SK281848B6 - Substituované azadioxacykloalkény, spôsob ich výroby, medziprodukty, fungicídne prostriedky tieto látky obsahujúce, spôsob potláčania nežiaducich húb a použitie uvedených zlúčenín - Google Patents
Substituované azadioxacykloalkény, spôsob ich výroby, medziprodukty, fungicídne prostriedky tieto látky obsahujúce, spôsob potláčania nežiaducich húb a použitie uvedených zlúčenín Download PDFInfo
- Publication number
- SK281848B6 SK281848B6 SK166-96A SK16696A SK281848B6 SK 281848 B6 SK281848 B6 SK 281848B6 SK 16696 A SK16696 A SK 16696A SK 281848 B6 SK281848 B6 SK 281848B6
- Authority
- SK
- Slovakia
- Prior art keywords
- group
- optionally
- substituted
- cyano
- carbon atoms
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract 6
- 238000002360 preparation method Methods 0.000 title claims abstract 4
- 239000000543 intermediate Substances 0.000 title claims 7
- 238000004519 manufacturing process Methods 0.000 title claims 5
- 241000233866 Fungi Species 0.000 title claims 3
- 230000000855 fungicidal effect Effects 0.000 title claims 2
- 230000002401 inhibitory effect Effects 0.000 title 1
- -1 cyano, nitro, amino, hydroxy, formyl Chemical group 0.000 claims 81
- 125000004432 carbon atom Chemical group C* 0.000 claims 36
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 22
- 229910052736 halogen Inorganic materials 0.000 claims 19
- 150000002367 halogens Chemical class 0.000 claims 18
- 125000004093 cyano group Chemical group *C#N 0.000 claims 16
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 16
- 125000000217 alkyl group Chemical group 0.000 claims 15
- 229910052801 chlorine Inorganic materials 0.000 claims 15
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 15
- 239000000460 chlorine Substances 0.000 claims 14
- 229910052731 fluorine Inorganic materials 0.000 claims 14
- 239000011737 fluorine Substances 0.000 claims 14
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 14
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 13
- 125000005843 halogen group Chemical group 0.000 claims 13
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 10
- 125000003545 alkoxy group Chemical group 0.000 claims 10
- 125000001153 fluoro group Chemical group F* 0.000 claims 10
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 10
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 10
- 125000004430 oxygen atom Chemical group O* 0.000 claims 10
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 10
- 150000001875 compounds Chemical class 0.000 claims 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 9
- 125000003342 alkenyl group Chemical group 0.000 claims 8
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims 7
- 229910052717 sulfur Inorganic materials 0.000 claims 7
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 7
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 7
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 6
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 6
- 229910052794 bromium Chemical group 0.000 claims 6
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 6
- 125000001188 haloalkyl group Chemical group 0.000 claims 6
- 229910052739 hydrogen Inorganic materials 0.000 claims 6
- 239000001257 hydrogen Substances 0.000 claims 6
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 5
- 125000003282 alkyl amino group Chemical group 0.000 claims 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims 5
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 5
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 5
- 125000004663 dialkyl amino group Chemical group 0.000 claims 5
- 239000003085 diluting agent Substances 0.000 claims 5
- 125000004438 haloalkoxy group Chemical group 0.000 claims 5
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims 5
- 229910052757 nitrogen Inorganic materials 0.000 claims 5
- 125000001424 substituent group Chemical group 0.000 claims 5
- 125000004434 sulfur atom Chemical group 0.000 claims 5
- 239000002253 acid Substances 0.000 claims 4
