 6
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 6
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 6
- 239000002202 Polyethylene glycol Substances 0.000 description 6
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 6
- 235000012211 aluminium silicate Nutrition 0.000 description 6
- 229910052740 iodine Inorganic materials 0.000 description 6
- 229920001223 polyethylene glycol Polymers 0.000 description 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 239000012312 sodium hydride Substances 0.000 description 6
- 229910000104 sodium hydride Inorganic materials 0.000 description 6
- 125000006526 (C1-C2) alkyl group Chemical group 0.000 description 5
- QWENRTYMTSOGBR-UHFFFAOYSA-N 1H-1,2,3-Triazole Chemical compound C=1C=NNN=1 QWENRTYMTSOGBR-UHFFFAOYSA-N 0.000 description 5
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 description 5
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 5
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 5
- 230000000895 acaricidal effect Effects 0.000 description 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 5
- 230000006378 damage Effects 0.000 description 5
- 230000018109 developmental process Effects 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 125000001841 imino group Chemical group [H]N=* 0.000 description 5
- 238000011534 incubation Methods 0.000 description 5
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 150000003254 radicals Chemical class 0.000 description 5
- 239000004094 surface-active agent Substances 0.000 description 5
- BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical compound C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 description 5
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 4
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 4
- 244000068988 Glycine max Species 0.000 description 4
- 240000005979 Hordeum vulgare Species 0.000 description 4
- 240000001307 Myosotis scorpioides Species 0.000 description 4
- 240000003768 Solanum lycopersicum Species 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 235000021307 Triticum Nutrition 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical group OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 230000002538 fungal effect Effects 0.000 description 4
- 230000000855 fungicidal effect Effects 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 4
- 230000003641 microbiacidal effect Effects 0.000 description 4
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 4
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 4
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 4
- IQHSSYROJYPFDV-UHFFFAOYSA-N 2-bromo-1,3-dichloro-5-(trifluoromethyl)benzene Chemical group FC(F)(F)C1=CC(Cl)=C(Br)C(Cl)=C1 IQHSSYROJYPFDV-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 241000335053 Beta vulgaris Species 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 241000813090 Rhizoctonia solani Species 0.000 description 3
- 235000007238 Secale cereale Nutrition 0.000 description 3
- 244000082988 Secale cereale Species 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 235000021536 Sugar beet Nutrition 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 125000001246 bromo group Chemical group Br* 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 235000008504 concentrate Nutrition 0.000 description 3
- 244000038559 crop plants Species 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 239000003337 fertilizer Substances 0.000 description 3
