DD202096A5 - Herbizides mittel - Google Patents

Herbizides mittel Download PDF

Info

Publication number: DD202096A5
Authority: DD; German Democratic Republic
Prior art keywords: methyl; yloxyacetic acid; benzoxazol; formula; herbicidal
Prior art date: 1981-01-26

Application number

DD82236878A

Other languages

German (de)

English (en)

Inventor

Masahiro Aya

Junichi Saito

Kazuomi Yasui

Kozo Shiokawa

Norihisa Morishima

Toshio Goto

Original Assignee

Nihon Tokushu Noyaku Seizo Kk

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1981-01-26

Filing date

1982-01-20

Publication date

1983-08-31

1981-01-26 Priority claimed from JP56008977A external-priority patent/JPS57123168A/ja

1981-06-20 Priority claimed from JP9457181A external-priority patent/JPS57212155A/ja

1982-01-20 Application filed by Nihon Tokushu Noyaku Seizo Kk filed Critical Nihon Tokushu Noyaku Seizo Kk

1983-08-31 Publication of DD202096A5 publication Critical patent/DD202096A5/de

Links

239000004009 herbicide Substances 0.000 title abstract description 5
241000196324 Embryophyta Species 0.000 claims abstract description 29
230000002363 herbicidal effect Effects 0.000 claims abstract description 23
239000000203 mixture Substances 0.000 claims abstract description 16
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 10
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims abstract description 5
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 5
238000004519 manufacturing process Methods 0.000 claims description 8
239000004094 surface-active agent Substances 0.000 claims description 6
239000004606 Fillers/Extenders Substances 0.000 claims description 3
238000002156 mixing Methods 0.000 claims description 3
LUBJCRLGQSPQNN-UHFFFAOYSA-N 1-Phenylurea Chemical class NC(=O)NC1=CC=CC=C1 LUBJCRLGQSPQNN-UHFFFAOYSA-N 0.000 claims 1
239000004744 fabric Substances 0.000 claims 1
GHDLZGOOOLEJKI-UHFFFAOYSA-N benzenesulfonylurea Chemical class NC(=O)NS(=O)(=O)C1=CC=CC=C1 GHDLZGOOOLEJKI-UHFFFAOYSA-N 0.000 abstract description 8
239000003795 chemical substances by application Substances 0.000 abstract description 7
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract description 3
231100000331 toxic Toxicity 0.000 abstract description 2
230000002588 toxic effect Effects 0.000 abstract description 2
101100242909 Streptococcus pneumoniae (strain ATCC BAA-255 / R6) pbpA gene Proteins 0.000 abstract 1
101100269618 Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) aliA gene Proteins 0.000 abstract 1
-1 4,6-dimethylpyrimidin-2-yl Chemical group 0.000 description 36
150000001875 compounds Chemical class 0.000 description 35
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238000006243 chemical reaction Methods 0.000 description 21
FWYULLXZQPHSAL-UHFFFAOYSA-N 2-(1,3-benzoxazol-2-yloxy)acetic acid Chemical compound C1=CC=C2OC(OCC(=O)O)=NC2=C1 FWYULLXZQPHSAL-UHFFFAOYSA-N 0.000 description 20
OPQIOIYLAKHILI-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-yloxy)acetic acid Chemical compound C1=CC=C2SC(OCC(=O)O)=NC2=C1 OPQIOIYLAKHILI-UHFFFAOYSA-N 0.000 description 17
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DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 2
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DROVNMHMVXRDSY-UHFFFAOYSA-N 2-[(5-ethyl-1,3,4-thiadiazol-2-yl)oxy]acetic acid Chemical compound CCC1=NN=C(OCC(O)=O)S1 DROVNMHMVXRDSY-UHFFFAOYSA-N 0.000 description 1
NXFQWRWXEYTOTK-UHFFFAOYSA-N 2-methyl-4-amino-6-methoxy-s-triazine Chemical compound COC1=NC(C)=NC(N)=N1 NXFQWRWXEYTOTK-UHFFFAOYSA-N 0.000 description 1
YMMHAIJRFWRDMG-UHFFFAOYSA-N 3,4,4a,5-tetrahydro-1h-quinolin-2-one Chemical compound C1C=CC=C2NC(=O)CCC21 YMMHAIJRFWRDMG-UHFFFAOYSA-N 0.000 description 1
KVHFZZUPCXCRIX-UHFFFAOYSA-N 4,6-dimethoxy-1,3,5-triazin-2-amine Chemical compound COC1=NC(N)=NC(OC)=N1 KVHFZZUPCXCRIX-UHFFFAOYSA-N 0.000 description 1
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NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
239000013543 active substance Substances 0.000 description 1
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QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
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239000000920 calcium hydroxide Substances 0.000 description 1
235000011116 calcium hydroxide Nutrition 0.000 description 1
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VNSBYDPZHCQWNB-UHFFFAOYSA-N calcium;aluminum;dioxido(oxo)silane;sodium;hydrate Chemical compound O.[Na].[Al].[Ca+2].[O-][Si]([O-])=O VNSBYDPZHCQWNB-UHFFFAOYSA-N 0.000 description 1
239000002775 capsule Substances 0.000 description 1
235000011089 carbon dioxide Nutrition 0.000 description 1