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 4
- 125000004414 alkyl thio group Chemical group 0.000 claims 4
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 3
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 claims 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 claims 3
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 239000001301 oxygen Substances 0.000 claims 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 2
- 125000004529 1,2,3-triazinyl group Chemical group N1=NN=C(C=C1)* 0.000 claims 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 2
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 claims 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 2
- 125000005277 alkyl imino group Chemical group 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 125000000304 alkynyl group Chemical group 0.000 claims 2
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 2
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims 2
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 2
- 125000006125 ethylsulfonyl group Chemical group 0.000 claims 2
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims 2
- 125000004995 haloalkylthio group Chemical group 0.000 claims 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
- 125000001624 naphthyl group Chemical group 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 claims 2
- 125000003373 pyrazinyl group Chemical group 0.000 claims 2
- 125000002098 pyridazinyl group Chemical group 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 2
- 239000011593 sulfur Substances 0.000 claims 2
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 claims 2
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims 1
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 1
- 125000004530 1,2,4-triazinyl group Chemical group N1=NC(=NC=C1)* 0.000 claims 1
- 125000002030 1,2-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([*:2])C([H])=C1[H] 0.000 claims 1
- 125000003363 1,3,5-triazinyl group Chemical group N1=C(N=CN=C1)* 0.000 claims 1
- 125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 claims 1
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 claims 1
- KDBIBHNDHQBKIE-UHFFFAOYSA-N 1-butoxy-N-(4-ethoxy-4-methoxy-4-propoxybutyl)sulfanyl-1-ethylsulfanyl-1-methylsulfanyl-N-propylsulfanylmethanamine Chemical compound COC(CCCSN(C(SCC)(SC)OCCCC)SCCC)(OCCC)OCC KDBIBHNDHQBKIE-UHFFFAOYSA-N 0.000 claims 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 150000001335 aliphatic alkanes Chemical class 0.000 claims 1
- 125000003302 alkenyloxy group Chemical group 0.000 claims 1
- 125000004666 alkoxyiminoalkyl group Chemical group 0.000 claims 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 1
- 125000005279 aryl sulfonyloxy group Chemical group 0.000 claims 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims 1
- 125000004618 benzofuryl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims 1
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims 1
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims 1
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 1
- 125000004850 cyclobutylmethyl group Chemical group C1(CCC1)C* 0.000 claims 1
- 125000004851 cyclopentylmethyl group Chemical group C1(CCCC1)C* 0.000 claims 1
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 claims 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 125000001634 furandiyl group Chemical group O1C(=C(C=C1)*)* 0.000 claims 1
- 125000002541 furyl group Chemical group 0.000 claims 1
- 125000000262 haloalkenyl group Chemical group 0.000 claims 1
- 125000005700 haloalkyleneoxy group Chemical group 0.000 claims 1
- 125000004970 halomethyl group Chemical group 0.000 claims 1
- 125000005549 heteroarylene group Chemical group 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 229910000039 hydrogen halide Inorganic materials 0.000 claims 1
- 239000012433 hydrogen halide Substances 0.000 claims 1
- 125000005027 hydroxyaryl group Chemical group 0.000 claims 1
