CZ304537B6 - Herbicidně selektivní kompozice a způsob kontroly nežádoucího rostlinného růstu - Google Patents
Herbicidně selektivní kompozice a způsob kontroly nežádoucího rostlinného růstu Download PDFInfo
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- CZ304537B6 CZ304537B6 CZ2002-2547A CZ20022547A CZ304537B6 CZ 304537 B6 CZ304537 B6 CZ 304537B6 CZ 20022547 A CZ20022547 A CZ 20022547A CZ 304537 B6 CZ304537 B6 CZ 304537B6
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- methyl
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- 239000000203 mixture Substances 0.000 title claims abstract description 157
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- -1 C 2 -C 6 haloalkynyl Chemical group 0.000 claims description 93
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 28
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims description 24
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 24
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- 229910052757 nitrogen Inorganic materials 0.000 claims description 16
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- UOTCXIMRODXHSV-UHFFFAOYSA-N [2,3-dihydroxy-4-(2-methylsulfonyloxyethylazaniumyl)butyl]-(2-methylsulfonyloxyethyl)azanium;dichloride Chemical group [Cl-].[Cl-].CS(=O)(=O)OCC[NH2+]CC(O)C(O)C[NH2+]CCOS(C)(=O)=O UOTCXIMRODXHSV-UHFFFAOYSA-N 0.000 claims description 8
- 239000000654 additive Substances 0.000 claims description 8
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 7
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- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims description 5
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- RZRJACCZWZTYJY-UHFFFAOYSA-N tert-butylsulfanyl n,n-dimethylcarbamodithioate Chemical compound CN(C)C(=S)SSC(C)(C)C RZRJACCZWZTYJY-UHFFFAOYSA-N 0.000 claims description 4
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- SOIIHESTBYNJRH-PMPSAXMXSA-N (3r,6r,8as)-6-(benzylsulfonylamino)-n-[3-(diaminomethylideneamino)propyl]-5-oxo-2,3,6,7,8,8a-hexahydro-[1,3]thiazolo[3,2-a]pyridine-3-carboxamide Chemical compound N([C@@H]1CC[C@@H]2SC[C@H](N2C1=O)C(=O)NCCCN=C(N)N)S(=O)(=O)CC1=CC=CC=C1 SOIIHESTBYNJRH-PMPSAXMXSA-N 0.000 claims 1
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- 125000000262 haloalkenyl group Chemical group 0.000 description 1
- 125000000232 haloalkynyl group Chemical group 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- 125000005059 halophenyl group Chemical group 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003707 hexyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
- RUCAXVJJQQJZGU-UHFFFAOYSA-M hydron;2-(phosphonatomethylamino)acetate;trimethylsulfanium Chemical compound C[S+](C)C.OP(O)(=O)CNCC([O-])=O RUCAXVJJQQJZGU-UHFFFAOYSA-M 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 description 1
- 125000006352 iso-propylthiomethyl group Chemical group [H]C([H])([H])C([H])(SC([H])([H])*)C([H])([H])[H] 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000005929 isobutyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])OC(*)=O 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 229940102253 isopropanolamine Drugs 0.000 description 1
- 125000006229 isopropoxyethyl group Chemical group [H]C([H])([H])C([H])(OC([H])([H])C([H])([H])*)C([H])([H])[H] 0.000 description 1
- 125000005928 isopropyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(OC(*)=O)C([H])([H])[H] 0.000 description 1
- OYIKARCXOQLFHF-UHFFFAOYSA-N isoxaflutole Chemical compound CS(=O)(=O)C1=CC(C(F)(F)F)=CC=C1C(=O)C1=C(C2CC2)ON=C1 OYIKARCXOQLFHF-UHFFFAOYSA-N 0.000 description 1
- 229940088649 isoxaflutole Drugs 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 150000004994 m-toluidines Chemical class 0.000 description 1
- 235000012254 magnesium hydroxide Nutrition 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- KPUREKXXPHOJQT-UHFFFAOYSA-N mesotrione Chemical compound [O-][N+](=O)C1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O KPUREKXXPHOJQT-UHFFFAOYSA-N 0.000 description 1
- 229910052987 metal hydride Inorganic materials 0.000 description 1
- 150000004681 metal hydrides Chemical class 0.000 description 1
- 229940087646 methanolamine Drugs 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 description 1
- JTHMVYBOQLDDIY-UHFFFAOYSA-N methyl 2-[(4-methyl-5-oxo-3-propoxy-1,2,4-triazole-1-carbonyl)sulfamoyl]benzoate Chemical compound O=C1N(C)C(OCCC)=NN1C(=O)NS(=O)(=O)C1=CC=CC=C1C(=O)OC JTHMVYBOQLDDIY-UHFFFAOYSA-N 0.000 description 1
- CXUNSFYXNQZSNS-UHFFFAOYSA-N methyl 2-methyl-4,6-dioxo-2-(trifluoromethyl)cyclohexane-1-carboxylate Chemical compound COC(=O)C1C(=O)CC(=O)CC1(C)C(F)(F)F CXUNSFYXNQZSNS-UHFFFAOYSA-N 0.000 description 1
- 125000004372 methylthioethyl group Chemical group [H]C([H])([H])SC([H])([H])C([H])([H])* 0.000 description 1
- 125000004092 methylthiomethyl group Chemical group [H]C([H])([H])SC([H])([H])* 0.000 description 1
- FOXFZRUHNHCZPX-UHFFFAOYSA-N metribuzin Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1N FOXFZRUHNHCZPX-UHFFFAOYSA-N 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- SRLHDBRENZFCIN-UHFFFAOYSA-N n,n-di(butan-2-yl)butan-2-amine Chemical compound CCC(C)N(C(C)CC)C(C)CC SRLHDBRENZFCIN-UHFFFAOYSA-N 0.000 description 1
- OOHAUGDGCWURIT-UHFFFAOYSA-N n,n-dipentylpentan-1-amine Chemical compound CCCCCN(CCCCC)CCCCC OOHAUGDGCWURIT-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000006095 n-butyl sulfinyl group Chemical group 0.000 description 1
- 125000006126 n-butyl sulfonyl group Chemical group 0.000 description 1
- DJUWKQYCYKRJNI-UHFFFAOYSA-N n-ethoxyaniline Chemical class CCONC1=CC=CC=C1 DJUWKQYCYKRJNI-UHFFFAOYSA-N 0.000 description 1
- QHCCDDQKNUYGNC-UHFFFAOYSA-N n-ethylbutan-1-amine Chemical compound CCCCNCC QHCCDDQKNUYGNC-UHFFFAOYSA-N 0.000 description 1
- IUZZLNVABCISOI-UHFFFAOYSA-N n-ethylheptan-1-amine Chemical compound CCCCCCCNCC IUZZLNVABCISOI-UHFFFAOYSA-N 0.000 description 1
- SDQCOADWEMMSGK-UHFFFAOYSA-N n-ethyloctan-1-amine Chemical compound CCCCCCCCNCC SDQCOADWEMMSGK-UHFFFAOYSA-N 0.000 description 1
- NJWMENBYMFZACG-UHFFFAOYSA-N n-heptylheptan-1-amine Chemical compound CCCCCCCNCCCCCCC NJWMENBYMFZACG-UHFFFAOYSA-N 0.000 description 1
- KLJUVCXLKBGKOY-UHFFFAOYSA-N n-hexylheptan-1-amine Chemical compound CCCCCCCNCCCCCC KLJUVCXLKBGKOY-UHFFFAOYSA-N 0.000 description 1
- PXSXRABJBXYMFT-UHFFFAOYSA-N n-hexylhexan-1-amine Chemical compound CCCCCCNCCCCCC PXSXRABJBXYMFT-UHFFFAOYSA-N 0.000 description 1
- SKLXFEQHEBALKG-UHFFFAOYSA-N n-hexyloctan-1-amine Chemical compound CCCCCCCCNCCCCCC SKLXFEQHEBALKG-UHFFFAOYSA-N 0.000 description 1
- NSBIQPJIWUJBBX-UHFFFAOYSA-N n-methoxyaniline Chemical class CONC1=CC=CC=C1 NSBIQPJIWUJBBX-UHFFFAOYSA-N 0.000 description 1
- OZIXTIPURXIEMB-UHFFFAOYSA-N n-methylnonan-1-amine Chemical compound CCCCCCCCCNC OZIXTIPURXIEMB-UHFFFAOYSA-N 0.000 description 1
- SZEGKVHRCLBFKJ-UHFFFAOYSA-N n-methyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCNC SZEGKVHRCLBFKJ-UHFFFAOYSA-N 0.000 description 1
- CNCBAEHAEKNSPZ-UHFFFAOYSA-N n-methylpentadecan-1-amine Chemical compound CCCCCCCCCCCCCCCNC CNCBAEHAEKNSPZ-UHFFFAOYSA-N 0.000 description 1
- JACMPVXHEARCBO-UHFFFAOYSA-N n-pentylpentan-1-amine Chemical compound CCCCCNCCCCC JACMPVXHEARCBO-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000005002 naphthylamines Chemical class 0.000 description 1
- RTCOGUMHFFWOJV-UHFFFAOYSA-N nicosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CN=2)C(=O)N(C)C)=N1 RTCOGUMHFFWOJV-UHFFFAOYSA-N 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- FJDUDHYHRVPMJZ-UHFFFAOYSA-N nonan-1-amine Chemical class CCCCCCCCCN FJDUDHYHRVPMJZ-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- NVGOPFQZYCNLDU-UHFFFAOYSA-N norflurazon Chemical compound O=C1C(Cl)=C(NC)C=NN1C1=CC=CC(C(F)(F)F)=C1 NVGOPFQZYCNLDU-UHFFFAOYSA-N 0.000 description 1
- 150000004993 o-toluidines Chemical class 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical class CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000006146 oximation reaction Methods 0.000 description 1
- 150000004995 p-toluidines Chemical class 0.000 description 1
- FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 description 1
- CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 description 1
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- CSWIKHNSBZVWNQ-UHFFFAOYSA-N pethoxamide Chemical compound CCOCCN(C(=O)CCl)C(=C(C)C)C1=CC=CC=C1 CSWIKHNSBZVWNQ-UHFFFAOYSA-N 0.000 description 1
- 125000005359 phenoxyalkyl group Chemical group 0.000 description 1
- 125000003884 phenylalkyl group Chemical group 0.000 description 1
- 150000004986 phenylenediamines Chemical class 0.000 description 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- UXCDUFKZSUBXGM-UHFFFAOYSA-N phosphoric tribromide Chemical compound BrP(Br)(Br)=O UXCDUFKZSUBXGM-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000004382 potting Methods 0.000 description 1
- YDJNPEDINFYMAD-UHFFFAOYSA-N propan-2-yl 4,4,4-trifluoro-3-methylbut-2-enoate Chemical compound CC(C)OC(=O)C=C(C)C(F)(F)F YDJNPEDINFYMAD-UHFFFAOYSA-N 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 125000004742 propyloxycarbonyl group Chemical group 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- SBYHFKPVCBCYGV-UHFFFAOYSA-N quinuclidine Chemical compound C1CC2CCN1CC2 SBYHFKPVCBCYGV-UHFFFAOYSA-N 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- MEFOUWRMVYJCQC-UHFFFAOYSA-N rimsulfuron Chemical compound CCS(=O)(=O)C1=CC=CN=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 MEFOUWRMVYJCQC-UHFFFAOYSA-N 0.000 description 1
- 238000002390 rotary evaporation Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000005930 sec-butyloxycarbonyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(OC(*)=O)C([H])([H])[H] 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 description 1
- OORLZFUTLGXMEF-UHFFFAOYSA-N sulfentrazone Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(NS(C)(=O)=O)=C(Cl)C=C1Cl OORLZFUTLGXMEF-UHFFFAOYSA-N 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-UHFFFAOYSA-N 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- CXPRGLWJJQBWRS-UHFFFAOYSA-N tert-butyl 3-cyclopropyl-3-oxopropanoate Chemical compound CC(C)(C)OC(=O)CC(=O)C1CC1 CXPRGLWJJQBWRS-UHFFFAOYSA-N 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- RKBCYCFRFCNLTO-UHFFFAOYSA-N triisopropylamine Chemical compound CC(C)N(C(C)C)C(C)C RKBCYCFRFCNLTO-UHFFFAOYSA-N 0.000 description 1
- PYIHTIJNCRKDBV-UHFFFAOYSA-L trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;dichloride Chemical compound [Cl-].[Cl-].C[N+](C)(C)CCCCCC[N+](C)(C)C PYIHTIJNCRKDBV-UHFFFAOYSA-L 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 239000008096 xylene Chemical class 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyridine Compounds (AREA)
- Pyrane Compounds (AREA)
Abstract
Řešení se týká herbicidně selektivní kompozice, jejíž podstata spočívá v tom, že kromě běžných inertních formulačních přísad obsahuje jako účinnou složku směs herbicidně účinného množství sloučeniny vzorce Ia nebo agrochemicky přijatelné soli takové sloučeniny a synergicky účinného množství jedné nebo více sloučenin zvolených ze souboru specificky definovaných sloučenin. Tato kompozice vykazuje výrazný synergický účinek, který umožňuje kontrolu širokého spektra plevelů. Řešení se týká i způsobu kontroly nežádoucího rostlinného růstu v kulturních užitkových rostlinách s využitím uvedené kompozice.
Description
Herbicidně selektivní kompozice a způsob kontroly nežádoucího rostlinného růstu
Oblast techniky
Vynález se týká nových herbicidně selektivních kompozic tvořených kombinacemi herbicidně aktivních sloučenin, které vykazují využitelný synergický účinek pro selektivní kontrolu plevele v plodinách užitkových rostlin, zejména v kukuřici, jakož i způsobu kontroly nežádoucího rostlinného růstu v uvedených užitkových plodinách.
Dosavadní stav techniky
V dokumentech dosavadního stavu techniky WO 00/00 029, WO 00/00 031 a US 4 995 902 jsou popsané některé strukturně blízké herbicidně účinné sloučeniny. V rámci vynálezu bylo překvapivě zjištěno, že kombinace určitých množství obdobných účinných sloučenin s alespoň jednou další známou a případně komerčně dostupnou definovanou účinnou sloučeninou vykazují oproti stavu techniky výrazný synergický účinek, který je schopen kontroly širokého spektra plevelů vyskytujících se zejména u plodin užitkových rostlin, a to jak při preemergentní, tak i při postemergentní aplikaci.
Podstata vynálezu
Předmětem vynálezu je takto herbicidně selektivní kompozice, jejíž podstata spočívá v tom, že kromě běžných inertních formulačních přísad obsahuje jako účinnou látku směs a) herbicidně účinného množství sloučeniny vzorce la
(la), ve kterém
R48 znamená Ci-C6alkyl, C2-C6alkenyl, C2-C6halogenalkenyl, C2-C6alkynyl, C2-C6halogenalkynyl, C3-C6cykloalkyl, Ci-C6halogenalkyl, Ci-C4alkoxy-Ci-C4alkyl nebo Ci-C4alkoxy-CiC4alkoxy-C i-C4alkyl;
R49 znamená vodík;
R5o znamená Ci-C6halogenalkyl a
Q znamená skupinu Q2
kde R23 znamená hydroxy a
- 1 CZ 304537 B6
Y znamená kyslík, síru, chemickou vazbu nebo C|-C4alky lenový můstek;
nebo agrochemicky přijatelné soli takové sloučeniny, a
b) synergicky účinného množství jedné nebo více sloučenin zvolených ze souboru zahrnujícího sloučeninu vzorce 2.1
(2.1), ve kterém R51 znamená CH2-OMe, ethyl nebo vodík; R52 znamená vodík nebo R51 a R52 dohromady znamenají skupinu -CH=CH-CH=CH-;
a sloučeninu vzorce 2.2
(2.2), ve kterém R53 znamená ethyl, R54 znamená methyl nebo ethyl a R55 znamená -CH(Me)CH2OMe, <S>-CH(Me)-CH2OMe, CH2OMe nebo CH2O-CH2CH3;
a sloučeninu vzorce 2.3
Me
ve kterém R56 znamená CH(Me)-CH2OMe nebo <S>CH(Me)-CH2OMe;
a sloučeninu vzorce 2.4 (2-4), '59 ve kterém R57 znamená chlor, methoxy nebo methylthio, R58 znamená ethyl a R59 znamená ethyl, isopropyl, -C(CN)(CH3)CH3 nebo terc-butyl;
-2CZ 304537 B6
ve kterém znamená vodík, methoxy nebo ethoxy, R^ znamená vodík, methyl, methoxy nebo fluor, Ró4 znamená COOMe, fluor nebo chlor, Rú5 znamená vodík nebo methyl, Y znamená methin, C-F nebo dusík, Z znamená methin nebo dusík a Róó znamená fluor nebo chlor;
a sloučeninu vzorce 2.7
(2-7), ve kterém R67 znamená vodík nebo -C(O)-S-n-oktyl;
a sloučeninu vzorce 2.12
(2.12), ve kterém R73 znamená NH2 nebo <S>NH2;
a sloučeninu vzorce 2.13
(2.13), ve kterém Yi znamená dusík, methin, NH-CHO nebo N-Me, Y2 znamená dusík, methin nebo CI, Y3 znamená methin, Y4 znamená methin nebo Y3 a Y4 společně tvoří síru nebo C-Cl, Y5 znamená dusík nebo methin, Y6 znamená methyl, difluormethoxy, trifluormethyl nebo methoxy, Y7 znamená methoxy nebo difluormethoxy a R74 znamená CONMe2, COOMe, COOC2H5, trifluormethyl, CH2-CH2CF3 nebo SO2CH2CH3, nebo její sodnou sůl; a sloučeninu vzorce 2.13.C
-3 CZ 304537 B6
Cl 0 CH,
/./ w
Ο'θΗ3 (2.13.C)
CH,
CH, a sloučeninu vzorce 2.14
(2.14), a sloučeninu vzorce 2.16
HOOC N PO(OH)2 H (2.16), a sloučeninu vzorce 2.18
(2.18), a sloučeninu vzorce 2.19
a sloučeninu vzorce 2.21
-4CZ 304537 B6
(2.21), a sloučeninu vzorce 2.25
(2.25), a sloučeninu vzorce 2.30
(2.30) a sloučeninu vzorce 2.33
O
II
OH
O
IL
Me—S—Me
I
Me (2.33).
Předmětem vynálezu je rovněž způsob kontroly nežádoucího rostlinného růstu v kulturách užitkových rostlin, jehož podstata spočívá v tom, že zahrnuje umožnění herbicidně účinnému množství kompozice podle nároku 1 působit na užitkovou rostlinu nebo na její lokalitu.
Výhodně je užitkovou rostlinou kukuřice nebo cukrová třtina. Výhodně se kultury užitkových rostlin ošetří uvedenou kompozicí v aplikačních množstvích odpovídajících celkovému množství účinné látky od 1 do 5000 g na hektar.
-5CZ 304537 B6
Ve výše uvedených vzorcích je „Me“ methylová skupina. Alkylové skupiny vyskytující se v definicích substituentů mohou být přímé nebo rozvětvené a jsou to například methylová skupina, ethylová skupina, n-propylová skupina, isopropylová skupina, n-butylová skupina, sec-butylová skupina, isobutylová skupina, terc-butylová skupina, pentylová skupina, hexylová skupina, heptylová skupina, oktylová skupina, nonylová skupina, decylová skupina, undecylová skupina a dodecylová skupina a také jejich rozvětvené isoformy. Alkoxyskupina, alkenylová skupina a alkynylová skupina jsou odvozeny od výše uvedených alkylových skupin. Alkenylová skupina a alkynylová skupina mohou být jednou nebo více, než jednou nenasycené.
Alkylenová skupina může být substituovaná jednou nebo více methylovými skupinami; s výhodou je taková alkylenová skupina v každém případě nesubstituovaná. Totéž platí pro všechny obsahující následující skupiny: skupinu cykloalkyl- obsahující 3 až 5 atomů uhlíku, skupinu oxacykloalkyl- obsahující 3 až 5 atomů uhlíku, skupinu thiacykloalkyl- obsahující 3 až 5 atomů uhlíku, skupinu dioxacykloalkyl- obsahující 3 až 4 atomy uhlíku, skupinu dithiacykloalkylobsahující 3 až 4 atomy uhlíku, skupinu thiacykloalkyl- obsahující 3 až 4 atomy uhlíku a skupinu N(CH2)-.
Atomem halogenu je obecně atom fluoru, chloru, bromu nebo jodu. Totéž platí pro atom halogenu v souvislosti s jinými definicemi, jako je halogenalkylová skupina nebo halogenfenylová skupina.
Halogenalkylovými skupinami obsahujícími 1 až 6 atomů uhlíku jsou například fluormethylová skupina, difluormethylová skupina, trifluormethylová skupina, chlormethylová skupina, dichlormethylová skupina, trichlormethylová skupina, 2,2,2-trifluorethylová skupina, 2-fluorethylová skupina, 2-chlorethylová skupina, pentafluorethylová skupina, l,l-difluor-2,2,2-trichlorethylová skupina, 2,2,3,3-tetrafluorethylová skupina a 2,2,2-trichlorethylová skupina, pentafluorethylová skupina, heptafluor-n-propylová skupina, perfluor-n-hexylová skupina; halogenalkylovými skupinami v definicích skupin R2, R3 a zejména R5 jsou s výhodou trichlormethylová skupina, dichlorfluormethylová skupina, difluorchlormethylová skupina, difluormethylová skupina, trifluormethylová skupina, pentafluorethylová skupina nebo heptafluor-n-propylová skupina.
Vhodnými halogenalkenylovými skupinami jsou alkenylové skupiny substituované jednou nebo vícekrát atomem halogenu, kdy atomy halogenu jsou atom fluoru, atom chloru, atom bromu nebo atom jodu a zejména atom fluoru nebo chloru, například 2,2-difluor-l-methylvinylová skupina, 3-fluorpropenylová skupina, 3-chlorpropenylová skupina, 3-brompropenylová skupina, 2,3,3— trifluorpropenylová skupina, 2,3,3-trichlorpropenylová skupina a 4,4,4-trifluorbut-2-en-lylová skupina. Výhodnými alkenylovými skupinami obsahujícími 2 až 12 atomů uhlíku substituovanými jednou, dvakrát nebo třikrát atomem halogenu jsou skupiny obsahující 2 až 5 atomů uhlíku v řetězci. Vhodnými halogenalkynylovými skupinami jsou například alkynylové skupiny substituované jednou nebo dvakrát atomem halogenu, kdy atomem halogenu je atom bromu nebo atom jodu a zejména atom fluoru nebo atom chloru, například 3-fluorpropynyl, 3-chlorpropynyl, 3-brompropynyl, 3,3,3-trifluorpropynylová skupina a 4,4,4-trifluor-but-2-yn-l-ylová skupina. Výhodnými alkynylovými skupinami substituovanými jednou nebo vícekrát atomem halogenu jsou skupiny obsahující 2 až 5 atomů uhlíku.
Alkoxyskupiny s výhodou obsahují 1 až 6 atomů uhlíku v řetězci. Alkoxyskupinou je například methoxyskupina, ethoxyskupina, propoxyskupina, isopropoxyskupina, n-butoxyskupina, isobutoxyskupina, sek-butoxyskupina nebo terc-butoxyskupina nebo pentyloxyskupina nebo hexyloxyskupina, s výhodou methoxyskupina a ethoxyskupina. Alkylkarbonylová skupina je s výhodou acetylová skupina nebo propionylová skupina. Alkoxykarbonylová skupina je například methoxykarbonylová skupina, ethoxykarbonylová skupina, propoxykarbonylová skupina, isopropoxykarbonylová skupina, n-butoxykarbonylová skupina, isobutoxykarbonylová skupina, sek-butoxykarbonylová skupina nebo terc-butoxykarbonylová skupina, s výhodou methoxykarbonylová skupina, ethoxykarbonylová skupina nebo terc-butoxykarbonylová skupina. Halogenalkoxyskupiny s výhodou obsahují řetězec o délce 1 až 8 atomů uhlíku.
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Halogenalkoxyskupinou je například fluormethoxyskupina, difluormethoxyskupina, trifluormethoxyskupina, 2,2,2-trifluorethoxyskupina, 1,1,2,2-tetrafluorethoxyskupina, 2-fluorethoxyskupina, 2-chlorethoxyskupina, 2,2-difluorethoxyskupina nebo 2,2,2-trichlorethoxyskupina, s výhodou difluormethoxyskupina, 2-chlorethoxyskupina nebo trifluormethoxyskupina. Alkylthioskupiny s výhodou obsahují řetězec o délce 1 až 8 atomů uhlíku.
Alkylthioskupinou je například methylthioskupina, ethylthioskupina, propylthioskupina, isopropylthioskupina, n-butylthioskupina, isobutylthioskupina, sek-butylthioskupina nebo tercbutylthioskupina, s výhodou methylthioskupina nebo ethylthioskupina. Alkylsulfínylovou skupinou je například methylsulfinylová skupina, ethylsulfínylová skupina, propylsulfinylová skupina, isopropylsulfmylová skupina, n-butylsulfinylová skupina, isobutylsulfmylová skupina, secbutylsulfínylová skupina nebo Zerc-butylsulfínylová skupina, s výhodou methylsulfinylová skupina nebo ethylsulfínylová skupina.
Alkylsulfonylovou skupinou je například methylsulfonylová skupina, ethylsulfonylová skupina, propylsulfonylová skupina, isopropylsulfonylová skupina, n-butylsulfonylová skupina, isobutylsulfonylová skupina, sek-butylsulfonylová skupina nebo terc-butylsulfonylová skupina, s výhodou methylsulfonylová skupina nebo ethylsulfonylová skupina.
Alkylaminoskupinou je například methylaminoskupina, ethylaminoskupina, n-propylaminoskupina, isopropy laminoskupina nebo buty laminoskupina. Dialkylaminoskupinou je například dimethylaminoskupina, methylethylaminoskupina, diethylaminoskupina, n-propylmethylaminoskupina, dibutylaminoskupina nebo diisopropylaminoskupina. Výhodné jsou alkylaminoskupiny obsahující řetězec o délce 1 až 4 atomy uhlíku. Alkoxyalkylové skupiny s výhodou obsahují 1 až 6 atomů uhlíku. Alkoxyalkylovou skupinou je například methoxymethylová skupina, methoxyethylová skupina, ethoxymethylová skupina, ethoxyethylová skupina, n-propoxymethylová skupina, n-propoxyethylová skupina, isopropoxymethylová skupina nebo isopropoxyethylová skupina. Alkylthioalkylové skupiny s výhodou obsahují 1 až 6 atomů uhlíku. Alkylthioalkylovou skupinou je například methylthiomethylová skupina, methylthioethylová skupina, ethylthiomethylová skupina, ethylthioethylová skupina, n-propylthiomethylová skupina, n-propylthioethylová skupina, isopropylthiomethylová skupina, isopropylthioethylová skupina, butylthiomethylová skupina, butylthioethylová skupina nebo butylthiobutylová skupina.
Cykloalkylové skupiny s výhodou obsahují 3 až 6 kruhových atomů uhlíku a mohou být substituované jednou nebo více methylovými skupinami; s výhodou jsou to nesubstituované skupiny, například cyklopropylová skupina, cyklobutylová skupina, cyklopentylová skupina nebo cyklohexylová skupina. Fenylová skupina, včetně feny lově skupiny, jako součásti substituentů, jako je fenoxyskupina, benzylová skupina, benzyloxyskupina, benzoyíová skupina, fenylthioskupina, fenylalkylová skupina, fenoxyalkylová skupina nebo tosylová skupina, může být v mono- nebo poly-substituované formě, kdy substituenty mohou podle toho, jak je to vhodné v polohách ortho-, meta- a/nebo para-.
Předkládaný vynález zahrnuje také soli, které mohou sloučeniny obecného vzorce I tvořit s aminy, bázemi na základě alkalických kovů a kovů alkalických zemin nebo kvartemími amoniovými bázemi. Mezi hydroxidy alkalických kovů a kovů alkalických zemin používanými jako sloučeniny pro tvorbu solí, jsou významné hydroxidy lithný, sodný, draselný, hořečnatý nebo vápenatý, ale zvláště hydroxid sodný nebo draselný.
Příklady vhodných aminů pro tvorbu amoniových solí, které přicházejí v úvahu, patří amoniak a také primární, sekundární a terciární alky laminy obsahující 1 až 18 atomů uhlíku, hydroxyalkylaminy obsahující 1 až 4 atomy uhlíku a alkoxyalkylaminy obsahující 1 až 4 atomy uhlíku, například methylamin, ethylamin, n-propylamin, isopropylamin, čtyři izomeiy butylaminu, namylamin, isoamylamin, hexylamin, heptylamin, oktylamin, nonylamin, decylamin, pentadecyl-7CZ 304537 B6 amin, hexadecylamin, heptadecylamin, oktadecylamin, methyl-ethylamin, methyl-isopropylamin, methyl-hexylamin, methyl-nonylamin, methyl-pentadecylamin, methyl-oktadecylamin, ethyl-butylamin, ethyl-heptylamin, ethyl-oktylamin, hexyl-heptylamin, hexyl-oktylamin, dimethylamin, diethylamin, di-n-propylamin, diisopropylamin, di-n-butylamin, di-n-amylamin, diisoamylamin, dihexylamin, diheptylamin, dioktylamin, ethanolamin, n-propanolamin, isopropanolamin, Ν,Ν-diethanolamin, N-ethylpropanolamin, N-butylethanolamin, allylamin, nbutenyI-2-amin, n-pentenyl-2-amin, 2,3-dimethylbutenyl-2-amin, dibutenyl-2-amin, nhexenyl-2-amin, propylendiamin, trimethylamin, triethylamin, tri-n-propylamin, triisopropylamin, tri-n-butylamin, triisobutylamin, tri-sec-butylamin, tri-n-amylamin, methoxyethylamin a ethoxyethylamin; heterocyklické aminy, například pyridin, chinolin, isochinolin, morfolin, piperidin, pyrrolidin, indolin, chinuklidin a azepin; primární arylaminy, například aniliny, methoxyaniliny, ethoxyaniliny, o-, m- a p-toluidiny, fenylendiaminy, benzidiny, naíitylaminy a o-, m- a p-chloraniliny; ale zejména triethylamin, isopropylamin a diisopropylamin.
Je mimořádně překvapivé, že kombinace aktivní složky obecného vzorce Ia s jednou nebo více aktivními složkami vybranými ze sloučenin vzorce 2.1 až 2.33 překračuje aditivní účinek na plevele, které se mají kontrolovat, jak by se dalo očekávat, a tak rozšiřuje rozsah působení jednotlivých aktivních složek zejména ve dvou ohledech: za prvé se snižuje aplikované množství sloučeniny obecného vzorce Ia a sloučenin 2.1 až 2.33 zatímco se zachová dobrá hladina působení a za druhé kompozice podle předkládaného vynálezu poskytuje vysokou úroveň kontroly plevele také v těch případech, ve kterých jednotlivé látky, při aplikaci v malém měřítku, byly z agronomického hlediska nepoužitelné. Výsledkem je značné rozšíření spektra plevele a další vzrůst selektivity vzhledem k plodinám užitečných rostlin, což je potřebné a žádoucí v případě neúmyslného předávkování aktivní složkou. Kompozice podle předkládaného vynálezu také umožňují vyšší flexibilitu při používání u plodin za zachování vynikající kontroly plevele u plodin užitečných rostlin.
Kompozice podle předkládaného vynálezu se mohou použít proti mnoha agronomicky významným plevelům, jako jsou Stellaria, Nasturtium, Agrostis, Digitaria, Avena, Setaria, Sinapis, Lolium, Solanum, Phaseolus, Echinochloa, Scirpus, Monochoria, Sagittaria, Bromus, Alopecurus, Sorghum halepense, Rottboellia, Cyperus, Abutilon, Sida, Xanthium, Amaranthus, Chenopodium, Ipomoea, Chrysanthemum, Galium, Viola a Veronica. Kompozice podle předkládaného vynálezu je také vhodná pro všechny způsoby aplikace běžně používané v zemědělství, například preemergentní aplikaci, postemergentní aplikaci a moření semen. Kompozice podle předkládaného vynálezu je vhodná zejména pro kontrolu plevele u plodin užitečných rostlin, jako jsou obiloviny, řepka, cukrová řepa, cukrová třtina, plantážní rostliny, rýže, kukuřice a sójové boby a také pro neselektivní kontrolu plevele.
„Plodinami“ se rozumí takové plodiny, u kterých vznikla odolnost k herbicidům nebo třídám herbicidů jako následek běžných postupů pěstování nebo genetického inženýrství.
Sloučeniny obecného vzorce Ia se mohou připravit analogickým způsobem, jako je popsáno v mezinárodní patentové přihlášce WO 97/46 530, pomocí a) reakce sloučeniny vzorce II
N (R) (II),
-8CZ 304537 B6 kde R a m jsou stejné, jako bylo definováno pro sloučeniny vzorce I a X je odstupující skupina, například atom halogenu, v inertním, organickém rozpouštědle v přítomnosti báze, se sloučeninou vzorce III, IV, V nebo VI
kde R2o, R23, R30 a Rto jsou hydroxylová skupina a ostatní substituenty jsou stejné, jako bylo definováno pro sloučeniny obecného vzorce I, za vzniku sloučenin vzorce VII, VIII, IX nebo X
a potom izomerací těchto sloučenin, například v přítomnosti báze a katalytického množství dimethylaminopyridinu (DMAP) nebo zdroje kyanidu; nebo
-9CZ 304537 B6
b) vzorce sloučeniny vzorce XI
OH (XI) , (R) kde R a m jsou stejné, jako bylo definováno pro sloučeniny vzorce I, se sloučeninami vzorce III, IV, V nebo VI v inertním, organickém rozpouštědle, v přítomnosti báze a kondenzačního činidla, za vzniku sloučeniny vzorce Vil, VIII, IX nebo X, a potom izomerací této sloučeniny, například způsobem popsaným u způsobu a).
Sloučeniny obecného vzorce I, kde Q je skupina Q5 kde Z je atom síry a R36 a Ri jsou stejné, jako bylo definováno pro sloučeniny obecného vzorce I, se mohou připravit způsoby, které jsou analogické známým postupům (například popsaným v mezinárodní patentové přihlášce WO 97/43 270), buď
a) převedením sloučeniny vzorce XII (R)m kde R36, R a m jsou definovány výše, v přítomnosti báze, sirouhlíku a alkylačního činidla vzorce XIII (XIII), kde Roi je stejná, jako bylo definováno pro sloučeniny obecného vzorce I a X] je odstupující skupina, například atom halogenu nebo sulfonátová skupina, na sloučeninu obecného vzorce XIV (R)m '36
- 10CZ 304537 B6 kde Z je atom síry a R, Roi, R36 a m jsou stejné, jako bylo definováno výše a potom cyklizací této sloučeniny hydrochloridem hydroxylaminů, popřípadě v rozpouštědle, v přítomnosti báze, za vzniku sloučeniny vzorce Ie
(Ie), kde Z je atom síry a R, R36, Rq] a m jsou stejné, jako bylo definováno výše, a potom oxidací této sloučeniny oxidačním činidlem, například meta-chlorperbenzoovou kyselinou (m-CPBA).
Příprava sloučenin obecného vzorce I je ilustrován podrobněji v následujících reakčních schématech 1 a 2.
Reakční schéma 1 způsob a):
(R)m-[— ' 11 + III, IV, V nebo VI
V
II báze, např. (C2H6)3N, rozpouštědlo, např. CH2CI2 0-110 °C
-► VII, Vlil, IX, nebo X
KCN kat.
isomerace báze, např. (C2HS)3N, —►
způsob b):
(R)m
XI báze, např. (C2H5)3N, kondenzace
OH III, IV. V nebo VI -—-► VII, Vlil, IX, nebo X + činidlo, např.
|-N+ Cl CH3 rozpouštědlo, např. CH2CI2 0-110°C
KCN kat isomerace: báze, např. (C2H5)3N
-11 CZ 304537 B6
Sloučeniny obecného vzorce I obsahující skupiny Qb Q2, Q3 a Q4, kde R2o, R23, R3o a R40 jsou hydroxylová skupina, se mohou připravit podle schématu uvedeného výše.
Reakční schéma 2
K2COj/CS2, Ro,-X„
XIII R(m) rozpouštědlo, např. DMF nebo^
KF/AI/CS2, R0,-x, *
XIII rozpouštědlo, např. CH3CN nebo NaH/CS2, R0,-Xv
XIII rozpouštědlo, např. DMSO
SR,
XIV
Pro přípravu sloučenin obecného vzorce I, kde Q je skupina Qi až Q4 a R2o, R23, R3o a Rto jsou hydroxylová skupina, se v souladu s reakčním schématem 1, způsob a) použijí jako výchozí látky deriváty karboxylové kyseliny obecného vzorce II, kde X je odstupující skupina, například atom halogenu, například atom jodu, bromu nebo zejména chloru, N-oxyftalimid nebo N,O-dimethyl/ N=C-NH hydroxylaminoskupina nebo aktivovaná esterová skupina, například ' ' o(vytvořená z dicyklohexylkarbodiimidu (DDC) a vhodné karboxylové kyseliny) nebo
C2H5N=C-NH(CH2)3N(CH3)2
O- (vytvořená z N-ethyl-N'-(3-dimethylaminopropyl)karbodiimidu (EDC) a vhodné karboxylové kyseliny). Tyto sloučeniny se reagují v inertním organickém rozpouštědle, například halogenovaném uhlovodíku, například dichlormethanu, nitrilu, například acetonitrilu, nebo v aromatickém uhlovodíku, například toluenu, a v přítomnosti báze, například alkylaminu, například triethylaminu, aromatickém aminu, například pyridinu nebo 4-dimethylaminopyridinu (DMAP), s derivátem dionu vzorce III, IV, V nebo VI za vzniku izomemích enoletherů vzorce VII, VIII, IX a X. Esterifikace se provádí při teplotách 0 až 110 °C.
Izomerace derivátů esterů vzorce VII, VIII, IX a X za vzniku derivátů dionu obecného vzorce I (kde R20, R23, R30 a Rto jsou hydroxylová skupina) se může provádět například analogickým způsobem, jako je popsáno v EP 369 803 v přítomnosti báze, například alkylaminu, například triethylaminu, uhličitanu, například uhličitanu draselného a katalytického množství DMAP nebo zdroje kyanidu, například kyanhydrinu acetonu nebo kyanidu draselného.
Podle reakčního schématu 1, způsob b) se může požadovaný dion obecného vzorce I (kde R2o, R23, R3o a Rto jsou hydroxylová skupina) získat například analogickým způsobem, jako je popsáno v Chem. Lett. 1975, 1045 pomocí esterifikace karboxylových kyselin vzorce XI deriváty dionů vzorce III, IV, V nebo VI v inertním rozpouštědle, například halogenovaném uhlovodíku, například dichlormethanu, nitrilu, například acetonitrilu, nebo aromatickém uhlovodíku, například toluenu, v přítomnosti báze, například alkylaminu, například triethylaminu, a kondenzačního činidla, například 2-chlor-l-methyl-pyridiniumjodidu. Esterifikace se provádí v závislosti na použitém rozpouštědle při teplotě 0 až 110 °C a poskytuje za prvé podle postupu popsaného ve způsobu a) k izomemímu esteru obecného vzorce I, který se může izomerovat podle postupu popsaného ve způsobu a), například v přítomnosti báze a katalytického množství DMAP, nebo
- 12CZ 304537 B6 zdroje kyanidu za vzniku požadovaného derivátu dionu vzorce I (kde R20, R23, R30 a R40 jsou hydroxylová skupina).
Příprava sloučenin obecného vzorce I, kde Q je skupina Q5, se může provádět podle postupu popsaného v reakčním schématu 2 reakcí derivátu b-diketonu vzorce XII, například analogickým způsobem, jako je popsáno v Synthesis 1991, 301; ibid. 1988, 793; nebo Tetrahedron 32, 3055 (1976), se sirouhlíkem v přítomnosti báze, například uhličitanu, například uhličitanu draselného, hydridu kovu, například hydridu sodného, nebo fluoridu draselného na alumině a alkylačního činidla vzorce XIII, kde Xj je odstupující skupina, například atom halogenu, například atom jodu, bromu nebo zejména atom chloru, skupina R25OSO2O-, skupina CH3SO2O- nebo skupina
CH \\ zz *
Reakce se s výhodou provádí v rozpouštědle, například amidu, například Ν,Ν-dimethylformamidu (DMF), sulfoxidu, například dimethylsulfoxidu (DMSO), nebo nitrilu, například acetonitrilu. Vznikající thioacetal ketenu vzorce XIV se cyklizuje za použití hydrochloridu hydroxylaminu v přítomnosti báze, například octanu sodného, v rozpouštědle, například alkoholu, například ethanolu nebo etheru, například tetrahydrofuranu, za vzniku sloučeniny obecného vzorce Ie, kde Z je S-. Cyklizační reakce se provádí při teplotách 0 až 100 °C. Sloučeniny obecného vzorce Ie (z = S) se mohou popřípadě oxidovat pomocí způsobů, které jsou analogické standardním postupům, například za použití peroxokyselin, například meta-chlorperbenzoové kyseliny (m-CPBA) nebo peroctové kyseliny, za vzniku odpovídajících sulfonů a sulfoxidů vzorce Ie (Z = SO- nebo SO2-), kde stupeň oxidace na atomu síry (Z = SO- nebo SO2-) se může kontrolovat pomocí množství použitého oxidačního činidla.
Oxidace sloučeniny obecného vzorce Ie (Z = SO- nebo SO2-) se provádí podle postupu popsaného například v H. O. House, „Modem Synthetic Reactions“ W. A. Benjamin, lne., Menlo Park, Califomia, 1972, strany 334-335 a 353-354.
Aktivované deriváty karboxylových kyselin obecného vzorce II v reakčním schématu 1 (způsob a), kde X je odstupující skupina, například atom halogenu, například atom bromu, atom jodu nebo zejména atom chloru, se mohou připravit podle známých standardních postupů, například jak je popsáno v C. Ferri „Reaktionen der organischen Synthese“, Georg Thieme Verlag, Stuttgart, 1978, strana 461 ff a jak je popsáno v reakčním schématu 3.
Reakční schéma 3
W,-X, DMF
Podle reakčního schématu 3 se příprava sloučenin obecného vzorce II (X je odstupující skupina) nebo II (X je atom halogenu) provádí například za použití halogenačního činidla, například thionylhalogenidu, například thionylchloridu nebo bromidu; a halogenidu fosforečného nebo oxyhalogenidu fosforečného, například chloridu fosforečného nebo oxychloridu fosforečného nebo bromidu fosforečného nebo bromidu fosforylu; nebo oxalylhalogenidu, například oxalylchloridu, nebo za použití činidla pro vznik aktivovaného esteru, například N,N'-dicyklohexylkarbodiimidu (DCC) nebo N-ethyl-N'-(3-dimethylaminopropyl)karbodiimidu (EDC) vzorce X. Ve sloučenině obecného vzorce X, to znamená halogenačním činidle, je X například odstupující skupina, napří- 13 CZ 304537 B6 klad atom halogenu, například atom fluoru, atom bromu nebo atom jodu a zejména atom chloru a W, je například PC12, SOCI, SOBr nebo C1COCO.
Způsob se výhodně provádí v inertním organickém rozpouštědle, například alifatickém, halogenovaném alifatickém, aromatickém nebo halogenovaném aromatickém uhlovodíku, například nhexanu, benzenu, toluenu, xylenech, dichlormethanu, 1,2-dichlorethanu nebo chlorbenzenu, při teplotě mezi -20 °C až teplotou varu reakční směsi, s výhodou při teplotě 40 až 150 °C, a v přítomnosti katalytického množství Ν,Ν-dimethylformamidu. Tyto reakce jsou obecně známé a popsané v literatuře v mnoha variantách s ohledem na odstupující skupinu X.
Sloučeniny obecného vzorce III, IV, V a VI jsou známé a mohou se připravit analogickým postupem, jako je popsáno například v patentových přihláškách WO 92/07 837, DE 3 818 958, EP 338 992 a DE 3 902 818.
Sloučeniny obecného vzorce XII v reakčním schématu 2 se mohou získat pomocí standardních postupů, například z odpovídajících sloučenin vzorce II
O
(R) kde R a m jsou stejné, jako bylo definováno pro sloučeniny vzorce I a X je odstupující skupina, například atom halogenu, například prostřednictvím Calisenovy kondenzace nebo ze sloučenin obecného vzorce II reakcí se solí ketokarboxylové kyseliny vzorce XV
COO'M+ z
(XV), kde R36 je stejná, jako bylo definováno pro sloučeniny vzorce I a M+je ion alkalického kovu (například podle WO 96/26 192).
Sloučeniny obecných vzorců II a XI jsou známé a mohou se připravit analogickým způsobem, jako je popsáno například v WO 97/46 530, Heterocykles, 48, 779 (1998), Heterocykles, 46, 129 (1997) nebo Tetrahedron Letters, 1749 (1998).
Pro přípravu všech dalších sloučenin obecného vzorce I funkcionalizovaných podle definice (R)m, je dostupných mnoho známých standardních postupů, například alkylace, halogenace, acylace, amidace, oximace, oxidace a redukce, přičemž výběr vhodného způsobu přípravy se řídí vlastnostmi (reaktivitou) substituentů v příslušných meziproduktech. Příklady takových reakcí jsou uvedeny v WO 97/46 353.
Všechny další sloučeniny spadající do rozsahu vzorce I se mohou připravit jednoduchými způsoby, s ohledem na chemické vlastnosti pyridilové skupiny a skupiny Q.
Cílové produkty obecného vzorce I se mohou izolovat pomocí běžných postupů pomocí koncentrace nebo odpaření rozpouštědla a mohou se čistit pomocí rekrystalizace nebo triturace pevného
- 14CZ 304537 B6 zbytku v rozpouštědle, ve kterém nejsou snadno rozpustné, jako jsou ethery, aromatické uhlovodíky nebo chlorované uhlovodíky, pomocí destilace nebo pomocí kolonové chromatografie a za použití vhodného rozpouštědla.
Dále budou odborníkovi pracujícímu v oblasti organické chemie zřejmé postupy, kterými se budou určité reakce s výhodou provádět, aby se zabránilo nežádoucím vedlejším reakcím.
Pokud není syntéza vedena k izolaci čistých izomerů, může být produkt ve formě směsi dvou nebo více izomerů. Izomery se mohou oddělit pomocí postupů, které jsou odborníkům pracujícím v této oblasti známé.
Příklady provedení vynálezu
Příklad Pl
Příprava 4-hydroxy-3-(2-methyl-6-trifluormethyl-pyridin-3-karbonyl)-bicyklo[3.2.1 ]okt-3en-2-onu:
6,68 g (0,0305 mol) methylesteru 2-methyl-6-trifluormethylnikotinové kyseliny (připraveného podle postupu popsaného v Heterocykles, 46, 129 (1997)) se rozpustí v 250 ml směsi methanol/voda (3:1) a po částech se při 22 °C přidá 1,92 g (0,046 mol) hydrátu hydroxidu lithného. Po 4 hodinách při 22 °C se reakční směs přidá k ethylacetátu a 2N roztoku kyseliny chlorovodíkové; organická fáze se třikrát promyje vodou, suší se nad síranem sodným a odpaří se. Zbytek se trituruje malým množstvím hexanu. Po filtraci se získá 5,69 g (90 % teoretického výtěžku) očekávané 2-methyl-6-trifluormethyl-nikotinové kyseliny o teplotě tání 147 až 149 °C.
2,0 g (0,0098 mol) získané 2-methyl-6-trifluormethylnikotinové kyseliny se rozpustí v 20 ml oxalylchloridu. Přidají se tři kapky dimethylformamidu a směs se zahřívá 1 hodinu kvaru pod zpětným chladičem. Směs se potom odpaří za použití rotační odparky a zbývající (2-methyl-6trifluormethylnikotinoylchlorid) se převede do 30 ml methylenchloridu. Při 0 °C se přikape 2,7 ml (0,0196 mol) triethylaminu a 0,12 g (0,00098 mol) dimethylaminopyridinu a potom 1,49 g (0,0108 mol) bicyklo [3,2,l]okt-2,4-dionu, rozpuštěného v 20 ml methylenchloridu. Po 3 hodinách při 22 °C se reakční směs extrahuje protřepáním s 2N roztokem kyseliny chlorovodíkové. Oddělená methylenchloridová fáze se promyje vodou a potom se extrahuje 10% vodným roztokem hydrogenuhličitanu sodného, suší se nad síranem sodným a odpaří se. Získá se 3,18 g (výtěžek 100 %) 4-oxo-bicyklo[3,2,l]okt-2-en-2-ylesteru 2-methyl-6-trifluormethyl-nikotinové kyseliny ve formě oleje, který se dále použije bez čištění.
3,02 g (0,0093 mol) 4-oxo-bicyklo[3,2,l]okt-2-en-2-ylesteru methyl-6-trifluormethyl-nikotinové kyseliny a 1,9 ml (0,0136 mol) triethylaminu se rozpustí v 45 ml acetonitrilu. Při 22 °C se přidá 0,01 ml kyanhydřinu acetonu. Po 18 hodinách při 22 °C se reakční směs nalije do směsi vody a 2N roztoku kyseliny chlorovodíkové a extrahuje se protřepáním s ethylacetátem. Ethylacetátová fáze se promyje vodou a potom solankou, suší se nad síranem sodným a odpaří se. Zbytek se rozpustí v malém množství horkého acetonu. Po stání produkt vykrystalizuje. Po filtraci se získá 0,99 g (výtěžek 33 %) očekávaného 4-hydroxy-3-(2-methyl-6-trifluormethylpyridin-3-karbonyl)bicyklo[3,2,l]okt-3-en-2-onu ve formě bílých krystalů (teplota tání 75 až 77 °C).
-15CZ 304537 B6
Příklad P2 (5-Cyklopropyl-3-methylsulfanylisoxazol-4-yl)(2-methyl-6-triíluormethylpyridin-3-yl)methanon
14,8 g (0,080 mol) terc-butylesteru 3-cyklopropyl-3-oxopropionové kyseliny se rozpustí v 25 ml methanolu a přidá se 1,93 g (0,080 mol) hořčíku. Za chlazení v ledové lázni se přikape 7 ml tetrachlormethanu a reakční směs se míchá 1 hodinu do dokončení reakce. Po odpaření se zbytek suspenduje ve 100 ml acetonitrilu a při 22 °C se přikape 16,31 g (0,073 mol) 2-methyl-6trifluormethylnikotinoylchloridu (připraveného způsobem popsaným v příkladu Pl), rozpuštěného v 50 ml acetonitrilu. Po 6 hodinách se reakční směs převede do ethylacetátu a promyje se nasyceným vodným roztokem hydrogenuhličitanu sodného. Ethylacetátová fáze se oddělí a promyje se vodou, suší se nad síranem sodným a odpaří se. Zbytek se rozpustí ve 160 ml dichlormethanu a při 22 °C se přikape 10 ml trifluoroctové kyseliny. Po 18 hodinách se reakční směs nalije do vody a extrahuje se dichlormethanem. Dichlormethanová fáze se promyje vodou a potom solankou, suší se nad síranem sodným a odpaří se. Získá se 17,3 g (výtěžek 88 %) l-eyklopropyl-3(2-methyl-6-trifluormethylpyridin-3-yl)propan-l,3-dionu ve formě oleje, který se dále použije bez čištění.
15,0 g (0,055 mol) získaného l-cyklopropyl-3-(2-niethyl-6-trifluormethylpyridin-3-yl)propan-l,3-dionu se rozpustí v 150 ml dimethylformamidu a při 0 °C se po částech přidá 50 g fluoridu draselného naneseného na nosiči z oxidu hlinitého (Alox) (0,0055 mol/g, 0,276 mol). Po 5 minutách se přidá 6,7 g (0,088 mol) sirouhlíku. Po 2 hodinách se přikape 23,6 g (0,166 mol) methyljodidu a reakční směs se zahřeje na 22 °C. Po 2 hodinách se Alox odfiltruje, filtrát se nalije do vody a extrahuje se protřepáním s ethylacetátem. Ethylacetátová fáze se promyje vodou a solankou, suší se nad síranem sodným a odpaří se. Zbytek se čistí pomocí chromatografie na silikagelu (eluent: ethylacetát/hexan 15/1). Získá se 12,0 g (výtěžek 60 %) 2-(bismethylsulfanylmethylen)-l-cyklopropyl-3-(2-methyl-6-trifluomiethylpyridin-3-yl)-propan-l,3-dionu ve formě pevné látky.
12,0 g (0,033 mol) získaného produktu se suspenduje v 120 ml ethanolu společně s 5,4 g (0,066 mol) bezvodého octanu sodného. Přidá se 4,6 g (0,066 mol) hydrochloridu hydroxylaminu a reakční směs zahřívá 5 hodin na 22 °C. Potom se přidá dalších 2,7 g bezvodého octanu sodného a 2,3 g hydrochloridu hydroxylaminu. Po 18 hodinách se reakční směs zředí vodou a extrahuje ethylacetátem. Ethylacetátová fáze se promyje vodou a solankou, suší se nad síranem sodným a odpaří se. Po trituraci malým množstvím ethylacetátu se získá 9,0 g (79,5 %) požadovaného produktu ve formě bílých krystalů (teplota tání 103 až 104 °C).
Příklad P3 (5-Cyklopropyl-3-methylsulfmylisoxazol-4-yl)-(2-methyl-6-trifluormethylpyridin-3-yl)methanon
1,50 g (0,0043 mol) (5-cyklopropyl-3-methylsulfanylisoxazoM-yl)(2-methyl-6-trifluormethylpyridin-3-yl)methanolu se rozpustí v 30 ml směsi aceton/voda (2:1) a po částech se při 22 °C přidá 1,02 g (0,0048 mol) jodistanu sodného. Po 5 hodinách se reakční směs odpaří pomocí rotační odparky. Zbytek se převede do vody a ethylacetátu. Ethylacetátová fáze se suší nad síranem sodným a odpaří se. Zbytek se čistí pomocí chromatografie na silikagelu (eluent: ethylacetát/hexan 3/1). Získá se 0,8 g (51 %) požadovaného produktu ve formě bílých krystalů o teplotě tání 96 až 97 °C.
-16CZ 304537 B6
Příklad P4
Příprava 3-hydroxy-4,4-dimethyl-2-{2-methyl-6-trifluormetliylpyridin-3-karbonyl)cyklohex2-enonu (A2-B24)
6,68 g (0,0305 mol) methylesterů 2-methyl-6-trifluormethylnikotinové kyseliny (připraveného podle postupu popsaného v Heterocykles, 46, 129 (1997)) se rozpustí v 250 ml směsi methanol/voda (3:1) a po částech se při 22 °C přidá 1,92 g (0,046 mol) hydrátu hydroxidu lithného. Po 4 hodinách při 22 °C se reakční směs přidá k ethylacetátu a 2N roztoku kyseliny chlorovodíkové; organické fáze se promyje třikrát vodou, suší se nad síranem sodným a odpaří se a zbytek se trituruje malým množstvím hexanu. Po filtraci se získá 5,69 g (výtěžek 90 %) očekávané 2methyl-6-trifluormethyl-nikotinové kyseliny o teplotě tání 147 až 149 °C.
Získaná 2-methyl-6-trifluormethylnikotinová kyselina (1,026 g, 0,005 mol) se rozpustí ve 20 ml oxalylchloridu. Přidají se tři kapky dimethylformamidu a směs se zahřívá 1 hodinu k varu pod zpětným chladičem. Směs se odpaří pomocí rotační odparky a zbytek (2-methyl-6-trifluormethylnikotinoylchlorid) se převede do 100 ml methylenchloridu. Při teplotě 0 °C se přidá 1,6 ml (0,0115 mol) triethylaminu a 0,7 g (0,005 mol) 4,4-dimethylcyklohexan-l,3-dionu. Po 2 hodinách při 22 °C se rozpouštědlo odpaří na rotační odparce a zbytek se rozpustí v 55 ml acetonitrilu a za účelem přesmyku meziproduktu se přidá 0,15 ml (0,0016 mol) kyanhydrinu acetonu a 0,79 ml (0,0057 mol) triethylaminu. Po 4 hodinách míchání při teplotě místnosti se reakční směs odpaří. Získaný sirup se čistí pomocí chromatografie na silikagelu. Světle žlutý viskózní olej, který se získá za eluce směsí toluen, ethylalkohol, dioxan, triethylamin a voda (100:40:20:20:5 objemově) (Rf=0,39 vzhledem ke jmenované směsi jako mobilní fázi), se rozpustí v dichlormethanu a promyje se postupně 75 ml 5% kyseliny chlorovodíkové a 75 ml vody. Po sušení organického roztoku síranem sodným a odpaření se získá 1,05 g (63 %) čisté sloučeniny uvedené v názvu.
*H NMR (de-DMSO, δ v ppm): 1,342, s, 6H: 2,088, t, J 9Hz, 2H: 2,685, s, 3H: 2,982, t, J 9Hz, 2H:8,030, d, J 8,1Hz, IH: 8,094, d, J 8,1Hz, 1H.
Příklad P5
Příprava 5-methyl-5-trifluormethylcyklohexan-l,3-dionu (příklad B1066):
0,64 g sodíku se umístí do 40 ml ethanolu, přidá se 3,23 ml methylesterů kyseliny octové a 4,9 g isopropylesteru 4,4,4-trifluor-3-methyl-but-2-enoové kyseliny a směs se zahřívá 18 hodin k varu pod zpětným chladičem. Po extrakci zředěnou kyselinou chlorovodíkovou a ethylacetátem se organická fáze odpaří. Získaný nečištěný methylester 2-methyl-4,6-dioxo-2-trifluormethylcyklohexankarboxylové kyseliny se za varu esterifikuje v přítomnosti 9,1 g hydroxidu sodného ve směsi methanolu a vody. Směs se potom okyselí kyselinou chlorovodíkovou a extrahuje se čerstvým ethylacetátem. Po rekiystalizaci z ethylacetátu se získá čistá 5-methyl-5-trifluormethyl-cyklohexan-l,3-dion o teplotě tání 150 až 152 °C.
Příklad P6
Příprava methylesterů 2-hydroxy-1 -methoxy-5-methy l-4-oxo-cyklohex-2-enkarboxylové kyseliny (B1069):
Během 20 minut se připraví 30% roztok 35,8 g methanolátu sodného v 65 ml dimethylsulfoxidu a při 30 až 35 °C se reaguje se směsí 16,7 g 3-methyl-3-buten-2-onu a 32,4 g dimethylesteru methoxymalonové kyseliny. Reakční směs se míchá 1 hodinu při 35 °C, okyselí se kyselinou chlorovodíkovou a potom se extrahuje několikrát dichlormethanem. Organické fáze se promyjí
- 17CZ 304537 B6 vodou a potom se extrahují několikrát dichlormethanem. Organické fáze se promyjí vodou, suší se a odpaří se. Po krystalizací z horkého ethylacetátu a hexanu se získá čistý methylester 2hydroxy-l-methoxy-5-methyl-4-oxocyklohex-2-enkarboxylové kyseliny o teplotě tání 117 až 117,5 °C.
Příklad P7
Příprava methylesteru 2-hydroxy-l-methoxy-5-methyl-3-(2-methyl-6-trifluormethylpyridin3-karbonyl)-4-oxocyklohex-2-en-karboxylové kyseliny (A2-B1069):
2,23 g čerstvého 2-methyl-6-trifluormethylnikotinoylchloridu se přidá ke směsi 2,14 g methylester 2-hydroxy-l-methoxy-5-methylA-oxo-cyklohex-2-enkarboxylové kyselin a 2,02 g triethylaminu v 30 ml acetonitrilu. Po 30 minutách se přidá 0,065 g kyanidu draselného a směs se míchá 18 hodin. Reakční směs se potom extrahuje při pH 2 vodou a ethylacetátem, suší se nad síranem hořečnatým a odpaří se. Po filtraci přes silikagel (mobilní fáze: ethylacetát/methanol/triethylamin 85:10:5), se získá čistý methylester 2-hydroxy-l_methoxy-5-methyl-3-(2-methyl6-trifluormethylpyridin-3-karbonyl)-4-oxocyklohex-2-en-karboxylové kyseliny ve formě viskózního oleje.
Příklad P8
Příprava 3-hydroxy-4-methoxy-6-methyl-2-(2-methyl-6-trifluormethylpyridin-3-karbonyl)cyklohex-2-enonu (A2-B1070)
0,586 g hydroxidu draselného se přidá k 1,4 g methylesteru 2-hydroxy-l-methoxy-5-methyl-3(2-methyl-6-trifluormethylpyridin-3-karbonyl)-4-oxocyklohex-2-enkarboxylové kyseliny ve směsi dioxan/voda (5:3) a reakční směs se míchá 3 hodiny. Směs se potom okyselí na pH 3 a extrahuje se čerstvým ethylacetátem. Surový produkt se čistí pomocí chromatografie analogickým způsobem, jako je popsáno v příkladu P7. Získá se 3-hydroxy-4-methoxy-6-methoxy-2(2-methyl-6-trifluormethylpyridin-3-karbonyl)cyklohex-2-enon ve formě viskózního oleje (podle NMR jako směs 3 tautomemích forem).
Sloučeniny uvedené v následujících tabulkách se mohou také připravit analogickým způsobem a za použití způsobů popsaných v obecných reakčních schématech 1 a 2 a v odkazech uvedených podle vynálezu. V následujících tabulkách znamená Ph fenylovou skupinu a CC je ethylenová skupina.
