DD258933A5 - Mikrobizide mittel - Google Patents

Mikrobizide mittel Download PDF

Info

Publication number: DD258933A5
Authority: DD; German Democratic Republic
Prior art keywords: formula; alkyl; stands; nitro; phenylsulfonylazoles
Prior art date: 1986-02-22

Application number

DD87300084A

Other languages

German (de)

English (en)

Inventor

Hans J Riebel

Yanagi Akihiko

Hirashima Akinori

Wilhelm Brandes

Paul Reinecke

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.)

1986-02-22

Filing date

1987-02-20

Publication date

1988-08-10

1987-02-20 Application filed by ��@��k�� filed Critical ��@��k��

1988-08-10 Publication of DD258933A5 publication Critical patent/DD258933A5/de

Links

239000002855 microbicide agent Substances 0.000 title claims abstract 4
230000003641 microbiacidal effect Effects 0.000 title claims description 5
229940124561 microbicide Drugs 0.000 title claims description 4
ZBFTZNKRTMPTDO-UHFFFAOYSA-N 2-(benzenesulfonyl)-1h-pyrrole Chemical compound C=1C=CC=CC=1S(=O)(=O)C1=CC=CN1 ZBFTZNKRTMPTDO-UHFFFAOYSA-N 0.000 claims abstract description 17
125000000217 alkyl group Chemical group 0.000 claims abstract description 17
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 7
239000001257 hydrogen Substances 0.000 claims abstract description 7
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 7
229910052736 halogen Inorganic materials 0.000 claims abstract description 4
150000002367 halogens Chemical group 0.000 claims abstract description 4
-1 Phenylsulfonylazolen Chemical compound 0.000 claims description 18
238000000034 method Methods 0.000 claims description 14
239000000203 mixture Substances 0.000 claims description 11
125000004432 carbon atom Chemical group C* 0.000 claims description 7
238000002360 preparation method Methods 0.000 claims description 7
239000000126 substance Substances 0.000 claims description 7
239000013543 active substance Substances 0.000 claims description 6
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 6
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
239000004606 Fillers/Extenders Substances 0.000 claims description 5
239000000460 chlorine Substances 0.000 claims description 5
229910052801 chlorine Inorganic materials 0.000 claims description 5
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
229910052794 bromium Inorganic materials 0.000 claims description 4
239000000417 fungicide Substances 0.000 claims description 4
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 3
229910052731 fluorine Inorganic materials 0.000 claims description 3
239000011737 fluorine Substances 0.000 claims description 3
230000000855 fungicidal effect Effects 0.000 claims description 3
244000005700 microbiome Species 0.000 claims description 3
UPTVJAJPBGIRLZ-UHFFFAOYSA-N 2-(trichloromethylsulfanyl)-3a,4,5,7a-tetrahydroisoindole-1,3-dione Chemical compound C1CC=CC2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C21 UPTVJAJPBGIRLZ-UHFFFAOYSA-N 0.000 claims description 2
230000000694 effects Effects 0.000 claims description 2
238000002156 mixing Methods 0.000 claims description 2
239000004094 surface-active agent Substances 0.000 claims description 2
BIJTZOHYNINMSE-UHFFFAOYSA-N 2-(benzenesulfonyl)-1h-imidazole Chemical class C=1C=CC=CC=1S(=O)(=O)C1=NC=CN1 BIJTZOHYNINMSE-UHFFFAOYSA-N 0.000 claims 1
YVGYDWSQWYUOKE-UHFFFAOYSA-N 4-(benzenesulfonyl)-2h-benzotriazole Chemical class C=1C=CC=2NN=NC=2C=1S(=O)(=O)C1=CC=CC=C1 YVGYDWSQWYUOKE-UHFFFAOYSA-N 0.000 claims 1
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RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Substances C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 1
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239000004480 active ingredient Substances 0.000 abstract description 10
150000002431 hydrogen Chemical group 0.000 abstract 1
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239000007788 liquid Substances 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
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UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
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239000011701 zinc Substances 0.000 description 3
RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
SGUVLZREKBPKCE-UHFFFAOYSA-N 1,5-diazabicyclo[4.3.0]-non-5-ene Chemical compound C1CCN=C2CCCN21 SGUVLZREKBPKCE-UHFFFAOYSA-N 0.000 description 2
LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 description 2
WPGVQDHXOUAJBW-UHFFFAOYSA-N 2-methyl-5-nitrobenzenesulfonyl chloride Chemical compound CC1=CC=C([N+]([O-])=O)C=C1S(Cl)(=O)=O WPGVQDHXOUAJBW-UHFFFAOYSA-N 0.000 description 2
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XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
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VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
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229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 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
235000014113 dietary fatty acids Nutrition 0.000 description 1
GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 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
150000002170 ethers Chemical class 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
238000005187 foaming Methods 0.000 description 1
239000000446 fuel Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000003630 growth substance Substances 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000004816 latex Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
239000000787 lecithin Substances 0.000 description 1
235000010445 lecithin Nutrition 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical class [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
239000004579 marble Substances 0.000 description 1
235000012054 meals Nutrition 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
SYBYTAAJFKOIEJ-UHFFFAOYSA-N methyl iso-propyl ketone Natural products CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
239000003595 mist Substances 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
229940042880 natural phospholipid Drugs 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
239000011368 organic material Substances 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
239000006072 paste Substances 0.000 description 1
244000052769 pathogen Species 0.000 description 1
150000003904 phospholipids Chemical class 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
239000000047 product Substances 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
239000003531 protein hydrolysate Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
239000010453 quartz Substances 0.000 description 1
239000011435 rock Substances 0.000 description 1
XMVJITFPVVRMHC-UHFFFAOYSA-N roxarsone Chemical group OC1=CC=C([As](O)(O)=O)C=C1[N+]([O-])=O XMVJITFPVVRMHC-UHFFFAOYSA-N 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
235000019355 sepiolite Nutrition 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
230000000391 smoking effect Effects 0.000 description 1
241000894007 species Species 0.000 description 1
125000001424 substituent group Chemical class 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- 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
- C07D233/60—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 with hydrocarbon radicals, substituted by oxygen or sulfur atoms, attached to ring nitrogen atoms
- 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
- 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
- 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
- C07D249/16—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
- C07D249/18—Benzotriazoles

