KR850002482A - 트리아졸릴메틸-피리딜옥시메틸-카비놀 유도체의 제조방법 - Google Patents
트리아졸릴메틸-피리딜옥시메틸-카비놀 유도체의 제조방법 Download PDFInfo
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- KR850002482A KR850002482A KR1019840005659A KR840005659A KR850002482A KR 850002482 A KR850002482 A KR 850002482A KR 1019840005659 A KR1019840005659 A KR 1019840005659A KR 840005659 A KR840005659 A KR 840005659A KR 850002482 A KR850002482 A KR 850002482A
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- carbon atoms
- phenyl
- chlorine
- fluorine
- alkyl
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- 125000004432 carbon atom Chemical group C* 0.000 claims 13
- 125000000217 alkyl group Chemical group 0.000 claims 11
- 229910052801 chlorine Inorganic materials 0.000 claims 10
- 239000000460 chlorine Chemical group 0.000 claims 10
- 229910052731 fluorine Inorganic materials 0.000 claims 10
- 239000011737 fluorine Substances 0.000 claims 10
- -1 methoxy, ethoxy, methylthio, ethylthio, trifluoromethoxy, trifluoromethylthio, vinyl Chemical group 0.000 claims 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 10
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 9
- 125000001424 substituent group Chemical group 0.000 claims 9
- 150000001875 compounds Chemical class 0.000 claims 7
- 229910052736 halogen Inorganic materials 0.000 claims 7
- 150000002367 halogens Chemical group 0.000 claims 7
- 125000004093 cyano group Chemical group *C#N 0.000 claims 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 6
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 5
- 125000003545 alkoxy group Chemical group 0.000 claims 5
- 125000001153 fluoro group Chemical group F* 0.000 claims 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 4
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 2
- 125000004414 alkyl thio group Chemical group 0.000 claims 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 2
- 229910052794 bromium Inorganic materials 0.000 claims 2
- 125000004438 haloalkoxy group Chemical group 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 229910052751 metal Chemical class 0.000 claims 2
- 239000002184 metal Chemical class 0.000 claims 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
- SCVJRXQHFJXZFZ-KVQBGUIXSA-N 2-amino-9-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3h-purine-6-thione Chemical compound C1=2NC(N)=NC(=S)C=2N=CN1[C@H]1C[C@H](O)[C@@H](CO)O1 SCVJRXQHFJXZFZ-KVQBGUIXSA-N 0.000 claims 1
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 claims 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- PEKZNJMAXNTZLF-UHFFFAOYSA-N O(C1=CC=CC=C1)[C]SC1=CC=CC=C1 Chemical class O(C1=CC=CC=C1)[C]SC1=CC=CC=C1 PEKZNJMAXNTZLF-UHFFFAOYSA-N 0.000 claims 1
- 229910052783 alkali metal Chemical group 0.000 claims 1
- 150000001340 alkali metals Chemical group 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000003282 alkyl amino group Chemical group 0.000 claims 1
- 239000002585 base Substances 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
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000000068 chlorophenyl group Chemical group 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 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 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 229910052740 iodine Chemical group 0.000 claims 1
- 239000011630 iodine Chemical group 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 1
- 125000002071 phenylalkoxy group Chemical group 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
- C07C45/511—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups
- C07C45/515—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups the singly bound functional group being an acetalised, ketalised hemi-acetalised, or hemi-ketalised hydroxyl group
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/63—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by introduction of halogen; by substitution of halogen atoms by other halogen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/20—Unsaturated compounds containing keto groups bound to acyclic carbon atoms
- C07C49/255—Unsaturated compounds containing keto groups bound to acyclic carbon atoms containing ether groups, groups, groups, or groups
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- C07—ORGANIC CHEMISTRY
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- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
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- Environmental Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
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Description
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Claims (4)
- 일반식(Ⅱ)의 옥시란을 희석제의 존재하 및 필요한 경우 염기의 존재하에서, 일반식(Ⅲ)의 1,2,4-트리아졸과 반응시키고, 필요한 경우, 생성된 일반식(Ⅰ)의 화합물에 산 또는 금속염을 가함을 특징으로 하여 일반식(Ⅰ)의 트리아졸릴메틸 -피리딜옥시 메틸-카비놀 유도체 및 그의 산부가염 및 금속염 복합체를 제조하는 방법.상기식에서, R은 임의로 치환된 알킬, 임의로 치환된 시클로알킬 또는 임의로 치환된 페닐이고; Y는 할로겐, 알킬, 알콕시 또는 시아노이며; m은 0,1,2,3 또는 4이고; M은 수소 또는 알칼리금속이다.
