DD208531A5 - Fungizide und pflanzenwuchsregulierende mittel - Google Patents

Fungizide und pflanzenwuchsregulierende mittel Download PDF

Info

Publication number: DD208531A5
Authority: DD; German Democratic Republic
Prior art keywords: formula; triazolyl; ketones; cycloalkyl; hydroxy
Prior art date: 1981-11-19

Application number

DD82244913A

Other languages

German (de)

English (en)

Inventor

Eckart Kranz

Karl H Buechel

Udo Kraatz

Erik Regel

Wilhelm Brandes

Paul-Ernst Frohberger

Klaus Luerssen

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.)

1981-11-19

Filing date

1982-11-16

Publication date

1984-04-04

1982-11-16 Application filed by Bayer Ag filed Critical Bayer Ag

1984-04-04 Publication of DD208531A5 publication Critical patent/DD208531A5/de

Links

239000000417 fungicide Substances 0.000 title claims abstract description 9
239000003795 chemical substances by application Substances 0.000 title claims description 9
150000003839 salts Chemical class 0.000 claims abstract description 36
239000002253 acid Substances 0.000 claims abstract description 23
229910052751 metal Chemical class 0.000 claims abstract description 18
239000002184 metal Chemical class 0.000 claims abstract description 18
125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 6
125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 5
125000001188 haloalkyl group Chemical group 0.000 claims abstract description 5
125000005346 substituted cycloalkyl group Chemical group 0.000 claims abstract description 3
101000588924 Anthopleura elegantissima Delta-actitoxin-Ael1a Proteins 0.000 claims description 36
238000002360 preparation method Methods 0.000 claims description 24
150000002576 ketones Chemical class 0.000 claims description 20
238000000034 method Methods 0.000 claims description 14
230000008569 process Effects 0.000 claims description 11
125000004432 carbon atom Chemical group C* 0.000 claims description 9
230000000855 fungicidal effect Effects 0.000 claims description 6
239000004606 Fillers/Extenders Substances 0.000 claims description 5
241000233866 Fungi Species 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 5
125000005843 halogen group Chemical group 0.000 claims description 4
230000008635 plant growth Effects 0.000 claims description 4
125000000262 haloalkenyl group Chemical group 0.000 claims description 3
230000001105 regulatory effect Effects 0.000 claims description 3
239000004094 surface-active agent Substances 0.000 claims description 3
125000003545 alkoxy group Chemical group 0.000 claims description 2
239000005648 plant growth regulator Substances 0.000 abstract description 4
241000196324 Embryophyta Species 0.000 description 58
150000001875 compounds Chemical class 0.000 description 53
-1 4- (i, 2,4-triazol-1-yl) -heptan-5-one Chemical compound 0.000 description 25
239000003630 growth substance Substances 0.000 description 20
230000012010 growth Effects 0.000 description 19
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239000002904 solvent Substances 0.000 description 15
239000003995 emulsifying agent Substances 0.000 description 14
238000012360 testing method Methods 0.000 description 14
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
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238000006243 chemical reaction Methods 0.000 description 10
238000003306 harvesting Methods 0.000 description 10
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239000013543 active substance Substances 0.000 description 4
150000001299 aldehydes Chemical class 0.000 description 4
125000002877 alkyl aryl group Chemical group 0.000 description 4
230000008901 benefit Effects 0.000 description 4
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ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
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ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
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229910052801 chlorine Inorganic materials 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
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OQBCJXUAQQMTRW-UHFFFAOYSA-N 1-(1-methylcyclopropyl)ethanone Chemical compound CC(=O)C1(C)CC1 OQBCJXUAQQMTRW-UHFFFAOYSA-N 0.000 description 2
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239000004113 Sepiolite Substances 0.000 description 1
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239000000853 adhesive Substances 0.000 description 1
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239000003513 alkali Substances 0.000 description 1
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150000008041 alkali metal carbonates Chemical class 0.000 description 1
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150000003973 alkyl amines Chemical group 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
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RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 1
229910001863 barium hydroxide Inorganic materials 0.000 description 1
230000001588 bifunctional effect Effects 0.000 description 1
238000009395 breeding Methods 0.000 description 1
230000001488 breeding effect Effects 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
230000001680 brushing effect Effects 0.000 description 1
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
AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
239000000920 calcium hydroxide Substances 0.000 description 1