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)

DD87300084A 1986-02-22 1987-02-20 Mikrobizide mittel DD258933A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19863605714 DE3605714A1 (de)	1986-02-22	1986-02-22	Mikrobizide mittel

Publications (1)

Publication Number	Publication Date
DD258933A5 true DD258933A5 (de)	1988-08-10

Family

ID=6294693

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD87300084A DD258933A5 (de)	1986-02-22	1987-02-20	Mikrobizide mittel

Country Status (12)

Country	Link
US (1)	US4734427A (pt)
EP (1)	EP0238824A1 (pt)
JP (1)	JPS62198667A (pt)
KR (1)	KR870007895A (pt)
BR (1)	BR8700826A (pt)
DD (1)	DD258933A5 (pt)
DE (1)	DE3605714A1 (pt)
DK (1)	DK87087A (pt)
HU (1)	HUT42761A (pt)
IL (1)	IL81625A0 (pt)
PT (1)	PT84293A (pt)
ZA (1)	ZA871248B (pt)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3833549A1 (de) *	1988-10-01	1990-04-12	Bayer Ag	Substituierte phenoxyphenylsulfonylazole, verfahren zu ihrer herstellung sowie ihre verwendung als herbizide und pflanzenwuchsregulatoren
EP0462931B1 (de) *	1990-06-21	1994-04-13	Ciba-Geigy Ag	Benzotriazol-1-sulfonylderivate mit mikrobiziden Eigenschaften
US5322853A (en) *	1990-06-21	1994-06-21	Ciba-Geigy Corporation	Microbicidal benzotriazole compounds
EP0549532A1 (de) *	1991-12-20	1993-06-30	Ciba-Geigy Ag	Benztriazolsulfonsäure-Derivate und ihre Verwendung als Mikrobizide
DE19523446A1 (de)	1995-06-28	1997-01-02	Bayer Ag	Benzotriazole
DE19623207A1 (de) *	1996-06-11	1997-12-18	Bayer Ag	Imidazolderivate
DE19708688A1 (de)	1997-03-04	1998-09-10	Bayer Ag	Annellierte Azolderivate
US6262100B1 (en)	1997-07-24	2001-07-17	Bayer Aktiengesellschaft	Nitrophenyl-sulfonyl-imidazoles and use thereof for controlling vegetable and animal pests
DE19844497A1 (de)	1998-09-29	2000-03-30	Bayer Ag	Sulfonyltriazol-Derivate

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE566599A (pt) *
FR1198995A (fr) *	1958-02-27	1959-12-10		Agents fongicides contenant des nu-sulfonyl-benzotriazols
US3294640A (en) *	1963-03-14	1966-12-27	American Home Prod	Controlling blood sugar with sulfonyl pyrazoles
US4115060A (en) *	1977-10-03	1978-09-19	Fmc Corporation	N-sulfonylimidazoles as peroxygen activators
DE3021834A1 (de) *	1980-06-11	1982-03-04	Basf Ag, 6700 Ludwigshafen	Azolyl-4-nitro-2-trichlormethyl-benzolsulfone, ihre herstellung und verwendung
JPS6160659A (ja) *	1984-09-03	1986-03-28	Nippon Tokushu Noyaku Seizo Kk	置換フエニルスルホニルアゾ−ル、その製法及び農園芸用殺菌剤