- 125000002883 imidazolyl group Chemical group 0.000 claims 1
- 238000011065 in-situ storage Methods 0.000 claims 1
- 238000002955 isolation Methods 0.000 claims 1
- 125000001786 isothiazolyl group Chemical group 0.000 claims 1
- 125000000842 isoxazolyl group Chemical group 0.000 claims 1
- 125000004957 naphthylene group Chemical group 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 125000001715 oxadiazolyl group Chemical group 0.000 claims 1
- 125000002971 oxazolyl group Chemical group 0.000 claims 1
- 125000000109 phenylethoxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])O* 0.000 claims 1
- 125000000168 pyrrolyl group Chemical group 0.000 claims 1
- 125000006413 ring segment Chemical group 0.000 claims 1
- 125000000547 substituted alkyl group Chemical class 0.000 claims 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims 1
- 125000001113 thiadiazolyl group Chemical group 0.000 claims 1
- 125000000335 thiazolyl group Chemical group 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 1
- 239000000417 fungicide Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D273/00—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/88—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with three ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Pest Control & Pesticides (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4326908 | 1993-08-11 | ||
| DE4408005A DE4408005A1 (de) | 1993-08-11 | 1994-03-10 | Substituierte Azadioxacycloalkene |
| PCT/EP1994/002533 WO1995004728A1 (de) | 1993-08-11 | 1994-07-29 | Substituierte azadioxacycloalkene und ihre verwendung als fungizide |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SK16696A3 SK16696A3 (en) | 1996-06-05 |
| SK281848B6 true SK281848B6 (sk) | 2001-08-06 |
Family
ID=25928507
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK166-96A SK281848B6 (sk) | 1993-08-11 | 1994-07-29 | Substituované azadioxacykloalkény, spôsob ich výroby, medziprodukty, fungicídne prostriedky tieto látky obsahujúce, spôsob potláčania nežiaducich húb a použitie uvedených zlúčenín |
Country Status (21)
| Country | Link |
|---|---|
| US (2) | US5679676A (cs) |
| EP (1) | EP0712396B1 (cs) |
| JP (2) | JP3887784B2 (cs) |
| CN (1) | CN1057762C (cs) |
| AT (1) | ATE172968T1 (cs) |
| AU (1) | AU682205B2 (cs) |
| BR (1) | BR9407239A (cs) |
| CA (1) | CA2169194C (cs) |
| CZ (1) | CZ293792B6 (cs) |
| DK (1) | DK0712396T3 (cs) |
| ES (1) | ES2124424T3 (cs) |
| HU (1) | HU222179B1 (cs) |
| IL (1) | IL110582A (cs) |
| MY (1) | MY111556A (cs) |
| NO (1) | NO308076B1 (cs) |
| NZ (1) | NZ271366A (cs) |
| PL (1) | PL187253B1 (cs) |
| SK (1) | SK281848B6 (cs) |
| TR (1) | TR27835A (cs) |
| WO (1) | WO1995004728A1 (cs) |
| ZW (1) | ZW8594A1 (cs) |
Families Citing this family (56)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6235887B1 (en) * | 1991-11-26 | 2001-05-22 | Isis Pharmaceuticals, Inc. | Enhanced triple-helix and double-helix formation directed by oligonucleotides containing modified pyrimidines |
| DE19501842A1 (de) * | 1995-01-23 | 1996-07-25 | Bayer Ag | Substituierte Arylazadioxacycloalkene |
| EP0837856B1 (en) * | 1995-06-22 | 2002-06-19 | Bayer Aktiengesellschaft | Pesticidal tris-oximino heterocyclic compounds |
| SK49498A3 (en) | 1995-10-18 | 1998-09-09 | Bayer Ag | Fluoromethoxyacrylic acid derivatives and their use as pest control agents |
| DE19611653A1 (de) * | 1995-10-18 | 1997-04-24 | Bayer Ag | Fluormethoxyacrylsäurederivate |
| US5739140A (en) * | 1995-11-03 | 1998-04-14 | Monsanto Company | Selected novel aryl acrylics |
| DE19602095A1 (de) * | 1996-01-22 | 1997-07-24 | Bayer Ag | Halogenpyrimidine |
| TW492962B (en) * | 1996-05-30 | 2002-07-01 | Bayer Ag | Process for preparing 3-(1-hydroxyphenyl-1-alkoximinomethyl)dioxazines |
| DE19642864A1 (de) * | 1996-10-17 | 1998-04-23 | Bayer Ag | Oximderivate |
| DE19706396A1 (de) * | 1996-12-09 | 1998-06-10 | Bayer Ag | Verfahren zur Herstellung von 3-(l-Hydroxiphenyl-l-alkoximinomethyl)dioxazinen |