239000003093 cationic surfactant Substances 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
VJYIFXVZLXQVHO-UHFFFAOYSA-N chlorsulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 VJYIFXVZLXQVHO-UHFFFAOYSA-N 0.000 description 1
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230000002939 deleterious effect Effects 0.000 description 1
SHFGJEQAOUMGJM-UHFFFAOYSA-N dialuminum dipotassium disodium dioxosilane iron(3+) oxocalcium oxomagnesium oxygen(2-) Chemical compound [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[Na+].[Na+].[Al+3].[Al+3].[K+].[K+].[Fe+3].[Fe+3].O=[Mg].O=[Ca].O=[Si]=O SHFGJEQAOUMGJM-UHFFFAOYSA-N 0.000 description 1
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238000009826 distribution Methods 0.000 description 1
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JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
238000010410 dusting Methods 0.000 description 1
230000008029 eradication Effects 0.000 description 1
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238000011156 evaluation Methods 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
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150000002334 glycols Chemical class 0.000 description 1
230000012010 growth Effects 0.000 description 1
239000010440 gypsum Substances 0.000 description 1
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WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
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150000002513 isocyanates Chemical class 0.000 description 1
238000002955 isolation Methods 0.000 description 1
QPPQHRDVPBTVEV-UHFFFAOYSA-N isopropyl dihydrogen phosphate Chemical compound CC(C)OP(O)(O)=O QPPQHRDVPBTVEV-UHFFFAOYSA-N 0.000 description 1
229910052622 kaolinite Inorganic materials 0.000 description 1
CYPPCCJJKNISFK-UHFFFAOYSA-J kaolinite Chemical compound [OH-].[OH-].[OH-].[OH-].[Al+3].[Al+3].[O-][Si](=O)O[Si]([O-])=O CYPPCCJJKNISFK-UHFFFAOYSA-J 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
239000004571 lime Substances 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
239000011419 magnesium lime Substances 0.000 description 1
XIGAUIHYSDTJHW-UHFFFAOYSA-N mefenacet Chemical compound N=1C2=CC=CC=C2SC=1OCC(=O)N(C)C1=CC=CC=C1 XIGAUIHYSDTJHW-UHFFFAOYSA-N 0.000 description 1
150000002736 metal compounds Chemical class 0.000 description 1
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
235000019713 millet Nutrition 0.000 description 1
235000010460 mustard Nutrition 0.000 description 1
MSLICLMCQYQNPK-UHFFFAOYSA-N n-(4-bromophenyl)acetamide Chemical compound CC(=O)NC1=CC=C(Br)C=C1 MSLICLMCQYQNPK-UHFFFAOYSA-N 0.000 description 1
UJYAZVSPFMJCLW-UHFFFAOYSA-N n-(oxomethylidene)benzenesulfonamide Chemical class O=C=NS(=O)(=O)C1=CC=CC=C1 UJYAZVSPFMJCLW-UHFFFAOYSA-N 0.000 description 1
230000001069 nematicidal effect Effects 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
150000004045 organic chlorine compounds Chemical class 0.000 description 1
150000002898 organic sulfur compounds Chemical class 0.000 description 1
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
239000010451 perlite Substances 0.000 description 1
235000019362 perlite Nutrition 0.000 description 1
239000005011 phenolic resin Substances 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
239000005648 plant growth regulator Substances 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
239000003380 propellant Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000000661 sodium alginate Substances 0.000 description 1
235000010413 sodium alginate Nutrition 0.000 description 1
229940005550 sodium alginate Drugs 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
238000003892 spreading Methods 0.000 description 1
238000004544 sputter deposition Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical class OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
238000004381 surface treatment Methods 0.000 description 1
239000000725 suspension Substances 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
238000010998 test method Methods 0.000 description 1
150000003573 thiols Chemical class 0.000 description 1
235000010487 tragacanth Nutrition 0.000 description 1
239000000196 tragacanth Substances 0.000 description 1
229940116362 tragacanth Drugs 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 1
150000003672 ureas Chemical class 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
239000010457 zeolite Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/65—N-sulfonylisocyanates
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D521/00—Heterocyclic compounds containing unspecified hetero rings