229910001861 calcium hydroxide Inorganic materials 0.000 description 1
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239000001569 carbon dioxide Substances 0.000 description 1
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235000016213 coffee Nutrition 0.000 description 1
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238000006731 degradation reaction Methods 0.000 description 1
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125000004774 dichlorofluoromethyl group Chemical group FC(Cl)(Cl)* 0.000 description 1
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235000014113 dietary fatty acids Nutrition 0.000 description 1
IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 description 1
XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
231100000676 disease causative agent Toxicity 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
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238000004049 embossing Methods 0.000 description 1
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238000005538 encapsulation 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
239000004744 fabric Substances 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
230000005089 fruit drop Effects 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
229960002598 fumaric acid Drugs 0.000 description 1
239000007789 gas Substances 0.000 description 1
230000035784 germination Effects 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
150000002373 hemiacetals Chemical class 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
150000004677 hydrates Chemical class 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
230000006872 improvement Effects 0.000 description 1
229910052738 indium Inorganic materials 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
230000036512 infertility Effects 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
229960000448 lactic acid Drugs 0.000 description 1
150000007517 lewis acids Chemical class 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
NXPHGHWWQRMDIA-UHFFFAOYSA-M magnesium;carbanide;bromide Chemical compound [CH3-].[Mg+2].[Br-] NXPHGHWWQRMDIA-UHFFFAOYSA-M 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
229940098895 maleic acid Drugs 0.000 description 1
239000004579 marble Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
230000002906 microbiologic effect Effects 0.000 description 1
244000005700 microbiome Species 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
239000011733 molybdenum Substances 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
230000017066 negative regulation of growth Effects 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000002420 orchard Substances 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
239000011368 organic material Substances 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
150000002902 organometallic compounds Chemical class 0.000 description 1
125000002524 organometallic group Chemical group 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
239000003208 petroleum Substances 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
235000010486 polyoxyethylene sorbitan monolaurate Nutrition 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
NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 1
BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 description 1
230000002028 premature Effects 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
125000006434 propyl cyclopropyl group Chemical group 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000010453 quartz Substances 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
230000002787 reinforcement Effects 0.000 description 1
230000010410 reperfusion Effects 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
235000019355 sepiolite Nutrition 0.000 description 1
238000004904 shortening Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
235000010265 sodium sulphite Nutrition 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
230000000638 stimulation Effects 0.000 description 1
238000003860 storage Methods 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 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
229960001367 tartaric acid Drugs 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
230000002123 temporal effect Effects 0.000 description 1
GIZSHQYTTBQKOQ-UHFFFAOYSA-N threo-Syringoylglycerol Chemical compound COC1=CC(C(O)C(O)CO)=CC(OC)=C1O GIZSHQYTTBQKOQ-UHFFFAOYSA-N 0.000 description 1
229910052718 tin Inorganic materials 0.000 description 1
239000011135 tin Substances 0.000 description 1
HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
230000005068 transpiration Effects 0.000 description 1
FEONEKOZSGPOFN-UHFFFAOYSA-K tribromoiron Chemical compound Br[Fe](Br)Br FEONEKOZSGPOFN-UHFFFAOYSA-K 0.000 description 1
FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 description 1
125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 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
238000010626 work up procedure Methods 0.000 description 1
239000008096 xylene 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
- A01N43/64—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
- 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
- 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)
Health & Medical Sciences (AREA)
Environmental Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