Tabulka 1: Sloučeniny obecného vzorce Ib:
(Ib)
Slouč. č. | R75 | R?6 | R77 |
1.001 | ch3 | cf3 | H |
1.002 | CH3CH2 | cf3 | H |
1.003 | (CH3)2CH | cf3 | H |
R78 t.t. (°C)
H 75-77
H
H 111-112
-18CZ 304537 B6
Slouč. | R75 | R76 | R77 | R78 | t.t. <°C) |
c. 1.004 | CH3(CH2)3 | cf3 | H | H | |
1.005 | Ph | cf3 | H | H | olej |
1.006 | CH2Br | cf3 | H | H | |
1.007 | CH2OCH3 | cf3 | H | H | 124-126 |
1.008 | CH2SMe | gf3 | H | H | olej |
1.009 | CH2S02Me | cf3 | H | H | 55-55 |
1.010 | SCH3 | cf3 | H | H | |
1.011 | soch3 | cf3 | H | H | |
1.012 | so2ch3 | cf3 | H | H | |
1.013 | SPh | cf3 | H | H | |
1.014 | SOPh | cf3 | H | H | |
1.015 | SO2Ph | cf3 | H | H | |
1.016 | ch3 | cf3cf2 | H | H | |
1.017 | ch3ch2 | cf3cf2 | H | H | |
1.018 | (CH3)2CH | cf3cf2 | H | H | |
1.019 | CH3(CH2)3 | cf3cf2 | H | H | |
1.020 | Ph | cf3cf2 | H | H | |
1.021 | CH2Br | cf3cf2 | H | H | |
1.022 | CH2OCH3 | cf3cf2 | H | H | |
1.023 | CH2SMe | cf3cf2 | H | H | |
1.024 | CH2SO2Me | cf3cf2 | H | H | |
1.025 | sch3 | cf3cf2 | H | H | |
1.026 | SOCH3 | cf3cf2 | H | H | |
1.027 | so2ch3 | cf3cf2 | H | H | |
1.028 | SPh | cf3cf2 | H | H | |
1.029 | SOPh | cf3cf2 | H | H | |
1.030 | SO2Ph | cf3cf2 | H | H | |
1.031 | ch3 | chf2 | H | H | |
1.032 | ch3ch2 | chf2 | H | H | |
1.033 | (CH3)2CH | chf2 | H | H | |
1.034 | CH3(CH2)3 | chf2 | H | H | |
1.035 | Ph | chf2 | H | H | |
1.036 | CH2Br | chf2 | H | H | |
1.037 | CH2OCH3 | chf2 | H | H | |
1.038 | CH2SMe | chf2 | H | H | |
1.039 | CH2SO2Me | chf2 | H | H | |
1.040 | sch3 | chf2 | H | H | |
1.041 | soch3 | chf2 | H | H | |
1.042 | so2ch3 | chf2 | H | H | |
1.043 | SPh | chf2 | H | H | |
1.044 | SOPh | chf2 | H | H | |
1.045 | SO2Ph | chf2 | H | H | |
1.046 | ch3 | cf3 | ch3 | H | |
1.047 | ch3ch2 | cf3 | ch3 | H | |
1.048 | (CH3)2CH | cf3 | ch3 | H | |
1.049 | CH3(CH2)3 | cf3 | ch3 | H | |
1.050 | Ph | cf3 | ch3 | H |
-19CZ 304537 B6
Slouč. | R75 | R76 | R77 R | |
1.051 | CH2Br | cf3 | ch3 | H |
1.052 | CH2OCH3 | cf3 | ch3 | H |
1.053 | CH2SMe | cf3 | ch3 | H |
1.054 | CH2SO2Me | cf3 | ch3 | H |
1.055 | sch3 | cf3 | ch3 | H |
1.056 | SOCH3 | cf3 | ch3 | H |
1.057 | SO2CH3 | cf3 | ch3 | H |
1.058 | SPh | cf3 | ch3 | H |
1.059 | SOPh | cf3 | ch3 | H |
1.060 | SO2Ph | cf3 | ch3 | H |
1.061 | ch3 | cf3cf2 | ch3 | H |
1.062 | CH3CH2 | cf3cf2 | ch3 | H |
1.063 | (CH3)2CH | cf3cf2 | ch3 | H |
1.064 | CH3(CH2)3 | cf3cf2 | ch3 | H |
1.065 | Ph | cf3cf2 | ch3 | H |
1.066 | CH2Br | cf3cf2 | ch3 | H |
1.067 | CH2OCH3 | cf3cf2 | ch3 | H |
1.068 | CH2SMe | cf3cf2 | ch3 | H |
1.069 | CH2SO2Me | cf3cf2 | ch3 | H |
1.070 | sch3 | cf3cf2 | ch3 | H |
1.071 | SOCH3 | cf3cf2 | ch3 | H |
1.072 | SO2CH3 | cf3cf2 | ch3 | H |
1.073 | SPh | cf3cf2 | ch3 | H |
1.074 | SOPh | cf3cf2 | ch3 | H |
1.075 | SO2Ph | cf3cf2 | ch3 | H |
1.076 | ch3 | chf2 | ch3 | H |
1.077 | CH3CH2 | chf2 | ch3 | H |
1.078 | (CH3)2CH | chf2 | ch3 | H |
1.079 | CH3(CH2)3 | chf2 | ch3 | H |
1.080 | Ph | chf2 | ch3 | H |
1.081 | CH2Br | chf2 | ch3 | H |
1.082 | CH2OCH3 | chf2 | ch3 | H |
1.083 | CH2SMe | chf2 | ch3 | H |
1.084 | CH2SO2Me | chf2 | ch3 | H |
1.085 | sch3 | chf2 | ch3 | H |
1.086 | soch3 | chf2 | ch3 | H |
1.087 | so2ch3 | chf2 | ch3 | H |
1.088 | SPh | chf2 | ch3 | H |
1.089 | SOPh | chf2 | ch3 | H |
1.090 | SO2Ph | chf2 | ch3 | H |
1.091 | ch3 | cf3 | H | ch3 |
1.092 | ch3ch2 | cf3 | H | ch3 |
1.093 | (CH3)2CH | cf3 | H | ch3 |
1.094 | ch3(ch2)3 | cf3 | H | ch3 |
1.095 | Ph | cf3 | H | ch3 |
1.096 | CH2Br | cf3 | H | ch3 |
1.097 | ch2och3 | cf3 | H | ch3 |
1.098 | CH2SMe | cf3 | H | ch3 |
t.t. (’C)
92-94
Slouč. | R75 | R76 | R77 | R78 |
1.099 | CH2SO2Me | cf3 | H | ch3 |
1.100 | sch3 | cf3 | H | ch3 |
1.101 | SOCH3 | cf3 | H | ch3 |
1.102 | SO2CH3 | cf3 | H | ch3 |
1.103 | SPh | cf3 | H | ch3 |
1.104 | SOPh | cf3 | H | ch3 |
1.105 | SO2Ph | cf3 | H | ch3 |
Tabulka 2: Sloučeniny obecného vzorce Ic:
T78 | O <75 0? | O Ϊ CHs (íT~«3 k Ά N 1 ch3 | (Ic) | |||
Slouč. | R75 | R76 | R77 | R78 | t.t.(°C) | |
č. | ||||||
2.001 | ch3 | cf3 | H | H | 107-109 | |
2.002 | ch3ch2 | cf3 | H | H | olej | |
2.003 | (CH3)2CH | cf3 | H | H | olej | |
2.004 | CH3(CH2)3 | cf3 | H | H | ||
2.005 | Ph | cf3 | H | H | olej | |
2.006 | CH2Br | cf3 | H | H | ||
2.007 | CH2OCH3 | cf3 | H | H | ||
2.008 | CH2SMe | cf3 | H | H | ||
2.009 | CH2SO2Me | cf3 | H | H | ||
2.010 | sch3 | cf3 | H | H | ||
2.011 | soch3 | cf3 | H | H | ||
2.012 | so2ch3 | cf3 | H | H | ||
2.013 | SPh | cf3 | H | H | ||
2.014 | SOPh | cf3 | H | H | ||
2.015 | SO2Ph | cf3 | H | H | ||
2.016 | ch3 | cf3cf2 | H | H | ||
2.017 | ch3ch2 | cf3cf2 | H | H | ||
2.018 | (CH3)2CH | cf3cf2 | H | H | ||
2.019 | ch3(ch2)3 | cf3cf2 | H | H | ||
2.020 | Ph | cf3cf2 | H | H | ||
2.021 | CH2Br | cf3cf2 | H | H | ||
2.022 | CH2OCH3 | cf3cf2 | H | H | ||
2.023 | CH2SMe | cf3cf2 | H | H |
Slouč. | R75 | R76 | R77 | R78 |
C · 2.024 | CH2SO2Me | CF3CF2 | H | H |
2.025 | sch3 | cf3cf2 | H | H |
2.026 | SOCH3 | cf3cf2 | H | H |
2.027 | SO2CH3 | cf3cf2 | H | H |
2.028 | SPh | cf3cf2 | H | H |
2.029 | SOPh | cf3cf2 | H | H |
2.030 | SO2Ph | cf3cf2 | H | H |
2.031 | ch3 | chf2 | H | H |
2.032 | ch3ch2 | chf2 | H | H |
2.033 | (CH3)2CH | chf2 | H | H |
2.034 | CH3(CH2)3 | chf2 | H | H |
2.035 | Ph | chf2 | H | H |
2.036 | CH2Br | chf2 | H | H |
2.037 | CH2OCH3 | chf2 | H | H |
2.038 | CH2SMe | chf2 | H | H |
2.039 | CH2SO2Me | chf2 | H | H |
2.040 | SCH3 | chf2 | H | H |
2.041 | soch3 | chf2 | H | H |
2.042 | so2ch3 | chf2 | H | H |
2.043 | SPh | chf2 | H | H |
2.044 | SOPh | chf2 | H | H |
2.045 | SO2Ph | chf2 | H | H |
2.046 | ch3 | cf3 | ch3 | H |
2.047 | ch3ch2 | cf3 | ch3 | H |
2.048 | (CH3)2CH | cf3 | ch3 | H |
2.049 | CH3(CH2)3 | cf3 | ch3 | H |
2.050 | Ph | cf3 | ch3 | H |
2.051 | CH2Br | cf3 | ch3 | H |
2.052 | CH2OCH3 | cf3 | ch3 | H |
2.053 | CH2SMe | cf3 | ch3 | H |
2.054 | CH2SO2Me | cf3 | ch3 | H |
2.055 | sch3 | cf3 | ch3 | H |
2.056 | SOCH3 | cf3 | ch3 | H |
2.057 | SO2CH3 | cf3 | ch3 | H |
2.058 | SPh | cf3 | ch3 | H |
2.059 | SOPh | cf3 | ch3 | H |
2.060 | SO2Ph | cf3 | ch3 | H |
2.061 | ch3 | cf3cf2 | ch3 | H |
2.062 | ch3ch2 | cf3cf2 | ch3 | H |
2.063 | (CH3)2CH | cf3cf2 | ch3 | H |
2.064 | ch3(ch2)3 | cf3cf2 | ch3 | H |
2.065 | Ph | cf3cf2 | ch3 | H |
2.066 | CH2Br | CF3CF2 | ch3 | H |
2.067 | CH2OCH3 | cf3cf2 | ch3 | H |
2.068 | CH2SMe | cf3cf2 | ch3 | H |
• t.(°C)
Slouč. | R75 | R76 | R77 | R78 |
C · 2.069 | CH2SO2Me | cf3cf2 | ch3 | H |
2.070 | sch3 | cf3cf2 | ch3 | H |
2.071 | SOCH3 | cf3cf2 | ch3 | H |
2.072 | SO2CH3 | cf3cf2 | ch3 | H |
2.073 | SPh | cf3cf2 | ch3 | H |
2.074 | SOPh | cf3cf2 | ch3 | H |
2.075 | SO2Ph | cf3cf2 | ch3 | H |
2.076 | ch3 | chf2 | ch3 | H |
2.077 | ch3ch2 | chf2 | ch3 | H |
2.078 | (CH3)2CH | chf2 | ch3 | H |
2.079 | ch3(ch2)3 | chf2 | ch3 | H |
2.080 | Ph | chf2 | ch3 | H |
2.081 | CH2Br | chf2 | ch3 | H |
2.082 | CH2OCH3 | chf2 | ch3 | H |
2.083 | CH2SMe | chf2 | ch3 | H |
2.084 | CH2SO2Me | chf2 | ch3 | H |
2.085 | sch3 | chf2 | ch3 | H |
2.086 | soch3 | chf2 | ch3 | H |
2.087 | so2ch3 | chf2 | ch3 | H |
2.088 | SPh | chf2 | ch3 | H |
2.089 | SOPh | chf2 | ch3 | H |
2.090 | SO2Ph | chf2 | ch3 | H |
2.091 | ch3 | cf3 | H | ch3 |
2.092 | ch3ch2 | cf3 | H | ch3 |
2.093 | (CH3)2CH | cf3 | H | ch3 |
2.094 | ch3(ch2)3 | cf3 | H | ch3 |
2.095 | Ph | cf3 | H | ch3 |
2.096 | CH2Br | cf3 | H | ch3 |
2.097 | CH2OCH3 | cf3 | H | ch3 |
2.098 | CH2SMe | cf3 | H | ch3 |
2.099 | CH2SO2Me | cf3 | H | ch3 |
2.100 | sch3 | cf3 | H | ch3 |
2.101 | soch3 | cf3 | H | ch3 |
2.102 | so2ch3 | cf3 | H | ch3 |
2.103 | SPh | cf3 | H | ch3 |
2.104 | SOPh | cf3 | H | ch3 |
2.105 | SO2Ph | cf3 | H | ch3 |
Tabulka 3: Sloučeniny obecného vzorce Id:
Slouč. c. | R75 | R76 | R77 | R78 |
3.001 | ch3 | cf3 | H | H |
3.002 | CH3CH2 | cf3 | H | H |
3.003 | (CH3)2CH | cf3 | H | H |
3.004 | CH3(CH2)3 | cf3 | H | H |
3.005 | Ph | cf3 | H | H |
3.006 | CH2Br | cf3 | H | H |
3.007 | CH2OCH3 | cf3 | H | H |
3.008 | CH2SMe | cf3 | H | H |
3.009 | CH2SO2Me | cf3 | H | H |
3.010 | sch3 | cf3 | H | H |
3.011 | soch3 | cf3 | H | H |
3.012 | so2ch3 | cf3 | H | H |
3.013 | SPh | cf3 | H | H |
3.014 | SOPh | cf3 | H | H |
3.015 | SO2Ph | cf3 | H | H |
3.016 | ch3 | cf3cf2 | H | H |
3.017 | ch3ch2 | cf3cf2 | H | H |
3.018 | (CH3)2CH | cf3cf2 | H | H |
3.019 | ch3(ch2)3 | cf3cf2 | H | H |
3.020 | Ph | cf3cf2 | H | H |
3.021 | CH2Br | cf3cf2 | H | H |
3.022 | CH2OCH3 | cf3cf2 | H | H |
3.023 | CH2SMe | cf3cf2 | H | H |
3.024 | CH2SO2Me | cf3cf2 | H | H |
3.025 | sch3 | cf3cf2 | H | H |
3.026 | soch3 | cf3cf2 | H | H |
3.027 | so2ch3 | cf3cf2 | H | H |
3.028 | SPh | cf3cf2 | H | H |
3.029 | SOPh | cf3cf2 | H | H |
3.030 | SO2Ph | cf3cf2 | H | H |
3.031 | ch3 | chf2 | H | H |
3.032 | ch3ch2 | chf2 | H | H |
3.033 | (CH3)2CH | chf2 | H | H |
3.034 | CH3(CH2)3 | chf2 | H | H |
3.035 | Ph | chf2 | H | H |
Slouč. | R75 | R76 | R77 | R78 |
G · 3.036 | CH2Br | chf2 | H | H |
3.037 | CH2OCH3 | chf2 | H | H |
3.038 | CH2SMe | chf2 | H | H |
3.039 | CH2SO2Me | chf2 | H | H |
3.040 | sch3 | chf2 | H | H |
3.041 | SOCH3 | chf2 | H | H |
3.042 | SO2CH3 | chf2 | H | H |
3.043 | SPh | chf2 | H | H |
3.044 | SOPh | chf2 | H | H |
3.045 | SO2Ph | chf2 | H | H |
3.046 | ch3 | cf3 | ch3 | H |
3.047 | CH3CH2 | cf3 | ch3 | H |
3.048 | (ch3)2ch | cf3 | ch3 | H |
3.049 | ch3(ch2)3 | cf3 | ch3 | H |
3.050 | Ph | cf3 | ch3 | H |
3.051 | CH2Br | cf3 | ch3 | H |
3.052 | CH2OCH3 | cf3 | ch3 | H |
3.053 | CH2SMe | cf3 | ch3 | H |
3.054 | CH2SO2Me | cf3 | ch3 | H |
3.055 | sch3 | cf3 | ch3 | H |
3.056 | SOCH3 | cf3 | ch3 | H |
3.057 | SO2CH3 | cf3 | ch3 | H |
3.058 | SPh | cf3 | ch3 | H |
3.059 | SOPh | cf3 | ch3 | H |
3.060 | SO2Ph | cf3 | ch3 | H |
3.061 | ch3 | cf3cf2 | ch3 | H |
3.062 | CH3CH2 | cf3cf2 | ch3 | H |
3.063 | (CH3)2CH | cf3cf2 | ch3 | H |
3.064 | CH3(CH2)3 | cf3cf2 | ch3 | H |
3.065 | Ph | cf3cf2 | ch3 | H |
3.066 | CH2Br | cf3cf2 | ch3 | H |
3.067 | CH2OCH3 | cf3cf2 | ch3 | H |
3.068 | CH2SMe | cf3cf2 | ch3 | H |
3.069 | CH2SO2Me | cf3cf2 | ch3 | H |
3.070 | sch3 | cf3cf2 | ch3 | H |
3.071 | SOCH3 | cf3cf2 | ch3 | H |
3.072 | SO2CH3 | cf3cf2 | ch3 | H |
3.073 | SPh | cf3cf2 | ch3 | H |
3.074 | SOPh | cf3cf2 | ch3 | H |
3.075 | SO2Ph | cf3cf2 | ch3 | H |
3.076 | ch3 | chf2 | ch3 | H |
3.077 | CH3CH2 | chf2 | ch3 | H |
3.078 | (CH3)2CH | chf2 | ch3 | H |
3.079 | CH3(CH2)3 | chf2 | ch3 | H |
3.080 | Ph | chf2 | ch3 | H |
3.081 | CH2Br | chf2 | ch3 | H |
3.082 | CH2OCH3 | chf2 | ch3 | H |
3.083 | CH2SMe | chf2 | ch3 | H |
Slouč. | R75 | R76 | R77 | R78 |
c · 3.084 | CH2SO2Me | chf2 | ch3 | H |
3.085 | sch3 | chf2 | ch3 | H |
3.086 | SOCH3 | chf2 | ch3 | H |
3.087 | SO2CH3 | chf2 | ch3 | H |
3.088 | SPh | chf2 | ch3 | H |
3.089 | SOPh | chf2 | ch3 | H |
3.090 | SO2Ph | chf2 | ch3 | H |
3.091 | ch3 | cf3 | H | ch3 |
3.092 | ch3ch2 | cf3 | H | ch3 |
3.093 | (CH3)2CH | cf3 | H | ch3 |
3.094 | CH3(CH2)3 | cf3 | H | ch3 |
3.095 | Ph | cf3 | H | ch3 |
3.096 | CH2Br | cf3 | H | ch3 |
3.097 | CH2OCH3 | cf3 | H | ch3 |
3.098 | CH2SMe | cf3 | H | ch3 |
3.099 | CH2S02Me | cf3 | H | ch3 |
3.100 | sch3 | cf3 | H | ch3 |
3.101 | soch3 | cf3 | H | ch3 |
3.102 | so2ch3 | cf3 | H | ch3 |
3.103 | SPh | cf3 | H | ch3 |
3.104 | SOPh | cf3 | H | ch3 |
3.105 | SO2Ph | cf3 | H | ch3 |
Tabulka 4: Sloučeniny obecného vzorce Ie: 5
(Ie)
Slouč. č. | R75 | R76 | R77 | R78 | Z |
4.001 | ch3 | cf3 | H | H | s |
4.002 | ch3ch2 | cf3 | H | H | s |
4.003 | (CH3)2CH | cf3 | H | H | s |
4.004 | ch3(ch2)3 | cf3 | H | H | s |
4.005 | Ph | cf3 | H | H | s |
4.006 | CH2Br | cf3 | H | H | s |
4.007 | ch2och3 | cf3 | H | H | s |
t.t.
(°C)
103104
-26CZ 304537 B6
Slouč. | R75 | R76 | R77 | R78 | Z |
G. 4.008 | CH2SMe | cf3 | H | H | s |
4.009 | CH2SO2Me | cf3 | H | H | s |
4.010 | sch3 | cf3 | H | H | s |
4.011 | SOCH3 | cf3 | H | H | s |
4.012 | SO2CH3 | cf3 | H | H | s |
4.013 | SPh | cf3 | H | H | s |
4.014 | SOPh | cf3 | H | H | s |
4.015 | SO2Ph | cf3 | H | H | s |
4.016 | ch3 | cf3cf2 | H | H | s |
4.017 | ch3ch2 | cf3cf2 | H | H | s |
4.018 | (CH3)2CH | cf3cf2 | H | H | s |
4.019 | CH3(CH2)3 | cf3cf2 | H | H | s |
4.020 | Ph | cf3cf2 | H | H | s |
4.021 | CH2Br | cf3cf2 | H | H | s |
4.022 | CH2OCH3 | cf3cf2 | H | H | s |
4.023 | CH2SMe | cf3cf2 | H | H | s |
4.024 | CH2SO2Me | cf3cf2 | H | H | s |
4.025 | sch3 | cf3cf2 | H | H | s |
4.026 | soch3 | cf3cf2 | H | H | s |
4.027 | so2ch3 | cf3cf2 | H | H | s |
4.028 | SPh | cf3cf2 | H | H | s |
4.029 | SOPh | CF3CF2 | H | H | s |
4.030 | SO2Ph | cf3cf2 | H | H | s |
4.031 | ch3 | chf2 | H | H | s |
4.032 | ch3ch2 | chf2 | H | H | s |
4.033 | (ch3)2ch | chf2 | H | H | s |
4.034 | CH3(CH2)3 | chf2 | H | H | s |
4.035 | Ph | chf2 | H | H | s |
4.036 | CH2Br | chf2 | H | H | s |
4.037 | CH2OCH3 | chf2 | H | H | s |
4.038 | CH2SMe | chf2 | H | H | s |
4.039 | CH2SO2Me | chf2 | H | H | s |
4.040 | SCH3 | chf2 | H | H | s |
4.041 | soch3 | chf2 | H | H | s |
4.042 | so2ch3 | chf2 | H | H | s |
4.043 | SPh | chf2 | H | H | s |
4.044 | SOPh | chf2 | H | H | s |
4.045 | SO2Ph | chf2 | H | H | s |
4.046 | ch3 | cf3 | ch3 | H | s |
4.047 | ch3ch2 | cf3 | ch3 | H | s |
4.048 | (CH3)2CH | cf3 | ch3 | H | s |
4.049 | ch3(ch2)3 | cf3 | ch3 | H | s |
4.050 | Ph | cf3 | ch3 | H | s |
4.051 | CH2Br | cf3 | ch3 | H | s |
4.052 | CH2OCH3 | cf3 | ch3 | H | s |
4.053 | CH2SMe | cf3 | ch3 | H | s |
4.054 | CH2SO2Me | cf3 | ch3 | H | s |
4.055 | sch3 | cf3 | ch3 | H | s |
27CZ 304537 B6
Slouč. v | R75 | R76 | R77 | R78 | z |
c · 4.056 | SOCH3 | cf3 | ch3 | H | S |
4.057 | SO2CH3 | cf3 | ch3 | H | s |
4.058 | SPh | cf3 | ch3 | H | s |
4.059 | SOPh | cf3 | ch3 | H | s |
4.060 | SO2Ph | cf3 | ch3 | H | s |
4.061 | ch3 | CF3CF2 | ch3 | H | s |
4.062 | CH3CH2 | CF3CF2 | ch3 | H | s |
4.063 | (CH3)2CH | CF3CF2 | ch3 | H | s |
4.064 | CH3(CH2)3 | CF3CF2 | ch3 | H | s |
4.065 | Ph | CF3CF2 | ch3 | H | s |
4.066 | CH2Br | CF3CF2 | ch3 | H | s |
4.067 | CH2OCH3 | CF3CF2 | ch3 | H | s |
4.068 | CH2SMe | CF3CF2 | ch3 | H | s |
4.069 | CH2SO2Me | CF3CF2 | ch3 | H | s |
4.070 | sch3 | CF3CF2 | ch3 | H | s |
4.071 | soch3 | CF3CF2 | ch3 | H | s |
4.072 | SO2CH3 | CF3CF2 | ch3 | H | s |
4.073 | SPh | cf3cf2 | ch3 | H | s |
4.074 | SOPh | CF3CF2 | ch3 | H | s |
4.075 | SO2Ph | CF3CF2 | ch3 | H | s |
4.076 | ch3 | chf2 | ch3 | H | s |
4.077 | CH3CH2 | chf2 | ch3 | H | s |
4.078 | (CH3)2CH | chf2 | ch3 | H | s |
4.079 | CH3(CH2)3 | chf2 | ch3 | H | s |
4.080 | Ph | chf2 | ch3 | H | s |
4.081 | CH2Br | chf2 | ch3 | H | s |
4.082 | CH2OCH3 | chf2 | ch3 | H | s |
4.083 | CH2SMe | chf2 | ch3 | H | s |
4.084 | CH2SO2Me | chf2 | ch3 | H | s |
4.085 | SCH3 | chf2 | ch3 | H | s |
4.086 | soch3 | chf2 | ch3 | H | s |
4.087 | SO2CH3 | chf2 | ch3 | H | s |
4.088 | SPh | chf2 | ch3 | H | s |
4.089 | SOPh | chf2 | ch3 | H | s |
4.090 | SO2Ph | chf2 | ch3 | H | s |
4.091 | ch3 | cf3 | H | CH3 | s |
4.092 | CH3CH2 | cf3 | H | ch3 | s |
4.093 | (CH3)2CH | cf3 | H | ch3 | s |
4.094 | CH3(CH2)3 | cf3 | H | ch3 | s |
4.095 | Ph | cf3 | H | ch3 | s |
4.096 | CH2Br | cf3 | H | ch3 | s |
4.097 | CH2OCH3 | cf3 | H | ch3 | s |
4.098 | CH2SMe | cf3 | H | ch3 | s |
4.099 | CH2SO2Me | cf3 | H | ch3 | s |
4.100 | SCH3 | cf3 | H | ch3 | s |
4.101 | SOCH3 | cf3 | H | ch3 | s |
4.102 | SO2CH3 | cf3 | H | ch3 | s |
4.103 | SPh | cf3 | H | ch3 | s |
28CZ 304537 B6
Slouč. v | R75 | R76 | R77 | R78 | Z |
c. 4.104 | SOPh | cf3 | H | ch3 | s |
4.105 | SO2Ph | cf3 | H | ch3 | s |
4.106 | ch3 | cf3 | H | H | so |
4.107 | CH3CH2 | cf3 | H | H | so |
4.108 | (CH3)2CH | cf3 | H | H | so |
4.109 | CH3(CH2)3 | cf3 | H | H | so |
4.110 | Ph | cf3 | H | H | so |
4.111 | CH2Br | cf3 | H | H | so |
4.112 | CH2OCH3 | cf3 | H | H | so |
4.113 | CH2SMe | cf3 | H | H | so |
4.114 | CH2SO2Me | cf3 | H | H | so |
4.115 | sch3 | cf3 | H | H | so |
4.116 | soch3 | cf3 | H | H | so |
4.117 | so2ch3 | cf3 | H | H | so |
4.118 | SPh | cf3 | H | H | so |
4.119 | SOPh | cf3 | H | H | so |
4.120 | SO2Ph | cf3 | H | H | so |
4.121 | ch3 | cf3cf2 | H | H | so |
4.122 | ch3ch2 | cf3cf2 | H | H | so |
4.123 | (CH3)2CH | cf3cf2 | H | H | so |
4.124 | CH3(CH2)3 | cf3cf2 | H | H | so |
4.125 | Ph | cf3cf2 | H | H | so |
4.126 | CH2Br | cf3cf2 | H | H | so |
4.127 | CH2OCH3 | cf3cf2 | H | H | so |
4.128 | CH2SMe | cf3cf2 | H | H | so |
4.129 | CH2SO2Me | cf3cf2 | H | H | so |
4.130 | sch3 | cf3cf2 | H | H | so |
4.131 | SOCH3 | cf3cf2 | H | H | so |
4.132 | so2ch3 | cf3cf2 | H | H | so |
4.133 | SPh | cf3cf2 | H | H | so |
4.134 | SOPh | cf3cf2 | H | H | so |
4.135 | SO2Ph | cf3cf2 | H | H | so |
4.136 | ch3 | chf2 | H | H | so |
4.137 | ch3ch2 | chf2 | H | H | so |
4.138 | (CH3)2CH | chf2 | H | H | so |
4.139 | CH3(CH2)3 | chf2 | H | H | so |
4.140 | Ph | chf2 | H | H | so |
4.141 | CH2Br | chf2 | H | H | so |
4.142 | CH2OCH3 | chf2 | H | H | so |
4.143 | CH2SMe | chf2 | H | H | so |
4.144 | CH2SO2Me | chf2 | H | H | so |
4.145 | sch3 | chf2 | H | H | so |
4.146 | soch3 | chf2 | H | H | so |
4.147 | so2ch3 | chf2 | H | H | so |
4.148 | SPh | chf2 | H | H | so |
4.149 | SOPh | chf2 | H | H | so |
4.150 | SO2Ph | chf2 | H | H | so |
4.151 | ch3 | cf3 | ch3 | H | so |
-29CZ 304537 B6
Slouč. w | R75 | R76 | R77 | R78 | Z |
G · 4.152 | ch3ch2 | cf3 | ch3 | H | so |
4.153 | (ch3)2ch | cf3 | ch3 | H | so |
4.154 | CH3(CH2)3 | cf3 | ch3 | H | so |
4.155 | Ph | cf3 | ch3 | H | so |
4.156 | CH2Br | cf3 | ch3 | H | so |
4.157 | CH2OCH3 | cf3 | ch3 | H | so |
4.158 | CH2SMe | cf3 | ch3 | H | so |
4.159 | CH2SO2Me | cf3 | ch3 | H | so |
4.160 | sch3 | cf3 | ch3 | H | so |
4.161 | soch3 | cf3 | ch3 | H | so |
4.162 | so2ch3 | cf3 | ch3 | H | so |
4.163 | SPh | cf3 | ch3 | H | so |
4.164 | SOPh | cf3 | ch3 | H | so |
4.165 | SO2Ph | cf3 | ch3 | H | so |
4.166 | ch3 | cf3cf2 | ch3 | H | so |
4.167 | ch3ch2 | cf3cf2 | ch3 | H | so |
4.168 | (ch3)2ch | cf3cf2 | ch3 | H | so |
4.169 | ch3(ch2)3 | cf3cf2 | ch3 | H | so |
4.170 | Ph | cf3cf2 | ch3 | H | so |
4.171 | CH2Br | cf3cf2 | ch3 | H | so |
4.172 | ch2och3 | cf3cf2 | ch3 | H | so |
4.173 | CH2SMe | cf3cf2 | ch3 | H | so |
4.174 | CH2S02Me | cf3cf2 | ch3 | H | so |
4.175 | sch3 | cf3cf2 | ch3 | H | so |
4.176 | soch3 | cf3cf2 | ch3 | H | so |
4.177 | so2ch3 | cf3cf2 | ch3 | H | so |
4.178 | SPh | cf3cf2 | ch3 | H | so |
4.179 | SOPh | cf3cf2 | ch3 | H | so |
4.180 | SO2Ph | cf3cf2 | ch3 | H | so |
4.181 | ch3 | chf2 | ch3 | H | so |
4.182 | ch3ch2 | chf2 | ch3 | H | so |
4.183 | (CH3)2CH | chf2 | ch3 | H | so |
4.184 | ch3(ch2)3 | chf2 | ch3 | H | so |
4.185 | Ph | chf2 | ch3 | H | so |
4.186 | CH2Br | chf2 | ch3 | H | so |
4.187 | CH2OCH3 | chf2 | ch3 | H | so |
4.188 | CH2SMe | chf2 | ch3 | H | so |
4.189 | CH2SO2Me | chf2 | ch3 | H | so |
4.190 | sch3 | chf2 | ch3 | H | so |
4.191 | soch3 | chf2 | ch3 | H | so |
4.192 | so2ch3 | chf2 | ch3 | H | so |
4.193 | SPh | chf2 | ch3 | H | so |
4.194 | SOPh | chf2 | ch3 | H | so |
4.195 | SO2Ph | chf2 | ch3 | H | so |
4.196 | ch3 | cf3 | H | ch3 | so |
4.197 | ch3ch2 | cf3 | H | ch3 | so |
4.198 | (CH3)2CH | cf3 | H | ch3 | so |
4.199 | ch3(ch2)3 | cf3 | H | ch3 | so |
-30CZ 304537 B6
Slouč. | R75 | R76 | R77 | R78 | Z |
c. 4.200 | Ph | cf3 | H | ch3 | SO |
4.201 | CH2Br | cf3 | H | ch3 | SO |
4.202 | CH2OCH3 | cf3 | H | ch3 | SO |
4.203 | CH2SMe | cf3 | H | ch3 | SO |
4.204 | CH2SO2Me | cf3 | H | ch3 | SO |
4.205 | sch3 | cf3 | H | ch3 | SO |
4.206 | soch3 | cf3 | H | ch3 | SO |
4.207 | so2ch3 | cf3 | H | ch3 | SO |
4.208 | SPh | cf3 | H | ch3 | SO |
4.209 | SOPh | cf3 | H | ch3 | SO |
4.210 | SO2Ph | cf3 | H | ch3 | SO |
4.211 | ch3 | cf3 | H | H | so2 |
4.212 | ch3ch2 | cf3 | H | H | so2 |
4.213 | (ch3)2ch | cf3 | H | H | so2 |
4.214 | ch3(ch2)3 | cf3 | H | H | so2 |
4.215 | Ph | cf3 | H | H | so2 |
4.216 | CH2Br | cf3 | H | H | so2 |
4.217 | CH2OCH3 | cf3 | H | H | so2 |
4.218 | CH2SMe | cf3 | H | H | so2 |
4.219 | CH2SO2Me | cf3 | H | H | so2 |
4.220 | sch3 | cf3 | H | H | so2 |
4.221 | soch3 | cf3 | H | H | so2 |
4.222 | so2ch3 | cf3 | H | H | so2 |
4.223 | SPh | cf3 | H | H | so2 |
4.224 | SOPh | cf3 | H | H | so2 |
4.225 | SO2Ph | cf3 | H | H | so2 |
4.226 | ch3 | cf3cf2 | H | H | so2 |
4.227 | ch3ch2 | cf3cf2 | H | H | so2 |
4.228 | (CH3)2CH | cf3cf2 | H | H | so2 |
4.229 | CH3(CH2)3 | cf3cf2 | H | H | so2 |
4.230 | Ph | cf3cf2 | H | H | so2 |
4.231 | CH2Br | cf3cf2 | H | H | so2 |
4.232 | CH2OCH3 | cf3cf2 | H | H | so2 |
4.233 | CH2SMe | cf3cf2 | H | H | so2 |
4.234 | CH2SO2Me | cf3cf2 | H | H | so2 |
4.235 | SCH3 | cf3cf2 | H | H | so2 |
4.236 | soch3 | cf3cf2 | H | H | so2 |
4.237 | so2ch3 | cf3cf2 | H | H | so2 |
4.238 | SPh | cf3cf2 | H | H | so2 |
4.239 | SOPh | cf3cf2 | H | H | so2 |
4.240 | SO2Ph | cf3cf2 | H | H | so2 |
4.241 | ch3 | chf2 | H | H | so2 |
4.242 | ch3ch2 | chf2 | H | H | so2 |
4.243 | (CH3)2CH | chf2 | H | H | so2 |
4.244 | CH3(CH2)3 | chf2 | H | H | so2 |
4.245 | Ph | chf2 | H | H | so2 |
4.246 | CH2Br | chf2 | H | H | so2 |
4.247 | CH2OCH3 | chf2 | H | H | so2 |
t.t.
Cc) amorf
-31 CZ 304537 B6
Slouč. | R75 | R76 | R77 | R78 | Z |
C · 4.248 | CH2SMe | chf2 | H | H | so2 |
4.249 | CH2SO2Me | chf2 | H | H | so2 |
4.250 | sch3 | chf2 | H | H | so2 |
4.251 | SOCH3 | chf2 | H | H | so2 |
4.252 | so2ch3 | chf2 | H | H | so2 |
4.253 | SPh | chf2 | H | H | so2 |
4.254 | SOPh | chf2 | H | H | so2 |
4.255 | SO2Ph | chf2 | H | H | so2 |
4.256 | ch3 | cf3 | ch3 | H | so2 |
4.257 | ch3ch2 | cf3 | ch3 | H | so2 |
4.258 | (CH3)2CH | cf3 | ch3 | H | so2 |
4.259 | CH3(CH2)3 | cf3 | ch3 | H | so2 |
4.260 | Ph | cf3 | ch3 | H | so2 |
4.261 | CH2Br | cf3 | ch3 | H | so2 |
4.262 | CH2OCH3 | cf3 | ch3 | H | so2 |
4.263 | CH2SMe | cf3 | ch3 | H | so2 |
4.264 | CH2SO2Me | cf3 | ch3 | H | so2 |
4.265 | sch3 | cf3 | ch3 | H | so2 |
4.266 | soch3 | cf3 | ch3 | H | so2 |
4.267 | so2ch3 | cf3 | ch3 | H | so2 |
4.268 | SPh | cf3 | ch3 | H | so2 |
4.269 | SOPh | cf3 | ch3 | H | so2 |
4.270 | SO2Ph | cf3 | ch3 | H | so2 |
4.271 | ch3 | cf3cf2 | ch3 | H | so2 |
4.272 | ch3ch2 | cf3cf2 | ch3 | H | so2 |
4.273 | (CH3)2CH | cf3cf2 | ch3 | H | so2 |
4.274 | CH3(CH2)3 | cf3cf2 | ch3 | H | so2 |
4.275 | Ph | cf3cf2 | ch3 | H | so2 |
4.276 | CH2Br | cf3cf2 | ch3 | H | so2 |
4.277 | CH2OCH3 | cf3cf2 | ch3 | H | so2 |
4.278 | CH2SMe | cf3cf2 | ch3 | H | so2 |
4.279 | CH2SO2Me | cf3cf2 | ch3 | H | so2 |
4.280 | sch3 | cf3cf2 | ch3 | H | so2 |
4.281 | soch3 | cf3cf2 | ch3 | H | so2 |
4.282 | so2ch3 | cf3cf2 | ch3 | H | so2 |
4.283 | SPh | cf3cf2 | ch3 | H | so2 |
4.284 | SOPh | cf3cf2 | ch3 | H | so2 |
4.285 | SO2Ph | cf3cf2 | ch3 | H | so2 |
4.286 | ch3 | chf2 | ch3 | H | so2 |
4.287 | ch3ch2 | chf2 | ch3 | H | so2 |
4.288 | (CH3)2CH | chf2 | ch3 | H | so2 |
4.289 | CH3(CH2)3 | chf2 | ch3 | H | S02 |
4.290 | Ph | chf2 | ch3 | H | SO2 |
4.291 | CH2Br | chf2 | ch3 | H | so2 |
4.292 | CH2OCH3 | chf2 | ch3 | H | SO2 |
4.293 | CH2SMe | chf2 | ch3 | H | so2 |
4.294 | CH2SO2Me | chf2 | ch3 | H | so2 |
4.295 | sch3 | chf2 | ch3 | H | SO2 |
32CZ 304537 B6
Slouč. | R75 | R76 | R77 | R78 | z |
C · 4.296 | SOCH3 | chf2 | ch3 | H | so2 |
4.297 | SO2CH3 | chf2 | ch3 | H | so2 |
4.298 | SPh | chf2 | ch3 | H | so2 |
4.299 | SOPh | chf2 | ch3 | H | so2 |
4.300 | SO2Ph | chf2 | ch3 | H | so2 |
4.301 | ch3 | cf3 | H | ch3 | so2 |
4.302 | CH3CH2 | cf3 | H | ch3 | so2 |
4.303 | (CH3)2CH | cf3 | H | ch3 | so2 |
4.304 | ch3(ch2)3 | cf3 | H | ch3 | so2 |
4.305 | Ph | cf3 | H | ch3 | so2 |
4.306 | CH2Br | cf3 | H | ch3 | so2 |
4.307 | CH2OCH3 | cf3 | H | ch3 | so2 |
4.308 | CH2SMe | cf3 | H | ch3 | so2 |
4.309 | CH2SO2Me | cf3 | H | ch3 | so2 |
4.310 | sch3 | cf3 | H | ch3 | so2 |
4.311 | SOCH3 | cf3 | H | ch3 | so2 |
4.312 | SO2CH3 | cf3 | H | ch3 | so2 |
4.313 | SPh | cf3 | H | ch3 | so2 |
4.314 | SOPh | cf3 | H | ch3 | so2 |
4.315 | SO2Ph | cf3 | H | ch3 | so2 |
Tabulka 5: Sloučeniny obecného vzorce XVI: | ||
? 80 | fl | |
R,’A | X)H | (XVI) |
R82 | K79 |
Sl. č. | R79 | Reo | Rei | R82 |
Al | H | H | H | cf3 |
A2 | ch3 | H | H | cf3 |
A3 | CH3CH2 | H | H | cf3 |
A4 | (CH3)2CH | H | H | cf3 |
A5 | (CH3)3C | H | H | cf3 |
A6 | cyklopropyl | H | H | cf3 |
A7 | CH3(CH2)2 | H | H | cf3 |
A8 | CH3OCH2 | H | H | cf3 |
A9 | CH3O(CH2)2 | H | H | cf3 |
A10 | Ph | H | H | cf3 |
All | PhO | H | H | cf3 |
A12 | PhS | H | H | cf3 |
A13 | PhSO | H | H | cf3 |
33CZ 304537 B6
Sl. č. A14 | R79 | Rbo | Rei | Rfl2 |
PhSO2 | H | H | cf3 | |
A15 | ch3s | H | H | cf3 |
A16 | ch3so | H | H | cf3 |
A17 | cf3 | H | H | cf3 |
A18 | f2ch | H | H | cf3 |
A19 | HCC | H | H | cf3 |
A20 | ch3cc | H | H | cf3 |
A21 | ch2=ch | H | H | cf3 |
A22 | ch2=chch2 | H | H | cf3 |
A23 | ch3so2n (CH3) | H | H | cf3 |
A24 | (CH3)2N | H | H | cf3 |
A25 | (CH3)2NSO2 | H | H | cf3 |
A26 | cich2 | H | H | cf3 |
A27 | ch3sch2 | H | H | cf3 |
A28 | ch3soch2 | H | H | cf3 |
A29 | ch3so2ch2 | H | H | cf3 |
A30 | [1,2,4]-triazol1-yl-methyl | H | H | cf3 |
A31 | ch3 | cf3 | H | ch3 |
A32 | ch3 | ch3 | H | cf3 |
A33 | H | H | H | cf3cf2 |
A34 | ch3 | H | H | cf3cf2 |
A35 | ch3ch2 | H | H | cf3cf2 |
A36 | cyklopropyl | H | H | cf3cf2 |
A37 | (CH3)3C | H | H | cf3cf2 |
A38 | (CH3)2CH | H | H | cf3cf2 |
A39 | CH3(CH2)2 | H | H | cf3cf2 |
A40 | ch3och2 | H | H | cf3cf2 |
A41 | CH3O(CH2)2 | H | H | cf3cf2 |
A42 | Ph | H | H | cf3cf2 |
A43 | PhO | H | H | cf3cf2 |
A44 | PhS | H | H | cf3cf2 |
A45 | PhSO | H | H | cf3cf2 |
A46 | PhSO2 | H | H | cf3cf2 |
A47 | ch3s | H | H | cf3cf2 |
A48 | ch3so | H | H | cf3cf2 |
A49 | cf3 | H | H | cf3cf2 |
A50 | f2ch | H | H | cf3cf2 |
A51 | HCC | H | H | cf3cf2 |
A52 | ch3cc | H | H | cf3cf2 |
A53 | ch2=ch | H | H | cf3cf2 |
A54 | ch2=chch2 | H | H | cf3cf2 |
A55 | CH3SO2N(CH3) | H | H | cf3cf2 |
A56 | (CH3)2N | H | H | cf3cf2 |
A57 | (CH3)2NSO2 | H | H | cf3cf2 |
A58 | cich2 | H | H | cf3cf2 |
A59 | ch3sch2 | H | H | cf3cf2 |
A60 | ch3soch2 | H | H | cf3cf2 |
A61 | ch3so2ch2 | H | H | cf3cf2 |
34CZ 304537 B6
Sl. w c. A62 | R79 | Reo | Rbi | Re2 |
[1,2,4]-triazol1-yl-methyl | H | H | cf3cf2 | |
A63 | H | H | H | cf3cf2cf2 |
A64 | ch3 | H | H | cf3cf2cf2 |
A65 | ch3ch2 | H | H | cf3cf2cf2 |
A66 | cyklopropyl | H | H | cf3cf2cf2 |
A67 | (CH3)3C | H | H | cf3cf2cf2 |
A68 | (CH3)2CH | H | H | cf3cf2cf2 |
A69 | CH3(CH2)2 | H | H | cf3cf2cf2 |
A70 | ch3och2 | H | H | cf3cf2cf2 |
A71 | CH3O(CH2)2 | H | H | cf3cf2cf2 |
A72 | Ph | H | H | cf3cf2cf2 |
A73 | PhO | H | H | cf3cf2cf2 |
A74 | PhS | H | H | cf3cf2cf2 |
A75 | PhSO | H | H | cf3cf2cf2 |
A76 | PhSO2 | H | H | cf3cf2cf2 |
A77 | ch3s | H | H | cf3cf2cf2 |
A78 | ch3so | H | H | cf3cf2cf2 |
A79 | cf3 | H | H | cf3cf2cf2 |
A80 | f2ch | H | H | cf3cf2cf2 |
A81 | HCC | H | H | cf3cf2cf2 |
A82 | ch3cc | H | H | cf3cf2cf2 |
A83 | ch2=ch | H | H | cf3cf2cf2 |
A84 | ch2=chch2 | H | H | cf3cf2cf2 |
A85 | CH3SO2N(CH3) | H | H | cf3cf2cf2 |
A86 | (CH3)2N | H | H | cf3cf2cf2 |
A87 | (CH3)2NSO2 | H | H | cf3cf2cf2 |
A88 | cich2 | H | H | cf3cf2cf2 |
A89 | ch3sch2 | H | H | cf3cf2cf2 |
A90 | ch3soch2 | H | H | cf3cf2cf2 |
A91 | ch3so2ch2 | H | H | cf3cf2cf2 |
A92 | [1,2,4]triazol-1ylmethyl | H | H | cf3cf2cf2 |
A93 | H | H | H | cf2ci |
A94 | ch3 | H | H | cf2ci |
A95 | ch3ch2 | H | H | CF2C1 |
A96 | cyklopropyl | H | H | CF2C1 |
A97 | (CH3)3C | H | H | cf2ci |
A98 | (CH3)2CH | H | H | CF2C1 |
A99 | CH3(CH2)2 | H | H | CF2C1 |
A100 | ch3och2 | H | H | cf2ci |
A101 | CH3O(CH2)2 | H | H | cf2ci |
A102 | Ph | H | H | cf2ci |
A103 | PhO | H | H | cf2ci |
A104 | PhS | H | H | cf2ci |
A105 | PhSO | H | H | cf2ci |
A106 | PhSO2 | H | H | cf2ci |
A107 | CH3S | H | H | cf2ci |
A108 | ch3so | H | H | cf2ci |
35CZ 304537 B6
Sl. č. A109 | R79 | Reo | Rei | R82 |
cf3 | H | H | CF2C1 | |
A110 | f2ch | H | H | cf2ci |
Alll | HCC | H | H | cf2ci |
A112 | CH3CC | H | H | cf2ci |
A113 | ch2=ch | H | H | CF2C1 |
A114 | ch2=chch2 | H | H | CF2C1 |
A115 | CH3SO2N(CH3) | H | H | cf2ci |
A116 | (CH3)2N | H | H | cf2ci |
A117 | (CH3)2NSO2 | H | H | cf2ci |
A118 | cich2 | H | H | CF2C1 |
A119 | ch3sch2 | H | H | CF2C1 |
A120 | ch3soch2 | H | H | cf2ci |
A121 | ch3so2ch2 | H | H | cf2ci |
A122 | [1,2,4]-triazol1-yl-methyl | H | H | cf2ci |
A123 | H | H | H | chf2 |
A124 | ch3 | H | H | chf2 |
A125 | ch3ch2 | H | H | chf2 |
A126 | cyklopropyl | H | H | chf2 |
A127 | (CH3)3C | H | H | chf2 |
A128 | (CH3)2CH | H | H | chf2 |
A129 | CH3(CH2)2 | H | H | chf2 |
A130 | ch3och2 | H | H | chf2 |
A131 | CH3O(CH2)2 | H | H | chf2 |
A132 | Ph | H | H | chf2 |
A133 | PhO | H | H | chf2 |
A134 | PhS | H | H | chf2 |
A135 | PhSO | H | H | chf2 |
A136 | PhSO2 | H | H | chf2 |
A137 | ch3s | H | H | chf2 |
A138 | ch3so | H | H | chf2 |
A139 | cf3 | H | H | chf2 |
A140 | f2ch | H | H | chf2 |
A141 | HCC | H | H | chf2 |
A142 | ch3cc | H | H | chf2 |
A143 | ch2=ch | Η | H | chf2 |
A144 | ch2=chch2 | H | H | chf2 |
A145 | CH3SO2N(CH3) | H | H | chf2 |
A146 | (CH3)2N | H | H | chf2 |
A147 | (CH3)2NSO2 | H | H | chf2 |
A148 | cich2 | H | H | chf2 |
A149 | ch3sch2 | H | H | chf2 |
A150 | ch3soch2 | H | H | chf2 |
A151 | ch3so2ch2 | H | H | chf2 |
A152 | [1,2,4]-triazol1-yl-methyl | H | H | chf2 |
A153 | H | H | H | CC13 |
A154 | ch3 | H | H | CC13 |
A155 | ch3ch2 | H | H | CC13 |
Sl. č. A156 | R79 | Reo | Rei | Rb2 |
cyklopropyl | H | H | CC13 | |
A157 | (CH3)3C | H | H | CC13 |
A158 | (CH3)2CH | H | H | CC13 |
A159 | CH3(CH2)2 | H | H | CC13 |
A160 | ch3och2 | H | H | CC13 |
A161 | CH3O(CH2)2 | H | H | CC13 |
A162 | Ph | H | H | CC13 |
A163 | PhO | H | H | CC13 |
A164 | PhS | H | H | CC13 |
A165 | PhSO | H | H | CC13 |
A166 | PhSO2 | H | H | CC13 |
A167 | CH3S | H | H | CC13 |
A168 | ch3so | H | H | CC13 |
A169 | cf3 | H | H | CC13 |
A170 | f2ch | H | H | CC13 |
A171 | HCC | H | H | CC13 |
A172 | ch3cc | H | H | CC13 |
A173 | ch2=ch | H | H | CC13 |
A174 | ch2=chch2 | H | H | CC13 |
A175 | CH3SO2N(CH3) | H | H | CC13 |
A176 | (CH3)2N | H | H | CC13 |
A177 | (CH3)2NSO2 | H | H | CC13 |
A178 | cich2 | H | H | CC13 |
A179 | ch3sch2 | H | H | CC13 |
A180 | ch3soch2 | H | H | CC13 |
A181 | ch3so2ch2 | H | H | CC13 |
A182 | [1,2,4]-triazol1-yl-methyl | H | H | CC13 |
A183 | H | H | ch3 | CF3 |
A184 | ch3 | H | ch3 | cf3 |
A185 | ch3ch2 | H | ch3 | cf3 |
A186 | cyklopropyl | H | ch3 | cf3 |
A187 | (CH3)3C | H | ch3 | cf3 |
A188 | (CH3)2CH | H | ch3 | cf3 |
A189 | CH3(CH2)2 | H | ch3 | cf3 |
A190 | ch3och2 | H | ch3 | cf3 |
A191 | CH3O(CH2)2 | H | ch3 | cf3 |
A192 | Ph | H | ch3 | cf3 |
A193 | PhO | H | ch3 | cf3 |
A194 | PhS | H | ch3 | cf3 |
A195 | PhSO | H | ch3 | cf3 |
A196 | PhSO2 | H | ch3 | cf3 |
A197 | CH3S | H | ch3 | cf3 |
A198 | ch3so | H | ch3 | cf3 |
A199 | cf3 | H | ch3 | cf3 |
A200 | f2ch | H | ch3 | cf3 |
A201 | HCC | H | ch3 | cf3 |
A202 | ch3cc | H | ch3 | cf3 |
A203 | ch2=ch | H | ch3 | cf3 |
Sl. | R79 | Reo | Rei | Rb2 |
C · A204 | ch2=chch2 | H | ch3 | cf3 |
A205 | CH3SO2N(CH3) | H | ch3 | cf3 |
A206 | (CH3)2N | H | ch3 | cf3 |
A207 | (CH3)2NSO2 | H | ch3 | cf3 |
A208 | cich2 | H | ch3 | cf3 |
A209 | ch3sch2 | H | ch3 | cf3 |
A210 | ch3soch2 | H | ch3 | cf3 |
A211 | ch3so2ch2 | H | ch3 | cf3 |
A212 | H | H | ch3 | cf3cf2 |
A213 | ch3 | H | ch3 | cf3cf2 |
A214 | ch3ch2 | H | ch3 | cf3cf2 |
A215 | cyklopropyl | H | ch3 | cf3cf2 |
A216 | (CH3)3C | H | ch3 | cf3cf2 |
A217 | (CH3)2CH | H | ch3 | cf3cf2 |
A218 | CH3(CH2)2 | H | ch3 | cf3cf2 |
A219 | ch3och2 | H | ch3 | cf3cf2 |
A220 | CH3O(CH2)2 | H | ch3 | cf3cf2 |
A221 | Ph | H | ch3 | cf3cf2 |
A222 | PhO | H | ch3 | cf3cf2 |
A223 | PhS | H | ch3 | cf3cf2 |
A224 | PhSO | H | ch3 | cf3cf2 |
A225 | PhSO2 | H | ch3 | cf3cf2 |
A226 | CH3S | H | ch3 | cf3cf2 |
A227 | ch3so | H | ch3 | cf3cf2 |
A228 | cf3 | H | ch3 | cf3cf2 |
A229 | f2ch | H | ch3 | cf3cf2 |
A230 | HCC | H | ch3 | cf3cf2 |
A231 | ch3cc | H | ch3 | cf3cf2 |
A232 | ch2=ch | H | ch3 | cf3cf2 |
A233 | ch2=chch2 | H | ch3 | cf3cf2 |
A234 | CH3SO2N(CH3) | H | ch3 | cf3cf2 |
A235 | (CH3)2N | H | ch3 | CF3CF2 |
A236 | (CH3)2NSO2 | H | ch3 | cf3cf2 |
A237 | cich2 | H | ch3 | cf3cf2 |
A238 | ch3sch2 | H | ch3 | CF3CF2 |
A239 | ch3soch2 | H | ch3 | cf3cf2 |
A240 | ch3so2ch2 | H | ch3 | cf3cf2 |
A241 | H | H | ch3 | cf3cf2cf2 |
A242 | ch3 | H | ch3 | cf3cf2cf2 |
A243 | ch3ch2 | H | ch3 | cf3cf2cf2 |
A244 | cyklopropyl | H | ch3 | cf3cf2cf2 |
A245 | (CH3)3C | H | ch3 | cf3cf2cf2 |
A246 | (ch3)2ch | H | ch3 | cf3cf2cf2 |
A247 | ch3(ch2)2 | H | ch3 | cf3cf2cf2 |
A248 | ch3och2 | H | ch3 | cf3cf2cf2 |
A249 | CH3O(CH2)2 | H | ch3 | cf3cf2cf2 |
A250 | Ph | H | ch3 | cf3cf2cf2 |
A251 | PhO | H | ch3 | cf3cf2cf2 |
A252 | PhS | H | ch3 | cf3cf2cf2 |
38CZ 304537 B6
Sl. | R79 | Reo | Rei | Rb2 |
c. A253 | PhSO | H | ch3 | cf3cf2cf2 |
A254 | PhSO2 | H | ch3 | cf3cf2cf2 |
A255 | ch3s | H | ch3 | cf3cf2cf2 |
A256 | ch3so | H | ch3 | cf3cf2cf2 |
A257 | cf3 | H | ch3 | cf3cf2cf2 |
A258 | f2ch | H | ch3 | cf3cf2cf2 |
A259 | HCC | H | ch3 | cf3cf2cf2 |
A260 | ch3cc | H | ch3 | cf3cf2cf2 |
A261 | ch2=ch | H | ch3 | cf3cf2cf2 |
A262 | ch2=chch2 | H | ch3 | cf3cf2cf2 |
A263 | CH3SO2N(CH3) | H | ch3 | cf3cf2cf2 |
A264 | (CH3)2N | H | ch3 | cf3cf2cf2 |
A265 | (CH3)2NSO2 | H | ch3 | cf3cf2cf2 |
A266 | cich2 | H | ch3 | cf3cf2cf2 |
A267 | ch3sch2 | H | ch3 | cf3cf2cf2 |
A268 | ch3soch2 | H | ch3 | cf3cf2cf2 |
A269 | ch3so2ch2 | H | ch3 | cf3cf2cf2 |
A270 | H | H | ch3 | cf2ci |
A271 | ch3 | H | ch3 | cf2ci |
A272 | ch3ch2 | H | ch3 | cf2ci |
A273 | cyklopropyl | H | ch3 | cf2ci |
A274 | (CH3)3C | H | ch3 | cf2ci |
A275 | (CH3)2CH | H | ch3 | cf2ci |
A276 | ch3(ch2)2 | H | ch3 | cf2ci |
A277 | ch3och2 | H | ch3 | cf2ci |
A278 | CH3O(CH2)2 | H | ch3 | cf2ci |
A279 | Ph | H | ch3 | cf2ci |
A280 | PhO | H | ch3 | cf2ci |
A281 | PhS | H | ch3 | cf2ci |
A282 | PhSO | H | ch3 | cf2ci |
A283 | PhSO2 | H | ch3 | cf2ci |
A284 | CH3S | H | ch3 | CF2C1 |
A285 | ch3so | H | ch3 | CF2C1 |
A28 6 | cf3 | H | ch3 | cf2ci |
A287 | f2ch | H | ch3 | cf2ci |
A288 | HCC | H | ch3 | cf2ci |
A289 | ch3cc | H | ch3 | cf2ci |
A290 | ch2=ch | H | ch3 | cf2ci |
A291 | ch2=chch2 | H | ch3 | cf2ci |
A292 | CH3SO2N(CH3) | H | ch3 | cf2ci |
A293 | (CH3)2N | H | ch3 | cf2ci |
A294 | (CH3)2NSO2 | H | ch3 | cf2ci |
A295 | cich2 | H | ch3 | cf2ci |
A296 | ch3sch2 | H | ch3 | cf2ci |
A297 | ch3soch2 | H | ch3 | cf2ci |
A298 | CH3SO2CH2 | H | ch3 | cf2ci |
A299 | H | H | ch3 | chf2 |
A300 | ch3 | H | ch3 | chf2 |
A301 | ch3ch2 | H | ch3 | chf2 |
39CZ 304537 B6
Sl. | R79 | Reo | Rei | Re2 |
c · A302 | cyklopropyl | H | ch3 | chf2 |
A303 | (CH3)3C | H | ch3 | chf2 |
A304 | (CH3)2CH | H | ch3 | chf2 |
A305 | CH3(CH2)2 | H | ch3 | chf2 |
A306 | ch3och2 | H | ch3 | chf2 |
A307 | CH3O(CH2)2 | H | ch3 | chf2 |
A308 | Ph | H | ch3 | chf2 |
A309 | PhO | H | ch3 | chf2 |
A310 | PhS | H | ch3 | chf2 |
A311 | PhSO | H | ch3 | chf2 |
A312 | PhSO2 | H | ch3 | chf2 |
A313 | CH3S | H | ch3 | chf2 |
A314 | ch3so | H | ch3 | chf2 |
A315 | cf3 | H | ch3 | chf2 |
A316 | f2ch | H | ch3 | chf2 |
A317 | HCC | H | ch3 | chf2 |
A318 | ch3cc | H | ch3 | chf2 |
A319 | ch2=ch | H | ch3 | chf2 |
A320 | ch2=chch2 | H | ch3 | chf2 |
A321 | CH3SO2N(CH3) | H | ch3 | chf2 |
A322 | (CH3)2N | H | ch3 | chf2 |
A323 | (CH3)2NSO2 | H | ch3 | chf2 |
A324 | cich2 | H | ch3 | chf2 |
A325 | ch3sch2 | H | ch3 | chf2 |
A326 | ch3soch2 | H | ch3 | chf2 |
A327 | ch3so2ch2 | H | ch3 | chf2 |
A328 | H | H | ch3 | CC13 |
A329 | ch3 | H | ch3 | CC13 |
A330 | ch3ch2 | H | ch3 | CC13 |
A331 | (CH3)3C | H | ch3 | CC13 |
A332 | (CH3)2CH | H | ch3 | CC13 |
A333 | cyklopropyl | H | ch3 | CC13 |
A334 | CH3(CH2)2 | H | ch3 | CC13 |
A335 | ch3och2 | H | ch3 | CC13 |
A336 | CH3O(CH2)2 | H | ch3 | CC13 |
A337 | Ph | H | ch3 | CC13 |
A338 | PhO | H | ch3 | CC13 |
A339 | PhS | H | ch3 | CC13 |
A340 | PhSO | H | ch3 | CC13 |
A341 | PhSO2 | H | ch3 | CC13 |
A342 | CH3S | H | ch3 | CC13 |
A343 | ch3so | H | ch3 | CC13 |
A344 | cf3 | H | ch3 | CC13 |
A345 | f2ch | H | ch3 | CC13 |
A346 | HCC | H | ch3 | CC13 |
A347 | ch3cc | H | ch3 | CC13 |
A348 | ch2=ch | H | ch3 | CC13 |
A349 | ch2=chch2 | H | ch3 | CC13 |
A350 | CH3SO2N(CH3) | H | ch3 | CC13 |
-40CZ 304537 B6
Sl. M ^a | R79 | Reo | Rei | R®2 |
c. A351 | (CH3)2N | H | ch3 | cci3 |
A352 | (CH3)2NSO2 | H | ch3 | CC13 |
A353 | cich2 | H | ch3 | CC13 |
A354 | ch3sch2 | H | ch3 | CC13 |
A355 | ch3soch2 | H | ch3 | cci3 |
A356 | ch3so2ch2 | H | ch3 | cci3 |
A357 | H | H | Ph | cf3 |
A358 | ch3 | H | Ph | cf3 |
A359 | ch3ch2 | H | Ph | cf3 |
A360 | cyklopropyl | H | Ph | cf3 |
A361 | (CH3)3C | H | Ph | cf3 |
A362 | (CH3)2CH | H | Ph | cf3 |
A363 | ch3(ch2)2 | H | Ph | cf3 |
A364 | ch3och2 | H | Ph | cf3 |
A365 | CH3O(CH2)2 | H | Ph | cf3 |
A366 | Ph | H | Ph | cf3 |
A367 | PhO | H | Ph | cf3 |
A368 | PhS | H | Ph | cf3 |
A369 | PhSO | H | Ph | cf3 |
A370 | PhSO2 | H | Ph | cf3 |
A371 | ch3s | H | Ph | cf3 |
A372 | ch3so | H | Ph | cf3 |
A373 | cf3 | H | Ph | cf3 |
A374 | f2ch | H | Ph | cf3 |
A375 | HCC | H | Ph | cf3 |
A376 | ch3cc | H | Ph | cf3 |
A377 | ch2=ch | H | Ph | cf3 |
A378 | ch2=chch2 | H | Ph | cf3 |
A379 | CH3SO2N(CH3) | H | Ph | cf3 |
A380 | (CH3)2N | H | Ph | cf3 |
A381 | (CH3)2NSO2 | H | Ph | cf3 |
A382 | C1CH2 | H | Ph | cf3 |
A383 | ch3sch2 | H | Ph | cf3 |
A384 | ch3soch2 | H | Ph | cf3 |
A385 | ch3so2ch2 | H | Ph | cf3 |
A386 | H | H | Ph | cf3cf2 |
A387 | ch3 | H | Ph | cf3cf2 |
A388 | ch3ch2 | H | Ph | cf3cf2 |
A389 | cyklopropyl | H | Ph | cf3cf2 |
A390 | (CH3)3C | H | Ph | cf3cf2 |
A391 | (CH3)2CH | H | Ph | cf3cf2 |
A392 | ch3(ch2)2 | H | Ph | cf3cf2 |
A393 | ch3och2 | H | Ph | cf3cf2 |
A394 | CH3O(CH2)2 | H | Ph | cf3cf2 |
A395 | Ph | H | Ph | cf3cf2 |
A396 | PhO | H | Ph | cf3cf2 |
A397 | PhS | H | Ph | cf3cf2 |
A398 | PhSO | H | Ph | cf3cf2 |
A399 | PhSO2 | H | Ph | cf3cf2 |
-41 CZ 304537 B6
Sl. | R79 | Reo | Rei | R82 |
C · A400 | ch3s | H | Ph | cf3cf2 |
A401 | ch3so | H | Ph | cf3cf2 |
A402 | cf3 | H | Ph | cf3cf2 |
A403 | f2ch | H | Ph | cf3cf2 |
A404 | HCC | H | Ph | cf3cf2 |
A405 | ch3cc | H | Ph | cf3cf2 |
A406 | ch2=ch | H | Ph | cf3cf2 |
A407 | ch2=chch2 | H | Ph | cf3cf2 |
A408 | CH3SO2N(CH3) | H | Ph | cf3cf2 |
A409 | (CH3)2N | H | Ph | cf3cf2 |
A410 | (CH3)2NSO2 | H | Ph | cf3cf2 |
A411 | cich2 | H | Ph | cf3cf2 |
A412 | ch3sch2 | H | Ph | cf3cf2 |
A413 | ch3soch2 | H | Ph | cf3cf2 |
A414 | ch3so2ch2 | H | Ph | cf3cf2 |
A415 | H | H | Ph | cf3cf2cf2 |
A416 | ch3 | H | Ph | cf3cf2cf2 |
A417 | ch3ch2 | H | Ph | cf3cf2cf2 |
A418 | cyklopropyl | H | Ph | cf3cf2cf2 |
A419 | (CH3)3C | H | Ph | cf3cf2cf2 |
A420 | (CH3)2CH | H | Ph | cf3cf2cf2 |
A421 | ch3(ch2)2 | H | Ph | cf3cf2cf2 |
A422 | ch3och2 | H | Ph | cf3cf2cf2 |
A423 | CH3O(CH2)2 | H | Ph | cf3cf2cf2 |
A424 | Ph | H | Ph | cf3cf2cf2 |
A425 | PhO | H | Ph | cf3cf2cf2 |
A426 | PhS | H | Ph | cf3cf2cf2 |
A427 | PhSO | H | Ph | cf3cf2cf2 |
A428 | PhSO2 | H | Ph | cf3cf2cf2 |
A429 | ch3s | H | Ph | cf3cf2cf2 |
A430 | ch3so | H | Ph | cf3cf2cf2 |
A431 | cf3 | H | Ph | cf3cf2cf2 |
A432 | f2ch | H | Ph | cf3cf2cf2 |
A433 | HCC | H | Ph | cf3cf2cf2 |
A434 | ch3cc | H | Ph | cf3cf2cf2 |
A435 | ch2=ch | H | Ph | cf3cf2cf2 |
A436 | ch2=chch2 | H | Ph | cf3cf2cf2 |
A437 | ch3so2n (CH3) | H | Ph | cf3cf2cf2 |
A438 | (ch3)2n | H | Ph | cf3cf2cf2 |
A439 | (CH3)2NSO2 | H | Ph | cf3cf2cf2 |
A440 | cich2 | H | Ph | cf3cf2cf2 |
A441 | ch3sch2 | H | Ph | cf3cf2cf2 |
A442 | ch3soch2 | H | Ph | cf3cf2cf2 |
A443 | ch3so2ch2 | H | Ph | cf3cf2cf2 |
A444 | H | H | Ph | cf2ci |
A445 | ch3 | H | Ph | cf2ci |
A446 | ch3ch2 | H | Ph | cf2ci |
A447 | cyklopropyl | H | Ph | cf2ci |
A448 | (CH3)3C | H | Ph | cf2ci |
42CZ 304537 B6
Sl. | R79 | Reo | Rex | Rfi2 |
c · A449 | (CH3)2CH | H | Ph | CF2C1 |
A450 | CH3(CH2)2 | H | Ph | CF2C1 |
A451 | ch3och2 | H | Ph | CF2C1 |
A452 | CH3O(CH2)2 | H | Ph | cf2ci |
A453 | Ph | H | Ph | cf2ci |
A454 | PhO | H | Ph | cf2ci |
A455 | PhS | H | Ph | cf2ci |
A456 | PhSO | H | Ph | cf2ci |
A457 | PhSO2 | H | Ph | CF2C1 |
A458 | ch3s | H | Ph | cf2ci |
A459 | ch3so | H | Ph | CF2C1 |
A4 60 | cf3 | H | Ph | CF2C1 |
A461 | f2ch | H | Ph | cf2ci |
A462 | HCC | H | Ph | cf2ci |
A463 | ch3cc | H | Ph | cf2ci |
A4 64 | ch2=ch | H | Ph | cf2ci |
A4 65 | ch2=chch2 | H | Ph | CF2C1 |
A466 | CH3SO2N(CH3) | H | Ph | CF2C1 |
A4 67 | (CH3)2N | H | Ph | cf2ci |
A468 | (CH3)2NSO2 | H | Ph | cf2ci |
A469 | cich2 | H | Ph | cf2ci |
A470 | ch3sch2 | H | Ph | cf2ci |
A471 | ch3soch2 | H | Ph | cf2ci |
A472 | ch3so2ch2 | H | Ph | cf2ci |
A473 | H | H | Ph | chf2 |
A474 | ch3 | H | Ph | chf2 |
A475 | ch3ch2 | H | Ph | chf2 |
A476 | cyklopropyl | H | Ph | chf2 |
A477 | (CH3)3C | H | Ph | chf2 |
A478 | (CH3)2CH | H | Ph | chf2 |
A479 | CH3(CH2)2 | H | Ph | chf2 |
A480 | ch3och2 | H | Ph | chf2 |
A481 | CH3O(CH2)2 | H | Ph | chf2 |
A482 | Ph | H | Ph | chf2 |
A483 | PhO | H | Ph | chf2 |
A484 | PhS | H | Ph | chf2 |
A485 | PhSO | H | Ph | chf2 |
A486 | PhSO2 | H | Ph | chf2 |
A487 | ch3s | H | Ph | chf2 |
A488 | ch3so | H | Ph | chf2 |
A489 | cf3 | H | Ph | chf2 |
A490 | f2ch | H | Ph | chf2 |
A491 | HCC | H | Ph | chf2 |
A492 | CH3CC | H | Ph | chf2 |
A493 | ch2=ch | H | Ph | chf2 |
A494 | ch2=chch2 | H | Ph | chf2 |
A495 | CH3SO2N(CH3) | H | Ph | chf2 |
A496 | (CH3)2N | H | Ph | chf2 |
A497 | (CH3)2NSO2 | H | Ph | chf2 |
43CZ 304537 B6
Sl. | R79 | Rbo | Rei | Re2 |
c. A498 | C1CH2 | H | Ph | chf2 |
A499 | CH3SCH2 | H | Ph | chf2 |
A500 | CH3SOCH2 | H | Ph | chf2 |
A501 | ch3so2ch2 | H | Ph | chf2 |
A502 | H | H | Ph | CC13 |
A503 | ch3 | H | Ph | CC13 |
A504 | ch3ch2 | H | Ph | CC13 |
A505 | cyklopropyl | H | Ph | CC13 |
A506 | (CH3)3C | H | Ph | CC13 |
A507 | (CH3)2CH | H | Ph | CC13 |
A508 | CH3(CH2)2 | H | Ph | CC13 |
A509 | ch3och2 | H | Ph | CC13 |
A510 | CH3O(CH2)2 | H | Ph | CC13 |
A511 | Ph | H | Ph | CC13 |
A512 | PhO | H | Ph | CC13 |
A513 | PhS | H | Ph | CC13 |
A514 | PhSO | H | Ph | CC13 |
A515 | PhSO2 | H | Ph | CC13 |
A516 | CH3S | H | Ph | CC13 |
A517 | ch3so | H | Ph | CC13 |
A518 | cf3 | H | Ph | CC13 |
A519 | f2ch | H | Ph | CC13 |
A520 | HCC | H | Ph | CC13 |
A521 | ch3cc | H | Ph | CC13 |
A522 | ch2=ch | H | Ph | CC13 |
A523 | ch2=chch2 | H | Ph | CC13 |
A524 | CH3SOzN(CH3) | H | Ph | CC13 |
A525 | (CH3)2N | H | Ph | CC13 |
A526 | (CH3)2NSO2 | H | Ph | CC13 |
A527 | C1CH2 | H | Ph | CC13 |
A528 | ch3sch2 | H | Ph | CC13 |
A529 | CH3SOCH2 | H | Ph | CC13 |
A530 | ch3so2ch2 | H | Ph | CC13 |
A531 | H | ch3 | H | cf3 |
A532 | H | ch3ch2 | H | cf3 |
A533 | H | cyklopropyl | H | cf3 |
A534 | H | (CH3)3CH | H | cf3 |
A535 | H | (CH3)2CH | H | cf3 |
A536 | H | CH3(CH2)2 | H | cf3 |
A537 | H | ch3och2 | H | cf3 |
A538 | H | CH3O(CH2)2 | H | cf3 |
A539 | H | Ph | H | cf3 |
A540 | H | PhO | H | cf3 |
A541 | H | PhS | H | cf3 |
A542 | H | PhSO | H | cf3 |
A543 | H | PhSO2 | H | cf3 |
A544 | H | ch3s | H | cf3 |
A545 | H | ch3so | H | cf3 |
A546 | H | cf3 | H | cf3 |
-44CZ 304537 B6
Sl. | R79 | Reo | Rei | Re2 |
c. A547 | H | f2ch | H | cf3 |
A548 | H | HCC | H | cf3 |
A549 | H | CH3CC | H | cf3 |
A550 | H | ch2=ch | H | cf3 |
A551 | H | ch2=chch2 | H | cf3 |
A552 | H | CH3SO2N(CH3) | H | cf3 |
A553 | H | (CH3)2N | H | cf3 |
A554 | H | (CH3)2NSO2 | H | cf3 |
A555 | H | ch3sch2 | H | cf3 |
A556 | H | ch3soch2 | H | cf3 |
A557 | H | ch3so2ch2 | H | cf3 |
A558 | H | ch3 | H | cf3cf2 |
A559 | H | ch3ch2 | H | cf3cf2 |
A560 | H | cyklopropyl | H | cf3cf2 |
A561 | H | (CH3)3C | H | cf3cf2 |
A562 | H | (CH3)2CH | H | cf3cf2 |
A563 | H | ch3(ch2)2 | H | cf3cf2 |
A564 | H | ch3och2 | H | cf3cf2 |
A565 | H | CH3O(CH2)2 | H | cf3cf2 |
A566 | H | Ph | H | cf3cf2 |
A567 | H | PhO | H | cf3cf2 |
A568 | H | PhS | H | cf3cf2 |
A569 | H | PhSO | H | cf3cf2 |
A570 | H | PhSO2 | H | cf3cf2 |
A571 | H | CH3S | H | cf3cf2 |
A572 | H | ch3so | H | cf3cf2 |
A573 | H | cf3 | H | cf3cf2 |
A574 | H | f2ch | H | cf3cf2 |
A575 | H | HCC | H | cf3cf2 |
A576 | H | ch3cc | H | cf3cf2 |
A577 | H | ch2=ch | H | cf3cf2 |
A578 | H | ch2=chch2 | H | cf3cf2 |
A579 | H | CH3SO2N(CH3) | H | cf3cf2 |
A580 | H | (ch3)2n | H | cf3cf2 |
A581 | H | (CH3)2NSO2 | H | cf3cf2 |
A582 | H | ch3sch2 | H | cf3cf2 |
A583 | H | ch3soch2 | H | cf3cf2 |
A584 | H | ch3so2ch2 | H | cf3cf2 |
A585 | H | ch3 | H | cf3cf2cf2 |
A586 | H | ch3ch2 | H | cf3cf2cf2 |
A587 | H | cyklopropyl | H | cf3cf2cf2 |
A588 | H | (CH3) 3c | H | cf3cf2cf2 |
A589 | H | (CH3)2CH | H | cf3cf2cf2 |
A590 | H | CH3(CH2)2 | H | cf3cf2cf2 |
A591 | H | CH3OCH2 | H | cf3cf2cf2 |
A592 | H | CH3O(CH2)2 | H | cf3cf2cf2 |
A593 | H | Ph | H | cf3cf2cf2 |
A594 | H | PhO | H | cf3cf2cf2 |
A595 | H | PhS | H | cf3cf2cf2 |
-45CZ 304537 B6
Sl. fl | R79 | Reo | Rei | Re2 |
s* · A596 | H | PhSO | H | CF3CF2CF2 |
A597 | H | PhSO2 | H | cf3cf2cf2 |
A598 | H | ch3s | H | CF3CF2CF2 |
A599 | H | ch3so | H | CF3CF2CF2 |
A600 | H | cf3 | H | cf3cf2cf2 |
A601 | H | f2ch | H | cf3cf2cf2 |
A602 | H | HCC | H | cf3cf2cf2 |
A603 | H | ch3cc | H | cf3cf2cf2 |
A604 | H | ch2=ch | H | cf3cf2cf2 |
A605 | H | ch2=chch2 | H | cf3cf2cf2 |
A606 | H | CH3SO2N(CH3) | H | CF3CF2CF2 |
A607 | H | (CH3)2N | H | cf3cf2cf2 |
A608 | H | (CH3)2NSO2 | H | cf3cf2cf2 |
A609 | H | ch3sch2 | H | cf3cf2cf2 |
A610 | H | ch3soch2 | H | cf3cf2cf2 |
A611 | H | ch3so2ch2 | H | cf3cf2cf2 |
A612 | H | ch3 | H | cf2ci |
A613 | H | ch3ch2 | H | cf2ci |
A614 | H | cyklopropyl | H | cf2ci |
A615 | H | (CH3)3C | H | cf2ci |
A616 | H | (CH3)2CH | H | cf2ci |
