DD146142A5 - Antagonistisch wirkendes mittel zum schuetzen von kulturpflanzen - Google Patents

Antagonistisch wirkendes mittel zum schuetzen von kulturpflanzen Download PDF

Info

Publication number: DD146142A5
Authority: DD; German Democratic Republic
Prior art keywords: radical; halogen; group; formula; substituted
Prior art date: 1978-08-28

Application number

DD215204A

Other languages

German (de)

English (en)

Inventor

Sturm

Schempp

Martin

Original Assignee

Ciba Geigy 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.)

1978-08-28

Filing date

1979-08-27

Publication date

1981-01-28

1979-08-27 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1981-01-28 Publication of DD146142A5 publication Critical patent/DD146142A5/de

Links

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235000010233 benzoic acid Nutrition 0.000 description 1
PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
KDPAWGWELVVRCH-UHFFFAOYSA-N bromoacetic acid Chemical class OC(=O)CBr KDPAWGWELVVRCH-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
150000001733 carboxylic acid esters Chemical class 0.000 description 1
235000019993 champagne Nutrition 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical class OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
CWJSHJJYOPWUGX-UHFFFAOYSA-N chlorpropham Chemical compound CC(C)OC(=O)NC1=CC=CC(Cl)=C1 CWJSHJJYOPWUGX-UHFFFAOYSA-N 0.000 description 1
229930016911 cinnamic acid Natural products 0.000 description 1
235000013985 cinnamic acid Nutrition 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
239000013078 crystal Substances 0.000 description 1
125000004966 cyanoalkyl group Chemical group 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
239000012973 diazabicyclooctane Substances 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
125000006371 dihalo methyl group Chemical group 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000006266 etherification reaction Methods 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
238000011049 filling Methods 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
230000035784 germination Effects 0.000 description 1
150000003977 halocarboxylic acids Chemical class 0.000 description 1
125000005059 halophenyl group Chemical group 0.000 description 1
230000009931 harmful effect Effects 0.000 description 1
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 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
238000003898 horticulture Methods 0.000 description 1
150000001469 hydantoins Chemical class 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
239000005457 ice water Substances 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
PGLTVOMIXTUURA-UHFFFAOYSA-N iodoacetamide Chemical compound NC(=O)CI PGLTVOMIXTUURA-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
YFYKPAWMOFQBKT-UHFFFAOYSA-N isocyanatobenzene;2-isocyanato-2-methylpropane Chemical compound CC(C)(C)N=C=O.O=C=NC1=CC=CC=C1 YFYKPAWMOFQBKT-UHFFFAOYSA-N 0.000 description 1
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000000155 melt Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
239000011707 mineral Substances 0.000 description 1
125000000896 monocarboxylic acid group Chemical group 0.000 description 1
PHWISQNXPLXQRU-UHFFFAOYSA-N n,n-dimethylcarbamothioyl chloride Chemical compound CN(C)C(Cl)=S PHWISQNXPLXQRU-UHFFFAOYSA-N 0.000 description 1
SHQJHXLWZDMQEJ-UHFFFAOYSA-N n-methoxy-n-methylcarbamoyl chloride Chemical compound CON(C)C(Cl)=O SHQJHXLWZDMQEJ-UHFFFAOYSA-N 0.000 description 1
CPGWSLFYXMRNDV-UHFFFAOYSA-N n-methyl-n-phenylcarbamoyl chloride Chemical compound ClC(=O)N(C)C1=CC=CC=C1 CPGWSLFYXMRNDV-UHFFFAOYSA-N 0.000 description 1
GRRYSIXDUIAUGY-UHFFFAOYSA-N n-methylcarbamoyl chloride Chemical compound CNC(Cl)=O GRRYSIXDUIAUGY-UHFFFAOYSA-N 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229920003052 natural elastomer Polymers 0.000 description 1
229920001194 natural rubber Polymers 0.000 description 1
229960003512 nicotinic acid Drugs 0.000 description 1
235000001968 nicotinic acid Nutrition 0.000 description 1
239000011664 nicotinic acid Substances 0.000 description 1
125000002560 nitrile group Chemical group 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
239000012044 organic layer Substances 0.000 description 1
238000006053 organic reaction Methods 0.000 description 1
235000020232 peanut Nutrition 0.000 description 1
239000008188 pellet Substances 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
KHUXNRRPPZOJPT-UHFFFAOYSA-N phenoxy radical Chemical compound O=C1C=C[CH]C=C1 KHUXNRRPPZOJPT-UHFFFAOYSA-N 0.000 description 1
239000002703 plant agrochemical Substances 0.000 description 1
239000004476 plant protection product Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
150000004672 propanoic acids Chemical class 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
235000018102 proteins Nutrition 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
230000001850 reproductive effect Effects 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
238000002791 soaking Methods 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
SRAWNDFHGTVUNZ-UHFFFAOYSA-M sodium;3,6-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(CCCC)=CC2=CC(CCCC)=CC=C21 SRAWNDFHGTVUNZ-UHFFFAOYSA-M 0.000 description 1
239000007921 spray Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000008107 starch Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
235000000346 sugar Nutrition 0.000 description 1
NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical class NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 description 1
108010057210 telomerase RNA Proteins 0.000 description 1
125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
QERYCTSHXKAMIS-UHFFFAOYSA-N thiophene-2-carboxylic acid Chemical compound OC(=O)C1=CC=CS1 QERYCTSHXKAMIS-UHFFFAOYSA-N 0.000 description 1
238000002054 transplantation Methods 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
125000004953 trihalomethyl group Chemical group 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
239000010455 vermiculite Substances 0.000 description 1
229910052902 vermiculite Inorganic materials 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
238000010626 work up procedure Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C327/00—Thiocarboxylic acids
- C07C327/60—Thiocarboxylic acids having sulfur atoms of thiocarboxyl groups further doubly-bound to oxygen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/38—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Zoology (AREA)
Pest Control & Pesticides (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Plant Pathology (AREA)
Environmental Sciences (AREA)
Toxicology (AREA)
Agronomy & Crop Science (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Heterocyclic Compounds Containing Sulfur Atoms (AREA)
Furan Compounds (AREA)