- 제1항에 있어서, R이 탄소수가 1 내지4인 직쇄 또는 측쇄알킬이거나, 탄소수가 3 내지 7이고, 할로겐, 탄소수 1내지 4인 알킬 및 탄소수가 1 내지 2인 알콕시로 이루어진 그룹 중에서 선택된 같거나 다른 치환체에 의해 임의로 1-치환 또는 다치환된 시클로 알킬이거나, 또는 같거나 다른 치환체(여기에서 언급될 수 있는 치환체는 하기에서 R3에 대해 언급되는 페닐상의 치환체이다)에 의해 임의로 1- 치환 또는 다치환된 페닐이거나, 또는의 그룹을 나타내며; R1은 수소 또는 할로겐이고; R2는 할로겐이며; R3는 각각 탄소수가 1 내지 4인 알킬, 알콕시 또는 알킬티오이거나, 각각의 경우에 탄소수가 1내지 2이고 같거나 다른 할로겐원자 1 내지 5개를 갖는 할로게노알콕시 또는 할로게노알킬티오이거나, 탄소수가 2내지 6인 알케닐, 알킬부위의 탄소수가 1내지 4인 알콕시카보닐 또는 시아노이거나, 각각의 경우에 할로겐 탄소수 1내지 4의 알킬, 각각의 경우에 탄소수가 1또는 2인 알콕시 및 알킬티오, 각각의 경우에 탄소수가 1 또는 2이고 같거나 다른 할로겐원자 1내지 5개를 갖는 할로게노알킬, 할로게노알콕시 및 할로게노알킬티오, 시클로헥실, 각 알킬부위의 탄소수가 1내지 4인 디알킬아미노, 니트로, 시아노, 알킬부위의 탄소수가 1내지 4인 알콕시카보닐 및 할로겐으로 임의로 치환된 페닐로 이루어진 그룹중에서 선택된 치환체에 의해 페닐환상에서 임의로 1치환 또는 다치환된 페닐, 펜옥시, 페닐티오, 알킬부위의 탄소수가 1 내지 4인 페닐알콕시 또는 알킬부위의 탄소수가 1 내지 4인 페틸알킬티오이고; n은 0.1 또는 2이며; Y는 할로겐, 각각의 경우에 탄소수가 1내지 4인 직쇄 또는 측쇄 알킬 및/또는 알콕시, 또는 시아노이고; m은 0,1,2,3 또는 4인 일반식(I)의 화합물을 제조하는 방법.
- 제1항에 있어서, R은 3급 부틸 또는 이소프로필이거나, 각각 메틸, 에틸, 이소프로필, 메톡시 및 에톡시로 이루어진 그룹중에서 선택된 같거나 다른 치환체에 의해 임의로 1-, 2- 또는 3-치환된 시클로프로필, 스클로펜틸 또는 시클로헥실이거나, 불소, 염소, 메틸, 트리플루오로메틸, 페닐 및 클로로페닐로 이루어진 그룹중에서 선택된 같거나 다른 치환체에 의해 임의로 1-, 2- 또는 3- 치환된 페닐이거나, 또는의 그룹을 나타내며; R1은 수소, 불소 또는 염소이고; R2는 불소 또는 염소이며; R3는 메틸, 에틸, 프로필, 메톡시, 에톡시, 메틸티오, 에틸티오, 트리플루오로메톡시, 트리플루오로메틸티오, 비닐, 메톡시카보닐, 에톡시카보닐 또는 시아노이거나, 각각 불소, 염소, 메틸, 에틸, 메톡시, 메틸티오, 트리플루오로메틸, 트리플루오로메톡시, 트리플루오로메틸티오, 디메틸아미노, 메톡시카보닐 또는 에톡시카보닐에 의해 임의로 치환된 페닐, 펜옥시, 페닐티오, 페닐메톡시 또는 페닐메틸티오이고, n은 0.1 또는 2이며; Y는 불소, 염소, 브롬, 요오드, 메틸, 에틸, 메톡시 또는 시아노이고; m은 0,1,2,3 또는 4인 일반식(I)의 화합물을 제조하는 방법.
