DD154519A5 - Pestizides mittel - Google Patents

Pestizides mittel Download PDF

Info

Publication number: DD154519A5
Authority: DD; German Democratic Republic
Prior art keywords: methyl; formula; ethyl; compounds; deep
Prior art date: 1979-11-16

Application number

DD80225205A

Other languages

German (de)

English (en)

Inventor

Adolf Hubele

Peter Riebli

Original Assignee

Janssen Pharmaceutica Nv

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.)

1979-11-16

Filing date

1980-11-14

Publication date

1982-03-31

1980-11-14 Application filed by Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv

1982-03-31 Publication of DD154519A5 publication Critical patent/DD154519A5/de

Links

239000000575 pesticide Substances 0.000 title description 2
150000001875 compounds Chemical class 0.000 claims abstract description 67
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229910052751 metal Chemical class 0.000 claims abstract description 22
239000002184 metal Chemical class 0.000 claims abstract description 22
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 22
241000233866 Fungi Species 0.000 claims abstract description 20
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 20
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 19
239000001257 hydrogen Substances 0.000 claims abstract description 19
239000002253 acid Substances 0.000 claims abstract description 13
244000005700 microbiome Species 0.000 claims abstract description 13
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 11
229910052760 oxygen Inorganic materials 0.000 claims abstract description 9
230000003032 phytopathogenic effect Effects 0.000 claims abstract description 9
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 8
239000001301 oxygen Substances 0.000 claims abstract description 8
229910052736 halogen Inorganic materials 0.000 claims abstract description 7
150000002367 halogens Chemical class 0.000 claims abstract description 7
150000002431 hydrogen Chemical class 0.000 claims abstract description 5
230000003449 preventive effect Effects 0.000 claims abstract description 4
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims abstract description 4
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 3
229910052717 sulfur Inorganic materials 0.000 claims abstract description 3
239000011593 sulfur Substances 0.000 claims abstract description 3
239000004305 biphenyl Substances 0.000 claims description 11
-1 trifluoromethyl-substituted phenyl Chemical group 0.000 claims description 11
RAXXELZNTBOGNW-UHFFFAOYSA-N 1H-imidazole Chemical compound C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 10
125000000217 alkyl group Chemical group 0.000 claims description 9
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125000004432 carbon atom Chemical group C* 0.000 claims description 3
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125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims description 2
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125000003342 alkenyl group Chemical group 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
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IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 2
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XLSZMDLNRCVEIJ-UHFFFAOYSA-N methylimidazole Natural products CC1=CNC=N1 XLSZMDLNRCVEIJ-UHFFFAOYSA-N 0.000 claims 2
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238000002844 melting Methods 0.000 description 6
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150000007522 mineralic acids Chemical class 0.000 description 4
239000003960 organic solvent Substances 0.000 description 4
238000012360 testing method Methods 0.000 description 4
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
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ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
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YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
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MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
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239000002585 base Substances 0.000 description 3
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150000008041 alkali metal carbonates Chemical class 0.000 description 1
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150000008046 alkali metal hydrides Chemical class 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
229910001516 alkali metal iodide Inorganic materials 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
238000005804 alkylation reaction Methods 0.000 description 1
235000020224 almond Nutrition 0.000 description 1
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230000000845 anti-microbial effect Effects 0.000 description 1
235000021016 apples Nutrition 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
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239000004359 castor oil Substances 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
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235000019693 cherries Nutrition 0.000 description 1
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239000011737 fluorine Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
235000013305 food Nutrition 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
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125000005843 halogen group Chemical group 0.000 description 1
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GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
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235000015243 ice cream Nutrition 0.000 description 1
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239000004615 ingredient Substances 0.000 description 1
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JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
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125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
235000021374 legumes Nutrition 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
235000009973 maize Nutrition 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
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150000002739 metals Chemical class 0.000 description 1
229940098779 methanesulfonic acid Drugs 0.000 description 1
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229910017604 nitric acid Inorganic materials 0.000 description 1
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239000003208 petroleum Substances 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
235000021018 plums Nutrition 0.000 description 1
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239000000843 powder Substances 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
235000015136 pumpkin Nutrition 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
239000012312 sodium hydride Substances 0.000 description 1
229910000104 sodium hydride Inorganic materials 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
229910052911 sodium silicate Inorganic materials 0.000 description 1
238000009331 sowing Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
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229940095064 tartrate Drugs 0.000 description 1
235000013616 tea Nutrition 0.000 description 1
ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 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)
Dentistry (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