DD215204A 1978-08-28 1979-08-27 Antagonistisch wirkendes mittel zum schuetzen von kulturpflanzen DD146142A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH908178		1978-08-28

Publications (1)

Publication Number	Publication Date
DD146142A5 true DD146142A5 (de)	1981-01-28

Family

ID=4348139

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD215204A DD146142A5 (de)	1978-08-28	1979-08-27	Antagonistisch wirkendes mittel zum schuetzen von kulturpflanzen

Country Status (13)

Country	Link
US (6)	US4278613A (fr)
EP (1)	EP0010588B1 (fr)
JP (1)	JPS5589258A (fr)
AT (1)	ATE12063T1 (fr)
AU (1)	AU533787B2 (fr)
CA (1)	CA1161452A (fr)
CS (1)	CS210697B2 (fr)
DD (1)	DD146142A5 (fr)
DE (1)	DE2967406D1 (fr)
HU (1)	HU184615B (fr)
IE (1)	IE49869B1 (fr)
IL (1)	IL58114A (fr)
ZA (1)	ZA794518B (fr)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4497648A (en) *	1978-09-01	1985-02-05	Ciba-Geigy Corporation	Oxime derivatives for protecting plant crops
US4347372A (en) *	1978-09-01	1982-08-31	Ciba-Geigy Corporation	Benzoxazolyl-glyoxylonitrile-2-oxime ether derivatives
US4954164A (en) *	1982-02-27	1990-09-04	Nissan Chemical Industries, Ltd.	Pyrazolesulfonylurea derivatives, preparation thereof, herbicide containing said derivative as active ingredient and herbicidal method by use thereof
DE3520943A1 (de) *	1985-06-12	1986-12-18	Bayer Ag, 5090 Leverkusen	Benzaldoxim-carbamat-derivate
DE3708320A1 (de) *	1987-03-14	1988-09-22	Bayer Ag	Benzaldoxim-derivate
DE3712632A1 (de) *	1987-04-14	1988-10-27	Bayer Ag	(alpha)-methylsulfonyl-benzaldoxim-carbamate
JPH01209513A (ja) *	1988-02-17	1989-08-23	Rinnai Corp	制御装置の作動補助装置
US5201933A (en) *	1988-08-01	1993-04-13	Monsanto Company	Safening herbicidal benzoic acid derivatives
IL94170A0 (en) *	1989-04-25	1991-01-31	Du Pont	Oxime carbamates and their use as fungicides
WO1991016299A1 (fr) *	1989-04-25	1991-10-31	E.I. Du Pont De Nemours And Company	Carbamates d'oxime fongicides
WO1992003050A1 (fr) *	1990-08-16	1992-03-05	E.I. Du Pont De Nemours And Company	Esters fongicides de sulfoneoxime
US7572249B2 (en) *	2006-12-01	2009-08-11	The Procter & Gamble Company	Merchandise display systems for baby care articles
US7582075B2 (en) *	2006-08-24	2009-09-01	The Procter & Gamble Company	Disposable absorbent article products with improved stages of development identification
CN103443072B (zh)	2011-01-28	2016-05-18	巴斯夫欧洲公司	包含肟磺酸酯作为热固化剂的可聚合组合物

