DD258741A5 - Fungizide und pflanzenwuchsregulierende mittel - Google Patents

Fungizide und pflanzenwuchsregulierende mittel Download PDF

Info

Publication number: DD258741A5
Authority: DD; German Democratic Republic
Prior art keywords: plants; formula; growth; compounds; acid
Prior art date: 1985-11-15

Application number

DD86296174A

Other languages

German (de)

English (en)

Inventor

Gerhard Jaeger

Manfred Jautelat

Wolfgang Kraemer

Karl H Buechel

Paul Reinecke

Wilhelm Brandes

Gerd Haenssler

Klaus Luerssen

Original Assignee

��@��k��

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.)

1985-11-15

Filing date

1986-11-11

Publication date

1988-08-03

1986-11-11 Application filed by ��@��k�� filed Critical ��@��k��

1988-08-03 Publication of DD258741A5 publication Critical patent/DD258741A5/de

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239000000417 fungicide Substances 0.000 title claims description 6
239000003795 chemical substances by application Substances 0.000 title claims description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 17
-1 Azolyl ether ketones Chemical class 0.000 abstract description 33
150000003839 salts Chemical class 0.000 abstract description 29
239000002253 acid Substances 0.000 abstract description 26
125000000217 alkyl group Chemical group 0.000 abstract description 25
150000001298 alcohols Chemical class 0.000 abstract description 15
229910052751 metal Chemical class 0.000 abstract description 14
239000002184 metal Chemical class 0.000 abstract description 14
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract description 9
150000007513 acids Chemical class 0.000 abstract description 9
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract description 9
229910052799 carbon Inorganic materials 0.000 abstract description 9
125000000468 ketone group Chemical group 0.000 abstract description 9
239000001301 oxygen Substances 0.000 abstract description 9
229910052760 oxygen Inorganic materials 0.000 abstract description 9
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract description 9
150000001721 carbon Chemical group 0.000 abstract description 7
229910052757 nitrogen Inorganic materials 0.000 abstract description 7
125000004433 nitrogen atom Chemical group N* 0.000 abstract description 7
241000233866 Fungi Species 0.000 abstract description 4
125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 abstract description 4
230000008635 plant growth Effects 0.000 abstract description 4
125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 abstract description 4
230000001105 regulatory effect Effects 0.000 abstract description 3
239000005864 Sulphur Chemical group 0.000 abstract 1
239000000543 intermediate Substances 0.000 abstract 1
241000196324 Embryophyta Species 0.000 description 64
150000001875 compounds Chemical class 0.000 description 59
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 51
ZMXDDKWLCZADIW-UHFFFAOYSA-N dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 31
239000000126 substance Substances 0.000 description 31
239000002904 solvent Substances 0.000 description 30
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 27
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 25
238000000034 method Methods 0.000 description 24
239000000203 mixture Substances 0.000 description 23
238000002360 preparation method Methods 0.000 description 23
239000000243 solution Substances 0.000 description 22
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 21
125000004432 carbon atom Chemical group C* 0.000 description 20
239000003630 growth substance Substances 0.000 description 20
239000000460 chlorine Substances 0.000 description 19
239000003995 emulsifying agent Substances 0.000 description 19
238000012360 testing method Methods 0.000 description 19
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 18
125000001424 substituent group Chemical group 0.000 description 17
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239000004480 active ingredient Substances 0.000 description 15
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 15
230000000694 effects Effects 0.000 description 13
230000012010 growth Effects 0.000 description 13
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ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 9
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 9
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
238000006243 chemical reaction Methods 0.000 description 9
229910052801 chlorine Inorganic materials 0.000 description 9
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 9
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235000011152 sodium sulphate Nutrition 0.000 description 9
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238000002844 melting Methods 0.000 description 8
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ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
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UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 6
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
125000002877 alkyl aryl group Chemical group 0.000 description 6
238000009835 boiling Methods 0.000 description 6
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 6
229910052794 bromium Inorganic materials 0.000 description 6
239000012141 concentrate Substances 0.000 description 6
238000011156 evaluation Methods 0.000 description 6
230000000855 fungicidal effect Effects 0.000 description 6
238000011081 inoculation Methods 0.000 description 6
239000003960 organic solvent Substances 0.000 description 6
229920000151 polyglycol Polymers 0.000 description 6
239000010695 polyglycol Substances 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
239000002689 soil Substances 0.000 description 6
239000007858 starting material Substances 0.000 description 6
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 6
230000009105 vegetative growth Effects 0.000 description 6
239000004606 Fillers/Extenders Substances 0.000 description 5
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125000003545 alkoxy group Chemical group 0.000 description 5
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125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
229910000027 potassium carbonate Inorganic materials 0.000 description 5
239000000047 product Substances 0.000 description 5
239000011701 zinc Substances 0.000 description 5
YSKKTGJIMXFBDK-UHFFFAOYSA-N 4,4-dichloro-1-(2,4-dichlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C(Cl)Cl)C)OC1=CC=C(Cl)C=C1Cl YSKKTGJIMXFBDK-UHFFFAOYSA-N 0.000 description 4
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 4
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
241000736122 Parastagonospora nodorum Species 0.000 description 4
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
235000021536 Sugar beet Nutrition 0.000 description 4
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
241000317942 Venturia <ichneumonid wasp> Species 0.000 description 4
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
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125000001309 chloro group Chemical group Cl* 0.000 description 4
229960001701 chloroform Drugs 0.000 description 4
150000002170 ethers Chemical class 0.000 description 4
229910052500 inorganic mineral Inorganic materials 0.000 description 4
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
235000010755 mineral Nutrition 0.000 description 4
238000003756 stirring Methods 0.000 description 4
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
229910052725 zinc Inorganic materials 0.000 description 4
WECXWSQRGGNCAL-UHFFFAOYSA-N 1-bromo-1-(2,4-dichlorophenoxy)-3-ethyl-3-methylpentan-2-one Chemical compound CCC(C)(CC)C(=O)C(Br)OC1=CC=C(Cl)C=C1Cl WECXWSQRGGNCAL-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
241001330975 Magnaporthe oryzae Species 0.000 description 3
244000061176 Nicotiana tabacum Species 0.000 description 3
235000002637 Nicotiana tabacum Nutrition 0.000 description 3
240000007594 Oryza sativa Species 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
241000317981 Podosphaera fuliginea Species 0.000 description 3
241000221300 Puccinia Species 0.000 description 3
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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
VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 3
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LGXVIGDEPROXKC-UHFFFAOYSA-N 1,1-dichloroethene Chemical compound ClC(Cl)=C LGXVIGDEPROXKC-UHFFFAOYSA-N 0.000 description 2
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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
239000004094 surface-active agent Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
230000002123 temporal effect Effects 0.000 description 1
229910052718 tin Inorganic materials 0.000 description 1
239000011135 tin Substances 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
230000005068 transpiration Effects 0.000 description 1
238000001665 trituration Methods 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
238000009369 viticulture Methods 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/20—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- 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

