DD285921A5 - Mittel mit herbizider und pflanzenwuchsregulierender wirkung - Google Patents

Mittel mit herbizider und pflanzenwuchsregulierender wirkung Download PDF

Info

Publication number: DD285921A5
Authority: DD; German Democratic Republic
Prior art keywords: group; alkyl; phenyl; halogen; alkoxy
Prior art date: 1987-07-01

Application number

DD88317312A

Other languages

German (de)

English (en)

Inventor

Martin Krueger

Juergen Westermann

Friedrich Arndt

Richard Rees

Russel G Hunt

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.)

1987-07-01

Filing date

1988-06-29

Publication date

1991-01-10

1988-06-29 Application filed by ��@��k�� filed Critical ��@��k��

1991-01-10 Publication of DD285921A5 publication Critical patent/DD285921A5/de

Links

230000008635 plant growth Effects 0.000 title abstract description 3
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229910052736 halogen Inorganic materials 0.000 claims description 26
150000002367 halogens Chemical class 0.000 claims description 21
125000000217 alkyl group Chemical group 0.000 claims description 14
125000005843 halogen group Chemical group 0.000 claims description 13
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 11
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JZNWSCPGTDBMEW-UHFFFAOYSA-N Glycerophosphorylethanolamin Natural products NCCOP(O)(=O)OCC(O)CO JZNWSCPGTDBMEW-UHFFFAOYSA-N 0.000 description 1
ZWZWYGMENQVNFU-UHFFFAOYSA-N Glycerophosphorylserin Natural products OC(=O)C(N)COP(O)(=O)OCC(O)CO ZWZWYGMENQVNFU-UHFFFAOYSA-N 0.000 description 1
241000219146 Gossypium Species 0.000 description 1
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235000021506 Ipomoea Nutrition 0.000 description 1
241000207783 Ipomoea Species 0.000 description 1
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240000009132 Sagittaria sagittifolia Species 0.000 description 1
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241000607479 Yersinia pestis Species 0.000 description 1
ATBOMIWRCZXYSZ-XZBBILGWSA-N [1-[2,3-dihydroxypropoxy(hydroxy)phosphoryl]oxy-3-hexadecanoyloxypropan-2-yl] (9e,12e)-octadeca-9,12-dienoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(COP(O)(=O)OCC(O)CO)OC(=O)CCCCCCC\C=C\C\C=C\CCCCC ATBOMIWRCZXYSZ-XZBBILGWSA-N 0.000 description 1
PQLVXDKIJBQVDF-UHFFFAOYSA-N acetic acid;hydrate Chemical compound O.CC(O)=O PQLVXDKIJBQVDF-UHFFFAOYSA-N 0.000 description 1
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DNEHKUCSURWDGO-UHFFFAOYSA-N aluminum sodium Chemical compound [Na].[Al] DNEHKUCSURWDGO-UHFFFAOYSA-N 0.000 description 1
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SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
150000008107 benzenesulfonic acids Chemical class 0.000 description 1
AGEZXYOZHKGVCM-UHFFFAOYSA-N benzyl bromide Chemical compound BrCC1=CC=CC=C1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 description 1
235000021028 berry Nutrition 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
229920005551 calcium lignosulfonate Polymers 0.000 description 1
RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
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238000007796 conventional method Methods 0.000 description 1
244000038559 crop plants Species 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000004821 distillation Methods 0.000 description 1
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230000001804 emulsifying effect Effects 0.000 description 1
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239000012442 inert solvent Substances 0.000 description 1
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239000011630 iodine Substances 0.000 description 1
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229920005610 lignin Polymers 0.000 description 1
239000006028 limestone Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