A617 | H | ch3(ch2)2 | H | cf2ci |
A618 | H | ch3och2 | H | cf2ci |
A619 | H | CH3O(CH2)2 | H | cf2ci |
A620 | H | Ph | H | cf2ci |
A621 | H | PhO | H | cf2ci |
A622 | H | PhS | H | cf2ci |
A623 | H | PhSO | H | cf2ci |
A624 | H | PhSO2 | H | cf2ci |
A625 | H | ch3s | H | cf2ci |
A626 | H | ch3so | H | cf2ci |
A627 | H | cf3 | H | cf2ci |
A628 | H | f2ch | H | cf2ci |
A629 | H | HCC | H | cf2ci |
A630 | H | ch3cc | H | cf2ci |
A631 | H | ch2=ch | H | cf2ci |
A632 | H | ch2=chch2 | H | cf2ci |
A633 | H | CH3SO2N(CH3) | H | cf2ci |
A634 | H | (CH3)2N | H | cf2ci |
A635 | H | (CH3)2NSO2 | H | cf2ci |
A636 | H | ch3sch2 | H | cf2ci |
A637 | H | ch3soch2 | H | cf2ci |
A638 | H | ch3so2ch2 | H | cf2ci |
A639 | H | ch3 | H | chf2 |
A640 | H | CH3CH2 | H | chf2 |
A641 | H | cyklopropyl | H | chf2 |
A642 | H | (CH3)3C | H | chf2 |
A643 | H | (CH3)2CH | H | chf2 |
A644 | H | CH3(CH2)2 | H | chf2 |
-46CZ 304537 B6
Sl. v | R79 | Reo | Rei | Re2 |
c · A645 | H | CH3OCH2 | H | chf2 |
A646 | H | CH3O(CH2)2 | H | chf2 |
A647 | H | Ph | H | CHF2 |
A648 | H | PhO | H | chf2 |
A649 | H | PhS | H | chf2 |
A650 | H | PhSO | H | chf2 |
A651 | H | PhSO2 | H | chf2 |
A652 | H | ch3s | H | chf2 |
A653 | H | ch3so | H | chf2 |
A654 | H | cf3 | H | chf2 |
A655 | H | f2ch | H | chf2 |
A656 | H | HCC | H | chf2 |
A657 | H | CH3CC | H | chf2 |
A658 | H | ch2=ch | H | chf2 |
A659 | H | ch2=chch2 | H | chf2 |
A660 | H | CH3SO2N(CH3) | H | chf2 |
A661 | H | (CH3)2N | H | chf2 |
A662 | H | (CH3)2NSO2 | H | chf2 |
A663 | H | ch3sch2 | H | chf2 |
A664 | H | ch3soch2 | H | chf2 |
A665 | H | ch3so2ch2 | H | chf2 |
A666 | H | ch3 | H | CC13 |
A667 | H | ch3ch2 | H | CC13 |
A668 | H | cyklopropyl | H | CC13 |
A669 | H | (CH3)3C | H | CC13 |
A670 | H | (CH3)2CH | H | CC13 |
A671 | H | ch3(ch2)2 | H | CC13 |
A672 | H | ch3och2 | H | CC13 |
A673 | H | CH3O(CH2)2 | H | CC13 |
A674 | H | Ph | H | CC13 |
A675 | H | PhO | H | CC13 |
A676 | H | PhS | H | CC13 |
A677 | H | PhSO | H | CC13 |
A678 | H | PhSO2 | H | CC13 |
A679 | H | ch3s | H | CC13 |
A680 | H | ch3so | H | CC13 |
A681 | H | cf3 | H | CC13 |
A682 | H | f2ch | H | CC13 |
A683 | H | HCC | H | CC13 |
A684 | H | CH3CC | H | CC13 |
A685 | H | ch2=ch | H | CC13 |
A686 | H | ch2=chch2 | H | CC13 |
A687 | H | CH3SO2N(CH3) | H | CC13 |
A688 | H | <ch3)2n | H | CC13 |
A689 | H | (CH3)2NSO2 | H | CC13 |
A690 | H | ch3sch2 | H | CC13 |
A691 | H | ch3soch2 | H | CC13 |
A692 | H | ch3so2ch2 | H | CC13 |
A693 | H | ch3 | ch3 | cf3 |
47CZ 304537 B6
Sl. | R79 | Reo | Rei | Rb2 |
c. A694 | H | ch3ch2 | ch3 | cf3 |
A695 | H | cyklopropyl | ch3 | cf3 |
A696 | H | (CH3)3C | ch3 | cf3 |
A697 | H | (CH3)2CH | ch3 | cf3 |
A698 | H | CH3(CH2)2 | ch3 | cf3 |
A699 | H | ch3och2 | ch3 | cf3 |
A700 | H | CH3O(CH2)2 | ch3 | cf3 |
A701 | H | Ph | ch3 | cf3 |
A702 | H | PhO | ch3 | cf3 |
A703 | H | PhS | ch3 | cf3 |
A704 | H | PhSO | ch3 | cf3 |
A705 | H | PhSO2 | ch3 | cf3 |
A706 | H | CH3S | ch3 | cf3 |
A707 | H | ch3so | ch3 | cf3 |
A708 | H | cf3 | ch3 | cf3 |
A709 | H | f2ch | ch3 | cf3 |
A710 | H | HCC | ch3 | cf3 |
A711 | H | ch3cc | ch3 | cf3 |
A712 | H | ch2=ch | ch3 | cf3 |
A713 | H | ch2=chch2 | ch3 | cf3 |
A714 | H | CH3SO2N(CH3) | ch3 | cf3 |
A715 | H | (CH3)2N | ch3 | cf3 |
A716 | H | (CH3)2NSO2 | ch3 | cf3 |
A717 | H | ch3sch2 | ch3 | cf3 |
A718 | H | ch3soch2 | ch3 | cf3 |
A719 | H | ch3so2ch2 | ch3 | cf3 |
A720 | H | ch3 | ch3 | cf3cf2 |
A721 | H | ch3ch2 | ch3 | cf3cf2 |
A722 | H | cyklopropyl | ch3 | cf3cf2 |
A723 | H | (CH3)3C | ch3 | cf3cf2 |
A724 | H | (CH3)2CH | ch3 | cf3cf2 |
A725 | H | ch3(ch2)2 | ch3 | cf3cf2 |
A726 | H | ch3och2 | ch3 | cf3cf2 |
A727 | H | CH3O(CH2)2 | ch3 | cf3cf2 |
A728 | H | Ph | ch3 | cf3cf2 |
A729 | H | PhO | ch3 | cf3cf2 |
A730 | H | PhS | ch3 | cf3cf2 |
A731 | H | PhSO | ch3 | cf3cf2 |
A732 | H | PhSO2 | ch3 | cf3cf2 |
A733 | H | ch3s | ch3 | cf3cf2 |
A734 | H | ch3so | ch3 | cf3cf2 |
A735 | H | cf3 | ch3 | cf3cf2 |
A736 | H | f2ch | ch3 | cf3cf2 |
A737 | H | HCC | ch3 | cf3cf2 |
A738 | H | ch3cc | ch3 | cf3cf2 |
A739 | H | ch2=ch | ch3 | cf3cf2 |
A740 | H | ch2=chch2 | ch3 | cf3cf2 |
A741 | H | CH3SO2N(CH3) | ch3 | cf3cf2 |
A742 | H | (CH3)2N | ch3 | cf3cf2 |
-48CZ 304537 B6
Sl. | R79 | Reo | Rex | Re2 |
c. A743 | H | (CH3)2NSO2 | ch3 | cf3cf2 |
A744 | H | ch3sch2 | ch3 | cf3cf2 |
A745 | H | ch3soch2 | ch3 | cf3cf2 |
A746 | H | ch3so2ch2 | ch3 | cf3cf2 |
A747 | H | ch3 | ch3 | cf3cf2cf2 |
A748 | H | ch3ch2 | ch3 | cf3cf2cf2 |
A749 | H | cyklopropyl | ch3 | cf3cf2cf2 |
A750 | H | (CH3)3C | ch3 | cf3cf2cf2 |
A751 | H | (CH3)2CH | ch3 | cf3cf2cf2 |
A752 | H | CH3(CH2)2 | ch3 | cf3cf2cf2 |
A753 | H | ch3och2 | ch3 | cf3cf2cf2 |
A754 | H | CH3O(CH2)2 | ch3 | cf3cf2cf2 |
A755 | H | Ph | ch3 | cf3cf2cf2 |
A756 | H | PhO | ch3 | cf3cf2cf2 |
A757 | H | PhS | ch3 | cf3cf2cf2 |
A758 | H | PhSO | ch3 | cf3cf2cf2 |
A759 | H | PhSO2 | ch3 | cf3cf2cf2 |
A7 60 | H | CH3S | ch3 | cf3cf2cf2 |
A761 | H | ch3so | ch3 | cf3cf2cf2 |
A762 | H | cf3 | ch3 | cf3cf2cf2 |
A763 | H | f2ch | ch3 | cf3cf2cf2 |
A764 | H | HCC | ch3 | cf3cf2cf2 |
A765 | H | ch3cc | ch3 | cf3cf2cf2 |
A766 | H | ch2=ch | ch3 | cf3cf2cf2 |
A7 67 | H | ch2=chch2 | ch3 | cf3cf2cf2 |
A768 | H | CH3SO2N(CH3) | ch3 | cf3cf2cf2 |
A7 69 | H | (CH3)2N | ch3 | cf3cf2cf2 |
A770 | H | (CH3)2NSO2 | ch3 | cf3cf2cf2 |
A771 | H | ch3sch2 | ch3 | cf3cf2cf2 |
A772 | H | ch3soch2 | ch3 | cf3cf2cf2 |
A773 | H | ch3so2ch2 | ch3 | cf3cf2cf2 |
A774 | H | ch3 | ch3 | CF2C1 |
A775 | H | ch3ch2 | ch3 | CF2C1 |
A776 | H | cyklopropyl | ch3 | cf2ci |
A777 | H | (CH3) 3c | ch3 | cf2ci |
A778 | H | (CH3)2CH | ch3 | cf2ci |
A779 | H | CH3(CH2)2 | ch3 | cf2ci |
A780 | H | ch3och2 | ch3 | cf2ci |
A781 | H | CH3O(CH2)2 | ch3 | cf2ci |
A782 | H | Ph | ch3 | cf2ci |
A783 | H | PhO | ch3 | cf2ci |
A784 | H | PhS | ch3 | cf2ci |
A785 | H | PhSO | ch3 | cf2ci |
A786 | H | PhSO2 | ch3 | cf2ci |
A787 | H | CH3S | ch3 | cf2ci |
A788 | H | ch3so | ch3 | cf2ci |
A789 | H | cf3 | ch3 | cf2ci |
A790 | H | f2ch | ch3 | CF2C1 |
A791 | H | HCC | ch3 | CF2C1 |
-49CZ 304537 B6
Sl. | R79 | Reo | Rbi | Rb2 |
č. A792 | H | CH3CC | ch3 | cf2ci |
A793 | H | ch2=ch | ch3 | cf2ci |
A794 | H | ch2=chch2 | ch3 | cf2ci |
A795 | H | CH3SO2N(CH3) | ch3 | cf2ci |
A796 | H | (CH3)2N | ch3 | cf2ci |
A797 | H | (CH3)2NSO2 | ch3 | cf2ci |
A798 | H | ch3sch2 | ch3 | cf2ci |
A799 | H | ch3soch2 | ch3 | cf2ci |
A800 | H | ch3so2ch2 | ch3 | cf2ci |
A801 | H | ch3 | ch3 | chf2 |
A802 | H | ch3ch2 | ch3 | chf2 |
A803 | H | cyklopropyl | ch3 | chf2 |
A804 | H | (CH3)3C | ch3 | chf2 |
A805 | H | (CH3)2CH | ch3 | chf2 |
A806 | H | CH3(CH2)2 | ch3 | chf2 |
A807 | H | ch3och2 | ch3 | chf2 |
A808 | H | CH3O(CH2)2 | ch3 | CHFz |
A809 | H | Ph | ch3 | chf2 |
A810 | H | PhO | ch3 | chf2 |
A811 | H | PhS | ch3 | chf2 |
A812 | H | PhSO | ch3 | chf2 |
A813 | H | PhSO2 | ch3 | chf2 |
A814 | H | ch3s | ch3 | chf2 |
A815 | H | CH3S0 | ch3 | chf2 |
A816 | H | cf3 | ch3 | chf2 |
A817 | H | f2ch | ch3 | chf2 |
A818 | H | HCC | ch3 | chf2 |
A819 | H | ch3cc | ch3 | chf2 |
A820 | H | ch2=ch | ch3 | chf2 |
A821 | H | ch2=chch2 | ch3 | chf2 |
A822 | H | CH3SO2N(CH3) | ch3 | chf2 |
A823 | H | (CH3)2N | ch3 | chf2 |
A824 | H | (CH3)2NSO2 | ch3 | chf2 |
A825 | H | ch3sch2 | ch3 | chf2 |
A826 | H | CH3SOCH2 | ch3 | chf2 |
A827 | H | CH3SO2CH2 | ch3 | chf2 |
A828 | H | ch3 | ch3 | CC13 |
A829 | H | ch3ch2 | ch3 | CC13 |
A830 | H | cyklopropyl | ch3 | CC13 |
A831 | H | (CH3)3C | ch3 | CC13 |
A832 | H | (CH3)2CH | ch3 | CC13 |
A833 | H | CH3(CH2)2 | ch3 | CC13 |
A834 | H | ch3och2 | ch3 | CC13 |
A835 | H | CH3O(CH2)2 | ch3 | CC13 |
A836 | H | Ph | ch3 | CC13 |
A837 | H | PhO | ch3 | CC13 |
A838 | H | PhS | ch3 | CC13 |
A839 | H | PhSO | ch3 | CC13 |
A840 | H | PhSO2 | ch3 | CC13 |
-50CZ 304537 B6
Sl. w c· | R79 | Reo | Rei | Re2 |
· A841 | H | CH3S | CH3 | CC13 |
A842 | H | ch3so | ch3 | CC13 |
A843 | H | cf3 | ch3 | CC13 |
A844 | H | f2ch | ch3 | CC13 |
A845 | H | HCC | ch3 | CC1-3 |
A846 | H | ch3cc | ch3 | CC13 |
A847 | H | ch2=ch | ch3 | CC13 |
A848 | H | ch2=chch2 | ch3 | CC13 |
A849 | H | CH3SO2N(CH3) | ch3 | CC13 |
A850 | H | (CH3)2N | ch3 | CC13 |
A851 | H | (CH3)2NSO2 | ch3 | CC13 |
A852 | H | ch3sch2 | ch3 | CC13 |
A853 | H | ch3soch2 | ch3 | CC13 |
A854 | H | ch3so2ch2 | ch3 | CC13 |
A855 | H | ch3 | Ph | cf3 |
A856 | H | ch3ch2 | Ph | cf3 |
A857 | H | (CH3)2CH | Ph | cf3 |
A858 | H | (CH3)2CH | Ph | cf3 |
A859 | H | cyklopropyl | Ph | cf3 |
A860 | H | CH3(CH2)2 | Ph | cf3 |
A861 | H | ch3och2 | Ph | cf3 |
A862 | H | CH3O(CH2)2 | Ph | cf3 |
A863 | H | Ph | Ph | cf3 |
A864 | H | PhO | Ph | cf3 |
A865 | H | PhS | Ph | cf3 |
A866 | H | PhSO | Ph | cf3 |
A867 | H | PhSO2 | Ph | cf3 |
A868 | H | CH3S | Ph | cf3 |
A869 | H | ch3so | Ph | cf3 |
A870 | H | cf3 | Ph | cf3 |
A871 | H | f2ch | Ph | cf3 |
A872 | H | HCC | Ph | cf3 |
A873 | H | CH3CC | Ph | cf3 |
A874 | H | ch2=ch | Ph | cf3 |
A875 | H | ch2=chch2 | Ph | cf3 |
A876 | H | CH3SO2N(CH3) | Ph | cf3 |
A877 | H | (CH3)2N | Ph | cf3 |
A878 | H | (CH3)2NSO2 | Ph | cf3 |
A879 | H | ch3sch2 | Ph | cf3 |
A880 | H | ch3soch2 | Ph | cf3 |
A881 | H | ch3so2ch2 | Ph | cf3 |
A882 | H | ch3 | Ph | cf3cf2 |
A883 | H | ch3ch2 | Ph | cf3cf2 |
A884 | H | cyklopropyl | Ph | cf3cf2 |
A885 | H | (CH3)3c | Ph | cf3cf2 |
A886 | H | (CH3)2CH | Ph | CF3CF2 |
A887 | H | CH3(CH2)2 | Ph | cf3cf2 |
A888 | H | ch3och2 | Ph | cf3cf2 |
A889 | H | CH3O(CH2)2 | Ph | cf3cf2 |
-51 CZ 304537 B6
Sl. v | R79 | Reo | Rei | Rfl2 |
c > A890 | H | Ph | Ph | cf3cf2 |
A891 | H | PhO | Ph | cf3cf2 |
A892 | H | PhS | Ph | cf3cf2 |
A893 | H | PhSO | Ph | cf3cf2 |
A894 | H | PhSO2 | Ph | cf3cf2 |
A895 | H | ch3s | Ph | cf3cf2 |
A896 | H | CH3SO | Ph | cf3cf2 |
A897 | H | cf3 | Ph | cf3cf2 |
A898 | H | f2ch | Ph | cf3cf2 |
A899 | H | HCC | Ph | cf3cf2 |
A900 | H | ch3cc | Ph | cf3cf2 |
A901 | H | ch2=ch | Ph | cf3cf2 |
A902 | H | ch2=chch2 | Ph | cf3cf2 |
A903 | H | CH3SO2N(CH3) | Ph | cf3cf2 |
A904 | H | (CH3)2N | Ph | cf3cf2 |
A905 | H | (CH3)2NSO2 | Ph | cf3cf2 |
A906 | H | ch3sch2 | Ph | cf3cf2 |
A907 | H | CH3SOCH2 | Ph | cf3cf2 |
A908 | H | ch3so2ch2 | Ph | cf3cf2 |
A909 | H | ch3 | Ph | cf3cf2cf2 |
A910 | H | ch3ch2 | Ph | cf3cf2cf2 |
A911 | H | cyklopropyl | Ph | cf3cf2cf2 |
A912 | H | (CH3)3C | Ph | cf3cf2cf2 |
A913 | H | (ch3)2ch | Ph | cf3cf2cf2 |
A914 | H | ch3(ch2)2 | Ph | cf3cf2cf2 |
A915 | H | ch3och2 | Ph | cf3cf2cf2 |
A916 | H | CH3O(CH2)2 | Ph | cf3cf2cf2 |
A917 | H | Ph | Ph | cf3cf2cf2 |
A918 | H | PhO | Ph | cf3cf2cf2 |
A919 | H | PhS | Ph | cf3cf2cf2 |
A920 | H | PhSO | Ph | cf3cf2cf2 |
A921 | H | PhSO2 | Ph | cf3cf2cf2 |
A922 | H | ch3s | Ph | cf3cf2cf2 |
A923 | H | ch3so | Ph | cf3cf2cf2 |
A924 | H | cf3 | Ph | cf3cf2cf2 |
A925 | H | f2ch | Ph | cf3cf2cf2 |
A926 | H | HCC | Ph | cf3cf2cf2 |
A927 | H | CH3CC | Ph | cf3cf2cf2 |
A928 | H | ch2=ch | Ph | cf3cf2cf2 |
A929 | H | ch2=chch2 | Ph | cf3cf2cf2 |
A930 | H | CH3SO2N(CH3) | Ph | cf3cf2cf2 |
A931 | H | (CH3)2N | Ph | cf3cf2cf2 |
A932 | H | (CH3)2NSO2 | Ph | cf3cf2cf2 |
A933 | H | CH3SCH2 | Ph | cf3cf2cf2 |
A934 | H | CH3SOCH2 | Ph | cf3cf2cf2 |
A935 | H | CH3SO2CH2 | Ph | cf3cf2cf2 |
A936 | H | ch3 | Ph | cf2ci |
A937 | H | ch3ch2 | Ph | cf2ci |
A938 | H | cyklopropyl | Ph | cf2ci |
-52CZ 304537 B6
Sl. M | R79 | Reo | Rei | R«2 |
w · A939 | H | (CH3)3C | Ph | cf2ci |
A940 | H | (ch3)2ch | Ph | cf2ci |
A941 | H | ch3(ch2)2 | Ph | cf2ci |
A942 | H | ch3och2 | Ph | cf2ci |
A943 | H | CH3O(CH2)2 | Ph | cf2ci |
A944 | H | Ph | Ph | cf2ci |
A945 | H | PhO | Ph | cf2ci |
A946 | H | PhS | Ph | cf2ci |
A947 | H | PhSO | Ph | cf2ci |
A948 | H | PhSO2 | Ph | cf2ci |
A949 | H | CH3S | Ph | cf2ci |
A950 | H | ch3so | Ph | cf2ci |
A951 | H | cf3 | Ph | cf2ci |
A952 | H | f2ch | Ph | cf2ci |
A953 | H | HCC | Ph | cf2ci |
A954 | H | ch3cc | Ph | cf2ci |
A955 | H | ch2=ch | Ph | cf2ci |
A956 | H | ch2=chch2 | Ph | cf2ci |
A957 | H | CH3SO2N(CH3) | Ph | cf2ci |
A958 | H | (CH3)2N | Ph | cf2ci |
A959 | H | (CH3)2NSO2 | Ph | cf2ci |
A960 | H | ch3sch2 | Ph | cf2ci |
A961 | H | ch3soch2 | Ph | cf2ci |
A962 | H | ch3so2ch2 | Ph | cf2ci |
A963 | H | ch3 | Ph | chf2 |
A964 | H | ch3ch2 | Ph | chf2 |
A965 | H | (CH3)3C | Ph | chf2 |
A966 | H | (CH3)2CH | Ph | chf2 |
A967 | H | cyklopropyl | Ph | chf2 |
A968 | H | CH3(CH2)2 | Ph | chf2 |
A969 | H | ch3och2 | Ph | chf2 |
A970 | H | CH3O(CH2)2 | Ph | chf2 |
A971 | H | Ph | Ph | chf2 |
A972 | H | PhO | Ph | chf2 |
A973 | H | PhS | Ph | chf2 |
A974 | H | PhSO | Ph | chf2 |
A975 | H | PhSO2 | Ph | chf2 |
A976 | H | CH3S | Ph | chf2 |
A977 | H | ch3so | Ph | chf2 |
A978 | H | cf3 | Ph | chf2 |
A979 | H | f2ch | Ph | chf2 |
A980 | H | HCC | Ph | chf2 |
A981 | H | CH3CC | Ph | chf2 |
A982 | H | ch2=ch | Ph | chf2 |
A983 | H | ch2=chch2 | Ph | chf2 |
A984 | H | CH3SO2N(CH3) | Ph | chf2 |
A985 | H | (CH3)2N | Ph | chf2 |
A986 | H | (CH3)2NSO2 | Ph | chf2 |
A987 | H | ch3sch2 | Ph | chf2 |
-53CZ 304537 B6
Sl. | R79 | Reo | Rei | R82 |
c. A988 | H | CH3SOCH2 | Ph | chf2 |
A989 | H | ch3so2ch2 | Ph | chf2 |
A990 | H | ch3 | Ph | CC13 |
A991 | H | ch3ch2 | Ph | CC13 |
A992 | H | (CH3)3C | Ph | CC13 |
A993 | H | (CH3)2CH | Ph | CC13 |
A994 | H | cyklopropyl | Ph | CC13 |
A995 | H | CH3(CH2)2 | Ph | CC13 |
A996 | H | ch3och2 | Ph | CC13 |
A997 | H | CH3O(CH2)2 | Ph | CC13 |
A998 | H | Ph | Ph | CC13 |
A999 | H | PhO | Ph | CC13 |
A1000 | H | PhS | Ph | CC13 |
A1001 | H | PhSO | Ph | CC13 |
A1002 | H | PhSO2 | Ph | CC13 |
A1003 | H | CH3S | Ph | CC13 |
A1004 | H | ch3so | Ph | CC13 |
A1005 | H | cf3 | Ph | CC13 |
A1006 | H | f2ch | Ph | CC13 |
A1007 | H | HCC | Ph | CC13 |
A1008 | H | ch3cc | Ph | CC13 |
A1009 | H | ch2=ch | Ph | CC13 |
A1010 | H | ch2=chch2 | Ph | CC13 |
A1011 | H | CH3SO2N(CH3) | Ph | CC13 |
A1012 | H | (CH3)2N | Ph | CC13 |
A1013 | H | (CH3)2NSO2 | Ph | CC13 |
A1014 | H | ch3sch2 | Ph | CC13 |
A1015 | H | ch3soch2 | Ph | CC13 |
A1016 | H | ch3so2ch2 | Ph | CC13 |
A1017 | F | H | H | cf3 |
A1018 | Cl | Η | H | cf3 |
A1019 | Br | H | H | cf3 |
A1020 | CN | H | H | cf3 |
A1021 | CH3SO2O | H | Η | cf3 |
A1022 | CH3O | H | H | cf3 |
A1023 | CH2CH3O | Η | H | cf3 |
A1024 | ch2ch=ch2o | Η | Η | cf3 |
A1025 | hccch2o | Η | Η | cf3 |
A1026 | S-benzyl | Η | Η | cf3 |
A1027 | SO2-benzyl | Η | Η | cf3 |
A1028 | C1CH2 | Η | Η | cf3 |
A1029 | BrCH2 | Η | Η | cf3 |
A1030 | fch2 | Η | Η | cf3 |
A1031 | chf2ch2 | Η | Η | cf3 |
A1032 | cf3ch2 | Η | Η | cf3 |
A1033 | triazolylmethyl | Η | Η | cf3 |
A1034 | CHC12CH2 | Η | Η | cf3 |
A1035 | C1CH=CH | Η | Η | cf3 |
A1036 | C12C=CH | Η | Η | cf3 |
Sl. v | R79 | Reo | Rei | Rb2 |
c · A1037 | cf3ch=ch | H | Η | cf3 |
A1038 | C1CC | H | Η | cf3 |
A1039 | Ph | H | Η | cf3 |
A1040 | ch3 | ch3 | Η | cf3 |
A1041 | ch3 | OH | Η | cf3 |
A1042 | ch3 | F | Η | cf3 |
A1043 | ch3 | Cl | Η | cf3 |
A1044 | f | ch3 | Η | cf3 |
A1045 | Cl | ch3 | Η | cf3 |
A1046 | H | F | Η | cf3 |
A1047 | H | Cl | Η | cf3 |
A1048 | H | Br | Η | cf3 |
A1049 | H | OH | Η | cf3 |
A1050 | H | och3 | Η | cf3 |
A1051 | H | OCHF2 | Η | cf3 |
A1052 | H | OSO2CH3 | Η | cf3 |
A1053 | H | oso2cf3 | Η | cf3 |
A1054 | H | cich2 | Η | cf3 |
A1055 | H | BrCH2 | Η | cf3 |
A1056 | H | fch2 | Η | cf3 |
A1057 | H | chf2ch2 | Η | cf3 |
A1058 | H | cf3ch2 | Η | cf3 |
A1059 | H | triazolylmet hyl | Η | cf3 |
A1060 | H | CHC12CH2 | Η | cf3 |
A1061 | H | C1CH=CH | Η | cf3 |
A1062 | H | ci2c=ch | Η | cf3 |
A1063 | H | cf3ch=ch | Η | cf3 |
A1064 | H | C1CC | Η | cf3 |
A1065 | H | CH3C(O) | Η | cf3 |
A1066 | H | fenyl | Η | cf3 |
A1067 | H | so2ch3 | Η | cf3 |
A1068 | H | so2cf3 | Η | cf3 |
A1069 | H | CN | Η | cf3 |
A1070 | H | no2 | Η | cf3 |
A1071 | ch3 | H | F | cf3 |
A1072 | ch3 | Η | C1 | cf3 |
A1073 | ch3 | Η | Br | cf3 |
A1074 | ch3 | Η | CN | cf3 |
A1075 | ch3 | Η | CH3O | cf3 |
A1076 | ch3 | Η | CH3S | cf3 |
A1077 | ch3 | Η | CH3SO | cf3 |
A1078 | ch3 | Η | ch3so2 | cf3 |
-55CZ 304537 B6
V následující tabulce 6 Q je Q3
a Q3 jsou následující skupiny B:
Tabulka 6: Skupiny B:
Sku- pina | R44 | R37 | R38 | R3g | R40 | W |
B1 | H | H | H | H | OH | ch2 |
B2 | ch3 | H | H | H | OH | ch2 |
B3 | ch3ch2 | H | H | H | OH | ch2 |
B4 | ch3ch2ch2 | H | H | H | OH | ch2 |
B5 | (ch3)2ch | H | H | H | OH | ch2 |
B6 | (CH3)3C | H | H | H | OH | ch2 |
B7 | ch3s | H | H | H | OH | ch2 |
B8 | ch3so | H | H | H | OH | ch2 |
B9 | ch3so2 | H | H | H | OH | ch2 |
BIO | Ph | H | H | H | OH | ch2 |
Bil | ch3o | H | H | H | OH | ch2 |
B12 | ch3co2 | H | H | H | OH | ch2 |
B13 | ch3ch2co2 | H | H | H | OH | ch2 |
B14 | ch2=chch2 | H | H | H | OH | ch2 |
B15 | hccch2 | H | H | H | OH | ch2 |
B16 | cf3 | H | H | H | OH | ch2 |
B17 | (CH3)2NSO2 | H | H | H | OH | ch2 |
B18 | (CH3)2N | H | H | H | OH | ch2 |
B19 | PhO | H | H | H | OH | ch2 |
B20 | PhS | H | H | H | OH | ch2 |
B21 | PhSO | H | H | H | OH | ch2 |
B22 | PhSO2 | H | H | H | OH | ch2 |
B23 | CN | H | H | H | OH | ch2 |
B24 | ch3 | ch3 | H | H | OH | ch2 |
B25 | ch3ch2 | ch3 | H | H | OH | ch2 |
B26 | ch3ch2ch2 | ch3 | H | H | OH | ch2 |
B27 | (ch3)2ch | ch3 | H | H | OH | ch2 |
B28 | (CH3)3C | ch3 | H | H | OH | ch2 |
B29 | ch3s | ch3 | H | H | OH | ch2 |
B30 | ch3so | ch3 | H | H | OH | ch2 |
B31 | ch3so2 | ch3 | H | H | OH | ch2 |
-56CZ 304537 B6
Sku- pina | R44 | R37 | R38 | R39 | R40 | W |
B32 | Ph | CH3 | H | H | OH | CH2 |
B33 | CH3O | ch3 | H | H | OH | ch2 |
B34 | CH3CO2 | ch3 | H | H | OH | ch2 |
B35 | CH3CH2CO2 | ch3 | H | H | OH | ch2 |
B36 | ch2=chch2 | ch3 | H | H | OH | ch2 |
B37 | hccch2 | ch3 | H | H | OH | ch2 |
B38 | cf3 | ch3 | H | H | OH | ch2 |
B39 | (CH3)2NSO2 | ch3 | H | H | OH | ch2 |
B40 | (CH3)2N | ch3 | H | H | OH | ch2 |
B41 | PhO | ch3 | H | H | OH | ch2 |
B42 | PhS | ch3 | H | H | OH | ch2 |
B43 | PhSO | ch3 | H | H | OH | ch2 |
B44 | PhSO2 | ch3 | H | H | OH | ch2 |
B45 | CN | ch3 | H | H | OH | ch2 |
B46 | ch3 | H | ch3 | H | OH | ch2 |
B47 | ch3ch2 | H | ch3 | H | OH | ch2 |
B48 | ch3ch2ch2 | H | ch3 | H | OH | ch2 |
B49 | (CH3)2CH | H | ch3 | H | OH | ch2 |
B50 | (CH3)3c | H | ch3 | H | OH | ch2 |
B51 | ch3s | H | ch3 | H | OH | ch2 |
B52 | ch3so | H | ch3 | H | OH | ch2 |
B53 | ch3so2 | H | ch3 | H | OH | ch2 |
B54 | Ph | H | ch3 | H | OH | ch2 |
B55 | CH3O | H | ch3 | H | OH | ch2 |
B56 | ch3co2 | H | ch3 | H | OH | ch2 |
B57 | ch3ch2co2 | H | ch3 | H | OH | ch2 |
B58 | ch2=chch2 | H | ch3 | H | OH | ch2 |
B59 | hccch2 | H | ch3 | H | OH | ch2 |
B60 | cf3 | H | ch3 | H | OH | ch2 |
B61 | (CH3)2NSO2 | H | ch3 | H | OH | ch2 |
B62 | (CH3)2N | H | ch3 | H | OH | ch2 |
B63 | PhO | H | ch3 | H | OH | ch2 |
B64 | PhS | H | ch3 | H | OH | ch2 |
B65 | PhSO | H | ch3 | H | OH | ch2 |
B66 | PhSO2 | H | ch3 | H | OH | ch2 |
B67 | CN | H | ch3 | H | OH | ch2 |
B68 | ch3 | ch3 | ch3 | H | OH | ch2 |
B69 | ch3ch2 | ch3 | ch3 | H | OH | ch2 |
B70 | ch3ch2ch2 | ch3 | ch3 | H | OH | ch2 |
B71 | (CH3)2CH | ch3 | ch3 | H | OH | ch2 |
B72 | (CH3)3C | ch3 | ch3 | H | OH | ch2 |
B73 | ch3s | ch3 | ch3 | H | OH | ch2 |
B74 | ch3so | ch3 | ch3 | H | OH | ch2 |
B75 | CH3SO2 | ch3 | ch3 | H | OH | ch2 |
B76 | Ph | ch3 | ch3 | H | OH | ch2 |
B77 | CH3O | ch3 | ch3 | H | OH | ch2 |
B78 | ch3co2 | ch3 | ch3 | H | OH | ch2 |
B79 | CH3CH2CO2 | ch3 | ch3 | H | OH | ch2 |
B80 | ch2=chch2 | ch3 | ch3 | H | OH | ch2 |
Sku- | R44 | R37 | R38 | R39 | R40 | W |
pina B81 | HCCCH2 | ch3 | ch3 | H | OH | ch2 |
B82 | cf3 | gh3 | ch3 | H | OH | ch2 |
B83 | (CH3)2NSO2 | ch3 | ch3 | H | OH | ch2 |
B84 | (CH3)2N | ch3 | ch3 | H | OH | ch2 |
B85 | PhO | ch3 | ch3 | H | OH | ch2 |
B86 | PhS | ch3 | ch3 | H | OH | ch2 |
B87 | PhSO | ch3 | ch3 | H | OH | ch2 |
B88 | PhSO2 | ch3 | ch3 | H | OH | ch2 |
B89 | CN | ch3 | ch3 | H | OH | ch2 |
B90 | ch3 | ch3 | ch3 | ch3 | OH | ch2 |
B91 | ch3ch2 | ch3 | ch3 | ch3 | OH | ch2 |
B92 | ch3ch2ch2 | ch3 | ch3 | ch3 | OH | ch2 |
B93 | (CH3)2CH | ch3 | ch3 | ch3 | OH | ch2 |
B94 | (CH3)3C | ch3 | ch3 | ch3 | OH | ch2 |
B95 | ch3s | ch3 | ch3 | ch3 | OH | ch2 |
B96 | ch3so | ch3 | ch3 | ch3 | OH | ch2 |
B97 | ch3so2 | ch3 | ch3 | ch3 | OH | ch2 |
B98 | Ph | ch3 | ch3 | ch3 | OH | ch2 |
B99 | ch3o | ch3 | ch3 | ch3 | OH | ch2 |
B100 | ch3co2 | ch3 | ch3 | ch3 | OH | ch2 |
B101 | ch3ch2co2 | ch3 | ch3 | ch3 | OH | ch2 |
B102 | ch2=chch2 | ch3 | ch3 | ch3 | OH | ch2 |
B103 | hccch2 | ch3 | ch3 | ch3 | OH | ch2 |
BIO 4 | cf3 | ch3 | ch3 | ch3 | OH | ch2 |
B105 | (CH3)2NSO2 | ch3 | ch3 | ch3 | OH | ch2 |
B106 | (CH3)2N | ch3 | ch3 | ch3 | OH | ch2 |
B107 | PhO | ch3 | ch3 | ch3 | OH | ch2 |
B108 | PhS | ch3 | ch3 | ch3 | OH | ch2 |
B109 | PhSO | ch3 | ch3 | ch3 | OH | ch2 |
B110 | PhSO2 | ch3 | ch3 | ch3 | OH | ch2 |
Blil | CN | ch3 | ch3 | ch3 | OH | ch2 |
B112 | ch3ch2 | ch3ch2 | H | H | OH | ch2 |
B113 | ch3ch2ch2 | ch3ch2 | H | H | OH | ch2 |
B114 | (CH3)2CH | ch3ch2 | H | H | OH | ch2 |
B115 | (CH3)3C | ch3ch2 | H | H | OH | ch2 |
B116 | ch3s | ch3ch2 | H | H | OH | ch2 |
B117 | ch3so | ch3ch2 | H | H | OH | ch2 |
B118 | ch3so2 | ch3ch2 | H | H | OH | ch2 |
B119 | Ph | ch3ch2 | H | H | OH | ch2 |
B120 | ch3o | ch3ch2 | H | H | OH | ch2 |
B121 | ch3co2 | ch3ch2 | H | H | OH | ch2 |
B122 | ch3ch2co2 | ch3ch2 | H | H | OH | ch2 |
B123 | ch2=chch2 | ch3ch2 | H | H | OH | ch2 |
B124 | hccch2 | ch3ch2 | H | H | OH | ch2 |
B125 | cf3 | ch3ch2 | H | H | OH | ch2 |
B126 | (CH3)2NSO2 | ch3ch2 | H | H | OH | ch2 |
B127 | (CH3)2N | ch3ch2 | H | H | OH | ch2 |
B128 | PhO | ch3ch2 | H | H | OH | ch2 |
B129 | PhS | ch3ch2 | H | H | OH | ch2 |
Sku- | R44 | Ra? | R38 | R39 | R40 | W |
pina B130 | PhSO | ch3ch2 | H | H | OH | ch2 |
B131 | PhSO2 | ch3ch2 | H | H | OH | ch2 |
B132 | CN | ch3ch2 | H | H | OH | ch2 |
B133 | H | H | H | H | OH | chch3 |
B134 | ch3 | H | H | H | OH | chch3 |
B135 | ch3ch2 | H | H | H | OH | chch3 |
B136 | ch3ch2ch2 | H | H | H | OH | CHCH3 |
B137 | (CH3)2CH | H | H | H | OH | chch3 |
B138 | (CH3)3C | H | H | H | OH | chch3 |
B139 | ch3s | H | H | H | OH | chch3 |
B140 | ch3so | H | H | H | OH | chch3 |
B141 | ch3so2 | H | H | H | OH | chch3 |
B142 | Ph | H | H | H | OH | chch3 |
B143 | ch3o | H | H | H | OH | chch3 |
B144 | ch3co2 | H | H | H | OH | chch3 |
B145 | ch3ch2co2 | H | H | H | OH | chch3 |
B146 | ch2=chch2 | H | H | H | OH | chch3 |
B147 | hccch2 | H | H | H | OH | chch3 |
B148 | cf3 | H | H | H | OH | chch3 |
B149 | (CH3)2NSO2 | H | H | H | OH | chch3 |
B150 | (CH3)2N | H | H | H | OH | chch3 |
B151 | PhO | H | H | H | OH | chch3 |
B152 | PhS | H | H | H | OH | chch3 |
B153 | PhSO | H | H | H | OH | CHCH3 |
B154 | PhSO2 | H | H | H | OH | CHCH3 |
B155 | CN | H | H | H | OH | chch3 |
B156 | ch3 | ch3 | H | H | OH | chch3 |
B157 | ch3ch2 | ch3 | H | H | OH | chch3 |
B158 | ch3ch2ch2 | ch3 | H | H | OH | chch3 |
B159 | (ch3)2ch | ch3 | H | H | OH | chch3 |
B160 | (CH3)3C | ch3 | H | H | OH | chch3 |
B161 | ch3s | ch3 | H | H | OH | chch3 |
B162 | CH3S0 | ch3 | H | H | OH | chch3 |
B163 | CH3SO2 | ch3 | H | H | OH | chch3 |
B164 | Ph | ch3 | H | H | OH | chch3 |
B165 | ch3o | ch3 | H | H | OH | chch3 |
B166 | ch3co2 | ch3 | H | H | OH | chch3 |
B167 | ch3ch2co2 | ch3 | H | H | OH | chch3 |
B168 | ch2=chch2 | ch3 | H | H | OH | chch3 |
B169 | hccch2 | ch3 | H | H | OH | chch3 |
B170 | cf3 | ch3 | H | H | OH | chch3 |
B171 | (CH3)2NSO2 | ch3 | H | H | OH | chch3 |
B172 | (CH3)2N | ch3 | H | H | OH | chch3 |
B173 | PhO | ch3 | H | H | OH | CHCH3 |
B174 | PhS | ch3 | H | H | OH | chch3 |
B175 | PhSO | ch3 | H | H | OH | CHCH3 |
B176 | PhSO2 | ch3 | H | H | OH | CHCH3 |
B177 | CN | ch3 | H | H | OH | chch3 |
B178 | ch3 | H | ch3 | H | OH | chch3 |
Sku- | R44 | R37 | R38 | R39 | R40 | W |
pina B179 | CH3CH2 | H | ch3 | H | OH | chch3 |
B180 | CH3CH2CH2 | H | ch3 | H | OH | chch3 |
B181 | (CH3)2CH | H | ch3 | H | OH | chch3 |
B182 | (CH3)3C | H | ch3 | H | OH | chch3 |
B183 | ch3s | H | ch3 | H | OH | chch3 |
B184 | CH3SO | H | ch3 | H | OH | chch3 |
B185 | CH3SO2 | H | ch3 | H | OH | chch3 |
B186 | Ph | H | ch3 | H | OH | CHCH3 |
B187 | CH3O | H | ch3 | H | OH | chch3 |
B188 | CH3CO2 | H | ch3 | H | OH | chch3 |
B189 | ch3ch2co2 | H | ch3 | H | OH | chch3 |
B190 | ch2=chch2 | H | ch3 | H | OH | chch3 |
B191 | hccch2 | H | ch3 | H | OH | chch3 |
B192 | cf3 | H | ch3 | H | OH | chch3 |
B193 | (CH3)2NSO2 | H | ch3 | H | OH | chch3 |
B194 | (CH3)2N | H | ch3 | H | OH | chch3 |
B195 | PhO | H | ch3 | H | OH | chch3 |
B196 | PhS | H | ch3 | H | OH | chch3 |
B197 | PhSO | H | ch3 | H | OH | chch3 |
B198 | PhSO2 | H | ch3 | H | OH | chch3 |
B199 | CN | H | ch3 | H | OH | chch3 |
B200 | ch3 | ch3 | ch3 | H | OH | chch3 |
B201 | ch3ch2 | ch3 | ch3 | H | OH | chch3 |
B202 | ch3ch2ch2 | ch3 | ch3 | H | OH | chch3 |
B203 | (CH3)2CH | ch3 | ch3 | H | OH | chch3 |
B204 | (CH3)3C | ch3 | ch3 | H | OH | CHCH3 |
B205 | ch3s | ch3 | ch3 | H | OH | CHCH3 |
B206 | ch3so | ch3 | ch3 | H | OH | CHCH3 |
B207 | ch3so2 | ch3 | ch3 | H | OH | CHCH3 |
B208 | Ph | ch3 | ch3 | H | OH | CHCH3 |
B209 | ch3o | ch3 | ch3 | H | OH | chch3 |
B210 | ch3co2 | ch3 | ch3 | H | OH | chch3 |
B211 | ch3ch2co2 | ch3 | ch3 | H | OH | chch3 |
B212 | ch2=chch2 | ch3 | ch3 | H | OH | chch3 |
B213 | hccch2 | ch3 | ch3 | H | OH | chch3 |
B214 | cf3 | ch3 | ch3 | H | OH | chch3 |
B215 | (CH3)2NSO2 | ch3 | ch3 | H | OH | chch3 |
B216 | (CH3)2N | ch3 | ch3 | H | OH | chch3 |
B217 | PhO | ch3 | ch3 | H | OH | chch3 |
B218 | PhS | ch3 | ch3 | H | OH | chch3 |
B219 | PhSO | ch3 | ch3 | H | OH | chch3 |
B220 | PhSO2 | ch3 | ch3 | H | OH | chch3 |
B221 | CN | ch3 | ch3 | H | OH | CHCH3 |
B222 | ch3 | ch3 | ch3 | ch3 | OH | CHCH3 |
B223 | ch3ch2 | ch3 | ch3 | ch3 | OH | chch3 |
B224 | ch3ch2ch2 | ch3 | ch3 | ch3 | OH | chch3 |
B225 | (CH3)2CH | ch3 | ch3 | ch3 | OH | CHCH3 |
B226 | (ch3)3c | ch3 | ch3 | ch3 | OH | CHCH3 |
B227 | ch3s | ch3 | ch3 | ch3 | OH | chch3 |
Sku- pina | R44 | R37 | R38 | R39 | R40 | W |
B228 | CH3SO | ch3 | ch3 | ch3 | OH | chch3 |
B229 | CH3SO2 | ch3 | ch3 | ch3 | OH | chch3 |
B230 | Ph | ch3 | ch3 | ch3 | OH | chch3 |
B231 | CH3O | ch3 | ch3 | ch3 | OH | chch3 |
B232 | CH3CO2 | ch3 | ch3 | ch3 | OH | chch3 |
B233 | CH3CH2CO2 | ch3 | ch3 | ch3 | OH | chch3 |
B234 | ch2=chch2 | ch3 | ch3 | ch3 | OH | chch3 |
B235 | HCCCH2 | ch3 | ch3 | ch3 | OH | chch3 |
B236 | cf3 | ch3 | ch3 | ch3 | OH | chch3 |
B237 | (CH3)2NSO2 | ch3 | ch3 | ch3 | OH | CHCH3 |
B238 | (CH3)2N | ch3 | ch3 | ch3 | OH | CHCH3 |
B239 | PhO | ch3 | ch3 | ch3 | OH | chch3 |
B240 | PhS | ch3 | ch3 | ch3 | OH | chch3 |
B241 | PhSO | ch3 | ch3 | ch3 | OH | chch3 |
B242 | PhSO2 | ch3 | ch3 | ch3 | OH | chch3 |
B243 | CN | ch3 | ch3 | ch3 | OH | chch3 |
B244 | CH3CH2 | ch3ch2 | H | H | OH | chch3 |
B245 | CH3CH2CH2 | ch3ch2 | H | H | OH | chch3 |
B246 | (CH3)2CH | ch3ch2 | H | H | OH | chch3 |
B247 | (ch3)3c | ch3ch2 | H | H | OH | chch3 |
B248 | ch3s | ch3ch2 | H | H | OH | chch3 |
B249 | ch3so | ch3ch2 | H | H | OH | chch3 |
B250 | ch3so2 | ch3ch2 | H | H | OH | chch3 |
B251 | Ph | ch3ch2 | H | H | OH | chch3 |
B252 | ch3o | ch3ch2 | H | H | OH | chch3 |
B253 | ch3co2 | ch3ch2 | H | H | OH | CHCH3 |
B254 | ch3ch2co2 | ch3ch2 | H | H | OH | CHCH3 |
B255 | ch2=chch2 | ch3ch2 | H | H | OH | CHCH3 |
B256 | HCCCHz | ch3ch2 | H | H | OH | chch3 |
B257 | cf3 | ch3ch2 | H | H | OH | CHCH3 |
B258 | (CH3)2NSO2 | ch3ch2 | H | H | OH | CHCH3 |
B259 | (CH3)2N | ch3ch2 | H | H | OH | CHCH3 |
B260 | PhO | ch3ch2 | H | H | OH | CHCHa |
B261 | PhS | ch3ch2 | H | H | OH | chch3 |
B262 | PhSO | ch3ch2 | H | H | OH | chch3 |
B263 | PhSO2 | ch3ch2 | H | H | OH | chch3 |
B264 | CN | ch3ch2 | H | H | OH | chch3 |
B265 | H | H | H | H | OH | c=o |
B266 | ch3 | H | H | H | OH | c=o |
B267 | CH3CH2 | H | H | H | OH | c=o |
B268 | CH3CH2CH2 | H | H | H | OH | c=o |
B269 | (CH3)2CH | H | H | H | OH | c=o |
B270 | (CH3)3c | H | H | H | OH | c=o |
B271 | ch3s | H | H | H | OH | c=o |
B272 | ch3so | H | H | H | OH | c=o |
B273 | CH3SO2 | H | H | H | OH | c=o |
B274 | Ph | H | H | H | OH | c=o |
B275 | ch3o | H | H | H | OH | c=o |
B276 | ch3co2 | H | H | H | OH | c=o |
Sku- | R44 | R37 | R38 | R39 | R40 | W |
pina B277 | CH3CH2CO2 | H | H | H | OH | C=O |
B278 | ch2=chch2 | H | H | H | OH | c=o |
B279 | hccch2 | H | H | H | OH | c=o |
B280 | cf3 | H | H | H | OH | c=o |
B281 | (CH3)2NSO2 | H | H | H | OH | c=o |
B282 | (CH3)2N | H | H | H | OH | c=o |
B283 | PhO | H | H | H | OH | c=o |
B284 | PhS | H | H | H | OH | c=o |
B285 | PhSO | H | H | H | OH | c=o |
B286 | PhSO2 | H | H | H | OH | c=o |
B287 | CN | H | H | H | OH | c=o |
B288 | ch3 | ch3 | H | H | OH | c=o |
B289 | ch3ch2 | ch3 | H | H | OH | c=o |
B290 | ch3ch2ch2 | ch3 | H | H | OH | c=o |
B291 | (ch3)2ch | ch3 | H | H | OH | c=o |
B292 | (ch3)3c | ch3 | H | H | OH | c=o |
B293 | ch3s | ch3 | H | H | OH | c=o |
B294 | ch3so | ch3 | H | H | OH | c=o |
B295 | ch3so2 | ch3 | H | H | OH | c=o |
B296 | Ph | ch3 | H | H | OH | c=o |
B297 | CH30 | ch3 | H | H | OH | c=o |
B298 | ch3co2 | ch3 | H | H | OH | c=o |
B299 | ch3ch2co2 | ch3 | H | H | OH | c=o |
B300 | ch2=chch2 | ch3 | H | H | OH | c=o |
B301 | hccch2 | ch3 | H | H | OH | c=o |
B302 | cf3 | ch3 | H | H | OH | c=o |
B303 | (CH3)2NSO2 | ch3 | H | H | OH | c=o |
B304 | (CH3)2N | ch3 | H | H | OH | c=o |
B305 | PhO | ch3 | H | H | OH | c=o |
B306 | PhS | ch3 | H | H | OH | c=o |
B307 | PhSO | ch3 | H | H | OH | c=o |
B308 | PhSO2 | ch3 | H | H | OH | c=o |
B309 | CN | ch3 | H | H | OH | c=o |
B310 | ch3 | H | ch3 | H | OH | c=o |
B311 | ch3ch2 | H | ch3 | H | OH | c=o |
B312 | ch3ch2ch2 | H | ch3 | H | OH | c=o |
B313 | (ch3)2ch | H | ch3 | H | OH | c=o |
B314 | (CH3)3C | H | ch3 | H | OH | c=o |
B315 | ch3s | H | ch3 | H | OH | c=o |
B316 | ch3so | H | ch3 | H | OH | c=o |
B317 | ch3so2 | H | ch3 | H | OH | c=o |
B318 | Ph | H | ch3 | H | OH | c=o |
B319 | ch3o | H | ch3 | H | OH | c=o |
B320 | ch3co2 | H | ch3 | H | OH | c=o |
B321 | ch3ch2co2 | H | ch3 | H | OH | c=o |
B322 | ch2=chch2 | H | ch3 | H | OH | c=o |
B323 | hccch2 | H | ch3 | H | OH | c=o |
B324 | cf3 | H | ch3 | H | OH | c=o |
B325 | (CH3)2NSO2 | H | ch3 | H | OH | c=o |
-62CZ 304537 B6
Sku- | R44 | R37 | R38 | R39 | R40 | W |
pina B326 | (CH3)2N | H | ch3 | H | OH | C=O |
B327 | PhO | H | ch3 | H | OH | C=O |
B328 | PhS | H | ch3 | H | OH | C=O |
B329 | PhSO | H | ch3 | H | OH | C=O |
B330 | PhSO2 | H | ch3 | H | OH | C=O |
B331 | CN | H | ch3 | H | OH | C=O |
B332 | ch3 | ch3 | ch3 | H | OH | C=O |
B333 | ch3ch2 | ch3 | ch3 | H | OH | C=O |
B334 | ch3ch2ch2 | ch3 | ch3 | H | OH | C=O |
B335 | (CH3)2CH | ch3 | ch3 | H | OH | C=O |
B336 | (CH3)3c | ch3 | ch3 | H | OH | c=o |
B337 | ch3s | ch3 | ch3 | H | OH | c=o |
B338 | ch3so | ch3 | ch3 | H | OH | c=o |
B339 | ch3so2 | ch3 | ch3 | H | OH | c=o |
B340 | Ph | ch3 | ch3 | H | OH | c=o |
B341 | ch3o | ch3 | ch3 | H | OH | c=o |
B342 | ch3co2 | ch3 | ch3 | H | OH | c=o |
B343 | ch3ch2co2 | ch3 | ch3 | H | OH | c=o |
B344 | ch2=chch2 | ch3 | ch3 | H | OH | c=o |
B345 | HCCCHz | ch3 | ch3 | H | OH | c=o |
B346 | cf3 | ch3 | ch3 | H | OH | c=o |
B347 | (CH3)2NSO2 | ch3 | ch3 | H | OH | c=o |
B348 | (CH3)2N | ch3 | ch3 | H | OH | c=o |
B349 | PhO | ch3 | ch3 | H | OH | c=o |
B350 | PhS | ch3 | ch3 | H | OH | c=o |
B351 | PhSO | ch3 | ch3 | H | OH | c=o |
B352 | PhSO2 | ch3 | ch3 | H | OH | c=o |
B353 | CN | ch3 | ch3 | H | OH | c=o |
B354 | ch3 | ch3 | ch3 | ch3 | OH | c=o |
B355 | ch3ch2 | ch3 | ch3 | ch3 | OH | c=o |
B356 | ch3ch2ch2 | ch3 | ch3 | ch3 | OH | c=o |
B357 | (CH3)2CH | ch3 | ch3 | ch3 | OH | c=o |
B358 | (CH3)3C | ch3 | ch3 | ch3 | OH | c=o |
B359 | ch3s | ch3 | ch3 | ch3 | OH | c=o |
B360 | ch3so | ch3 | ch3 | ch3 | OH | c=o |
B361 | ch3so2 | ch3 | ch3 | ch3 | OH | c=o |
B362 | Ph | ch3 | ch3 | ch3 | OH | c=o |
B363 | ch3o | ch3 | ch3 | ch3 | OH | c=o |
B364 | ch3co2 | ch3 | ch3 | ch3 | OH | c=o |
B365 | ch3ch2co2 | ch3 | ch3 | ch3 | OH | c=o |
B366 | ch2=chch2 | ch3 | ch3 | ch3 | OH | c=o |
B367 | hccch2 | ch3 | ch3 | ch3 | OH | c=o |
B368 | cf3 | ch3 | ch3 | ch3 | OH | c=o |
B369 | (CH3)2NSO2 | ch3 | ch3 | ch3 | OH | c=o |
B370 | (CH3)2N | ch3 | ch3 | ch3 | OH | c=o |
B371 | PhO | ch3 | ch3 | ch3 | OH | c=o |
B372 | PhS | ch3 | ch3 | ch3 | OH | c=o |
B373 | PhSO | ch3 | ch3 | ch3 | OH | c=o |
B374 | PhSO2 | ch3 | ch3 | ch3 | OH | c=o |
Sku- | R44 | R37 | R38 | R39 | R40 | W |
pina B375 | CN | CH3 | ch3 | ch3 | OH | C-0 |
B376 | ch3ch2 | ch3ch2 | H | H | OH | C=O |
B377 | ch3ch2ch2 | ch3ch2 | H | H | OH | C=O |
B378 | (CH3)2CH | ch3ch2 | H | H | OH | C=O |
B379 | (CH3)3C | ch3ch2 | H | H | OH | c=o |
B380 | ch3s | ch3ch2 | H | H | OH | c=o |
B381 | ch3so | ch3ch2 | H | H | OH | c=o |
B382 | ch3so2 | ch3ch2 | H | H | OH | c=o |
B383 | Ph | ch3ch2 | H | H | OH | c=o |
B384 | ch3o | ch3ch2 | H | H | OH | c=o |
B385 | ch3co2 | ch3ch2 | H | H | OH | c=o |
B386 | ch3ch2co2 | CH3CH2 | H | H | OH | c=o |
B387 | ch2=chch2 | ch3ch2 | H | H | OH | c=o |
B388 | hccch2 | ch3ch2 | H | H | OH | c=o |
B389 | cf3 | ch3ch2 | H | H | OH | c=o |
B390 | (CH3)2NSO2 | ch3ch2 | H | H | OH | c=o |
B391 | (CH3)2N | ch3ch2 | H | H | OH | c=o |
B392 | PhO | ch3ch2 | H | H | OH | c=o |
B393 | PhS | ch3ch2 | H | H | OH | c=o |
B394 | PhSO | ch3ch2 | H | H | OH | c=o |
B395 | PhSO2 | ch3ch2 | H | H | OH | c=o |
B396 | CN | ch3ch2 | H | H | OH | c=o |
B397 | H | H | H | H | OH | n-ch3 |
B398 | ch3 | H | H | H | OH | n-ch3 |
B399 | ch3ch2 | H | H | H | OH | n-ch3 |
B400 | ch3ch2ch2 | H | H | H | OH | n-ch3 |
B401 | (CH3)2CH | H | H | H | OH | n-ch3 |
B402 | (CH3)3c | H | H | H | OH | n-ch3 |
B403 | ch3s | H | H | H | OH | n-ch3 |
B404 | ch3so | H | H | H | OH | n-ch3 |
B405 | ch3so2 | H | H | H | OH | n-ch3 |
B406 | Ph | H | H | H | OH | n-ch3 |
B407 | ch3o | H | H | H | OH | n-ch3 |
B408 | ch3co2 | H | H | H | OH | n-ch3 |
B409 | ch3ch2co2 | H | H | H | OH | N-CH3 |
B410 | ch2=chch2 | H | H | H | OH | N-CH3 |
B411 | hccch2 | H | H | H | OH | n-ch3 |
B412 | cf3 | H | H | H | OH | n-ch3 |
B413 | (CH3)2NSO2 | H | H | H | OH | n-ch3 |
B414 | (CH3)2N | H | H | H | OH | n-ch3 |
B415 | PhO | H | H | H | OH | n-ch3 |
B416 | PhS | H | H | H | OH | n-ch3 |
B417 | PhSO | H | H | H | OH | n-ch3 |
B418 | PhSO2 | H | H | H | OH | n-ch3 |
B419 | CN | H | H | H | OH | n-ch3 |
B420 | ch3 | ch3 | H | H | OH | n-ch3 |
B421 | ch3ch2 | ch3 | H | H | OH | n-ch3 |
B422 | ch3ch2ch2 | ch3 | H | H | OH | N-CH3 |
B423 | (CH3)2CH | ch3 | H | H | OH | n-ch3 |
Sku- | R44 | R37 | R38 | R39 | R40 | W |
pina B424 | (CH3)3C | ch3 | H | H | OH | n-ch3 |
B425 | ch3s | ch3 | H | H | OH | n-ch3 |
B426 | ch3so | ch3 | H | H | OH | n-ch3 |
B427 | ch3so2 | ch3 | H | H | OH | n-ch3 |
B428 | Ph | ch3 | H | H | OH | n-ch3 |
B429 | ch3o | ch3 | H | H | OH | n-ch3 |
B430 | ch3co2 | ch3 | H | H | OH | n-ch3 |
B431 | ch3ch2co2 | ch3 | H | H | OH | n-ch3 |
B432 | ch2=chch2 | ch3 | H | H | OH | n-ch3 |
B433 | hccch2 | ch3 | H | H | OH | n-ch3 |
B434 | cf3 | ch3 | H | H | OH | n-ch3 |
B435 | (CH3)2NSO2 | ch3 | H | H | OH | n-ch3 |
B436 | (CH3)2N | ch3 | H | H | OH | n-ch3 |
B437 | PhO | ch3 | H | H | OH | n-ch3 |
B438 | PhS | ch3 | H | H | OH | n-ch3 |
B439 | PhSO | ch3 | H | H | OH | n-ch3 |
B440 | PhSO2 | ch3 | H | H | OH | n-ch3 |
B441 | CN | ch3 | H | H | OH | n-ch3 |
B442 | ch3 | H | ch3 | H | OH | n-ch3 |
B443 | ch3ch2 | H | ch3 | H | OH | n-ch3 |
B444 | ch3ch2ch2 | H | ch3 | H | OH | n-ch3 |
B445 | (CH3)2CH | H | ch3 | H | OH | n-ch3 |
B446 | (CH3)3C | H | ch3 | H | OH | N-CH3 |
B447 | ch3s | H | ch3 | H | OH | n-ch3 |
B448 | ch3so | H | ch3 | H | OH | n-ch3 |
B449 | ch3so2 | H | ch3 | H | OH | n-ch3 |
B450 | Ph | H | ch3 | H | OH | n-ch3 |
B451 | ch3o | H | ch3 | H | OH | n-ch3 |
B452 | ch3co2 | H | ch3 | H | OH | n-ch3 |
B453 | ch3ch2co2 | H | ch3 | H | OH | n-ch3 |
B454 | ch2=chch2 | H | ch3 | H | OH | n-ch3 |
B455 | HCCCH2 | H | ch3 | H | OH | n-ch3 |
B456 | cf3 | H | ch3 | H | OH | n-ch3 |
B457 | (CH3)2NS02 | H | ch3 | H | OH | n-ch3 |
B458 | (CH3)2N | H | ch3 | H | OH | n-ch3 |
B459 | PhO | H | ch3 | H | OH | n-ch3 |
B460 | PhS | H | ch3 | H | OH | n-ch3 |
B461 | PhSO | H | ch3 | H | OH | n-ch3 |
B462 | PhSO2 | H | ch3 | H | OH | n-ch3 |
B463 | CN | H | ch3 | H | OH | n-ch3 |
B464 | ch3 | ch3 | ch3 | H | OH | n-ch3 |
B465 | ch3ch2 | ch3 | ch3 | H | OH | n-ch3 |
B466 | ch3ch2ch2 | ch3 | ch3 | H | OH | n-ch3 |
B467 | (CH3)2CH | ch3 | ch3 | H | OH | n-ch3 |
B468 | (CH3)3C | ch3 | ch3 | H | OH | n-ch3 |
B469 | ch3s | ch3 | ch3 | H | OH | n-ch3 |
B470 | ch3so | ch3 | ch3 | H | OH | n-ch3 |
B471 | ch3so2 | ch3 | ch3 | H | OH | n-ch3 |
B472 | Ph | ch3 | ch3 | H | OH | n-ch3 |
Sku- | R44 | R37 | R38 | R3g | R40 | W |
pina B473 | CH3O | ch3 | ch3 | H | OH | N-CH3 |
B474 | CH3CO2 | ch3 | ch3 | H | OH | n-ch3 |
B475 | CH3CH2CO2 | ch3 | ch3 | H | OH | n-ch3 |
B476 | ch2=chch2 | ch3 | ch3 | H | OH | n-ch3 |
B477 | hccch2 | ch3 | ch3 | H | OH | n-ch3 |
B478 | cf3 | ch3 | ch3 | H | OH | n-ch3 |
B479 | (CH3)2NSO2 | ch3 | ch3 | H | OH | n-ch3 |
B480 | (CH3)2N | ch3 | ch3 | H | OH | n-ch3 |
B481 | PhO | ch3 | ch3 | H | OH | n-ch3 |
B482 | PhS | ch3 | ch3 | H | OH | n-ch3 |
B483 | PhSO | ch3 | ch3 | H | OH | n-ch3 |
B484 | PhSO2 | ch3 | ch3 | H | OH | n-ch3 |
B485 | CN | ch3 | ch3 | H | OH | n-ch3 |
B486 | ch3 | ch3 | ch3 | ch3 | OH | n-ch3 |
B487 | ch3ch2 | ch3 | ch3 | ch3 | OH | n-ch3 |
B488 | ch3ch2ch2 | ch3 | ch3 | ch3 | OH | n-ch3 |
B489 | (CH3)2CH | ch3 | ch3 | ch3 | OH | n-ch3 |
B490 | (CH3)3c | ch3 | ch3 | ch3 | OH | n-ch3 |
B491 | ch3s | ch3 | ch3 | ch3 | OH | n-ch3 |
B492 | ch3so | ch3 | ch3 | ch3 | OH | n-ch3 |
B493 | ch3so2 | ch3 | ch3 | ch3 | OH | N-CH3 |
B494 | Ph | ch3 | ch3 | ch3 | OH | n-ch3 |
B495 | CH3O | ch3 | ch3 | ch3 | OH | n-ch3 |
B496 | ch3co2 | ch3 | ch3 | ch3 | OH | n-ch3 |
B497 | ch3ch2co2 | ch3 | ch3 | ch3 | OH | n-ch3 |
B498 | ch2=chch2 | ch3 | ch3 | ch3 | OH | n-ch3 |
B499 | HCCCHz | ch3 | ch3 | ch3 | OH | n-ch3 |
B500 | cf3 | ch3 | ch3 | ch3 | OH | n-ch3 |
B501 | (CH3)2NS02 | ch3 | ch3 | ch3 | OH | n-ch3 |
B502 | (CH3)2N | ch3 | ch3 | ch3 | OH | n-ch3 |
B503 | PhO | ch3 | ch3 | ch3 | OH | n-ch3 |
B504 | PhS | ch3 | ch3 | ch3 | OH | n-ch3 |
B505 | PhSO | ch3 | ch3 | ch3 | OH | n-ch3 |
B506 | PhSO2 | ch3 | ch3 | ch3 | OH | n-ch3 |
B507 | CN | ch3 | ch3 | ch3 | OH | n-ch3 |
B508 | ch3ch2 | ch3ch2 | H | H | OH | n-ch3 |
B509 | ch3ch2ch2 | ch3ch2 | H | H | OH | n-ch3 |
B510 | (CH3)2CH | ch3ch2 | H | H | OH | n-ch3 |
B511 | (CH3)3c | ch3ch2 | H | H | OH | n-ch3 |
B512 | ch3s | ch3ch2 | H | H | OH | n-ch3 |
B513 | ch3so | ch3ch2 | H | H | OH | n-ch3 |
B514 | ch3so2 | ch3ch2 | H | H | OH | n-ch3 |
B515 | Ph | ch3ch2 | H | H | OH | n-ch3 |
B516 | ch3o | ch3ch2 | H | H | OH | n-ch3 |
B517 | ch3co2 | ch3ch2 | H | H | OH | N-CH3 |
B518 | ch3ch2co2 | ch3ch2 | H | H | OH | n-ch3 |
B519 | ch2=chch2 | ch3ch2 | H | H | OH | n-ch3 |
B520 | hccch2 | ch3ch2 | H | H | OH | n-ch3 |
B521 | cf3 | ch3ch2 | H | H | OH | n-ch3 |
Sku- | R44 | R37 | R38 | R39 | R40 | W |
pina B522 | (CH3)2NSO2 | CH3CH2 | H | H | OH | n-ch3 |
B523 | (CH3)2N | ch3ch2 | H | H | OH | n-ch3 |
B524 | PhO | ch3ch2 | H | H | OH | n-ch3 |
B525 | PhS | ch3ch2 | H | H | OH | n-ch3 |
B526 | PhSO | ch3ch2 | H | H | OH | n-ch3 |
B527 | PhSO2 | ch3ch2 | H | H | OH | n-ch3 |
B528 | CN | ch3ch2 | H | H | OH | N-CH3 |
B529 | H | H | H | H | OH | 0 |
B530 | ch3 | H | H | H | OH | 0 |
B531 | ch3ch2 | H | H | H | OH | 0 |
B532 | ch3ch2ch2 | H | H | H | OH | 0 |
B533 | (CH3)2CH | H | H | H | OH | 0 |
B534 | (CH3)3C | H | H | H | OH | 0 |
B535 | ch3s | H | H | H | OH | 0 |
B536 | ch3so | H | H | H | OH | 0 |
B537 | ch3so2 | H | H | H | OH | 0 |
B538 | Ph | H | H | H | OH | 0 |
B539 | ch3o | H | H | H | OH | 0 |
B540 | ch3co2 | H | H | H | OH | 0 |
B541 | ch3ch2co2 | H | H | H | OH | 0 |
B542 | ch2=chch2 | H | H | H | OH | 0 |
B543 | hccch2 | H | H | H | OH | 0 |
B544 | cf3 | H | H | H | OH | 0 |
B545 | (CH3)2NSO2 | H | H | H | OH | 0 |
B546 | (CH3)2N | H | H | H | OH | 0 |
B547 | PhO | H | H | H | OH | 0 |
B548 | PhS | H | H | H | OH | 0 |
B549 | PhSO | H | H | H | OH | 0 |
B550 | PhSO2 | H | H | H | OH | 0 |
B551 | CN | H | H | H | OH | 0 |
B552 | CH3 | ch3 | H | H | OH | 0 |
B553 | ch3ch2 | ch3 | H | H | OH | 0 |
B554 | ch3ch2ch2 | ch3 | H | H | OH | 0 |
B555 | <ch3)2ch | ch3 | H | H | OH | 0 |
B556 | (CH3)3C | ch3 | H | H | OH | 0 |
B557 | ch3s | ch3 | H | H | OH | 0 |
B558 | ch3so | ch3 | H | H | OH | 0 |
B559 | ch3so2 | ch3 | H | H | OH | 0 |
B560 | Ph | ch3 | H | H | OH | 0 |
B561 | ch3o | ch3 | H | H | OH | 0 |
B562 | ch3co2 | ch3 | H | H | OH | 0 |
B563 | ch3ch2co2 | ch3 | H | H | OH | 0 |
B564 | ch2=chch2 | ch3 | H | H | OH | 0 |
B565 | hccch2 | ch3 | H | H | OH | 0 |
B566 | cf3 | ch3 | H | H | OH | 0 |
B567 | (CH3)2NSO2 | ch3 | H | H | OH | 0 |
B568 | (CH3)2N | ch3 | H | H | OH | 0 |
B569 | PhO | ch3 | H | H | OH | 0 |
B570 | PhS | ch3 | H | H | OH | 0 |
-67CZ 304537 B6
Sku- | R44 | R37 | R38 | R39 | R40 | W |
pina B571 | PhSO | ch3 | H | H | OH | 0 |
B572 | PhSO2 | ch3 | H | H | OH | 0 |
B573 | CN | ch3 | H | H | OH | 0 |
B574 | ch3 | H | ch3 | H | OH | 0 |
B575 | ch3ch2 | H | ch3 | H | OH | 0 |
B576 | ch3ch2ch2 | H | ch3 | H | OH | 0 |
B577 | (CH3)2CH | H | ch3 | H | OH | 0 |
B578 | (CH3)3c | H | ch3 | H | OH | 0 |
B579 | ch3s | H | ch3 | H | OH | 0 |
B580 | ch3so | H | ch3 | H | OH | 0 |
B581 | ch3so2 | H | ch3 | H | OH | 0 |
B582 | Ph | H | ch3 | H | OH | 0 |
B583 | ch3o | H | ch3 | H | OH | 0 |
B584 | ch3co2 | H | ch3 | H | OH | 0 |
B585 | ch3ch2co2 | H | ch3 | H | OH | 0 |
B586 | ch2=chch2 | H | ch3 | H | OH | 0 |
B587 | hccch2 | H | ch3 | H | OH | 0 |
B588 | cf3 | H | ch3 | H | OH | 0 |
B589 | (CH3)2NSO2 | H | ch3 | H | OH | 0 |
B590 | (CH3)2N | H | ch3 | H | OH | 0 |
B591 | PhO | H | ch3 | H | OH | 0 |
B592 | PhS | H | ch3 | H | OH | 0 |
B593 | PhSO | H | ch3 | H | OH | 0 |
B594 | PhSO2 | H | ch3 | H | OH | 0 |
B595 | CN | H | ch3 | H | OH | 0 |
B596 | ch3 | ch3 | ch3 | H | OH | 0 |
B597 | ch3ch2 | ch3 | ch3 | H | OH | 0 |
B598 | ch3ch2ch2 | ch3 | ch3 | H | OH | 0 |
B599 | (ch3)2ch | ch3 | ch3 | H | OH | 0 |
B600 | (CH3)3C | ch3 | ch3 | H | OH | 0 |
B601 | ch3s | ch3 | ch3 | H | OH | 0 |
B602 | ch3so | ch3 | ch3 | H | OH | 0 |
B603 | ch3so2 | ch3 | ch3 | H | OH | 0 |
B604 | Ph | ch3 | ch3 | H | OH | 0 |
B605 | ch3o | ch3 | ch3 | H | OH | 0 |
B606 | ch3co2 | ch3 | ch3 | H | OH | 0 |
B607 | ch3ch2co2 | ch3 | ch3 | H | OH | 0 |
B608 | ch2=chch2 | ch3 | ch3 | H | OH | 0 |
B609 | hccch2 | ch3 | ch3 | H | OH | 0 |
B610 | cf3 | ch3 | ch3 | H | OH | 0 |
B611 | (CH3)2NSO2 | ch3 | ch3 | H | OH | 0 |
B612 | (CH3)2N | ch3 | ch3 | H | OH | 0 |
B613 | PhO | ch3 | ch3 | H | OH | 0 |
B614 | PhS | ch3 | ch3 | H | OH | 0 |
B615 | PhSO | ch3 | ch3 | H | OH | 0 |
B616 | PhSO2 | ch3 | ch3 | H | OH | 0 |
B617 | CN | ch3 | ch3 | H | OH | 0 |
B618 | ch3 | ch3 | ch3 | ch3 | OH | 0 |
B619 | ch3ch2 | ch3 | ch3 | ch3 | OH | 0 |
-68CZ 304537 B6
Sku- | R44 | R37 | R38 | R39 | R40 | W |
pina B620 | CH3CH2CH2 | ch3 | ch3 | ch3 | OH | 0 |
B621 | (CH3)2CH | ch3 | ch3 | ch3 | OH | 0 |
B622 | (CH3)3C | ch3 | ch3 | ch3 | OH | 0 |
B623 | ch3s | ch3 | ch3 | ch3 | OH | 0 |
B624 | ch3so | ch3 | ch3 | ch3 | OH | 0 |
B625 | ch3so2 | ch3 | ch3 | ch3 | OH | 0 |
B626 | Ph | ch3 | ch3 | ch3 | OH | 0 |
B627 | ch3o | ch3 | ch3 | ch3 | OH | 0 |
B628 | ch3co2 | ch3 | ch3 | ch3 | OH | 0 |
B629 | ch3ch2co2 | ch3 | ch3 | ch3 | OH | 0 |
B630 | ch2=chch2 | ch3 | ch3 | ch3 | OH | 0 |
B631 | hccch2 | ch3 | ch3 | ch3 | OH | 0 |
B632 | cf3 | ch3 | ch3 | ch3 | OH | 0 |
B633 | (CH3)2NSO2 | ch3 | ch3 | ch3 | OH | 0 |
B634 | (CH3)2N | ch3 | ch3 | ch3 | OH | 0 |
B635 | PhO | ch3 | ch3 | ch3 | OH | 0 |
B636 | PhS | ch3 | ch3 | ch3 | OH | 0 |
B637 | PhSO | ch3 | ch3 | ch3 | OH | 0 |
B638 | PhSO2 | ch3 | ch3 | ch3 | OH | 0 |
B639 | CN | ch3 | ch3 | ch3 | OH | 0 |
B640 | CH3CH2 | ch3ch2 | H | H | OH | 0 |
B641 | ch3ch2ch2 | ch3ch2 | H | H | OH | 0 |
B642 | (CH3)2CH | ch3ch2 | H | H | OH | 0 |
B643 | (ch3)3c | ch3ch2 | H | H | OH | 0 |
B644 | ch3s | ch3ch2 | H | H | OH | 0 |
B645 | ch3so | ch3ch2 | H | H | OH | 0 |
B646 | ch3so2 | ch3ch2 | H | H | OH | 0 |
B647 | Ph | ch3ch2 | H | H | OH | 0 |
B648 | ch3o | ch3ch2 | H | H | OH | 0 |
B649 | ch3co2 | ch3ch2 | H | H | OH | 0 |
B650 | ch3ch2co2 | ch3ch2 | H | H | OH | 0 |
B651 | ch2=chch2 | ch3ch2 | H | H | OH | 0 |
B652 | hccch2 | ch3ch2 | H | H | OH | 0 |
B653 | cf3 | ch3ch2 | H | H | OH | 0 |
B654 | (CH3)2NSO2 | ch3ch2 | H | H | OH | 0 |
B655 | (CH3)2N | ch3ch2 | H | H | OH | 0 |
B656 | PhO | ch3ch2 | H | H | OH | 0 |
B657 | PhS | ch3ch2 | H | H | OH | 0 |
B658 | PhSO | ch3ch2 | H | H | OH | 0 |
B659 | PhSO2 | ch3ch2 | H | H | OH | 0 |
B660 | CN | ch3ch2 | H | H | OH | 0 |
B661 | H | H | H | H | OH | s |
B662 | ch3 | H | H | H | OH | s |
B663 | ch3ch2 | H | H | H | OH | s |
B664 | ch3ch2ch2 | H | H | H | OH | s |
B665 | (ch3)2ch | H | H | H | OH | s |
B666 | (CH3)3C | H | H | H | OH | s |
B667 | ch3s | H | H | H | OH | s |
B668 | ch3so | H | H | H | OH | s |
-69CZ 304537 B6
Sku- | R44 | R37 | R38 | R39 | R40 |
pina B669 | CH3SO2 | H | H | H | OH |
B670 | Ph | H | H | H | OH |
B671 | CH3O | H | H | H | OH |
B672 | CH3CO2 | H | H | H | OH |
B673 | ch3ch2co2 | H | H | H | OH |
B674 | ch2=chch2 | H | H | H | OH |
B675 | hccch2 | H | H | H | OH |