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1141487B (de)	1960-04-23	1962-12-20	Merck Ag E	Fungizides Mittel
US3131509A (en) *	1961-05-08	1964-05-05	Spencer Chem Co	Compositions and methods for reducing herbicidal injury
US3483246A (en) *	1966-12-05	1969-12-09	Mobil Oil Corp	Aromatic glyoxynitrile oximino carbanates
US3819700A (en)	1970-04-23	1974-06-25	R Bellina	2-(hydrocarbylthio)-2-(hydroxyimino)-acetamide s-oxides and derivatives
CH624552A5 (fr) *	1975-09-04	1981-08-14	Ciba Geigy Ag

1979
- 1979-08-20 US US06/068,123 patent/US4278613A/en not_active Expired - Lifetime
- 1979-08-24 CA CA000334431A patent/CA1161452A/fr not_active Expired
- 1979-08-27 AU AU50308/79A patent/AU533787B2/en not_active Ceased
- 1979-08-27 IE IE1633/79A patent/IE49869B1/en unknown
- 1979-08-27 DE DE7979103164T patent/DE2967406D1/de not_active Expired
- 1979-08-27 EP EP79103164A patent/EP0010588B1/fr not_active Expired
- 1979-08-27 HU HU79CI1956A patent/HU184615B/hu not_active IP Right Cessation
- 1979-08-27 DD DD215204A patent/DD146142A5/de unknown
- 1979-08-27 IL IL58114A patent/IL58114A/xx unknown
- 1979-08-27 ZA ZA00794518A patent/ZA794518B/xx unknown
- 1979-08-27 AT AT79103164T patent/ATE12063T1/de not_active IP Right Cessation
- 1979-08-28 JP JP10962679A patent/JPS5589258A/ja active Granted
- 1979-08-28 CS CS795844A patent/CS210697B2/cs unknown
1981
- 1981-05-04 US US06/260,537 patent/US4425151A/en not_active Expired - Fee Related
- 1981-05-04 US US06/260,534 patent/US4394152A/en not_active Expired - Lifetime
- 1981-05-04 US US06/260,539 patent/US4382893A/en not_active Expired - Lifetime
- 1981-05-04 US US06/260,536 patent/US4451279A/en not_active Expired - Fee Related
- 1981-05-04 US US06/260,648 patent/US4449999A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
IE791633L (en)	1980-02-28
AU533787B2 (en)	1983-12-08
JPS5589258A (en)	1980-07-05
HU184615B (en)	1984-09-28
US4451279A (en)	1984-05-29
ZA794518B (en)	1980-09-24
EP0010588A2 (fr)	1980-05-14
US4382893A (en)	1983-05-10
DE2967406D1 (en)	1985-04-18
CA1161452A (fr)	1984-01-31
EP0010588A3 (en)	1980-10-01
ATE12063T1 (de)	1985-03-15
US4425151A (en)	1984-01-10
EP0010588B1 (fr)	1985-03-13
AU5030879A (en)	1980-03-06
US4278613A (en)	1981-07-14
IL58114A (en)	1984-12-31
US4394152A (en)	1983-07-19
IE49869B1 (en)	1986-01-08
IL58114A0 (en)	1979-12-30
JPS6252743B2 (fr)	1987-11-06
US4449999A (en)	1984-05-22
CS210697B2 (en)	1982-01-29