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Agronomy & Crop Science (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)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

DD82236878A 1981-01-26 1982-01-20 Herbizides mittel DD202096A5 (de)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
JP56008977A JPS57123168A (en)	1981-01-26	1981-01-26	Substituted phenylsulfonylurea derivative, its preparation and herbicide containing the same as active constituent
JP9457181A JPS57212155A (en)	1981-06-20	1981-06-20	Substituted phenylsulfonyl isocyanate and its preparation

Publications (1)

Publication Number	Publication Date
DD202096A5 true DD202096A5 (de)	1983-08-31

Family

ID=26343610

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD82236878A DD202096A5 (de)	1981-01-26	1982-01-20	Herbizides mittel

Country Status (16)

Country	Link
US (3)	US4500342A (fr)
EP (1)	EP0056969B1 (fr)
AR (1)	AR228636A1 (fr)
AU (1)	AU543150B2 (fr)
BR (1)	BR8200386A (fr)
DD (1)	DD202096A5 (fr)
DE (1)	DE3267205D1 (fr)
DK (1)	DK31782A (fr)
ES (2)	ES8305338A1 (fr)
GR (1)	GR74765B (fr)
IL (1)	IL64845A0 (fr)
NZ (1)	NZ199547A (fr)
PH (1)	PH17499A (fr)
PL (1)	PL130861B1 (fr)
PT (1)	PT74294B (fr)
TR (1)	TR21378A (fr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5846071A (ja) *	1981-09-16	1983-03-17	Nippon Tokushu Noyaku Seizo Kk	置換フエニルスルホニルウレア誘導体、その中間体、それらの製法、及び除草剤
US4579583A (en) *	1982-09-08	1986-04-01	Ciba-Geigy Corporation	Novel sulfonylureas
US4515626A (en) *	1982-10-06	1985-05-07	Ciba Geigy Corporation	N-(Cyclopropyl-triazinyl-n'-(arylsulfonyl) ureas having herbicidal activity
JPS606654A (ja) *	1983-06-24	1985-01-14	Nippon Tokushu Noyaku Seizo Kk	置換フエニルスルホニルグアニジン誘導体、その中間体、それらの製法及び除草剤
JPS6036467A (ja) *	1983-08-10	1985-02-25	Nippon Tokushu Noyaku Seizo Kk	置換フエニルスルホニルグアニジン誘導体、その中間体、それらの製法及び雑草防除剤
EP0151554A1 (fr) *	1984-02-03	1985-08-14	Ciba-Geigy Ag	Dérivés de phénylsulfonamide
US5306825A (en) *	1984-03-01	1994-04-26	Consiglio Nazionale Delle Ricerche	Physostigmine derivatives with acetylcholinesterase inhibition properties, and the relative production process
JPS60215660A (ja) *	1984-04-11	1985-10-29	Nippon Tokushu Noyaku Seizo Kk	ビフエニリルスルホニルウレア誘導体の製法、その中間体及び該中間体の製法
GB8719730D0 (en) *	1987-08-20	1987-09-30	Vickers Plc	Radiation sensitive compounds
US5179207A (en) *	1991-08-19	1993-01-12	Eastman Kodak Company	Substituted 2-amino-5-maleimido thiophenes and substituted 2-amino-maleimido thiazoles
DE69221698T2 (de) *	1991-10-15	1998-02-19	Du Pont	Verfahren zur Herstellung von Sulfonylharnstoffen