B676 | cf3 | H | H | H | OH |
B677 | (CH3)2NSO2 | H | H | H | OH |
B678 | (CH3)2N | H | H | H | OH |
B679 | PhO | H | H | H | OH |
B680 | PhS | H | H | H | OH |
B681 | PhSO | H | H | H | OH |
B682 | PhSO2 | H | H | H | OH |
B683 | CN | H | H | H | OH |
B684 | ch3 | ch3 | H | H | OH |
B685 | ch3ch2 | ch3 | H | H | OH |
B686 | ch3ch2ch2 | ch3 | H | H | OH |
B687 | (CH3)2CH | ch3 | H | H | OH |
B688 | (CH3)3C | ch3 | H | H | OH |
B689 | ch3s | ch3 | H | H | OH |
B690 | ch3so | ch3 | H | H | OH |
B691 | ch3so2 | ch3 | H | H | OH |
B692 | Ph | ch3 | H | H | OH |
B693 | ch3o | ch3 | H | H | OH |
B694 | ch3co2 | ch3 | H | H | OH |
B695 | ch3ch2co2 | ch3 | H | H | OH |
B696 | ch2=chch2 | ch3 | H | H | OH |
B697 | hccch2 | ch3 | H | H | OH |
B698 | cf3 | ch3 | H | H | OH |
B699 | (CH3)2NSO2 | ch3 | H | H | OH |
B700 | (CH3)2N | ch3 | H | H | OH |
B701 | PhO | ch3 | H | H | OH |
B702 | PhS | ch3 | H | H | OH |
B703 | PhSO | ch3 | H | H | OH |
B704 | PhSO2 | ch3 | H | H | OH |
B705 | CN | ch3 | H | H | OH |
B706 | CH3 | H | ch3 | H | OH |
B707 | ch3ch2 | H | ch3 | H | OH |
B708 | ch3ch2ch2 | H | ch3 | H | OH |
B709 | (CH3)2CH | H | ch3 | H | OH |
B710 | (CH3)3C | H | ch3 | H | OH |
B711 | ch3s | H | ch3 | H | OH |
B712 | ch3so | H | ch3 | H | OH |
B713 | ch3so2 | H | ch3 | H | OH |
B714 | Ph | H | ch3 | H | OH |
B715 | ch3o | H | ch3 | H | OH |
B716 | ch3co2 | H | ch3 | H | OH |
B717 | ch3ch2co2 | H | ch3 | H | OH |
W
S
S s
s s
s s
s s
s s
s s
s s
s s
s cn cn s
s s
s s
s s
s s
s s
s s
s s
s s
s s
s s
s s
s s
s s
s s
Sku- | R44 | R37 | R38 | R39 | R40 |
pina | |||||
B718 | ch2=chch2 | H | ch3 | H | OH |
B719 | hccch2 | H | ch3 | H | OH |
B720 | cf3 | H | ch3 | H | OH |
B721 | (CH3)2NSO2 | H | ch3 | H | OH |
B722 | (ch3)2n | H | ch3 | H | OH |
B723 | PhO | H | ch3 | H | OH |
B724 | PhS | H | ch3 | H | OH |
B725 | PhSO | H | ch3 | H | OH |
B726 | PhSO2 | H | ch3 | H | OH |
B727 | CN | H | ch3 | H | OH |
B728 | ch3 | ch3 | ch3 | H | OH |
B729 | ch3ch2 | ch3 | ch3 | H | OH |
B730 | ch3ch2ch2 | ch3 | ch3 | H | OH |
B731 | (ch3)2ch | ch3 | ch3 | H | OH |
B732 | (CH3)3C | ch3 | ch3 | H | OH |
B733 | ch3s | ch3 | ch3 | H | OH |
B734 | ch3so | ch3 | ch3 | H | OH |
B735 | ch3so2 | ch3 | ch3 | H | OH |
B736 | Ph | ch3 | ch3 | H | OH |
B737 | ch3o | ch3 | ch3 | H | OH |
B738 | ch3co2 | ch3 | ch3 | H | OH |
B739 | ch3ch2co2 | ch3 | ch3 | H | OH |
B740 | ch2=chch2 | ch3 | ch3 | H | OH |
B741 | hccch2 | ch3 | ch3 | H | OH |
B742 | cf3 | ch3 | ch3 | H | OH |
B743 | (CH3)2NSO2 | ch3 | ch3 | H | OH |
B744 | (CH3)2N | ch3 | ch3 | H | OH |
B745 | PhO | ch3 | ch3 | H | OH |
B746 | PhS | ch3 | ch3 | H | OH |
B747 | PhSO | ch3 | ch3 | H | OH |
B748 | PhSO2 | ch3 | ch3 | H | OH |
B749 | CN | ch3 | ch3 | H | OH |
B750 | ch3 | ch3 | ch3 | CH3 | OH |
B751 | ch3ch2 | ch3 | ch3 | ch3 | OH |
B752 | ch3ch2ch2 | ch3 | ch3 | ch3 | OH |
B753 | (CH3)2CH | ch3 | ch3 | ch3 | OH |
B754 | (CH3)3C | ch3 | ch3 | ch3 | OH |
B755 | ch3s | ch3 | ch3 | ch3 | OH |
B756 | ch3so | ch3 | ch3 | ch3 | OH |
B757 | ch3so2 | ch3 | ch3 | ch3 | OH |
B758 | Ph | ch3 | ch3 | ch3 | OH |
B759 | ch3o | ch3 | ch3 | ch3 | OH |
B760 | ch3co2 | ch3 | ch3 | ch3 | OH |
B761 | ch3ch2co2 | ch3 | ch3 | ch3 | OH |
B762 | ch2=chch2 | ch3 | ch3 | ch3 | OH |
B763 | hccch2 | ch3 | ch3 | ch3 | OH |
B764 | cf3 | ch3 | ch3 | ch3 | OH |
B765 | (CH3)2NSO2 | ch3 | ch3 | ch3 | OH |
B766 | (CH3)2N | ch3 | ch3 | ch3 | OH |
tnwtncntnmmwcntntnmcncncncnmtn s
s s
s s
s s
s s
s s
s s
s s
s s
s s
s s
s s
s s
s s
s s
Sku- | R44 | R37 | R38 | R39 | R40 | W |
pina B7 67 | PhO | ch3 | ch3 | ch3 | OH | S |
B768 | PhS | ch3 | ch3 | ch3 | OH | S |
B769 | PhSO | ch3 | ch3 | ch3 | OH | S |
B770 | PhSO2 | ch3 | ch3 | ch3 | OH | S |
B771 | CN | ch3 | ch3 | ch3 | OH | S |
B772 | ch3ch2 | ch3ch2 | H | H | OH | S |
B773 | ch3ch2ch2 | ch3ch2 | H | H | OH | S |
B774 | (CH3)2CH | ch3ch2 | H | H | OH | S |
B775 | (CH3)3C | ch3ch2 | H | H | OH | S |
B776 | ch3s | ch3ch2 | H | H | OH | S |
B777 | ch3so | ch3ch2 | H | H | OH | S |
B778 | ch3so2 | ch3ch2 | H | H | OH | S |
B779 | Ph | ch3ch2 | H | H | OH | S |
B780 | CH3O | ch3ch2 | H | H | OH | S |
B781 | CH3CO2 | ch3ch2 | H | H | OH | S |
B782 | ch3ch2co2 | ch3ch2 | H | H | OH | S |
B783 | ch2=chch2 | ch3ch2 | H | H | OH | s |
B784 | hccch2 | ch3ch2 | H | H | OH | s |
B785 | cf3 | ch3ch2 | H | H | OH | s |
B786 | (CH3)2NSO2 | ch3ch2 | H | H | OH | s |
B787 | (CH3)zN | ch3ch2 | H | H | OH | s |
B788 | PhO | ch3ch2 | H | H | OH | s |
B789 | PhS | ch3ch2 | H | H | OH | s |
B790 | PhSO | ch3ch2 | H | H | OH | s |
B791 | PhSO2 | ch3ch2 | H | H | OH | s |
B792 | CN | ch3ch2 | H | H | OH | s |
B793 | H | H | H | H | OH | so2 |
B794 | ch3 | H | H | H | OH | so2 |
B795 | ch3ch2 | H | H | H | OH | so2 |
B796 | ch3ch2ch2 | H | H | H | OH | so2 |
B797 | (CH3)2CH | H | H | H | OH | so2 |
B798 | (CH3)3C | H | H | H | OH | so2 |
B799 | ch3s | H | H | H | OH | so2 |
B800 | ch3so | H | H | H | OH | so2 |
B801 | ch3so2 | H | H | H | OH | so2 |
B802 | Ph | H | H | H | OH | so2 |
B803 | CH3O | H | H | H | OH | so2 |
B804 | CH3CO2 | H | H | H | OH | so2 |
B805 | ch3ch2co2 | H | H | H | OH | so2 |
B806 | ch2=chch2 | H | H | H | OH | so2 |
B807 | hccch2 | H | H | H | OH | so2 |
B808 | cf3 | H | H | H | OH | so2 |
B809 | (CH3)2NSO2 | H | H | H | OH | so2 |
B810 | (CH3)2N | H | H | H | OH | so2 |
B811 | PhO | H | H | H | OH | so2 |
B812 | PhS | H | H | H | OH | so2 |
B813 | PhSO | H | H | H | OH | so2 |
B814 | PhSO2 | H | H | H | OH | so2 |
B815 | CN | H | H | H | OH | so2 |
-72CZ 304537 B6
Sku- | R44 | R37 | R38 | R39 | R40 | W |
pina B816 | ch3 | ch3 | H | H | OH | SO2 |
B817 | ch3ch2 | ch3 | H | H | OH | SO2 |
B818 | ch3ch2ch2 | ch3 | H | H | OH | SO2 |
B819 | (CH3)2CH | ch3 | H | H | OH | SO2 |
B820 | (CH3)3C | ch3 | H | H | OH | SO2 |
B821 | ch3s | ch3 | H | H | OH | SO2 |
B822 | ch3so | ch3 | H | H | OH | SO2 |
B823 | ch3so2 | ch3 | H | H | OH | S02 |
B824 | Ph | ch3 | H | H | OH | SO2 |
B825 | ch3o | ch3 | H | H | OH | SO2 |
B826 | ch3co2 | ch3 | H | H | OH | SO2 |
B827 | ch3ch2co2 | ch3 | H | H | OH | so2 |
B828 | ch2=chch2 | ch3 | H | H | OH | S02 |
B829 | hccch2 | ch3 | H | H | OH | so2 |
B830 | cf3 | ch3 | H | H | OH | SO2 |
B831 | (CH3)2NSO2 | ch3 | H | H | OH | SO2 |
B832 | (CH3)2N | ch3 | H | H | OH | so2 |
B833 | PhO | ch3 | H | H | OH | so2 |
B834 | PhS | ch3 | H | H | OH | so2 |
B835 | PhSO | ch3 | H | H | OH | so2 |
B836 | PhSO2 | ch3 | H | H | OH | so2 |
B837 | CN | ch3 | H | H | OH | so2 |
B838 | ch3 | H | ch3 | H | OH | so2 |
B839 | ch3ch2 | H | ch3 | H | OH | so2 |
B840 | ch3ch2ch2 | H | ch3 | H | OH | so2 |
B841 | (CH3)2CH | H | ch3 | H | OH | so2 |
B842 | (CH3)3C | H | ch3 | H | OH | so2 |
B843 | ch3s | H | ch3 | H | OH | so2 |
B844 | ch3so | H | ch3 | H | OH | so2 |
B845 | ch3so2 | H | ch3 | H | OH | so2 |
B846 | Ph | H | ch3 | H | OH | so2 |
B847 | ch3o | H | ch3 | H | OH | so2 |
B848 | ch3co2 | H | ch3 | H | OH | so2 |
B849 | ch3ch2co2 | H | ch3 | H | OH | so2 |
B850 | ch2=chch2 | H | ch3 | H | OH | so2 |
B851 | hccch2 | H | ch3 | H | OH | so2 |
B852 | cf3 | H | ch3 | H | OH | so2 |
B853 | (CH3)2NSO2 | H | ch3 | H | OH | so2 |
B854 | (CH3)2N | H | ch3 | H | OH | so2 |
B855 | PhO | H | ch3 | H | OH | so2 |
B856 | PhS | H | ch3 | H | OH | so2 |
B857 | PhSO | H | ch3 | H | OH | so2 |
B858 | PhSO2 | H | ch3 | H | OH | so2 |
B859 | CN | H | ch3 | H | OH | so2 |
B860 | CH3 | ch3 | ch3 | H | OH | so2 |
B861 | ch3ch2 | ch3 | ch3 | H | OH | so2 |
B862 | ch3ch2ch2 | ch3 | ch3 | H | OH | so2 |
B863 | (CH3)2CH | ch3 | ch3 | H | OH | so2 |
B864 | (CH3)3C | ch3 | ch3 | H | OH | so2 |
Sku- | R44 | R37 | R38 | R3g | R40 | W |
pina B865 | ch3s | ch3 | ch3 | H | OH | SO2 |
B866 | ch3so | ch3 | ch3 | H | OH | so2 |
B867 | ch3so2 | ch3 | ch3 | H | OH | so2 |
B868 | Ph | ch3 | ch3 | H | OH | so2 |
B869 | ch3o | ch3 | ch3 | H | OH | so2 |
B870 | ch3co2 | ch3 | ch3 | H | OH | so2 |
B871 | ch3ch2co2 | ch3 | ch3 | H | OH | so2 |
B872 | ch2=chch2 | ch3 | ch3 | H | OH | so2 |
B873 | hccch2 | ch3 | ch3 | H | OH | so2 |
B874 | cf3 | ch3 | ch3 | H | OH | so2 |
B875 | (CH3)2NSO2 | ch3 | ch3 | H | OH | so2 |
B876 | (CH3)2N | ch3 | ch3 | H | OH | so2 |
B877 | PhO | ch3 | ch3 | H | OH | so2 |
B878 | PhS | ch3 | ch3 | H | OH | so2 |
B879 | PhSO | ch3 | ch3 | H | OH | so2 |
B880 | PhSO2 | ch3 | ch3 | H | OH | so2 |
B881 | CN | ch3 | ch3 | H | OH | so2 |
B882 | ch3 | ch3 | ch3 | ch3 | OH | so2 |
B883 | ch3ch2 | ch3 | ch3 | ch3 | OH | so2 |
B884 | ch3ch2ch2 | ch3 | ch3 | ch3 | OH | so2 |
B885 | (CH3)2CH | ch3 | ch3 | ch3 | OH | so2 |
B886 | (CH3)3C | ch3 | ch3 | ch3 | OH | so2 |
B887 | ch3s | ch3 | ch3 | ch3 | OH | so2 |
B888 | ch3so | ch3 | ch3 | ch3 | OH | so2 |
B889 | ch3so2 | ch3 | ch3 | ch3 | OH | so2 |
B890 | Ph | ch3 | ch3 | ch3 | OH | so2 |
B891 | ch3o | ch3 | ch3 | ch3 | OH | so2 |
B892 | ch3co2 | ch3 | ch3 | ch3 | OH | so2 |
B893 | ch3ch2co2 | ch3 | ch3 | ch3 | OH | so2 |
B894 | ch2=chch2 | ch3 | ch3 | ch3 | OH | so2 |
B895 | hccch2 | ch3 | ch3 | ch3 | OH | so2 |
B896 | cf3 | ch3 | ch3 | ch3 | OH | so2 |
B897 | (CH3)2NSO2 | ch3 | ch3 | ch3 | OH | so2 |
B898 | (CH3)2N | ch3 | ch3 | ch3 | OH | so2 |
B899 | PhO | ch3 | ch3 | ch3 | OH | so2 |
B900 | PhS | ch3 | ch3 | ch3 | OH | so2 |
B901 | PhSO | ch3 | ch3 | ch3 | OH | so2 |
B902 | PhSO2 | ch3 | ch3 | ch3 | OH | so2 |
B903 | CN | ch3 | ch3 | ch3 | OH | so2 |
B904 | CH3CH2 | ch3ch2 | H | H | OH | so2 |
B905 | ch3ch2ch2 | ch3ch2 | H | H | OH | so2 |
B906 | (CH3)2CH | ch3ch2 | H | H | OH | so2 |
B907 | (CH3)3C | ch3ch2 | H | H | OH | so2 |
B908 | ch3s | ch3ch2 | H | H | OH | so2 |
B909 | ch3so | ch3ch2 | H | H | OH | so2 |
B910 | ch3so2 | ch3ch2 | H | H | OH | so2 |
B911 | Ph | ch3ch2 | H | H | OH | so2 |
B912 | ch3o | ch3ch2 | H | H | OH | so2 |
B913 | ch3co2 | ch3ch2 | H | H | OH | so2 |
-74CZ 304537 B6
Sku- | R44 | R37 | R38 | R39 | R40 | W |
pina B914 | CH3CH2CO2 | ch3ch2 | H | H | OH | SO2 |
B915 | ch2=chch2 | ch3ch2 | H | H | OH | so2 |
B916 | HCCCH2 | ch3ch2 | H | H | OH | so2 |
B917 | cf3 | ch3ch2 | H | H | OH | so2 |
B918 | (CH3)2NSO2 | ch3ch2 | H | H | OH | so2 |
B919 | (CH3)2N | ch3ch2 | H | H | OH | so2 |
B920 | PhO | ch3ch2 | H | H | OH | so2 |
B921 | PhS | ch3ch2 | H | H | OH | so2 |
B922 | PhSO | ch3ch2 | H | H | OH | so2 |
B923 | PhSO2 | ch3ch2 | H | H | OH | so2 |
B924 | CN | ch3ch2 | H | H | OH | so2 |
B925 | H | H | H | H | OH | CH(CO2CH2CH3) |
B926 | CH3 | H | H | H | OH | CH(CO2CH2CH3) |
B927 | ch3ch2 | H | H | H | OH | CH(CO2CH2CH3) |
B928 | ch3ch2ch2 | H | H | H | OH | CH(CO2CH2CH3) |
B929 | (CH3)2CH | H | H | H | OH | CH(CO2CH2CH3) |
B930 | (CH3)3C | H | H | H | OH | CH(CO2CH2CH3) |
B931 | ch3s | H | H | H | OH | CH(CO2CH2CH3) |
B932 | ch3so | H | H | H | OH | CH(CO2CH2CH3) |
B933 | ch3so2 | H | H | H | OH | CH(CO2CH2CH3) |
B934 | Ph | H | H | H | OH | CH(CO2CH2CH3) |
B935 | ch3o | H | H | H | OH | CH(CO2CH2CH3) |
B936 | ch3co2 | H | H | H | OH | CH(CO2CH2CH3) |
B937 | ch3ch2co2 | H | H | H | OH | CH(CO2CH2CH3) |
B938 | ch2=chch2 | H | H | H | OH | CH(CO2CH2CH3) |
B939 | hccch2 | H | H | H | OH | CH(CO2CH2CH3) |
B940 | cf3 | H | H | H | OH | CH(CO2CH2CH3) |
B941 | (CH3)2NSO2 | H | H | H | OH | CH(CO2CH2CH3) |
B942 | (CH3)2N | H | H | H | OH | CH(CO2CH2CH3) |
B943 | PhO | H | H | H | OH | CH(CO2CH2CH3) |
B944 | PhS | H | H | H | OH | CH(CO2CH2CH3) |
B945 | PhSO | H | H | H | OH | CH(CO2CH2CH3) |
B946 | PhSO2 | H | H | H | OH | CH(CO2CH2CH3) |
B947 | CN | H | H | H | OH | CH(CO2CH2CH3) |
B948 | ch3 | ch3 | H | H | OH | CH(CO2CH2CH3) |
B949 | ch3ch2 | ch3 | H | H | OH | CH(CO2CH2CH3) |
B95O | ch3ch2ch2 | ch3 | H | H | OH | CH(CO2CH2CH3) |
B951 | (CH3)2CH | ch3 | H | H | OH | CH(CO2CH2CH3) |
B952 | (CH3)3c | ch3 | H | H | OH | CH(CO2CH2CH3) |
B953 | ch3s | ch3 | H | H | OH | CH(CO2CH2CH3) |
B954 | ch3so | ch3 | H | H | OH | CH(CO2CH2CH3) |
B95.5 | ch3so2 | ch3 | H | H | OH | CH(CO2CH2CH3) |
B956 | Ph | ch3 | H | H | OH | CH (CO2CH2CH3) |
B957 | ch3o | ch3 | H | H | OH | CH(CO2CH2CH3) |
B958 | ch3co2 | ch3 | H | H | OH | CH(CO2CH2CH3) |
B959 | ch3ch2co2 | ch3 | H | H | OH | CH(CO2CH2CH3) |
B960 | ch2=chch2 | ch3 | H | H | OH | CH(CO2CH2CH3) |
B961 | hccch2 | ch3 | H | H | OH | CH(CO2CH2CH3) |
B962 | cf3 | ch3 | H | H | OH | CH(CO2CH2CH3) |
Sku- | R44 | R37 | R38 | R3g | R40 | W |
pina | ||||||
B963 | (CH3)2NSO2 | ch3 | H | H | OH | CH(CO2CH2CH3) |
B964 | (CH3)2N | ch3 | H | H | OH | CH(CO2CH2CH3) |
B965 | PhO | ch3 | H | H | OH | CH(CO2CH2CH3) |
B966 | PhS | ch3 | H | H | OH | CH(CO2CH2CH3) |
B967 | PhSO | ch3 | H | H | OH | CH(CO2CH2CH3) |
B968 | PhSO2 | ch3 | H | H | OH | CH (CO2CH2CH3) |
B969 | CN | ch3 | H | H | OH | CH(CO2CH2CH3) |
B970 | CH3 | H | ch3 | H | OH | CH(CO2CH2CH3) |
B971 | ch3ch2 | H | ch3 | H | OH | CH(CO2CH2CH3) |
B972 | ch3ch2ch2 | H | ch3 | H | OH | CH(CO2CH2CH3) |
B973 | (CH3)2CH | H | ch3 | H | OH | CH(CO2CH2CH3) |
B974 | (CH3)3C | H | ch3 | H | OH | CH(CO2CH2CH3) |
B975 | ch3s | H | ch3 | H | OH | CH(CO2CH2CH3) |
B976 | ch3so | H | ch3 | H | OH | CH(CO2CH2CH3) |
B977 | ch3so2 | H | ch3 | H | OH | CH(CO2CH2CH3) |
B978 | Ph | H | ch3 | H | OH | CH(CO2CH2CH3) |
B979 | ch3o | H | ch3 | H | OH | CH(CO2CH2CH3) |
B980 | ch3co2 | H | ch3 | H | OH | CH(CO2CH2CH3) |
B981 | ch3ch2co2 | H | ch3 | H | OH | CH(CO2CH2CH3) |
B982 | ch2=chch2 | H | ch3 | H | OH | CH(CO2CH2CH3) |
B983 | hccch2 | H | ch3 | H | OH | CH(CO2CH2CH3) |
B984 | cf3 | H | ch3 | H | OH | CH(CO2CH2CH3) |
B985 | (CH3)2NSO2 | H | ch3 | H | OH | CH(CO2CH2CH3) |
B986 | (CH3)2N | H | ch3 | H | OH | CH(CO2CH2CH3) |
B987 | PhO | H | ch3 | H | OH | CH(CO2CH2CH3) |
B988 | PhS | H | ch3 | H | OH | CH(CO2CH2CH3) |
B989 | PhSO | H | ch3 | H | OH | CH(CO2CH2CH3) |
B990 | PhSO2 | H | ch3 | H | OH | CH(CO2CH2CH3) |
B991 | CN | H | ch3 | H | OH | CH(CO2CH2CH3) |
B992 | ch3 | ch3 | ch3 | H | OH | CH(CO2CH2CH3) |
B993 | ch3ch2 | ch3 | ch3 | H | OH | CH(CO2CH2CH3) |
B994 | ch3ch2ch2 | ch3 | ch3 | H | OH | CH(CO2CH2CH3) |
B995 | (CH3)2CH | ch3 | ch3 | H | OH | CH(CO2CH2CH3) |
B996 | (CH3)3c | ch3 | ch3 | H | OH | CH(CO2CH2CH3) |
B997 | ch3s | ch3 | ch3 | H | OH | CH(CO2CH2CH3) |
B998 | ch3so | ch3 | ch3 | H | OH | CH(CO2CH2CH3) |
B999 | ch3so2 | ch3 | ch3 | H | OH | CH(CO2CH2CH3) |
B1000 | Ph | ch3 | ch3 | H | OH | CH (CO2CH2CH3) |
B1001 | ch3o | ch3 | ch3 | H | OH | CH(CO2CH2CH3) |
B1002 | ch3co2 | ch3 | ch3 | H | OH | CH(CO2CH2CH3) |
B1003 | ch3ch2co2 | ch3 | ch3 | H | OH | CH(CO2CH2CH3) |
B1004 | ch2=chch2 | ch3 | ch3 | H | OH | CH(CO2CH2CH3) |
B1005 | hccch2 | ch3 | ch3 | H | OH | CH(CO2CH2CH3) |
B1006 | cf3 | ch3 | ch3 | H | OH | CH(CO2CH2CH3) |
B1007 | (CH3)2NS02 | ch3 | ch3 | H | OH | CH(CO2CH2CH3) |
B1008 | (CH3)2N | ch3 | ch3 | H | OH | CH(CO2CH2CH3) |
B1009 | PhO | ch3 | ch3 | H | OH | CH(CO2CH2CH3) |
B1010 | PhS | ch3 | ch3 | H | OH | CH(CO2CH2CH3) |
B1011 | PhSO | ch3 | ch3 | H | OH | CH(CO2CH2CH3) |
Sku- | R44 | R37 |
pina B1012 | PhSO2 | CH3 |
B1013 | CN | ch3 |
B1014 | ch3 | ch3 |
B1015 | ch3ch2 | ch3 |
B1016 | ch3ch2ch2 | ch3 |
B1017 | (CH3)2CH | ch3 |
B1018 | (CH3)3C | ch3 |
B1019 | ch3s | ch3 |
B1020 | ch3so | ch3 |
B1021 | ch3so2 | ch3 |
B1022 | Ph | ch3 |
B1023 | ch3o | ch3 |
B1024 | ch3co2 | ch3 |
B1025 | ch3ch2co2 | ch3 |
B1026 | ch2=chch2 | ch3 |
B1027 | hccch2 | ch3 |
B1028 | cf3 | ch3 |
B1029 | (CH3)2NSO2 | ch3 |
B1030 | (CH3)2N | ch3 |
B1031 | PhO | ch3 |
B1032 | PhS | ch3 |
B1033 | PhSO | ch3 |
B1034 | PhSO2 | ch3 |
B1035 | CN | ch3 |
B1036 | ch3ch2 | ch3ch2 |
B1037 | ch3ch2ch2 | ch3ch2 |
B1038 | (CH3)2CH | ch3ch2 |
B1039 | (CH3)3C | ch3ch2 |
B1040 | ch3s | ch3ch2 |
B1041 | ch3so | ch3ch2 |
B1042 | ch3so2 | ch3ch2 |
B1043 | Ph | ch3ch2 |
B1044 | ch3o | ch3ch2 |
B1045 | ch3co2 | CH3CH2 |
B1046 | ch3ch2co2 | ch3ch2 |
B1047 | ch2=chch2 | ch3ch2 |
B1048 | hccch2 | ch3ch2 |
B1049 | cf3 | ch3ch2 |
B1050 | (CH3)2NSO2 | ch3ch2 |
B1051 | (CH3)2N | ch3ch2 |
B1052 | PhO | ch3ch2 |
B1053 | PhS | ch3ch2 |
B1054 | PhSO | ch3ch2 |
B1055 | PhSO2 | ch3ch2 |
B1056 | CN | ch3ch2 |
B1057 | ch3oco | H |
B1O58 | H | H |
B1059 | H | H |
B1060 | H | H |
R38 | R39 | R40 | W |
ch3 | H | OH | CH(CO2CH2CH3) |
ch3 | H | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH (CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH(CO2CH2CH3) |
ch3 | ch3 | OH | CH (CO2CH2CH3) |
H | H | OH | CH(CO2CH2CH3) |
H | H | OH | CH(CO2CH2CH3) |
H | H | OH | CH{CO2CH2CH3) |
H | H | OH | CH(CO2CH2CH3) |
H | H | OH | CH(CO2CH2CH3) |
H | H | OH | CH(CO2CH2CH3) |
H | H | OH | CH(CO2CH2CH3) |
H | H | OH | CH(CO2CH2CH3) |
H | H | OH | CH(CO2CH2CH3) |
H | H | OH | CH(CO2CH2CH3) |
H | H | OH | CH (CO2CH2CH3) |
H | H | OH | CH(CO2CH2CH3) |
H | H | OH | CH(CO2CH2CH3) |
H | H | OH | CH(CO2CH2CH3) |
H | H | OH | CH(CO2CH2CH3) |
H | H | OH | CH(CO2CH2CH3) |
H | H | OH | CH(CO2CH2CH3) |
H | H | OH | CH(CO2CH2CH3) |
H | H | OH | CH(CO2CH2CH3) |
H | H | OH | CH(CO2CH2CH3) |
H | H | OH | CH(CO2CH2CH3) |
H | H | OH | CHPh |
H | H | OH | CHPh |
H | H | OH | CH(CH2CH3) |
H | H | OH | CH(CH2CH2CH3) |
Sku- | R44 | R37 | R38 | R39 | R40 | W |
pina B1061 | H | H | H | H | OH | CH(CH(CH3)2) |
B1062 | H | H | H | H | OH | CH(C(CH3)3) |
B1063 | H | H | H | H | OH | C(CH3)2 |
B1064 | H | H | H | H | OH | CH(CF3) |
B1065 | CH3OCO | H | H | H | OH | C(CH3) (CF3) |
B1066 | H | H | H | H | OH | C(CH3) (CF3) |
B1067 | CH3OCO | CH30 | H | H | OH | ch2 |
B1068 | H | CH30 | H | H | OH | ch2 |
B1069 | CH30 | CH3OCO | H | ch3 | OH | ch2 |
B1070 | CH30 | H | CH3 | H | OH | ch2 |
B1071 | Cl | H | H | H | OH | ch2 |
B1072 | F | H | H | H | OH | ch2 |
B1073 | H | H | H | H | OH | CH(OCH3)2 |
B1074 | H | H | H | H | OH | ch2oso2ch3 |
B1075 | ch3 | CH3 | ch3 | ch3 | OH | S(O) |
B1076 | cich2ch2 | H | H | H | OH | ch2 |
B1077 | HO(CH2)2 | H | H | H | OH | ch2 |
B1078 | MsO(CH2)2 | H | H | H | OH | ch2 |
B1079 | HOCH(CH3)CH2 | H | H | H | OH | ch2 |
B1080 | MsOCH(CH3)CH2 | H | H | H | OH | ch2 |
B1081 | (CH3)2CH | H | ch3 | ch3 | OH | ch2 |
B1082 | hccch2 | H | ch3 | ch3 | OH | ch2 |
B1083 | h2c=cch2 | H | ch3 | ch3 | OH | ch2 |
V následující tabulce 7 Q je Q6
R
a Qg jsou následující skupiny C:
78CZ 304537 B6
Tabulka 7: Skupiny C:
Sku- pina | Rb4 | Res | R86 | R83 | P | w |
Cl | H | H | H | OH | 1 | ch2 |
C2 | ch3 | H | H | OH | 1 | ch2 |
C3 | ch3ch2 | H | H | OH | 1 | ch2 |
C4 | ch3ch2ch2 | H | H | OH | 1 | ch2 |
C5 | (CH3)2CH | H | H | OH | 1 | ch2 |
C6 | (CH3)3C | H | H | OH | 1 | ch2 |
C7 | ch3s | H | H | OH | 1 | ch2 |
C8 | ch3so | H | H | OH | 1 | ch2 |
C9 | ch3so2 | H | H | OH | 1 | ch2 |
CIO | Ph | H | H | OH | 1 | ch2 |
Cil | ch3o | H | H | OH | 1 | ch2 |
C12 | ch3oco2 | H | H | OH | 1 | ch2 |
C13 | ch3ch2oco2 | H | H | OH | 1 | ch2 |
C14 | ch2=chch2 | H | H | OH | 1 | ch2 |
C15 | hccch2 | H | H | OH | 1 | ch2 |
C16 | cf3 | H | H | OH | 1 | ch2 |
C17 | (CH3)2NSO2 | H | H | OH | 1 | ch2 |
C18 | (CH3)2N | H | H | OH | 1 | ch2 |
C19 | PhO | H | H | OH | 1 | ch2 |
C20 | PhS | H | H | OH | 1 | ch2 |
C21 | PhSO | H | H | OH | 1 | ch2 |
C22 | PhSO2 | H | H | OH | 1 | ch2 |
C23 | CN | H | H | OH | 1 | ch2 |
C24 | CH3 | ch3 | H | OH | 1 | ch2 |
C25 | ch3ch2 | ch3 | H | OH | 1 | ch2 |
C26 | ch3ch2ch2 | ch3 | H | OH | 1 | ch2 |
C27 | (CH3)2CH | ch3 | H | OH | 1 | ch2 |
C28 | (CH3)3C | ch3 | H | OH | 1 | ch2 |
C29 | ch3s | ch3 | H | OH | 1 | ch2 |
C30 | ch3so | ch3 | H | OH | 1 | ch2 |
C31 | CH3SO2 | ch3 | H | OH | 1 | ch2 |
C32 | Ph | ch3 | H | OH | 1 | ch2 |
C33 | ch3o | ch3 | H | OH | 1 | ch2 |
C34 | ch3oco2 | ch3 | H | OH | 1 | ch2 |
C35 | ch3ch2oco2 | ch3 | H | OH | 1 | ch2 |
C36 | ch2=chch2 | ch3 | H | OH | 1 | ch2 |
C37 | hccch2 | ch3 | H | OH | 1 | ch2 |
C38 | cf3 | ch3 | H | OH | 1 | ch2 |
C39 | (CH3)2NSO2 | ch3 | H | OH | 1 | ch2 |
C40 | (CH3)2N | ch3 | H | OH | 1 | ch2 |
C41 | PhO | ch3 | H | OH | 1 | ch2 |
C42 | PhS | ch3 | H | OH | 1 | ch2 |
C43 | PhSO | ch3 | H | OH | 1 | ch2 |
-79CZ 304537 B6
Sku- | Re 4 | Rb5 | Re 6 | Re 3 | P | W |
pina C44 | PhSO2 | ch3 | H | OH | 1 | ch2 |
C45 | CN | ch3 | H | OH | 1 | ch2 |
C46 | H | H | H | OH | 4 | ch2 |
C47 | ch3 | H | H | OH | 4 | ch2 |
C48 | ch3ch2 | H | H | OH | 4 | ch2 |
C49 | ch3ch2ch2 | H | H | OH | 4 | ch2 |
C50 | (CH3)2CH | H | H | OH | 4 | ch2 |
C51 | (CH3)3C | H | H | OH | 4 | ch2 |
C52 | ch3s | H | H | OH | 4 | ch2 |
C53 | ch3so | H | H | OH | 4 | ch2 |
C54 | ch3so2 | H | H | OH | 4 | ch2 |
C55 | Ph | H | H | OH | 4 | ch2 |
C56 | ch3o | H | H | OH | 4 | ch2 |
C57 | ch3oco2 | H | H | OH | 4 | ch2 |
C58 | ch3ch2oco2 | H | H | OH | 4 | ch2 |
C59 | ch2=chch2 | H | H | OH | 4 | ch2 |
C60 | hccch2 | H | H | OH | 4 | ch2 |
C61 | cf3 | H | H | OH | 4 | ch2 |
C62 | (CH3)2NSO2 | H | H | OH | 4 | ch2 |
C63 | (CH3)2N | H | H | OH | 4 | ch2 |
C64 | PhO | H | H | OH | 4 | ch2 |
C65 | PhS | H | H | OH | 4 | ch2 |
C66 | PhSO | H | H | OH | 4 | ch2 |
C67 | PhSO2 | H | H | OH | 4 | ch2 |
C68 | CN | H | H | OH | 4 | ch2 |
C69 | ch3 | ch3 | H | OH | 4 | ch2 |
C70 | ch3ch2 | ch3 | H | OH | 4 | ch2 |
C71 | ch3ch2ch2 | ch3 | H | OH | 4 | ch2 |
C72 | (CH3)2CH | ch3 | H | OH | 4 | ch2 |
C73 | (CH3)3C | ch3 | H | OH | 4 | ch2 |
C74 | ch3s | ch3 | H | OH | 4 | ch2 |
C75 | ch3so | ch3 | H | OH | 4 | ch2 |
C76 | ch3so2 | ch3 | H | OH | 4 | ch2 |
C77 | Ph | ch3 | H | OH | 4 | ch2 |
C78 | ch3o | ch3 | H | OH | 4 | ch2 |
C79 | ch3oco2 | ch3 | H | OH | 4 | ch2 |
C80 | ch3ch2oco2 | ch3 | H | OH | 4 | ch2 |
C81 | ch2=chch2 | ch3 | H | OH | 4 | ch2 |
C82 | HCCCHz | ch3 | H | OH | 4 | ch2 |
C83 | cf3 | ch3 | H | OH | 4 | ch2 |
C84 | (CH3)2NSO2 | ch3 | H | OH | 4 | ch2 |
C85 | (CH3)2N | ch3 | H | OH | 4 | ch2 |
C86 | PhO | ch3 | H | OH | 4 | ch2 |
C87 | PhS | ch3 | H | OH | 4 | ch2 |
C88 | PhSO | ch3 | H | OH | 4 | ch2 |
C89 | PhSO2 | ch3 | H | OH | 4 | ch2 |
C90 | CN | ch3 | H | OH | 4 | ch2 |
C91 | H | H | H | OH | 3 | ch2 |
C92 | ch3 | H | H | OH | 3 | ch2 |
-80CZ 304537 B6
Sku- | Re 4 | Res | Re 6 | R83 | P | W |
pina C93 | CH3CH2 | H | H | OH | 3 | ch2 |
C94 | CH3CH2CH2 | H | H | OH | 3 | ch2 |
C95 | (CH3)2CH | H | H | OH | 3 | ch2 |
C96 | (CH3)3c | H | H | OH | 3 | ch2 |
C97 | ch3s | H | H | OH | 3 | ch2 |
C98 | ch3so | H | H | OH | 3 | ch2 |
C99 | ch3so2 | H | H | OH | 3 | ch2 |
C100 | Ph | H | H | OH | 3 | ch2 |
C101 | CH3O | H | H | OH | 3 | ch2 |
C102 | CH3OCO2 | H | H | OH | 3 | ch2 |
C103 | ch3ch2oco2 | H | H | OH | 3 | ch2 |
C1O4 | ch2=chch2 | H | H | OH | 3 | ch2 |
C105 | hccch2 | H | H | OH | 3 | ch2 |
C106 | cf3 | H | H | OH | 3 | ch2 |
C107 | (CH3)2NSO2 | H | H | OH | 3 | ch2 |
C108 | (CH3)2N | H | H | OH | 3 | ch2 |
C109 | PhO | H | H | OH | 3 | ch2 |
C110 | PhS | H | H | OH | 3 | ch2 |
Clil | PhSO | H | H | OH | 3 | ch2 |
C112 | PhSO2 | H | H | OH | 3 | ch2 |
C113 | CN | H | H | OH | 3 | ch2 |
C114 | ch3 | ch3 | H | OH | 3 | ch2 |
C115 | CH3CH2 | ch3 | H | OH | 3 | ch2 |
C116 | CH3CH2CH2 | ch3 | H | OH | 3 | ch2 |
C117 | (CH3)2CH | ch3 | H | OH | 3 | ch2 |
C118 | (CH3)3C | ch3 | H | OH | 3 | ch2 |
C119 | ch3s | ch3 | H | OH | 3 | ch2 |
C120 | ch3so | ch3 | H | OH | 3 | ch2 |
C121 | ch3so2 | ch3 | H | OH | 3 | ch2 |
C122 | Ph | ch3 | H | OH | 3 | ch2 |
C123 | ch3o | ch3 | H | OH | 3 | ch2 |
C124 | ch3oco2 | ch3 | H | OH | 3 | ch2 |
C125 | ch3ch2oco2 | ch3 | H | OH | 3 | ch2 |
C126 | ch2=chch2 | ch3 | H | OH | 3 | ch2 |
C127 | hccch2 | ch3 | H | OH | 3 | ch2 |
C128 | cf3 | ch3 | H | OH | 3 | ch2 |
C129 | (CH3)2NSO2 | ch3 | H | OH | 3 | ch2 |
C130 | (CH3)2N | ch3 | H | OH | 3 | ch2 |
C131 | PhO | ch3 | H | OH | 3 | ch2 |
C132 | PhS | ch3 | H | OH | 3 | ch2 |
C133 | PhSO | ch3 | H | OH | 3 | ch2 |
C134 | PhSO2 | ch3 | H | OH | 3 | ch2 |
C135 | CN | ch3 | H | OH | 3 | ch2 |
C136 | ch3ch2 | ch3ch2 | H | OH | 1 | ch2 |
C137 | H | H | H | OH | 1 | CH(CH3) |
C138 | ch3 | H | H | OH | 1 | CH(CH3) |
C139 | ch3 | ch3 | H | OH | 1 | CH(CH3) |
C140 | ch2ch3 | H | H | OH | 1 | CH(CH3) |
C141 | ch2ch3 | ch3 | H | OH | 1 | CH(CH3) |
Sku- pina | Re 4 | Res | Re 6 | R83 | P | W |
C142 | ch3ch2 | ch3ch2 | H | OH | 1 | CH(CH3) |
C143 | H | H | ch3 | OH | 1 | ch2 |
C144 | ch3 | ch3 | ch3 | OH | 1 | ch2 |
C145 | ch3ch2 | ch3ch2 | ch3 | OH | 1 | ch2 |
C146 | H | H | H | OH | 2 | ch2 |
C147 | ch3 | ch3 | H | OH | 2 | ch2 |
C148 | ch3ch2 | ch3ch2 | H | OH | 2 | ch2 |
C149 | H | H | H | OH | 5 | ch2 |
C150 | ch3 | ch3 | H | OH | 5 | ch2 |
C151 | ch3ch2 | ch3ch2 | H | OH | 5 | ch2 |
V následující tabulce 8 Q je Q8
a Q8 jsou následující skupiny D:
Tabulka 8: Skupiny D:
Skupi- na | Res | Re9 | R90 | R91 | R87 | 0 |
Dl | Η | H | H | H | OH | 2 |
D2 | ch3 | H | H | H | OH | 2 |
D3 | ch3ch2 | H | H | H | OH | 2 |
D4 | ch3ch2ch2 | H | H | H | OH | 2 |
D5 | (CH3)2CH | H | H | H | OH | 2 |
D6 | (CH3)3c | H | H | H | OH | 2 |
D7 | ch3s | H | H | H | OH | 2 |
D8 | ch3so | H | H | H | OH | 2 |
D9 | ch3so2 | H | H | H | OH | 2 |
D10 | Ph | H | H | H | OH | 2 |
Dli | ch3o | H | H | H | OH | 2 |
D12 | ch2=chch2 | H | H | H | OH | 2 |
D13 | hccch2 | H | H | H | OH | 2 |
D14 | cf3 | H | H | H | OH | 2 |
D15 | PhO | H | H | H | OH | 2 |
D16 | PhS | H | H | H | OH | 2 |
D17 | PhSO | H | H | H | OH | 2 |
D18 | PhSO2 | H | H | H | OH | 2 |
D19 | ch3 | CH3 | H | H | OH | 2 |
D20 | ch3ch2 | ch3 | H | H | OH | 2 |
-82CZ 304537 B6
Skupi- | Ree | Re 9 | R90 | R91 | R87 | 0 |
na | ||||||
D21 | CH3CH2CH2 | ch3 | H | H | OH | 2 |
D22 | (CH3)2CH | ch3 | H | H | OH | 2 |
D23 | (CH3)3C | ch3 | H | H | OH | 2 |
D24 | ch3s | ch3 | H | H | OH | 2 |
D25 | ch3so | ch3 | H | H | OH | 2 |
D26 | ch3so2 | ch3 | H | H | OH | 2 |
D27 | Ph | ch3 | H | H | OH | 2 |
D28 | ch3o | ch3 | H | H | OH | 2 |
D29 | ch2=chch2 | ch3 | H | H | OH | 2 |
D30 | HCCCH2 | ch3 | H | H | OH | 2 |
D31 | cf3 | ch3 | H | H | OH | 2 |
D32 | PhO | ch3 | H | H | OH | 2 |
D33 | PhS | ch3 | H | H | OH | 2 |
D34 | PhSO | ch3 | H | H | OH | 2 |
D35 | PhSO2 | ch3 | H | H | OH | 2 |
D36 | H | H | H | H | OH | 3 |
D37 | ch3 | H | H | H | OH | 3 |
D38 | ch3ch2 | H | H | H | OH | 3 |
D39 | ch3ch2ch2 | H | H | H | OH | 3 |
D40 | (CH3)2CH | H | H | H | OH | 3 |
D41 | (ch3)3c | H | H | H | OH | 3 |
D42 | ch3s | H | H | H | OH | 3 |
D43 | ch3so | H | H | H | OH | 3 |
D44 | ch3so2 | H | H | H | OH | 3 |
D45 | Ph | H | H | H | OH | 3 |
D4 6 | ch3o | H | H | H | OH | 3 |
D47 | ch2=chch2 | H | H | H | OH | 3 |
D48 | hccch2 | H | H | H | OH | 3 |
D49 | cf3 | H | H | H | OH | 3 |
D50 | PhO | H | H | H | OH | 3 |
D51 | PhS | H | H | H | OH | 3 |
D52 | PhSO | H | H | H | OH | 3 |
D53 | PhSO2 | H | H | H | OH | 3 |
D54 | ch3 | ch3 | H | H | OH | 3 |
D55 | ch3ch2 | ch3 | H | H | OH | 3 |
D56 | ch3ch2ch2 | ch3 | H | H | OH | 3 |
D57 | (CH3)2CH | ch3 | H | H | OH | 3 |
D58 | (CH3)3C | ch3 | H | H | OH | 3 |
D59 | ch3s | ch3 | H | H | OH | 3 |
D60 | ch3so | ch3 | H | H | OH | 3 |
D61 | ch3so2 | ch3 | H | H | OH | 3 |
D62 | Ph | ch3 | H | H | OH | 3 |
D63 | ch3o | ch3 | H | H | OH | 3 |
D64 | ch2=chch2 | ch3 | H | H | OH | 3 |
D65 | hccch2 | ch3 | H | H | OH | 3 |
D66 | cf3 | ch3 | H | H | OH | 3 |
D67 | PhO | ch3 | H | H | OH | 3 |
D68 | PhS | ch3 | H | H | OH | 3 |
D69 | PhSO | ch3 | H | H | OH | 3 |
-83CZ 304537 B6
Skupi- | Ree | Re9 | R90 | R91 | R87 | 0 |
na | ||||||
D70 | PhSO2 | ch3 | H | H | OH | 3 |
D71 | H | H | H | H | OH | 4 |
D72 | ch3 | H | H | H | OH | 4 |
D73 | ch3ch2 | H | H | H | OH | 4 |
D74 | ch3ch2ch2 | H | H | H | OH | 4 |
D75 | (CH3)2CH | H | H | H | OH | 4 |
D76 | (CH3)3C | H | H | H | OH | 4 |
D77 | ch3s | H | H | H | OH | 4 |
D78 | ch3so | H | H | H | OH | 4 |
D79 | ch3so2 | H | H | H | OH | 4 |
D80 | Ph | H | H | H | OH | 4 |
D81 | ch3o | H | H | H | OH | 4 |
D82 | ch2=chch2 | H | H | H | OH | 4 |
D83 | hccch2 | H | H | H | OH | 4 |
D84 | cf3 | H | H | H | OH | 4 |
D85 | PhO | H | H | H | OH | 4 |
D86 | PhS | H | H | H | OH | 4 |
D87 | PhSO | H | H | H | OH | 4 |
D88 | PhSO2 | H | H | H | OH | 4 |
D89 | ch3 | ch3 | H | H | OH | 4 |
D90 | ch3ch2 | ch3 | H | H | OH | 4 |
D91 | ch3ch2ch2 | ch3 | H | H | OH | 4 |
D92 | (CH3)2CH | ch3 | H | H | OH | 4 |
D93 | (CH3)3c | ch3 | H | H | OH | 4 |
D94 | ch3s | ch3 | H | H | OH | 4 |
D95 | ch3so | ch3 | H | H | OH | 4 |
D96 | ch3so2 | ch3 | H | H | OH | 4 |
D97 | Ph | ch3 | H | H | OH | 4 |
D98 | CH3O | ch3 | H | H | OH | 4 |
D99 | ch2=chch2 | ch3 | H | H | OH | 4 |
D100 | hccch2 | ch3 | H | H | OH | 4 |
D101 | cf3 | ch3 | H | H | OH | 4 |
D102 | PhO | ch3 | H | H | OH | 4 |
D103 | PhS | ch3 | H | H | OH | 4 |
D104 | PhSO | ch3 | H | H | OH | 4 |
D105 | PhSO2 | ch3 | H | H | OH | 4 |
D106 | H | H | H | ch3 | OH | 4 |
D107 | H | H | H | ch3 | OH | 3 |
D108 | H | H | H | H | OH | 1 |
D109 | ch3 | H | H | H | OH | 1 |
DUO | CH3OCO | ch3 | H | H | OH | 1 |
Din | ch3ch2oco | ch3 | H | H | OH | 1 |
D112 | ch3o | ch3 | H | H | OH | 1 |
D113 | ch3s | ch3 | H | H | OH | 1 |
D114 | ch3so | ch3 | H | H | OH | 1 |
D115 | ch3so2 | ch3 | H | H | OH | 1 |
D116 | ch3ch2 | H | H | H | OH | 1 |
D117 | ch3oco | ch3ch2 | H | H | OH | 1 |
D118 | ch3ch2oco | ch3ch2 | H | H | OH | 1 |
-84CZ 304537 B6
Skupi- na D119 | Re 8 ch3o | Re 9 ch3ch2 | R90 H | R91 H | Re7 O | |
OH | 1 | |||||
D120 | ch3s | ch3ch2 | H | H | OH | 1 |
D121 | ch3so | ch3ch2 | H | H | OH | 1 |
D122 | ch3so2 | ch3ch2 | H | H | OH | 1 |
D123 | ch3ch2s | ch3 | H | H | OH | 1 |
D124 | ch3ch2so | ch3 | H | H | OH | 1 |
D125 | ch3ch2so2 | ch3 | H | H | OH | 1 |
D126 | ch3ch2s | ch3ch2 | H | H | OH | 1 |
D127 | ch3ch2so | ch3ch2 | H | H | OH | 1 |
D128 | ch3ch2so2 | ch3ch2 | H | H | OH | 1 |
D129 | H | H | ch3 | H | OH | 1 |
D130 | ch3 | H | ch3 | H | OH | 1 |
D131 | ch3oco | ch3 | ch3 | H | OH | 1 |
D132 | ch3ch2oco | ch3 | ch3 | H | OH | 1 |
D133 | ch3o | ch3 | ch3 | H | OH | 1 |
D134 | ch3s | ch3 | ch3 | H | OH | 1 |
D135 | ch3so | ch3 | ch3 | H | OH | 1 |
D136 | ch3so2 | ch3 | ch3 | H | OH | 1 |
D137 | H | H | H | ch3 | OH | 1 |
D138 | ch3 | H | H | ch3 | OH | 1 |
D139 | H | H | ch3 | ch3 | OH | 1 |
D140 | ch3ch2oco | ch3 | H | H | OH | 4 |
Tabulka 9: Sloučeniny obecného vzorce lf:
? 93 θ
e R 92 | (lf) | ||||
Sl. č. | R92 | R93 | R94 | R95 | q3 |
Al | H | H | H | cf3 | B24 |
A2 | ch3 | H | H | cf3 | B24 |
A3 | ch3ch2 | H | H | cf3 | B24 |
A4 | (CH3)2CH | H | H | cf3 | B24 |
A5 | (CH3)3C | H | H | cf3 | B24 |
A6 | cyklopropyl | H | H | cf3 | B24 |
A7 | CH3(CH2)2 | H | H | cf3 | B24 |
A8 | ch3och2 | H | H | cf3 | B24 |
A9 | CH3O(CH2)2 | H | H | cf3 | B24 |
A10 | Ph | H | H | cf3 | B24 |
-85CZ 304537 B6
Sl. č. All | R92 | R93 | R94 | R95 | q3 |
PhO | H | H | cf3 | B24 | |
A12 | PhS | H | H | cf3 | B24 |
A13 | PhSO | H | H | cf3 | B24 |
A14 | PhSO2 | H | H | cf3 | B24 |
A15 | ch3s | H | H | cf3 | B24 |
A16 | ch3so | H | H | cf3 | B24 |
A17 | cf3 | H | H | cf3 | B24 |
A18 | f2ch | H | H | cf3 | B24 |
A19 | HCC | H | H | cf3 | B24 |
A20 | CH3CC | H | H | cf3 | B24 |
A21 | ch2=ch | H | H | cf3 | B24 |
A22 | ch2=chch2 | H | H | cf3 | B24 |
A23 | CH3SO2N(CH3) | H | H | cf3 | B24 |
A24 | (CH3)2N | H | H | cf3 | B24 |
A25 | (CH3)2NSO2 | H | H | cf3 | B24 |
A26 | cich2 | H | H | cf3 | B24 |
A27 | ch3sch2 | H | H | cf3 | B24 |
A28 | ch3soch2 | H | H | cf3 | B24 |
A29 | ch3so2ch2 | H | H | cf3 | B24 |
A30 | [1,2,4]-triazol-1yl-methyl | H | H | cf3 | B24 |
A31 | ch3 | cf3 | H | ch3 | B24 |
A32 | ch3 | ch3 | H | cf3 | B24 |
A33 | H | H | H | cf3cf2 | B24 |
A34 | ch3 | H | H | cf3cf2 | B24 |
A35 | ch3ch2 | H | H | cf3cf2 | B24 |
A36 | cyklopropyl | H | H | cf3cf2 | B24 |
A37 | (CH3)3C | H | H | cf3cf2 | B24 |
A38 | (CH3)2CH | H | H | cf3cf2 | B24 |
A39 | CH3(CH2)2 | H | H | cf3cf2 | B24 |
A40 | CH3OCH2 | H | H | cf3cf2 | B24 |
A41 | CH3O(CH2)2 | H | H | CF3CF2 | B24 |
A42 | Ph | H | H | cf3cf2 | B24 |
A43 | PhO | H | H | cf3cf2 | B24 |
A44 | PhS | H | H | cf3cf2 | B24 |
A45 | PhSO | H | H | cf3cf2 | B24 |
A46 | PhSO2 | H | H | cf3cf2 | B24 |
A47 | ch3s | H | H | cf3cf2 | B24 |
A48 | ch3so | H | H | cf3cf2 | B24 |
A49 | cf3 | H | H | cf3cf2 | B24 |
A50 | f2ch | H | H | cf3cf2 | B24 |
A51 | HCC | H | H | cf3cf2 | B24 |
A52 | CH3CC | H | H | cf3cf2 | B24 |
A53 | ch2=ch | H | H | cf3cf2 | B24 |
A54 | ch2=chch2 | H | H | cf3cf2 | B24 |
A55 | CH3SO2N(CH3) | H | H | cf3cf2 | B24 |
A56 | (ch3)2n | H | H | cf3cf2 | B24 |
A57 | (CH3)2NSO2 | H | H | cf3cf2 | B24 |
A58 | C1CH2 | H | H | cf3cf2 | B24 |
-86CZ 304537 B6
Sl. X | R92 | R93 | R94 | R95 | q3 |
c. A59 | ch3sch2 | Η | H | cf3cf2 | B24 |
A60 | ch3soch2 | H | H | cf3cf2 | B24 |
A61 | ch3so2ch2 | H | H | cf3cf2 | B24 |
A62 | [1,2,4]-triazol-1yl-methyl | H | H | CF3CF2 | B24 |
A63 | H | H | H | CF3CF2CF2 | B24 |
A64 | ch3 | H | H | cf3cf2cf2 | B24 |
A65 | ch3ch2 | H | H | cf3cf2cf2 | B24 |
A66 | cyklopropyl | H | H | cf3cf2cf2 | B24 |
A67 | (CH3)3C | H | H | cf3cf2cf2 | B24 |
A68 | (CH3)2CH | H | H | cf3cf2cf2 | B24 |
A69 | CH3{CH2)2 | H | H | cf3cf2cf2 | B24 |
A70 | ch3och2 | H | H | cf3cf2cf2 | B24 |
A71 | CH3O(CH2)2 | H | H | cf3cf2cf2 | B24 |
A72 | Ph | H | H | cf3cf2cf2 | B24 |
A73 | PhO | H | H | cf3cf2cf2 | B24 |
A74 | PhS | H | H | cf3cf2cf2 | B24 |
A75 | PhSO | H | H | cf3cf2cf2 | B24 |
A76 | PhSO2 | H | H | cf3cf2cf2 | B24 |
A77 | CH3S | H | H | cf3cf2cf2 | B24 |
A78 | ch3so | H | H | cf3cf2cf2 | B24 |
A79 | cf3 | H | H | cf3cf2cf2 | B24 |
A80 | f2ch | H | H | cf3cf2cf2 | B24 |
A81 | HCC | H | H | cf3cf2cf2 | B24 |
A82 | CH3CC | H | H | cf3cf2cf2 | B24 |
A83 | ch2=ch | H | H | cf3cf2cf2 | B24 |
A84 | ch2=chch2 | H | H | cf3cf2cf2 | B24 |
A85 | CH3SO2N(CH3) | H | H | cf3cf2cf2 | B24 |
A86 | (ch3)2n | H | H | cf3cf2cf2 | B24 |
A87 | (CH3)2NSO2 | H | H | cf3cf2cf2 | B24 |
A88 | C1CH2 | H | H | cf3cf2cf2 | B24 |
A89 | CH3SCH2 | H | H | cf3cf2cf2 | B24 |
A90 | CH3SOCH2 | H | H | cf3cf2cf2 | B24 |
A91 | CH3SO2CH2 | H | H | cf3cf2cf2 | B24 |
A92 | [1,2,4]-triazol-1yl-methyl | H | H | cf3cf2cf2 | B24 |
A93 | H | H | H | cf2ci | B24 |
A94 | CH3 | H | H | cf2ci | B24 |
A95 | ch3ch2 | H | H | cf2ci | B24 |
A96 | cyklopropyl | H | H | cf2ci | B24 |
A97 | (CH3)3C | H | H | cf2ci | B24 |
A98 | (CH3)2CH | H | H | cf2ci | B24 |
A99 | CH3(CH2)2 | H | H | cf2ci | B24 |
A100 | ch3och2 | H | H | cf2ci | B24 |
A101 | CH3O(CH2)2 | H | H | cf2ci | B24 |
A102 | Ph | H | H | cf2ci | B24 |
A103 | PhO | H | H | cf2ci | B24 |
A104 | PhS | H | H | cf2ci | B24 |
A105 | PhSO | H | H | cf2ci | B24 |
87CZ 304537 B6
Sl. č. A106 | R92 | R93 | R94 | R95 | q3 |
PhS02 | Η | Η | CF2C1 | B24 | |
A107 | CH3S | Η | Η | cf2ci | B24 |
A108 | ch3so | Η | Η | cf2ci | B24 |
A109 | cf3 | Η | Η | cf2ci | B24 |
A110 | f2ch | Η | Η | cf2ci | B24 |
Alll | HCC | Η | Η | cf2ci | B24 |
A112 | ch3cc | Η | Η | CF2C1 | B24 |
A113 | ch2=ch | Η | Η | cf2ci | B24 |
A114 | ch2=chch2 | Η | Η | cf2ci | B24 |
A115 | CH3SO2N(CH3) | Η | Η | cf2ci | B24 |
A116 | <ch3)2n | Η | Η | cf2ci | B24 |
A117 | (CH3)2NSO2 | Η | Η | cf2ci | B24 |
A118 | cich2 | Η | Η | cf2ci | B24 |
A119 | ch3sch2 | Η | Η | cf2ci | B24 |
A120 | ch3soch2 | Η | Η | cf2ci | B24 |
A121 | ch3so2ch2 | Η | Η | cf2ci | B24 |
A122 | [1,2,4]-triazol-1yl-methyl | Η | Η | cf2ci | B24 |
A123 | H | Η | Η | chf2 | B24 |
A124 | ch3 | Η | Η | chf2 | B24 |
A125 | ch3ch2 | Η | Η | chf2 | B24 |
A126 | cyklopropyl | Η | Η | chf2 | B24 |
A127 | (CH3)3C | Η | Η | chf2 | B24 |
A128 | (CH3)2CH | Η | Η | chf2 | B24 |
A129 | ch3(ch2)2 | Η | Η | chf2 | B24 |
A130 | ch3och2 | Η | Η | chf2 | B24 |
A131 | CH3O(CH2)2 | Η | Η | chf2 | B24 |
A132 | Ph | Η | Η | chf2 | B24 |
A133 | PhO | Η | Η | chf2 | B24 |
A134 | PhS | Η | Η | chf2 | B24 |
A135 | PhSO | Η | Η | chf2 | B24 |
A136 | PhSO2 | Η | Η | chf2 | B24 |
A137 | CH3S | Η | Η | chf2 | B24 |
A138 | ch3so | Η | Η | chf2 | B24 |
A139 | cf3 | Η | Η | chf2 | B24 |
A140 | f2ch | Η | Η | chf2 | B24 |
A141 | HCC | Η | Η | chf2 | B24 |
A142 | CH3CC | Η | Η | chf2 | B24 |
A143 | ch2=ch | Η | Η | chf2 | B24 |
A144 | ch2=chch2 | Η | Η | chf2 | B24 |
A145 | CH3SO2N(CH3) | Η | Η | chf2 | B24 |
A146 | (CH3)2N | Η | Η | chf2 | B24 |
A147 | (CH3)2NSO2 | Η | Η | chf2 | B24 |
A148 | C1CH2 | Η | Η | chf2 | B24 |
A149 | CH3SCH2 | Η | Η | chf2 | B24 |
A150 | ch3soch2 | Η | Η | chf2 | B24 |
A151 | ch3so2ch2 | Η | Η | chf2 | B24 |
A152 | [1,2,4]-triazol-1- | Η | Η | chf2 | B24 |
yl-methyl
-88CZ 304537 B6
Sl. | R92 | R93 | R94 | R95 | q3 |
č. A153 | H | Η | H | CC13 | B24 |
A154 | ch3 | H | H | CC13 | B24 |
A155 | ch3ch2 | H | H | CC13 | B24 |
A156 | cyklopropyl | H | H | CC13 | B24 |
A157 | (CH3)3C | H | H | CC13 | B24 |
A158 | (CH3)2CH | H | H | CC13 | B24 |
A159 | CH3(CH2)2 | H | H | CC13 | B24 |
A160 | ch3och2 | H | H | CC13 | B24 |
A161 | CH3O(CH2)2 | H | H | CC13 | B24 |
A162 | Ph | H | H | CC13 | B24 |
A163 | PhO | H | H | CC13 | B24 |
A164 | PhS | H | H | CC13 | B24 |
A165 | PhSO | H | H | CC13 | B24 |
A166 | PhSO2 | H | H | CC13 | B24 |
A167 | ch3s | H | H | CC13 | B24 |
A168 | ch3so | H | H | CC13 | B24 |
A169 | cf3 | H | H | CC13 | B24 |
A170 | f2ch | H | H | CC13 | B24 |
A171 | HCC | H | H | CC13 | B24 |
A172 | ch3cc | H | H | CC13 | B24 |
A173 | ch2=ch | H | H | CC13 | B24 |
A174 | ch2=chch2 | H | H | CC13 | B24 |
A175 | CH3SO2N (CH3) | H | H | CC13 | B24 |
A176 | (CH3)2N | H | H | CC13 | B24 |
A177 | (CH3)2NSO2 | H | H | CC13 | B24 |
A178 | cich2 | H | H | CC13 | B24 |
A179 | ch3sch2 | H | H | CC13 | B24 |
A180 | ch3soch2 | H | H | CC13 | B24 |
A181 | ch3so2ch2 | H | H | CC13 | B24 |
A182 | [1,2,4]-triazol-1yl-methyl | H | H | CC13 | B24 |
A183 | H | H | ch3 | cf3 | B24 |
A184 | ch3 | H | ch3 | cf3 | B24 |
A185 | ch3ch2 | H | ch3 | cf3 | B24 |
A186 | cyklopropyl | H | ch3 | cf3 | B24 |
A187 | (CH3)3C | H | ch3 | cf3 | B24 |
A188 | (CH3)2CH | H | ch3 | cf3 | B24 |
A189 | CH3(CH2)2 | H | ch3 | cf3 | B24 |
A190 | ch3och2 | H | ch3 | cf3 | B24 |
A191 | CH3O(CH2)2 | H | ch3 | cf3 | B24 |
A192 | Ph | H | ch3 | cf3 | B24 |
A193 | PhO | H | ch3 | cf3 | B24 |
A194 | PhS | H | ch3 | cf3 | B24 |
A195 | PhSO | H | ch3 | cf3 | B24 |
A196 | PhSO2 | H | ch3 | cf3 | B24 |
A197 | ch3s | H | ch3 | cf3 | B24 |
A198 | ch3so | H | ch3 | cf3 | B24 |
A199 | cf3 | H | ch3 | cf3 | B24 |
A200 | f2ch | H | ch3 | cf3 | B24 |
89CZ 304537 B6
Sl. % | R92 | R93 | R94 | R95 | q3 |
c · A201 | HCC | H | CH3 | cf3 | B24 |
A202 | CH3CC | H | ch3 | cf3 | B24 |
A203 | ch2=ch | H | ch3 | cf3 | B24 |
A204 | ch2=chch2 | H | ch3 | cf3 | B24 |
A205 | CH3SO2N(CH3) | H | ch3 | cf3 | B24 |
A206 | (CH3)2N | H | ch3 | cf3 | B24 |
A207 | (CH3)2NSO2 | H | ch3 | cf3 | B24 |
A208 | cich2 | H | ch3 | cf3 | B24 |
A209 | ch3sch2 | H | ch3 | cf3 | B24 |
A210 | ch3soch2 | H | ch3 | cf3 | B24 |
A211 | ch3so2ch2 | H | ch3 | cf3 | B24 |
A212 | H | H | ch3 | CF3CF2 | B24 |
A213 | ch3 | H | ch3 | cf3cf2 | B24 |
A214 | ch3ch2 | H | ch3 | cf3cf2 | B24 |
A215 | cyklopropyl | H | ch3 | cf3cf2 | B24 |
A216 | (CH3)3C | H | ch3 | cf3cf2 | B24 |
A217 | (CH3)2CH | H | ch3 | cf3cf2 | B24 |
A218 | CH3(CH2)2 | H | ch3 | cf3cf2 | B24 |
A219 | ch3och2 | H | ch3 | CF3CF2 | B24 |
A220 | CH3O(CH2)2 | H | ch3 | cf3cf2 | B24 |
A221 | Ph | H | ch3 | cf3cf2 | B24 |
A222 | PhO | H | ch3 | cf3cf2 | B24 |
A223 | PhS | H | ch3 | cf3cf2 | B24 |
A224 | PhSO | H | ch3 | cf3cf2 | B24 |
A225 | PhSO2 | H | ch3 | cf3cf2 | B24 |
A226 | CH3S | H | ch3 | cf3cf2 | B24 |
A227 | ch3so | H | ch3 | cf3cf2 | B24 |
A228 | cf3 | H | ch3 | cf3cf2 | B24 |
A229 | f2ch | H | ch3 | cf3cf2 | B24 |
A230 | HCC | H | ch3 | cf3cf2 | B24 |
A231 | ch3cc | H | ch3 | cf3cf2 | B24 |
A232 | ch2=ch | H | ch3 | cf3cf2 | B24 |
A233 | ch2=chch2 | H | ch3 | cf3cf2 | B24 |
A234 | CH3SO2N(CH3) | H | ch3 | cf3cf2 | B24 |
A235 | (CH3)2N | H | ch3 | cf3cf2 | B24 |
A236 | (CH3)2NSO2 | H | ch3 | cf3cf2 | B24 |
A237 | cich2 | H | ch3 | cf3cf2 | B24 |
A238 | ch3sch2 | H | ch3 | cf3cf2 | B24 |
A239 | ch3soch2 | H | ch3 | cf3cf2 | B24 |
A240 | ch3so2ch2 | H | ch3 | cf3cf2 | B24 |
A241 | H | H | ch3 | cf3cf2cf2 | B24 |
A242 | ch3 | H | ch3 | cf3cf2cf2 | B24 |
A243 | ch3ch2 | H | ch3 | cf3cf2cf2 | B24 |
A244 | cyklopropyl | H | ch3 | cf3cf2cf2 | B24 |
A245 | (CH3)3C | H | ch3 | cf3cf2cf2 | B24 |
A246 | (CH3)2CH | H | ch3 | cf3cf2cf2 | B24 |
A247 | ch3(ch2)2 | H | ch3 | cf3cf2cf2 | B24 |
A248 | ch3och2 | H | ch3 | cf3cf2cf2 | B24 |
A249 | CH30(CH2)2 | H | ch3 | cf3cf2cf2 | B24 |
-90CZ 304537 B6
Sl. | R92 | R93 | R94 | R95 | q3 |
c - A250 | Ph | Η | ch3 | cf3cf2cf2 | B24 |
A251 | PhO | H | ch3 | cf3cf2cf2 | B24 |
A252 | PhS | H | ch3 | cf3cf2cf2 | B24 |
A253 | PhSO | H | ch3 | cf3cf2cf2 | B24 |
A254 | PhSO2 | H | ch3 | cf3cf2cf2 | B24 |
A255 | CH3S | H | ch3 | cf3cf2cf2 | B24 |
A256 | ch3so | H | ch3 | cf3cf2cf2 | B24 |
A257 | cf3 | H | ch3 | CF3CF2CF2 | B24 |
A258 | f2ch | H | ch3 | CF3CF2CF2 | B24 |
A259 | HCC | H | ch3 | cf3cf2cf2 | B24 |
A260 | CH3CC | H | ch3 | cf3cf2cf2 | B24 |
A261 | ch2=ch | H | ch3 | cf3cf2cf2 | B24 |
A262 | ch2=chch2 | H | ch3 | cf3cf2cf2 | B24 |
A263 | CH3SO2N{CH3) | H | ch3 | cf3cf2cf2 | B24 |
A264 | (CH3)2N | H | ch3 | cf3cf2cf2 | B24 |
A265 | (CH3)2NSO2 | H | ch3 | cf3cf2cf2 | B24 |
A266 | cich2 | H | ch3 | cf3cf2cf2 | B24 |
A267 | ch3sch2 | H | ch3 | cf3cf2cf2 | B24 |
A268 | ch3soch2 | H | ch3 | cf3cf2cf2 | B24 |
A269 | ch3so2ch2 | H | ch3 | cf3cf2cf2 | B24 |
A270 | H | H | ch3 | CFzCl | B24 |
A271 | ch3 | H | ch3 | CF2C1 | B24 |
A272 | ch3ch2 | H | ch3 | cf2ci | B24 |
A273 | cyklopropyl | H | ch3 | cf2ci | B24 |
A274 | (CH3)3C | H | ch3 | cf2ci | B24 |
A275 | (CH3)2CH | H | ch3 | cf2ci | B24 |
A276 | ch3(ch2)2 | H | ch3 | CFzCl | B24 |
A277 | ch3och2 | H | ch3 | CF2C1 | B24 |
A278 | CH3O(CH2)2 | H | ch3 | CF2C1 | B24 |
A279 | Ph | H | ch3 | cf2ci | B24 |
A280 | PhO | H | ch3 | CF2C1 | B24 |
A281 | PhS | H | ch3 | CF2C1 | B24 |
A282 | PhSO | H | ch3 | cf2ci | B24 |
A283 | PhSO2 | H | ch3 | cf2ci | B24 |
A284 | ch3s | H | ch3 | cf2ci | B24 |
A285 | ch3so | H | ch3 | CF2C1 | B24 |
A286 | cf3 | H | ch3 | CFzCl | B24 |
A287 | f2ch | H | ch3 | CF2C1 | B24 |
A288 | HCC | H | ch3 | CF2C1 | B24 |
A289 | CH3CC | H | ch3 | cf2ci | B24 |
A290 | ch2=ch | H | ch3 | cf2ci | B24 |
A291 | ch2=chch2 | H | ch3 | cf2ci | B24 |
A292 | CH3SO2N(CH3) | H | ch3 | cf2ci | B24 |
A293 | (CH3)2N | H | ch3 | cf2ci | B24 |
A294 | (CH3)2NSO2 | H | ch3 | cf2ci | B24 |
A295 | CICHz | H | ch3 | CF2C1 | B24 |
A296 | CH3SCH2 | H | ch3 | CF2C1 | B24 |
A297 | ch3soch2 | H | ch3 | CF2C1 | B24 |
A298 | ch3so2ch2 | H | ch3 | CFzCl | B24 |
-91 CZ 304537 B6
Sl. | Rg2 | R93 | R94 | R95 | q3 |
č. A299 | H | H | ch3 | chf2 | B24 |
A300 | ch3 | H | ch3 | chf2 | B24 |
A301 | CH3CH2 | H | ch3 | chf2 | B24 |
A302 | cyklopropyl | H | ch3 | chf2 | B24 |
A303 | (CH3)3C | H | ch3 | chf2 | B24 |
A304 | (CH3)2CH | H | ch3 | chf2 | B24 |
A305 | CH3(CH2)2 | H | ch3 | chf2 | B24 |
A306 | CH3OCH2 | H | ch3 | chf2 | B24 |
A307 | CH3O(CH2)2 | H | ch3 | chf2 | B24 |
A308 | Ph | H | ch3 | chf2 | B24 |
A309 | PhO | H | ch3 | chf2 | B24 |
A310 | PhS | H | ch3 | chf2 | B24 |
A311 | PhSO | H | ch3 | chf2 | B24 |
A312 | PhSO2 | H | ch3 | chf2 | B24 |
A313 | ch3s | H | ch3 | chf2 | B24 |
A314 | ch3so | H | ch3 | chf2 | B24 |
A315 | cf3 | H | ch3 | chf2 | B24 |
A316 | f2ch | H | ch3 | chf2 | B24 |
A317 | HCC | H | ch3 | chf2 | B24 |
A318 | ch3cc | H | ch3 | chf2 | B24 |
A319 | ch2=ch | H | ch3 | chf2 | B24 |
A320 | ch2=chch2 | H | ch3 | chf2 | B24 |
A321 | CH3SO2N(CH3) | H | ch3 | chf2 | B24 |
A322 | (CH3)2N | H | ch3 | chf2 | B24 |
A323 | (CH3)2NSO2 | H | ch3 | chf2 | B24 |
A324 | cich2 | H | ch3 | chf2 | B24 |
A325 | ch3sch2 | H | ch3 | chf2 | B24 |
A326 | ch3soch2 | H | ch3 | chf2 | B24 |
A327 | ch3so2ch2 | H | ch3 | chf2 | B24 |
A328 | H | H | ch3 | CC13 | B24 |
A329 | CH3 | H | ch3 | CC13 | B24 |
A330 | ch3ch2 | H | ch3 | CC13 | B24 |
A331 | (CH3)3C | H | ch3 | CC13 | B24 |
A332 | (CH3)2CH | H | ch3 | CC13 | B24 |
A333 | cyklopropyl | H | ch3 | CC13 | B24 |
A334 | CH3(CH2)2 | H | ch3 | CC13 | B24 |
A335 | ch3och2 | H | ch3 | CC13 | B24 |
A336 | CH3O(CH2)2 | H | ch3 | CC13 | B24 |
A337 | Ph | H | ch3 | CC13 | B24 |
A338 | PhO | H | ch3 | CC13 | B24 |
A339 | PhS | H | ch3 | CC13 | B24 |
A340 | PhSO | H | ch3 | CC13 | B24 |
A341 | PhSO2 | H | ch3 | CC13 | B24 |
A342 | ch3s | H | ch3 | CC13 | B24 |
A343 | ch3so | H | ch3 | CC13 | B24 |
A344 | cf3 | H | ch3 | CC13 | B24 |
A345 | f2ch | H | ch3 | CC13 | B24 |
A346 | HCC | H | ch3 | CC13 | B24 |
A347 | ch3cc | H | ch3 | CC13 | B24 |
92CZ 304537 B6
Sl. | R92 | R93 | R94 | R95 | q3 |
č. A348 | ch2=ch | Η | ch3 | CC13 | B24 |
A349 | ch2=chch2 | H | ch3 | CC13 | B24 |
A350 | CH3SO2N(CH3) | H | ch3 | cci3 | B24 |
A351 | (CH3)2N | H | ch3 | CC13 | B24 |
A352 | (CH3)2NSO2 | H | ch3 | CC13 | B24 |
A353 | cich2 | H | ch3 | CC13 | B24 |
A354 | ch3sch2 | H | ch3 | CC13 | B24 |
A355 | ch3soch2 | H | ch3 | CC13 | B24 |
A356 | ch3so2ch2 | H | ch3 | CC13 | B24 |
A357 | H | H | Ph | cf3 | B24 |
A358 | ch3 | H | Ph | cf3 | B24 |
A359 | ch3ch2 | H | Ph | cf3 | B24 |
A360 | cyklopropyl | H | Ph | cf3 | B24 |
A361 | (CH3)3C | H | Ph | cf3 | B24 |
A362 | (CH3)2CH | H | Ph | cf3 | B24 |
A363 | ch3(ch2)2 | H | Ph | cf3 | B24 |
A364 | ch3och2 | H | Ph | cf3 | B24 |
A365 | CH3O(CH2)2 | H | Ph | cf3 | B24 |
A366 | Ph | H | Ph | cf3 | B24 |
A367 | PhO | H | Ph | cf3 | B24 |
A368 | PhS | H | Ph | cf3 | B24 |
A369 | PhSO | H | Ph | cf3 | B24 |
A370 | PhSO2 | H | Ph | cf3 | B24 |
A371 | ch3s | H | Ph | cf3 | B24 |
A372 | ch3so | H | Ph | cf3 | B24 |
A373 | cf3 | H | Ph | cf3 | B24 |
A374 | f2ch | H | Ph | cf3 | B24 |
A375 | HCC | H | Ph | cf3 | B24 |
A376 | ch3cc | H | Ph | cf3 | B24 |
A377 | ch2=ch | H | Ph | cf3 | B24 |