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- 239000000417 fungicide Substances 0.000 description 3
- 238000003898 horticulture Methods 0.000 description 3
- 239000005457 ice water Substances 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- 230000000749 insecticidal effect Effects 0.000 description 3
- 239000002917 insecticide Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000012074 organic phase Substances 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 229910000027 potassium carbonate Inorganic materials 0.000 description 3
- 239000000741 silica gel Substances 0.000 description 3
- 229910002027 silica gel Inorganic materials 0.000 description 3
- 229920005552 sodium lignosulfonate Polymers 0.000 description 3
- 235000013311 vegetables Nutrition 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- PPNCOQHHSGMKGI-UHFFFAOYSA-N 1-cyclononyldiazonane Chemical compound C1CCCCCCCC1N1NCCCCCCC1 PPNCOQHHSGMKGI-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 241001124076 Aphididae Species 0.000 description 2
- 241000952611 Aphis craccivora Species 0.000 description 2
- 244000105624 Arachis hypogaea Species 0.000 description 2
- 235000004535 Avena sterilis Nutrition 0.000 description 2
- 241001647031 Avena sterilis Species 0.000 description 2
- 235000016068 Berberis vulgaris Nutrition 0.000 description 2
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
- 240000008067 Cucumis sativus Species 0.000 description 2
- 241001529600 Diabrotica balteata Species 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- 241000256244 Heliothis virescens Species 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 2
- 241000257303 Hymenoptera Species 0.000 description 2
- 229930194542 Keto Natural products 0.000 description 2
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
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- C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
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Applications Claiming Priority (4)
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CH1294 | 1994-01-05 | ||
CH211794 | 1994-07-01 | ||
PCT/EP1994/004318 WO1995018789A1 (en) | 1994-01-05 | 1994-12-27 | Pesticides |
US08/526,859 US5756426A (en) | 1994-01-05 | 1995-09-11 | Phenyl acetic acid derivatives as pesticides |
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LV11684A LV11684A (lv) | 1997-02-20 |
LV11684B true LV11684B (en) | 1997-06-20 |
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LVP-96-314A LV11684B (en) | 1994-01-05 | 1996-07-24 | Pesticides |
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US (3) | US5756426A (hu) |
EP (1) | EP0738260B2 (hu) |
CN (1) | CN1152007C (hu) |
AP (1) | AP654A (hu) |
AU (1) | AU690190B2 (hu) |
CA (1) | CA2179418C (hu) |
CZ (1) | CZ291625B6 (hu) |
FI (1) | FI962712A (hu) |
HU (1) | HU219157B (hu) |
IL (1) | IL112227A (hu) |
LV (1) | LV11684B (hu) |
MD (1) | MD1315C2 (hu) |
NO (1) | NO307045B1 (hu) |
SK (1) | SK88096A3 (hu) |
WO (1) | WO1995018789A1 (hu) |
Families Citing this family (69)
Publication number | Priority date | Publication date | Assignee | Title |
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US5965613A (en) * | 1989-12-12 | 1999-10-12 | Novartis Finance Corporation | Derivatives of acrylic acid |
CZ291625B6 (cs) * | 1994-01-05 | 2003-04-16 | Bayer Aktiengesellschaft | Oximové deriváty |