Publication	Publication Date	Title
EP0012158B1 (fr)	1984-08-15	Dérivés d'oxime et leur utilisation dans la protection des cultures de plantes
DE2808317C2 (fr)	1991-05-08
DE69227527T2 (de)	1999-06-24	Fluoroalkenyl verbindungen und ihre verwendung als schädlingsbekämpfungsmittel
DE2639405A1 (de)	1977-03-17	Neuer oximaether, verfahren zu dessen herstellung und seine verwendung als gegenmittel fuer kulturpflanzen schaedigende herbizide
EP0004931A2 (fr)	1979-10-31	Utilisation de derivés du furanne et du thiophène comme agents de régulation de croissance des plantes
EP0010588B1 (fr)	1985-03-13	Composés d'oxime contenant du soufre et leur utilisation pour la protection des plantes cultivées
DD147904A5 (de)	1981-04-29	Verfahren zum schutz von pflanzenkulturen
EP0010143B1 (fr)	1983-09-28	Dérivés d'oxime pour la protection de plantes cultivées
DE2837204A1 (de)	1980-03-06	Oxim-carbamate und -carbonate zum schuetzen von pflanzenkulturen
EP0310558A2 (fr)	1989-04-05	Agent microbicide
CH637268A5 (de)	1983-07-29	Mittel zum schutz von pflanzenkulturen.
EP0010058B1 (fr)	1983-06-22	Procédé et compositions pour la protection de cultures de plantes contre l'action phytotoxique des herbicides forts; dérivés d'oxime-éthers
EP0062254A1 (fr)	1982-10-13	Acétanilides substitués, procédé pour leur préparation et leur utilisation comme herbicides
CH615805A5 (fr)	1980-02-29
DE2601376A1 (de)	1977-07-21	Phenoxycarbonsaeure-aryloxy(thio)carbonylaminomethylester, verfahren zu ihrer herstellung sowie ihre verwendung zur regulierung des pflanzenwachstums
EP0230260B1 (fr)	1990-12-27	Dérivés de cyclohexénone, leur procédé de préparation et leur utilisation comme herbiciole et régulateur de croissance des plantes
CH635083A5 (de)	1983-03-15	1-alkylcarbonyl-3-(3,5-dihalogenphenyl)-imidazolidin-2,4-dione mit verzweigter alkylgruppe im alkylcarbonylrest.
DD145362A5 (de)	1980-12-10	Verfahren zum schutz von kulturpflanzen
DE2201500A1 (de)	1972-08-17	Substituierte Azabicycloalkane
EP0033516A1 (fr)	1981-08-12	Anilides substitués, préparation de ces composés, agents fongicides les contenant comme matières actives et utilisation de ces composés et agents dans la lutte contre les fungi en agriculture et horticulture
EP0016985A1 (fr)	1980-10-15	Anilides substitués, procédés pour leur préparation, fongicides contenant de tels composés et utilisation de tels composés ou fongicides dans la lutte contre les champignons des plantes
DE2106872A1 (de)	1971-09-02	Herbizide, mitizide und fungizide Mittel
DE3322662A1 (de)	1983-12-29	1,2,4-thiadiazolverbindungen und sie enthaltendes fungizides mittel
DD251125A5 (de)	1987-11-04	Verfahren zur herstellung von substituierten propargyloxyacetonitrilderivaten
CH644354A5 (en)	1984-07-31	Oxime ethers and esters, and processes for their preparation