DD80225205A 1979-11-16 1980-11-14 Pestizides mittel DD154519A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH1025279		1979-11-16

Publications (1)

Publication Number	Publication Date
DD154519A5 true DD154519A5 (de)	1982-03-31

Family

ID=4361145

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD80225205A DD154519A5 (de)	1979-11-16	1980-11-14	Pestizides mittel

Country Status (11)

Country	Link
EP (1)	EP0029355B1 (fr)
JP (1)	JPS5683488A (fr)
AU (1)	AU534772B2 (fr)
BR (1)	BR8007460A (fr)
CA (1)	CA1173449A (fr)
DD (1)	DD154519A5 (fr)
DE (1)	DE3064447D1 (fr)
IE (1)	IE50211B1 (fr)
IL (1)	IL61487A (fr)
NZ (1)	NZ195375A (fr)
ZA (1)	ZA807104B (fr)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5266585A (en) *	1981-05-12	1993-11-30	Ciba-Geigy Corporation	Arylphenyl ether derivatives, compositions containing these compounds and use thereof
FI77458C (fi) *	1981-05-12	1989-03-10	Ciba Geigy Ag	Nya mikrobicida arylfenyleterderivat, foerfarande foer deras framstaellning och deras anvaendning.
DE3144318A1 (de) *	1981-11-07	1983-05-19	Bayer Ag, 5090 Leverkusen	2-imidazolylmethyl-2-phenyl-1, 3-dioxolane, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide
ZA832373B (en) *	1982-04-05	1984-11-28	Syntex Inc	Anticonvulsant active substituted n-alkyl imidazoles
US4568678A (en) *	1982-04-05	1986-02-04	Syntex (U.S.A.) Inc.	Substituted N-alkyl imidazoles to treat convulsions
DE3232737A1 (de) *	1982-09-03	1984-03-08	Bayer Ag, 5090 Leverkusen	2-aryl-2-azolylmethyl-1,3-dioxepine
FI834141A7 (fi) *	1982-11-16	1984-05-17	Ciba Geigy Ag	Foerfarande foer framstaellning av nya arylfenyleterderivat.
US4533670A (en) *	1983-09-21	1985-08-06	Eli Lilly And Company	Anti-convulsant fluorenylalkylimidazole derivatives, compositions, and method of use
CS253719B2 (en) *	1984-03-07	1987-12-17	Janssen Pharmaceutica Nv	Emulsible concentrate with fungicide activity and process for preparing thereof
EP0296518A1 (fr) *	1987-06-22	1988-12-28	Ciba-Geigy Ag	Dérivés de phényléthers comme microbicide, procédé de leur préparation et leur application
US4943311A (en) *	1988-05-09	1990-07-24	Uniroyal Chemical Company, Inc.	Azole derivatives of spiroheterocycles
WO2010146116A1 (fr) *	2009-06-18	2010-12-23	Basf Se	Composés de triazole portant un substituant soufré
WO2010146115A1 (fr) *	2009-06-18	2010-12-23	Basf Se	Composés de triazole portant un substituant de soufre
AU2010261822A1 (en) *	2009-06-18	2012-01-19	Basf Se	Triazole compounds carrying a sulfur substituent
EP2745691A1 (fr)	2012-12-19	2014-06-25	Basf Se	Composés d'imidazole substitués et leur utilisation comme fongicides
EP2746274A1 (fr)	2012-12-19	2014-06-25	Basf Se	Composés de [1,2,4] triazole substitué
EP3519404A1 (fr)	2016-09-29	2019-08-07	Bayer CropScience Aktiengesellschaft	Dérivés d'imidazolylméthyldioxolane à substitution en position 5 en tant que fongicides

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3575999A (en) *	1968-08-19	1971-04-20	Janssen Pharmaceutica Nv	Ketal derivatives of imidazole
NZ179111A (en) *	1974-11-18	1978-03-06	Janssen Pharmaceutica Nv	I-(aryl)-ethyl-1h-1,2,4-triazole ketals,anti-microbial and plant growth controlling compositions
US3936470A (en) *	1975-01-27	1976-02-03	Janssen Pharmaceutica N.V.	1,3-Dioxolan-2-ylmethylimidazoles
US4101665A (en) *	1975-10-06	1978-07-18	Janssen Pharmaceutica N.V.	1-(2-Ar-4-aryloxymethyl-1,3-dioxolan-2-ylmethyl)imidazoles
US4141908A (en) *	1976-10-15	1979-02-27	Janssen Pharmaceutica N.V.	2-Aryl-1,3-dioxolanes
US4160838A (en) *	1977-06-02	1979-07-10	Janssen Pharmaceutica N.V.	Antimicrobial and plant-growth-regulating triazole derivatives

