JPS60246302A - 除草剤活性ヘテロアリールオキシアセトアミド類の作物植物による耐性を改良するためのアミド類の使用 - Google Patents

除草剤活性ヘテロアリールオキシアセトアミド類の作物植物による耐性を改良するためのアミド類の使用

Info

Publication number: JPS60246302A
Authority: JP; Japan
Prior art keywords: case; formula; optionally; optionally substituted; active compound
Prior art date: 1984-05-16
Legal status (The legal status 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 status listed.): Pending

Application number

JP60099759A

Other languages

English (en)

Japanese (ja)

Inventor

ハンス‐ヨアヒム・リーベル

イエルク・シユテツター

ビンフリート・ルンケンハイマー

クラウス・デイトゲンス

ウルリツヒ・ハイネマン

ルドルフ・トーマス

カルル・フエトケ

ハンス‐ヨアヒム・ザンテル

ルウトウイツヒ・オイエ

ロベルト・アール・シユミツト

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Bayer AG

Original Assignee

Bayer 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.)

1984-05-16

Filing date

1985-05-13

Publication date

1985-12-06

1985-05-13 Application filed by Bayer AG filed Critical Bayer AG

1985-12-06 Publication of JPS60246302A publication Critical patent/JPS60246302A/ja

Status Pending legal-status Critical Current

Links

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HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical class [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
241001148683 Zostera marina Species 0.000 description 1
239000000205 acacia gum Substances 0.000 description 1
235000010489 acacia gum Nutrition 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
150000008061 acetanilides Chemical class 0.000 description 1
125000001539 acetonyl group Chemical group [H]C([H])([H])C(=O)C([H])([H])* 0.000 description 1
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
150000001263 acyl chlorides Chemical class 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
125000004183 alkoxy alkyl group Chemical group 0.000 description 1
125000005194 alkoxycarbonyloxy group Chemical group 0.000 description 1
125000000676 alkoxyimino group Chemical group 0.000 description 1
125000003282 alkyl amino group Chemical group 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
125000005278 alkyl sulfonyloxy group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
230000003042 antagnostic effect Effects 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
244000269888 azena Species 0.000 description 1
239000000987 azo dye Substances 0.000 description 1
125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 description 1
150000005350 bicyclononyls Chemical group 0.000 description 1
229910052796 boron Inorganic materials 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000002775 capsule Substances 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
239000003610 charcoal Substances 0.000 description 1
VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical compound NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 description 1
125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
239000010941 cobalt Chemical class 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical class [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Chemical class 0.000 description 1
125000001651 cyanato group Chemical group [*]OC#N 0.000 description 1
CPPKAGUPTKIMNP-UHFFFAOYSA-N cyanogen fluoride Chemical compound FC#N CPPKAGUPTKIMNP-UHFFFAOYSA-N 0.000 description 1
125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 1
125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
NLUNLVTVUDIHFE-UHFFFAOYSA-N cyclooctylcyclooctane Chemical group C1CCCCCCC1C1CCCCCCC1 NLUNLVTVUDIHFE-UHFFFAOYSA-N 0.000 description 1
125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
125000004663 dialkyl amino group Chemical group 0.000 description 1
125000005202 dialkylaminocarbonyloxy group Chemical group 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
125000004774 dichlorofluoromethyl group Chemical group FC(Cl)(Cl)* 0.000 description 1
125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
125000006125 ethylsulfonyl group Chemical group 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
238000005469 granulation Methods 0.000 description 1
230000003179 granulation Effects 0.000 description 1
230000012010 growth Effects 0.000 description 1
239000003102 growth factor Substances 0.000 description 1
230000009931 harmful effect Effects 0.000 description 1
125000006343 heptafluoro propyl group Chemical group 0.000 description 1
125000005980 hexynyl group Chemical group 0.000 description 1
239000010903 husk Substances 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
125000001841 imino group Chemical group [H]N=* 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
DCYOBGZUOMKFPA-UHFFFAOYSA-N iron(2+);iron(3+);octadecacyanide Chemical compound [Fe+2].[Fe+2].[Fe+2].[Fe+3].[Fe+3].[Fe+3].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] DCYOBGZUOMKFPA-UHFFFAOYSA-N 0.000 description 1
125000005956 isoquinolyl group Chemical group 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000000787 lecithin Substances 0.000 description 1
235000010445 lecithin Nutrition 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 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
239000000463 material Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
239000011785 micronutrient Substances 0.000 description 1
235000013369 micronutrients Nutrition 0.000 description 1
239000011733 molybdenum Chemical class 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
229940042880 natural phospholipid Drugs 0.000 description 1
229920005615 natural polymer Polymers 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
JVJQPDTXIALXOG-UHFFFAOYSA-N nitryl fluoride Chemical compound [O-][N+](F)=O JVJQPDTXIALXOG-UHFFFAOYSA-N 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
125000005981 pentynyl group Chemical group 0.000 description 1
239000003209 petroleum derivative Substances 0.000 description 1
150000003904 phospholipids Chemical class 0.000 description 1
239000001007 phthalocyanine dye Substances 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000573 polyethylene 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
229960003351 prussian blue Drugs 0.000 description 1
239000013225 prussian blue Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000010453 quartz Substances 0.000 description 1
239000011435 rock Substances 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
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
238000004381 surface treatment Methods 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
238000010998 test method Methods 0.000 description 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 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
229960000278 theophylline Drugs 0.000 description 1
150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
125000000858 thiocyanato group Chemical group *SC#N 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
125000005034 trifluormethylthio group Chemical group FC(S*)(F)F 0.000 description 1
125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
239000011701 zinc Chemical class 0.000 description 1
229910052725 zinc Chemical class 0.000 description 1