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
OA05625A (fr) *	1976-04-07	1981-04-30	Du Pont	N-(hétérocyclique aminocarbonyl) aryl sulfonamides herbicides, compositions les contenant et procédés les utilisant .
US4169719A (en) *	1976-04-07	1979-10-02	E. I. Du Pont De Nemours And Co.	Herbicidal sulfonamides
US4257802A (en) *	1977-10-06	1981-03-24	E. I. Du Pont De Nemours And Company	Herbicidal sulfonamides
US4368069A (en) *	1980-07-11	1983-01-11	E. I. Du Pont De Nemours And Company	Herbicidal sulfonamides
US4378991A (en) *	1980-07-11	1983-04-05	E. I. Du Pont De Nemours And Company	Herbicidal o-aryl or alkarylsulfonylureas
JPS5846071A (ja) *	1981-09-16	1983-03-17	Nippon Tokushu Noyaku Seizo Kk	置換フエニルスルホニルウレア誘導体、その中間体、それらの製法、及び除草剤
US4514213A (en) *	1984-03-19	1985-04-30	E. I. Du Pont De Nemours And Company	Herbicidal sulfonamides

1981
- 1981-01-21 TR TR21378A patent/TR21378A/xx unknown
1982
- 1982-01-18 DE DE8282100319T patent/DE3267205D1/de not_active Expired
- 1982-01-18 EP EP82100319A patent/EP0056969B1/fr not_active Expired
- 1982-01-18 PT PT74294A patent/PT74294B/pt unknown
- 1982-01-19 AU AU79607/82A patent/AU543150B2/en not_active Ceased
- 1982-01-20 US US06/340,903 patent/US4500342A/en not_active Expired - Fee Related
- 1982-01-20 DD DD82236878A patent/DD202096A5/de unknown
- 1982-01-22 NZ NZ199547A patent/NZ199547A/en unknown
- 1982-01-22 PL PL1982234803A patent/PL130861B1/pl unknown
- 1982-01-22 AR AR288211A patent/AR228636A1/es active
- 1982-01-22 IL IL64845A patent/IL64845A0/xx unknown
- 1982-01-25 GR GR67110A patent/GR74765B/el unknown
- 1982-01-25 BR BR8200386A patent/BR8200386A/pt unknown
- 1982-01-25 ES ES509044A patent/ES8305338A1/es not_active Expired
- 1982-01-25 DK DK31782A patent/DK31782A/da not_active Application Discontinuation
- 1982-01-26 PH PH26786A patent/PH17499A/en unknown
- 1982-12-30 ES ES518710A patent/ES518710A0/es active Granted
1984
- 1984-07-19 US US06/632,555 patent/US4586951A/en not_active Expired - Fee Related
- 1984-08-31 US US06/646,553 patent/US4602941A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
AU543150B2 (en)	1985-04-04
NZ199547A (en)	1984-07-31
EP0056969A2 (fr)	1982-08-04
ES509044A0 (es)	1983-04-01
US4586951A (en)	1986-05-06
ES8305338A1 (es)	1983-04-01
PL234803A1 (fr)	1982-10-25
PL130861B1 (en)	1984-09-29
TR21378A (tr)	1984-04-26
IL64845A0 (en)	1982-03-31
PT74294A (en)	1982-02-01
ES8402566A1 (es)	1984-02-01
US4500342A (en)	1985-02-19
PT74294B (en)	1983-06-28
AU7960782A (en)	1982-08-05
DE3267205D1 (en)	1985-12-12
EP0056969A3 (en)	1982-11-24
DK31782A (da)	1982-07-27
AR228636A1 (es)	1983-03-30
PH17499A (en)	1984-09-07
EP0056969B1 (fr)	1985-11-06
US4602941A (en)	1986-07-29
ES518710A0 (es)	1984-02-01
BR8200386A (pt)	1982-11-23
GR74765B (fr)	1984-07-12