1980
- 1980-10-23 CA CA000363086A patent/CA1173449A/fr not_active Expired
- 1980-10-24 AU AU63685/80A patent/AU534772B2/en not_active Ceased
- 1980-10-28 NZ NZ195375A patent/NZ195375A/xx unknown
- 1980-11-13 JP JP15891780A patent/JPS5683488A/ja active Pending
- 1980-11-14 DD DD80225205A patent/DD154519A5/de unknown
- 1980-11-14 ZA ZA00807104A patent/ZA807104B/xx unknown
- 1980-11-14 IL IL61487A patent/IL61487A/xx unknown
- 1980-11-14 IE IE2370/80A patent/IE50211B1/en unknown
- 1980-11-14 DE DE8080304094T patent/DE3064447D1/de not_active Expired
- 1980-11-14 EP EP80304094A patent/EP0029355B1/fr not_active Expired
- 1980-11-14 BR BR8007460A patent/BR8007460A/pt unknown

Also Published As

Publication number	Publication date
ZA807104B (en)	1982-06-30
IL61487A0 (en)	1980-12-31
DE3064447D1 (en)	1983-09-01
IE50211B1 (en)	1986-03-05
AU534772B2 (en)	1984-02-16
AU6368580A (en)	1981-05-21
JPS5683488A (en)	1981-07-08
EP0029355A1 (fr)	1981-05-27
IE802370L (en)	1981-05-16
BR8007460A (pt)	1981-05-26
IL61487A (en)	1984-06-29
EP0029355B1 (fr)	1983-07-27
NZ195375A (en)	1982-12-07
CA1173449A (fr)	1984-08-28

Publication	Publication Date	Title
EP0065485B1 (fr)	1990-04-18	Dérivés d'arylphényléthers comme microbicide, procédé pour leur préparation et leur application
EP0332579B1 (fr)	1994-08-10	Méthode de protection de plantes contre des maladies
DD154519A5 (de)	1982-03-31	Pestizides mittel
DE3801233A1 (de)	1988-08-04	Mikrobizides mittel
DD279671A5 (de)	1990-06-13	Mikrobizides mittel
DD145105A5 (de)	1980-11-19	Verfahren zur herstellung von 1-(2 aryl-4,5-disubstituierten-1,3-dioxolan-2-ylmethyl)-1h-i idazolen und-1h-1,2,4-triazolen
EP0198797B1 (fr)	1990-01-31	Parasiticide
DE2930196C2 (fr)	1992-10-22
EP0149426B1 (fr)	1988-05-04	Microbicides
DE3234624C2 (fr)	1992-04-30
EP0130149B1 (fr)	1989-04-12	Dérivés de 3-phényl-4-cyanopyrrol, procédé de préparation et utilisation comme microbicides
EP0221844A1 (fr)	1987-05-13	Dérivés de la pyridine à activité microbicide
EP0163606A2 (fr)	1985-12-04	Dérivés de 1-fluoro-1-azolyl-2,2-diaryléthane à activité microbicide
EP0334813B1 (fr)	1994-02-02	Agents pour la protection de plantes contre des maladies
EP0183217B1 (fr)	1990-06-13	Agents microbicides
EP0517660B1 (fr)	1997-04-23	Dérivés de benzo-1,2,3-thiadiazole
DE2943631A1 (de)	1980-05-14	Azolylketale, verfahren zu ihrer herstellung und ihre verwendung als mikrobizide
EP0288976B1 (fr)	1994-06-01	Agent protecteur contre les maladies de plantes
EP0079856A1 (fr)	1983-05-25	Microbicide triazolyl-vinyl éthers
EP0060962B1 (fr)	1985-08-07	Triazolylméthyldioxolanes microbicides et leur préparation
EP0065483A1 (fr)	1982-11-24	Dérivés d'acylanilines et de acylnaphtylamines à activité microbicide, procédés de leur préparation et leur utilisation
EP0228343A2 (fr)	1987-07-08	Dérivés microbiens de 2-(1-triazolyl)-1-phényl-éthanone-(1)-cétals
EP0296518A1 (fr)	1988-12-28	Dérivés de phényléthers comme microbicide, procédé de leur préparation et leur application
EP0443980A1 (fr)	1991-08-28	Microbicides
DE3505869A1 (de)	1985-08-22	2-((arylthio)phenyl)-2-(1h-azolylmethyl)-diox(ol)ane als mikrobizide