DD208295A5 - Pflanzenwachstumsregulierende und fungizide mittel - Google Patents

Pflanzenwachstumsregulierende und fungizide mittel Download PDF

Info

Publication number: DD208295A5
Authority: DD; German Democratic Republic
Prior art keywords: carbon atoms; alkyl; halogen; formula; phenyl
Prior art date: 1981-11-10

Application number

DD82244614A

Other languages

German (de)

English (en)

Inventor

Hans-Ludewig Elbe

Karl H Buechel

Klaus Luerssen

Paul-Ernst Frohberger

Original Assignee

Bayer Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1981-11-10

Filing date

1982-11-05

Publication date

1984-05-02

1982-11-05 Application filed by Bayer Ag filed Critical Bayer Ag

1984-05-02 Publication of DD208295A5 publication Critical patent/DD208295A5/de

Links

239000000417 fungicide Substances 0.000 title claims description 8
230000008635 plant growth Effects 0.000 title claims description 8
230000001105 regulatory effect Effects 0.000 title claims description 7
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 52
125000000217 alkyl group Chemical group 0.000 claims abstract description 40
150000003839 salts Chemical class 0.000 claims abstract description 27
239000002253 acid Substances 0.000 claims abstract description 22
229910052736 halogen Inorganic materials 0.000 claims abstract description 21
150000002367 halogens Chemical class 0.000 claims abstract description 20
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 17
229910052751 metal Chemical class 0.000 claims abstract description 13
239000002184 metal Chemical class 0.000 claims abstract description 13
125000001188 haloalkyl group Chemical group 0.000 claims abstract description 9
125000001424 substituent group Chemical group 0.000 claims abstract description 9
229910052757 nitrogen Inorganic materials 0.000 claims abstract description 8
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims abstract description 7
125000003545 alkoxy group Chemical group 0.000 claims abstract description 6
125000004414 alkyl thio group Chemical group 0.000 claims abstract description 6
125000005843 halogen group Chemical group 0.000 claims abstract description 6
125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 6
125000004663 dialkyl amino group Chemical group 0.000 claims abstract description 5
125000004438 haloalkoxy group Chemical group 0.000 claims abstract description 5
125000001316 cycloalkyl alkyl group Chemical group 0.000 claims abstract description 4
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
239000001257 hydrogen Substances 0.000 claims abstract description 3
125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 3
125000000753 cycloalkyl group Chemical group 0.000 claims abstract 3
238000002360 preparation method Methods 0.000 claims description 22
239000003921 oil Substances 0.000 claims description 19
239000000203 mixture Substances 0.000 claims description 17
238000000034 method Methods 0.000 claims description 13
230000008569 process Effects 0.000 claims description 8
239000013543 active substance Substances 0.000 claims description 5
239000004606 Fillers/Extenders Substances 0.000 claims description 4
241000233866 Fungi Species 0.000 claims description 4
125000004995 haloalkylthio group Chemical group 0.000 claims description 4
239000005648 plant growth regulator Substances 0.000 claims description 4
125000003943 azolyl group Chemical group 0.000 claims description 3
125000005346 substituted cycloalkyl group Chemical group 0.000 claims description 3
230000001276 controlling effect Effects 0.000 claims description 2
238000002156 mixing Methods 0.000 claims description 2
125000003282 alkyl amino group Chemical group 0.000 abstract 2
150000001875 compounds Chemical class 0.000 description 60
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-1 oxime ethers Chemical class 0.000 description 21
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RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 15
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241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 4
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SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 description 3
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
230000008901 benefit Effects 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
230000035613 defoliation Effects 0.000 description 3
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POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 3
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RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
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NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 description 2
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HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
230000000954 anitussive effect Effects 0.000 description 1
230000000545 anti-microbicidal effect Effects 0.000 description 1
229940124584 antitussives Drugs 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
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238000005815 base catalysis Methods 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
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239000001273 butane Substances 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
230000034303 cell budding Effects 0.000 description 1
230000008859 change Effects 0.000 description 1
239000003638 chemical reducing agent Substances 0.000 description 1
150000008422 chlorobenzenes Chemical class 0.000 description 1