| DE19710355A1 (de) * | 1997-03-13 | 1998-09-17 | Bayer Ag | Alkoximinomethyldioxazinderivate |
| DE19710609A1 (de) | 1997-03-14 | 1998-09-17 | Bayer Ag | Substituierte Aminosalicylsäureamide |
| DE19713762A1 (de) * | 1997-04-03 | 1998-10-08 | Bayer Ag | Methoximinomethyldioxazine |
| IL134002A0 (en) * | 1997-08-14 | 2001-04-30 | Bayer Ag | Methoximinomethyloxadiazines used as pesticides |
| AU9541898A (en) * | 1997-10-14 | 1999-05-03 | Bayer Aktiengesellschaft | Azines containing the 5,6-di-hydro-(1,4,2) dioxazine-3-yl group and the use thereof as fungicides |
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| DE3100728A1 (de) * | 1981-01-13 | 1982-08-26 | Bayer Ag, 5090 Leverkusen | Hydroximsaeureester, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide |
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| JP3188286B2 (ja) * | 1991-08-20 | 2001-07-16 | 塩野義製薬株式会社 | フェニルメトキシイミノ化合物およびそれを用いる農業用殺菌剤 |
-
1994
- 1994-07-11 ZW ZW8594A patent/ZW8594A1/xx unknown
- 1994-07-29 BR BR9407239A patent/BR9407239A/pt not_active IP Right Cessation
- 1994-07-29 CZ CZ1996370A patent/CZ293792B6/cs not_active IP Right Cessation
- 1994-07-29 JP JP50620595A patent/JP3887784B2/ja not_active Expired - Lifetime
- 1994-07-29 SK SK166-96A patent/SK281848B6/sk not_active IP Right Cessation
- 1994-07-29 WO PCT/EP1994/002533 patent/WO1995004728A1/de active IP Right Grant
- 1994-07-29 ES ES94924825T patent/ES2124424T3/es not_active Expired - Lifetime
- 1994-07-29 CN CN94193669A patent/CN1057762C/zh not_active Expired - Lifetime
- 1994-07-29 DK DK94924825T patent/DK0712396T3/da active
- 1994-07-29 AT AT94924825T patent/ATE172968T1/de active
- 1994-07-29 EP EP94924825A patent/EP0712396B1/de not_active Expired - Lifetime
- 1994-07-29 NZ NZ271366A patent/NZ271366A/en not_active IP Right Cessation
- 1994-07-29 AU AU74972/94A patent/AU682205B2/en not_active Expired
- 1994-07-29 HU HU9600299A patent/HU222179B1/hu active IP Right Grant
- 1994-07-29 US US08/596,175 patent/US5679676A/en not_active Expired - Lifetime
- 1994-07-29 CA CA002169194A patent/CA2169194C/en not_active Expired - Lifetime
- 1994-07-29 PL PL94312965A patent/PL187253B1/pl unknown
- 1994-08-04 TR TR00764/94A patent/TR27835A/xx unknown
- 1994-08-08 IL IL11058294A patent/IL110582A/xx not_active IP Right Cessation
- 1994-08-11 MY MYPI94002100A patent/MY111556A/en unknown
-
1996
- 1996-02-08 NO NO960514A patent/NO308076B1/no not_active IP Right Cessation
-
1997
- 1997-05-15 US US08/857,119 patent/US5883250A/en not_active Expired - Lifetime
-
2004
- 2004-12-15 JP JP2004363426A patent/JP2005162760A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| JPH10507998A (ja) | 1998-08-04 |
| CA2169194C (en) | 2005-05-24 |
| CZ293792B6 (cs) | 2004-08-18 |
| AU7497294A (en) | 1995-02-28 |
| US5679676A (en) | 1997-10-21 |
| MY111556A (en) | 2000-08-30 |
| IL110582A (en) | 2000-07-26 |
| IL110582A0 (en) | 1994-11-11 |
| BR9407239A (pt) | 1996-09-24 |
| ATE172968T1 (de) | 1998-11-15 |
| CN1132507A (zh) | 1996-10-02 |
| HUT74937A (en) | 1997-03-28 |
| WO1995004728A1 (de) | 1995-02-16 |
| US5883250A (en) | 1999-03-16 |
| NO308076B1 (no) | 2000-07-17 |
| CN1057762C (zh) | 2000-10-25 |
| TR27835A (tr) | 1995-08-31 |
| CA2169194A1 (en) | 1995-02-16 |
| CZ37096A3 (en) | 1996-05-15 |
| SK16696A3 (en) | 1996-06-05 |
| PL312965A1 (en) | 1996-05-27 |
| NO960514L (no) | 1996-02-08 |
| DK0712396T3 (da) | 1999-07-19 |
| JP3887784B2 (ja) | 2007-02-28 |
| HU222179B1 (hu) | 2003-04-28 |
| HU9600299D0 (en) | 1996-04-29 |
| EP0712396B1 (de) | 1998-11-04 |
| PL187253B1 (pl) | 2004-06-30 |
| JP2005162760A (ja) | 2005-06-23 |
| EP0712396A1 (de) | 1996-05-22 |
| NO960514D0 (no) | 1996-02-08 |
| ES2124424T3 (es) | 1999-02-01 |
| NZ271366A (en) | 1996-10-28 |
| AU682205B2 (en) | 1997-09-25 |
| ZW8594A1 (en) | 1994-10-12 |
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Legal Events
| Date | Code | Title | Description |
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| MK4A | Patent expired |
Expiry date: 20140729 |