229910052987 metal hydride Inorganic materials 0.000 description 1
150000004681 metal hydrides Chemical class 0.000 description 1
229910000000 metal hydroxide Inorganic materials 0.000 description 1
150000004692 metal hydroxides Chemical class 0.000 description 1
KOSMBCOUJWPIJF-UHFFFAOYSA-N methyl 3-acetamido-5-[(2,6-difluorophenyl)sulfamoyl]-1h-pyrazole-4-carboxylate Chemical compound CC(=O)NC1=NNC(S(=O)(=O)NC=2C(=CC=CC=2F)F)=C1C(=O)OC KOSMBCOUJWPIJF-UHFFFAOYSA-N 0.000 description 1
FYGAWJLIPBLHGE-UHFFFAOYSA-N methyl 3-amino-5-[(2,6-difluorophenyl)sulfamoyl]-1h-pyrazole-4-carboxylate Chemical compound NC1=NNC(S(=O)(=O)NC=2C(=CC=CC=2F)F)=C1C(=O)OC FYGAWJLIPBLHGE-UHFFFAOYSA-N 0.000 description 1
HAMGRBXTJNITHG-UHFFFAOYSA-N methyl isocyanate Chemical compound CN=C=O HAMGRBXTJNITHG-UHFFFAOYSA-N 0.000 description 1
238000003801 milling Methods 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
GMFWJTPXSOGDQT-UHFFFAOYSA-N o-methyl 3-amino-5-benzyl-1h-pyrazole-4-carbothioate Chemical compound NC1=NNC(CC=2C=CC=CC=2)=C1C(=S)OC GMFWJTPXSOGDQT-UHFFFAOYSA-N 0.000 description 1
230000009965 odorless effect Effects 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
125000000913 palmityl 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])C([H])([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
229910052625 palygorskite Inorganic materials 0.000 description 1
KHUXNRRPPZOJPT-UHFFFAOYSA-N phenoxy radical Chemical compound O=C1C=C[CH]C=C1 KHUXNRRPPZOJPT-UHFFFAOYSA-N 0.000 description 1
WTJKGGKOPKCXLL-RRHRGVEJSA-N phosphatidylcholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCCCC WTJKGGKOPKCXLL-RRHRGVEJSA-N 0.000 description 1
150000008105 phosphatidylcholines Chemical class 0.000 description 1
150000008104 phosphatidylethanolamines Chemical class 0.000 description 1
150000003905 phosphatidylinositols Chemical class 0.000 description 1
150000003904 phospholipids Chemical class 0.000 description 1
230000008654 plant damage Effects 0.000 description 1
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239000010695 polyglycol Substances 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
238000000746 purification Methods 0.000 description 1
JUXWUYWPUDKPSD-UHFFFAOYSA-N pyrazolo[1,5-a][1,3,5]triazine Chemical compound N1=CN=CN2N=CC=C21 JUXWUYWPUDKPSD-UHFFFAOYSA-N 0.000 description 1
125000004076 pyridyl group Chemical group 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
BCELSKZIQVOBEH-UHFFFAOYSA-N s-benzylthiohydroxylamine Chemical group NSCC1=CC=CC=C1 BCELSKZIQVOBEH-UHFFFAOYSA-N 0.000 description 1
OEBIHOVSAMBXIB-SJKOYZFVSA-N selitrectinib Chemical compound C[C@@H]1CCC2=NC=C(F)C=C2[C@H]2CCCN2C2=NC3=C(C=NN3C=C2)C(=O)N1 OEBIHOVSAMBXIB-SJKOYZFVSA-N 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
238000009331 sowing Methods 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
RUPAXCPQAAOIPB-UHFFFAOYSA-N tert-butyl formate Chemical compound CC(C)(C)OC=O RUPAXCPQAAOIPB-UHFFFAOYSA-N 0.000 description 1
229960000278 theophylline Drugs 0.000 description 1
ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-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
238000009736 wetting Methods 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000002023 wood Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
- 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
Environmental Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Cosmetics (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

DD88317312A 1987-07-01 1988-06-29 Mittel mit herbizider und pflanzenwuchsregulierender wirkung DD285921A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19873722072 DE3722072A1 (de)	1987-07-01	1987-07-01	6,7-dihydro-pyrazolo(1,5-a)(1,3,5) triazin-2-sulfonsaeureamide, verfahren zu ihrer herstellung und ihre verwendung als mittel mit herbizider und pflanzenwuchsregulierender wirkung

Publications (1)