235000020971 citrus fruits Nutrition 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000008199 coating composition Substances 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
235000016213 coffee Nutrition 0.000 description 1
235000013353 coffee beverage Nutrition 0.000 description 1
229940126086 compound 21 Drugs 0.000 description 1
230000001143 conditioned effect Effects 0.000 description 1
239000000470 constituent Substances 0.000 description 1
239000013256 coordination polymer Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
238000005520 cutting process Methods 0.000 description 1
125000001995 cyclobutyl group Chemical class [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
125000004850 cyclobutylmethyl group Chemical class C1(CCC1)C* 0.000 description 1
125000000113 cyclohexyl group Chemical class [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000004210 cyclohexylmethyl group Chemical class [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
125000001511 cyclopentyl group Chemical class [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
125000004851 cyclopentylmethyl group Chemical class C1(CCCC1)C* 0.000 description 1
125000001559 cyclopropyl group Chemical class [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
125000004186 cyclopropylmethyl group Chemical class [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
PCHPORCSPXIHLZ-UHFFFAOYSA-N diphenhydramine hydrochloride Chemical compound [Cl-].C=1C=CC=CC=1C(OCC[NH+](C)C)C1=CC=CC=C1 PCHPORCSPXIHLZ-UHFFFAOYSA-N 0.000 description 1
231100000676 disease causative agent Toxicity 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
239000013583 drug formulation Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000010410 dusting Methods 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
238000005538 encapsulation Methods 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
238000005187 foaming Methods 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
RUJLJMUWUVTHEU-UHFFFAOYSA-N hex-5-en-3-one Chemical compound CCC(=O)CC=C RUJLJMUWUVTHEU-UHFFFAOYSA-N 0.000 description 1
150000007857 hydrazones Chemical class 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000005457 ice water Substances 0.000 description 1
230000006872 improvement Effects 0.000 description 1
239000012535 impurity Substances 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
230000036512 infertility Effects 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
238000011081 inoculation Methods 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
239000004816 latex Substances 0.000 description 1
229910052744 lithium Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
239000004579 marble Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
244000005700 microbiome Species 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
239000002420 orchard Substances 0.000 description 1
239000011368 organic material Substances 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
150000002901 organomagnesium compounds Chemical class 0.000 description 1
150000002923 oximes Chemical class 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
239000006072 paste Substances 0.000 description 1
244000052769 pathogen Species 0.000 description 1
230000001717 pathogenic effect Effects 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000003495 polar organic solvent Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
230000002028 premature Effects 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
239000010453 quartz Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
230000009467 reduction Effects 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
230000014284 seed dormancy process Effects 0.000 description 1
239000010865 sewage Substances 0.000 description 1
238000004904 shortening Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000004334 sorbic acid Substances 0.000 description 1
235000010199 sorbic acid Nutrition 0.000 description 1
229940075582 sorbic acid Drugs 0.000 description 1
238000009331 sowing Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
208000024891 symptom Diseases 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000011975 tartaric acid Substances 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
230000002123 temporal effect Effects 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
239000011135 tin Substances 0.000 description 1
229910052718 tin Inorganic materials 0.000 description 1
239000010936 titanium Substances 0.000 description 1
229910052719 titanium Inorganic materials 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
238000009827 uniform distribution Methods 0.000 description 1
238000009369 viticulture Methods 0.000 description 1
238000005406 washing Methods 0.000 description 1
229910052727 yttrium Inorganic materials 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1

Classifications

- 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
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
- 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
- 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
- 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

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

DD82244614A 1981-11-10 1982-11-05 Pflanzenwachstumsregulierende und fungizide mittel DD208295A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19813144670 DE3144670A1 (de)	1981-11-10	1981-11-10	Azolyl-alkenone und -ole, verfahren zu ihrer herstellung sowie ihre verwendung als pflanzenwachstumsregulatoren und fungizide

Publications (1)