AU681932B2 (en) | 1994-02-04 | 1997-09-11 | Basf Aktiengesellschaft | Phenyl acetic acid derivatives, process and intermediate products for their production and agents containing them |
EP0945431A3 (de) * | 1994-02-04 | 2004-08-18 | Basf Aktiengesellschaft | Verfahren und Zwischenprodukte zur Herstellung von Phenylessigsäurederivaten |
CH689228A5 (de) * | 1994-10-07 | 1998-12-31 | Novartis Ag | Oximether, sowie diese enthaltende Pflanzenschutzmittel. |
MX9703616A (es) * | 1994-11-17 | 1997-08-30 | Novartis Ag | Derivados de eter de oxima o-bencilica y su uso como pesticidas. |
CN1078202C (zh) * | 1995-04-08 | 2002-01-23 | 巴斯福股份公司 | 基本上异构体纯的α-双肟的制备方法 |
AU5735096A (en) * | 1995-05-17 | 1996-11-29 | E.I. Du Pont De Nemours And Company | Fungicidal cyclic amides |
EA001223B1 (ru) * | 1995-06-22 | 2000-12-25 | Новартис Аг | Пестицидные трис-оксимино гетероциклические соединения |
PL323311A1 (en) * | 1995-07-04 | 1998-03-16 | Ciba Geigy Ag | Bis-oximie derivatives of triazolin and isoxazolin and their application as pesticides |
SK10298A3 (en) * | 1995-07-27 | 1998-11-04 | Basf Ag | Phenyl acetic acid derivatives, process and intermediate products for their production and their use as parasiticides and fungicides |
DE19528651A1 (de) * | 1995-08-04 | 1997-02-06 | Basf Ag | Hydroximsäurederivate, Verfahren zu ihrer Herstellung und sie enthaltende Mittel |
ATE374188T1 (de) * | 1995-08-15 | 2007-10-15 | Bayer Cropscience Ag | Pestizide indazol-derivate |
KR19990037655A (ko) * | 1995-08-17 | 1999-05-25 | 스타르크, 카르크 | 옥심에테르 카르복실산 아미드와 아닐리노피리미딘의 살진균성혼합물 |
WO1997006678A1 (de) * | 1995-08-17 | 1997-02-27 | Basf Aktiengesellschaft | Fungizide mischungen eines oximethercarbonsäureamids mit azolderivaten |
BR9610420A (pt) * | 1995-08-17 | 1999-07-06 | Basf Ag | Mistura fungicida processo para controlar fungos nocivos e uso de um composto |
AU6788196A (en) * | 1995-08-17 | 1997-03-12 | Basf Aktiengesellschaft | Fungicidal mixtures |
JP3883575B2 (ja) * | 1995-08-17 | 2007-02-21 | ビーエーエスエフ アクチェンゲゼルシャフト | 殺菌剤混合物 |
AU6740896A (en) * | 1995-08-17 | 1997-03-12 | Basf Aktiengesellschaft | Fungicidal mixtures of an oxime ether carboxylic acid amide with a morpholine or piperidine derivative |
AR004012A1 (es) | 1995-10-10 | 1998-09-30 | Basf Ag | Derivados de acido fenilacetico, procedimientos para su obtencion, su uso para preparar composiciones para combatir animales u hongos nocivos, lascomposiciones asi obtenidas y los procedimientos de aplicacion de dichas composiciones. |
DE19539324A1 (de) * | 1995-10-23 | 1997-04-24 | Basf Ag | Phenylessigsäurederivate, Verfahren und Zwischenprodukte zu ihrer Herstellung und sie enthaltende Mittel |
DE19540361A1 (de) * | 1995-10-30 | 1997-05-07 | Basf Ag | Phenylessigsäurederivate, Verfahren und Zwischenprodukte zu ihrer Herstellung und ihre Verwendung zur Bekämpfung von Schadpilzen und tierischen Schädlingen |
AU7297196A (en) * | 1995-11-02 | 1997-05-22 | Basf Aktiengesellschaft | Pyridylacetic acid derivatives, process and intermediate products for their preparation, and their use |
DE19540989A1 (de) * | 1995-11-03 | 1997-05-07 | Basf Ag | Pyridylessigsäurederivate, Verfahren und Zwischenprodukte zu ihrer Herstellung und sie enthaltende Mittel |
DE19542629A1 (de) * | 1995-11-15 | 1997-05-22 | Basf Ag | Azinooximether, Verfahren und Zwischenprodukte zu ihrer Herstellung und ihre Verwendung zur Bekämpfung von Schadpilzen und tierischen Schädlingen |
DE19545094A1 (de) * | 1995-12-04 | 1997-06-05 | Basf Ag | Phenylessigsäurederivate, Verfahren und Zwischenprodukte zu ihrer Herstellung und sie enthaltende Mittel |