Publication Number	Publication Date
DD285921A5 true DD285921A5 (de)	1991-01-10

Family

ID=6330887

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD88317312A DD285921A5 (de)	1987-07-01	1988-06-29	Mittel mit herbizider und pflanzenwuchsregulierender wirkung

Country Status (15)

Country	Link
US (1)	US4892576A (da)
EP (1)	EP0297490A1 (da)
JP (1)	JPS6470489A (da)
KR (1)	KR890002154A (da)
CN (1)	CN1030419A (da)
AU (1)	AU606697B2 (da)
BR (1)	BR8803293A (da)
DD (1)	DD285921A5 (da)
DE (1)	DE3722072A1 (da)
DK (1)	DK368088A (da)
FI (1)	FI883168A7 (da)
HU (1)	HUT47393A (da)
IL (1)	IL86901A0 (da)
SU (1)	SU1616507A3 (da)
ZA (1)	ZA884744B (da)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4970142A (en) *	1989-02-16	1990-11-13	Konica Corporation	Silver halide photographic light-sensitive material containing cyan coupler
US6191131B1 (en)	1997-07-23	2001-02-20	Dupont Pharmaceuticals Company	Azolo triazines and pyrimidines
HU229024B1 (en) *	1996-07-24	2013-07-29	Bristol Myers Squibb Pharma Co	Azolo-pyridimidines, pharmaceutical compositions containing the same and use thereof
US6313124B1 (en)	1997-07-23	2001-11-06	Dupont Pharmaceuticals Company	Tetrazine bicyclic compounds
US7094782B1 (en)	1996-07-24	2006-08-22	Bristol-Myers Squibb Company	Azolo triazines and pyrimidines
US6124289A (en)	1996-07-24	2000-09-26	Dupont Pharmaceuticals Co.	Azolo triazines and pyrimidines
US6060478A (en) *	1996-07-24	2000-05-09	Dupont Pharmaceuticals	Azolo triazines and pyrimidines
AU4203500A (en)	1999-04-06	2000-10-23	Du Pont Pharmaceuticals Company	Pyrazolopyrimidines as crf antagonists
AU4331500A (en)	1999-04-06	2000-10-23	Du Pont Pharmaceuticals Company	Pyrazolotriazines as crf antagonists
KR20020001958A (ko) *	2000-06-22	2002-01-09	황성호	아스팔트 및 시멘트 콘크리트 도로의 검지선 보호용실란트 조성물과 그 제조방법
US6630476B2 (en)	2000-07-07	2003-10-07	Bristol-Myers Squibb Pharma Company	Pyrrolo [3,4-d] pyrimidines as corticotropin releasing factor (CRF) antagonists
DE10116399A1 (de) *	2001-04-03	2002-10-10	Bayer Ag	Substituierte Azolazin(thi)one
FR2842809A1 (fr) *	2002-07-26	2004-01-30	Greenpharma Sas	NOUVELLES PYRAZOLO[1,5-a]-1,3,5-TRIAZINES SUBSTITUEES ET LEURS ANALOGUES, COMPOSITIONS PHARMACEUTIQUES LES CONTENANT, UTILISATION A TITRE DE MEDICAMENT ET PROCEDES POUR LEUR PREPARATION
US7208596B2 (en) *	2003-11-25	2007-04-24	Bristol-Myers Squibb Pharma Company	Processes for the preparation of pyrazolo[1,5-a]-1,3,5-triazines and intermediates thereof
US7153961B2 (en) *	2003-11-25	2006-12-26	Bristol-Myers Squibb Pharma Co.	Salt and crystalline form thereof of a corticotropin releasing factor receptor antagonist
PE20141468A1 (es)	2010-12-21	2014-11-05	Bayer Cropscience Lp	Mutantes tipo papel de lija de bacillus y metodos de uso de los mismo para mejorar el crecimiento vegetal, promover la salud de plantas y controlar enfermedades y plagas
US8809328B2 (en) *	2011-04-27	2014-08-19	National University Corporation Shizuoka University	Imidazole derivative
MX2014002890A (es)	2011-09-12	2015-01-19	Bayer Cropscience Lp	Metodo para mejorar la salud y/o promover el crecimiento de una planta y/o mejorar la maduracion de frutos.
KR20150130491A (ko) *	2013-03-13	2015-11-23	제넨테크, 인크.	피라졸로 화합물 및 그것의 용도