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

DD86296174A 1985-11-15 1986-11-11 Fungizide und pflanzenwuchsregulierende mittel DD258741A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19853540523 DE3540523A1 (de)	1985-11-15	1985-11-15	Azolyletherketone und -alkohole

Publications (1)

Publication Number	Publication Date
DD258741A5 true DD258741A5 (de)	1988-08-03

Family

ID=6286057

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD86296174A DD258741A5 (de)	1985-11-15	1986-11-11	Fungizide und pflanzenwuchsregulierende mittel

Country Status (14)

Country	Link
US (2)	US4917720A (da)
EP (1)	EP0224076B1 (da)
JP (1)	JPS62181265A (da)
KR (1)	KR870004968A (da)
AT (1)	ATE47848T1 (da)
AU (1)	AU6480586A (da)
BR (1)	BR8605623A (da)
DD (1)	DD258741A5 (da)
DE (2)	DE3540523A1 (da)
DK (1)	DK546086A (da)
HU (1)	HUT42683A (da)
IL (1)	IL80608A0 (da)
PT (1)	PT83687B (da)
ZA (1)	ZA868652B (da)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3825867A1 (de) *	1988-03-04	1989-09-14	Bayer Ag	Heterocyclisch substituierte sulfonylaminoazole und ihre verwendung als herbizide
DE4415049A1 (de) *	1994-04-29	1995-11-02	Hoechst Schering Agrevo Gmbh	Acylierte Aminophenylsulfonylharnstoffe, Verfahren zu deren Herstellung und Verwendung als Herbizide und Wachstumsregulatoren
ITMI20061573A1 (it) *	2006-08-04	2008-02-05	F I S Fabbrica Italiana Sintetici Spa	Processo per la preparazione di 1,1-dicloro-2-alchiletilene