A378 | ch2=chch2 | H | Ph | cf3 | B24 |
A379 | CH3SO2N(CH3) | H | Ph | cf3 | B24 |
A380 | (CH3)2N | H | Ph | cf3 | B24 |
A381 | (CH3)2NSO2 | H | Ph | cf3 | B24 |
A382 | cich2 | H | Ph | cf3 | B24 |
A383 | ch3sch2 | H | Ph | cf3 | B24 |
A384 | ch3soch2 | H | Ph | cf3 | B24 |
A385 | ch3so2ch2 | H | Ph | cf3 | B24 |
A386 | H | H | Ph | cf3cf2 | B24 |
A387 | ch3 | H | Ph | cf3cf2 | B24 |
A388 | ch3ch2 | H | Ph | cf3cf2 | B24 |
A389 | cyklopropyl | H | Ph | cf3cf2 | B24 |
A390 | (CH3)3c | H | Ph | cf3cf2 | B24 |
A391 | (CH3)2CH | H | Ph | cf3cf2 | B24 |
A392 | CH3(CH2)2 | H | Ph | cf3cf2 | B24 |
A393 | ch3och2 | H | Ph | cf3cf2 | B24 |
A394 | CH3O(CH2)2 | H | Ph | cf3cf2 | B24 |
A395 | Ph | H | Ph | cf3cf2 | B24 |
A396 | PhO | H | Ph | cf3cf2 | B24 |
-93CZ 304537 B6
Sl. | R92 | R93 | R94 | R95 | q3 |
C · A397 | PhS | H | Ph | cf3cf2 | B24 |
A398 | PhSO | H | Ph | cf3cf2 | B24 |
A399 | PhSO2 | H | Ph | cf3cf2 | B24 |
A400 | CH3S | H | Ph | cf3cf2 | B24 |
A401 | ch3so | H | Ph | cf3cf2 | B24 |
A402 | cf3 | H | Ph | cf3cf2 | B24 |
A403 | f2ch | H | Ph | cf3cf2 | B24 |
A404 | HCC | H | Ph | cf3cf2 | B24 |
A405 | ch3cc | H | Ph | cf3cf2 | B24 |
A406 | ch2=ch | H | Ph | cf3cf2 | B24 |
A407 | ch2=chch2 | H | Ph | cf3cf2 | B24 |
A4O8 | CH3S02N(CH3) | H | Ph | cf3cf2 | B24 |
A409 | (CH3)2N | H | Ph | cf3cf2 | B24 |
A41O | (CH3)2NSO2 | H | Ph | cf3cf2 | B24 |
A411 | cich2 | H | Ph | cf3cf2 | B24 |
A412 | ch3sch2 | H | Ph | cf3cf2 | B24 |
A413 | ch3soch2 | H | Ph | cf3cf2 | B24 |
A414 | ch3so2ch2 | H | Ph | cf3cf2 | B24 |
A415 | H | H | Ph | cf3cf2cf2 | B24 |
A416 | ch3 | H | Ph | cf3cf2cf2 | B24 |
A417 | ch3ch2 | H | Ph | cf3cf2cf2 | B24 |
A418 | cyklopropyl | H | Ph | cf3cf2cf2 | B24 |
A419 | (CH3)3C | H | Ph | cf3cf2cf2 | B24 |
A420 | (CH3)2CH | H | Ph | cf3cf2cf2 | B24 |
A421 | ch3(ch2)2 | H | Ph | cf3cf2cf2 | B24 |
A422 | ch3och2 | H | Ph | cf3cf2cf2 | B24 |
A423 | CH3O(CH2)2 | H | Ph | CF3CF2CF2 | B24 |
A424 | Ph | H | Ph | cf3cf2cf2 | B24 |
A425 | PhO | H | Ph | cf3cf2cf2 | B24 |
A426 | PhS | H | Ph | cf3cf2cf2 | B24 |
A427 | PhSO | H | Ph | cf3cf2cf2 | B24 |
A428 | PhSO2 | H | Ph | cf3cf2cf2 | B24 |
A429 | CH3S | H | Ph | cf3cf2cf2 | B24 |
A430 | ch3so | H | Ph | cf3cf2cf2 | B24 |
A431 | cf3 | H | Ph | cf3cf2cf2 | B24 |
A432 | f2ch | H | Ph | cf3cf2cf2 | B24 |
A433 | HCC | H | Ph | cf3cf2cf2 | B24 |
A434 | ch3cc | H | Ph | cf3cf2cf2 | B24 |
A435 | ch2=ch | H | Ph | cf3cf2cf2 | B24 |
A436 | ch2=chch2 | H | Ph | cf3cf2cf2 | B24 |
A437 | CH3S02N(CH3) | H | Ph | cf3cf2cf2 | B24 |
A438 | (CH3)2N | H | Ph | cf3cf2cf2 | B24 |
A439 | (CH3)2NSO2 | H | Ph | cf3cf2cf2 | B24 |
A440 | cich2 | H | Ph | cf3cf2cf2 | B24 |
A441 | ch3sch2 | H | Ph | cf3cf2cf2 | B24 |
A442 | ch3soch2 | H | Ph | cf3cf2cf2 | B24 |
A443 | ch3so2ch2 | H | Ph | cf3cf2cf2 | B24 |
A444 | H | H | Ph | cf2ci | B24 |
A445 | ch3 | H | Ph | cf2ci | B24 |
-94CZ 304537 B6
Sl. X | R92 | R93 | R94 | R95 | q3 |
c · A446 | CH3CH2 | H | Ph | cf2ci | B24 |
A447 | cyklopropyl | H | Ph | cf2ci | B24 |
A448 | (CH3)3C | H | Ph | cf2ci | B24 |
A449 | (CH3)2CH | H | Ph | cf2ci | B24 |
A450 | CH3(CH2)2 | H | Ph | cf2ci | B24 |
A451 | CH3OCH2 | H | Ph | cf2ci | B24 |
A452 | CH3O(CH2)2 | H | Ph | cf2ci | B24 |
A453 | Ph | H | Ph | cf2ci | B24 |
A454 | PhO | H | Ph | CF2C1 | B24 |
A455 | PhS | H | Ph | CF2C1 | B24 |
A456 | PhSO | H | Ph | cf2ci | B24 |
A457 | PhSO2 | H | Ph | CF2C1 | B24 |
A458 | CH3S | H | Ph | CF2C1 | B24 |
A459 | ch3so | H | Ph | cf2ci | B24 |
A460 | cf3 | H | Ph | cf2ci | B24 |
A461 | f2ch | H | Ph | cf2ci | B24 |
A462 | HCC | H | Ph | cf2ci | B24 |
A463 | CH3CC | H | Ph | cf2ci | B24 |
A4 64 | CH2=CH | H | Ph | cf2ci | B24 |
A465 | ch2=chch2 | H | Ph | cf2ci | B24 |
A466 | CH3SO2N(CH3) | H | Ph | cf2ci | B24 |
A467 | <ch3)2n | H | Ph | cf2ci | B24 |
A468 | (CH3)2NSO2 | H | Ph | cf2ci | B24 |
A469 | cich2 | H | Ph | cf2ci | B24 |
A470 | ch3sch2 | H | Ph | cf2ci | B24 |
A471 | ch3soch2 | H | Ph | cf2ci | B24 |
A472 | ch3so2ch2 | H | Ph | cf2ci | B24 |
A473 | Η | H | Ph | chf2 | B24 |
A474 | ch3 | H | Ph | chf2 | B24 |
A475 | ch3ch2 | H | Ph | chf2 | B24 |
A476 | cyklopropyl | H | Ph | chf2 | B24 |
A477 | (CH3)3C | H | Ph | chf2 | B24 |
A478 | (CH3)2CH | H | Ph | chf2 | B24 |
A479 | CH3(CH2)2 | H | Ph | chf2 | B24 |
A480 | ch3och2 | H | Ph | chf2 | B24 |
A481 | CH30(CH2)2 | H | Ph | chf2 | B24 |
A482 | Ph | H | Ph | chf2 | B24 |
A483 | PhO | H | Ph | chf2 | B24 |
A484 | PhS | H | Ph | chf2 | B24 |
A485 | PhSO | H | Ph | chf2 | B24 |
A486 | PhSO2 | H | Ph | chf2 | B24 |
A487 | ch3s | H | Ph | chf2 | B24 |
A488 | CH3SO | H | Ph | chf2 | B24 |
A489 | cf3 | H | Ph | chf2 | B24 |
A490 | f2ch | H | Ph | chf2 | B24 |
A491 | HCC | H | Ph | chf2 | B24 |
A492 | CH3CC | H | Ph | chf2 | B24 |
A493 | ch2=ch | H | Ph | chf2 | B24 |
A494 | ch2=chch2 | H | Ph | chf2 | B24 |
95CZ 304537 B6
Sl. | R92 | R93 | R94 | R95 | q3 |
c. A495 | CH3SO2N (CH3) | H | Ph | CHF2 | B24 |
A496 | (CH3)2N | H | Ph | chf2 | B24 |
A497 | (CH3)2NSO2 | H | Ph | cbf2 | B24 |
A498 | cich2 | H | Ph | chf2 | B24 |
A499 | ch3sch2 | H | Ph | chf2 | B24 |
A500 | ch3soch2 | H | Ph | chf2 | B24 |
A501 | ch3so2ch2 | H | Ph | chf2 | B24 |
A502 | H | H | Ph | CC13 | B24 |
A503 | ch3 | H | Ph | CC13 | B24 |
A504 | ch3ch2 | H | Ph | CC13 | B24 |
A505 | cyklopropyl | H | Ph | CC13 | B24 |
A506 | (CH3)3C | H | Ph | CC13 | B24 |
A507 | (CH3)2CH | H | Ph | CC13 | B24 |
A508 | ch3(ch2)2 | H | Ph | CC13 | B24 |
A509 | ch3och2 | H | Ph | CC13 | B24 |
A510 | CH3O(CH2)2 | H | Ph | CC13 | B24 |
A511 | Ph | H | Ph | CC13 | B24 |
A512 | PhO | H | Ph | CC13 | B24 |
A513 | PhS | H | Ph | CC13 | B24 |
A514 | PhSO | H | Ph | CC13 | B24 |
A515 | PhSO2 | H | Ph | CC13 | B24 |
A516 | CH3S | H | Ph | CC13 | B24 |
A517 | ch3so | H | Ph | CC13 | B24 |
A518 | cf3 | H | Ph | CC13 | B24 |
A519 | f2ch | H | Ph | CC13 | B24 |
A520 | HCC | H | Ph | CC13 | B24 |
A521 | CH3CC | H | Ph | CC13 | B24 |
A522 | ch2=ch | H | Ph | CC13 | B24 |
A523 | ch2=chch2 | H | Ph | CC13 | B24 |
A524 | CH3SO2N(CH3) | H | Ph | CC13 | B24 |
A525 | (CH3)2N | H | Ph | CC13 | B24 |
A526 | (CH3)2NSO2 | H | Ph | CC13 | B24 |
A527 | cich2 | H | Ph | CC13 | B24 |
A528 | ch3sch2 | H | Ph | CC13 | B24 |
A529 | CH3SOCH2 | H | Ph | CC13 | B24 |
A530 | ch3so2ch2 | H | Ph | CC13 | B24 |
A531 | Η | ch3 | H | CF3 | B24 |
A532 | H | ch3ch2 | H | cf3 | B24 |
A533 | H | cyklopropyl | H | cf3 | B24 |
A534 | H | (CH3)3CH | H | cf3 | B24 |
A535 | H | (CH3)2CH | H | cf3 | B24 |
A536 | H | CH3(CH2)2 | H | cf3 | B24 |
A537 | H | ch3och2 | H | cf3 | B24 |
A538 | H | CH3O(CH2)2 | H | cf3 | B24 |
A539 | H | Ph | H | cf3 | B24 |
A540 | H | PhO | H | cf3 | B24 |
A541 | H | PhS | H | cf3 | B24 |
A542 | H | PhSO | H | cf3 | B24 |
A543 | H | PhSO2 | H | cf3 | B24 |
-96CZ 304537 B6
Sl. X | R92 | R93 | R94 | R95 | q3 |
· A544 | H | ch3s | Η | cf3 | B24 |
A545 | H | ch3so | H | cf3 | B24 |
A546 | H | cf3 | H | cf3 | B24 |
A547 | H | f2ch | H | cf3 | B24 |
A548 | H | HCC | H | cf3 | B24 |
A549 | H | ch3cc | Η | cf3 | B24 |
A550 | H | ch2=ch | Η | cf3 | B24 |
A551 | H | ch2=chch2 | Η | cf3 | B24 |
A552 | H | CH3SO2N (CH3) | Η | cf3 | B24 |
A553 | H | (ch3)2n | Η | cf3 | B24 |
A554 | H | (CH3)2NSO2 | Η | cf3 | B24 |
A555 | H | ch3sch2 | Η | cf3 | B24 |
A556 | H | ch3soch2 | Η | cf3 | B24 |
A557 | H | ch3so2ch2 | Η | cf3 | B24 |
A558 | H | ch3 | Η | cf3cf2 | B24 |
A559 | H | ch3ch2 | Η | cf3cf2 | B24 |
A560 | H | cyklopropyl | Η | cf3cf2 | B24 |
A561 | H | (CH3)3C | Η | cf3cf2 | B24 |
A562 | H | (CH3)2CH | Η | cf3cf2 | B24 |
A563 | H | ch3(ch2)2 | Η | cf3cf2 | B24 |
A564 | H | ch3och2 | Η | cf3cf2 | B24 |
A565 | H | CH3O(CH2)2 | Η | cf3cf2 | B24 |
A566 | H | Ph | Η | cf3cf2 | B24 |
A567 | H | PhO | Η | cf3cf2 | B24 |
A568 | H | PhS | Η | cf3cf2 | B24 |
A569 | H | PhSO | Η | cf3cf2 | B24 |
A570 | H | PhSO2 | Η | cf3cf2 | B24 |
A571 | H | CH3S | Η | cf3cf2 | B24 |
A572 | H | ch3so | Η | cf3cf2 | B24 |
A573 | H | cf3 | Η | cf3cf2 | B24 |
A574 | H | f2ch | Η | cf3cf2 | B24 |
A575 | H | HCC | Η | cf3cf2 | B24 |
A576 | H | ch3cc | Η | cf3cf2 | B24 |
A577 | H | ch2=ch | Η | cf3cf2 | B24 |
A578 | H | ch2=chch2 | Η | cf3cf2 | B24 |
A579 | H | CH3S02N(CH3) | Η | cf3cf2 | B24 |
A580 | H | (CH3)2N | Η | cf3cf2 | B24 |
A581 | H | (CH3)2NSO2 | Η | cf3cf2 | B24 |
A582 | H | CH3SCH2 | Η | cf3cf2 | B24 |
A583 | H | ch3soch2 | Η | cf3cf2 | B24 |
A584 | H | ch3so2ch2 | Η | CF3CF2 | B24 |
A585 | H | ch3 | Η | cf3cf2cf2 | B24 |
A586 | H | ch3ch2 | Η | cf3cf2cf2 | B24 |
A587 | H | cyklopropyl | Η | cf3cf2cf2 | B24 |
A588 | H | (CH3)3C | Η | cf3cf2cf2 | B24 |
A589 | H | (CH3)2CH | Η | cf3cf2cf2 | B24 |
A590 | H | ch3(ch2)2 | Η | cf3cf2cf2 | B24 |
A591 | H | ch3och2 | Η | cf3cf2cf2 | B24 |
A592 | H | CH3O(CH2)2 | Η | cf3cf2cf2 | B24 |
-97CZ 304537 B6
Sl. Λ | R92 | R93 | R94 | R95 | q3 |
Q·» · A593 | H | Ph | Η | cf3cf2cf2 | B24 |
A594 | H | PhO | H | cf3cf2cf2 | B24 |
A595 | H | PhS | Η | cf3cf2cf2 | B24 |
A596 | H | PhSO | H | cf3cf2cf2 | B24 |
A597 | H | PhSO2 | H | cf3cf2cf2 | B24 |
A598 | H | CH3S | H | cf3cf2cf2 | B24 |
A599 | H | ch3so | H | cf3cf2cf2 | B24 |
A600 | H | cf3 | H | cf3cf2cf2 | B24 |
A601 | H | f2ch | H | cf3cf2cf2 | B24 |
A602 | H | HCC | H | cf3cf2cf2 | B24 |
A603 | H | ch3cc | H | cf3cf2cf2 | B24 |
A604 | H | ch2=ch | H | cf3cf2cf2 | B24 |
A605 | H | ch2=chch2 | H | cf3cf2cf2 | B24 |
A606 | H | CH3SO2N(CH3) | H | cf3cf2cf2 | B24 |
A607 | H | (CH3)2N | H | cf3cf2cf2 | B24 |
A608 | H | (CH3)2NSO2 | H | cf3cf2cf2 | B24 |
A609 | H | ch3sch2 | H | cf3cf2cf2 | B24 |
A610 | H | ch3soch2 | H | cf3cf2cf2 | B24 |
A611 | H | ch3so2ch2 | H | cf3cf2cf2 | B24 |
A612 | H | ch3 | H | cf2ci | B24 |
A613 | H | ch3ch2 | H | cf2ci | B24 |
A614 | H | cyklopropyl | H | cf2ci | B24 |
A615 | H | (CH3)3C | H | cf2ci | B24 |
A616 | H | (CH3)2CH | H | CF2C1 | B24 |
A617 | H | ch3(ch2)2 | H | CF2C1 | B24 |
A618 | H | ch3och2 | H | cf2ci | B24 |
A619 | H | CH3O(CH2)2 | H | cf2ci | B24 |
A620 | H | Ph | H | cf2ci | B24 |
A621 | H | PhO | H | cf2ci | B24 |
A622 | H | PhS | H | cf2ci | B24 |
A623 | H | PhSO | H | cf2ci | B24 |
A624 | H | PhSO2 | H | cf2ci | B24 |
A625 | H | ch3s | H | cf2ci | B24 |
A626 | H | ch3so | H | cf2ci | B24 |
A627 | H | cf3 | H | cf2ci | B24 |
A628 | H | f2ch | H | cf2ci | B24 |
A629 | H | HCC | H | CF2C1 | B24 |
A630 | H | ch3cc | H | CF2C1 | B24 |
A631 | H | ch2=ch | H | cf2ci | B24 |
A632 | H | ch2=chch2 | H | cf2ci | B24 |
A633 | H | CH3SO2N(CH3) | H | cf2ci | B24 |
A634 | H | (CH3)2N | H | CF2C1 | B24 |
A635 | H | (CH3)2NSO2 | H | CF2C1 | B24 |
A636 | H | ch3sch2 | H | CF2C1 | B24 |
A637 | H | ch3soch2 | H | CF2C1 | B24 |
A638 | H | ch3so2ch2 | H | CF2C1 | B24 |
A639 | H | ch3 | H | chf2 | B24 |
A640 | H | ch3ch2 | H | chf2 | B24 |
A641 | H | cyklopropyl | H | chf2 | B24 |
-98CZ 304537 B6
Sl. | R92 | R93 | R94 | R95 | q3 |
v · A642 | H | (CH3)3C | H | chf2 | B24 |
A643 | H | (CH3)2CH | H | chf2 | B24 |
A644 | H | ch3(ch2)2 | H | chf2 | B24 |
A645 | H | ch3och2 | H | chf2 | B24 |
A646 | H | CH3O(CH2)2 | H | chf2 | B24 |
A647 | H | Ph | H | chf2 | B24 |
A648 | H | PhO | H | chf2 | B24 |
A649 | H | PhS | H | chf2 | B24 |
A650 | H | PhSO | H | chf2 | B24 |
A651 | H | PhSO2 | H | chf2 | B24 |
A652 | H | CH3S | H | chf2 | B24 |
A653 | H | ch3so | H | chf2 | B24 |
A654 | H | cf3 | H | chf2 | B24 |
A655 | H | f2ch | H | chf2 | B24 |
A656 | H | HCC | H | chf2 | B24 |
A657 | H | CH3CC | H | chf2 | B24 |
A658 | H | ch2=ch | H | chf2 | B24 |
A659 | H | ch2=chch2 | H | chf2 | B24 |
A660 | H | ch3so2n (CH3) | H | chf2 | B24 |
A661 | H | (CH3)2N | H | chf2 | B24 |
A662 | H | (CH3)2NSO2 | H | chf2 | B24 |
A663 | H | ch3sch2 | H | chf2 | B24 |
A664 | H | ch3soch2 | H | chf2 | B24 |
A665 | H | ch3so2ch2 | H | chf2 | B24 |
A666 | H | ch3 | H | CC13 | B24 |
A667 | H | ch3ch2 | H | CC13 | B24 |
A668 | H | cyklopropyl | H | CC13 | B24 |
A669 | H | (CH3)3C | H | CC13 | B24 |
A670 | H | (CH3)2CH | H | CC13 | B24 |
A671 | H | CH3(CH2)2 | H | CC13 | B24 |
A672 | H | ch3och2 | H | CC13 | B24 |
A673 | H | CH3O(CH2)2 | H | CC13 | B24 |
A674 | H | Ph | H | CC13 | B24 |
A675 | H | PhO | H | CC13 | B24 |
A676 | H | PhS | H | CC13 | B24 |
A677 | H | PhSO | H | CC13 | B24 |
A678 | H | PhSO2 | H | CC13 | B24 |
A679 | H | CH3S | H | CC13 | B24 |
A680 | H | ch3so | H | CC13 | B24 |
A681 | H | cf3 | H | CC13 | B24 |
A682 | H | f2ch | H | CC13 | B24 |
A683 | H | HCC | H | CC13 | B24 |
A684 | H | ch3cc | H | CC13 | B24 |
A685 | H | ch2=ch | H | CC13 | B24 |
A686 | H | ch2=chch2 | H | CC13 | B24 |
A687 | H | CH3SO2N{CH3) | H | CC13 | B24 |
A688 | H | (CH3)2N | H | CC13 | B24 |
A689 | H | (CH3)2NSO2 | H | CC13 | B24 |
A690 | H | ch3sch2 | H | CC13 | B24 |
-99CZ 304537 B6
Sl. | R92 | R93 | R94 | R95 | q3 |
č. A691 | H | CH3SOCH2 | H | CC13 | B24 |
A692 | H | CH3SO2CH2 | H | CC13 | B24 |
A693 | H | ch3 | CH3 | cf3 | B24 |
A694 | H | ch3ch2 | ch3 | cf3 | B24 |
A695 | H | cyklopropyl | ch3 | cf3 | B24 |
A696 | H | (CH3)3C | ch3 | cf3 | B24 |
A697 | H | (CH3)2CH | ch3 | cf3 | B24 |
A698 | H | CH3(CH2)2 | ch3 | cf3 | B24 |
A699 | H | ch3och2 | ch3 | cf3 | B24 |
A700 | H | CH3O(CH2)2 | ch3 | cf3 | B24 |
A701 | H | Ph | ch3 | cf3 | B24 |
A702 | H | PhO | ch3 | cf3 | B24 |
A703 | H | PhS | ch3 | cf3 | B24 |
A704 | H | PhSO | ch3 | cf3 | B24 |
A705 | H | PhSO2 | ch3 | cf3 | B24 |
A706 | H | CH3S | ch3 | cf3 | B24 |
A707 | H | ch3so | ch3 | cf3 | B24 |
A708 | H | cf3 | ch3 | cf3 | B24 |
A709 | H | f2ch | ch3 | cf3 | B24 |
A710 | H | HCC | ch3 | cf3 | B24 |
A711 | H | ch3cc | ch3 | cf3 | B24 |
A712 | H | ch2=ch | ch3 | cf3 | B24 |
A713 | H | ch2=chch2 | ch3 | cf3 | B24 |
A714 | H | CH3SO2N (CH3) | ch3 | cf3 | B24 |
A715 | H | (CH3)2N | ch3 | cf3 | B24 |
A716 | H | (CH3)2NSO2 | ch3 | cf3 | B24 |
A717 | H | ch3sch2 | ch3 | cf3 | B24 |
A718 | H | ch3soch2 | ch3 | cf3 | B24 |
A719 | H | CH3SO2CH2 | ch3 | cf3 | B24 |
A720 | H | ch3 | ch3 | cf3cf2 | B24 |
A721 | H | ch3ch2 | ch3 | cf3cf2 | B24 |
A722 | H | cyklopropyl | ch3 | cf3cf2 | B24 |
A723 | H | (CH3)3C | ch3 | cf3cf2 | B24 |
A724 | H | (CH3)2CH | ch3 | cf3cf2 | B24 |
A725 | H | CH3(CH2)2 | ch3 | cf3cf2 | B24 |
A726 | H | ch3och2 | ch3 | cf3cf2 | B24 |
A727 | H | CH30(CH2)2 | ch3 | cf3cf2 | B24 |
A728 | H | Ph | ch3 | cf3cf2 | B24 |
A729 | H | PhO | ch3 | cf3cf2 | B24 |
A730 | H | PhS | ch3 | cf3cf2 | B24 |
A731 | H | PhSO | ch3 | cf3cf2 | B24 |
A732 | H | PhSO2 | ch3 | cf3cf2 | B24 |
A733 | H | CH3S | ch3 | cf3cf2 | B24 |
A734 | H | ch3so | ch3 | cf3cf2 | B24 |
A735 | H | cf3 | ch3 | cf3cf2 | B24 |
A736 | H | f2ch | ch3 | cf3cf2 | B24 |
A737 | H | HCC | ch3 | cf3cf2 | B24 |
A738 | H | ch3cc | ch3 | cf3cf2 | B24 |
A739 | H | ch2=ch | ch3 | cf3cf2 | B24 |
-100CZ 304537 B6
Sl. A | R92 | R93 | R94 | R95 | q3 |
u · A740 | H | ch2=chch2 | CH3 | cf3cf2 | B24 |
A741 | H | CH3SO2N(CH3) | ch3 | cf3cf2 | B24 |
A742 | H | (CH3)2N | ch3 | cf3cf2 | B24 |
A743 | H | (CH3)2NSO2 | ch3 | cf3cf2 | B24 |
A744 | H | ch3sch2 | ch3 | cf3cf2 | B24 |
A745 | H | ch3soch2 | ch3 | cf3cf2 | B24 |
A746 | H | ch3so2ch2 | ch3 | cf3cf2 | B24 |
A747 | H | ch3 | ch3 | cf3cf2cf2 | B24 |
A748 | H | ch3ch2 | ch3 | cf3cf2cf2 | B24 |
A749 | H | cyklopropyl | ch3 | cf3cf2cf2 | B24 |
A750 | H | (CH3)3c | ch3 | cf3cf2cf2 | B24 |
A751 | H | (CH3)2CH | ch3 | cf3cf2cf2 | B24 |
A752 | H | ch3(ch2)2 | ch3 | cf3cf2cf2 | B24 |
A753 | H | ch3och2 | ch3 | cf3cf2cf2 | B24 |
A754 | H | CH3O(CH2)2 | ch3 | cf3cf2cf2 | B24 |
A755 | H | Ph | ch3 | cf3cf2cf2 | B24 |
A756 | H | PhO | ch3 | cf3cf2cf2 | B24 |
A757 | H | PhS | ch3 | cf3cf2cf2 | B24 |
A758 | H | PhSO | ch3 | cf3cf2cf2 | B24 |
A759 | H | PhSO2 | ch3 | cf3cf2cf2 | B24 |
A760 | H | ch3s | ch3 | cf3cf2cf2 | B24 |
A761 | H | CH3S0 | ch3 | cf3cf2cf2 | B24 |
A762 | H | cf3 | ch3 | cf3cf2cf2 | B24 |
A763 | H | f2ch | ch3 | cf3cf2cf2 | B24 |
A764 | H | HCC | ch3 | CF3CF2CF2 | B24 |
A765 | H | CH3CC | ch3 | cf3cf2cf2 | B24 |
A766 | H | ch2=ch | ch3 | cf3cf2cf2 | B24 |
A767 | H | ch2=chch2 | ch3 | cf3cf2cf2 | B24 |
A768 | H | CH3SO2N(CH3) | ch3 | cf3cf2cf2 | B24 |
A769 | H | (CH3)2N | ch3 | cf3cf2cf2 | B24 |
A770 | H | (CH3)2NSO2 | ch3 | cf3cf2cf2 | B24 |
A771 | H | ch3sch2 | ch3 | CF3CF2CF2 | B24 |
A772 | H | ch3soch2 | ch3 | CF3CF2CF2 | B24 |
A773 | H | ch3so2ch2 | ch3 | cf3cf2cf2 | B24 |
A774 | H | ch3 | ch3 | cf2ci | B24 |
A775 | H | ch3ch2 | ch3 | cf2ci | B24 |
A776 | H | cyklopropyl | ch3 | cf2ci | B24 |
A777 | H | (CH3)3C | ch3 | cf2ci | B24 |
A778 | H | (CH3)2CH | ch3 | cf2ci | B24 |
A779 | H | ch3(ch2)2 | ch3 | cf2ci | B24 |
A780 | H | ch3och2 | ch3 | cf2ci | B24 |
A781 | H | CH30(CH2)2 | ch3 | cf2ci | B24 |
A782 | H | Ph | ch3 | cf2ci | B24 |
A783 | H | PhO | ch3 | cf2ci | B24 |
A784 | H | PhS | ch3 | cf2ci | B24 |
A785 | H | PhSO | ch3 | cf2ci | B24 |
A786 | H | PhSO2 | ch3 | cf2ci | B24 |
A787 | H | CH3S | ch3 | cf2ci | B24 |
A788 | H | ch3so | ch3 | cf2ci | B24 |
-101 CZ 304537 B6
Sl. Č · | R92 | R93 | R94 | R95 | Qs |
A789 | H | cf3 | ch3 | CF2C1 | B24 |
A790 | H | f2ch | ch3 | cf2ci | B24 |
A791 | H | HCC | ch3 | cf2ci | B24 |
A792 | H | ch3cc | ch3 | cf2ci | B24 |
A793 | H | ch2=ch | ch3 | cf2ci | B24 |
A794 | H | ch2=chch2 | ch3 | cf2ci | B24 |
A795 | H | CH3SO2N(CH3) | ch3 | cf2ci | B24 |
A796 | H | (CH3)2N | ch3 | cf2ci | B24 |
A797 | H | (CH3)2NSO2 | ch3 | cf2ci | B24 |
A798 | H | ch3sch2 | ch3 | cf2ci | B24 |
A799 | H | ch3soch2 | ch3 | cf2ci | B24 |
A800 | H | ch3so2ch2 | ch3 | cf2ci | B24 |
A801 | H | ch3 | ch3 | chf2 | B24 |
A802 | H | ch3ch2 | ch3 | chf2 | B24 |
A803 | H | cyklopropyl | ch3 | chf2 | B24 |
A804 | H | (CH3)3c | ch3 | chf2 | B24 |
A805 | H | (CH3)2CH | ch3 | chf2 | B24 |
A806 | H | ch3(ch2)2 | ch3 | chf2 | B24 |
A807 | H | ch3och2 | ch3 | chf2 | B24 |
A808 | H | CH3O(CH2)2 | ch3 | chf2 | B24 |
A809 | H | Ph | ch3 | chf2 | B24 |
A810 | H | PhO | ch3 | chf2 | B24 |
A811 | H | PhS | ch3 | chf2 | B24 |
A812 | H | PhSO | ch3 | chf2 | B24 |
A813 | H | PhSO2 | ch3 | chf2 | B24 |
A814 | H | ch3s | ch3 | chf2 | B24 |
A815 | H | ch3so | ch3 | chf2 | B24 |
A816 | H | cf3 | ch3 | chf2 | B24 |
A817 | H | f2ch | ch3 | chf2 | B24 |
A818 | H | HCC | ch3 | chf2 | B24 |
A819 | H | CH3CC | ch3 | chf2 | B24 |
A820 | H | ch2=ch | ch3 | chf2 | B24 |
A821 | H | ch2=chch2 | ch3 | chf2 | B24 |
A822 | H | CH3SO2N(CH3) | ch3 | chf2 | B24 |
A823 | H | (CH3)2N | ch3 | chf2 | B24 |
A824 | H | (CH3)2NSO2 | ch3 | chf2 | B24 |
A825 | H | CH3SCH2 | ch3 | chf2 | B24 |
A826 | H | ch3soch2 | ch3 | chf2 | B24 |
A827 | H | ch3so2ch2 | ch3 | chf2 | B24 |
A828 | H | ch3 | ch3 | CC13 | B24 |
A829 | H | ch3ch2 | ch3 | CC13 | B24 |
A830 | H | cyklopropyl | ch3 | CC13 | B24 |
A831 | H | (CH3)3c | ch3 | CC13 | B24 |
A832 | H | (CH3)2CH | ch3 | CC13 | B24 |
A833 | H | ch3(ch2)2 | ch3 | CC13 | B24 |
A834 | H | ch3och2 | ch3 | CC13 | B24 |
A835 | H | CH3O(CH2)2 | ch3 | CC13 | B24 |
A836 | H | Ph | ch3 | CC13 | B24 |
A837 | H | PhO | ch3 | CC13 | B24 |
- 102CZ 304537 B6
Sl. | R92 | R93 | R94 | R95 | q3 |
c. A838 | H | PhS | CH3 | CC13 | B24 |
A839 | H | PhSO | ch3 | CC13 | B24 |
A84O | H | PhSO2 | ch3 | CC13 | B24 |
A841 | H | ch3s | ch3 | CC13 | B24 |
A842 | H | ch3so | ch3 | CC13 | B24 |
A843 | H | cf3 | ch3 | CC13 | B24 |
A844 | H | f2ch | ch3 | CC13 | B24 |
A845 | H | HCC | ch3 | CC13 | B24 |
A846 | H | ch3cc | ch3 | CC1-3 | B24 |
A847 | H | ch2=ch | ch3 | CC13 | B24 |
A848 | H | ch2=chch2 | ch3 | CC13 | B24 |
A849 | H | CH3SO2N(CH3) | ch3 | cc13 | B24 |
A850 | H | (CH3)2N | ch3 | CC13 | B24 |
A851 | H | (CH3)zNSO2 | ch3 | CC13 | B24 |
A852 | H | ch3sch2 | ch3 | CC13 | B24 |
A853 | H | ch3soch2 | ch3 | CC13 | B24 |
A854 | H | ch3so2ch2 | ch3 | CC13 | B24 |
A855 | H | ch3 | Ph | cf3 | B24 |
A856 | H | ch3ch2 | Ph | cf3 | B24 |
A857 | H | (ch3)2ch | Ph | cf3 | B24 |
A858 | H | (ch3)2ch | Ph | cf3 | B24 |
A859 | H | cyklopropyl | Ph | cf3 | B24 |
A860 | H | CH3(CH2)2 | Ph | cf3 | B24 |
A861 | H | ch3och2 | Ph | cf3 | B24 |
A862 | H | CH3O(CH2)z | Ph | cf3 | B24 |
A863 | H | Ph | Ph | cf3 | B24 |
A864 | H | PhO | Ph | cf3 | B24 |
A865 | H | PhS | Ph | cf3 | B24 |
A866 | H | PhSO | Ph | cf3 | B24 |
A867 | H | PhSO2 | Ph | cf3 | B24 |
A868 | H | ch3s | Ph | cf3 | B24 |
A869 | H | CH3SO | Ph | cf3 | B24 |
A870 | H | cf3 | Ph | cf3 | B24 |
A871 | H | f2ch | Ph | cf3 | B24 |
A872 | H | HCC | Ph | cf3 | B24 |
A873 | H | ch3cc | Ph | cf3 | B24 |
A874 | H | ch2=ch | Ph | cf3 | B24 |
A875 | H | ch2=chch2 | Ph | cf3 | B24 |
A876 | H | CH3SO2N(CH3) | Ph | cf3 | B24 |
A877 | H | (CH3)2N | Ph | cf3 | B24 |
A878 | H | (CH3)2NSO2 | Ph | cf3 | B24 |
A879 | H | ch3sch2 | Ph | cf3 | B24 |
A880 | H | ch3soch2 | Ph | cf3 | B24 |
A881 | H | ch3so2ch2 | Ph | cf3 | B24 |
A882 | H | ch3 | Ph | cf3cf2 | B24 |
A883 | H | CH3CH2 | Ph | CF3CF2 | B24 |
A884 | H | cyklopropyl | Ph | cf3cf2 | B24 |
A885 | H | (CH3)3C | Ph | cf3cf2 | B24 |
A886 | H | (CH3)2CH | Ph | cf3cf2 | B24 |
-103CZ 304537 B6
Sl. | R92 | R93 | R94 | R95 | q3 |
Vo · A887 | H | CH3(CH2)2 | Ph | cf3cf2 | B24 |
A888 | H | ch3och2 | Ph | cf3cf2 | B24 |
A889 | H | CH3O(CH2)2 | Ph | cf3cf2 | B24 |
A890 | H | Ph | Ph | cf3cf2 | B24 |
A891 | H | PhO | Ph | cf3cf2 | B24 |
A892 | H | PhS | Ph | cf3cf2 | B24 |
A893 | H | PhSO | Ph | cf3cf2 | B24 |
A894 | H | PhSO2 | Ph | cf3cf2 | B24 |
A895 | H | ch3s | Ph | cf3cf2 | B24 |
A896 | H | ch3so | Ph | cf3cf2 | B24 |
A897 | H | cf3 | Ph | cf3cf2 | B24 |
A898 | H | f2ch | Ph | cf3cf2 | B24 |
A899 | H | HCC | Ph | cf3cf2 | B24 |
A900 | H | ch3cc | Ph | cf3cf2 | B24 |
A901 | H | ch2=ch | Ph | cf3cf2 | B24 |
A902 | H | ch2=chch2 | Ph | cf3cf2 | B24 |
A903 | H | CH3SO2N(CH3) | Ph | cf3cf2 | B24 |
A904 | H | (CH3)2N | Ph | cf3cf2 | B24 |
A905 | H | (CH3)2NSO2 | Ph | cf3cf2 | B24 |
A906 | H | CH3SCH2 | Ph | cf3cf2 | B24 |
A907 | H | CH3SOCH2 | Ph | CF3CF2 | B24 |
A908 | H | ch3so2ch2 | Ph | cf3cf2 | B24 |
A909 | H | ch3 | Ph | cf3cf2cf2 | B24 |
A910 | H | ch3ch2 | Ph | cf3cf2cf2 | B24 |
A911 | H | cyklopropyl | Ph | cf3cf2cf2 | B24 |
A912 | H | (CH3)3C | Ph | cf3cf2cf2 | B24 |
A913 | H | (CH3)2CH | Ph | cf3cf2cf2 | B24 |
A914 | H | CH3(CH2)2 | Ph | cf3cf2cf2 | B24 |
A915 | H | CH3OCH2 | Ph | cf3cf2cf2 | B24 |
A916 | H | CH3O(CH2)2 | Ph | cf3cf2cf2 | B24 |
A917 | H | Ph | Ph | cf3cf2cf2 | B24 |
A918 | H | PhO | Ph | cf3cf2cf2 | B24 |
A919 | H | PhS | Ph | cf3cf2cf2 | B24 |
A920 | H | PhSO | Ph | cf3cf2cf2 | B24 |
A921 | H | PhSO2 | Ph | cf3cf2cf2 | B24 |
A922 | H | CH3S | Ph | cf3cf2cf2 | B24 |
A923 | H | CH3SO | Ph | cf3cf2cf2 | B24 |
A924 | H | cf3 | Ph | cf3cf2cf2 | B24 |
A925 | H | f2ch | Ph | cf3cf2cf2 | B24 |
A926 | H | HCC | Ph | cf3cf2cf2 | B24 |
A927 | H | ch3cc | Ph | cf3cf2cf2 | B24 |
A928 | H | ch2=ch | Ph | cf3cf2cf2 | B24 |
A929 | H | ch2=chch2 | Ph | cf3cf2cf2 | B24 |
A930 | H | CH3SO2N(CH3) | Ph | cf3cf2cf2 | B24 |
A931 | H | (CH3)2N | Ph | cf3cf2cf2 | B24 |
A932 | H | (CH3)2NSO2 | Ph | cf3cf2cf2 | B24 |
A933 | H | ch3sch2 | Ph | cf3cf2cf2 | B24 |
A934 | H | ch3soch2 | Ph | cf3cf2cf2 | B24 |
A935 | H | ch3so2ch2 | Ph | cf3cf2cf2 | B24 |
-104CZ 304537 B6
Sl. X | R92 | R93 | R94 | R95 | Q3 |
· A936 | H | ch3 | Ph | CF2C1 | B24 |
A937 | H | ch3ch2 | Ph | cf2ci | B24 |
A938 | H | cyklopropyl | Ph | CF2C1 | B24 |
A939 | H | (CH3)3C | Ph | CF2C1 | B24 |
A940 | H | (CH3)2CH | Ph | CF2C1 | B24 |
A941 | H | CH3(CH2)2 | Ph | cf2ci | B24 |
A942 | H | ch3och2 | Ph | cf2ci | B24 |
A943 | H | CH3O(CH2)2 | Ph | cf2ci | B24 |
A944 | H | Ph | Ph | cf2ci | B24 |
A945 | H | PhO | Ph | cf2ci | B24 |
A946 | H | PhS | Ph | CF2C1 | B24 |
A947 | H | PhSO | Ph | CF2C1 | B24 |
A948 | H | PhSO2 | Ph | cf2ci | B24 |
A949 | H | CH3S | Ph | cf2ci | B24 |
A950 | H | ch3so | Ph | cf2ci | B24 |
A951 | H | cf3 | Ph | cf2ci | B24 |
A952 | H | f2ch | Ph | cf2ci | B24 |
A953 | H | HCC | Ph | cf2ci | B24 |
A954 | H | ch3cc | Ph | cf2ci | B24 |
A955 | H | ch2=ch | Ph | cf2ci | B24 |
A956 | H | ch2=chch2 | Ph | cf2ci | B24 |
A957 | H | CH3SO2N(CH3) | Ph | cf2ci | B24 |
A958 | H | (CH3)2N | Ph | cf2ci | B24 |
A959 | H | (CH3)2NSO2 | Ph | CF2C1 | B24 |
A960 | H | ch3sch2 | Ph | CF2C1 | B24 |
A961 | H | ch3soch2 | Ph | CF2C1 | B24 |
A962 | H | ch3so2ch2 | Ph | cf2ci | B24 |
A963 | H | ch3 | Ph | chf2 | B24 |
A964 | H | ch3ch2 | Ph | chf2 | B24 |
A965 | H | (CH3)3c | Ph | chf2 | B24 |
A966 | H | (CH3)2CH | Ph | chf2 | B24 |
A967 | H | cyklopropyl | Ph | chf2 | B24 |
A968 | H | CH3(CH2)2 | Ph | chf2 | B24 |
A969 | H | ch3och2 | Ph | chf2 | B24 |
A970 | H | CH3O(CH2)2 | Ph | chf2 | B24 |
A971 | H | Ph | Ph | chf2 | B24 |
A972 | H | PhO | Ph | chf2 | B24 |
A973 | H | PhS | Ph | chf2 | B24 |
A974 | H | PhSO | Ph | chf2 | B24 |
A975 | H | PhSO2 | Ph | chf2 | B24 |
A976 | H | CH3S | Ph | chf2 | B24 |
A977 | H | ch3so | Ph | chf2 | B24 |
A978 | H | cf3 | Ph | chf2 | B24 |
A979 | H | f2ch | Ph | chf2 | B24 |
A980 | H | HCC | Ph | chf2 | B24 |
A981 | H | ch3cc | Ph | chf2 | B24 |
A982 | H | ch2=ch | Ph | chf2 | B24 |
A983 | H | ch2=chch2 | Ph | chf2 | B24 |
A984 | H | CH3SO2N(CH3) | Ph | chf2 | B24 |
-105CZ 304537 B6
Sl. | R92 | R93 | R94 | R95 | q3 |
č. A985 | H | (CH3)2N | Ph | chf2 | B24 |
A986 | H | (CH3)2NSO2 | Ph | chf2 | B24 |
A987 | H | ch3sch2 | Ph | chf2 | B24 |
A988 | H | ch3soch2 | Ph | chf2 | B24 |
A989 | H | ch3so2ch2 | Ph | chf2 | B24 |
A990 | H | ch3 | Ph | cci3 | B24 |
A991 | H | ch3ch2 | Ph | CC13 | B24 |
A992 | H | (CH3)3C | Ph | CC13 | B24 |
A993 | H | (CH3)2CH | Ph | CC13 | B24 |
A994 | H | cyklopropyl | Ph | CC13 | B24 |
A995 | H | CH3(CH2)2 | Ph | CC13 | B24 |
A996 | H | ch3och2 | Ph | CC13 | B24 |
A997 | H | CH3O(CH2)2 | Ph | CC13 | B24 |
A998 | H | Ph | Ph | CC13 | B24 |
A999 | H | PhO | Ph | CC13 | B24 |
A1000 | H | PhS | Ph | CC13 | B24 |
A1001 | H | PhSO | Ph | CC13 | B24 |
A1002 | H | PhSO2 | Ph | CC13 | B24 |
A1003 | H | ch3s | Ph | CC13 | B24 |
A1004 | H | ch3so | Ph | CC13 | B24 |
A1005 | H | cf3 | Ph | CC13 | B24 |
A1006 | H | f2ch | Ph | CC13 | B24 |
A1007 | H | HCC | Ph | CC13 | B24 |
A1008 | H | ch3cc | Ph | CC13 | B24 |
A1009 | H | ch2=ch | Ph | CC13 | B24 |
A1010 | H | ch2=chch2 | Ph | CC13 | B24 |
A1011 | H | CH3SO2N(CH3) | Ph | CC13 | B24 |
A1012 | H | (CH3)2N | Ph | CC13 | B24 |
A1013 | H | (CH3)2NSO2 | Ph | CC13 | B24 |
A1014 | H | ch3sch2 | Ph | CC13 | B24 |
A1015 | H | ch3soch2 | Ph | CC13 | B24 |
A1016 | H | ch3so2ch2 | Ph | CC13 | B24 |
A1017 | F | H | H | cf3 | B24 |
A1018 | Cl | H | H | cf3 | B24 |
A1019 | Br | H | H | cf3 | B24 |
A1020 | CN | H | H | cf3 | B24 |
A1021 | CH3SO2O | H | H | cf3 | B24 |
A1022 | CH3O | H | H | cf3 | B24 |
A1023 | CH2CH3O | H | H | cf3 | B24 |
A1024 | ch2ch=ch2o | H | H | cf3 | B24 |
A1025 | hccch2o | H | H | cf3 | B24 |
A1026 | S-benzyl | H | H | cf3 | B24 |
A1027 | SO2-benzyl | H | H | cf3 | B24 |
A1028 | C1CH2 | H | H | cf3 | B24 |
A1029 | BrCH2 | H | H | cf3 | B24 |
A1030 | fch2 | H | H | cf3 | B24 |
A1031 | chf2ch2 | H | H | cf3 | B24 |
A1032 | cf3ch2 | H | H | cf3 | B24 |
A1033 | triazolylmethyl | H | H | cf3 | B24 |
-106CZ 304537 B6
Sl. | R92 | R93 | R94 | R95 | q3 |
c - A1034 | CHCI2CH2 | H | H | cf3 | B24 |
A1035 | C1CH=CH | H | H | cf3 | B24 |
A1036 | Cl2C=CH | H | H | cf3 | B24 |
A1037 | cf3ch=ch | H | H | cf3 | B24 |
A1038 | C1CC | H | H | cf3 | B24 |
A1039 | Ph | H | H | cf3 | B24 |
A1040 | ch3 | ch3 | H | cf3 | B24 |
A1041 | ch3 | OH | H | cf3 | B24 |
A1042 | ch3 | F | H | cf3 | B24 |
A1043 | ch3 | Cl | H | cf3 | B24 |
A1O44 | F | ch3 | H | cf3 | B24 |
A1045 | Cl | ch3 | H | cf3 | B24 |
A1046 | H | F | H | cf3 | B24 |
A1047 | H | Cl | H | cf3 | B24 |
A1048 | H | Br | H | cf3 | B24 |
A1049 | H | OH | H | cf3 | B24 |
A1050 | H | och3 | H | cf3 | B24 |
A1051 | H | OCHF2 | H | cf3 | B24 |
A1052 | H | oso2ch3 | H | cf3 | B24 |
A1053 | H | oso2cf3 | H | cf3 | B24 |
A1054 | H | cich2 | H | cf3 | B24 |
A1055 | H | BrCH2 | H | cf3 | B24 |
A1056 | H | fch2 | H | cf3 | B24 |
A1057 | H | chf2ch2 | H | cf3 | B24 |
A1058 | H | cf3ch2 | H | cf3 | B24 |
A1059 | H | triazolyl- methyl | H | cf3 | B24 |
A1060 | H | CHC12CH2 | H | cf3 | B24 |
A1061 | H | C1CH=CH | H | cf3 | B24 |
A1062 | H | C12C=CH | H | cf3 | B24 |
A1063 | H | cf3ch=ch | H | cf3 | B24 |
A1064 | H | C1CC | H | cf3 | B24 |
A1065 | H | CH3C(O) | H | cf3 | B24 |
A1066 | H | fenyl | H | cf3 | B24 |
A1067 | H | so2ch3 | H | cf3 | B24 |
A1068 | H | so2cf3 | H | cf3 | B24 |
A1069 | H | CN | H | cf3 | B24 |
A1070 | H | no2 | H | cf3 | B24 |
A1071 | ch3 | H | F | cf3 | B24 |
A1072 | ch3 | H | Cl | cf3 | B24 |
A1073 | ch3 | H | Br | cf3 | B24 |
A1074 | ch3 | H | CN | cf3 | B24 |
A1075 | ch3 | H | CH3O | cf3 | B24 |
A1076 | ch3 | H | ch3s | cf3 | B24 |
A1077 | ch3 | H | ch3so | cf3 | B24 |
A1078 | ch3 | H | ch3so2 | cf3 | B24 |
-107CZ 304537 B6
Tabulka 9a: Sloučeniny obecného vzorce lg:
Os | 03 | 03 | Q3 | 2l | Ol | Ol | Ol | Ol | & | Ol | |
B1 | B2 | B3 | B4 | B5 | B6 | B7 | B8 | B9 | BIO | Bil | B12 |
B13 | B14 | B15 | B16 | B17 | B18 | B19 | B20 | B21 | B22 | B23 | B24 |
B25 | B26 | B27 | B28 | B29 | B30 | B31 | B32 | B33 | B34 | B35 | B36 |
B37 | B38 | B39 | B40 | B41 | B42 | B43 | B44 | B45 | B46 | B47 | B48 |
B49 | B50 | B51 | B52 | B53 | B54 | B55 | B56 | B57 | B58 | B59 | B60 |
B61 | B62 | B63 | B64 | B65 | B66 | B67 | B68 | B69 | B70 | B71 | B72 |
B73 | B74 | B75 | B76 | B77 | B78 | B7 9 | B80 | B81 | B82 | B83 | B84 |
B85 | B86 | B87 | B88 | B89 | B90 | B91 | B92 | B93 | B94 | B95 | B96 |
B97 | B98 | B99 | B100 | B101 | B102 | B103 | B104 | B105 | B106 | B107 | B108 |
B109 | B110 | Blil | B112 | B113 | B114 | B115 | B116 | B117 | B118 | B119 | B120 |
B121 | B122 | B123 | B124 | B125 | B126 | B127 | B128 | B129 | B130 | B131 | B132 |
B133 | B134 | B135 | B136 | B137 | B138 | B139 | B140 | B141 | B142 | B143 | B144 |
B145 | B146 | B147 | B148 | B149 | B150 | B151 | B152 | B153 | B154 | B155 | B156 |
B157 | B158 | B159 | B160 | B161 | B162 | B163 | B164 | B165 | B166 | B167 | B168 |
B169 | B170 | B171 | B172 | B173 | B174 | B175 | B176 | B177 | B178 | B179 | B180 |
B181 | B182 | B183 | B184 | B185 | B186 | B187 | B188 | B189 | B190 | B191 | B192 |
B193 | B194 | B195 | B196 | B197 | B198 | B199 | B200 | B201 | B202 | B203 | B204 |
B205 | B206 | B207 | B208 | B209 | B210 | B211 | B212 | B213 | B214 | B215 | B216 |
B217 | B218 | B219 | B220 | B221 | B222 | B223 | B224 | B225 | B226 | B227 | B228 |
B229 | B230 | B231 | B232 | B233 | B234 | B235 | B236 | B237 | B238 | B239 | B240 |
B241 | B242 | B243 | B244 | B245 | B246 | B247 | B248 | B249 | B250 | B251 | B252 |
B253 | B254 | B255 | B256 | B257 | B258 | B259 | B260 | B261 | B262 | B263 | B264 |
B265 | B266 | B267 | B268 | B269 | B270 | B271 | B272 | B273 | B274 | B275 | B276 |
B277 | B278 | B279 | B280 | B281 | B282 | B283 | B284 | B285 | B286 | B287 | B288 |
B289 | B290 | B291 | B292 | B293 | B294 | B295 | B296 | B297 | B298 | B299 | B300 |
B301 | B302 | B303 | B304 | B305 | B306 | B307 | B308 | B309 | B310 | B311 | B312 |
B313 | B314 | B315 | B316 | B317 | B318 | B319 | B320 | B321 | B322 | B323 | B324 |
B325 | B326 | B327 | B328 | B329 | B330 | B331 | B332 | B333 | B334 | B335 | B336 |
B337 | B338 | B339 | B340 | B341 | B342 | B343 | B344 | B345 | B346 | B347 | B348 |
B349 | B350 | B351 | B352 | B353 | B354 | B355 | B356 | B357 | B358 | B359 | B360 |
B361 | B362 | B363 | B364 | B365 | B366 | B367 | B368 | B369 | B370 | B371 | B372 |
B373 | B374 | B375 | B376 | B377 | B378 | B379 | B380 | B381 | B382 | B383 | B384 |
B385 | B386 | B387 | B388 | B389 | B390 | B391 | B392 | B393 | B394 | B395 | B396 |
B397 | B398 | B399 | B400 | B401 | B402 | B403 | B404 | B405 | B406 | B407 | B408 |
B409 | B410 | B411 | B412 | B413 | B414 | B415 | B416 | B417 | B418 | B419 | B420 |
B421 | B422 | B423 | B424 | B425 | B426 | B427 | B428 | B429 | B430 | B431 | B432 |
B433 | B434 | B435 | B436 | B437 | B438 | B439 | B440 | B441 | B442 | B443 | B444 |
B445 | B446 | B447 | B448 | B449 | B450 | B451 | B452 | B453 | B454 | B455 | B456 |
B457 | B4.58 | B459 | B460 | B461 | B462 | B463 | B464 | B465 | B466 | B467 | B468 |
B469 | B470 | B471 | B472 | B473 | B474 | B475 | B476 | B477 | B478 | B479 | B480 |
-108CZ 304537 B6
23 B481 | q3 B482 | B483 | q3 B484 | q3 B485 | q3 B486 | B487 | 2l B488 | Qs B489 | Qi B490 | 2i B491 | q3 B492 |
B493 | B494 | B495 | B496 | B497 | B498 | B499 | B500 | B501 | B502 | B503 | B504 |
B505 | B506 | B507 | B508 | B509 | B510 | B511 | B512 | B513 | B514 | B515 | B516 |
B517 | B518 | B519 | B520 | B521 | B522 | B523 | B524 | B525 | B526 | B527 | B528 |
B529 | B530 | B531 | B532 | B533 | B534 | B535 | B536 | B537 | B538 | B539 | B540 |
B541 | B542 | B543 | B544 | B545 | B54 6 | B547 | B548 | B549 | B550 | B551 | B552 |
B553 | B554 | B555 | B556 | B557 | B558 | B559 | B560 | B561 | B562 | B563 | B564 |
B565 | B566 | B567 | B568 | B569 | B570 | B571 | B572 | B573 | B574 | B575 | B576 |
B577 | B578 | B579 | B580 | B581 | B582 | B583 | B584 | B585 | B586 | B587 | B588 |
B589 | B590 | B591 | B592 | B593 | B594 | B595 | B596 | B597 | B598 | B599 | B600 |
B601 | B602 | B603 | B604 | B605 | B606 | B607 | B608 | B609 | B610 | B611 | B612 |
B613 | B614 | B615 | B616 | B617 | B618 | B619 | B620 | B621 | B622 | B623 | B624 |
B625 | B626 | B627 | B628 | B629 | B630 | B631 | B632 | B633 | B634 | B635 | B636 |
B637 | B638 | B639 | B640 | B641 | B642 | B643 | B644 | B645 | B646 | B647 | B648 |
B649 | B650 | B651 | B652 | B653 | B654 | B655 | B656 | B657 | B658 | B659 | B660 |
B661 | B662 | B663 | B664 | B665 | B666 | B667 | B668 | B669 | B670 | B671 | B672 |
B773 | B774 | B775 | B776 | B777 | B778 | B779 | B780 | B781 | B782 | B783 | B784 |
B785 | B786 | B787 | B788 | B789 | B790 | B791 | B792 | B793 | B794 | B795 | B796 |
B797 | B798 | B799 | B800 | B801 | B802 | B803 | B804 | B805 | B806 | B807 | B808 |
B809 | B810 | B811 | B812 | B813 | B814 | B815 | B816 | B817 | B818 | B819 | B820 |
B821 | B822 | B823 | B824 | B825 | B826 | B827 | B828 | B829 | B830 | B831 | B832 |
B833 | B834 | B835 | B836 | B837 | B838 | B839 | B840 | B841 | B842 | B843 | B844 |
B845 | B846 | B847 | B848 | B849 | B850 | B851 | B852 | B853 | B854 | B855 | B856 |
B857 | B858 | B859 | B860 | B861 | B862 | B863 | B864 | B865 | B866 | B867 | B868 |
B869 | B870 | B871 | B872 | B873 | B874 | B875 | B876 | B877 | B878 | B879 | B880 |
B881 | B882 | B883 | B884 | B885 | B886 | B887 | B888 | B889 | B890 | B891 | B892 |
B893 | B894 | B895 | B896 | B897 | B898 | B899 | B900 | B901 | B902 | B903 | B904 |
B905 | B906 | B907 | B908 | B909 | B910 | B911 | B912 | B913 | B914 | B915 | B916 |
B917 | B918 | B919 | B920 | B921 | B922 | B923 | B924 | B925 | B926 | B927 | B928 |
B929 | B930 | B931 | B932 | B933 | B934 | B935 | B936 | B937 | B938 | B939 | B940 |
B941 | B942 | B943 | B944 | B945 | B946 | B947 | B948 | B949 | B950 | B951 | B952 |
B953 | B954 | B955 | B956 | B957 | B958 | B959 | B960 | B961 | B962 | B963 | B964 |
B965 | B966 | B967 | B968 | B969 | B970 | B971 | B972 | B973 | B974 | B975 | B976 |
B977 | B978 | B979 | B980 | B981 | B982 | B983 | B984 | B985 | B986 | B987 | B988 |
B989 | B990 | B991 | B992 | B993 | B994 | B995 | B996 | B997 | B998 | B999 | B100 n |
B100 | B100 | B100 | B100 | B100 | B100 | B100 | B100 | B100 | B101 | B101 | u B101 |
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 |
ΒΙΟΙ | ΒΙΟΙ | B101 | B101 | B101 | B101 | B101 | B102 | B102 | B102 | B102 | B102 |
3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 |
B102 | B102 | B102 | B102 | B102 | B103 | B103 | B103 | B103 | B103 | B103 | B103 |
5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 |
B103 | B103 | B103 | B104 | B104 | B104 | B104 | B104 | B104 | B104 | B104 | B104 |
7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 |
B104 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B106 |
9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 |
B106 | B106 | BIOS | B106 | B106 | B106 | B106 | B106 | B106 | B107 | B107 | B107 |
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 |
B107 | B107 | B107 | B107 | B107 | B107 | B107 | B108 | B108 | B108 | B108 | |
3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 |
-109CZ 304537 B6
Tabulka 10: Sloučeniny obecného vzorce Ih:
03 | Ql | Ql | Ql | Ql | 03 | 03 | Ql | Sl | Ql | 03 | |
Bl | B2 | B3 | B4 | B5 | B6 | B7 | B8 | B9 | BIO | Bil | B12 |
B13 | B14 | B15 | B16 | B17 | B18 | B19 | B20 | B21 | B22 | B23 | B24 |
B25 | B26 | B27 | B28 | B29 | B30 | B31 | B32 | B33 | B34 | B35 | B36 |
B37 | B38 | B39 | B40 | B41 | B42 | B43 | B44 | B45 | B4 6 | B47 | B48 |
B49 | B50 | B51 | B52 | B53 | B54 | B55 | B56 | B57 | B58 | B59 | B60 |
B61 | B62 | B63 | B64 | B65 | B66 | B67 | B68 | B69 | B70 | B71 | B72 |
B73 | B74 | B75 | B76 | B77 | B78 | B79 | B80 | B81 | B82 | B83 | B84 |
B85 | B86 | B87 | B88 | B89 | B90 | B91 | B92 | B93 | B94 | B95 | B96 |
B97 | B98 | B99 | B100 | B101 | B102 | B103 | B104 | B105 | B106 | B107 | B108 |
B109 | B110 | Blil | B112 | B113 | B114 | B115 | B116 | B117 | B118 | B119 | B120 |
B121 | B122 | B123 | B124 | B125 | B126 | B127 | B128 | B129 | B130 | B131 | B132 |
B133 | B134 | B135 | B136 | B137 | B138 | B139 | B140 | B141 | B142 | B143 | B144 |
B145 | B146 | B147 | B148 | B149 | B150 | B151 | B152 | B153 | B154 | B155 | B156 |
B157 | B158 | B159 | B160 | B161 | B162 | B163 | B164 | B165 | B166 | B167 | B168 |
B169 | B170 | B171 | B172 | B173 | B174 | B175 | B176 | B177 | B178 | B179 | B180 |
B181 | B182 | B183 | B184 | B185 | B186 | B187 | B188 | B189 | B190 | B191 | B192 |
B193 | B194 | B195 | B196 | B197 | B198 | B199 | B200 | B201 | B202 | B203 | B204 |
B205 | B206 | B207 | B208 | B209 | B210 | B211 | B212 | B213 | B214 | B215 | B216 |
B217 | B218 | B219 | B220 | B221 | B222 | B223 | B224 | B225 | B226 | B227 | B228 |
B229 | B230 | B231 | B232 | B233 | B234 | B235 | B236 | B237 | B238 | B239 | B240 |
B241 | B242 | B243 | B244 | B245 | B246 | B247 | B248 | B249 | B250 | B251 | B252 |
B253 | B254 | B255 | B256 | B257 | B258 | B259 | B260 | B261 | B262 | B263 | B264 |
B265 | B266 | B267 | B268 | B269 | B270 | B271 | B272 | B273 | B274 | B275 | B276 |
B277 | B278 | B279 | B280 | B281 | B282 | B283 | B284 | B285 | B286 | B287 | B288 |
B289 | B290 | B291 | B292 | B293 | B294 | B295 | B296 | B297 | B298 | B299 | B300 |
B301 | B302 | B303 | B304 | B305 | B306 | B307 | B308 | B309 | B310 | B311 | B312 |
B313 | B314 | B315 | B316 | B317 | B318 | B319 | B320 | B321 | B322 | B323 | B324 |
B325 | B326 | B327 | B328 | B329 | B330 | B331 | B332 | B333 | B334 | B335 | B336 |
B337 | B338 | B339 | B340 | B341 | B342 | B343 | B344 | B345 | B346 | B347 | B348 |
B349 | B350 | B351 | B352 | B353 | B354 | B355 | B356 | B357 | B358 | B359 | B360 |
B361 | B362 | B363 | B364 | B365 | B366 | B367 | B368 | B369 | B370 | B371 | B372 |
B373 | B374 | B375 | B376 | B377 | B378 | B379 | B380 | B381 | B382 | B383 | B384 |
B385 | B386 | B387 | B388 | B389 | B390 | B391 | B392 | B393 | B394 | B395 | B396 |
B397 | B398 | B399 | B400 | B401 | B402 | B403 | B404 | B405 | B406 | B407 | B408 |
B409 | B410 | B411 | B412 | B413 | B414 | B415 | B416 | B417 | B418 | B419 | B420 |
B421 | B422 | B423 | B424 | B425 | B426 | B427 | B428 | B429 | B430 | B431 | B432 |
B433 | B434 | B435 | B436 | B437 | B438 | B439 | B440 | B441 | B442 | B443 | B444 |
-110CZ 304537 B6
q3 B445 | Qs B446 | q3 B447 | q3 B448 | q3 B449 | q3 B450 | q3 B451 | q3 B452 | q3 B453 | q3 B454 | q3 B455 | q3 B456 |
B457 | B458 | B459 | B460 | B461 | B462 | B463 | B464 | B465 | B466 | B467 | B468 |
B469 | B470 | B471 | B472 | B473 | B474 | B475 | B476 | B477 | B478 | B479 | B480 |
B481 | B482 | B483 | B484 | B485 | B486 | B487 | B488 | B489 | B490 | B491 | B492 |
B493 | B494 | B4 95 | B496 | B497 | B498 | B499 | B500 | B501 | B502 | B503 | B504 |
B505 | B506 | B507 | B508 | B509 | B510 | B511 | B512 | B513 | B514 | B515 | B516 |
B517 | B518 | B519 | B520 | B521 | B522 | B523 | B524 | B525 | B526 | B527 | B528 |
B529 | B530 | B531 | B532 | B533 | B534 | B535 | B536 | B537 | B538 | B539 | B540 |
B541 | B542 | B543 | B544 | B545 | B546 | B547 | B548 | B549 | B550 | B551 | B552 |
B553 | B554 | B555 | B556 | B557 | B558 | B559 | B560 | B561 | B562 | B563 | B564 |
B565 | B566 | B567 | B568 | B569 | B570 | B571 | B572 | B573 | B574 | B575 | B576 |
B577 | B578 | B579 | B580 | B581 | B582 | B583 | B584 | B585 | B586 | B587 | B588 |
B589 | B590 | B591 | B592 | B593 | B594 | B595 | B596 | B597 | B598 | B599 | B600 |
B601 | B602 | B603 | B604 | B605 | B606 | B607 | B608 | B609 | B610 | B611 | B612 |
B613 | B614 | B615 | B616 | B617 | B618 | B619 | B620 | B621 | B622 | B623 | B624 |
B625 | B626 | B627 | B628 | B629 | B630 | B631 | B632 | B633 | B634 | B635 | B636 |
B637 | B638 | B639 | B640 | B641 | B642 | B643 | B644 | B645 | B646 | B647 | B648 |
B649 | B650 | B651 | B652 | B653 | B654 | B655 | B656 | B657 | B658 | B659 | B660 |
B661 | B662 | B663 | B664 | B665 | B666 | B667 | B668 | B669 | B670 | B671 | B672 |
B773 | B774 | B775 | B776 | B777 | B778 | B779 | B780 | B781 | B782 | B783 | B784 |
B785 | B786 | B787 | B788 | B789 | B790 | B791 | B792 | B793 | B794 | B795 | B796 |
B797 | B798 | B799 | B800 | B801 | B802 | B803 | B804 | B805 | B806 | B807 | B808 |
B809 | B810 | B811 | B812 | B813 | B814 | B815 | B816 | B817 | B818 | B819 | B820 |
B821 | B822 | B823 | B824 | B825 | B826 | B827 | B828 | B829 | B830 | B831 | B832 |
B833 | B834 | B835 | B836 | B837 | B838 | B839 | B840 | B841 | B842 | B843 | B844 |
B845 | B846 | B847 | B848 | B849 | B850 | B851 | B852 | B853 | B854 | B855 | B856 |
B857 | B858 | B859 | B860 | B861 | B862 | B863 | B864 | B865 | B866 | B867 | B868 |
B869 | B870 | B871 | B872 | B873 | B874 | B875 | B876 | B877 | B878 | B879 | B880 |
B881 | B882 | B883 | B884 | B885 | B886 | B887 | B888 | B889 | B890 | B891 | B892 |
B893 | B894 | B895 | B896 | B897 | B898 | B899 | B900 | B901 | B902 | B903 | B904 |
B905 | B906 | B907 | B908 | B909 | B910 | B911 | B912 | B913 | B914 | B915 | B916 |
B917 | B918 | B919 | B920 | B921 | B922 | B923 | B924 | B925 | B926 | B927 | B928 |
B929 | B930 | B931 | B932 | B933 | B934 | B935 | B936 | B937 | B938 | B939 | B940 |
B941 | B942 | B943 | B944 | B945 | B946 | B947 | B948 | B949 | B950 | B951 | B952 |
B953 | B954 | B955 | B956 | B957 | B958 | B959 | B960 | B961 | B962 | B963 | B964 |
B965 | B966 | B967 | B968 | B969 | B970 | B971 | B972 | B973 | B974 | B975 | B976 |
B977 | B978 | B979 | B980 | B981 | B982 | B983 | B984 | B985 | B986 | B987 | B988 |
B989 | B990 | B991 | B992 | B993 | B994 | B995 | B996 | B997 | B998 | B999 | B100 fi |
B100 | B100 | B100 | B100 | B100 | B100 | B100 | B100 | B100 | B101 | B101 | v B101 |
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 |
B101 | B101 | B101 | B101 | B101 | B101 | B101 | B102 | B102 | B102 | B102 | B102 |
3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 |
B102 | B102 | B102 | B102 | B102 | B103 | B103 | B103 | B103 | B103 | B103 | B103 |
5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 |
B103 | B103 | B103 | B104 | B104 | B104 | B104 | B104 | B104 | B104 | BIO 4 | B104 |
7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 |
BIO 4 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B106 |
9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 |
B106 | B106 | B106 | B106 | B106 | B106 | B106 | B106 | B106 | B107 | B107 | B107 |
- 111 CZ 304537 B6
q3 | q3 | q3 | q3 | q3 | q3 | q3 | q3 | q3 | q3 | q3 | q3 |
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 |
B107 | B107 | B107 | B107 | B107 | B107 | B107 | B108 | B108 | B108 | B108 | |
3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 |
Tabulka 11: Sloučeniny obecného vzorce lk:
Os | 23 | q3 | Os | 03 | q3 | Ol | Ol | 03 | Ol | Ol | Ol |
Bl | B2 | B3 | B4 | B5 | B6 | B7 | B8 | B9 | BIO | Bil | B12 |
B13 | B14 | B15 | B16 | B17 | B18 | B19 | B20 | B21 | B22 | B23 | B24 |
B25 | B26 | B27 | B28 | B29 | B30 | B31 | B32 | B33 | B34 | B35 | B36 |
B37 | B38 | B39 | B40 | B41 | B42 | B43 | B44 | B45 | B46 | B47 | B48 |
B4 9 | B50 | B51 | B52 | B53 | B54 | B55 | B56 | B57 | B58 | B59 | B60 |
B61 | B62 | B63 | B64 | B65 | B66 | B67 | B68 | B69 | B70 | B71 | B72 |
B73 | B74 | B75 | B76 | B77 | B78 | B79 | B80 | B81 | B82 | B83 | B84 |
B85 | B86 | B87 | B88 | B89 | B90 | B91 | B92 | B93 | B94 | B95 | B96 |
B97 | B98 | B99 | B100 | B101 | B102 | B103 | B104 | B105 | B106 | B107 | B108 |
B109 | B110 | Blil | B112 | B113 | B114 | B115 | B116 | B117 | B118 | B119 | B120 |
B121 | B122 | B123 | B124 | B125 | B126 | B127 | B128 | B129 | B130 | B131 | B132 |
B133 | B134 | B135 | B136 | B137 | B138 | B139 | B140 | B141 | B142 | B143 | B144 |
B145 | B146 | B147 | B148 | B149 | B150 | B151 | B152 | B153 | B154 | B155 | B156 |
B157 | B158 | B159 | B160 | B161 | B162 | B163 | B164 | B165 | B166 | B167 | B168 |
B169 | B170 | B171 | B172 | B173 | B174 | B175 | B176 | B177 | B178 | B179 | B180 |
B181 | B182 | B183 | B184 | B185 | B186 | B187 | B188 | B189 | B190 | B191 | B192 |
B193 | B194 | B195 | B196 | B197 | B198 | B199 | B200 | B201 | B202 | B203 | B204 |
B205 | B206 | B207 | B208 | B209 | B210 | B211 | B212 | B213 | B214 | B215 | B216 |
B217 | B218 | B219 | B220 | B221 | B222 | B223 | B224 | B225 | B226 | B227 | B228 |
B229 | B230 | B231 | B232 | B233 | B234 | B235 | B236 | B237 | B238 | B239 | B240 |
B241 | B242 | B243 | B244 | B245 | B246 | B247 | B248 | B249 | B250 | B251 | B252 |