Publication Number	Publication Date
DD208295A5 true DD208295A5 (de)	1984-05-02

Family

ID=6146061

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD82244614A DD208295A5 (de)	1981-11-10	1982-11-05	Pflanzenwachstumsregulierende und fungizide mittel

Country Status (18)

Country	Link
EP (1)	EP0079006B1 (cs)
JP (1)	JPS5890559A (cs)
AT (1)	ATE16930T1 (cs)
AU (1)	AU9033582A (cs)
BR (1)	BR8206503A (cs)
CA (1)	CA1185608A (cs)
CS (1)	CS236691B2 (cs)
DD (1)	DD208295A5 (cs)
DE (2)	DE3144670A1 (cs)
DK (1)	DK499982A (cs)
ES (1)	ES517235A0 (cs)
GR (1)	GR78400B (cs)
HU (1)	HU189189B (cs)
IL (1)	IL67198A0 (cs)
NZ (1)	NZ202416A (cs)
PL (1)	PL133825B1 (cs)
PT (1)	PT75774B (cs)
ZA (1)	ZA828195B (cs)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
IT1150706B (it) *	1982-03-19	1986-12-17	Montedison Spa	Derivati di eterociclici azotati dotati di attivita' fitoregolatrice
DE3224129A1 (de) *	1982-06-29	1983-12-29	Bayer Ag, 5090 Leverkusen	Substituierte azolyl-ketone und -alkohole
DE3229273A1 (de) *	1982-08-05	1984-02-09	Bayer Ag, 5090 Leverkusen	Substituierte azolylallyl-ketone und -carbinole
JPS6058965A (ja) *	1983-09-13	1985-04-05	Kaken Pharmaceut Co Ltd	新規なイミダゾール誘導体
DE3511922A1 (de)	1985-04-01	1986-10-09	Basf Ag, 6700 Ludwigshafen	Azolverbindungen, verfahren zu ihrer herstellung und mittel zur regulierung des pflanzenwachstums
WO2010029065A1 (de) *	2008-09-10	2010-03-18	Basf Se	Imidazol- und triazolverbindungen, ihre verwendung sowie sie enthaltende mittel
WO2010029066A1 (de) *	2008-09-10	2010-03-18	Basf Se	Imidazol- und triazolverbindungen, ihre verwendung sowie sie enthaltende mittel
US20110166020A1 (en) *	2008-09-10	2011-07-07	Basf Se	Imidazole and Triazole Compounds, Use Thereof and Agents Containing Said Compounds
WO2010031843A1 (de) *	2008-09-22	2010-03-25	Basf Se	Imidazol- und triazolverbindungen, ihre verwendung sowie sie enthaltende mittel
EA030024B1 (ru)	2013-04-12	2018-06-29	Байер Кропсайенс Акциенгезельшафт	Новые производные триазола для борьбы с фитопатогенными вредоносными грибами
WO2014167009A1 (en)	2013-04-12	2014-10-16	Bayer Cropscience Ag	Novel triazole derivatives
EP2984080B1 (en)	2013-04-12	2017-08-30	Bayer CropScience Aktiengesellschaft	Novel triazolinthione derivatives
BR112017021109A2 (pt)	2015-04-02	2018-07-03	Bayer Cropscience Ag	derivados de triazol como fungicidas

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2905981A1 (de) *	1979-02-16	1980-10-30	Bayer Ag	1-allyltriazol-derivate, verfahren zu ihrer herstellung und ihre verwendung als pflanzenschutzmittel