DK0876333T3 (da) | 1995-12-07 | 2002-07-22 | Bayer Ag | Fremgangsmåde til fremstilling af pesticider |
CA2238632A1 (en) * | 1995-12-07 | 1997-06-12 | Novartis Ag | Pesticides |
DE19548783A1 (de) * | 1995-12-27 | 1997-07-03 | Basf Ag | Cyaniminooximether, Verfahren und Zwischenprodukte zu ihrer Herstellung und ihre Verwendung zur Bekämpfung von Schadpilzen und tierischen Schädlingen |
DK0782982T3 (da) | 1996-01-03 | 2000-10-09 | Novartis Ag | Fremgangsmåde til fremstilling af o-chlormethyl-phenylglyoxylsyrederivater |
WO1997037968A1 (fr) * | 1996-04-11 | 1997-10-16 | Shionogi & Co., Ltd. | DERIVES D'α-ALCOXYIMINOBENZYLE ET PRODUITS CHIMIQUES A USAGE AGRICOLE CONTENANT CES DERIVES COMME PRINCIPES ACTIFS |
DE69709112T2 (de) * | 1996-06-12 | 2002-04-25 | Bayer Ag | Pestizide |
US5973001A (en) * | 1996-08-05 | 1999-10-26 | Basf Aktiengesellshcaft | Fungicidal mixtures of an oxime ether carboxylic acid amide with cymoxanil |
AU5760098A (en) * | 1996-12-20 | 1998-07-17 | Novartis Ag | O-benzyl oxime ether derivatives as pecticides |
DE19708940A1 (de) | 1997-03-05 | 1998-09-10 | Basf Ag | Hydroximsäurehalogenide, Verfahren zur ihrer Herstellung und ihre Verwendung |
JP2002501515A (ja) * | 1997-05-27 | 2002-01-15 | バイエル アクチェンゲゼルシャフト | O−ベンジルオキシムエーテルおよび農薬としてのそれらの使用 |
AR015821A1 (es) * | 1997-05-27 | 2001-05-30 | Bayer Ag | Compuestos organicos |
CO5050364A1 (es) | 1997-05-28 | 2001-06-27 | Basf Ag | Metodo para controlar hongos nocivos |
NZ501241A (en) | 1997-05-30 | 2001-10-26 | Basf Ag | Fungicidal mixtures comprising a carbamate and an oxime ether carboxamide |
PL337157A1 (en) | 1997-06-04 | 2000-07-31 | Basf Ag | Fungicidal mixtures |
GB9718366D0 (en) | 1997-08-29 | 1997-11-05 | Ciba Geigy Ag | Novel combinations |
EP1077953A2 (de) * | 1998-05-14 | 2001-02-28 | Basf Aktiengesellschaft | Bisoximetherderivate, zwischenprodukte und verwendung zur bekämpfung von schadpilzen und tierischen schädlingen |
US6313344B1 (en) | 1998-05-27 | 2001-11-06 | Bayer Aktiengesellschaft | Organic compounds |
GB9820582D0 (en) * | 1998-09-22 | 1998-11-11 | Novartis Ag | Organic compounds |
WO2000017155A1 (en) * | 1998-09-22 | 2000-03-30 | Bayer Aktiengesellschaft | Pesticidal bis-oxime compounds |
BR9915423A (pt) * | 1998-11-20 | 2001-08-07 | Basf Ag | Processo para preparar derivados de bis (éter de oxima) substituìdos por alquenila. |
WO2000034229A1 (en) * | 1998-12-10 | 2000-06-15 | Bayer Aktiengesellschaft | Process for the preparation of strobilurin intermediates |
GB9827163D0 (en) | 1998-12-10 | 1999-02-03 | Novartis Ag | Organic compounds |
AU1007400A (en) * | 1999-01-27 | 2000-08-03 | Dow Agrosciences Llc | Aryl and heteroarylcyclopropyl oxime ethers and their use as fungicides and insecticides |
GB9908530D0 (en) | 1999-04-14 | 1999-06-09 | Novartis Ag | Organic compounds |
EP1237852A1 (de) * | 1999-12-06 | 2002-09-11 | Bayer Aktiengesellschaft | N-phenylcarbamate mit mikrobizider, insektizider und akarizider wirkung |
EP1265837B1 (de) | 1999-12-07 | 2004-06-09 | Basf Aktiengesellschaft | Verfahren zur herstellung von o-chlormethylbenzoesäurechloriden |
US6313339B1 (en) | 2000-02-17 | 2001-11-06 | Ronald Ross, Jr. | Aryl and heteroarylcylopropyl oxime ethers and their use as fungicides and insecticides |
DE60102308T2 (de) * | 2000-01-21 | 2004-07-29 | Dow Agrosciences Llc, Indianapolis | Aryl und heteroarylcyclopropyl oxime Ether und ihre Verwendung als Fungicide und Insektizide |