B253 | B254 | B255 | B256 | B257 | B258 | B259 | B260 | B261 | B262 | B263 | B264 |
B265 | B266 | B267 | B268 | B269 | B270 | B271 | B272 | B273 | B274 | B275 | B27 6 |
B277 | B278 | B279 | B280 | B281 | B282 | B283 | B284 | B285 | B286 | B287 | B288 |
B289 | B290 | B291 | B292 | B293 | B294 | B295 | B296 | B297 | B298 | B299 | B300 |
B301 | B302 | B303 | B304 | B305 | B306 | B307 | B308 | B309 | B310 | B311 | B312 |
B313 | B314 | B315 | B316 | B317 | B318 | B319 | B320 | B321 | B322 | B323 | B324 |
B325 | B326 | B327 | B328 | B329 | B330 | B331 | B332 | B333 | B334 | B335 | B336 |
B337 | B338 | B339 | B340 | B341 | B342 | B343 | B344 | B345 | B346 | B347 | B348 |
B349 | B350 | B351 | B352 | B353 | B354 | B355 | B356 | B357 | B358 | B359 | B360 |
B361 | B362 | B363 | B364 | B365 | B366 | B367 | B368 | B369 | B370 | B371 | B372 |
B373 | B374 | B375 | B376 | B377 | B378 | B379 | B380 | B381 | B382 | B383 | B384 |
- 112CZ 304537 B6
q3 B385 | Os B386 | Qa B387 | q3 B388 | q3 B389 | q3 B390 | q3 B391 | 23 B392 | q3 B393 | q3 B394 | q3 B395 | q3 B396 |
B397 | B398 | B399 | B400 | B401 | B402 | B403 | B404 | B405 | B406 | B407 | B408 |
B409 | B410 | B411 | B412 | B413 | B414 | B415 | B416 | B417 | B418 | B419 | B420 |
B421 | B422 | B423 | B424 | B425 | B426 | B427 | B428 | B429 | B430 | B431 | B432 |
B433 | B434 | B435 | B436 | B437 | B438 | B439 | B440 | B441 | B442 | B443 | B444 |
B445 | B446 | B447 | B448 | B449 | B450 | B451 | B452 | B453 | B454 | B455 | B456 |
B457 | B458 | B459 | B460 | B461 | B462 | B463 | B464 | B465 | B466 | B467 | B468 |
B469 | B470 | B471 | B472 | B473 | B474 | B475 | B476 | B477 | B478 | B479 | B480 |
B481 | B482 | B483 | B484 | B485 | B486 | B487 | B488 | B489 | B490 | B491 | B492 |
B493 | B494 | B495 | B496 | B497 | B498 | B499 | B500 | B501 | B502 | B503 | B504 |
B505 | B506 | B507 | B508 | B509 | B510 | B511 | B512 | B513 | B514 | B515 | B516 |
B517 | B518 | B519 | B520 | B521 | B522 | B523 | B524 | B525 | B526 | B527 | B528 |
B529 | B530 | B531 | B532 | B533 | B534 | B535 | B536 | B537 | B538 | B539 | B540 |
B541 | B542 | B543 | B544 | B545 | B546 | B547 | B548 | B549 | B550 | B551 | B552 |
B553 | B554 | B555 | B556 | B557 | B558 | B559 | B560 | B561 | B562 | B563 | B564 |
B565 | B566 | B567 | B568 | B569 | B570 | B571 | B572 | B573 | B574 | B575 | B576 |
B577 | B578 | B579 | B580 | B581 | B582 | B583 | B584 | B585 | B586 | B587 | B588 |
B589 | B590 | B591 | B592 | B593 | B594 | B595 | B596 | B597 | B598 | B599 | B600 |
B601 | B602 | B603 | B604 | B605 | B606 | B607 | B608 | B609 | B610 | B611 | B612 |
B613 | B614 | B615 | B616 | B617 | B618 | B619 | B620 | B621 | B622 | B623 | B624 |
B625 | B626 | B627 | B628 | B629 | B630 | B631 | B632 | B633 | B634 | B635 | B636 |
B637 | B638 | B639 | B640 | B641 | B642 | B643 | B644 | B645 | B646 | B647 | B648 |
B649 | B650 | B651 | B652 | B653 | B654 | B655 | B656 | B657 | B658 | B659 | B660 |
B661 | B662 | B663 | B664 | B665 | B666 | B667 | B668 | B669 | B670 | B671 | B672 |
B773 | B774 | B775 | B776 | B777 | B778 | B779 | B780 | B781 | B782 | B783 | B784 |
B785 | B786 | B787 | B788 | B789 | B790 | B791 | B792 | B793 | B794 | B795 | B796 |
B7 97 | B798 | B799 | B800 | B801 | B802 | B803 | B804 | B805 | B806 | B807 | B808 |
B809 | B810 | B811 | B812 | B813 | B814 | B815 | B816 | B817 | B818 | B819 | B820 |
B821 | B822 | B823 | B824 | B825 | B826 | B827 | B828 | B829 | B830 | B831 | B832 |
B833 | B834 | B835 | B836 | B837 | B838 | B839 | B840 | B841 | B842 | B843 | B844 |
B845 | B846 | B847 | B848 | B849 | B850 | B851 | B852 | B853 | B854 | B855 | B856 |
B857 | B858 | B859 | B860 | B861 | B862 | B863 | B864 | B865 | B866 | B867 | B868 |
B869 | B870 | B871 | B872 | B873 | B874 | B875 | B876 | B877 | B878 | B879 | B880 |
B881 | B882 | B883 | B884 | B885 | B886 | B887 | B888 | B889 | B890 | B891 | B892 |
B893 | B894 | B895 | B896 | B897 | B898 | B899 | B900 | B901 | B902 | B903 | B904 |
B905 | B906 | B907 | B908 | B909 | B910 | B911 | B912 | B913 | B914 | B915 | B916 |
B917 | B918 | B919 | B920 | B921 | B922 | B923 | B924 | B925 | B926 | B927 | B928 |
B929 | B930 | B931 | B932 | B933 | B934 | B935 | B936 | B937 | B938 | B939 | B940 |
B941 | B942 | B943 | B944 | B945 | B946 | B947 | B948 | B949 | B950 | B951 | B952 |
B953 | B954 | B955 | B956 | B957 | B958 | B959 | B960 | B961 | B962 | B963 | B964 |
B965 | B966 | B967 | B968 | B969 | B970 | B971 | B972 | B973 | B974 | B975 | B976 |
B977 | B978 | B979 | B980 | B981 | B982 | B983 | B984 | B985 | B986 | B987 | B988 |
B989 | B990 | B991 | B992 | B993 | B994 | B995 | B996 | B997 | B998 | B999 | B100 n |
B100 | B100 | B100 | B100 | B100 | B100 | B100 | B100 | B100 | B101 | B101 | B101 |
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 |
B101 | B101 | B101 | B101 | B101 | B101 | B101 | B102 | B102 | B102 | B102 | B102 |
3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 |
B102 | B102 | B102 | B102 | B102 | B103 | B103 | B103 | B103 | B103 | B103 | B103 |
5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 |
- 113 CZ 304537 B6
q3 | q3 | q3 | q3 | q3 | q3 | q3 | 03 | q3 | q3 | q3 | q3 |
B103 | B103 | B103 | B104 | B104 | B104 | B104 | B104 | B104 | B104 | B104 | B104 |
7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 |
B104 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B106 |
9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 |
B106 | B106 | B106 | B106 | B106 | B106 | B106 | B106 | B106 | B107 | B107 | B107 |
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 |
B107 | B107 | B107 | B107 | B107 | B107 | B107 | B108 | B108 | B108 | B108 | |
3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 |
Tabulka 12: Sloučeniny obecného vzorce Im:
03 | 03 | 03 | Ql | Ql | 03 | q3 | O? | Os | 03 | 03 | 03 |
B1 | B2 | B3 | B4 | B5 | B6 | B7 | B8 | B9 | BIO | Bil | B12 |
B13 | B14 | B15 | B16 | B17 | B18 | B19 | B20 | B21 | B22 | B23 | B24 |
B25 | B26 | B27 | B28 | B29 | B30 | B31 | B32 | B33 | B34 | B35 | B36 |
B37 | B38 | B39 | B40 | B41 | B42 | B43 | B44 | B45 | B46 | B47 | B48 |
B49 | B50 | B51 | B52 | B53 | B54 | B55 | B56 | B57 | B58 | B59 | B60 |
B61 | B62 | B63 | B64 | B65 | B66 | B67 | B68 | B69 | B70 | B71 | B72 |
B73 | B74 | B75 | B76 | B77 | B78 | B79 | B80 | B81 | B82 | B83 | B84 |
B85 | B86 | B87 | B88 | B89 | B90 | B91 | B92 | B93 | B94 | B95 | B96 |
B97 | B98 | B99 | B100 | B101 | B102 | B103 | B104 | B105 | B106 | B107 | B108 |
B109 | B110 | Blil | B112 | B113 | B114 | B115 | B116 | B117 | B118 | B119 | B120 |
B121 | B122 | B123 | B124 | B125 | B126 | B127 | B128 | B129 | B130 | B131 | B132 |
B133 | B134 | B135 | B136 | B137 | B138 | B139 | B140 | B141 | B142 | B143 | B144 |
B145 | B146 | B147 | B148 | B149 | B150 | B151 | B152 | B153 | B154 | B155 | B156 |
ΒΊ57 | B158 | B159 | B160 | B161 | B162 | B163 | B164 | B165 | B166 | B167 | B168 |
B169 | B170 | B171 | B172 | B173 | B174 | B175 | B176 | B177 | B178 | B179 | B180 |
B181 | B182 | B183 | B184 | B185 | B186 | B187 | B188 | B189 | B190 | B191 | B192 |
B193 | B194 | B195 | B196 | B197 | B198 | B199 | B200 | B201 | B202 | B203 | B204 |
B205 | B206 | B207 | B208 | B209 | B210 | B211 | B212 | B213 | B214 | B215 | B216 |
B217 | B218 | B219 | B220 | B221 | B222 | B223 | B224 | B225 | B226 | B227 | B228 |
B229 | B230 | B231 | B232 | B233 | B234 | B235 | B236 | B237 | B238 | B239 | B240 |
B241 | B242 | B243 | B244 | B245 | B246 | B247 | B24 8 | B249 | B250 | B251 | B252 |
B253 | B254 | B255 | B256 | B257 | B258 | B259 | B260 | B261 | B262 | B263 | B264 |
B265 | B266 | B267 | B268 | B269 | B270 | B271 | B272 | B273 | B274 | B275 | B276 |
B277 | B278 | B279 | B280 | B281 | B282 | B283 | B284 | B285 | B286 | B287 | B288 |
B289 | B290 | B291 | B292 | B293 | B294 | B295 | B296 | B297 | B298 | B299 | B300 |
B301 | B302 | B303 | B304 | B305 | B306 | B307 | B308 | B309 | B310 | B311 | B312 |
B313 | B314 | B315 | B316 | B317 | B318 | B319 | B320 | B321 | B322 | B323 | B324 |
B325 | B326 | B327 | B328 | B329 | B330 | B331 | B332 | B333 | B334 | B335 | B336 |
- 114CZ 304537 B6
Qa B337 | q3 B338 | Os B339 | q3 B340 | q3 B341 | q3 B342 | q3 B343 | q3 B344 | q3 B345 | q3 B346 | q3 B347 | 03 B348 |
B349 | B350 | B351 | B352 | B353 | B354 | B355 | B356 | B357 | B358 | B359 | B360 |
B361 | B362 | B363 | B364 | B365 | B366 | B367 | B368 | B369 | B370 | B371 | B372 |
B373 | B374 | B375 | B376 | B377 | B378 | B379 | B380 | B381 | B382 | B383 | B384 |
B385 | B386 | B387 | B388 | B389 | B390 | B391 | B392 | B393 | B394 | B395 | B396 |
B397 | B398 | B399 | B400 | B401 | B402 | B403 | B404 | B405 | B406 | B407 | B408 |
B409 | B410 | B411 | B412 | B413 | B414 | B415 | B416 | B417 | B418 | B419 | B420 |
B421 | B422 | B423 | B424 | B425 | B426 | B427 | B428 | B429 | B430 | B431 | B432 |
B433 | B434 | B435 | B436 | B437 | B438 | B439 | B440 | B441 | B442 | B443 | B444 |
B445 | B446 | B447 | B448 | B449 | B450 | B451 | B452 | B453 | B454 | B455 | B456 |
B457 | B458 | B459 | B460 | B461 | B462 | B463 | B464 | B465 | B466 | B467 | B468 |
B469 | B470 | B471 | B472 | B473 | B474 | B475 | B476 | B477 | B478 | B479 | B480 |
B481 | B482 | B483 | B484 | B485 | B486 | B487 | B488 | B489 | B490 | B491 | B492 |
B493 | B494 | B495 | B496 | B497 | B498 | B499 | B500 | B501 | B502 | B503 | B504 |
B505 | B506 | B507 | B508 | B509 | B510 | B511 | B512 | B513 | B514 | B515 | B516 |
B517 | B518 | B519 | B520 | B521 | B522 | B523 | B524 | B525 | B526 | B527 | B528 |
B529 | B530 | B531 | B532 | B533 | B534 | B535 | B536 | B537 | B538 | B539 | B540 |
B541 | B542 | B543 | B544 | B545 | B546 | B547 | B548 | B549 | B550 | B551 | B552 |
B553 | B554 | B555 | B556 | B557 | B558 | B559 | B560 | B561 | B562 | B563 | B564 |
B565 | B566 | B567 | B568 | B569 | B570 | B571 | B572 | B573 | B574 | B575 | B576 |
B577 | B578 | B579 | B580 | B581 | B582 | B583 | B584 | B585 | B586 | B587 | B588 |
B589 | B590 | B591 | B592 | B593 | B594 | B595 | B596 | B597 | B598 | B599 | B600 |
B601 | B602 | B603 | B604 | B605 | B606 | B607 | B608 | B609 | B610 | B611 | B612 |
B613 | B614 | B615 | B616 | B617 | B618 | B619 | B620 | B621 | B622 | B623 | B624 |
B625 | B626 | B627 | B628 | B629 | B630 | B631 | B632 | B633 | B634 | B635 | B636 |
B637 | B638 | B639 | B640 | B641 | B642 | B643 | B644 | B645 | B646 | B647 | B648 |
B649 | B650 | B651 | B652 | B653 | B654 | B655 | B656 | B657 | B658 | B659 | B660 |
B661 | B662 | B663 | B664 | B665 | B666 | B667 | B668 | B669 | B670 | B671 | B672 |
B773 | B774 | B775 | B776 | B777 | B778 | B779 | B780 | B781 | B782 | B783 | B784 |
B785 | B786 | B787 | B788 | B789 | B790 | B791 | B792 | B793 | B794 | B795 | B796 |
B797 | B798 | B799 | B800 | B801 | B802 | B803 | B804 | B805 | B806 | B807 | B808 |
B809 | B810 | B811 | B812 | B813 | B814 | B815 | B816 | B817 | B818 | B819 | B820 |
B821 | B822 | B823 | B824 | B825 | B826 | B827 | B828 | B829 | B830 | B831 | B832 |
B833 | B834 | B835 | B836 | B837 | B838 | B839 | B840 | B841 | B842 | B843 | B844 |
B845 | B846 | B847 | B848 | B849 | B850 | B851 | B852 | B853 | B854 | B855 | B856 |
B857 | B858 | B859 | B860 | B861 | B862 | B863 | B864 | B865 | B866 | B867 | B868 |
B869 | B870 | B871 | B872 | B873 | B874 | B875 | B876 | B877 | B878 | B879 | B880 |
B881 | B882 | B883 | B884 | B885 | B886 | B887 | B888 | B889 | B890 | B891 | B892 |
B893 | B894 | B895 | B896 | B897 | B898 | B899 | B900 | B901 | B902 | B903 | B904 |
B905 | B906 | B907 | B908 | B909 | B910 | B911 | B912 | B913 | B914 | B915 | B916 |
B917 | B918 | B919 | B920 | B921 | B922 | B923 | B924 | B925 | B926 | B927 | B928 |
B929 | B930 | B931 | B932 | B933 | B934 | B935 | B936 | B937 | B938 | B939 | B940 |
B941 | B942 | B943 | B944 | B945 | B946 | B947 | B948 | B949 | B950 | B951 | B952 |
B953 | B954 | B955 | B956 | B957 | B958 | B959 | B960 | B961 | B962 | B963 | B964 |
B965 | B966 | B967 | B968 | B969 | B970 | B971 | B972 | B973 | B974 | B975 | B976 |
B977 | B978 | B979 | B980 | B981 | B982 | B983 | B984 | B985 | B986 | B987 | B988 |
B989 | B990 | B991 | B992 | B993 | B994 | B995 | B996 | B997 | B998 | B999 | B100 0 |
B100 | B100 | B100 | B100 | B100 | B100 | B100 | B100 | B100 | B101 | B101 | V B101 |
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 |
- 115CZ 304537 B6
Qs | Qs | Qs | Qs | Qs | Qs | Qs | Qs | Qs | Qs | Qs | Qs |
B101 | B101 | B101 | B101 | B101 | B101 | B101 | B102 | B102 | B102 | B102 | B102 |
3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 |
B102 | B102 | B102 | B102 | B102 | B103 | B103 | B103 | B103 | B103 | B103 | B103 |
5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 |
B103 | B103 | B103 | B104 | B104 | B104 | B104 | B104 | B104 | B104 | B104 | B104 |
7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 |
B104 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B106 |
9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 |
B106 | B106 | B106 | B106 | B106 | B106 | B106 | B106 | B106 | B107 | B107 | B107 |
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 |
B107 | B107 | B107 | B107 | B107 | B107 | B107 | B108 | B108 | B108 | B108 | |
3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 |
Tabulka 13: Sloučeniny obecného vzorce In:
Qs | Qs | Qs | Qs | Qs | Qs | Qs | Qs | Qs | Qs | Qs | Qs |
Bl | B2 | B3 | B4 | B5 | B6 | B7 | B8 | B9 | BIO | Bil | B12 |
B13 | B14 | B15 | B16 | B17 | B18 | B19 | B20 | B21 | B22 | B23 | B24 |
B25 | B26 | B27 | B28 | B29 | B30 | B31 | B32 | B33 | B34 | B35 | B36 |
B37 | B38 | B39 | B40 | B41 | B42 | B43 | B44 | B45 | B46 | B47 | B48 |
B49 | B50 | B51 | B52 | B53 | B54 | B55 | B56 | B57 | B58 | B59 | B60 |
B61 | B62 | B63 | B64 | B65 | B66 | B67 | B68 | B69 | B70 | B71 | B72 |
B73 | B74 | B75 | B76 | B77 | B78 | B79 | B80 | B81 | B82 | B83 | B84 |
B85 | B86 | B87 | B88 | B89 | B90 | B91 | B92 | B93 | B94 | B95 | B96 |
B97 | B98 | B99 | B100 | B101 | B102 | B103 | B104 | B105 | B106 | BIO 7 | B108 |
B109 | B110 | Blil | B112 | B113 | B114 | B115 | B116 | B117 | B118 | B119 | B120 |
B121 | B122 | B123 | B124 | B125 | B126 | B127 | B128 | B129 | B130 | B131 | B132 |
B133 | B134 | B135 | B136 | B137 | B138 | B139 | B140 | B141 | B142 | B143 | B144 |
B145 | B146 | B147 | B148 | B149 | B150 | B151 | B152 | B153 | B154 | B155 | B156 |
B157 | B158 | B159 | B160 | B161 | B162 | B163 | B164 | B165 | B166 | B167 | B168 |
B169 | B170 | B171 | B172 | B173 | B174 | B175 | B176 | B177 | B178 | B179 | B180 |
B181 | B182 | B183 | B184 | B185 | B186 | B187 | B188 | B189 | B190 | B191 | B192 |
B193 | B194 | B195 | B196 | B197 | B198 | B199 | B200 | B201 | B202 | B203 | B204 |
B205 | B206 | B207 | B208 | B209 | B210 | B211 | B212 | B213 | B214 | B215 | B216 |
B217 | B218 | B219 | B220 | B221 | B222 | B223 | B224 | B225 | B226 | B227 | B228 |
B229 | B230 | B231 | B232 | B233 | B234 | B235 | B236 | B237 | B238 | B239 | B240 |
B241 | B242 | B243 | B244 | B245 | B246 | B247 | B248 | B249 | B250 | B251 | B252 |
B253 | B254 | B255 | B256 | B257 | B258 | B259 | B260 | B261 | B262 | B263 | B264 |
B265 | B266 | B267 | B268 | B269 | B270 | B271 | B272 | B273 | B274 | B275 | B276 |
-116CZ 304537 B6
q3 B277 | q3 B278 | Qa B279 | q3 B280 | q3 B281 | q3 B282 | q3 B283 | q3 B284 | q3 B285 | q3 B286 | q3 B287 | q3 B288 |
B289 | B290 | B291 | B292 | B293 | B294 | B295 | B296 | B297 | B298 | B299 | B300 |
B301 | B302 | B303 | B304 | B305 | B306 | B307 | B308 | B309 | B310 | B311 | B312 |
B313 | B314 | B315 | B316 | B317 | B318 | B319 | B320 | B321 | B322 | B323 | B324 |
B325 | B326 | B327 | B328 | B329 | B330 | B331 | B332 | B333 | B334 | B335 | B336 |
B337 | B338 | B339 | B340 | B341 | B342 | B343 | B344 | B345 | B346 | B347 | B348 |
B349 | B350 | B351 | B352 | B353 | B354 | B355 | B356 | B357 | B358 | B359 | B360 |
B361 | B362 | B363 | B364 | B365 | B366 | B367 | B368 | B369 | B370 | B371 | B372 |
B373 | B374 | B375 | B376 | B377 | B378 | B379 | B380 | B381 | B382 | B383 | B384 |
B385 | B386 | B387 | B388 | B389 | B390 | B391 | B392 | B393 | B394 | B395 | B396 |
B397 | B398 | B399 | B400 | B401 | B402 | B403 | B404 | B405 | B406 | B407 | B408 |
B409 | B410 | B411 | B412 | B413 | B414 | B415 | B416 | B417 | B418 | B419 | B420 |
B421 | B422 | B423 | B424 | B425 | B426 | B427 | B428 | B429 | B430 | B431 | B432 |
B433 | B434 | B435 | B436 | B437 | B438 | B439 | B440 | B441 | B442 | B443 | B444 |
B445 | B446 | B447 | B448 | B449 | B450 | B451 | B452 | B453 | B454 | B455 | B456 |
B457 | B458 | B459 | B4 60 | B461 | B462 | B463 | B464 | B465 | B466 | B467 | B468 |
B469 | B470 | B471 | B472 | B473 | B474 | B475 | B476 | B477 | B478 | B479 | B480 |
B481 | B482 | B483 | B484 | B485 | B486 | B487 | B488 | B489 | B490 | B491 | B492 |
B493 | B494 | B495 | B496 | B497 | B498 | B499 | B500 | B501 | Β5Ό2 | B503 | B504 |
B505 | B506 | B507 | B508 | B509 | B510 | B511 | B512 | B513 | B514 | B515 | B516 |
B517 | B518 | B519 | B520 | B521 | B522 | B523 | B524 | B525 | B526 | B527 | B528 |
B529 | B530 | B531 | B532 | B533 | B534 | B535 | B536 | B537 | B538 | B539 | B540 |
B541 | B542 | B543 | B544 | B545 | B546 | B547 | B548 | B549 | B550 | B551 | B552 |
B553 | B554 | B555 | B556 | B557 | B558 | B559 | B560 | B561 | B562 | B563 | B564 |
B565 | B566 | B567 | B568 | B569 | B570 | B571 | B572 | B573 | B574 | B575 | B576 |
B577 | B578 | B579 | B580 | B581 | B582 | B583 | B584 | B585 | B586 | B587 | B588 |
B589 | B590 | B591 | B592 | B593 | B594 | B595 | B596 | B597 | B598 | B599 | B600 |
B601 | B602 | B603 | B604 | B605 | B606 | B607 | B608 | B609 | B610 | B611 | B612 |
B613 | B614 | B615 | B616 | B617 | B618 | B619 | B620 | B621 | B622 | B623 | B624 |
B625 | B626 | B627 | B628 | B629 | B630 | B631 | B632 | B633 | B634 | B635 | B636 |
B637 | B638 | B639 | B640 | B641 | B642 | B643 | B644 | B645 | B646 | B647 | B648 |
B649 | B650 | B651 | B652 | B653 | B654 | B655 | B656 | B657 | B658 | B659 | B660 |
B661 | B662 | B663 | B664 | B665 | B666 | B667 | B668 | B669 | B670 | B671 | B672 |
B773 | B774 | B775 | B776 | B777 | B778 | B779 | B780 | B781 | B782 | B783 | B784 |
B785 | B786 | B787 | B788 | B789 | B790 | B791 | B792 | B793 | B794 | B795 | B796 |
B797 | B798 | B799 | B800 | B801 | B802 | B803 | B804 | B805 | B806 | B807 | B808 |
B809 | B810 | B811 | B812 | B813 | B814 | B815 | B816 | B817 | B818 | B819 | B820 |
B821 | B822 | B823 | B824 | B825 | B826 | B827 | B828 | B829 | B830 | B831 | B832 |
B833 | B834 | B835 | B836 | B837 | B838 | B839 | B840 | B841 | B842 | B843 | B844 |
B845 | B846 | B847 | B848 | B849 | B85O | B851 | B852 | B853 | B854 | B855 | B856 |
B857 | B858 | B859 | B860 | B861 | B862 | B863 | B864 | B865 | B866 | B867 | B868 |
B869 | B870 | B871 | B872 | B873 | B874 | B875 | B876 | B877 | B878 | •B879 | B880 |
B881 | B882 | B883 | B884 | B885 | B886 | B887 | B888 | B889 | B890 | B891 | B892 |
B893 | B894 | B895 | B896 | B897 | B898 | B899 | B900 | B901 | B902 | B903 | B904 |
B905 | B906 | B907 | B908 | B909 | B910 | B911 | B912 | B913 | B914 | B915 | B916 |
B917 | B918 | B919 | B920 | B921 | B922 | B923 | B924 | B925 | B926 | B927 | B928 |
B929 | B930 | B931 | B932 | B933 | B934 | B935 | B936 | B937 | B938 | B939 | B940 |
B941 | B942 | B943 | B944 | B945 | B946 | B947 | B948 | B949 | B950 | B951 | B952 |
B953 | B954 | B955 | B956 | B957 | B958 | B959 | B960 | B961 | B962 | B963 | B964 |
B965 | B966 | B967 | B968 | B969 | B970 | B971 | B972 | B973 | B974 | B975 | B976 |
- 117CZ 304537 B6
Qa B977 | Qa B978 | Qa B979 | Qa B980 | q3 B981 | Qa B982 | Qa B983 | Qa B984 | Qa B985 | Qa B986 | Qa B987 | Qa B988 |
B989 | B990 | B991 | B992 | B993 | B994 | B995 | B996 | B997 | B998 | B999 | B100 |
B100 | B100 | B100 | B100 | B100 | B100 | B100 | B100 | B100 | B101 | B101 | U B101 |
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 |
B101 | B101 | B101 | B101 | B101 | B101 | B101 | B102 | B102 | B102 | B102 | B102 |
3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 |
B102 | B102 | B102 | B102 | B102 | B103 | B103 | B103 | B103 | B103 | B103 | B103 |
5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 |
B103 | B103 | B103 | B104 | B104 | B104 | B104 | B104 | B104 | B104 | B104 | B104 |
7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 |
B104 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | BIOS | B105 | B106 |
9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 |
B106 | B106 | B106 | B106 | B106 | B106 | B106 | B106 | B106 | B107 | B107 | B107 |
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 |
B107 | B107 | B107 | B107 | B107 | B107 | B107 | B108 | B108 | B108 | B108 | |
3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 |
Tabulka 14: Sloučeniny obecného vzorce Io:
Qa | 2l | 23 | Qa | 23 | Qa | Qa | Qa | Qa | 23 | Qa | |
BI | B2 | B3 | B4 | B5 | B6 | B7 | B8 | B9 | BIO | Bil | B12 |
B13 | B14 | B15 | B16 | B17 | B18 | B19 | B20 | B21 | B22 | B23 | B24 |
B25 | B26 | B27 | B28 | B29 | B30 | B31 | B32 | B33 | B34 | B35 | B36 |
B37 | B38 | B39 | B40 | B41 | B42 | B43 | B44 | B45 | B46 | B47 | B48 |
B49 | B50 | B51 | B52 | B53 | B54 | B55 | B56 | B57 | B58 | B59 | B60 |
B61 | B62 | B63 | B64 | B65 | B66 | B67 | B68 | B69 | B70 | B71 | B72 |
B73 | B74 | B75 | B76 | B77 | B78 | B79 | B80 | B81 | B82 | B83 | B84 |
B85 | B86 | B87 | B88 | B89 | B90 | B91 | B92 | B93 | B94 | B95 | B96 |
B97 | B98 | B99 | B100 | B101 | B102 | B103 | B104 | B105 | B106 | B107 | B108 |
B109 | B110 | Blil | B112 | B113 | B114 | B115 | B116 | B117 | B118 | B119 | B120 |
B121 | B122 | B123 | B124 | B125 | B126 | B127 | B128 | B129 | B130 | B131 | B132 |
B133 | B134 | B135 | B136 | B137 | B138 | B139 | B140 | B141 | B142 | B143 | B144 |
B145 | B146 | B147 | B148 | B149 | B150 | B151 | B152 | B153 | B154 | B155 | B156 |
B157 | B158 | B159 | B160 | B161 | B162 | B163 | B164 | B165 | B166 | B167 | B168 |
B169 | B170 | B171 | B172 | B173 | B174 | B175 | B176 | B177 | B178 | B179 | B180 |
B181 | B182 | B183 | B184 | B185 | B186 | B187 | B188 | B189 | B190 | B191 | B192 |
B193 | B194 | B195 | B196 | B197 | B198 | B199 | B200 | B201 | B202 | B203 | B204 |
B205 | B206 | B207 | B208 | B209 | B210 | B211 | B212 | B213 | B214 | B215 | B216 |
B217 | B218 | B219 | B220 | B221 | B222 | B223 | B224 | B225 | B226 | B227 | B228 |
-118CZ 304537 B6
q3 B229 | 23 B230 | q3 B231 | Qa B232 | q3 B233 | q3 B234 | q3 B235 | q3 B236 | q3 B237 | q3 B238 | q3 B239 | q3 B240 |
B241 | B242 | B243 | B244 | B245 | B246 | B247 | B248 | B249 | B250 | B251 | B252 |
B253 | B254 | B255 | B256 | B257 | B258 | B259 | B260 | B261 | B262 | B263 | B264 |
B265 | B266 | B267 | B268 | B269 | B270 | B271 | B272 | B273 | B274 | B275 | B276 |
B277 | B278 | B279 | B280 | B281 | B282 | B283 | B284 | B285 | B286 | B287 | B288 |
B289 | B290 | B291 | B292 | B293 | B294 | B295 | B296 | B297 | B298 | B299 | B300 |
B301 | B302 | B303 | B304 | B305 | B306 | B307 | B308 | B309 | B310 | B311 | B312 |
B313 | B314 | B315 | B316 | B317 | B318 | B319 | B320 | B321 | B322 | B323 | B324 |
B325 | B326 | B327 | B328 | B329 | B330 | B331 | B332 | B333 | B334 | B335 | B336 |
B337 | B338 | B339 | B340 | B341 | B342 | B343 | B344 | B345 | B346 | B347 | B348 |
B349 | B350 | B351 | B352 | B353 | B354 | B355 | B356 | B357 | B358 | B359 | B360 |
B361 | B362 | B363 | B364 | B365 | B366 | B367 | B368 | B369 | B370 | B371 | B372 |
B373 | B374 | B375 | B376 | B377 | B378 | B379 | B380 | B381 | B382 | B383 | B384 |
B385 | B386 | B387 | B388 | B389 | B390 | B391 | B392 | B393 | B394 | B395 | B396 |
B397 | B398 | B399 | B400 | B401 | B402 | B403 | B404 | B405 | B406 | B407 | B408 |
B409 | B410 | B411 | B412 | B413 | B414 | B415 | B416 | B417 | B418 | B419 | B420 |
B421 | B422 | B423 | B424 | B425 | B426 | B427 | B428 | B429 | B430 | B431 | B432 |
B433 | B434 | B435 | B436 | B437 | B438 | B439 | B440 | B441 | B442 | B443 | B444 |
B445 | B446 | B447 | B448 | B449 | B450 | B451 | B452 | B453 | B454 | B455 | B456 |
B457 | B458 | B459 | B460 | B461 | B4 62 | B463 | B464 | B465 | B466 | B467 | B468 |
B469 | B470 | B471 | B472 | B473 | B474 | B475 | B476 | B477 | B478 | B479 | B480 |
B481 | B482 | B483 | B484 | B485 | B486 | B487 | B488 | B489 | B490 | B491 | B492 |
B493 | B494 | B495 | B496 | B497 | B498 | B499 | B500 | B501 | B502 | B503 | B504 |
B505 | B506 | B507 | B508 | B509 | B510 | B511 | B512 | B513 | B514 | B515 | B516 |
B517 | B518 | B519 | B520 | B521 | B522 | B523 | B524 | B525 | B526 | B527 | B528 |
B529 | B530 | B531 | B532 | B533 | B534 | B535 | B536 | B537 | B538 | B539 | B540 |
B541 | B542 | B543 | B544 | B545 | B546 | B547 | B548 | B549 | B550 | B551 | B552 |
B553 | B554 | B555 | B556 | B557 | B558 | B559 | B560 | B561 | B562 | B563 | B564 |
B565 | B566 | B567 | B568 | B569 | B570 | B571 | B572 | B573 | B574 | B575 | B576 |
B577 | B578 | B579 | B580 | B581 | B582 | B583 | B584 | B585 | B586 | B587 | B588 |
B589 | B590 | B591 | B592 | B593 | B594 | B595 | B596 | B597 | B598 | B599 | B600 |
B601 | B602 | B603 | B604 | B605 | B606 | B607 | B608 | B609 | B61O | B611 | B612 |
B613 | B614 | B615 | B616 | B617 | B618 | B619 | B620 | B621 | B622 | B623 | B624 |
B625 | B626 | B627 | B628 | B629 | B630 | B631 | B632 | B633 | B634 | B635 | B636 |
B637 | B638 | B639 | B640 | B641 | B642 | B643 | B644 | B645 | B646 | B647 | B648 |
B649 | B650 | B651 | B652 | B653 | B654 | B655 | B656 | B657 | B658 | B659 | B660 |
B661 | B662 | B663 | B664 | B665 | B666 | B667 | B668 | B669 | B670 | B671 | B672 |
B773 | B774 | B775 | B77G | B777 | B778 | B779 | B780 | B781 | B782 | B783 | B784 |
B785 | B786 | B787 | B788 | B789 | B790 | B791 | B792 | B793 | B794 | B795 | B796 |
B797 | B798 | B799 | B800 | B801 | B802 | B803 | B804 | B805 | B806 | B807 | B808 |
B809 | B810 | B811 | B812 | B813 | B814 | B815 | B816 | B817 | B818 | B819 | B820 |
B821 | B822 | B823 | B824 | B825 | B826 | B827 | B828 | B829 | B830 | B831 | B832 |
B833 | B834 | B835 | B836 | B837 | B838 | B839 | B840 | B841 | B842 | B843 | B844 |
B845 | B846 | B847 | B848 | B849 | B850 | B851 | B852 | B853 | B854 | B855 | B856 |
B857 | B858 | B859 | B860 | B861 | B862 | B863 | B864 | B865 | B866 | B867 | B868 |
B869 | B870 | B871 | B872 | B873 | B874 | B875 | B876 | B877 | B878 | B879 | B880 |
B881 | B882 | B883 | B884 | B885 | B886 | B887 | B888 | B889 | B890 | B891 | B892 |
B893 | B894 | B895 | B896 | B897 | B898 | B899 | B900 | B901 | B902 | B903 | B904 |
B905 | B906 | B907 | B908 | B909 | B910 | B911 | B912 | B913 | B914 | B915 | B916 |
B917 | B918 | B919 | B920 | B921 | B922 | B923 | B924 | B925 | B926 | B927 | B928 |
-119CZ 304537 B6
Qa B929 | Qa B930 | Q3 B931 | Qa B932 | Qa B933 | Qa B934 | Qa B935 | Qa B936 | Qa B937 | Qa B938 | Qa B939 | Qa B940 |
B941 | B942 | B943 | B944 | B945 | B946 | B947 | B948 | B949 | B950 | B951 | B952 |
B953 | B954 | B955 | B956 | B957 | B958 | B959 | B960 | B961 | B962 | B963 | B964 |
B965 | B966 | B967 | B968 | B969 | B970 | B971 | B972 | B973 | B974 | B975 | B976 |
B977 | B978 | B979 | B980 | B981 | B982 | B983 | B984 | B985 | B986 | B987 | B988 |
B989 | B990 | B991 | B992 | B993 | B994 | B995 | B996 | B997 | B998 | B999 | B100 π |
B100 | B100 | B100 | B100 | B100 | B100 | B100 | B100 | B100 | B101 | B101 | u B101 |
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 |
B101 | B101 | B101 | B101 | B101 | B101 | B101 | B102 | B102 | B102 | B102 | B102 |
3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 |
B102 | B102 | B102 | B102 | B102 | B103 | B103 | B103 | B103 | B103 | B103 | B103 |
5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 |
B103 | B103 | B103 | B104 | B104 | B104 | B104 | B104 | B104 | B104 | B104 | B104 |
7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 |
B104 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B106 |
9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 |
B106 | B106 | B106 | B106 | B106 | B106 | B106 | B106 | B106 | B107 | B107 | B107 |
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 |
B107 | B107 | B107 | B107 | B107 | B107 | B107 | B108 | B108 | B108 | B108 | |
3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 |
Tabulka 15: Sloučeniny obecného vzorce Ip:
Qa | Qa | Qa | Qa | 03 | Qa | Qa | Qa | Qa | Qa | Qa | Qa |
Bl | B2 | B3 | B4 | B5 | B6 | B7 | B8 | B9 | BIO | Bil | B12 |
B13 | B14 | B15 | B16 | B17 | B18 | B19 | B20 | B21 | B22 | B23 | B24 |
B25 | B26 | B27 | B28 | B29 | B30 | B31 | B32 | B33 | B34 | B35 | B36 |
B37 | B38 | B39 | B40 | B41 | B42 | B43 | B44 | B45 | B46 | B47 | B48 |
B49 | B50 | B51 | B52 | B53 | B54 | B55 | B56 | B57 | B58 | B59 | B60 |
B61 | B62 | B63 | B64 | B65 | B66 | B67 | B68 | B69 | B70 | B71 | B72 |
B73 | B74 | B75 | B76 | B77 | B78 | B79 | B80 | B81 | B82 | B83 | B84 |
B85 | B86 | B87 | B88 | B89 | B90 | B91 | B92 | B93 | B94 | B95 | B96 |
B97 | B98 | B99 | B100 | B101 | B102 | B103 | B104 | B105 | B106 | B107 | B108 |
B109 | B110 | Blil | B112 | B113 | B114 | B115 | B116 | B117 | B118 | B119 | B120 |
B121 | B122 | B123 | B124 | B125 | B126 | B127 | B128 | B129 | B130 | B131 | B132 |
B133 | B134 | B135 | B136 | B137 | B138 | B139 | B140 | B141 | B142 | B143 | B144 |
B145 | B146 | B147 | B148 | B149 | B150 | B151 | B152 | B153 | B154 | B155 | B156 |
-120CZ 304537 B6
q3 B157 | q3 B158 | q3 B159 | q3 B160 | q3 B161 | q3 B162 | q3 B163 | q3 B164 | q3 B165 | q3 B166 | q3 B167 | q3 B168 |
B169 | B170 | B171 | B172 | B173 | B174 | B175 | B176 | B177 | B178 | B179 | B180 |
B181 | B182 | B183 | B184 | B185 | B186 | B187 | B188 | B189 | B190 | B191 | B192 |
B193 | B194 | B195 | B196 | B197 | B198 | B199 | B200 | B201 | B202 | B203 | B204 |
B205 | B206 | B207 | B208 | B209 | B210 | B211 | B212 | B213 | B214 | B215 | B216 |
B217 | B218 | B219 | B220 | B221 | B222 | B223 | B224 | B225 | B226 | B227 | B228 |
B229 | B230 | B231 | B232 | B233 | B234 | B235 | B236 | B237 | B238 | B239 | B240 |
B241 | B242 | B243 | B244 | B245 | B246 | B247 | B248 | B249 | B250 | B251 | B252 |
B253 | B254 | B255 | B256 | B257 | B258 | B259 | B260 | B261 | B262 | B263 | B264 |
B265 | B266 | B267 | B268 | B269 | B270 | B271 | B272 | B273 | B274 | B275 | B276 |
B277 | B278 | B279 | B280 | B281 | B282 | B283 | B284 | B285 | B286 | B287 | B288 |
B289 | B290 | B291 | B292 | B293 | B294 | B295 | B296 | B297 | B298 | B299 | B300 |
B301 | B302 | B303 | B304 | B305 | B306 | B307 | B308 | B309 | B310 | B311 | B312 |
B313 | B314 | B315 | B316 | B317 | B318 | B319 | B320 | B321 | B322 | B323 | B324 |
B325 | B326 | B327 | B328 | B329 | B330 | B331 | B332 | B333 | B334 | B335 | B336 |
B337 | B338 | B339 | B340 | B341 | B342 | B343 | B344 | B345 | B346 | B347 | B348 |
B349 | B350 | B351 | B352 | B353 | B354 | B355 | B356 | B357 | B358 | B359 | B360 |
B361 | B362 | B363 | B364 | B365 | B366 | B367 | B368 | B369 | B370 | B371 | B372 |
B373 | B374 | B375 | B376 | B377 | B378 | B379 | B380 | B381 | B382 | B383 | B384 |
B385 | B386 | B387 | B388 | B389 | B390 | B391 | B392 | B393 | B394 | B395 | B396 |
B397 | B398 | B399 | B400 | B401 | B402 | B403 | B404 | B405 | B406 | B407 | B408 |
B409 | B410 | B411 | B412 | B413 | B414 | B415 | B416 | B417 | B418 | B419 | B420 |
B421 | B422 | B423 | B424 | B425 | B426 | B427 | B428 | B429 | B430 | B431 | B432 |
B433 | B434 | B435 | B436 | B437 | B438 | B439 | B440 | B441 | B442 | B443 | B444 |
B445 | B446 | B447 | B448 | B449 | B450 | B451 | B452 | B453 | B454 | B455 | B456 |
B457 | B458 | B459 | B460 | B461 | B462 | B463 | B464 | B465 | B466 | B467 | B468 |
B469 | B470 | B471 | B472 | B473 | B474 | B475 | B476 | B477 | B478 | B479 | B480 |
B481 | B482 | B483 | B484 | B485 | B486 | B487 | B488 | B489 | B490 | B491 | B492 |
B493 | B494 | B495 | B496 | B497 | B498 | B499 | B500 | B501 | B502 | B503 | B504 |
B505 | B506 | B507 | B508 | B509 | B510 | B511 | B512 | B513 | B514 | B515 | B516 |
B517 | B518 | B519 | B520 | B521 | B522 | B523 | B524 | B525 | B526 | B527 | B528 |
B529 | B530 | B531 | B532 | B533 | B534 | B535 | B536 | B537 | B538 | B539 | B540 |
B541 | B542 | B543 | B544 | B545 | B546 | B547 | B548 | B549 | B550 | B551 | B552 |
B553 | B554 | B555 | B556 | B557 | B558 | B559 | B560 | B561 | B562 | B563 | B564 |
B565 | B566 | B567 | B568 | B569 | B570 | B571 | B572 | B573 | B574 | B575 | B576 |
B577 | B578 | B579 | B580 | B581 | B582 | B583 | B584 | B585 | B586 | B587 | B588 |
B589 | B590 | B591 | B592 | B593 | B594 | B595 | B596 | B597 | B598 | B599 | B600 |
B601 | B602 | B603 | B604 | B605 | B606 | B607 | B608 | B609 | B610 | B611 | B612 |
B613 | B614 | B615 | B616 | B617 | B618 | B619 | B620 | B621 | B622 | B623 | B624 |
B625 | B626 | B627 | B628 | B629 | B630 | B631 | B632 | B633 | B634 | B635 | B636 |
B637 | B638 | B639 | B640 | B641 | B642 | B643 | B644 | B645 | B646 | B647 | B648 |
B649 | B650 | B651 | B652 | B653 | B654 | B655 | B656 | B657 | B658 | B659 | B660 |
B661 | B662 | B663 | B664 | B665 | B666 | B667 | B668 | B669 | B670 | B671 | B672 |
B773 | B774 | B775 | B776 | B777 | B778 | B779 | B780 | B781 | B782 | B783 | B784 |
B785 | B786 | B787 | B788 | B789 | B790 | B791 | B792 | B793 | B794 | B795 | B796 |
B797 | B798 | B799 | B800 | B801 | B802 | B803 | B804 | B805 | B806 | B807 | B808 |
B809 | B810 | B811 | B812 | B813 | B814 | B815 | B816 | B817 | B818 | B819 | B820 |
B821 | B822 | B823 | B824 | B825 | B826 | B827 | B828 | B829 | B830 | B831 | B832 |
B833 | B834 | B835 | B836 | B837 | B838 | B839 | B840 | B841 | B842 | B843 | B844 |
B845 | B846 | B847 | B848 | B849 | B850 | B851 | B852 | B853 | B854 | B855 | B856 |
- 121 CZ 304537 B6
Qa B857 | q3 B858 | q3 B859 | q3 B860 | q3 B861 | q3 B862 | q3 B863 | q3 B864 | q3 B865 | Qa B866 | q3 B867 | q3 B868 |
B869 | B870 | B871 | B872 | B873 | B874 | B875 | B876 | B877 | B878 | B879 | B880 |
B881 | B882 | B883 | B884 | B885 | B886 | B887 | B888 | B889 | B890 | B891 | B892 |
B893 | B894 | B895 | B896 | B897 | B898 | B899 | B900 | B901 | B902 | B903 | B904 |
B905 | B906 | B907 | B908 | B909 | B910 | B911 | B912 | B913 | B914 | B915 | B916 |
B917 | B918 | B919 | B920 | B921 | B922 | B923 | B924 | B925 | B926 | B927 | B928 |
B929 | B930 | B931 | B932 | B933 | B934 | B935 | B936 | B937 | B938 | B939 | B940 |
B941 | B942 | B943 | B944 | B945 | B946 | B947 | B948 | B949 | B950 | B951 | B952 |
B953 | B954 | B955 | B956 | B957 | B958 | B959 | B960 | B961 | B962 | B963 | B964 |
B965 | B966 | B967 | B968 | B969 | B970 | B971 | B972 | B973 | B974 | B975 | B97 6 |
B977 | B978 | B979 | B980 | B981 | B982 | B983 | B984 | B985 | B986 | B987 | B988 |
B989 | B990 | B991 | B992 | B993 | B994 | B995 | B996 | B997 | B998 | B999 | B100 n |
B100 | B100 | B100 | B100 | B100 | B100 | B100 | B100 | B100 | B101 | B101 | B101 |
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 |
B1O1 | B101 | B1O1 | B101 | B101 | B101 | B101 | B102 | B102 | B102 | B102 | B102 |
3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 |
B102 | B102 | B102 | B102 | B102 | B103 | B103 | B103 | B103 | B103 | B103 | B103 |
5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 |
B103 | B103 | B103 | B104 | B104 | B104 | B1O4 | B1O4 | B104 | B104 | B104 | B104 |
7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 |
B104 | B105 | B105 | B105 | B105 | B105 | B105 | B1O5 | B105 | B105 | B105 | B106 |
9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 |
B106 | B106 | B106 | B106 | B106 | B106 | B106 | B106 | B106 | B107 | B107 | B107 |
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 |
B107 | B107 | B107 | B107 | B107 | B107 | B107 | B108 | B108 | B108 | B108 | |
3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 | |
Tabulka 16: Sloučeniny obecného vzorce Iq: |
Qa | Qa | Qa | 03 | Qa | 03 | 03 | Ol | 03 | Qa | 03 | Qa |
Bl | B2 | B3 | B4 | B5 | B6 | B7 | B8 | B9 | BIO | Bil | B12 |
B13 | B14 | B15 | B16 | B17 | B18 | B19 | B20 | B21 | B22 | B23 | B24 |
B25 | B26 | B27 | B28 | B29 | B30 | B31 | B32 | B33 | B34 | B35 | B36 |
B37 | B38 | B39 | B40 | B41 | B42 | B43 | B44 | B45 | B46 | B47 | B48 |
B49 | B50 | B51 | B52 | B53 | B54 | B55 | B56 | B57 | B58 | B59 | B60 |
B61 | B62 | B63 | B64 | B65 | B66 | B67 | B68 | B69 | B70 | B71 | B72 |
- 122CZ 304537 B6
q3 | q3 | q3 | q3 | q3 | Sl | q3 | q3 | q3 | q3 | q3 | Si |
B73 | B74 | B75 | B76 | B77 | B78 | B7 9 | B80 | B81 | B82 | B83 | B84 |
B85 | B86 | B87 | B88 | B89 | B90 | B91 | B92 | B93 | B94 | B95 | B96 |
B97 | B98 | B99 | B100 | B101 | B102 | B103 | B104 | B105 | B106 | B107 | B108 |
B109 | B110 | Blil | B112 | B113 | B114 | B115 | B116 | B117 | B118 | B119 | B120 |
B121 | B122 | B123 | B124 | B125 | B126 | B127 | B128 | B129 | B130 | B131 | B132 |
B133 | B134 | B135 | B136 | B137 | B138 | B139 | B140 | B141 | B142 | B143 | B144 |
B145 | B146 | B147 | B148 | B149 | B150 | B151 | B152 | B153 | B154 | B155 | B156 |
B157 | B158 | B159 | B160 | B161 | B162 | B163 | B164 | B165 | B166 | B167 | B168 |
B169 | B170 | B171 | B172 | B173 | B174 | B175 | B176 | B177 | B178 | B179 | B180 |
B181 | B182 | B183 | B184 | B185 | B186 | B187 | B188 | B189 | B190 | B191 | B192 |
B193 | B194 | B195 | B196 | B197 | B198 | B199 | B200 | B201 | B202 | B203 | B204 |
B205 | B206 | B207 | B208 | B209 | B210 | B211 | B212 | B213 | B214 | B215 | B216 |
B217 | B218 | B219 | B220 | B221 | B222 | B223 | B224 | B225 | B226 | B227 | B228 |
B229 | B230 | B231 | B232 | B233 | B234 | B235 | B236 | B237 | B238 | B239 | B240 |
B241 | B242 | B243 | B244 | B245 | B246 | B247 | B248 | B249 | B250 | B251 | B252 |
B253 | B254 | B255 | B256 | B257 | B258 | B259 | B260 | B261 | B262 | B263 | B264 |
B265 | B266 | B267 | B268 | B269 | B270 | B271 | B272 | B273 | B274 | B275 | B27 6 |
B277 | B278 | B279 | B280 | B281 | B282 | B283 | B284 | B285 | B286 | B287 | B288 |
B289 | B290 | B291 | B292 | B293 | B294 | B295 | B296 | B297 | B298 | B299 | B300 |
B301 | B302 | B303 | B304 | B305 | B306 | B307 | B308 | B309 | B310 | B311 | B312 |
B313 | B314 | B315 | B316 | B317 | B318 | B319 | B320 | B321 | B322 | B323 | B324 |
B325 | B326 | B327 | B328 | B329 | B330 | B331 | B332 | B333 | B334 | B335 | B336 |
B337 | B338 | B339 | B340 | B341 | B342 | B343 | B344 | B345 | B346 | B347 | B348 |
B349 | B350 | B351 | B352 | B353 | B354 | B355 | B356 | B357 | B358 | B359 | B360 |
B361 | B362 | B363 | B364 | B365 | B366 | B367 | B368 | B369 | B370 | B371 | B372 |
B373 | B374 | B375 | B376 | B377 | B378 | B379 | B380 | B381 | B382 | B383 | B384 |
B385 | B386 | B387 | B388 | B389 | B390 | B391 | B392 | B393 | B394 | B395 | B396 |
B397 | B398 | B399 | B400 | B401 | B402 | B403 | B404 | B405 | B406 | B407 | B408 |
B409 | B410 | B411 | B412 | B413 | B414 | B415 | B416 | B417 | B418 | B419 | B420 |
B421 | B422 | B423 | B424 | B425 | B426 | B427 | B428 | B429 | B430 | B431 | B432 |
B433 | B434 | B435 | B436 | B437 | B438 | B439 | B440 | B441 | B442 | B443 | B444 |
B445 | B446 | B447 | B448 | B449 | B450 | B451 | B452 | B453 | B454 | B455 | B456 |
B457 | B458 | B459 | B460 | B4 61 | B462 | B463 | B4 64 | B465 | B466 | B467 | B4 68 |
B469 | B470 | B471 | B472 | B473 | B474 | B475 | B476 | B477 | B478 | B479 | B480 |
B481 | B482 | B483 | B484 | B485 | B486 | B487 | B488 | B489 | B490 | B491 | B4 92 |
B493 | B494 | B495 | B496 | B497 | B498 | B499 | B500 | B501 | B502 | B503 | B504 |
B505 | B506 | B507 | B508 | B509 | B510 | B511 | B512 | B513 | B514 | B515 | B516 |
B517 | B518 | B519 | B520 | B521 | B522 | B523 | B524 | B525 | B526 | B527 | B528 |
B529 | B530 | B531 | B532 | B533 | B534 | B535 | B536 | B537 | B538 | B539 | B540 |
B541 | B542 | B543 | B544 | B545 | B546 | B547 | B548 | B549 | B550 | B551 | B552 |
B553 | B554 | B555 | B556 | B557 | B558 | B559 | B560 | B561 | B562 | B563 | B564 |
B565 | B566 | B567 | B568 | B569 | B570 | B571 | B572 | B573 | B574 | B575 | B576 |
B577 | B578 | B579 | B580 | B581 | B582 | B583 | B584 | B585 | B586 | B587 | B588 |
B589 | B590 | B591 | B592 | B593 | B594 | B595 | B596 | B597 | B598 | B599 | B600 |
B601 | B602 | B603 | B604 | B605 | B606 | B607 | B608 | B609 | B610 | B611 | B612 |
B613 | B614 | B615 | B616 | B617 | B618 | B619 | B620 | B621 | B622 | B623 | B624 |
B625 | B626 | B627 | B628 | B629 | B630 | B631 | B632 | B633 | B634 | B635 | B636 |
B637 | B638 | B639 | B640 | B641 | B642 | B643 | B644 | B645 | B646 | B647 | B648 |
B649 | B650 | B651 | B652 | B653 | B654 | B655 | B656 | B657 | B658 | B659 | B660 |
B661 | B662 | B663 | B664 | B665 | B666 | B667 | B668 | B669 | B670 | B671 | B672 |
- 123CZ 304537 B6
q3 B773 | Qs B774 | q3 B775 | q3 B776 | q3 B777 | q3 B778 | q3 B779 | q3 B780 | q3 B781 | q3 B782 | q3 B783 | q3 B784 |
B785 | B786 | B787 | B788 | B789 | B790 | B791 | B792 | B793 | B794 | B795 | B796 |
B797 | B798 | B799 | B800 | B801 | B802 | B803 | B804 | B805 | B806 | B807 | B808 |
B809 | B810 | B811 | B812 | B813 | B814 | B815 | B816 | B817 | B818 | B819 | B820 |
B821 | B822 | B823 | B824 | B825 | B826 | B827 | B828 | B829 | B830 | B831 | B832 |
B833 | B834 | B835 | B836 | B837 | B838 | B839 | B840 | B841 | B842 | B843 | B844 |
B845 | B846 | B847 | B848 | B849 | B850 | B851 | B852 | B853 | B854 | B855 | B856 |
B857 | B858 | B859 | B860 | B861 | B862 | B863 | B864 | B865 | B866 | B867 | B868 |
B869 | B870 | B871 | B872 | B873 | B874 | B875 | B876 | B877 | B878 | B879 | B880 |
B881 | B882 | B883 | B884 | B885 | B886 | B887 | B888 | B889 | B890 | B891 | B892 |
B893 | B894 | B895 | B896 | B897 | B898 | B899 | B900 | B901 | B902 | B903 | B904 |
B905 | B906 | B907 | B908 | B909 | B910 | B911 | B912 | B913 | B914 | B915 | B916 |
B917 | B918 | B919 | B920 | B921 | B922 | B923 | B924 | B925 | B926 | B927 | B928 |
B929 | B930 | B931 | B932 | B933 | B934 | B935 | B936 | B937 | B938 | B939 | B940 |
B941 | B942 | B943 | B944 | B945 | B946 | B947 | B948 | B949 | B950 | B951 | B952 |
B953 | B954 | B955 | B956 | B957 | B958 | B959 | B960 | B961 | B962 | B963 | B964 |
B965 | B966 | B967 | B968 | B969 | B970 | B971 | B972 | B973 | B974 | B975 | B976 |
B977 | B978 | B979 | B980 | B981 | B982 | B983 | B984 | B985 | B986 | B987 | B988 |
B989 | B990 | B991 | B992 | B993 | B994 | B995 | B996 | B997 | B998 | B999 | B100 0 B101 |
B100 | B100 | B100 | B100 | B100 | B100 | B100 | B100 | B100 | B101 | B101 | |
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 |
B101 | B101 | B101 | B101 | B101 | B101 | B101 | B102 | B102 | B102 | B102 | B102 |
3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 |
B102 | B102 | B102 | B102 | B102 | B103 | B103 | B103 | B103 | B103 | B103 | B103 |
5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 |
B103 | B103 | B103 | B104 | B104 | B104 | B104 | B104 | B104 | B104 | B104 | B104 |
7 | 8 | 9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 |
B104 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B105 | B106 |
9 | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 |
B106 | B106 | B106 | B106 | B106 | B106 | B106 | B106 | B106 | B107 | B107 | B107 |
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 |
B107 | B107 | B107 | B107 | B107 | B107 | B107 | B108 | B108 | B108 | BIOS | |
3 | 4 | 5 | 6 | 7 | 8 | 9 | 0 | 1 | 2 | 3 |
Tabulka 17: Sloučeniny obecného vzorce Ir:
O
Qe | Qe | Qg | Qg | Qg | Qg | Qg | Qg | Qg | Qg | Qg | Qg |
Cl | C2 | C3 | C4 | C5 | C6 | C7 | C8 | C9 | CIO | Cil | C12 |
C13 | C14 | C15 | C16 | C17 | C18 | C19 | C20 | C21 | C22 | C23 | C24 |
C25 | C26 | C27 | C28 | C29 | C30 | C31 | C32 | C33 | C34 | C35 | C36 |
C37 | C38 | C39 | C40 | C41 | C42 | C43 | C44 | C45 | C46 | C47 | C48 |
- 124CZ 304537 B6
Qe | Qe | Qe | Qe | Qe | Qe | Qe | Qe | Qe | Qe | Qe | Qe |
C49 | C50 | C51 | C52 | C53 | C54 | C55 | C56 | C57 | C58 | C59 | C60 |
C61 | C62 | C63 | C64 | C65 | C66 | C67 | C68 | C69 | C70 | C71 | C72 |
C73 | C74 | C75 | C76 | C77 | C78 | C79 | C80 | C81 | C82 | C83 | C84 |
C85 | C86 | C87 | C88 | C89 | C90 | C91 | C92 | C93 | C94 | C95 | C96 |
C97 | C98 | C99 | C100 | C101 | C102 | C103 | C104 | C105 | C106 | C107 | C108 |
C109 | C110 | Clil | C112 | C113 | C114 | C115 | C116 | C117 | C118 | C119 | C120 |
C121 | C122 | C123 | C124 | C125 | C126 | C127 | C128 | C129 | C130 | C131 | C132 |
C133 | C134 | C135 | C136 | C137 | C138 | C139 | C140 | C141 | C142 | C143 | C144 |
C145 | C146 | C147 | C148 | C149 | C150 | C151 |
Tabulka 18: Sloučeniny obecného vzorce Is:
Q7 | Qz | 2z | 2z | 2z | Qz | Qz | Q7 | Q7 | Q7 | Q7 | Q7 |
Dl | D2 | D3 | D4 | D5 | D6 | D7 | D8 | D9 | D10 | Dli | D12 |
D13 | D14 | D15 | D16 | D17 | D18 | D19 | D20 | D21 | D22 | D2.3 | D24 |
D25 | D26 | D27 | D28 | D29 | D30 | D31 | D32 | D33 | D34 | D35 | D36 |
D37 | D38 | D39 | D40 | D41 | D42 | D43 | D44 | D45 | D46 | D47 | D48 |
D4 9 | D50 | D51 | D52 | D53 | D54 | D55 | D56 | D57 | D58 | D59 | D60 |
D61 | D62 | D63 | D64 | D65 | D66 | D67 | D68 | D69 | D70 | D71 | D72 |
D73 | D74 | D75 | D76 | D77 | D78 | D79 | D80 | D81 | D82 | D83 | D84 |
D85 | D86 | D87 | D88 | D89 | D90 | D91 | D92 | D93 | D94 | D95 | D96 |
D97 | D98 | D99 | D100 | D101 | D102 | D103 | D104 | D105 | D106 | D107 | Dl 08 |
D109 | DUO | Dl 11 | D112 | D113 | D114 | D115 | D116 | D117 | Dl 18 | D119 | D120 |
D121 | D122 | D123 | D124 | D125 | D126 | D127 | D128 | D129 | Dl 30 | D131 | D132 |
D133 | D134 | D135 | D136 | D137 | D138 | D139 | D140 |
Tabulka 19: Sloučeniny obecného vzorce Iv:
- 125CZ 304537 B6
Slouč
č.