1981
- 1981-11-10 DE DE19813144670 patent/DE3144670A1/de not_active Withdrawn
1982
- 1982-10-29 DE DE8282109999T patent/DE3267941D1/de not_active Expired
- 1982-10-29 AT AT82109999T patent/ATE16930T1/de not_active IP Right Cessation
- 1982-10-29 EP EP82109999A patent/EP0079006B1/de not_active Expired
- 1982-11-02 PT PT75774A patent/PT75774B/pt unknown
- 1982-11-05 DD DD82244614A patent/DD208295A5/de unknown
- 1982-11-08 PL PL1982238928A patent/PL133825B1/pl unknown
- 1982-11-08 IL IL67198A patent/IL67198A0/xx unknown
- 1982-11-08 GR GR69759A patent/GR78400B/el unknown
- 1982-11-08 NZ NZ202416A patent/NZ202416A/en unknown
- 1982-11-09 ZA ZA828195A patent/ZA828195B/xx unknown
- 1982-11-09 JP JP57195416A patent/JPS5890559A/ja active Pending
- 1982-11-09 CS CS827975A patent/CS236691B2/cs unknown
- 1982-11-09 HU HU823605A patent/HU189189B/hu unknown
- 1982-11-09 DK DK499982A patent/DK499982A/da not_active Application Discontinuation
- 1982-11-09 CA CA000415219A patent/CA1185608A/en not_active Expired
- 1982-11-09 BR BR8206503A patent/BR8206503A/pt unknown
- 1982-11-10 AU AU90335/82A patent/AU9033582A/en not_active Abandoned
- 1982-11-10 ES ES517235A patent/ES517235A0/es active Granted

Also Published As

Publication number	Publication date
PT75774A (en)	1982-12-01
PL133825B1 (en)	1985-07-31
PT75774B (en)	1985-07-26
DE3144670A1 (de)	1983-05-19
ES8401756A1 (es)	1983-12-16
EP0079006B1 (de)	1985-12-11
PL238928A1 (en)	1983-06-20
DK499982A (da)	1983-05-11
JPS5890559A (ja)	1983-05-30
CA1185608A (en)	1985-04-16
ATE16930T1 (de)	1985-12-15
GR78400B (cs)	1984-09-27
ES517235A0 (es)	1983-12-16
EP0079006A1 (de)	1983-05-18
AU9033582A (en)	1983-05-19
BR8206503A (pt)	1983-09-27
IL67198A0 (en)	1983-03-31
DE3267941D1 (en)	1986-01-23
ZA828195B (en)	1983-09-28
HU189189B (en)	1986-06-30
CS236691B2 (en)	1985-05-15
NZ202416A (en)	1985-07-12

Publication	Publication Date	Title
DD205602A5 (de)	1984-01-04	Pflanzenwachstumsregulierende und fungizide mittel
EP0015387A2 (de)	1980-09-17	1-Vinyltriazol-Derivate, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Wachstumsregulatoren und Fungizide
DE2951163A1 (de)	1981-07-16	Substituierte triazolylmethyl-tert.-butyl-carbinole, verfahren zu ihrer herstellung und ihre verwendung als pflanzenschutzmittel sowie als zwischenprodukte
DD210193A5 (de)	1984-06-06	Pflanzenschutzmittel
EP0044993B1 (de)	1985-05-29	Triazolylpropenol-Derivate, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Pflanzenwachstumsregulatoren und Fungizide
EP0044425B1 (de)	1985-09-18	Halogenierte Triazolylvinyl-keto- und -carbinol-Derivate, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Pflanzenwachstumsregulatoren und Fungizide
DD208295A5 (de)	1984-05-02	Pflanzenwachstumsregulierende und fungizide mittel
DD149010A5 (de)	1981-06-24	Pflanzenschutzmittel
DE2951164A1 (de)	1981-07-16	Substituierte triazolylmethyl-tert.-butyl-ketone, verfahren zu ihrer herstellung und ihre verwendung als pflanzenschutzmittel sowie als zwischenprodukte
EP0058347B1 (de)	1984-09-12	Benzyl-pyrimidinylalkyl-ether, Verfahren zu ihrer Herstellung, ihre Verwendung als Pflanzenwachstumsregulatoren und Fungizide sowie Zwischenprodukte und deren Herstellung
EP0080102B1 (de)	1986-05-28	Cycloalkyl-(alpha-triazolyl-beta-hydroxy)-ketone, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Fungizide und Pflanzenwachstumsregulatoren
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