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2105490C3 (de)	1971-02-05	1979-06-13	Bayer Ag, 5090 Leverkusen	1 -Imidazolylketonderivate
US3912752A (en) *	1972-01-11	1975-10-14	Bayer Ag	1-Substituted-1,2,4-triazoles
DE2324010C3 (de)	1973-05-12	1981-10-08	Bayer Ag, 5090 Leverkusen	1-Substituierte 2-Triazolyl-2-phenoxyäthanol-Verbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung von Pilzen
DE2325156A1 (de)	1973-05-18	1974-12-05	Bayer Ag	Fungizide und mikrobizide mittel
DE2333355C2 (de)	1973-06-30	1984-01-19	Bayer Ag, 5090 Leverkusen	Antimikrobielle Mittel
GB1533375A (en) *	1976-07-20	1978-11-22	Bayer Ag	Halogenated 1-azolyl-butane derivatives and their use as fungicides
DE2632603A1 (de)	1976-07-20	1978-01-26	Bayer Ag	Halogenierte 1-triazolyl-butan-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide
DE2632601A1 (de)	1976-07-20	1978-01-26	Bayer Ag	Antimikrobielle mittel
DE2811919A1 (de) *	1978-03-18	1979-09-27	Bayer Ag	Acylierte 1-azolyl-2-hydroxy-butan- derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide
DE2842137A1 (de)	1978-09-28	1980-04-17	Bayer Ag	Halogenierte 1-azolyl-1-fluorphenoxy- butan-derivate, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide
DE2951164A1 (de) *	1979-12-19	1981-07-16	Bayer Ag, 5090 Leverkusen	Substituierte triazolylmethyl-tert.-butyl-ketone, verfahren zu ihrer herstellung und ihre verwendung als pflanzenschutzmittel sowie als zwischenprodukte
EP0158741A3 (en) *	1980-11-19	1986-02-12	Imperial Chemical Industries Plc	Intermediates for fungicidal triazole and imidazole compounds
AR228764A1 (es) *	1980-12-20	1983-04-15	Bayer Ag	1-azolil-3,3-dimetilalcan(c3-4)-2-onas y-2-oles,sustituidos,procedimiento para su produccion y composiciones protectoras de plantas fungicidas y reguladoras del crecimiento de las plantas a base de dichos compuestos
DE3049461A1 (de)	1980-12-30	1982-09-09	Bayer Ag, 5090 Leverkusen	Verfahren zur herstellung von monochlormethylketonen
DE3108770A1 (de) *	1981-03-07	1982-09-16	Bayer Ag, 5090 Leverkusen	Triazolylalkyl-thioether, verfahren zu ihrer herstellung sowie ihre verwendung als pflanzenwachstumsregulatoren und fungizide