El
E2
E3
E4
E5
E6
E7
E8
E9
E10
Eli
E12
E13
E14
E15
E16
E17
R75
CH2OCH3 CH2OC2H5 CH20-n-propyl CH2O-i s opropy1 CH2O-n-butyl CH20-isobutyl CH2O-terc-butyl (CH2)2OCH3 (CH2) 2O-ethyl (CH2)2O-npropyl (CH2)2Oisopropyl (CH2) 20-n-butyl (CH2)2Oisobutyl (CH2) 2O-tercbutyl (CH2)2O(CH2)2OCH (CH2)2O(CH2)2OCH
C2H5
Tabulka 20: Fyzikální údaje pro tabulky 5 až 19 (t.t. ve °C)
Slouč.
Fyz. údaj e
Slouč. Fyz. údaje Slouč.
A2 | 150-151 | C46 | 159-161 | A2-B1058 |
A3 | 148-149 | C91 | 141-143 | A2-B1066 |
A4 | 143-144 | C146 | 99-101 | A2-B1067 |
A5 | 81-82 | C149 | 148-150 | A2-B1069 |
A6 | 148-150 | A2-B1 | 90-92 | A2-B1069 |
A7 | 105-106 | A2-B68 | 120-121 | A8-B1 |
A8 | 123-124 | A2-B2 | pryskyřice | A7-B1 |
A9 | 73-74 | A2-B90 | pryskyřice | A3-B1 |
A10 | 165-167 | A2-B93 | 95-96 | A94-B1 |
A15 | 164-166 | A2-B46 | 61-62 cis— rac | A66-B24 |
A17 | 99-100 | A2-B46 | 83-84 trans-rac | A64-B1 |
A26 | 143-144 | A2-B91 | pryskyřice | A154-B1 |
A27 | 107-108 | A2-B1081 | olej | A6-B1 |
Fyz.
údaje
88-89 viskózní pryskyř.
olej olej viskózní olej
97-98 olej
42-44
57-58
80-82
49-51
94-95
123-124
- 126CZ 304537 B6
Slouč. A29 | Fyz. údaje 173-174 | Slouč. A2-B1082 | Fyz. údaje Slouč. | Fyz. údaje olej | |
pryskyřice | A6-B24 | ||||
A30 | 178-181 | A2-B1083 | pryskyřice | A34-B1 | 53-54 |
A31 | 209-210 | A2-B29 | 87-88 | A2-B25 | olej |
A32 | 145-146 | A2-B73 | pryskyřice | A2-B925 | olej |
A34 | 170-171 | A2-B95 | 106-107 | E8 | 55-56 |
A64 | 134-135 | A2-B31 | 151-153 | E17 | 99-101 |
A94 | 134-135 | A2-B75 | amorfní | ||
A154 | 108-110 | A2-B24 | olej | ||
B1057 | 166-167 | A2-B5 | pryskyřice | ||
B1058 | krysta- | A2-C91 | pryskyřice | ||
lický | |||||
B1061 | krysta- | A2-C146 | olej | ||
lický | |||||
B1063 | krysta- | A2-B112 | pryskyřice | ||
lický | |||||
B1065 | olej | A2-D140 | olej | ||
B1066 | 150-152 | A2-B1057 | amorfní | ||
B1067 | 122-123 | A2-B1063 | olej | ||
B1069 | 117-118 | A2-B1061 | olej | ||
B1070 | krysta- | A2-B133 | olej | ||
lický |
Sloučeniny vzorce 2.1 a 2.3 až 2.13.C jsou známé pod názvy imazamox, imazethapyr, imazachin, imazapyr, dimethenamid, atrazin, terbuthylazin, simazin, terbutym, cyanazin, ametryn, terbu5 meton, prohexadione calcium, sethoxydim, clethodim, tepraloxydim, flumetsulam, metosulam, pyridate, bromxynil, ioxynil, sulcotrione, carfentrazone, sulfentrazone, isoxaflutole, glufosinate, primisulfuron, prosulfuron, rimsulfuron, halogensulfuron, nicosulfuron, ethoxysulfuron, flazasulfuron a thifensulfuron a jsou popsané v Pesticide Manual, jedenácté vydání, British Crop Protection Council, 1997 pod přístupovými čísly 412, 415, 414, 413, 240, 34, 692, 651, 693, 168, 20, io 691, 595, 648, 146, 49, 339, 495, 626, 88, 425, 664, 112, 665, 436, 382, 589, 613, 644, 389, 519, 287, 325 a 704. Sloučenina vzorce 2.13, kde Yb Y3 a Y4 jsou methinová skupina, Y2 je skupina C-I, R74 je skupina COOMe, Y5 je atom dusíku, Y6 je methylová skupina a Y7 je methoxyskupina je známá pod názvem jodsulfuron (zejména sodná sůl) z AGROW No. 296, 16. ledna 1998, strana 22. sloučenina vzorce 2.13, kde Yb Y2, Y3 a Y4 jsou methinové skupiny, R74 je trifluor15 methylová skupina, Y5 je atom dusíku, Yé je trifluormethylová skupina a Y7 je methoxyskupina, je známá pod názvem tritosulíuron aje popsaná v DE-A 40 38 430. Sloučenina vzorce 2.13, kde Yi je skupina NH-CHO, Y2, Y3 a Y4 jsou methinová skupina, R74 je skupina CONMe2, Y5 je methinová skupina a Y6 a Y7 jsou methoxyskupina je popsaná například v WO 95/29 899.
S enantiomer sloučeniny vzorce 2.12 je registrován pod číslem CAS-Reg. No. [35597-44-5]. Sloučenina obecného vzorce 2.2, aRS,l'S(-)N-(r-methyl-2'-methoxyethyl)-N-chloracetyl-2ethyl-6-methylanilin, a sloučenina obecného vzorce 2.3, (lS,aRS)-2-chlor-N-(2,4-dimethyl-3thienyl)-N-(2-methoxy-l-methylethyl)acetamid, jsou popsané například v WO 97/34 485. Sloučenina vzorce 2.9, kde R09 je skupina NO2 je známá pod názvem mesotrione aje popsaná na25 příklad v US-A 5 006 158. Sloučenina vzorce 2.6, kde Re2 je ethoxyskupina, R^ je atom fluoru, Y je methinová skupina, Ré4 je methoxykarbonylová skupina, R je atom vodíku a R^ je atom chloru, je známá pod názvem cloransulam, například z AGROW No. 261, 2. srpna 1996, strana 21. Sloučenina vzorce 2.6, kde R2 je methoxyskupina, R^ je atom vodíku, Y je skupina C-F, Rs4 je atom fluoru, R5 je atom vodíku a Róó je atom fluoru, je známá pod názvem florasulam a je popsaná v US-A 5 163 995.
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Dále jsou následující sloučeniny z kompozice podle předkládaného vynálezu popsané v Pesticide Manual, jedenácté vydání, British Crop Protection Council, 1997:
Sloučenina vzorce (název) Pesticide Manual jedenácté vydání, přístupové číslo:
2.14 | (metribuzin) | 497 |
2.15 | (aclonifen) | 8 |
2.16 | (glyphosate) | 383 |
2.17 | (bentazone) | 65 |
2.18 | (pendimethalin) | 557 |
2.19 | (dicamba) | 210 |
2.20 | (butylate) | 100 |
2.22 | (clomazone) | 150 |
2.23 | (2,4-D) | 192 |
2.24 | (flumiclorac) | 340 |
2.25 | (fluthiacet-methyl) | 359 |
2.26 | (flurtamone) | 356 |
2.27 | (flumioxazin) | 341 |
2.28 | (paraquat) | 550 |
2.29 | (azafenidin) | 37 |
2.30 | (fluthiamid) | 51 |
2.33 | (sulfosate) | 383 |
2.34 | (asulam) | 33 |
2.35 | (norflurazon) | 526 |
2.36 | (terbacil) | 689 |
2.37 | (thiazopyr) | 702 |
2.38 | (dithiopyr) | 259 |
2.39 | (hexazinone) | 400 |
2.40 | (diuron) | 260 |
2.41 | (MCPA) | 455 |
2.42 | (mecoprop) | 459 |
2.43 | (tebuthiuron) | 683 |
Sloučenina vzorce 2.7, kde R<57 je atom vodíku a její příprava, jsou popsány v US-A 3 790 571; sloučenina vzorce 2.6, kde Ró2 je ethoxyskupina, Z je atom dusíku, je atom fluoru, R^ je atom chloru, R^ je atom vodíku a R^6 je atom chloruje popsaná v US-A 5 498 773.
Sloučenina vzorce 2.21 a její příprava, jsou popsány v US-A 5 183 492; sloučenina vzorce 2.22 je známá pod názvem isoxachlortole a je popsaná v AGROW č. 296, 16. ledna 1998, strana 22. Sloučenina vzorce 2.31 je popsaná pod názvem fentrazamide v The 1997 British Crop Protection Conference - Weeds, Conference Proceedings Vol. 1, 2-8, strany 67 až 72; sloučenina vzorce
2.32 je popsaná pod názvem JV 485 (isoxapropazol) v The 1997 British Crop Protection Conference - Weeds, Conference Proceedings Vol. 1, 3A-2, strany 93 až 98. Sloučenina vzorce 2.44 je známá pod názvem pethoxamid a je popsaná například v EP-A 0 206 251. Sloučenina vzorce 2.45 je známá pod názvem prokarbazone je popsaná například v EP-A 0 507 171; sloučenina vzorce 2.46 je známá pod názvem fluazolate a je popsaná například v US-A 5 530 126. Sloučeni20 na vzorce 2.47 je známá pod názvem cinidon-ethyl a je popsaná například v DE-A 4 037 840. Sloučenina vzorce 2.48 je známá pod názvem benzfendizone a je popsaná například v WO 97/08 953. Sloučenina vzorce 2.49 je známá jako diflufenzopyr a je popsaná například v EP-A 0 646 315. Sloučenina vzorce 2.50 (amikarbazone) a její příprava, jsou popsány v DD 298 393 a v US-A 5 194 085. Sloučenina vzorce 2.51 (flufenpyr-ethyl) je popsaná v Abstracts of
Papers American Chemical Society, (2000) Vol. 220, č. díl 1, str. AGRO 174.
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Je mimořádně překvapivé, že kombinace aktivní složky vzorce I s jednou nebo více aktivními složkami vybranými ze sloučenin vzorce 2.1 až 2.51 převyšuje principielně obecně očekávaný aditivní účinek na plevel, který se má kontrolovat, a tak rozšiřuje rozsah působení jednotlivých aktivních složek zejména ve dvou ohledech: za prvé aplikovaná množství jednotlivých sloučenin vzorce I a 2.1 až 2.51 se sníží, za současného zachování dobré hladiny působení, za druhé kompozice podle předkládaného vynálezu poskytuje vysokou úroveň kontroly plevele také v případech, kdy jednotlivé látky (v rozsahu nízkých aplikovaných množství) se staly z agronomického hlediska neúčinnými. Výsledkem je značné rozšíření spektra plevele a další vzrůst selektivity ve smyslu plodin užitečných rostlin, což je nutné a žádoucí v případě nežádoucího předávkování aktivní složkou. Kompozice podle předkládaného vynálezu za současné vynikající kontroly plevele u plodin užitečných rostlin také umožňuje vyšší flexibilitu při ochraně plodin.
Kompozice podle předkládaného vynálezu se mohou použít proti mnoha agronomicky významným plevelům, jako je Stellaria, Nasturtium, Agrostis, Digitaria, Avena, Setaria, Sinapis, Lolium, Solanum, Phaseolus, Echinochloa, Scirpus, Monochoria, Sagittaria, Bromus, Alopecurus, Sorghum halepense, Rottboellia, Cyperus, Abutilon, Sida, Xanthium, Amaranthus, Chenopodium, Ipomoea, Chrysanthemum, Galium, Viola a Veronica. Kompozice podle předkládaného vynálezu je vhodná pro všechny způsoby aplikace běžně používané v zemědělství, například preemergentní aplikaci, postemergentní aplikaci a prostředek na moření semen. Kompozice podle předkládaného vynálezu je vhodná zejména pro kontrolu plevele u plodin užitečných rostlin, jako jsou obiloviny, řepa, cukrová řepa, cukrová třtina, plantážní plodiny, rýže, kukuřice a sójové boby a také pro neselektivní kontrolu plevele. „Plodinami“ se rozumí také plodiny, které se staly odolnými vůči herbicidům nebo třídám herbicidů, jako důsledek běžných způsobů pěstování nebo generického inženýrství. Předkládaný vynález se také týká způsobů kontroly růstu nežádoucích rostlin u plodin užitečných rostlin, který zahrnuje nechání herbicidně účinného množství kompozice podle předkládaného vynálezu působit na rostlinu plodiny nebo na její stanoviště.
Kompozice podle předkládaného vynálezu obsahuje aktivní složku vzorce I a aktivní složky vzorce 2.1 až 2.51 v jakémkoli směšovacím poměru, ale obvykle obsahují přebytek jedné složky oproti druhé. Obvykle jsou směšovací poměry (hmotnostní poměry) aktivní složky obecného vzorce I a směsných partnerů vzorce 2.1 až 2.51 1:2000 až 2000:1, zejména 200:1 až 1:200. Aplikované množství se může měnit v širokých mezích a závisí na povaze půdy, způsobu aplikace (preemergentní nebo postemergentní; moření semen; aplikace do výsetbové brázdy; aplikace do nezorané půdy a tak dále); plodině, plevelu, který se má kontrolovat, převažujících klimatických podmínkách a dalších faktorech ovlivňujících způsob aplikace, době aplikace a cílové plodině. Směs aktivních složek podle předkládaného vynálezu se může obecně aplikovat v množství 1 až 5000 g směsi aktivních složek na hektar. Směsi sloučenin obecného vzorce I se sloučeninami vzorce 2.1 až 2.51 se mohou použít v neupravené formě, to znamená tak, jak se získají při syntéze. S výhodou se však upravují běžným způsobem, společně s běžně používanými přísadami, jako jsou rozpouštědla, pevné nosiče nebo povrchově aktivní látky, například do formy emulgovatelných koncentrátů, přímo rozstřikovatelných nebo ředitelných roztoků, zředěných emulzí, smáčivých prášků, rozpustných prášků, popráší, granulí nebo mikrokapsulí. Podle povahy kompozice se vybere způsob aplikace, jako je postřikování, atomizace, práškování, máčení, rozptylování nebo zalévání, v souladu s požadovaným účelem a podle převažujících okolností.
Prostředky, tj. kompozice, přípravky nebo směsi obsahující sloučeniny (aktivní složky) vzorce I a2.1 až2.51 a, pokud je to vhodné, jednu nebo více pevných nebo kapalných přísad, se připraví způsobem, který je odborníkům v této oblasti známý, například dokonalým smísením a/nebo mletím aktivních složek s přísadami, například rozpouštědly nebo pevnými nosiči. Dále se mohou v prostředcích použít povrchově aktivní sloučeniny (surfaktanty).
Příklady rozpouštědel a pevných nosičů jsou uvedené například v Mezinárodní patentové přihlášce WO 97/34 485, strana 6.
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V závislosti na povaze sloučeniny obecného vzorce I, která se má formulovat, jsou povrchově aktivní látky neionogenní, kationtové a/nebo aniontové povrchově aktivní látky a směsi povrchově aktivních látek, které mají dobré emulgační, dispergační a smáčivé vlastnosti.
Příklady vhodných aniontových, neionogenních a kationtových povrchově aktivních látek jsou uvedeny například v Mezinárodní patentové přihlášce WO 97/34 485, strany 7 a 8.
Při přípravě herbicidních kompozic podle předkládaného vynálezu jsou také vhodné povrchově aktivní látky běžně používané ve formulační technologii, které jsou mimo jiné popsány v „McCutcheon's Detergents and Emulsifiers Annual“ MC Publishing Corp., Ridgewood New Jersey, 1981, Stache, H., „Tensid-Taschenbuch“, Carl Hanser Verlag, Munich/Vienna, 1981 and M. and J. Ash, „Encyclopedia of Surfactants“, Vol I—III, Chemical Publishing Co., New York, 1980-81.
Herbicidní kompozice obvykle obsahují 0,1 až 99 % hmotnostních, zejména 0,1 až 95 % hmotnostních, aktivní složky, kterou je směs sloučeniny obecného vzorce I a sloučenin vzorců 2.1 až 2.51, 1 až 99,9 % hmotnostních pevných nebo kapalných přísad a 0 až 25 % hmotnostních, zejména 0,1 až 25 % hmotnostních povrchově aktivních látek.
Zatímco se komerční produkty obvykle formulují jako koncentráty, koncový uživatel bude běžně používat zředěné prostředky. Kompozice mohou obsahovat také další složky, jako jsou stabilizátory, například rostlinné oleje nebo epoxidované rostlinné oleje (epoxidovaný kokosový olej, řepkový olej nebo sójový olej), činidla proti tvorbě pěny, například silikonový olej, konzervační látky, látky upravující viskozitu, pojivá, zahušťovadla, a také hnojivá nebo jiné aktivní složky. Výhodné kompozice mají zejména následující složení:
(% = procenta hmotnostní)
Emulgovatelné koncentráty směs aktivních složek: surfaktant: kapalný nosič:
Popraše směs aktivních složek: pevný nosič:
Suspenzní koncentráty směs aktivních složek:
voda:
surfaktant:
Smáčivé prášky směs aktivních složek:
surfaktant:
pevný nosič:
až 90 %, s výhodou 5 až 20 % až 30 %, s výhodou 10 až 20 % 5 až 94 %, s výhodou 70 až 85 %
0,1 až 10 %, s výhodou 0,1 až 5 % 99,9 až 90 %, s výhodou 99,9 až 99 % až 75 %, s výhodou 10 až 50 % 94 až 24 %, s výhodou 88 až 30 % 1 až 40 %, s výhodou 2 až 30 %
0,5 až 90 %, s výhodou 1 až 80 % 0,5 až 20 %, s výhodou 1 až 15 % 5 až 95 %, s výhodou 15 až 90 %
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Granule směs aktivních složek: 0,1 až 30 %, s výhodou 0,1 až 15 % pevný nosič: 99,5 až 70 %, s výhodou 97 až 85 %
Následující příklady dále ilustrují vynález, ale v žádném ohledu jej neomezují.
Fl. Emulgovatelné koncentráty | a) | b) | c) | d) |
směs aktivních složek | 5% | 10% | 25% | 50% |
dodecylbenzensulfonát vápenatý | 6% | 8% | 6% | 8% |
polyglykolether ricínového oleje | 4% | - | 4% | 4% |
(36 mol ethylenoxidu) oktylfenolpolyglykolether | 4% | — | 2% | |
(7 až 8 mol ethylenoxidu) cyklohexanon | 10% | 20% | ||
směs arom. uhlovodíků C9-C12 | 85% | 78% | 55% | 16% |
Emulze 0 jakýchkoli požadovaných koncentracích vodou. | se mohou | získat z koncentrátů zředěním | ||
F2. Roztoky | a) | b) | c) | d) |
směs aktivních složek | 5% | 10% | 50% | 90% |
1 -methoxy-3-(3-methoxypropoxy)propan | _ | 20% | 20% | _ |
polyethyethylenglykol MH 400 | 20% | 10% | - | - |
N-methyl-2-pyrrolidon | - | - | 30% | 10% |
směs arom. uhlovodíků C9-C12 | 75% | 60% | — | — |
Roztoky jsou vhodné pro použití ve formě mikrokapiček.
F3. Smáčivé prášky | a) | b) | c) | d) |
směs aktivních složek | 5% | 25% | 50% | 80% |
lignosulfonát sodný | 4% | - | 3 % | - |
laurylsulfát sodný | 2% | 3% | - | 4% |
diisobutylnaftalen sulfonát sodný | - | 6% | 5% | 6% |
oktylfenolpolyglykolether | - | 1 % | 2% | - |
(7 až 8 mol ethylenoxidu) vysoce dispergovaná kys. křemičitá | 1 % | 3 % | 5% | 10% |
kaolin | 88% | 62% | 35% | — |
Aktivní složka se dokonale smísí s přísadami a směs se důkladně rozemele ve vhodném mlýnu a získají se smáčivé prášky, které se mohou zředit vodou za získání suspenzí o jakékoli požadované koncentraci.
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F4. Potahované granule | a) | b) | c) |
směs aktivních složek | 0,1 % | 5% | 15% |
vysoce disperg. kys. křemičitá | 0,9 % | 2% | 2% |
anorganický nosič | 99,0 % | 93 % | 83 % |
(AE 0,1 až 1 mm) například CaCCý nebo SiO2
Aktivní složka se rozpustí v dichlormethanu a aplikuje se na nosič pomocí postřikování a roz-
pouštědlo se potom odpaří ve vakuu. | ||||
F5. Potahované granule | a) | b) | c) | |
směs aktivních složek | 0,1 % | 5% | 15% | |
polyethylenglykol MH 200 | 1,0 % | 2% | 3% | |
vysoce disperg. kys. křemičitá | 0,9 % | 1 % | 2% | |
anorganický nosič (AE 0,1 až 1 mm) například CaCCý nebo SiO2 | 98,0 % | 92% | 80% | |
Jemně rozemletá aktivní složka se homogenně nanese v míchačce na nosič zvlhčený polyethylenglykolem. Tímto způsobem se získají bezprašné potažené granule. | ||||
F6. extrudované granule | a) | b) | c) | d) |
směs aktivních složek | 0,1 % | 3% | 5% | 15% |
lignosulfonát sodný | 1,5 % | 2% | 3 % | 4% |
karboxymethylcelulóza | 1,4 % | 2% | 2% | 2% |
kaolin | 97,0 % | 93 % | 90% | 79% |
Aktivní složky se smísí a rozemelou s přísadami a a potom suší v proudu vzduchu. | směs se zvlhčí vodou. Směs se extrahuje | |||
F7. Popraše | a) | b) | c) | |
směs aktivních složek | 0,1 % | 1 % | 5 % | |
mastek | 39,9 % | 49% | 35% | |
kaolin | 60,0 % | 50% | 60% | |
Popraše připravené k okamžitému použití se mletím směsi ve vhodném mlýnu. | získají | smísením aktivních složek s nosiči a roze- | ||
F8. Suspenzní koncentráty | a) | b) | c) | d) |
směs aktivních složek | 3 % | 10% | 25% | 50% |
ethylenglykol | 5% | 5% | 5% | 5% |
nonylfenolpolyglykolether (15 mol ethylenoxidu) | — | 1 % | 2% | — |
lignosulfonát sodný | 3% | 3% | 4% | 5% |
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karboxymethylcelulóza | 1 % | 1 % | 1 % | 1 % |
37% vodný roztok | 0,2 % | 0,2 % | 0,2 % | 0,2 % |
formaldehydu emulze silikonového oleje | 0,8 % | 0,8 % | 0,8 % | 0,8 % |
voda | 87% | 79% | 62% | 38% |
Jemně rozemleté aktivní složky se dobře promíchají s přísadami a získá se suspenzní koncentrát, ze kterého lze zředěním vodou připravit suspenze o jakékoli požadované koncentraci.
Často je praktičtější, aby se sloučeniny obecného vzorce I a směsný partner nebo partneři vzorce 2.1 až 2.51 formulovali odděleně a smísili se ve vhodném směsném poměru v aplikátoru ve formě „směsi v tanku“ ve vodě krátce před aplikací.
Příklady biologického testování
K synergickému efektu dochází vždy, když působení kombinace aktivních složek, a to sloučeniny vzorce I a 2.1 až 2.51 je vyšší, než součet působení aktivních složek aplikovaných odděleně.
Očekávané herbicidní působení WE pro danou kombinaci dvou herbicidů se může vypočítat následujícím způsobem (viz. COLBY, S.R., „Calculating synergistic and antagonistic response of herbicide combinations“, Weeds 15, strany 20-22, 1967):
We=X+[Y· (100-X)/100\ kde:
X = procentuální herbicidní působení při ošetření sloučeninou obecného vzorce I v aplikovaném množství p kg na hektar, v porovnání s neošetřenou kontrolou (= 0 %).
Y = procentuální herbicidní působení při ošetření sloučeninou vzorce 2.1 až 2.51 v aplikovaném množství q kg na hektar, v porovnání s neošetřenou kontrolou.
We = očekávané herbicidní působení (procentuální herbicidní působení v porovnání s neošetřenou kontrolou) po ošetření sloučeninami obecného vzorce I a 2.1 až 2.51 v aplikovaném množství p + kg aktivní složky na hektar.
Pokud je konkrétní pozorované působení vyšší, než očekávaná hodnota WE, jedná se o synergický účinek.
Synergický efekt kombinace sloučeniny obecného vzorce I se sloučeninami vzorce 2.1 až2.51je demonstrován na následujících příkladech.
Popis experimentu - preemergentní test:
Jednoděložné a dvouděložné testované rostliny se vysejí do standardní půdy v plastových květináčích. Ihned po vysetí se aplikují testované látky ve vodné suspenzi pomocí rozstříkání (500 vody/ha). Aplikované množství závisí na optimální dávce zjištěné za podmínek na poli a za podmínek ve skleníku. Testované rostliny se pěstují ve skleníku za optimálních podmínek. Testy se vyhodnotí po 36 dnech (% působení, 100 % = rostlina zahynula, 0 % = žádný fytotoxický účinek). Příklady synergického působení kompozic podle předkládaného vynálezu jsou uvedeny v následujících tabulkách Bl až B6.
Směs A obsahuje jako aktivní látky 915 g/litr sloučeniny vzorce 2.2a a 45 g/litr sloučeniny vzorce 3.1.
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Tabulka Bl
Testovaná rostlina: | Slouč. 1.001 [25 g/ha] | Směs A [900 g/ha] | Slouč. 1.001 [25 g/ha] + směs A [900 g/ha] | We podle Colbyho |
Čirok | 30 | 20 | 90 | 44 |
Merlík | 0 | 0 | 100 | 0 |
Sida | 0 | 70 | 100 | 70 |
Tabulka B2:
Testovaná rostlina: | Slouč. 1.001 [12.5 g/ha] | Směs A [900 g/ha] | Slouč. 1.001 [12.5 g/ha] + směs A [900 g/ha] | We podle Colbyho |
Čirok | 0 | 20 | 80 | 20 |
Merlík | 0 | 0 | 95 | 0 |
Sida | 0 | 70 | 95 | 70 |
Tabulka B3:
Testovaná rostlina: | Slouč. 1.001 [6.25 g/ha] | Směs A [900 g/ha] | Slouč. 1.001 [6.25 g/ha] + směs A [900 g/ha] | We podle Colbyho |
Čirok | 0 | 20 | 70 | 20 |
Merlik | 0 | 0 | 95 | 0 |
Sida | 0 | 70 | 95 | 70 |
Tabulka B4:
Testovaná rostlina: | Slouč. 1.001 [25 g/ha] | Směs A [300 g/ha] | Slouč. 1.001 [25 g/ha] + směs A [300 g/ha] | We podle Colbyho |
Merlík | 0 | 0 | 90 | 0 |
Povijnice | 30 | 0 | 100 | 30 |
Sida | 0 | 0 | 40 | 0 |
Tabulka B5:
Testovaná rostlina: | Slouč. 1.001 [12.5 g/ha] | Směs A [300 g/ha] | Slouč. 1.001 [12.5 g/ha] + směs A [300 g/ha] | We podle Colbyho |
Merlík | 0 | 0 | 80 | 0 |
Povijnice | 0 | 0 | 60 | 0 |
Sida | 0 | 0 | 40 | 0 |
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Tabulka B6:
Testovaná rostlina | Slouč. 1.001 [6.25 g/ha] | Směs A [300 g/ha] | Slouč. 1.001 [6.25 g/ha] + směs A [300 g/ha] | We podle Colbyho |
Merlík | 0 | 0 | 80 | 0 |
Povijnice | 0 | 0 | 60 | 0 |
Sida | 0 | 0 | 40 | 0 |
Popis experimentu - postemergentní test
Testované rostliny se pěstují do stádia 2 a 3 listů v plastových květináčích za podmínek skleníku. Jako kultivační substrát se použije standardní půda. Ve stádiu 2 až 3 listů se herbicid aplikuje na testované rostliny tak, jak je nebo ve směsi. Aplikace se provádí za použití vodné suspenze testovaných látek v 500 litrech vody na ha. Aplikovaná množství závisí na optimální dávce určené za podmínek na poli a za podmínek ve skleníku. Testy se vyhodnotí po 33 dnech (% působení, 100 % = rostlina zahynula, 0 % = žádný fytotoxický účinek). Příklady synergického působení kompozic podle předkládaného vynálezu jsou uvedeny v následujících tabulkách B7 až BIO.
Směs A obsahuje jako aktivní složky 915 g/litr sloučeniny vzorce 2.2a a 45 g/litr sloučeniny vzorce 3.1.
Tabulka B7: Postemergentní test:
Testovaná rostlina: | Slouč. 1.001 [12.5 g/ha] | Směs A [900 g/ha] | Slouč. 1.001 [12.5 g/ha] + směs A [900 g/ha] | We podle Colbyho |
Povijnice | 0 | 0 | 80 | 0 |
Rdesno | 0 | 20 | 100 | 20 |
Xanthium | 80 | 0 | 100 | 80 |
Tabulka B8: Postemergentní test:
Testovaná rostlina: | Slouč. 1.001 [12.5 g/ha] | Směs A [300 g/ha] | Slouč. 1.001 [12.5 g/ha] + směs A [300 g/ha] | We podle Colbyho |
Povijnice | 0 | 0 | 80 | 0 |
Rdesno | 0 | 0 | 70 | 0 |
Xanthium | 80 | 0 | 98 | 80 |
Tabulka B9: postemergentní test:
Testovaná rostlina: | Slouč. 1.001 [6.25 g/ha] | Směs A [900 g/ha] | Slouč. 1.001 [6.25 g/ha] + směs A [900 g/ha] | We podle Colbyho |
Povijnice | 0 | 0 | 70 | 0 |
Rdesno | 0 | 20 | 70 | 20 |
Xanthium | 70 | 0 | 80 | 70 |
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Tabulka BIO: Postemergentní test:
Testovaná rostlina: | Slouč. 1.001 [6.25 g/ha] | Směs A [300 g/ha] | Slouč. 1.001 [6.25 g/ha] + směs A [300 g/ha] | We podle Colbyho |
Povijnice | 0 | 0 | 80 | 0 |
Rdesno | 0 | 0 | 70 | 0 |
Xanthium | 70 | 0 | 70 | 70 |
V následujících tabulkách se hodnocení provádí po 14 dnech:
Tabulka Bil: Preemergentní působení:
Testovaná rostlina: | Slouč. E8 [50 g/ha] | Slouč. 2.18 [500 g/ha] | Slouč. E8 [50 g/ha] + slouč. 2.18 [500 g/ha] | We podle Colbyho |
Rdesno | 50 | 80 | 95 | 90 |
Tabulka B12: Preemergentní působení:
Testovaná rostlina: | Slouč. E8 [100 g/ha] | Slouč. 2.14 [250 g/ha] | Slouč. E8 [100 g/ha] + slouč. 2.14 [250 g/ha] | We podle Colbyho |
Rdesno | 50 | 50 | 90 | 75 |
Tabulka B13: Preemergentní působení:
Testovaná rostlina: | Slouč. E8 [100 g/ha] | Slouč. 2.14 [125 g/ha] | Slouč. E8 [100 g/ha] + slouč. 2.14 [125 g/ha] | We podle Colbyho |
Rdesno | 50 | 30 | 90 | 65 |
Tabulka B14: Preemergentní působení: Sloučenina č. 2.13a odpovídá vzorci 2.13, kde R74 je skupina -CH2CH2CF3, Yb Y2, Y3 a Y4 jsou každá methinová skupina, Y5 je atom dusíku a Y6 je methylová skupina.
Testovaná rostlina: | Slouč. E8 [100 g/ha] | Slouč. 2.13a [60 g/ha] | Slouč. E8 [100 g/ha] + slouč. 2.13a [60 g/ha] | We podle Colbyho |
Rdesno | 50 | 80 | 95 | 90 |
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Tabulka B15: Preemergentní působení:
Testovaná rostlina: | Slouč. E8 [50 g/ha] | Slouč. 2.30 [60 g/ha] | Slouč. E8 [50 g/ha] + slouč. 2.30 [60 g/ha] | We podle Colbyho |
Rdesno | 50 | 30 | 90 | 65 |
Tabulka B16: Preemergentní působení:
Testovaná rostlina: | Slouč. E8 [50 g/ha] | Slouč. 2.21 [30 g/ha] | Slouč. E8 [50 g/ha] + slouč. 2.21 [30 g/ha] | We podle Colbyho |
Rdesno | 50 | 50 | 100 | 75 |
Tabulka B17: Preemergentní působení: Sloučenina č. 2.4.a odpovídá vzorci 2.4, kde R57 je atom chloru, R5g je ethylová skupina a R59 je terc-butylová skupina.
Testovaná rostlina: | Slouč. E8 [50 g/ha] | Slouč. 2.4.a [125 g/ha] | Slouč. E8 [50 g/ha] + slouč. 2.4.a [125 g/ha] | We podle Colbyho |
Rdesno | 50 | 30 | 85 | 65 |
Tabulka B18: Preemergentní působení:
Testovaná rostlina: | Slouč. 1.001 [25 g/ha] | Slouč. 2.2.b [300 g/ha] | Slouč. 1.001 [25 g/ha] + slouč. 2.2.b [300 g/ha] | We podle Colbyho |
Merlik | 80 | 0 | 95 | 80 |
Solanum | 80 | 40 | 98 | 88 |
Šáchor | 0 | 0 | 50 | 0 |
Tabulka B19: Preemergentní působení:
Sloučenina č. 2.3.a odpovídá vzorci 2.3, kde R56 je skupina CH(Me)-CH2OMe.
Testovaná rostlina: | Slouč. 1.001 [12.5 g/ha] | Slouč. 2.3.a [100 g/ha] | Slouč. 1.001 [12.5 g/ha] + slouč. 2.3.a [100 g/ha] | We podle Colbyho |
Merlik | 80 | 20 | 90 | 84 |
Solanum | 75 | 60 | 90 | 90 |
Šáchor | 0 | 20 | 60 | 20 |
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Tabulka B20: Preemergentní působení:
Sloučenina č. 2.2.c odpovídá vzorci 2.2, kde R53 a R54 jsou ethylová skupina a R55 je skupina CH2OMe.
Testovaná rostlina: | Slouč. 1.001 [12.5 g/ha] | Slouč. 2.2.C [100 g/ha] | Slouč. 1.001 [12.5 g/ha] + slouč. 2.2.c [100 g/ha] | We podle Colbyho |
Merlík | 80 | 20 | 90 | 84 |
Solanum | 75 | 50 | 95 | 88 |
Šáchor | 0 | 0 | 30 | 0 |
Tabulka B21: Preemergentní působení:
Sloučenina č. 2.2.d odpovídá vzorci 2.2, kde R53 je ethylová skupina, R54 je methylová skupina a R55 je skupina CH2O-CH2CH3.
Testovaná rostlina: | Slouč. 1.001 [12.5 g/ha] | Slouč. 2.2.d [100 g/ha] | Slouč. 1.001 [12.5 g/ha] + slouč. 2.2.d [100 g/ha] | We podle Colbyho |
Solanum | 75 | 60 | 95 | 90 |
Tabulka B22: Preemergentní působení:
Testovaná rostlina: | Slouč. 1.001 [25 g/ha] | Slouč. 2.30 [100 g/ha] | Slouč. 1.001 [25 g/ha] + slouč. 2.30 [100 g/ha] | We podle Colbyho |
Šáchor | 10 | 0 | 60 | 10 |
V následujících tabulkách se hodnocení provádí po 31 dnech:
Tabulka B23: Preemergentní působení: Sloučenina č. 2.4.a odpovídá sloučenině vzorce 2.4, kde R57 je atom chloru, R58 je ethylová skupina a R59 je isopropylová skupina.
Testovaná rostlina: | Slouč. 1.001 [25 g/ha] | Slouč. 2.4.a [250 g/ha] | Slouč. 1.001 [25 g/ha] + slouč. 2.4.a [250 g/ha] | We podle Colbyho |
Rdesno | 0 | 20 | 80 | 20 |
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Tabulka B24: Preemergentní působení: Sloučenina č. 2.4.b odpovídá sloučenině vzorce 2.4, kde R57 je atom chloru, R58 je ethylová skupina a R59 je ethylová skupina.
Testovaná rostlina: | Slouč. 1.001 [25 g/ha] | Slouč. 2.4.b [125 g/ha] | Slouč. 1.001 [25 g/ha] + slouč. 2.4.b [125 g/ha] | We podle Colby |
Šáchor | 0 | 0 | 40 | 0 |
Tabulka B25: Preemergentní působení: Sloučenina č. 2.4.c odpovídá sloučenině vzorce 2.4, kde R57 je atom chloru, R58 je ethylová skupina a R59 je terc-butylová skupina.
Testovaná rostlina: | Slouč. 1.001 [25 g/ha] | Slouč. 2.4.c [250 g/ha] | Slouč. 1.001 [25 g/ha] + slouč. 2.4.C [250 g/ha] | We podle Colbyho |
Povijnice | 70 | 0 | 90 | 70 |
Xanthium | 80 | 0 | 100 | 80 |
Tabulka B26: Preemergentní působení: Sloučenina č. 2.4.d odpovídá sloučenině vzorce 2.4, kde R57 je methylthioskupina, R58 je ethylová skupina a R59 je terc-butylová skupina.
Testovaná rostlina: | Slouč. 1.001 [25 g/ha] | Slouč. 2.4.d [250 g/ha] | Slouč. 1.001 [25 g/ha] + slouč. 2.4.d [250 g/ha] | We podle Colbyho |
Povijnice | 70 | 0 | 80 | 70 |
Xanthium | 80 | 10 | 95 | 82 |
Tabulka B27: Preemergentní působení:
Testovaná rostlina: | Slouč. 1.001 [25 g/ha] | Slouč. 2.14 [125 g/ha] | Slouč. 1.001 [25 g/ha] + slouč. 2.14 [125 g/ha] | We podle Colbyho |
Povijnice | 70 | 0 | 85 | 70 |
Xanthium | 80 | 20 | 100 | 84 |
Tabulka B28: Preemergentní působení: Sloučenina č. 2.6.a odpovídá sloučenině vzorce 2.6, kde Ré2 je atom fluoru, R« je atom vodíku, Y je atom dusíku, Z je methinová skupina a R^ je atom fluoru.
Testovaná | Slouč. 1.001 | Slouč. | Slouč. 1.001 | We |
rostlina: | [50 g/ha] | 2.6.a [30 g/ha] | [50 g/ha] + slouč. 2.6.a [30 g/ha] | podle Colbyho |
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I Rdesno
V následujících tabulkách se hodnocení provádí po 21 dnech:
Tabulka B29: Postemergentní působení: Sloučenina č. 2.7.a odpovídá sloučenině vzorce 2.7, kde R<>7 kde Ré7 je -C(O)-S-n-oktylová skupina.
Testovaná rostlina: | Slouč. 1.001 [25 g/ha] | Slouč. 2.7.a [250 g/ha] | Slouč. 1.001 [25 g/ha] + slouč. 2.7.a [250 g/ha] | We podle Colbyho |
Povijnice | 30 | 10 | 80 | 30 |
Rdesno | 75 | 0 | 95 | 75 |
Xanthium | 90 | 10 | 100 | 91 |
Tabulka B30: Postemergentní působení:
Testovaná rostlina: | Slouč. 1.001 [25 g/ha] | Slouč. 2.19 [250 g/ha] | Slouč. 1.001 [25 g/ha] + slouč. 2.19 [250 g/ha] | We podle Colbyho |
Povijnice | 30 | 60 | 95 | 72 |
Tabulka B31: Postemergentní působení:
Testovaná rostlina: | Slouč. 1.001 [25 g/ha] | Slouč. 2.16 [360 g/ha] | Slouč. 1.001 [25 g/ha] + slouč. 2.16 [360 g/ha] | We podle Colbyho |
Povijnice | 30 | 20 | 70 | 46 |
Rdesno | 75 | 10 | 90 | 84 |
Tabulka B32: Postemergentní působení:
Testovaná rostlina: | Slouč. 1.001 [12.5 g/ha] | Slouč. 2.33 [360 g/ha] | Slouč. 1.001 [12.5 g/ha] + slouč. 2.33 [360 g/ha] | We podle Colbyho |
Rdesno | 30 | 0 | 90 | 30 |
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Tabulka B33: Postemergentní působení: Sloučenina č. 2.12.a odpovídá sloučenině vzorce 2.12, kde R73 je NH2.
Testovaná rostlina: | Slouč. 1.001 [25 g/ha] | Slouč. 2.12.a [400 g/ha] | Slouč. 1.001 [25 g/ha] + slouč. 2.33 [400 g/ha] | We podle to Colby |
Povijnice | 30 | 20 | 90 | 44 |
Tabulka B34: Postemergentní působení:
Testovaná rostlina: | Slouč. 1.001 [12.5 g/ha] | Slouč. 2.25 [2 g/ha] | Slouč. 1.001 [12.5 g/ha] + slouč. 2.25 [2 g/ha] | We podle Colbyho |
Povijnice | 30 | 0 | 50 | 30 |
Rdesno | 30 | 0 | 40 | 30 |
Tabulka B35: Postemergentní působení: Sloučenina č. 2.1.a odpovídá sloučenině vzorce 2.1, kde R_52 je atom vodíku a R5j je ethylová skupina.
Testovaná rostlina: | Slouč. 1.001 [12.5 g/ha] | Slouč. 2.1.a [30 g/ha] | Slouč. 1.001 [12.5 g/ha] + slouč. 2.1.a [30 g/ha] | We podle Colbyho |
Rdesno | 30 | 30 | 70 | 51 |
Tabulka B36: Postemergentní působení: Sloučenina č. 2.1.b odpovídá sloučenině vzorce 2.1, kde R5i je skupina CH2OMe a R52 je atom vodíku.
Testovaná rostlina: | Slouč. 1.001 [25 g/ha] | Slouč. 2.1.b [30 g/ha] | Slouč. 1.001 [25 g/ha] + slouč. 2.1.b [30 g/ha] | We podle Colbyho |
Rdesno | 75 | 30 | 90 | 83 |
V následujících tabulkách se hodnocení provádí po 23 dnech:
Tabulka B37: Preemergentní působení: Sloučenina č. 2.13.b odpovídá vzorci 2.13, kde R74 je skupina -COOMe, Yb Y2, Y3 a Y4 jsou každá methinová skupina, Y5 je methinová skupina a Y6 a Y7 jsou difluormethoxyskupina.
Testovaná rostlina: | Slouč. 1.001 [6 g/ha] | Slouč. 2.13.b [15 g/ha] | Slouč. 1.001 [6 g/ha] + slouč. 2.13.b [15 g/ha] | We podle Colbyho |
Merlík | 50 | 70 | 35 | 85 |
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Tabulka B38: Preemergentní působení:
Testovaná rostlina: | Slouč. 1.001 [6 g/ha] | Slouč. 2.13.C [60 g/ha] | Slouč. 1.001 [6 g/ha] + slouč. 2.13.C [60 g/ha] | We podle Colbyho |
Merlík | 50 | 10 | 85 | 55 |
Tabulka B39: Preemergentní působení: Sloučenina č. 2.13.d odpovídá sloučenině vzorce 2.13, kde Yb Y2, Y3 aY4jsou methinová skupina, R74 je trifluormethylová skupina, Y5 je atom dusíku, Y6 je trifluormethylová skupina a Y7 je methoxyskupina.
Testovaná rostlina: | Slouč. 1.001 [6 g/ha] | Slouč. 2.13d [7.5 g/ha] | Slouč. 1.001 [6 g/ha] + slouč. 2.13.d [7.5 g/ha] | We podle Colbyho |
Amaranthus | 10 | 80 | 95 | 82 |
Překvapivě bylo zjištěno, že určité protilátky jsou vhodné pro smísení se synergickou kompozicí podle předkládaného vynálezu. Předkládaný vynález se tedy také týká herbicidně selektivní kompozice pro kontrolu trávy a plevele u plodin užitečných rostlin, zejména u plodin kukuřice, která obsahuje sloučeninu obecného vzorce I, jednu nebo více sloučenin vybraných ze sloučenin vzorce 2.1 až 2.51, a protilátku, a kdy tato kompozice chrání užitečné rostliny, ale nikoli plevel, proti fytotoxickému působení herbicidu, a také se týká použití této kompozice pro kontrolu plevele u plodin užitečných rostlin.
Předkládaný vynález také poskytuje herbicidně selektivní kompozici, která kromě toho, že obsahuje běžné inertní přísady, jako jsou nosiče, rozpouštědla a smáčedla, obsahuje jako aktivní složku směs
a) herbicidně synergického účinného množství sloučeniny obecného vzorce I a jedné nebo více sloučenin vybraných ze sloučenin vzorce 2.1 až 2.51 a
b) herbicidně antagonisticky účinného množství sloučeniny vybrané ze sloučeniny vzorce 3.1
a sloučeniny vzorce 3.2
- 142CZ 304537 B6 a sloučeniny vzorce 3.3
Cl
O-CHj-CíOJ-O-CHíCHaJCsH^-n a sloučeniny vzorce 3.4
- 143 CZ 304537 B6
a sloučeniny vzorce 3.9
C12CHCON(CH2CH=CH2)2 (3.9), a sloučeniny vzorce 3.10
a sloučeniny vzorce 3.13
-144CZ 304537 B6 a sloučeniny vzorce 3.14
Předkládaný vynález se také týká herbicidně selektivní kompozice, která kromě toho, že obsahuje běžné inertní přísady, jako jsou nosiče, rozpouštědla a smáčedla, obsahuje jako aktivní složku směs
a) herbicidně účinného množství sloučeniny obecného vzorce I a
b) herbicidně antagonisticky účinného množství sloučeniny vybrané ze sloučenin vzorce 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 3.10, 3.11, 3.12, 3.13, 3.14, 3.15 a 3.16.
Výhodné kompozice podle předkládaného vynálezu obsahují jako protilátku sloučeninu vybranou ze sloučenin vzorce 3.1, 3.3 a 3.8. Tyto protilátky jsou zvláště vhodné pro kompozice podle předkládaného vynálezu, které obsahují výše uvedené výhodné sloučeniny vzorce I a popřípadě vzorce 2.1 až 2.51.
Ukázalo se, že kombinace sloučenin obecného vzorce I se sloučeninou 3.1 je zvláště účinnou kompozicí, přičemž zvláště výhodná je sloučenina číslo 1.001 jako sloučenina vzorce I. Tato kompozice se s výhodou použije společně se sloučeninou vzorce 2.2a
- 145CZ 304537 B6
chloracetyl-2-ethyl-6-methylanilin).
aRS, 1 'S(-)N-( 1 '-Methyl-2'-methoxyethyl)-NPředkládaný vynález se také týká způsobu selektivní kontroly plevele u plodin užitečných rostlin, který zahrnuje ošetření užitečných rostlin, jejich semen nebo řízků, nebo místa jejich pěstování, herbicidně účinným množstvím herbicidu obecného vzorce I, pokud je to vhodné, jedním nebo více herbicidy vybranými ze sloučenin vzorců 2.1 až 2.51, a herbicidně antagonisticky účinným množstvím protilátky vzorce 3.1 až 3.16.
Sloučeniny vzorce 3.1 až 3.16 jsou známé a jsou popsány například v Pesticide Manual, eleventh ed., British Crop Protection Council, 1997 pod příslušnými čísly 61 (vzorec 3.1, benoxacor), 304 (vzorec 3.2, fenclorim), 154 (vzorec 3.3, clochintocet), 462 (vzorec 3.4, mefenpyr-diethyl), 377 (vzorec 3.5, furilazol), 363 (vzorec 3.8, fluxofenim), 213 (vzorec 3.9, dichlormid) a 350 (vzorec 3.10, flurazole). Sloučenina vzorce 3.11 je známá pod názvem MON 4660 (Monsanto) a je popsaná například v EP-A 0 436 483.
Sloučenina vzorce 3.6 (AC 304 415) je popsaná například v EP-A 0 613 618, sloučenina vzorce 3.7 v DE-A 2 948 535. Sloučeniny vzorce 3.12 jsou popsány v DE-A 4 331 448, a sloučenina vzorce 3.13 v DE-A 3 525 205. Sloučenina vzorce 3.14 je známá například zUS-A 5 215 570 a sloučenina vzorce 3.15 z EP-A 0 929 543. Sloučenina vzorce 3.16 je popsaná v WO 99/00 020. Kromě sloučeniny vzorce 3.16, jsou další 3-(5-tetrazolylkarbonyl)-2-chinolony popsány v WO 99/00 020, přičemž zejména sloučeniny konkrétně popsané v tabulkách 1 a 2 na stranách 21 až 29 jsou vhodné pro ochranu plodin proti fytotoxickému působení sloučenin vzorce I.
Jako plodiny, které se mohou chránit protilátkami vzorce 3.1 až 3.16 proti poškození výše uvedenými herbicidy, přicházejí v úvahu zejména obiloviny, řepa, kukuřice a rýže, zejména kukuřice. „Plodinami“ se rozumí také takové plodiny, které se staly odolnými vůči herbicidům nebo třídám herbicidů jako důsledek běžných způsobů pěstování nebo genetického inženýrství.
Plevely, které se mohou kontrolovat, jsou jak jednoděložné, tak dvouděložné plevele, například Stellaria, Agrostis, Digitaria, Avena, Apera, Brachiaria, Phalaris, Setaria, Sinapis, Lolium, Solanum, Echinochloa, Scirpus, Monochoria, Segittaria, Panicům, Bromus, Alopecurus, Sorghum halepense (čirok), Sorghum bicolor, Rottboellia, Cyperus (šáchor), Abutilon, Sida, Xanthium, Amaranthus, Chenopodium (merlík), Ipomoea (podvijnice), Chrystanthemum, Galium, Viola a Veronica.
Mezi místa pěstování patří plochy půdy, na kterých se plodiny obvykle pěstují nebo které již byly osety semeny těchto plodin a také půda určená pro pěstování těchto rostlin.
V závislosti na účelu použití se mohou protilátky vzorce 3.1 až 3.16 použít pro předběžné ošetření semen plodin (moření semen nebo řízků) nebo se mohou umístit do půdy před nebo po vysetí. Mohou se však také aplikovat buď samotné, nebo s herbicidem po vyklíčení rostliny. Ošetření rostlin nebo semen protilátkami se může proto v principu provádět nezávisle na době, ve které se aplikuje herbicid. Rostliny se však mohou také ošetřit současnou aplikací herbicidu a protilátky (například ve formě směsi v tanku). Poměr aplikovaného množství protilátky k množství aplikovaného herbicidu závisí zejména na způsobu aplikace. V případě ošetření pole, které se provádí buď za použití směsi v tanku obsahující kombinaci protilátky a herbicidu, nebo pomocí oddělené
-146CZ 304537 B6 aplikace protilátky a herbicidu, se poměr herbicidů ku protilátce bude obvykle pohybovat mezi 100:1 až 1:10, s výhodou 20:1 až 1:1. V případě ošetření pole se obvykle aplikuje 0,001 až 0,5 kg protilátky/ha, s výhodou 0,001 až 0,25 kg protilátky/ha.
Množství aplikovaného herbicidu se obvykle pohybuje mezi 0,001 až 5 kg/ha, ale s výhodou 0,005 až 0,5 kg/ha. Kompozice podle předkládaného vynálezu jsou vhodné pro všechny způsoby aplikace, které se běžně používají v zemědělství, například preemergentní aplikaci, postemergentní aplikaci a moření semene. V případě moření semen se obvykle aplikuje 0,001 až 10 g protilátky/kg semen, s výhodou 0,05 až 2 g protilátky/kg semen. Pokud se protilátka aplikuje v kapalné formě krátce před vysetím, při sáknutí semen, potom s výhodou použité roztoky protilátek obsahují aktivní složku v koncentraci 1 až 10 000 ppm, s výhodou 100 až 1000 ppm.
Pro účel aplikace se protilátky vzorce 3.1 až 3.16 nebo kombinace těchto protilátek s herbicidem vzorce I a pokud je to vhodné, sjedním nebo více herbicidy vybranými ze sloučenin vzorce 2.1 až 2.51, s výhodou formulují společně s přísadami běžně používanými ve formulační technologii, například do formy emulgovatelných koncentrátů, potahovacích past, přímo rozprašovatelných nebo ředitelných roztoků, zředěných emulzí, smáčivých prášků, rozpustných prášků, popráší, granulí a mikrokapsulí.
Tyto prostředky jsou popsány například v WO 97/34 485, strany 9 až 13. Prostředky se připraví známými postupy, například dokonalým smísením a/nebo rozemletím aktivních složek s kapalnými nebo pevnými přísadami, například rozpouštědly nebo pevnými nosiči. Kromě toho se mohou také při přípravě prostředků použít povrchově aktivní sloučeniny (surfaktanty). Rozpouštědla a pevné nosiče, které jsou vhodné pro tento účel, jsou uvedeny například v WO 97/34 485, strana 6.
V závislosti na povaze sloučenin vzorce I, 2.1 až 2.51 a 3.1 až 3.16, které se mají formulovat, přichází v úvahu jako povrchově aktivní sloučeniny neionogenní, kationtové a/nebo aniontové povrchově aktivní látky a směsi povrchově aktivních látek, které mají dobré emulgační, dispergační a smáčivé vlastnosti. Příklady vhodných aniontových, neionogenních a kationtových povrchově aktivních látek jsou uvedeny například na stranách 7 a 8 v WO 97/34 485. Pro přípravu herbicidních kompozic podle předkládaného vynálezu jsou také vhodné povrchově aktivní látky běžně používané ve formulační technologii, které jsou popsané mimo jiné v „McCutcheon's Detergents and Emulsifiers Annual“ MC Publishing Corp., Ridgewood New Jersey, 1981, Stache, H., „Tensid-Taschenbuch“, Carl Hanser Verlag, Munich/Vienna, 1981 a M. a J. Ash, „Encyklopedia of Surfactants“, Vol. I—III, Chemical Publishing Co., New York, 1980-81.
Herbicidní kompozice obvykle obsahují 0,1 až 99 % hmotnostních, zejména 0,1 až 95 % hmotnostních, aktivní složky, kterou je směs obsahující sloučeninu obecného vzorce I, sloučeninu vybranou ze sloučenin vzorce 2.1 až 2.51 a sloučeniny vzorce 3.1 až 3.16, 1 až 99,9 % hmotnostních pevných nebo kapalných přísad a 0 až 25 % hmotnostních, zejména 0,1 až 25 % hmotnostních, povrchově aktivních látek. Zatímco se komerční produkty budou obvykle formulovat jako koncentráty, koncový uživatel bude běžně používat zředěné prostředky.
Kompozice mohou také obsahovat další přísady, jako jsou stabilizátory, například rostlinné oleje nebo epoxidované rostlinné oleje (epoxidovaný kokosový olej, řepkový olej nebo sójový olej), činidla proti tvorbě pěny, například silikonový olej, konzervační látky, regulátory viskozity, pojivá, zahušťovadla a také hnojivá nebo další aktivní složky. Pro použití protilátek vzorce 3.1 až 3.16, nebo kompozice, kteréje obsahují, při ochraně plodin proti poškození herbicidy vzorce 2.1 až 2.51, přicházejí v úvahu různé způsoby a techniky, jako jsou například následující:
i) Moření semen
a) Moření semen smáčivým práškovým prostředkem obsahujícím sloučeninu vzorce 3.1 až 3.16 se provádí protřepáním v nádobě, dokud se nedosáhne homogenního potažení povrchu semen
-147CZ 304537 B6 (suché moření). Při tomto způsobu se použije přibližně 1 až 500 g sloučeniny vzorce 3.1 až 3.16 (4 g až 23 kg smáčivého prášku) na 100 kg semen.
b) Moření semen emulgovatelným koncentrátem obsahujícím sloučeninu vzorce 3.1 až 3.16 se provádí podle způsobu a) (moření za mokra).
c) Moření ponořením semen se provádí ponořením semen na 1 až 72 hodin do kapaliny obsahující 100 až 1000 ppm sloučeniny vzorce 3.1 až 3.16 a popřípadě pomocí následného sušení semen (moření za ponoření).
Moření semen nebo ošetření vyklíčených semenáčků jsou samozřejmě výhodné způsoby aplikace, protože ošetření aktivními složkami je vedeno pouze na cílovou plodinu. Obecně se použije 1 až 1000 g protilátky, s výhodou 5 až 250 g protilátky, na 100 kg semen, ale množství závisí na způsobu, který také umožňuje přidání dalších aktivních látek nebo mikrohnojiv, přičemž zjištěné koncentrační limity se mohou měnit směrem vzhůru i dolů (opakované moření).
ii) Aplikace jako směs v tanku
Použije se kapalný prostředek obsahující směs protilátky a herbicidu (hmotnostní poměr jedné látky ke druhé je 10:1 až 1:100), přičemž aplikované množství herbicidu se pohybuje mezi 0,005 až 5,0 kg na hektar. Tyto směsi v tanku se aplikují před nebo po vysetí.
iii) Aplikace do výsevové brázdy
Sloučeniny vzorce 3.1 až 3.16 se umístí do otevřené, výsevové brázdy obsahující semena ve formě emulgovatelného koncentrátu, smáčivého prášku nebo granulí. Jakmile se výsevová brázda zahrne, aplikuje se pomocí způsobu, který je běžný při preemergentních procesech, herbicid.
iv) Kontrolované uvolňování aktivní látky
Sloučeniny vzorce 3.1 až 3.16 se aplikují v roztoku na granule minerálního nosiče nebo polymerované granule (močovina/formaldehyd) a suší se. Pokud je to vhodné, je také možné aplikovat povlak, který umožňuje, aby se aktivní látka uvolňovala v odměřeném množství v průběhu určitého časového úseku (potažené granule).
Výhodné kompozice mají zejména následující složení:
(% = procenta hmotnostní)
Emulgovatelné koncentráty směs aktivních složek: surfaktant: kapalný nosič:
Popraše směs aktivních složek: pevný nosič:
až 90 %, s výhodou 5 až 20 % až 30 %, s výhodou 10 až 20 % 5 až 94 %, s výhodou 70 až 85 %
0,1 až 10 %, s výhodou 0,1 až 5 % 99,9 až 90 %, s výhodou 99,9 až 99 %
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Suspenzní koncentráty směs aktivních složek:
voda:
surfaktant:
Smáčivé prášky směs aktivních složek:
surfaktant:
pevný nosič:
Granule až 75 %, s výhodou 10 až 50 % 94 až 24 %, s výhodou 88 až 30 % 1 až 40 %, s výhodou 2 až 30 %
0,5 až 90 %, s výhodou 1 až 80 % 0,5 až 20 %, s výhodou 1 až 15 % 5 až 95 %, s výhodou 15 až 90 % směs aktivních složek: pevný nosič:
0,1 až 30 %, s výhodou 0,1 až 15 % 99,5 až 70 %, s výhodou 97 až 85 %
Následující příklady dále ilustrují vynález, ale v žádném ohledu jej neomezují.
Fl. Emulgovatelné koncentráty | a) | b) | c) | d) |
směs aktivních složek | 5% | 10% | 25% | 50% |
dodecylbenzensulfonát vápenatý | 6% | 8% | 6% | 8% |
polyglykolether ricínového oleje | 4% | - | 4% | 4% |
(36 mol ethylenoxidu) oktylfenolpolyglykolether | _ | 4% | _ | 2% |
(7 až 8 mol ethylenoxidu) cyklohexanon | _ | _ | 10% | 20% |
směs arom. uhlovodíků C9-C12 | 85% | 78% | 55% | 16% |
Emulze o jakýchkoli požadovaných koncentracích se mohou získat z koncentrátů zředěním vodou.
F2. Roztoky | a) | b) | c) | d) |
směs aktivních složek | 5% | 10% | 50% | 90% |
1 -methoxy-3-(3-methoxypropoxy)propan | _ | 20% | 20% | _ |
polyethyethylenglykol MH 400 | 20% | 10% | - | - |
N-methyl-2-pyrrolidon | - | - | 30% | 10% |
směs arom. uhlovodíků C9-C12 | 75% | 60% | — | — |
Roztoky jsou vhodné pro použití ve formě mikrokapiček.
F3. Smáčivé prášky | a) | b) | c) | d) |
směs aktivních složek | 5% | 25% | 50% | 80% |
lignosulfonát sodný | 4% | - | 3% | - |
laurylsulfát sodný | 2% | 3 % | - | 4% |
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diisobutylnaftalen sulfonát sodný - | 6% | 5% | 6% |
oktylfenolpolyglykolether - | 1 % | 2% | - |
(7 až 8 mol ethylenoxidu) vysoce dispergovaná kys. křemičitá 1 % | 3% | 5% | 10% |
kaolin 88 % | 62% | 35 % | — |
Aktivní složka se dokonale smísí s přísadami a směs se důkladně rozemele ve vhodném mlýnu a získají se smáčivé prášky, které se mohou zředit vodou za získání suspenzí o jakékoli požadované koncentraci.
F4. Potahované granule | a) | b) | c) |
směs aktivních složek | 0,1 % | 5% | 15% |
vysoce disperg. kys. křemičitá | 0,9 % | 2% | 2% |
anorganický nosič | 99,0 % | 93 % | 83 % |
(AE 0,1 až 1 mm) například CaCO3 nebo SiO2
Aktivní složka se rozpustí v dichlormethanu a aplikuje se na nosič pomocí postřikování a roz-
pouštědlo se potom odpaří ve vakuu. | ||||
F5. Potahované granule | a) | b) | c) | |
směs aktivních složek | 0,1 % | 5% | 15% | |
polyethylenglykol MH 200 | 1,0 % | 2% | 3 % | |
vysoce disperg. kys. křemičitá | 0,9 % | 1 % | 2% | |
anorganický nosič (AE 0,1 až 1 mm) například CaCO3 nebo SiO2 | 98,0 % | 92% | 80% | |
Jemně rozemletá aktivní složka se homogenně nanese v míchačce na nosič zvlhčený polyethylenglykolem. Tímto způsobem se získají bezprašné potažené granule. | ||||
F6. extrudované granule | a) | b) | c) | d) |
směs aktivních složek | 0,1 % | 3 % | 5% | 15% |
lignosulfonát sodný | 1,5 % | 2% | 3 % | 4% |
karboxymethylcelulóza | 1,4 % | 2% | 2% | 2% |
kaolin | 97,0 % | 93 % | 90% | 79% |
Aktivní složky se smísí a rozemelou s přísadami a a potom suší v proudu vzduchu. | směs se zvlhčí vodou. Směs se extrahuje | |||
F7. Popraše | a) | b) | c) | |
směs aktivních složek | 0,1 % | 1 % | 5% | |
mastek | 39,9 % | 49% | 35% | |
kaolin | 60,0 % | 50% | 60% |
Popraše připravené k okamžitému použití se získají smísením aktivních složek s nosiči a rozemletím směsi ve vhodném mlýnu.