- 제1항에 있어서, R은 3급부틸이거나, 불소, 염소, 메틸, 트리플루오로메틸, 페닐 및 클로로페닐로 이루어진 그룹중에서 선택된 같거나 다른 치환체에 의해 임의로 1-, 2- 또는 3-치환된 페닐이거나, 또는의 그룹을 나타내며; R1은 수소, 불소 또는 염소이고; R2는 불소 또는 염소이며; R3는 각각 불소, 염소, 메틸, 메톡시, 메틸티오, 트리플루오로메틸, 트리플루오로메톡시, 트리플루오로메칠티오, 메톡시카보닐 및 에톡시 카보닐로 이루어진 그룹중에서 선택된 같거나 다른 치환체에 의해 임의로 1- 또는 2- 치환된 펜옥시, 페닐티오, 페닐메톡시 또는 페기메틸티오이고; Y는 불소, 염소, 브롬, 또는 요오드이며; m은 0,1,2 또는 3인 일반식(I)의 화합물을 제조하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19833334409 DE3334409A1 (de) | 1983-09-23 | 1983-09-23 | Triazolylmethyl-pyridyloxymethyl-carbinol-derivate |
| DEP3334409.4 | 1983-09-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR850002482A true KR850002482A (ko) | 1985-05-13 |
Family
ID=6209841
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019840005659A KR850002482A (ko) | 1983-09-23 | 1984-09-17 | 트리아졸릴메틸-피리딜옥시메틸-카비놀 유도체의 제조방법 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4631288A (ko) |
| EP (1) | EP0142654A1 (ko) |
| JP (1) | JPS6087286A (ko) |
| KR (1) | KR850002482A (ko) |
| AU (1) | AU3339584A (ko) |
| BR (1) | BR8404742A (ko) |
| DE (1) | DE3334409A1 (ko) |
| DK (1) | DK452884A (ko) |
| ES (1) | ES536137A0 (ko) |
| GR (1) | GR80442B (ko) |
| HU (1) | HUT35932A (ko) |
| IL (1) | IL73006A0 (ko) |
| ZA (1) | ZA847444B (ko) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01199378A (ja) * | 1988-02-03 | 1989-08-10 | Hitachi Maxell Ltd | テープカートリッジ |
| BR112014000108A2 (pt) * | 2011-07-08 | 2017-04-18 | Dow Global Technologies Llc | processo e tubo curado in situ |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2908378A1 (de) * | 1979-03-03 | 1980-09-11 | Hoechst Ag | Derivate des 1,2,4-triazols |
| DE2921168A1 (de) * | 1979-05-25 | 1980-12-11 | Basf Ag | Triazolylderivate und verfahren zu ihrer herstellung sowie diese enthaltende mittel zur beeinflussung des pflanzenwachstums |
| DE3000244A1 (de) * | 1980-01-05 | 1981-07-09 | Bayer Ag, 5090 Leverkusen | Triazolylphenacyl-pyridyl-ether-derivate, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide |
| DE3018866A1 (de) * | 1980-05-16 | 1981-11-26 | Bayer Ag, 5090 Leverkusen | 1-hydroxyethyl-azol-derivate, verfahren zu ihrer herstellung sowie ihre verwendung als pflanzenwachstumsregulatoren und fungizide |
| DE3028669A1 (de) * | 1980-07-29 | 1982-02-25 | Bayer Ag, 5090 Leverkusen | Substituierte triazolylalkyl-pyridylether, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide |
| NZ198085A (en) * | 1980-08-18 | 1985-09-13 | Ici Plc | Regulation of plant growth with certain 2,2-di(hydrocarbyl)-1-(1,2,4-triazol-1-yl)ethan-2-ols |
| EP0061835B1 (en) * | 1981-03-18 | 1989-02-01 | Imperial Chemical Industries Plc | Triazole compounds, a process for preparing them, their use as plant fungicides and fungicidal compositions containing them |
| DK157135C (da) * | 1982-04-07 | 1990-04-02 | Pfizer | Analogifremgangsmaade til fremstilling af 1,2,4-triazol-forbindelser eller farmaceutisk acceptable syreadditionssalte deraf |
-
1983
- 1983-09-23 DE DE19833334409 patent/DE3334409A1/de not_active Withdrawn
-
1984
- 1984-09-08 EP EP84110734A patent/EP0142654A1/de not_active Withdrawn
- 1984-09-14 US US06/651,002 patent/US4631288A/en not_active Expired - Fee Related
- 1984-09-17 KR KR1019840005659A patent/KR850002482A/ko not_active Application Discontinuation
- 1984-09-20 IL IL73006A patent/IL73006A0/xx unknown
- 1984-09-21 AU AU33395/84A patent/AU3339584A/en not_active Abandoned
- 1984-09-21 ZA ZA847444A patent/ZA847444B/xx unknown
- 1984-09-21 DK DK452884A patent/DK452884A/da not_active Application Discontinuation
- 1984-09-21 HU HU843581A patent/HUT35932A/hu unknown
- 1984-09-21 JP JP59196939A patent/JPS6087286A/ja active Pending
- 1984-09-21 GR GR80442A patent/GR80442B/el unknown
- 1984-09-21 ES ES536137A patent/ES536137A0/es active Granted
- 1984-09-21 BR BR8404742A patent/BR8404742A/pt unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BR8404742A (pt) | 1985-08-13 |
| EP0142654A1 (de) | 1985-05-29 |
| DE3334409A1 (de) | 1985-04-18 |
| DK452884D0 (da) | 1984-09-21 |
| GR80442B (en) | 1985-01-21 |
| AU3339584A (en) | 1985-03-28 |
| ES8505669A1 (es) | 1985-06-01 |
| DK452884A (da) | 1985-03-24 |
| JPS6087286A (ja) | 1985-05-16 |
| US4631288A (en) | 1986-12-23 |
| IL73006A0 (en) | 1984-12-31 |
| ES536137A0 (es) | 1985-06-01 |
| ZA847444B (en) | 1985-05-29 |
| HUT35932A (en) | 1985-08-28 |
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