1986
- 1986-02-22 DE DE19863605714 patent/DE3605714A1/de not_active Withdrawn
1987
- 1987-02-10 US US07/012,988 patent/US4734427A/en not_active Expired - Fee Related
- 1987-02-10 EP EP87101794A patent/EP0238824A1/de not_active Withdrawn
- 1987-02-13 PT PT84293A patent/PT84293A/pt unknown
- 1987-02-19 IL IL81625A patent/IL81625A0/xx unknown
- 1987-02-20 ZA ZA871248A patent/ZA871248B/xx unknown
- 1987-02-20 JP JP62035992A patent/JPS62198667A/ja active Pending
- 1987-02-20 HU HU87667A patent/HUT42761A/hu unknown
- 1987-02-20 DD DD87300084A patent/DD258933A5/de unknown
- 1987-02-20 BR BR8700826A patent/BR8700826A/pt unknown
- 1987-02-20 DK DK087087A patent/DK87087A/da not_active Application Discontinuation
- 1987-02-20 KR KR870001429A patent/KR870007895A/ko not_active Withdrawn

Also Published As

Publication number	Publication date
US4734427A (en)	1988-03-29
JPS62198667A (ja)	1987-09-02
EP0238824A1 (de)	1987-09-30
DK87087A (da)	1987-08-23
HUT42761A (en)	1987-08-28
ZA871248B (en)	1987-08-12
DK87087D0 (da)	1987-02-20
IL81625A0 (en)	1987-09-16
PT84293A (en)	1987-03-01
KR870007895A (ko)	1987-09-22
DE3605714A1 (de)	1987-08-27
BR8700826A (pt)	1987-12-22

Publication	Publication Date	Title
DE3618662A1 (de)	1987-12-10	Trisubstituierte 1,3,5-triazin-2,4,6-trione
DD258933A5 (de)	1988-08-10	Mikrobizide mittel
EP0334134A1 (de)	1989-09-27	3,7-Disubstituierte Benzthiazolone
EP0554729B1 (de)	1995-12-06	Substituierte Aminosäureamide
EP0226051A1 (de)	1987-06-24	Fungizide Verwendung von Tetrahydrobenzothienylharnstoff-Derivaten
EP0670836B1 (de)	2001-10-04	3-pyridyl-1,2,4-thiadiazole als pestizide
EP0590458B1 (de)	1999-02-24	Substituierte Thiophencarbonsäureamide
DD247373A5 (de)	1987-07-08	Schaedlingsbekaempfungsmittel
EP0586386A1 (de)	1994-03-16	Substituierte salicylamide, mittel gegen pflanzenkrankheiten
DD246697A5 (de)	1987-06-17	Fungizide mittel
DE3728277A1 (de)	1989-03-09	N,n'-diacylaminale
DE3716023A1 (de)	1988-12-08	Azolyl-tetrahydrofuran-2-yliden-methane
EP0422461A2 (de)	1991-04-17	Trisubstituierte 1,3,5-Triazin-2,4,6-trione
DE3708320A1 (de)	1988-09-22	Benzaldoxim-derivate
DE3911226A1 (de)	1990-10-11	Fungizide mittel auf basis von nitrosubstituierten benzthiazolonen, neue nitrosubstituierte benzthiazolone und verfahren zu deren herstellung
DE3911227A1 (de)	1990-10-11	Nitrosubstituierte benzthiazolone, verfahren zu ihrer herstellung und ihre verwendung in schaedlingsbekaempfungsmitteln und neue zwischenprodukte
DE4321029A1 (de)	1995-01-05	Aralkylaminochinazoline
WO1994004529A1 (de)	1994-03-03	Pyridylsubstituierte 1,3-oxazolidin-derivate und ihre verwendung als schädlingsbekämpfungsmittel
DE3707687A1 (de)	1988-09-22	Benzaldoxim-carbamat-derivate
EP0269929A1 (de)	1988-06-08	Chlor-1,2,4-oxadiazole
DE3921502A1 (de)	1991-01-10	Imidazolyl-propin-derivate
DE3809776A1 (de)	1989-10-05	Hetaryl-1,10-phenanthrolin-derivate
DE3806490A1 (de)	1989-09-14	Substituierte pyridylbenzoxazine
EP0272430A1 (de)	1988-06-29	Saccharin-Salze von substituierten Aminen
EP0320775A2 (de)	1989-06-21	Substituierte Pyrimidine