Classifications

- 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

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Toxicology (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Agronomy & Crop Science (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)

JP60099759A 1984-05-16 1985-05-13 除草剤活性ヘテロアリールオキシアセトアミド類の作物植物による耐性を改良するためのアミド類の使用 Pending JPS60246302A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE3418167A DE3418167A1 (de)	1984-05-16	1984-05-16	Verwendung von amiden zur verbesserung der kulturpflanzen-vertraeglichkeit von herbizid wirksamen heteroaryloxyacetamiden
DE3418167.9		1984-05-16

Publications (1)

Publication Number	Publication Date
JPS60246302A true JPS60246302A (ja)	1985-12-06

Family

ID=6236005

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP60099759A Pending JPS60246302A (ja)	1984-05-16	1985-05-13	除草剤活性ヘテロアリールオキシアセトアミド類の作物植物による耐性を改良するためのアミド類の使用

Country Status (6)

Country	Link
JP (1)	JPS60246302A (it)
BR (1)	BR8502281A (it)
DE (1)	DE3418167A1 (it)
FR (1)	FR2564288A1 (it)
IT (1)	IT8520607A0 (it)
ZA (1)	ZA853686B (it)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2003528809A (ja) *	1999-07-30	2003-09-30	バイエルアクチェンゲゼルシャフト	除草性５−クロロジフルオロメチル−１，３，４−チアジアゾール−２−イル−オキシアセトアニリド類
JP2009534302A (ja) *	2006-03-22	2009-09-24	シンジェンタリミテッド	製剤
CN113336731A (zh) *	2020-03-02	2021-09-03	西湖大学	一种Flavagliness天然产物不对称多样性导向合成方法

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0236268A1 (de) *	1986-02-25	1987-09-09	Ciba-Geigy Ag	Halogenacylierte Amine zum Schützen von Kulturpflanzen vor der phytotoxischen Wirkung von stark wirksamen Halogenacyl-Herbiziden
CA1308352C (en) *	1986-08-15	1992-10-06	James V. Peck	Compositions comprising 1-oxohydrocarbyl-substituted azacyclohexanes
DE19546751B4 (de) *	1994-12-23	2005-02-17	Bayer Cropscience Ag	Selektive Herbizide auf Basis von Heteroaryloxy-acetamiden
SK287461B6 (sk)	2000-05-22	2010-10-07	Bayer Cropscience Ag	Prostriedok na ničenie nežiaducich rastlín, jeho použitie, spôsob ničenia a spôsob jeho výroby
DE10041619A1 (de)	2000-05-22	2001-11-29	Bayer Ag	Selektive Herbizide auf Basis von Heteroaryloxyacetamiden
BRPI0815591B8 (pt)	2007-08-22	2021-05-25	Astrazeneca Ab	composto, composição farmacêutica, e, uso de um composto.
TW201039825A (en)	2009-02-20	2010-11-16	Astrazeneca Ab	Cyclopropyl amide derivatives 983
FR2951447B1 (fr)	2009-10-19	2012-10-19	Rhodia Operations	Composes de type ether-amide et utilisattions
AU2011218491C1 (en)	2010-02-18	2015-05-14	Astrazeneca Ab	Processes for making cyclopropyl amide derivatives and intermediates associated therewith