KR100422883B1 (ko) * | 2001-03-26 | 2004-03-12 | 학교법인고려중앙학원 | 항균물질 페닐아세틱 에시드 및 소디움 페닐아세테이트을유효성분으로 하는 고추역병 방제용 살균제 조성물 |
DE10209145A1 (de) * | 2002-03-01 | 2003-09-04 | Bayer Cropscience Ag | Halogenbenzole |
ES2309392T3 (es) | 2002-11-12 | 2008-12-16 | Basf Se | Procedimiento para el aumento del rendimiento en leguminosas resistentes a los glifosatos. |
US7161026B1 (en) | 2005-07-08 | 2007-01-09 | Property Development Corporation International, Ltd, Inc. | Method of preparation of methyl-benzyl-ketone |
DE602006012716D1 (de) * | 2005-10-28 | 2010-04-15 | Basf Se | Verfahren zur induktion von resistenz gegen schadpilze |
AU2007224578A1 (en) * | 2006-03-10 | 2007-09-20 | Basf Se | Method for improving the tolerance of plants to chilling temperatures and/or frost |
AU2007224576A1 (en) * | 2006-03-14 | 2007-09-20 | Basf Se | Method of inducing tolerance of plants against bacterioses |
UA94093C2 (ru) | 2006-03-24 | 2011-04-11 | Басф Се | Применение активного соединения для борьбы с комплексом грибных фитопатогенов эска и способ борьбы с эска |
EP2076602A2 (en) | 2007-04-23 | 2009-07-08 | Basf Se | Plant produtivity enhancement by combining chemical agents with transgenic modifications |
WO2011005325A1 (en) * | 2009-07-09 | 2011-01-13 | Spray Away Bed Bugs Llc | Compositions and methods of use pertaining to insecticide |
PE20121128A1 (es) | 2009-07-28 | 2012-08-16 | Basf Se | Un metodo para aumentar el nivel de aminoacidos libres en tejidos de almacenamiento de plantas perennes |
EP2480073A2 (en) | 2009-09-25 | 2012-08-01 | Basf Se | Method for reducing pistillate flower abortion in plants |
WO2011151261A2 (en) * | 2010-05-31 | 2011-12-08 | Basf Se | Method for increasing the health of a plant |
EP3047731A1 (en) | 2015-01-21 | 2016-07-27 | Basf Se | Method for combating soybean rust comprising treating soybean with (2E)-2-[3-substituted-2 [[(E)-[(2E)-2-alkoxyimino-1-methyl-2-phenyl-ethylidene]amino]oxymethyl]phenyl]-2-methoxy-imino-N-methyl-acetamides |
AR115870A1 (es) | 2018-07-31 | 2021-03-10 | Sumitomo Chemical Co | MÉTODO PARA CONTROLAR EL HONGO DE LA ROYA DE LA SOJA QUE TIENE RESISTENCIA AL INHIBIDOR DE SITIO Qₒ |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2621102A1 (de) * | 1976-05-10 | 1977-11-24 | Schering Ag | Propan-1,2-diondioxime, schaedlingsbekaempfungsmittel enthaltend diese verbindungen sowie verfahren zu ihrer herstellung |
DE3039269A1 (de) * | 1980-10-17 | 1982-05-19 | Bayer Ag, 5090 Leverkusen | Hydroxamsaeureester, verfahren zu ihrer herstellung, ihre verwendung in schaedlingsbekaempfungsmitteln und zwischenprodukte dafuer |
EP0506149B1 (en) * | 1988-11-21 | 1998-08-12 | Zeneca Limited | Intermediate compounds for the preparation of fungicides |
HUT52421A (en) * | 1988-12-23 | 1990-07-28 | Janos Puglits | Control gear for automatic operating the clutch of motor vehicles |
EP0403618B2 (de) * | 1988-12-29 | 2004-04-28 | Bayer Aktiengesellschaft | Aldimino- oder ketimino-oxy-ortho-tolylacrylsäure-methylester, ihre herstellung und diese enthaltende fungizide |
US5104872A (en) * | 1989-08-22 | 1992-04-14 | Nihon Hohyaku Co., Ltd. | N-(substituted benzyloxy) imine derivatives and method of use thereof |
PH11991042549B1 (hu) * | 1990-06-05 | 2000-12-04 | ||
DE59109047D1 (de) * | 1990-06-27 | 1998-10-08 | Basf Ag | O-Benzyl-Oximether und diese Verbindungen enthaltende Pflanzenschutzmittel |
GB9018408D0 (en) * | 1990-08-22 | 1990-10-03 | Ici Plc | Fungicides |