1985
- 1985-11-15 DE DE19853540523 patent/DE3540523A1/de not_active Withdrawn
1986
- 1986-11-03 EP EP86115194A patent/EP0224076B1/de not_active Expired
- 1986-11-03 DE DE8686115194T patent/DE3666817D1/de not_active Expired
- 1986-11-03 AT AT86115194T patent/ATE47848T1/de not_active IP Right Cessation
- 1986-11-04 AU AU64805/86A patent/AU6480586A/en not_active Abandoned
- 1986-11-05 PT PT83687A patent/PT83687B/pt unknown
- 1986-11-11 JP JP61266771A patent/JPS62181265A/ja active Pending
- 1986-11-11 DD DD86296174A patent/DD258741A5/de unknown
- 1986-11-12 IL IL80608A patent/IL80608A0/xx unknown
- 1986-11-14 DK DK546086A patent/DK546086A/da not_active Application Discontinuation
- 1986-11-14 BR BR8605623A patent/BR8605623A/pt unknown
- 1986-11-14 HU HU864700A patent/HUT42683A/hu unknown
- 1986-11-14 ZA ZA868652A patent/ZA868652B/xx unknown
- 1986-11-15 KR KR860009657A patent/KR870004968A/ko not_active Withdrawn
1988
- 1988-10-12 US US07/256,808 patent/US4917720A/en not_active Expired - Fee Related
- 1988-10-13 US US07/258,108 patent/US4878939A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
DE3540523A1 (de)	1987-05-27
IL80608A0 (en)	1987-02-27
EP0224076B1 (de)	1989-11-08
JPS62181265A (ja)	1987-08-08
DK546086A (da)	1987-05-16
ZA868652B (en)	1987-07-29
EP0224076A1 (de)	1987-06-03
ATE47848T1 (de)	1989-11-15
PT83687A (en)	1986-12-01
KR870004968A (ko)	1987-06-02
DK546086D0 (da)	1986-11-14
US4878939A (en)	1989-11-07
AU6480586A (en)	1987-05-21
HUT42683A (en)	1987-08-28
PT83687B (en)	1988-12-05
US4917720A (en)	1990-04-17
DE3666817D1 (en)	1989-12-14
BR8605623A (pt)	1987-08-18

Publication	Publication Date	Title
EP0297345B1 (de)	1991-09-25	Azolylmethyl-cyclopropyl-Derivate
DD208752A5 (de)	1984-04-11	Pflanzenschutzmittel, verfahren zu ihrer herstellung sowie verwendung von substituierten 1--hydroxyalkyl-azolyl-derivaten
DE3716558A1 (de)	1988-12-01	Hydroxyalkyl-azolyl-derivate
DD155292A5 (de)	1982-06-02	Pflanzenschutzmittel
EP0298332A1 (de)	1989-01-11	Hydroxyalkyl-azolyl-Derivate
EP0044993A2 (de)	1982-02-03	Triazolylpropenol-Derivate, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Pflanzenwachstumsregulatoren und Fungizide
EP0079006B1 (de)	1985-12-11	Azolyl-alkenone und -ole, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Pflanzenwachstumsregulatoren und Fungizide
DD205812A5 (de)	1984-01-11	Pflanzenwachstumsregulierende und fungizide mittel
EP0311892B1 (de)	1991-01-02	Subtituierte Azolylmethylcarbinole
EP0080102B1 (de)	1986-05-28	Cycloalkyl-(alpha-triazolyl-beta-hydroxy)-ketone, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Fungizide und Pflanzenwachstumsregulatoren
EP0180838A2 (de)	1986-05-14	Substituierte Azolylcyclopropyl-azolylmethyl-carbinol-Derivate
EP0327913B1 (de)	1994-04-06	Substituierte Azolylmethyloxirane
DE3702301A1 (de)	1987-09-10	2-hydroxyethyl-azol-derivate
EP0224076B1 (de)	1989-11-08	Azolyletherketone und -alkohole
DE3045182A1 (de)	1982-07-01	Pflanzenwachstumsregulierende und fungizide mittel
EP0254797B1 (de)	1990-07-04	2-Hydroxyethyl-azol-Derivate
EP0298300A1 (de)	1989-01-11	Azolyl-tetrahydropyran-Derivate
EP0296452A1 (de)	1988-12-28	Azolylmethyl-cyclopropyl-carbinol-Derivate
EP0384246A2 (de)	1990-08-29	Cyclopropyl-hydroxyethyl-azolyl-Derivate
DE3905317A1 (de)	1990-08-23	Cyclopropyl-hydroxyalkyl-azolyl-derivate
EP0291798B1 (de)	1992-03-18	Hydroxyalkyl-triazolyl-Derivate
DE3422244A1 (de)	1985-12-19	1-azolyl-2-phenyl-cyclopropan-derivate
DD274164A5 (de)	1989-12-13	Fungizide und pflanzenregulierende mittel
DD281745A5 (de)	1990-08-22	Fungizide und pflanzenwuchsregulierende mittel
DD274163A5 (de)	1989-12-13	Fungizide und pflanzenwuchsregulierende mittel