DD82244913A 1981-11-19 1982-11-16 Fungizide und pflanzenwuchsregulierende mittel DD208531A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19813145846 DE3145846A1 (de)	1981-11-19	1981-11-19	Cycloalkyl-((alpha)-triazolyl-ss-hydroxy)-ketone, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide und pflanzenwachstumsregulatoren

Publications (1)

Publication Number	Publication Date
DD208531A5 true DD208531A5 (de)	1984-04-04

Family

ID=6146717

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD82244913A DD208531A5 (de)	1981-11-19	1982-11-16	Fungizide und pflanzenwuchsregulierende mittel

Country Status (19)

Country	Link
US (1)	US4530715A (fr)
EP (1)	EP0080102B1 (fr)
JP (1)	JPS5892668A (fr)
AT (1)	ATE20059T1 (fr)
AU (1)	AU554279B2 (fr)
BR (1)	BR8206678A (fr)
CA (1)	CA1185246A (fr)
CS (1)	CS236695B2 (fr)
DD (1)	DD208531A5 (fr)
DE (2)	DE3145846A1 (fr)
DK (1)	DK514582A (fr)
ES (1)	ES8307767A1 (fr)
GR (1)	GR77760B (fr)
HU (1)	HU188524B (fr)
IL (1)	IL67274A (fr)
NZ (1)	NZ202515A (fr)
PL (1)	PL131544B1 (fr)
PT (1)	PT75818B (fr)
ZA (1)	ZA828493B (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3145857A1 (de) *	1981-11-19	1983-05-26	Bayer Ag, 5090 Leverkusen	Alkylcyloalkyl-triazolylmethyl-ketone und verfahreen zu ihrer herstellung
DE3702920A1 (de) *	1987-01-31	1988-08-11	Bayer Ag	Substituierte hydroxy-azolyl-ketone
ATA136687A (de) *	1987-05-27	1993-09-15	Technica Entwicklung	Verfahren und vorrichtung zum beheben von durch naehrstoff-ueberschuss bedingten belastungen von kulturpflanzen
DE3812967A1 (de) *	1987-06-24	1989-01-05	Bayer Ag	Azolylmethyl-cyclopropyl-derivate
DE4208050A1 (de) *	1992-03-13	1993-09-23	Bayer Ag	Azolylmethyl-fluorcyclopropyl-derivate
TW200307539A (en) *	2002-02-01	2003-12-16	Bristol Myers Squibb Co	Cycloalkyl inhibitors of potassium channel function
EP2654433B1 (fr)	2010-12-21	2017-08-30	Bayer Cropscience LP	Les mutants "papier émeri" de bacillus et des méthodes d'application pour la promotion de la croissance des plantes, de la santé des plants et pour le contrôl des maladies et des parasites
MX2014002890A (es)	2011-09-12	2015-01-19	Bayer Cropscience Lp	Metodo para mejorar la salud y/o promover el crecimiento de una planta y/o mejorar la maduracion de frutos.

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1601453A (en) *	1977-05-05	1981-10-28	Ici Ltd	Triazole and imidazole derivatives useful in agriculture
DE2832233A1 (de) *	1978-07-21	1980-01-31	Bayer Ag	Alpha -azolyl- beta -hydroxy-ketone, verfahren zu ihrer herstellung und ihre verwendung als fungizide
DE3002430A1 (de) *	1980-01-24	1981-07-30	Bayer Ag, 5090 Leverkusen	Triazolyl-alkandiol-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide

1981
- 1981-11-19 DE DE19813145846 patent/DE3145846A1/de not_active Withdrawn
1982
- 1982-11-02 US US06/438,448 patent/US4530715A/en not_active Expired - Fee Related
- 1982-11-09 PT PT75818A patent/PT75818B/pt unknown
- 1982-11-09 DE DE8282110296T patent/DE3271447D1/de not_active Expired
- 1982-11-09 AT AT82110296T patent/ATE20059T1/de not_active IP Right Cessation
- 1982-11-09 EP EP82110296A patent/EP0080102B1/fr not_active Expired
- 1982-11-16 DD DD82244913A patent/DD208531A5/de unknown
- 1982-11-16 JP JP57199847A patent/JPS5892668A/ja active Pending
- 1982-11-16 NZ NZ202515A patent/NZ202515A/en unknown
- 1982-11-16 IL IL67274A patent/IL67274A/xx unknown
- 1982-11-17 PL PL1982239079A patent/PL131544B1/pl unknown
- 1982-11-17 GR GR69836A patent/GR77760B/el unknown
- 1982-11-18 BR BR8206678A patent/BR8206678A/pt unknown
- 1982-11-18 CA CA000415878A patent/CA1185246A/fr not_active Expired
- 1982-11-18 ZA ZA828493A patent/ZA828493B/xx unknown
- 1982-11-18 AU AU90706/82A patent/AU554279B2/en not_active Ceased
- 1982-11-18 DK DK514582A patent/DK514582A/da not_active Application Discontinuation
- 1982-11-19 ES ES517513A patent/ES8307767A1/es not_active Expired
- 1982-11-19 HU HU823736A patent/HU188524B/hu unknown
- 1982-11-19 CS CS828295A patent/CS236695B2/cs unknown