GB9200635D0 (en) * | 1991-01-30 | 1992-03-11 | Ici Plc | Fungicides |
NZ242290A (en) * | 1991-04-15 | 1994-12-22 | Zeneca Ltd | Pyridyl and pyrimidinyl substituted oxime-o-benzyl ether derivatives; preparatory processes, fungicidal compositions and an intermediate |
CH686307A5 (de) * | 1991-04-19 | 1996-02-29 | Ciba Geigy Ag | Oximether des 3-Methoxy-2-(o-tolyl)acrylsouremethylesters, Verfahren zu ihrer Herstellung und fungizide Mittel, die diese als Wirkstoffe enthalten. |
CZ291625B6 (cs) * | 1994-01-05 | 2003-04-16 | Bayer Aktiengesellschaft | Oximové deriváty |
EP0945431A3 (de) * | 1994-02-04 | 2004-08-18 | Basf Aktiengesellschaft | Verfahren und Zwischenprodukte zur Herstellung von Phenylessigsäurederivaten |
AU681932B2 (en) † | 1994-02-04 | 1997-09-11 | Basf Aktiengesellschaft | Phenyl acetic acid derivatives, process and intermediate products for their production and agents containing them |
DK0765304T4 (da) * | 1994-06-10 | 2007-12-03 | Bayer Cropscience Ag | Fremgangsmåde og mellemprodukter til fremstilling af a-methoxyiminocarboxylsyremethylamider |
-
1994
- 1994-12-27 CZ CZ19961990A patent/CZ291625B6/cs not_active IP Right Cessation
- 1994-12-27 SK SK880-96A patent/SK88096A3/sk unknown
- 1994-12-27 EP EP95905110A patent/EP0738260B2/en not_active Expired - Lifetime
- 1994-12-27 CN CNB941947785A patent/CN1152007C/zh not_active Expired - Fee Related
- 1994-12-27 WO PCT/EP1994/004318 patent/WO1995018789A1/en active IP Right Grant
- 1994-12-27 MD MD96-0291A patent/MD1315C2/ro unknown
- 1994-12-27 CA CA002179418A patent/CA2179418C/en not_active Expired - Fee Related
- 1994-12-27 HU HU9601839A patent/HU219157B/hu not_active IP Right Cessation
- 1994-12-27 AP APAP/P/1996/000820A patent/AP654A/en active
- 1994-12-27 AU AU13851/95A patent/AU690190B2/en not_active Ceased
-
1995
- 1995-01-03 IL IL11222795A patent/IL112227A/xx not_active IP Right Cessation
- 1995-09-11 US US08/526,859 patent/US5756426A/en not_active Expired - Lifetime
-
1996
- 1996-07-01 FI FI962712A patent/FI962712A/fi unknown
- 1996-07-04 NO NO962823A patent/NO307045B1/no not_active IP Right Cessation
- 1996-07-24 LV LVP-96-314A patent/LV11684B/en unknown
-
1997
- 1997-11-12 US US08/968,143 patent/US5981585A/en not_active Expired - Fee Related
-
1999
- 1999-06-22 US US09/338,236 patent/US6313166B1/en not_active Expired - Fee Related
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FI962712A (fi) | 1996-08-16 |
AU1385195A (en) | 1995-08-01 |
US6313166B1 (en) | 2001-11-06 |
US5981585A (en) | 1999-11-09 |
HU219157B (hu) | 2001-02-28 |
AU690190B2 (en) | 1998-04-23 |
HUT74980A (en) | 1997-03-28 |
CN1141032A (zh) | 1997-01-22 |
IL112227A (en) | 1999-11-30 |
SK88096A3 (en) | 1996-12-04 |
MD1315C2 (ro) | 2000-06-30 |
LV11684A (lv) | 1997-02-20 |
FI962712A0 (fi) | 1996-07-01 |
CZ291625B6 (cs) | 2003-04-16 |
NO962823D0 (no) | 1996-07-04 |
CZ199096A3 (en) | 1996-10-16 |
EP0738260B2 (en) | 2006-12-13 |
WO1995018789A1 (en) | 1995-07-13 |
HU9601839D0 (en) | 1996-10-28 |
EP0738260B1 (en) | 2001-08-29 |
CN1152007C (zh) | 2004-06-02 |
CA2179418A1 (en) | 1995-07-13 |
NO962823L (no) | 1996-07-04 |
AP9600820A0 (en) | 1996-07-31 |
NO307045B1 (no) | 2000-01-31 |
AP654A (en) | 1998-07-31 |
MD1315B1 (en) | 1999-09-30 |
EP0738260A1 (en) | 1996-10-23 |
MD960291A (en) | 1997-10-31 |
IL112227A0 (en) | 1995-03-30 |
US5756426A (en) | 1998-05-26 |
CA2179418C (en) | 2004-06-22 |
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