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* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB951652A (en) *	1960-06-28	1964-03-11	Wallace Broadbent	Sulphamyl triazolopyrimidines and their preparation
WO1979000733A1 (en) *	1978-03-10	1979-10-04	Ici Ltd	Heterocyclic compounds
IL83139A (en) *	1983-11-14	1993-01-14	Dow Chemical Co	1,2,4-triazolo (1,5-a) pyrimidine-2-sulfonyl chlorides and their preparation
CA1244826A (en) *	1984-01-26	1988-11-15	William A. Kleschick	Sulfonamides derived from substituted 2-amino-1,2,4- triazolo(1,5-a)-pyrimidines and compositions and methods of controlling undesired vegetation
US4734414A (en) *	1985-06-06	1988-03-29	Biomeasure, Inc.	Anti-inflammatory and anti-arthritic pyrazolo-[1,5-a]-1,3,5-triazine derivatives, compositions, and method of use therefor
DE3616681A1 (de) *	1986-05-16	1987-11-19	Bayer Ag	1-aralkylpyrazole

1987
- 1987-07-01 DE DE19873722072 patent/DE3722072A1/de not_active Withdrawn
1988
- 1988-06-28 IL IL86901A patent/IL86901A0/xx unknown
- 1988-06-28 EP EP88110245A patent/EP0297490A1/de not_active Withdrawn
- 1988-06-29 DD DD88317312A patent/DD285921A5/de unknown
- 1988-06-30 HU HU883386A patent/HUT47393A/hu unknown
- 1988-06-30 AU AU18564/88A patent/AU606697B2/en not_active Withdrawn - After Issue
- 1988-06-30 US US07/213,905 patent/US4892576A/en not_active Expired - Fee Related
- 1988-06-30 CN CN88104008A patent/CN1030419A/zh active Pending
- 1988-06-30 SU SU884356000A patent/SU1616507A3/ru active
- 1988-06-30 KR KR1019880007968A patent/KR890002154A/ko not_active Withdrawn
- 1988-06-30 JP JP63161090A patent/JPS6470489A/ja active Pending
- 1988-07-01 DK DK368088A patent/DK368088A/da not_active Application Discontinuation
- 1988-07-01 FI FI883168A patent/FI883168A7/fi not_active Application Discontinuation
- 1988-07-01 BR BR8803293A patent/BR8803293A/pt unknown
- 1988-07-01 ZA ZA884744A patent/ZA884744B/xx unknown

Also Published As

Publication number	Publication date
KR890002154A (ko)	1989-04-08
US4892576A (en)	1990-01-09
IL86901A0 (en)	1988-11-30
DK368088D0 (da)	1988-07-01
SU1616507A3 (ru)	1990-12-23
JPS6470489A (en)	1989-03-15
HUT47393A (en)	1989-03-28
DK368088A (da)	1989-01-02
EP0297490A1 (de)	1989-01-04
FI883168A0 (fi)	1988-07-01
AU606697B2 (en)	1991-02-14
FI883168A7 (fi)	1989-01-11
BR8803293A (pt)	1989-01-24
DE3722072A1 (de)	1989-01-12
AU1856488A (en)	1989-01-05
CN1030419A (zh)	1989-01-18
ZA884744B (en)	1989-04-26