1984
- 1984-05-16 DE DE3418167A patent/DE3418167A1/de not_active Withdrawn
1985
- 1985-05-07 IT IT8520607A patent/IT8520607A0/it unknown
- 1985-05-13 JP JP60099759A patent/JPS60246302A/ja active Pending
- 1985-05-15 ZA ZA853686A patent/ZA853686B/xx unknown
- 1985-05-15 BR BR8502281A patent/BR8502281A/pt unknown
- 1985-05-15 FR FR8507478A patent/FR2564288A1/fr not_active Withdrawn

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2003528809A (ja) *	1999-07-30	2003-09-30	バイエルアクチェンゲゼルシャフト	除草性５−クロロジフルオロメチル−１，３，４−チアジアゾール−２−イル−オキシアセトアニリド類
JP4936622B2 (ja) *	1999-07-30	2012-05-23	バイエルアクチェンゲゼルシャフト	除草性５−クロロジフルオロメチル−１，３，４−チアジアゾール−２−イル−オキシアセトアニリド類
JP2009534302A (ja) *	2006-03-22	2009-09-24	シンジェンタリミテッド	製剤
CN113336731A (zh) *	2020-03-02	2021-09-03	西湖大学	一种Flavagliness天然产物不对称多样性导向合成方法

Also Published As

Publication number	Publication date
BR8502281A (pt)	1986-01-14
IT8520607A0 (it)	1985-05-07
ZA853686B (en)	1985-12-24
FR2564288A1 (fr)	1985-11-22
DE3418167A1 (de)	1985-11-21

Publication	Publication Date	Title
JP3728324B2 (ja)	2005-12-21	１−置換−４−カルバモイル−１，２，４−トリアゾール−５−オン誘導体及び除草剤
JPH03190859A (ja)	1991-08-20	２―イミノピリジン誘導体、その製法及び該誘導体からなる除草剤
MXPA02001459A (es)	2002-07-02	Fungicidas.
JPH0717620B2 (ja)	1995-03-01	６‐クロロベンゾアゾリルオキシアセトアミド
DE4228000A1 (de)	1994-03-03	3-Aryl-triazin-2,4-dione
JPH04283578A (ja)	1992-10-08	置換スルホニルアミノトリアゾリルピリミジン
JPH04305577A (ja)	1992-10-28	置換ピリジン類
JP2641518B2 (ja)	1997-08-13	ハロゲン化チアジアゾリル−オキシ酢酸アミド、その製造方法及び新規中間体並びに除草剤としてのその使用
JPH0369906B2 (it)	1991-11-05
EP0459243A2 (de)	1991-12-04	Substituierte Azine
JP2909098B2 (ja)	1999-06-23	ジフルオロメチル‐チアジアゾリル‐オキシアセトアミドの選択除草剤としての使用
DE69110157T2 (de)	1995-10-19	Iminothiazoline, ihre Herstellung und Anwendung als Herbizide und Zwischenprodukte für ihre Herstellung.
JPS5933273A (ja)	1984-02-23	置換３−トリクロロメチル−１，２，４−チアジアゾ−ル−５−イル−オキシアセタミド、その製法及び農薬
US4384881A (en)	1983-05-24	Herbicidally active novel benzazol-2-yloxyacetanilides
JPH0245479A (ja)	1990-02-15	置換チアジアゾリルオキシアセトアミド
JPH04234352A (ja)	1992-08-24	スルホニル化（チオ）カルバミン酸に基づく除草剤
JPS6326757B2 (it)	1988-05-31
JPS6314711B2 (it)	1988-04-01
JPH0358974A (ja)	1991-03-14	２ｈ―ピリダジノン誘導体
EP0510479A1 (de)	1992-10-28	7-Chlor-Benzthiazolyloxyacetamide
JPS63287782A (ja)	1988-11-24	アネル化（チオ）ヒダントイン類
JPS6314713B2 (it)	1988-04-01
JPH029588B2 (it)	1990-03-02
JPS58126872A (ja)	1983-07-28	置換フエニルスルホニルウレア誘導体、その製法及び除草剤
JPH0393771A (ja)	1991-04-18	Ｎ―（５―アルキルチオフエニル）置換された窒素複素環類