Publication	Publication Date	Title
DE69410141T2 (de)	1998-09-03	1-(substituiertes Phenyl)-Tetrazolinon Derivate, deren Herstellung und deren Verwendung als Herbizide
DE69306866T2 (de)	1997-05-07	Tetrazolinone als Herbizide für das Reisfeld
EP0074595B1 (fr)	1986-07-23	Dérivés de phénylsulfonylurées substituées, procédé et nouveaux intermédiaires pour leur préparation et leur utilisation comme herbicide
DE69126836T2 (de)	1998-01-02	Herbizide
EP0056969B1 (fr)	1985-11-06	Dérivés substitués de phénylsulfonylurées, intermédiaires et procédé pour leur préparation et compositions herbicides contenant les dérivés
EP0353641B1 (fr)	1994-12-07	Sulfonylurées substituées avec des hétérocycles, procédé pour leur préparation et leur utilisation comme herbicides et régulateurs de croissance des plantes
EP0136455A1 (fr)	1985-04-10	Dérivés de phénylsulfonylguanidines substituées
DD224760A5 (de)	1985-07-17	Herbizide mittel
EP0058868B1 (fr)	1984-04-11	Dérivés de tétrahydropyrimidinone, procédé pour leur préparation et herbicides contenant ces dérivés comme produits actifs
EP0141319B1 (fr)	1988-05-25	Esters d'acides phénoxyalcanoiques substitués
EP0062254A1 (fr)	1982-10-13	Acétanilides substitués, procédé pour leur préparation et leur utilisation comme herbicides
EP0342568A1 (fr)	1989-11-23	Phénoxysulfonylurées substituées par un hétérocycle, procédé pour leur préparation et leur utilisation comme herbicides ou comme régulateurs de croissance des plantes
EP0153601B1 (fr)	1987-04-01	Dérivés d'alcoxyaminosulfonyle-2-benzènesulfonylurées
EP0319689B1 (fr)	1993-12-15	N-sultam-sulfonamides substitutées par un hétérocycle, procédé pour leur préparation et leur utilisation comme herbicide et comme régulateurs de croissance de plantes
EP0303114B1 (fr)	1994-08-24	Phénylesters d'acide sulfamique hétérocycliquement substitués, procédé pour leur préparation et leur utilisation comme herbicides et régulateurs de croissance des plantes
DE2436108A1 (de)	1975-02-13	Substituierte phenylharnstoffe, verfahren zu ihrer herstellung und herbizide mittel
DE2044735A1 (de)	1971-05-06	Schädlingsbekämpfungsmittel
EP0057367B1 (fr)	1983-12-28	2-Pyridyloxyacétanilides, procédé pour leur préparation et leur utilisation
EP0092112A1 (fr)	1983-10-26	Phénoxypropionates substitués
EP0409114A1 (fr)	1991-01-23	Sulfonylurées à groupement hétérocycliques, leur procédé de préparation et leur application comme herbicides ou régulateurs de croissance des végétaux
EP0148498A1 (fr)	1985-07-17	Dérivés de sulfonylguanidines
DD235996A5 (de)	1986-05-28	Pesticide benzoylharnstoffverbindung
DE68913686T2 (de)	1994-06-16	Benzamidverbindungen, deren Herstellung und deren Verwendung als Pestizide.
EP0388771A1 (fr)	1990-09-26	Phénoxysulfonylurées à base d'esters alkyl d'acide salicyclique, procédés pour leur préparation et leur utilisation comme herbicides et régulateurs de croissance des plantes
EP0086411A2 (fr)	1983-08-24	Tétrahydropyrimidin-2-ones substituées par un ou plusieurs méthyles procédé pour leur préparation et leur utilisation comme herbicides et intermédiaires pour leur préparation