Also Published As

Publication number	Publication date
AU9070682A (en)	1983-05-26
CA1185246A (fr)	1985-04-09
HU188524B (en)	1986-04-28
EP0080102A1 (fr)	1983-06-01
CS236695B2 (en)	1985-05-15
DK514582A (da)	1983-05-20
ATE20059T1 (de)	1986-06-15
IL67274A0 (en)	1983-03-31
DE3145846A1 (de)	1983-05-26
ZA828493B (en)	1983-09-28
PL239079A1 (en)	1983-08-15
JPS5892668A (ja)	1983-06-02
PT75818A (en)	1982-12-01
GR77760B (fr)	1984-09-25
AU554279B2 (en)	1986-08-14
DE3271447D1 (en)	1986-07-03
BR8206678A (pt)	1983-10-04
PL131544B1 (en)	1984-11-30
ES517513A0 (es)	1983-08-16
PT75818B (en)	1985-07-26
US4530715A (en)	1985-07-23
IL67274A (en)	1986-02-28
EP0080102B1 (fr)	1986-05-28
ES8307767A1 (es)	1983-08-16
NZ202515A (en)	1985-05-31

Publication	Publication Date	Title
EP0297345B2 (fr)	1993-10-13	Dérivés ayant des groupes azolylméthyl-cyclopropyles
DD205602A5 (de)	1984-01-04	Pflanzenwachstumsregulierende und fungizide mittel
DE2951163A1 (de)	1981-07-16	Substituierte triazolylmethyl-tert.-butyl-carbinole, verfahren zu ihrer herstellung und ihre verwendung als pflanzenschutzmittel sowie als zwischenprodukte
DE3413996A1 (de)	1985-10-24	Tetrahydrofuran-2-ylmethylamine
EP0044993B1 (fr)	1985-05-29	Dérivés triazolylpropénols, leur procédé de préparation ainsi que leur application comme fongicides et régulateurs de croissance des plantes
EP0044425B1 (fr)	1985-09-18	Dérivés triazolylvinyl-céto- et -carbinol-halogénés, leur procédé de préparation et leur application comme fongicides et régulateurs de croissance des plantes
EP0079006B1 (fr)	1985-12-11	Azolyl-alkénones et -ols, leur procédé de préparation et leur application comme agents régulateurs de croissance des plantes et fongicides
EP0080102B1 (fr)	1986-05-28	Cycloalkyl-(alpha-triazolyl-bêta-hydroxy)-cétones, leur procédé de préparation et leur application comme fongicides et régulateurs de croissance des plantes
DE2951164A1 (de)	1981-07-16	Substituierte triazolylmethyl-tert.-butyl-ketone, verfahren zu ihrer herstellung und ihre verwendung als pflanzenschutzmittel sowie als zwischenprodukte
EP0180838B1 (fr)	1990-05-16	Dérivés d'azolylcyclopropyl-azolylméthyl-carbinol substitués
EP0058347B1 (fr)	1984-09-12	Benzyl-pyrimidinylalkyl-éthers, leur procédé de préparation, leur utilisation comme régulateurs de croissance des plantes et comme fongicides et intermédiaires et leur préparation
EP0059894A1 (fr)	1982-09-15	Triazolylalkylthio éthers, procédé pour leur préparation et leur application comme agent régulateur de la croissance des plantes et comme agent fongicide
EP0131867B1 (fr)	1988-06-01	Aryloxy-pyrimidinyl alcanols
EP0094572B1 (fr)	1986-03-12	Dérivés de l'1-azolyl-2-oximino-butane, leur procédé de fabrication et leur application comme fongicides et agents régulateurs de croissance des plantes
DE3200414A1 (de)	1983-07-21	Azolyl-thioether-derivate, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide und pflanzenwachstumsregulatoren
EP0224076B1 (fr)	1989-11-08	Azolyléthercétones et alcools
EP0297393A2 (fr)	1989-01-04	Dérivés de 1-phénoxy-3-triazolyl-hex-1-ènes
DE3045182A1 (de)	1982-07-01	Pflanzenwachstumsregulierende und fungizide mittel
EP0053311A2 (fr)	1982-06-09	Phényl-1-triazolyl-2-penten-1-oles-3, leur préparation et leur emploi comme fongicides et régulateurs de croissance des plantes
DD209957A5 (de)	1984-05-30	Pflanzenschutzmittel
DE3028330A1 (de)	1982-04-08	Triazolylpropenol-derivate, verfahren zu ihrer herstellung sowie ihre verwendung als pflanzenwachstumsregulatoren und fungizide
DE3422244A1 (de)	1985-12-19	1-azolyl-2-phenyl-cyclopropan-derivate
DD209100A5 (de)	1984-04-25	Pflanzenschutzmittel
DE3111013A1 (de)	1982-09-30	Triazolylpropenol-derivate, verfahren zu ihrer herstellung sowie ihre verwendung als pflanzenwachstumsregulatoren und fungizide
DD274163A5 (de)	1989-12-13	Fungizide und pflanzenwuchsregulierende mittel