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F8. Suspenzní koncentráty | a) | b) | c) | d) |
směs aktivních složek | 3 % | 10% | 25% | 50% |
ethylenglykol | 5% | 5% | 5% | 5% |
nonylfenolpolyglykolether (15 mol ethylenoxidu) | — | 1 % | 2% | — |
lignosulfonát sodný | 3% | 3 % | 4% | 5% |
karboxymethylcelulóza | 1 % | 1 % | 1 % | 1 % |
37% vodný roztok formaldehydu | 0,2 % | 0,2 % | 0,2 % | 0,2 % |
emulze silikonového oleje | 0,8 % | 0,8 % | 0,8 % | 0,8 % |
voda | 87% | 79% | 62% | 38% |
Jemně rozemleté aktivní složky se dobře promíchají s přísadami a získá se suspenzní koncentrát, ze které lze zředěním vodou připravit suspenze o jakékoli požadované koncentraci.
Často je praktičtější, aby se sloučeniny obecného vzorce 12.1 až2.51 a3.1 až3.16 formulovali odděleně a smísili se ve vhodném směsném poměru v aplikátoru ve formě „směsi v tanku“ ve vodě krátce před aplikací.
Schopnost protilátek vzorce 3.1 až 3.16 chránit rostliny zemědělských plodin proti fytotoxickému působení herbicidů vzorce I je ilustrována v následujících příkladech.
Příklady biologického testování
Ochranné působení
Testované rostliny se pěstují v plastových květináčích za podmínek skleníku do stádia 4 listů. V tomto stádiu se na testované rostliny aplikují samotné herbicidy, a směs herbicidů se sloučeninami, které se mají testovat jako protilátky. Aplikace se provádí ve formě vodné suspenze testovaných sloučenin připravené z 25 % smáčivého prášku (příklad F3 b)) s 500 litry vody/ha. 4 týdny po aplikaci se hodnotí fýtotoxické působení herbicidů na testované rostliny, například kukuřici a obiloviny, za použití procentuální stupnice. 100 % znamená, že testovaná rostlina zahynula, 0 % znamená žádné fýtotoxické působení.
Výsledky získané při tomto testu ukazují, že poškození rostlin zemědělských plodin způsobené herbicidem vzorce I v kombinaci s jedním nebo více herbicidy vzorce 2.1 až 2.51 může být významně sníženo pomocí sloučenin vzorce 3.1 až 3.16. Příklady ochranného působení jsou uvedeny v tabulce B40.
Tabulka B40
Testova- | Slouč. | Slouč. 1.001 | Slouč. 1.001 | Slouč. 1.001 |
ná rost- | 1.001 | [50 g/ha] + | [50 g/ha] + | [50 g/ha] + |
lina | [50 | slouč. 3.3 | slouč. 3.1 [50 | slouč. 3.8 |
g/ha] | [50 g/ha] | g/ha] | [50 g/ha] | |
Kukuřice | 50 | 5 | 5 | 0 |
Mračňák | 100 | 100 | 100 | 100 |
Setaria | 100 | 100 | 100 | 100 |
Stejných výsledků se dosáhlo, když se připravily směsi podle příkladů Fl, F2 a F4 až F8.
Claims (4)
- PATENTOVÉ NÁROKY1. Herbicidně selektivní kompozice, vyznačená tím, že kromě běžných inertních formulačních přísad obsahuje jako účinnou látku směs a) herbicidně účinného množství sloučeniny vzorce IaOCa) ve kterémR48 znamená Ci-C6alkyl, C2-C6alkenyl, C2-C6halogenalkenyl, C2-C6alkynyl, C2-C6halogenalkynyl, C3-C6cykloalkyl, Ci-C6halogenalkyl, Ci-C4alkoxy-Ci-C4alkyl nebo Ci-C4alkoxy-CiC4alkoxy-Ci-C4alkyl;R49 znamená vodík;R50 znamená Ci-C6halogenalkyl aQ znamená skupinu Q2 kde R23 znamená hydroxy aY znamená kyslík, síru, chemickou vazbu nebo Ci-C4alkylenový můstek;nebo agrochemicky přijatelné soli takové sloučeniny, ab) synergicky účinného množství jedné nebo více sloučenin zvolených ze souboru zahrnujícího sloučeninu vzorce 2.1Me ve kterém R5i znamená CH2-OMe, ethyl nebo vodík; R52 znamená vodík nebo R5] a R52 dohromady znamenají skupinu -CH=CH-CH=CH-;-152CZ 304537 B6 a sloučeninu vzorce 2.2 ve kterém R53 znamená ethyl, R54 znamená methyl nebo ethyl a R55 znamená -CH(Me)CH2OMe, <S>-CH(Me)-CH2OMe, CH2OMe nebo CH2O-CH2CH3;a sloučeninu vzorce 2.3Me '56 ch2ci (23),Me 0 ve kterém R56 znamená CH(Me)-CH2OMe nebo <S>CH(Me)-CH2OMe;a sloučeninu vzorce 2.4 ^57 '58 'XNAA (2.4), '59 ve kterém R57 znamená chlor, methoxy nebo methylthio, R58 znamená ethyl a R59 znamená ethyl, isopropyl, -C(CN)(CH3)CH3 nebo terc-butyl;ve kterém R^ znamená vodík, methoxy nebo ethoxy, R$3 znamená vodík, methyl, methoxy nebo fluor, Ré4 znamená COOMe, fluor nebo chlor, R^ znamená vodík nebo methyl, Y znamená methin, C-F nebo dusík, Z znamená methin nebo dusík a R56 znamená fluor nebo chlor;- 153 CZ 304537 B6 a sloučeninu vzorce 2.7 (2-7), ve kterém fU7 znamená vodík nebo -C(O)-S-n-oktyl;a sloučeninu vzorce 2.12 (2.12), ve kterém R73 znamená NH2 nebo <S>NH2;a sloučeninu vzorce 2.13 (2.13), ve kterém Y] znamená dusík, methin, NH-CHO nebo N-Me, Y2 znamená dusík, methin nebo ΟΙ, Y3 znamená methin, Y4 znamená methin nebo Y3 a Y4 společně tvoří síru nebo C-Cl, Y5 zna mená dusík nebo methin, Y6 znamená methyl, difluormethoxy, trifluormethyl nebo methoxy, Y znamená methoxy nebo difluormethoxy a R74 znamená CONMe2, COOMe, COOC2H5, trifluor methyl, CH2-CH2CF3 nebo SO2CH2CH3, nebo její sodnou sůl;a sloučeninu vzorce 2.13.CClN iCHO '\ 3 /Ό /o Zz \?'NHO L OCH, crCH3 (2.13.C), /CH3- 154CZ 304537 B6 a sloučeninu vzorce 2.14 (2.14),5 a sloučeninu vzorce 2.16HOCKT N PO(OH)2 (2.16), H a sloučeninu vzorce 2.18 (2.18), a sloučeninu vzorce 2.19 (2.21),- 155CZ 304537 B6 a sloučeninu vzorce 2.25 (2.30) a sloučeninu vzorce 2.33HOOCOMe—S—Me (2·33)· IMe
- 2. Způsob kontroly nežádoucího rostlinného růstu v kulturách užitkových rostlin, vyznačený tím, že zahrnuje umožnění herbicidně účinnému množství kompozice podle nároku 1 působit na užitkovou rostlinu nebo na její lokalitu.
- 3. Způsob podle nároku 2, vyznačený tím, že užitkovou rostlinou je kukuřice nebo cukrová třtina.
- 4. Způsob podle nároku 2, vyznačený tím, že kultury užitkových rostlin se ošetří uvedenou kompozicí v aplikačních množstvích odpovídajících celkovému množství účinné látky od 1 do 5000 g na hektar.
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Families Citing this family (368)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU773363B2 (en) * | 2000-01-25 | 2004-05-20 | Syngenta Participations Ag | Herbicidal composition |
GT200100103A (es) * | 2000-06-09 | 2002-02-21 | Nuevos herbicidas | |
MXPA04005264A (es) * | 2001-12-03 | 2004-10-11 | Syngenta Participations Ag | Composicion herbicida. |
WO2003047343A1 (en) * | 2001-12-03 | 2003-06-12 | Syngenta Participations Ag | Herbicidal composition |
DE10219036A1 (de) | 2002-04-29 | 2003-11-06 | Bayer Cropscience Ag | Substituierte Pyridylketone |
AU2003213473A1 (en) * | 2002-08-07 | 2004-02-26 | Syngenta Participations Ag | Herbicidal composition |
WO2005077178A2 (en) * | 2004-02-16 | 2005-08-25 | Syngenta Participations Ag | Herbicidal composition |
US8883683B2 (en) * | 2005-12-06 | 2014-11-11 | Bayer Cropscience Lp | Stabilized herbicidal composition |
US20070129250A1 (en) * | 2005-12-06 | 2007-06-07 | Tai-Teh Wu | Stabilized herbicidal composition |
US8883689B2 (en) | 2005-12-06 | 2014-11-11 | Bayer Cropscience Lp | Stabilized herbicidal compositions |
EP2102181B1 (en) * | 2006-12-14 | 2014-06-18 | Syngenta Participations AG | 4-phenyl-pyrane-3,5-diones, 4-phenyl-thiopyrane-3,5-diones and cyclohexanetriones as novel herbicides |
JP5300225B2 (ja) * | 2007-08-03 | 2013-09-25 | バイエル・クロップサイエンス・アーゲー | 除草剤トリアゾリルピリジンケトン類 |
US9480252B2 (en) * | 2007-08-06 | 2016-11-01 | Syngenta Crop Protection Llc | Herbicidal compositions |
JP5596541B2 (ja) * | 2007-08-06 | 2014-09-24 | シンジェンタ リミテッド | 除草用組成物及びその使用法 |
EA019698B1 (ru) * | 2008-06-09 | 2014-05-30 | Зингента Партисипейшнс Аг | Способ борьбы с сорняками и гербицидная композиция |
TW201002202A (en) * | 2008-06-27 | 2010-01-16 | Du Pont | Fungicidal pyridines |
WO2010103065A1 (en) | 2009-03-11 | 2010-09-16 | Basf Se | Fungicidal compositions and their use |
US9232785B2 (en) | 2009-04-02 | 2016-01-12 | Basf Se | Method for reducing sunburn damage in plants |
US20120077676A1 (en) | 2009-06-12 | 2012-03-29 | Basf Se | Antifungal 1,2,4-Triazolyl Derivatives Having a 5-Sulfur Substituent |
WO2010146032A2 (de) | 2009-06-16 | 2010-12-23 | Basf Se | Fungizide mischungen |
WO2010146115A1 (en) | 2009-06-18 | 2010-12-23 | Basf Se | Triazole compounds carrying a sulfur substituent |
EP2443097A1 (en) | 2009-06-18 | 2012-04-25 | Basf Se | Antifungal 1, 2, 4-triazolyl derivatives |
EP2442653A2 (de) | 2009-06-18 | 2012-04-25 | Basf Se | Fungizide mischungen |
EP2443098A1 (en) | 2009-06-18 | 2012-04-25 | Basf Se | Antifungal 1, 2, 4-triazolyl derivatives |
EP2443099A1 (en) | 2009-06-18 | 2012-04-25 | Basf Se | Antifungal 1, 2, 4-triazolyl derivatives having a 5- sulfur substituent |
WO2010146116A1 (en) | 2009-06-18 | 2010-12-23 | Basf Se | Triazole compounds carrying a sulfur substituent |
KR20120062679A (ko) | 2009-06-18 | 2012-06-14 | 바스프 에스이 | 황 치환기를 보유하는 트리아졸 화합물 |
WO2010149758A1 (en) | 2009-06-25 | 2010-12-29 | Basf Se | Antifungal 1, 2, 4-triazolyl derivatives |
BR112012001001A2 (pt) | 2009-07-14 | 2016-11-16 | Basf Se | compositos azol das formulas i e ii, compostos das formulas i e i, compostos de formula ix, composição agricola, uso de um composto farmaceutica, metodo para tratar infecções de câncer ou virus para combater fungos zoopatigênicos ou humanopatogenicos |
MX2012000421A (es) | 2009-07-28 | 2012-02-08 | Basf Se | Composiciones plaguicidas de suspo - emulsiones. |
WO2011026796A1 (en) | 2009-09-01 | 2011-03-10 | Basf Se | Synergistic fungicidal mixtures comprising lactylates and method for combating phytopathogenic fungi |
WO2011069912A1 (de) | 2009-12-07 | 2011-06-16 | Basf Se | Triazolverbindungen, ihre verwendung sowie sie enthaltende mittel |
WO2011069916A1 (de) | 2009-12-08 | 2011-06-16 | Basf Se | Triazolverbindungen, ihre verwendung als fungizide sowie sie enthaltende mittel |
WO2011069894A1 (de) | 2009-12-08 | 2011-06-16 | Basf Se | Triazolverbindungen, ihre verwendung sowie sie enthaltende mittel |
WO2011110583A2 (en) | 2010-03-10 | 2011-09-15 | Basf Se | Fungicidal mixtures comprising triazole derivatives |
EP2547209B1 (en) | 2010-03-18 | 2021-05-12 | Basf Se | Fungicidal compositions comprising a phosphate solubilizing microorganism and a fungicidally active compound |
EP2366289A1 (en) | 2010-03-18 | 2011-09-21 | Basf Se | Synergistic fungicidal mixtures |
DE102011017716A1 (de) | 2010-04-29 | 2011-11-03 | Basf Se | Synergistische fungizide Mischungen |
DE102011017715A1 (de) | 2010-04-29 | 2012-03-08 | Basf Se | Synergistische fungizide Mischungen |
DE102011017670A1 (de) | 2010-04-29 | 2011-11-03 | Basf Se | Synergistische fungizide Mischungen |
DE102011017669A1 (de) | 2010-04-29 | 2011-11-03 | Basf Se | Synergistische fungizide Mischungen |
EP2402345A1 (en) | 2010-06-29 | 2012-01-04 | Basf Se | Pyrazole fused bicyclic compounds |
EP2402335A1 (en) | 2010-06-29 | 2012-01-04 | Basf Se | Pyrazolopyridine compounds |
EP2402336A1 (en) | 2010-06-29 | 2012-01-04 | Basf Se | Pyrazolopyridine compounds |
EP2401915A1 (en) | 2010-06-29 | 2012-01-04 | Basf Se | Pyrazolopyridine compounds |
EP2402339A1 (en) | 2010-06-29 | 2012-01-04 | Basf Se | Pyrazolopyridine compounds |
EP2402344A1 (en) | 2010-06-29 | 2012-01-04 | Basf Se | Pyrazole fused bicyclic compounds |
EP2402343A1 (en) | 2010-06-29 | 2012-01-04 | Basf Se | Pyrazole-fused bicyclic compounds |
EP2402338A1 (en) | 2010-06-29 | 2012-01-04 | Basf Se | Pyrazolopyridine compounds |
EP2402337A1 (en) | 2010-06-29 | 2012-01-04 | Basf Se | Pyrazolopyridine compounds |
EP2402340A1 (en) | 2010-06-29 | 2012-01-04 | Basf Se | Pyrazolopyridine compounds |
KR20130101003A (ko) | 2010-08-03 | 2013-09-12 | 바스프 에스이 | 살진균 조성물 |
JP5753178B2 (ja) * | 2010-09-24 | 2015-07-22 | クミアイ化学工業株式会社 | 6−アシルピリジン−2−オン誘導体及び除草剤 |
EP2447261A1 (en) | 2010-10-29 | 2012-05-02 | Basf Se | Pyrrole, furane and thiophene derivatives and their use as fungicides |
EP2447262A1 (en) | 2010-10-29 | 2012-05-02 | Basf Se | Pyrrole, furane and thiophene derivatives and their use as fungicides |
EP2465350A1 (en) | 2010-12-15 | 2012-06-20 | Basf Se | Pesticidal mixtures |
EP2481284A3 (en) | 2011-01-27 | 2012-10-17 | Basf Se | Pesticidal mixtures |
EP2686316B1 (de) | 2011-03-15 | 2015-04-22 | Bayer Intellectual Property GmbH | N-(1,2,5-oxadiazol-3-yl)pyridincarboxamide und ihre verwendung als herbizide |
PL2688405T3 (pl) | 2011-03-23 | 2018-05-30 | Basf Se | Kompozycje zawierające polimerowe, jonowe związki zawierające grupy imidazoliowe |
US9253980B2 (en) | 2011-04-15 | 2016-02-09 | Basf Se | Use of substituted dithiine-tetracarboximides for combating phytopathogenic fungi |
CN103501615A (zh) | 2011-04-15 | 2014-01-08 | 巴斯夫欧洲公司 | 取代的二噻烯-二羧酰亚胺在防治植物病原性真菌中的用途 |
CN103491775A (zh) | 2011-04-21 | 2014-01-01 | 巴斯夫欧洲公司 | 3,4-二取代的吡咯-2,5-二酮及其作为杀真菌剂的用途 |
UY34136A (es) | 2011-06-17 | 2013-01-03 | Basf Se | Mezclas fungicidas sinérgicas que comprenden 2,3,5,6-tetraciano-[1,4]ditiína |
EP2731935B1 (en) | 2011-07-13 | 2016-03-09 | BASF Agro B.V. | Fungicidal substituted 2-[2-halogenalkyl-4-(phenoxy)-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds |
US20140141974A1 (en) | 2011-07-15 | 2014-05-22 | Basf Se | Fungicidal phenylalkyl-substituted 2-[2-chloro-4-(4-chloro-phenoxy)-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds |
KR20140057550A (ko) | 2011-07-15 | 2014-05-13 | 바스프 에스이 | 살진균성의 알킬-치환된 2-[2-클로로-4-(4-클로로-페녹시)-페닐]-1-[1,2,4]트리아졸-1-일-에탄올 화합물 |
WO2013010885A1 (en) | 2011-07-15 | 2013-01-24 | Basf Se | Fungicidal alkyl- and aryl-substituted 2-[2-chloro-4-(dihalo-phenoxy)-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds |
US9247746B2 (en) | 2011-08-15 | 2016-02-02 | Basf Se | Fungicidal substituted 1-{2-cyclyloxy-2-[2-halo-4-(4-halogen-phenoxy)-phenyl]-ethyl}-1H-[1,2,4]triazole compounds |
EP2559688A1 (en) | 2011-08-15 | 2013-02-20 | Basf Se | Fungicidal substituted 1-{2-[2-halo-4-(4-halogen-phenoxy)-phenyl]-2-butoxy-ethyl}-1h [1,2,4]triazole compounds |
JP2014524430A (ja) | 2011-08-15 | 2014-09-22 | ビーエーエスエフ ソシエタス・ヨーロピア | 殺菌性置換1−{2−[2−ハロ−4−(4−ハロゲン−フェノキシ)−フェニル]−2−エトキシ−エチル}−1h−[1,2,4]トリアゾール化合物 |
EP2744791B1 (en) | 2011-08-15 | 2015-10-28 | Basf Se | Fungicidal substituted 1-{2-[2-halo-4-(4-halogen-phenoxy)-phenyl]-2-alkoxy-3-methyl-butyl}-1h-[1,2,4]triazole compounds |
CN103827096A (zh) | 2011-08-15 | 2014-05-28 | 巴斯夫欧洲公司 | 杀真菌的取代的1-{2-[2-卤代-4-(4-卤代苯氧基)苯基]-2-烷氧基己基}-1h-[1,2,4]三唑化合物 |
EP2744792B1 (en) | 2011-08-15 | 2016-10-12 | Basf Se | Fungicidal substituted 1-{2-[2-halo-4-(4-halogen-phenoxy)-phenyl]-2-alkynyloxy-ethyl}-1h-[1,2,4]triazole compounds |
CN103857662B (zh) | 2011-08-15 | 2017-02-15 | 巴斯夫欧洲公司 | 杀真菌的取代的1‑{2‑[2‑卤代‑4‑(4‑卤代苯氧基)苯基]‑2‑烷氧基‑2‑炔基/链烯基乙基}‑1h‑[1,2,4]三唑化合物 |
KR20140054235A (ko) | 2011-08-15 | 2014-05-08 | 바스프 에스이 | 살진균 치환된 1-{2-[2-할로-4-(4-할로겐-페녹시)-페닐]-2-알콕시-2-시클릴-에틸}-1h-[1,2,4]트리아졸 화합물 |
SI2776038T1 (en) | 2011-11-11 | 2018-06-29 | Gilead Apollo, Llc | ACC INHIBITORS AND THEIR USE |
JP6093367B2 (ja) * | 2011-11-30 | 2017-03-08 | シンジェンタ リミテッド | 2−(置換フェニル)−シクロペンタン−1,3−ジオン化合物、およびその誘導体 |
CA2856954C (en) | 2011-12-21 | 2020-09-22 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi resistant to qo inhibitors |
WO2013113773A1 (en) | 2012-02-03 | 2013-08-08 | Basf Se | Fungicidal pyrimidine compounds |
WO2013113719A1 (en) | 2012-02-03 | 2013-08-08 | Basf Se | Fungicidal pyrimidine compounds ii |
WO2013113791A1 (en) | 2012-02-03 | 2013-08-08 | Basf Se | Fungicidal pyrimidine compounds |
WO2013113720A1 (en) | 2012-02-03 | 2013-08-08 | Basf Se | Fungicidal pyrimidine compounds |
WO2013113782A1 (en) | 2012-02-03 | 2013-08-08 | Basf Se | Fungicidal pyrimidine compounds |
WO2013113781A1 (en) | 2012-02-03 | 2013-08-08 | Basf Se | Fungicidal pyrimidine compounds i |
WO2013113776A1 (en) | 2012-02-03 | 2013-08-08 | Basf Se | Fungicidal pyrimidine compounds |
WO2013113716A1 (en) | 2012-02-03 | 2013-08-08 | Basf Se | Fungicidal pyrimidine compounds |
WO2013113778A1 (en) | 2012-02-03 | 2013-08-08 | Basf Se | Fungicidal pyrimidine compounds |
IN2014DN07220A (cs) | 2012-02-03 | 2015-04-24 | Basf Se | |
CA2862346A1 (en) | 2012-02-03 | 2013-08-08 | Basf Se | Fungicidal pyrimidine compounds |
WO2013124250A2 (en) | 2012-02-20 | 2013-08-29 | Basf Se | Fungicidal substituted thiophenes |
WO2013135672A1 (en) | 2012-03-13 | 2013-09-19 | Basf Se | Fungicidal pyrimidine compounds |
US9462809B2 (en) | 2012-03-13 | 2016-10-11 | Basf Se | Fungicidal pyrimidine compounds |
WO2013144223A1 (en) | 2012-03-30 | 2013-10-03 | Basf Se | N-substituted pyrimidinylidene compounds and derivatives for combating animal pests |
ES2626360T3 (es) | 2012-03-30 | 2017-07-24 | Basf Se | Compuestos de piridinilideno tiocarbonilo N-sustituidos y su uso para combatir plagas de animales |
US20150065343A1 (en) | 2012-04-02 | 2015-03-05 | Basf Se | Acrylamide compounds for combating invertebrate pests |
WO2013149903A1 (en) | 2012-04-03 | 2013-10-10 | Basf Se | N- substituted hetero - bicyclic furanone derivatives for combating animal |
WO2013150115A1 (en) | 2012-04-05 | 2013-10-10 | Basf Se | N- substituted hetero - bicyclic compounds and derivatives for combating animal pests |
EA201401213A1 (ru) | 2012-05-04 | 2015-04-30 | Басф Се | Замещенные пиразолсодержащие соединения и их применение в качестве пестицидов |
CN104487439B (zh) | 2012-05-24 | 2017-06-09 | 巴斯夫欧洲公司 | N‑硫代邻氨基苯甲酰胺化合物及其作为杀害虫剂的用途 |
WO2013186089A2 (en) | 2012-06-14 | 2013-12-19 | Basf Se | Pesticidal methods using substituted 3-pyridyl thiazole compounds and derivatives for combating animal pests |
WO2014009137A1 (en) | 2012-07-13 | 2014-01-16 | Basf Se | Substituted thiadiazoles and their use as fungicides |
WO2014009293A1 (en) | 2012-07-13 | 2014-01-16 | Basf Se | New substituted thiadiazoles and their use as fungicides |
WO2014053406A1 (en) | 2012-10-01 | 2014-04-10 | Basf Se | Method of controlling ryanodine-modulator insecticide resistant insects |
CN104768377A (zh) | 2012-10-01 | 2015-07-08 | 巴斯夫欧洲公司 | 包含邻氨基苯甲酰胺类化合物的农药活性混合物 |
AR094139A1 (es) | 2012-10-01 | 2015-07-15 | Basf Se | Mezclas activas como plaguicidas, que comprenden compuestos de antranilamida |
WO2014053407A1 (en) | 2012-10-01 | 2014-04-10 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
WO2014053403A1 (en) | 2012-10-01 | 2014-04-10 | Basf Se | Method of controlling insecticide resistant insects |
WO2014053401A2 (en) | 2012-10-01 | 2014-04-10 | Basf Se | Method of improving plant health |
JP2015532274A (ja) | 2012-10-01 | 2015-11-09 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | 栽培植物へのn−チオ−アントラニルアミド化合物の使用 |
US20150257383A1 (en) | 2012-10-12 | 2015-09-17 | Basf Se | Method for combating phytopathogenic harmful microbes on cultivated plants or plant propagation material |
WO2014079820A1 (en) | 2012-11-22 | 2014-05-30 | Basf Se | Use of anthranilamide compounds for reducing insect-vectored viral infections |
CN104955813A (zh) | 2012-11-27 | 2015-09-30 | 巴斯夫欧洲公司 | 取代的[1,2,4]三唑化合物 |
WO2014082871A1 (en) | 2012-11-27 | 2014-06-05 | Basf Se | Substituted 2-[phenoxy-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds and their use as fungicides |
WO2014082879A1 (en) | 2012-11-27 | 2014-06-05 | Basf Se | Substituted [1,2,4]triazole compounds |
WO2014082881A1 (en) | 2012-11-27 | 2014-06-05 | Basf Se | Substituted 2-[phenoxy-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds and their use as fungicides |
WO2014086856A1 (en) | 2012-12-04 | 2014-06-12 | Basf Agro B.V., Arnhem (Nl) | Compositions comprising a quillay extract and a biopesticide |
KR20150093750A (ko) | 2012-12-04 | 2015-08-18 | 바스프 에스이 | 신규 치환된 1,4-디티인 유도체 및 살진균제로서의 이들의 용도 |
WO2014086850A1 (en) | 2012-12-04 | 2014-06-12 | Basf Agro B.V., Arnhem (Nl) | Compositions comprising a quillay extract and a fungicidal inhibitor of respiratory complex ii |
WO2014086854A1 (en) | 2012-12-04 | 2014-06-12 | Basf Agro B.V., Arnhem (Nl) | Compositions comprising a quillay extract and a plant growth regulator |
EP2746278A1 (en) | 2012-12-19 | 2014-06-25 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
CN105164111B (zh) | 2012-12-19 | 2018-11-20 | 巴斯夫欧洲公司 | 取代[1,2,4]三唑及其作为杀真菌剂的用途 |
EP2746256A1 (en) | 2012-12-19 | 2014-06-25 | Basf Se | Fungicidal imidazolyl and triazolyl compounds |
EP2746277A1 (en) | 2012-12-19 | 2014-06-25 | Basf Se | Fungicidal imidazolyl and triazolyl compounds |
EP2746276A1 (en) | 2012-12-19 | 2014-06-25 | Basf Se | New substituted triazoles and imidazoles and their use as fungicides |
EP2746274A1 (en) | 2012-12-19 | 2014-06-25 | Basf Se | Substituted [1,2,4]triazole compounds |
EP2746263A1 (en) | 2012-12-19 | 2014-06-25 | Basf Se | Alpha-substituted triazoles and imidazoles |
WO2014095555A1 (en) | 2012-12-19 | 2014-06-26 | Basf Se | New substituted triazoles and imidazoles and their use as fungicides |
EP2746275A1 (en) | 2012-12-19 | 2014-06-25 | Basf Se | New substituted triazoles and imidazoles and their use as fungicides |
WO2014095534A1 (en) | 2012-12-19 | 2014-06-26 | Basf Se | New substituted triazoles and imidazoles and their use as fungicides |
EP2746279A1 (en) | 2012-12-19 | 2014-06-25 | Basf Se | Fungicidal imidazolyl and triazolyl compounds |
EP2746255A1 (en) | 2012-12-19 | 2014-06-25 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
WO2014095547A1 (en) | 2012-12-19 | 2014-06-26 | Basf Se | New substituted triazoles and imidazoles and their use as fungicides |
EP2746264A1 (en) | 2012-12-19 | 2014-06-25 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
EP2746262A1 (en) | 2012-12-19 | 2014-06-25 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds for combating phytopathogenic fungi |
EP2935237A1 (en) | 2012-12-19 | 2015-10-28 | Basf Se | Substituted [1,2,4]triazole compounds and their use as fungicides |
EP2745691A1 (en) | 2012-12-19 | 2014-06-25 | Basf Se | Substituted imidazole compounds and their use as fungicides |
EP2746266A1 (en) | 2012-12-19 | 2014-06-25 | Basf Se | New substituted triazoles and imidazoles and their use as fungicides |
WO2014095381A1 (en) | 2012-12-19 | 2014-06-26 | Basf Se | Fungicidal imidazolyl and triazolyl compounds |
EA030875B1 (ru) | 2012-12-20 | 2018-10-31 | Басф Агро Б.В. | Композиции, содержащие триазольное соединение |
EP2746260A1 (en) | 2012-12-21 | 2014-06-25 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
EP2746259A1 (en) | 2012-12-21 | 2014-06-25 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
EP2746257A1 (en) | 2012-12-21 | 2014-06-25 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
EP2746258A1 (en) | 2012-12-21 | 2014-06-25 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
US20150368236A1 (en) | 2012-12-27 | 2015-12-24 | Basf Se | 2-(pyridin-3-yl)-5-hetaryl-thiazole compounds carrying an imine or imine-derived substituent for combating invertebrate pests |
WO2014118099A1 (en) | 2013-01-30 | 2014-08-07 | Basf Se | Fungicidal naphthoquinones and derivatives |
WO2014124850A1 (en) | 2013-02-14 | 2014-08-21 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
US20160270405A1 (en) | 2013-03-20 | 2016-09-22 | Basf Corporation | Synergistic Compositions Comprising a Bacillus Subtilis Strain and a Pesticide |
CA2898583C (en) | 2013-03-20 | 2023-09-26 | Basf Corporation | Synergistic compositions comprising a bacillus subtilis strain and a biopesticide |
EP2783569A1 (en) | 2013-03-28 | 2014-10-01 | Basf Se | Compositions comprising a triazole compound |
US20160050923A1 (en) | 2013-04-19 | 2016-02-25 | Basf Se | N-substituted acyl-imino-pyridine compounds and derivatives for combating animal pests |
AU2014262638A1 (en) | 2013-05-10 | 2015-11-26 | Gilead Apollo, Llc | ACC inhibitors and uses thereof |
CA2911818A1 (en) | 2013-05-10 | 2014-11-13 | Nimbus Apollo, Inc. | Acc inhibitors and uses thereof |
EP2813499A1 (en) | 2013-06-12 | 2014-12-17 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
EP2815647A1 (en) | 2013-06-18 | 2014-12-24 | Basf Se | Novel strobilurin-type compounds for combating phytopathogenic fungi |
EP2815649A1 (en) | 2013-06-18 | 2014-12-24 | Basf Se | Fungicidal mixtures II comprising strobilurin-type fungicides |
BR112015031439A2 (pt) | 2013-06-21 | 2017-07-25 | Basf Se | métodos para o combate ou controle das pragas, para o tratamento, prevenção e proteção de culturas de soja, para o controle e proteção do material de propagação dos vegetais de soja, para o combate ou controle das pragas e utilização de um composto de fórmula i |
AR097138A1 (es) | 2013-07-15 | 2016-02-24 | Basf Se | Compuestos plaguicidas |
WO2015011615A1 (en) | 2013-07-22 | 2015-01-29 | Basf Corporation | Mixtures comprising a trichoderma strain and a pesticide |
EP2835052A1 (en) | 2013-08-07 | 2015-02-11 | Basf Se | Fungicidal mixtures comprising pyrimidine fungicides |
EP2839745A1 (en) | 2013-08-21 | 2015-02-25 | Basf Se | Agrochemical formulations comprising a 2-ethyl-hexanol alkoxylate |
WO2015036059A1 (en) | 2013-09-16 | 2015-03-19 | Basf Se | Fungicidal pyrimidine compounds |
CA2923101A1 (en) | 2013-09-16 | 2015-03-19 | Basf Se | Fungicidal pyrimidine compounds |
CA2922506A1 (en) | 2013-09-19 | 2015-03-26 | Basf Se | N-acylimino heterocyclic compounds |
WO2015055757A1 (en) | 2013-10-18 | 2015-04-23 | Basf Se | Use of pesticidal active carboxamide derivative in soil and seed application and treatment methods |
EP3080092B1 (en) | 2013-12-12 | 2019-02-06 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
US20160318897A1 (en) | 2013-12-18 | 2016-11-03 | Basf Se | Azole compounds carrying an imine-derived substituent |
EP3083581A1 (en) | 2013-12-18 | 2016-10-26 | Basf Se | N-substituted imino heterocyclic compounds |
WO2015104422A1 (en) | 2014-01-13 | 2015-07-16 | Basf Se | Dihydrothiophene compounds for controlling invertebrate pests |
PL3122732T3 (pl) | 2014-03-26 | 2018-08-31 | Basf Se | Podstawione związki [1,2,4]triazolowe i imidazolowe jako fungicydy |
EP2924027A1 (en) | 2014-03-28 | 2015-09-30 | Basf Se | Substituted [1,2,4]triazole and imidazole fungicidal compounds |
EP2949649A1 (en) | 2014-05-30 | 2015-12-02 | Basf Se | Fungicide substituted [1,2,4]triazole and imidazole compounds |
EP2949216A1 (en) | 2014-05-30 | 2015-12-02 | Basf Se | Fungicidal substituted alkynyl [1,2,4]triazole and imidazole compounds |
AR100743A1 (es) | 2014-06-06 | 2016-10-26 | Basf Se | Compuestos de [1,2,4]triazol sustituido |
EP2952512A1 (en) | 2014-06-06 | 2015-12-09 | Basf Se | Substituted [1,2,4]triazole compounds |
EP2952507A1 (en) | 2014-06-06 | 2015-12-09 | Basf Se | Substituted [1,2,4]triazole compounds |
EP3151669B1 (en) | 2014-06-06 | 2020-10-28 | Basf Se | Use of substituted oxadiazoles for combating phytopathogenic fungi |
EP2952506A1 (en) | 2014-06-06 | 2015-12-09 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
EP2979549A1 (en) | 2014-07-31 | 2016-02-03 | Basf Se | Method for improving the health of a plant |
EP3204390B1 (en) | 2014-10-06 | 2019-06-05 | Basf Se | Substituted pyrimidinium compounds for combating animal pests |
JP2017538860A (ja) | 2014-10-24 | 2017-12-28 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | 固体粒子の表面荷電を改変するための、非両性の四級化可能な水溶性ポリマー |
BR112017009513A2 (pt) | 2014-11-06 | 2018-02-06 | Basf Se | utilização de um composto heterobicíclico, utilização dos compostos i, compostos, composição agrícola ou veterinária, método para o combate ou controle de pragas, método para a proteção de culturas e sementes |
EP3028573A1 (en) | 2014-12-05 | 2016-06-08 | Basf Se | Use of a triazole fungicide on transgenic plants |
AU2016214305B2 (en) | 2015-02-06 | 2020-10-08 | Basf Se | Pyrazole compounds as nitrification inhibitors |
WO2016128240A1 (en) | 2015-02-11 | 2016-08-18 | Basf Se | Pesticidal mixture comprising a pyrazole compound and two fungicides |
CA3170386A1 (en) | 2015-02-11 | 2016-08-18 | Basf Se | Pesticidal mixture comprising a pyrazole compound, an insecticide and a fungicide |
CA2980505A1 (en) | 2015-04-07 | 2016-10-13 | Basf Agrochemical Products B.V. | Use of an insecticidal carboxamide compound against pests on cultivated plants |
AU2016260805A1 (en) | 2015-05-12 | 2017-11-23 | Basf Se | Thioether compounds as nitrification inhibitors |
WO2016198611A1 (en) | 2015-06-11 | 2016-12-15 | Basf Se | N-(thio)acylimino heterocyclic compounds |
WO2016198613A1 (en) | 2015-06-11 | 2016-12-15 | Basf Se | N-(thio)acylimino compounds |
WO2017016883A1 (en) | 2015-07-24 | 2017-02-02 | Basf Se | Process for preparation of cyclopentene compounds |
EP3356341B1 (en) | 2015-10-02 | 2020-04-01 | Basf Se | Imino compounds with a 2-chloropyrimidin-5-yl substituent as pest-control agents |
US20180279615A1 (en) | 2015-10-05 | 2018-10-04 | Basf Se | Pyridine derivatives for combating phytopathogenic fungi |
EP3371177A1 (en) | 2015-11-02 | 2018-09-12 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
EP3165094A1 (en) | 2015-11-03 | 2017-05-10 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
BR112018008288A2 (pt) | 2015-11-04 | 2018-10-30 | Basf Se | uso de compostos de fórmula, compostos de fórmula, mistura, composição agroquímica e método para combater fungos |
EP3165093A1 (en) | 2015-11-05 | 2017-05-10 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
EP3167716A1 (en) | 2015-11-10 | 2017-05-17 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
WO2017081312A1 (en) | 2015-11-13 | 2017-05-18 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
EP3373732A1 (en) | 2015-11-13 | 2018-09-19 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
CA3003946A1 (en) | 2015-11-19 | 2017-05-26 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
WO2017085100A1 (en) | 2015-11-19 | 2017-05-26 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
HUE053175T2 (hu) | 2015-11-25 | 2021-06-28 | Gilead Apollo Llc | ACC-gátló észterek és azok alkalmazása |
EP3380480B1 (en) | 2015-11-25 | 2022-12-14 | Gilead Apollo, LLC | Pyrazole acc inhibitors and uses thereof |
ES2939977T3 (es) | 2015-11-25 | 2023-04-28 | Gilead Apollo Llc | Inhibidores de triazol ACC y usos de los mismos |
EP3383183B1 (en) | 2015-11-30 | 2020-05-27 | Basf Se | Compositions containing cis-jasmone and bacillus amyloliquefaciens |
CN108290840A (zh) | 2015-12-01 | 2018-07-17 | 巴斯夫欧洲公司 | 作为杀真菌剂的吡啶化合物 |
BR112018010140A8 (pt) | 2015-12-01 | 2019-02-26 | Basf Se | compostos de fórmula, composição, utilização de um composto de fórmula, método para o combate de fungos fitopatogênicos e semente |
EP3205208A1 (en) | 2016-02-09 | 2017-08-16 | Basf Se | Mixtures and compositions comprising paenibacillus strains or fusaricidins and chemical pesticides |
EP3426660A1 (en) | 2016-03-09 | 2019-01-16 | Basf Se | Spirocyclic derivatives |
US20190098899A1 (en) | 2016-03-10 | 2019-04-04 | Basf Se | Fungicidal mixtures iii comprising strobilurin-type fungicides |
US20190082696A1 (en) | 2016-03-11 | 2019-03-21 | Basf Se | Method for controlling pests of plants |
UA123912C2 (uk) | 2016-04-01 | 2021-06-23 | Басф Се | Біциклічні сполуки |
BR112018069897B1 (pt) | 2016-04-11 | 2023-01-17 | Basf Se | Composto de fórmula i, composição agroquímica, processo para a preparação de compostos de fórmula i, uso não terapêutico de compostos e método para o combate de fungos fitopatogênicos nocivos |
US20190276376A1 (en) | 2016-05-18 | 2019-09-12 | Basf Se | Capsules comprising benzylpropargylethers for use as nitrification inhibitors |
WO2018050421A1 (en) | 2016-09-13 | 2018-03-22 | Basf Se | Fungicidal mixtures i comprising quinoline fungicides |
WO2018054711A1 (en) | 2016-09-26 | 2018-03-29 | Basf Se | Pyridine compounds for controlling phytopathogenic harmful fungi |
WO2018054723A1 (en) | 2016-09-26 | 2018-03-29 | Basf Se | Pyridine compounds for controlling phytopathogenic harmful fungi |
WO2018054721A1 (en) | 2016-09-26 | 2018-03-29 | Basf Se | Pyridine compounds for controlling phytopathogenic harmful fungi |
WO2018065182A1 (en) | 2016-10-04 | 2018-04-12 | Basf Se | Reduced quinoline compounds as antifuni agents |
WO2018073110A1 (en) | 2016-10-20 | 2018-04-26 | Basf Se | Quinoline compounds as fungicides |
EP3555050A1 (en) | 2016-12-16 | 2019-10-23 | Basf Se | Pesticidal compounds |
EP3555056A1 (en) | 2016-12-19 | 2019-10-23 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
EP3339297A1 (en) | 2016-12-20 | 2018-06-27 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
EP3338552A1 (en) | 2016-12-21 | 2018-06-27 | Basf Se | Use of a tetrazolinone fungicide on transgenic plants |
EP3571190A1 (en) | 2017-01-23 | 2019-11-27 | Basf Se | Fungicidal pyridine compounds |
WO2018149754A1 (en) | 2017-02-16 | 2018-08-23 | Basf Se | Pyridine compounds |
BR112019015338B1 (pt) | 2017-02-21 | 2023-03-14 | Basf Se | Compostos de fórmula i, composição agroquímica, semente revestida, uso dos compostos e método para combater fungos nocivos fitopatogênicos |
WO2018162312A1 (en) | 2017-03-10 | 2018-09-13 | Basf Se | Spirocyclic derivatives |
WO2018166855A1 (en) | 2017-03-16 | 2018-09-20 | Basf Se | Heterobicyclic substituted dihydroisoxazoles |
KR102596592B1 (ko) | 2017-03-28 | 2023-10-31 | 바스프 에스이 | 살충 화합물 |
AU2018241628B2 (en) | 2017-03-31 | 2022-03-17 | Basf Se | Pyrimidinium compounds and their mixtures for combating animal pests |
US20200187500A1 (en) | 2017-04-06 | 2020-06-18 | Basf Se | Pyridine compounds |
US20200045974A1 (en) | 2017-04-07 | 2020-02-13 | Basf Se | Substituted Oxadiazoles for Combating Phytopathogenic Fungi |
WO2018188962A1 (en) | 2017-04-11 | 2018-10-18 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
TW201838965A (zh) | 2017-04-20 | 2018-11-01 | 印度商Pi工業公司 | 新穎的苯胺化合物 |
WO2018192793A1 (en) | 2017-04-20 | 2018-10-25 | Basf Se | Substituted rhodanine derivatives |
MX2019012813A (es) | 2017-04-26 | 2020-01-14 | Basf Se | Derivados de succinimida sustituida como plaguicidas. |
US20210084902A1 (en) | 2017-05-02 | 2021-03-25 | Basf Se | Fungicidal mixture comprising substituted 3-phenyl-5-(trifluoromethyl)-1,2,4-oxadiazoles |
WO2018202491A1 (en) | 2017-05-04 | 2018-11-08 | Basf Se | Substituted trifluoromethyloxadiazoles for combating phytopathogenic fungi |
CN110621669A (zh) | 2017-05-04 | 2019-12-27 | 巴斯夫欧洲公司 | 防除植物病原性真菌的取代5-卤代烷基-5-羟基异噁唑类 |
BR112019022206A2 (pt) | 2017-05-05 | 2020-05-12 | Basf Se | Misturas fungicidas, composição agroquímica, uso da mistura, métodos para controlar fungos nocivos fitopatogênicos e para a proteção de material de propagação de plantas e material de propagação vegetal |
CA3059282A1 (en) | 2017-05-10 | 2018-11-15 | Basf Se | Bicyclic pesticidal compounds |
WO2018210661A1 (en) | 2017-05-15 | 2018-11-22 | Basf Se | Heteroaryl compounds as agrochemical fungicides |
WO2018210658A1 (en) | 2017-05-15 | 2018-11-22 | Basf Se | Heteroaryl compounds as agrochemical fungicides |
WO2018210659A1 (en) | 2017-05-15 | 2018-11-22 | Basf Se | Heteroaryl compounds as agrochemical fungicides |
WO2018210660A1 (en) | 2017-05-15 | 2018-11-22 | Basf Se | Heteroaryl compounds as agrochemical fungicides |
EP3625215B1 (en) | 2017-05-18 | 2023-09-13 | PI Industries Ltd | Formimidamidine compounds useful against phytopathogenic microorganisms |
EP3630731B1 (en) | 2017-05-30 | 2023-08-09 | Basf Se | Pyridine and pyrazine compounds for combating phytopathogenic fungi |
WO2018219797A1 (en) | 2017-06-02 | 2018-12-06 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
WO2018224455A1 (en) | 2017-06-07 | 2018-12-13 | Basf Se | Substituted cyclopropyl derivatives |
CN110770235A (zh) | 2017-06-16 | 2020-02-07 | 巴斯夫欧洲公司 | 用于防除动物害虫的介离子咪唑鎓化合物和衍生物 |
US20200190043A1 (en) | 2017-06-19 | 2020-06-18 | Basf Se | 2-[[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]aryloxy](thio)acetamides for combating phytopathogenic fungi |
EP3642203A1 (en) | 2017-06-19 | 2020-04-29 | Basf Se | Substituted pyrimidinium compounds and derivatives for combating animal pests |
WO2018234488A1 (en) | 2017-06-23 | 2018-12-27 | Basf Se | SUBSTITUTED CYCLOPROPYL DERIVATIVES |
WO2019002158A1 (en) | 2017-06-30 | 2019-01-03 | Basf Se | SUBSTITUTED TRIFLUOROMETHYLOXADIAZOLES FOR THE CONTROL OF PHYTOPATHOGENIC FUNGI |
WO2019025250A1 (en) | 2017-08-04 | 2019-02-07 | Basf Se | SUBSTITUTED TRIFLUOROMETHYLOXADIAZOLES FOR COMBATING PHYTOPATHOGENIC FUNGI |
WO2019038042A1 (en) | 2017-08-21 | 2019-02-28 | Basf Se | SUBSTITUTED TRIFLUOROMETHYLOXADIAZOLES FOR THE CONTROL OF PHYTOPATHOGENIC FUNGI |
EP3915379A1 (en) | 2017-08-29 | 2021-12-01 | Basf Se | Pesticidal mixtures |
WO2019042932A1 (en) | 2017-08-31 | 2019-03-07 | Basf Se | METHOD FOR CONTROLLING RICE PARASITES IN RICE |
EP3453706A1 (en) | 2017-09-08 | 2019-03-13 | Basf Se | Pesticidal imidazole compounds |
US11076596B2 (en) | 2017-09-18 | 2021-08-03 | Basf Se | Substituted trifluoromethyloxadiazoles for combating phytopathogenic fungi |
WO2019057660A1 (en) | 2017-09-25 | 2019-03-28 | Basf Se | INDOLE AND AZAINDOLE COMPOUNDS HAVING 6-CHANNEL SUBSTITUTED ARYL AND HETEROARYL CYCLES AS AGROCHEMICAL FUNGICIDES |
BR112020006037A2 (pt) | 2017-10-13 | 2020-10-06 | Basf Se | compostos, misturas pesticidas, composição agroquímica, métodos para controlar pragas de invertebrados, para proteger plantas e para proteção de material de propagação de plantas, semente e uso de compostos de fórmula (i) |
EP3713936B1 (en) | 2017-11-23 | 2021-10-20 | Basf Se | Substituted trifluoromethyloxadiazoles for combating phytopathogenic fungi |
WO2019115511A1 (en) | 2017-12-14 | 2019-06-20 | Basf Se | Fungicidal mixture comprising substituted 3-phenyl-5-(trifluoromethyl)-1,2,4-oxadiazoles |
CA3084405A1 (en) | 2017-12-15 | 2019-06-20 | Basf Se | Fungicidal mixture comprising substituted pyridines |
EP3728204A1 (en) | 2017-12-20 | 2020-10-28 | PI Industries Ltd. | Fluoralkenyl compounds, process for preparation and use thereof |
WO2019121143A1 (en) | 2017-12-20 | 2019-06-27 | Basf Se | Substituted cyclopropyl derivatives |
UA127604C2 (uk) | 2017-12-21 | 2023-11-01 | Басф Се | Пестицидні сполуки |
BR112020012706A2 (pt) | 2018-01-09 | 2020-11-24 | Basf Se | uso de um composto de silietinil hetarila, composição para uso na redução de nitrificação, mistura agroquímica, métodos para reduzir a nitrificação e para tratamento de um fertilizante ou de uma composição |
WO2019137995A1 (en) | 2018-01-11 | 2019-07-18 | Basf Se | Novel pyridazine compounds for controlling invertebrate pests |
EP3746439A2 (en) | 2018-01-30 | 2020-12-09 | PI Industries Ltd. | Oxadiazoles for use in controlling phytopathogenic fungi |
WO2019150311A1 (en) | 2018-02-02 | 2019-08-08 | Pi Industries Ltd. | 1-3 dithiol compounds and their use for the protection of crops from phytopathogenic microorganisms |
US20200354321A1 (en) | 2018-02-07 | 2020-11-12 | Basf Se | New pyridine carboxamides |
WO2019154665A1 (en) | 2018-02-07 | 2019-08-15 | Basf Se | New pyridine carboxamides |
EP3530118A1 (en) | 2018-02-26 | 2019-08-28 | Basf Se | Fungicidal mixtures |
EP3530116A1 (en) | 2018-02-27 | 2019-08-28 | Basf Se | Fungicidal mixtures comprising xemium |
WO2019166561A1 (en) | 2018-02-28 | 2019-09-06 | Basf Se | Use of alkoxypyrazoles as nitrification inhibitors |
EP3758491A1 (en) | 2018-02-28 | 2021-01-06 | Basf Se | Use of pyrazole propargyl ethers as nitrification inhibitors |
WO2019166252A1 (en) | 2018-02-28 | 2019-09-06 | Basf Se | Fungicidal mixtures comprising fenpropidin |
IL276745B2 (en) | 2018-02-28 | 2023-10-01 | Basf Se | Use of N-functional alkoxy pyrazole compounds as nitrification inhibitors |
WO2019166257A1 (en) | 2018-03-01 | 2019-09-06 | BASF Agro B.V. | Fungicidal compositions of mefentrifluconazole |
EP3533331A1 (en) | 2018-03-02 | 2019-09-04 | Basf Se | Fungicidal mixtures comprising pydiflumetofen |
EP3533333A1 (en) | 2018-03-02 | 2019-09-04 | Basf Se | Fungicidal mixtures comprising pydiflumetofen |
EP3536150A1 (en) | 2018-03-06 | 2019-09-11 | Basf Se | Fungicidal mixtures comprising fluxapyroxad |
WO2019171234A1 (en) | 2018-03-09 | 2019-09-12 | Pi Industries Ltd. | Heterocyclic compounds as fungicides |
WO2019175713A1 (en) | 2018-03-14 | 2019-09-19 | Basf Corporation | New catechol molecules and their use as inhibitors to p450 related metabolic pathways |
WO2019175712A1 (en) | 2018-03-14 | 2019-09-19 | Basf Corporation | New uses for catechol molecules as inhibitors to glutathione s-transferase metabolic pathways |
WO2019185413A1 (en) | 2018-03-27 | 2019-10-03 | Basf Se | Pesticidal substituted cyclopropyl derivatives |
WO2019202459A1 (en) | 2018-04-16 | 2019-10-24 | Pi Industries Ltd. | Use of 4-substituted phenylamidine compounds for controlling disease rust diseases in plants |
WO2019219464A1 (en) | 2018-05-15 | 2019-11-21 | Basf Se | Substituted trifluoromethyloxadiazoles for combating phytopathogenic fungi |
WO2019219529A1 (en) | 2018-05-15 | 2019-11-21 | Basf Se | Mixtures comprising benzpyrimoxan and oxazosulfyl and uses and methods of applying them |
WO2019224092A1 (en) | 2018-05-22 | 2019-11-28 | Basf Se | Pesticidally active c15-derivatives of ginkgolides |
WO2020002472A1 (en) | 2018-06-28 | 2020-01-02 | Basf Se | Use of alkynylthiophenes as nitrification inhibitors |
WO2020020777A1 (en) | 2018-07-23 | 2020-01-30 | Basf Se | Use of substituted 2-thiazolines as nitrification inhibitors |
ES2969872T3 (es) | 2018-07-23 | 2024-05-23 | Basf Se | Uso de un compuesto de tiazolidina sustituida como inhibidor de la nitrificación |
TW202009235A (zh) | 2018-08-17 | 2020-03-01 | 印度商皮埃企業有限公司 | 1,2-二硫醇酮化合物及其用途 |
EP3613736A1 (en) | 2018-08-22 | 2020-02-26 | Basf Se | Substituted glutarimide derivatives |
EP3628158A1 (en) | 2018-09-28 | 2020-04-01 | Basf Se | Pesticidal mixture comprising a mesoionic compound and a biopesticide |
EP3628156A1 (en) | 2018-09-28 | 2020-04-01 | Basf Se | Method for controlling pests of sugarcane, citrus, rapeseed, and potato plants |
CA3112042A1 (en) | 2018-09-28 | 2020-04-02 | Basf Se | Method of controlling pests by seed treatment application of a mesoionic compound or mixture thereof |
EP3628157A1 (en) | 2018-09-28 | 2020-04-01 | Basf Se | Method of controlling insecticide resistant insects and virus transmission to plants |
WO2020070611A1 (en) | 2018-10-01 | 2020-04-09 | Pi Industries Ltd | Oxadiazoles as fungicides |
EP3860992A1 (en) | 2018-10-01 | 2021-08-11 | PI Industries Ltd. | Novel oxadiazoles |
EP3643705A1 (en) | 2018-10-24 | 2020-04-29 | Basf Se | Pesticidal compounds |
WO2020095161A1 (en) | 2018-11-05 | 2020-05-14 | Pi Industries Ltd. | Nitrone compounds and use thereof |
EP3887357A1 (en) | 2018-11-28 | 2021-10-06 | Basf Se | Pesticidal compounds |
EP3670501A1 (en) | 2018-12-17 | 2020-06-24 | Basf Se | Substituted [1,2,4]triazole compounds as fungicides |
WO2020126591A1 (en) | 2018-12-18 | 2020-06-25 | Basf Se | Substituted pyrimidinium compounds for combating animal pests |
EP3696177A1 (en) | 2019-02-12 | 2020-08-19 | Basf Se | Heterocyclic compounds for the control of invertebrate pests |
CN113784958B (zh) | 2019-04-08 | 2024-04-30 | Pi工业有限公司 | 用于控制或预防植物病原性真菌的噁二唑化合物 |
WO2020208509A1 (en) | 2019-04-08 | 2020-10-15 | Pi Industries Limited | Novel oxadiazole compounds for controlling or preventing phytopathogenic fungi |
BR112021020231A2 (pt) | 2019-04-08 | 2021-12-07 | Pi Industries Ltd | Compostos de oxadiazol inovadores para controlar ou prevenir fungos fitopatogênicos |
EP3730489A1 (en) | 2019-04-25 | 2020-10-28 | Basf Se | Heteroaryl compounds as agrochemical fungicides |
EP3769623A1 (en) | 2019-07-22 | 2021-01-27 | Basf Se | Mesoionic imidazolium compounds and derivatives for combating animal pests |
WO2020239517A1 (en) | 2019-05-29 | 2020-12-03 | Basf Se | Mesoionic imidazolium compounds and derivatives for combating animal pests |
WO2020244970A1 (en) | 2019-06-06 | 2020-12-10 | Basf Se | New carbocyclic pyridine carboxamides |
BR112021021028A2 (pt) | 2019-06-06 | 2021-12-14 | Basf Se | Uso dos compostos de fórmula i, compostos da fórmula i, composição e método para combater fungos fitopatogênicos |
WO2020244969A1 (en) | 2019-06-06 | 2020-12-10 | Basf Se | Pyridine derivatives and their use as fungicides |
EP3766879A1 (en) | 2019-07-19 | 2021-01-20 | Basf Se | Pesticidal pyrazole derivatives |
AR119774A1 (es) | 2019-08-19 | 2022-01-12 | Pi Industries Ltd | Compuestos de oxadiazol que contienen un anillo heteroaromático de 5 miembros para controlar o prevenir hongos fitopatogénicos |
WO2021063736A1 (en) | 2019-10-02 | 2021-04-08 | Basf Se | Bicyclic pyridine derivatives |
WO2021063735A1 (en) | 2019-10-02 | 2021-04-08 | Basf Se | New bicyclic pyridine derivatives |
AR120374A1 (es) | 2019-11-08 | 2022-02-09 | Pi Industries Ltd | Compuestos de oxadiazol que contienen anillos de heterociclilo fusionados para controlar o prevenir hongos fitopatogénicos |
CA3162521A1 (en) | 2019-12-23 | 2021-07-01 | Basf Se | Enzyme enhanced root uptake of agrochemical active compound |
US20230106291A1 (en) | 2020-02-28 | 2023-04-06 | BASF Agro B.V. | Methods and uses of a mixture comprising alpha-cypermethrin and dinotefuran for controlling invertebrate pests in t |
WO2021175669A1 (en) | 2020-03-04 | 2021-09-10 | Basf Se | Use of substituted 1,2,4-oxadiazoles for combating phytopathogenic fungi |
BR112022020612A2 (pt) | 2020-04-14 | 2022-11-29 | Basf Se | Mistura fungicida, composição agroquímica, uso não terapêutico da mistura e método para controlar fungos fitopatogênicos nocivos |
EP3903584A1 (en) | 2020-04-28 | 2021-11-03 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors iv |
EP3903581A1 (en) | 2020-04-28 | 2021-11-03 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors i |
EP4143167B1 (en) | 2020-04-28 | 2024-05-15 | Basf Se | Pesticidal compounds |
EP3903583A1 (en) | 2020-04-28 | 2021-11-03 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors iii |
EP3903582A1 (en) | 2020-04-28 | 2021-11-03 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors ii |
EP3909950A1 (en) | 2020-05-13 | 2021-11-17 | Basf Se | Heterocyclic compounds for the control of invertebrate pests |
EP3945089A1 (en) | 2020-07-31 | 2022-02-02 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors v |
WO2021249800A1 (en) | 2020-06-10 | 2021-12-16 | Basf Se | Substituted [1,2,4]triazole compounds as fungicides |
EP3939961A1 (en) | 2020-07-16 | 2022-01-19 | Basf Se | Strobilurin type compounds and their use for combating phytopathogenic fungi |
WO2022017836A1 (en) | 2020-07-20 | 2022-01-27 | BASF Agro B.V. | Fungicidal compositions comprising (r)-2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1- (1,2,4-triazol-1-yl)propan-2-ol |
EP3970494A1 (en) | 2020-09-21 | 2022-03-23 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors viii |
AR123264A1 (es) | 2020-08-18 | 2022-11-16 | Pi Industries Ltd | Nuevos compuestos heterocíclicos para combatir los hongos fitopatógenos |
UY39424A (es) | 2020-09-15 | 2022-03-31 | Pi Industries Ltd | Nuevos compuestos de picolinamida para combatir hongos fitopatógenos |
AR123501A1 (es) | 2020-09-15 | 2022-12-07 | Pi Industries Ltd | Nuevos compuestos de picolinamida para combatir hongos fitopatógenos |
AR123594A1 (es) | 2020-09-26 | 2022-12-21 | Pi Industries Ltd | Compuestos nematicidas y uso de los mismos |
CN116209355A (zh) | 2020-10-27 | 2023-06-02 | 巴斯夫农业公司 | 包含氯氟醚菌唑的组合物 |
EP4018830A1 (en) | 2020-12-23 | 2022-06-29 | Basf Se | Pesticidal mixtures |
EP4043444A1 (en) | 2021-02-11 | 2022-08-17 | Basf Se | Substituted isoxazoline derivatives |
TW202309047A (zh) | 2021-05-05 | 2023-03-01 | 印度商皮埃企業有限公司 | 用以防治植物病原真菌的新穎稠合雜環化合物 |
EP4337012A1 (en) | 2021-05-11 | 2024-03-20 | Basf Se | Fungicidal mixtures comprising substituted 3-phenyl-5-(trifluoromethyl)-1,2,4-oxadiazoles |
CN117355520A (zh) | 2021-05-18 | 2024-01-05 | 巴斯夫欧洲公司 | 用作杀真菌剂的新型取代喹啉类 |
BR112023024017A2 (pt) | 2021-05-18 | 2024-02-06 | Basf Se | Compostos, composição, método para combater fungos fitopatogênicos e semente |
AR125925A1 (es) | 2021-05-26 | 2023-08-23 | Pi Industries Ltd | Composicion fungicida que contiene compuestos de oxadiazol |
EP4094579A1 (en) | 2021-05-28 | 2022-11-30 | Basf Se | Pesticidal mixtures comprising metyltetraprole |
EP4119547A1 (en) | 2021-07-12 | 2023-01-18 | Basf Se | Triazole compounds for the control of invertebrate pests |
WO2023011958A1 (en) | 2021-08-02 | 2023-02-09 | Basf Se | (3-pirydyl)-quinazoline |
EP4140986A1 (en) | 2021-08-23 | 2023-03-01 | Basf Se | Pyrazine compounds for the control of invertebrate pests |
EP4140995A1 (en) | 2021-08-27 | 2023-03-01 | Basf Se | Pyrazine compounds for the control of invertebrate pests |
EP4151631A1 (en) | 2021-09-20 | 2023-03-22 | Basf Se | Heterocyclic compounds for the control of invertebrate pests |
WO2023072670A1 (en) | 2021-10-28 | 2023-05-04 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors x |
WO2023072671A1 (en) | 2021-10-28 | 2023-05-04 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors ix |
EP4194453A1 (en) | 2021-12-08 | 2023-06-14 | Basf Se | Pyrazine compounds for the control of invertebrate pests |
EP4198033A1 (en) | 2021-12-14 | 2023-06-21 | Basf Se | Heterocyclic compounds for the control of invertebrate pests |
EP4198023A1 (en) | 2021-12-16 | 2023-06-21 | Basf Se | Pesticidally active thiosemicarbazone compounds |
AR127972A1 (es) | 2021-12-17 | 2024-03-13 | Pi Industries Ltd | Novedosos compuestos de piridina carboxamida bicíclica sustituida fusionada para combatir hongos fitopatogénicos |
EP4238971A1 (en) | 2022-03-02 | 2023-09-06 | Basf Se | Substituted isoxazoline derivatives |
WO2023203066A1 (en) | 2022-04-21 | 2023-10-26 | Basf Se | Synergistic action as nitrification inhibitors of dcd oligomers with alkoxypyrazole and its oligomers |
WO2024028243A1 (en) | 2022-08-02 | 2024-02-08 | Basf Se | Pyrazolo pesticidal compounds |
EP4361126A1 (en) | 2022-10-24 | 2024-05-01 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors xv |
EP4389210A1 (en) | 2022-12-21 | 2024-06-26 | Basf Se | Heteroaryl compounds for the control of invertebrate pests |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4995902A (en) * | 1988-07-25 | 1991-02-26 | Ciba-Geigy Corporation | Novel herbicides |
WO2000000031A1 (de) * | 1998-06-26 | 2000-01-06 | Novartis Pharma Ag. | Herbizides mittel |
WO2000000029A1 (en) * | 1998-06-26 | 2000-01-06 | Novartis Pharma Ag. | Herbicidal composition |
WO2000015615A1 (en) * | 1998-09-15 | 2000-03-23 | Syngenta Participations Ag | Pyridine ketones useful as herbicides |
EP1250047B9 (en) * | 2000-01-25 | 2005-05-18 | Syngenta Participations AG | Herbicidal composition |
Family Cites Families (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2129109C3 (de) | 1971-06-11 | 1979-06-07 | Lentia Gmbh | Phenylpyridazine, ihre Herstellung und sie enthaltende herbizide Mittel |
DE2948535A1 (de) | 1979-12-03 | 1981-06-25 | Basf Ag, 6700 Ludwigshafen | Dichloracetamide, herbizide mittel, die acetanilide als herbizide wirkstoffe und diese dichloracetamide als antagonistische mittel enthalten, sowie ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses |
DE3525205A1 (de) | 1984-09-11 | 1986-03-20 | Hoechst Ag, 6230 Frankfurt | Pflanzenschuetzende mittel auf basis von 1,2,4-triazolderivaten sowie neue derivate des 1,2,4-triazols |
JPS61293956A (ja) | 1985-06-21 | 1986-12-24 | Tokuyama Soda Co Ltd | クロロアセトアミド化合物及びその製造方法 |
US5194085A (en) | 1987-06-12 | 1993-03-16 | Bayer Aktiengesellschaft | Herbicidal substituted triazolinones |
US5256625A (en) | 1987-08-13 | 1993-10-26 | Monsanto Company | Safening imidazolinone herbicides |
DK184489A (da) * | 1988-04-18 | 1989-10-19 | Sandoz Ag | Bicyclodioner |
HU206242B (en) * | 1988-04-18 | 1992-10-28 | Sandoz Ag | Herbicidal compositions comprising substituted benzoyl bicyclodione derivatives as active ingredient |
DE4110795A1 (de) | 1991-04-04 | 1992-10-08 | Bayer Ag | Sulfonylaminocarbonyltriazolinone mit ueber sauerstoff gebundenen substituenten |
US5215570A (en) | 1988-10-20 | 1993-06-01 | Ciba-Geigy Corporation | Sulfamoylphenylureas |
DK0436680T3 (da) | 1989-06-29 | 1994-10-10 | Ciba Geigy Ag | Heterocycliske forbindelser |
JPH0352862A (ja) * | 1989-07-20 | 1991-03-07 | Nippon Soda Co Ltd | 置換ピリジン誘導体、その製造法及び除草剤 |
US5281571A (en) | 1990-10-18 | 1994-01-25 | Monsanto Company | Herbicidal benzoxazinone- and benzothiazinone-substituted pyrazoles |
DE4037840A1 (de) | 1990-11-28 | 1992-06-11 | Basf Ag | 2-amino-zimtsaeureester |
US5498773A (en) | 1991-05-03 | 1996-03-12 | Dowelanco | Herbicidal compositions with increased crop safety |
DE59209933D1 (de) * | 1991-12-31 | 2001-12-20 | Aventis Cropscience Gmbh | Kombinationen aus Herbiziden und pflanzenschützenden Stoffen |
DE59309481D1 (de) | 1992-05-15 | 1999-05-06 | Hoechst Schering Agrevo Gmbh | Synergistisch wirksame Herbizidkombinationen |
US5674810A (en) | 1995-09-05 | 1997-10-07 | Fmc Corporation | Herbicidal compositions comprising 2- (4-heterocyclic-phenoxymethyl)Phenoxy!-alkanoates |
EP0646315B1 (en) | 1992-11-05 | 1999-05-12 | Novartis AG | Novel compositions containing an auxin transport inhibitor and another herbicide |
US5407897A (en) | 1993-03-03 | 1995-04-18 | American Cyanamid Company | Method for safening herbicides in crops using substituted benzopyran and tetrahydronaphthalene compounds |
DE4331448A1 (de) | 1993-09-16 | 1995-03-23 | Hoechst Schering Agrevo Gmbh | Substituierte Isoxazoline, Verfahren zu deren Herstellung, diese enthaltende Mittel und deren Verwendung als Safener |
US5741756A (en) * | 1995-07-19 | 1998-04-21 | Zeneca Limited | Synergistic herbicidal composition comprising triketones and chloroacetanilides, and method of use thereof |
PL186631B1 (pl) * | 1996-03-15 | 2004-02-27 | Syngenta Participations Ag | Synergistyczna kompozycja herbicydowa oraz sposóbzwalczania niepożądanych roślin |
WO1998013361A1 (en) | 1996-09-26 | 1998-04-02 | Novartis Ag | Herbicidal composition |
DE19727410A1 (de) | 1997-06-27 | 1999-01-07 | Hoechst Schering Agrevo Gmbh | 3-(5-Tetrazolylcarbonyl)-2-chinolone und diese enthaltende nutzpflanzenschützende Mittel |
-
2001
- 2001-01-23 AU AU37335/01A patent/AU773363B2/en not_active Expired
- 2001-01-23 CA CA002396587A patent/CA2396587C/en not_active Expired - Lifetime
- 2001-01-23 CN CNB018040896A patent/CN100488362C/zh not_active Expired - Lifetime
- 2001-01-23 DK DK01909680T patent/DK1250047T3/da active
- 2001-01-23 EP EP04029625A patent/EP1520472A3/en not_active Withdrawn
- 2001-01-23 PT PT01909680T patent/PT1250047E/pt unknown
- 2001-01-23 MX MXPA02006931A patent/MXPA02006931A/es active IP Right Grant
- 2001-01-23 PL PL356434A patent/PL202070B1/pl unknown
- 2001-01-23 EP EP01909680A patent/EP1250047B9/en not_active Expired - Lifetime
- 2001-01-23 BR BRPI0107811-9A patent/BR0107811B1/pt not_active IP Right Cessation
- 2001-01-23 SK SK1082-2002A patent/SK10822002A3/sk not_active Application Discontinuation
- 2001-01-23 ES ES01909680T patent/ES2238425T3/es not_active Expired - Lifetime
- 2001-01-23 HU HU0301083A patent/HU230041B1/hu not_active IP Right Cessation
- 2001-01-23 AT AT01909680T patent/ATE290785T1/de active
- 2001-01-23 JP JP2001555490A patent/JP4880161B2/ja not_active Expired - Fee Related
- 2001-01-23 DE DE60109411T patent/DE60109411T2/de not_active Expired - Lifetime
- 2001-01-23 WO PCT/EP2001/000720 patent/WO2001054501A2/en active IP Right Grant
- 2001-01-23 AR ARP010100287A patent/AR027928A1/es active IP Right Grant
- 2001-01-23 RU RU2002121642/04A patent/RU2260949C2/ru not_active IP Right Cessation
- 2001-01-23 CZ CZ2002-2547A patent/CZ304537B6/cs not_active IP Right Cessation
-
2002
- 2002-07-23 US US10/201,405 patent/US6890885B2/en not_active Expired - Lifetime
- 2002-08-13 HR HR20020669A patent/HRP20020669B1/xx not_active IP Right Cessation
-
2007
- 2007-07-05 AR ARP070103002A patent/AR061831A2/es unknown
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4995902A (en) * | 1988-07-25 | 1991-02-26 | Ciba-Geigy Corporation | Novel herbicides |
WO2000000031A1 (de) * | 1998-06-26 | 2000-01-06 | Novartis Pharma Ag. | Herbizides mittel |
WO2000000029A1 (en) * | 1998-06-26 | 2000-01-06 | Novartis Pharma Ag. | Herbicidal composition |
WO2000015615A1 (en) * | 1998-09-15 | 2000-03-23 | Syngenta Participations Ag | Pyridine ketones useful as herbicides |
EP1250047B9 (en) * | 2000-01-25 | 2005-05-18 | Syngenta Participations AG | Herbicidal composition |
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