Publication	Publication Date	Title
EP0131258B1 (de)	1989-08-30	Neue N-Alkoxy- N-Alkylsulfonylaminosulfonylharnstoffe, und neue (Pyrimido) Triazino-thiatriazinoxide als Vorprodukte
DD285921A5 (de)	1991-01-10	Mittel mit herbizider und pflanzenwuchsregulierender wirkung
EP1209973B1 (de)	2004-02-25	Herbizides mittel
EP0342569B1 (de)	1994-06-22	Heterocyclische 2-Alkoxyphenoxysulfonylharnstoffe und ihre Verwendung als Herbizide oder Pflanzenwachstumsregulatoren
EP0521500A1 (de)	1993-01-07	Salze von Pyridylsulfonylharnstoffen als Herbizide und Pflanzenwachstumsregulatoren, Verfahren zu ihrer Herstellung und ihre Verwendung
DE60221921T2 (de)	2008-05-15	Herbizide Zusammensetzung
EP0272594A1 (de)	1988-06-29	Bicyclische Imide, Verfahren zu ihrer Herstellung sowie ihre Verwendung im Pflanzenschutz
DE3813885A1 (de)	1989-11-02	1-chlorpyrimidinyl-1h-1,2,4-triazol-3-sulfonsaeureamide, verfahren zu ihrer herstellung und ihre verwendung als mittel mit herbizider, fungizider und pflanzenwachstumsregulierender wirkung
EP0074595B1 (de)	1986-07-23	Substituierte Phenylsulfonylharnstoff- Derivate, Verfahren und neue Zwischenprodukte zu ihrer Herstellung und ihre Verwendung als Herbizide
EP0071958A1 (de)	1983-02-16	Heterocyclisch substituierte Sulfonylharnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung in der Landwirtschaft
EP0165572A2 (de)	1985-12-27	Neue herbizid wirksame Sulfonylharnstoffe
DE3826609A1 (de)	1990-02-08	Heterocyclisch substituierte sulfonylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung als herbizide oder pflanzenwachstumsregulatoren
EP0347788A2 (de)	1989-12-27	Substituierte Sulfonyldiamide, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide und Pflanzenwachstumsregulatoren
EP0272628B1 (de)	1992-04-29	6,7-Dihydro-[1,2,4]triazolo[1,5-a][1,3,5]triazin-2-sulfonsäureamide, Verfahren zu ihrer Herstellung und ihre Verwendung als Mittel mit herbizider und wachstumsregulierender Wirkung
DE3825041A1 (de)	1990-02-15	Pyrido(3,2-e)(1,2,4)triazolo(1,5-a)pyrimidin- 2-sulfonsaeureamide, verfahren zu ihrer herstellung und ihre verwendung als mittel mit herbizider, pflanzenwachstumsregulierender und fungizider wirkung
DE3813886A1 (de)	1989-11-02	1-triazinyl-1h-1,2,4-triazol-3- sulfonsaeureamide, verfahren zu ihrer herstellung und ihre verwendung als mittel mit herbizider, fungizider und pflanzenwachstumsregulierender wirkung
DE3737748A1 (de)	1989-05-18	3-arylsulfonylamino-1h-1,2,4-triazole, verfahren zu ihrer herstellung und ihre verwendung als mittel mit herbizider und wachstumsregulierender wirkung
DE3811777A1 (de)	1989-10-19	Heterocyclisch substituierte alkyl- und alkenylsulfonylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung als herbizide oder pflanzenwachstumsregulatoren
DD261084A5 (de)	1988-10-19	1,2-disubstituierte piperidine, verfahren zu ihrer herstellung sowie ihre verwendung im pflanzenschutz
EP0216243A2 (de)	1987-04-01	N-Substituierte 3,4,5,6-Tetrahydrophthalimide, Verfahren zu ihrer Herstellung sowie ihre Verwendung im Pflanzenschutz
DD283762A5 (de)	1990-10-24	Herbizide und pflanzenwuchsregulierende mittel
EP0319689B1 (de)	1993-12-15	Heterocyclisch substituierte N-Sultam-sulfonamide, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide und Pflanzenwachstumsregulatoren
EP0303114B1 (de)	1994-08-24	Heterocyclisch substituierte Sulfamidsäurephenylester, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide und Pflanzenwachstumsregulatoren
DD256449A5 (de)	1988-05-11	Pyrazolo(3,4-b)pyridinderivate enthaltende mittel mit herbizider wirkung
DE4241658A1 (de)	1994-06-09	Substituierte 2-Thiobenzthiazole, Verfahren zu ihrer Herstellung und ihre Verwendung als herbizide Mittel