Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
KR910019996A - 시클로헥센온 옥심 에테르, 그것의 제조방법 및 제초제로서의 이용 - Google Patents
[go: Go Back, main page]

KR910019996A - 시클로헥센온 옥심 에테르, 그것의 제조방법 및 제초제로서의 이용 - Google Patents

시클로헥센온 옥심 에테르, 그것의 제조방법 및 제초제로서의 이용 Download PDF

Info

Publication number
KR910019996A
KR910019996A KR1019910007479A KR910007479A KR910019996A KR 910019996 A KR910019996 A KR 910019996A KR 1019910007479 A KR1019910007479 A KR 1019910007479A KR 910007479 A KR910007479 A KR 910007479A KR 910019996 A KR910019996 A KR 910019996A
Authority
KR
South Korea
Prior art keywords
alkyl
alkoxy
group
halogen
substituted
Prior art date
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.)
Granted
Application number
KR1019910007479A
Other languages
English (en)
Other versions
KR0175318B1 (ko
Inventor
미슬리츠 울프
메이어 노르베르트
카스트 위르겐
괴츠 노르베르트
하르로이스 알브레히트
뷔르쩌 브루노
발터 헬무트
베스트팔렌 카를-오토
게르버 마트히아스
Original Assignee
라이싱어, 바르츠
바스프 악티엔게젤샤프트
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.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=25893053&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=KR910019996(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from DE4014986A external-priority patent/DE4014986A1/de
Priority claimed from DE4033423A external-priority patent/DE4033423A1/de
Application filed by 라이싱어, 바르츠, 바스프 악티엔게젤샤프트 filed Critical 라이싱어, 바르츠
Publication of KR910019996A publication Critical patent/KR910019996A/ko
Application granted granted Critical
Publication of KR0175318B1 publication Critical patent/KR0175318B1/ko
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/14Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N35/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
    • A01N35/08Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen
    • A01N35/10Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen containing a carbon-to-nitrogen double bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C239/00Compounds containing nitrogen-to-halogen bonds; Hydroxylamino compounds or ethers or esters thereof
    • C07C239/08Hydroxylamino compounds or their ethers or esters
    • C07C239/20Hydroxylamino compounds or their ethers or esters having oxygen atoms of hydroxylamino groups etherified
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/04Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no 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
    • C07D309/06Radicals substituted by oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D335/00Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom
    • C07D335/02Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/12Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/16Systems containing only non-condensed rings with a six-membered ring the ring being unsaturated

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (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)
  • Pest Control & Pesticides (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pyridine Compounds (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Furan Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

내용 없음

Description

시클로헥센온 옥심 에테르, 그것의 제조방법 및 제조체로서의 이용
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (7)

  1. 다음 일반식(Ⅰ)의 시클로헥센은 옥심 에테르, 및 그것의 농업적으로 유용한 염 및 C1-C10-카르복실산과 무기산의 에스테르:
  2. 상기식에서, R1은 C1-C5-알킬이고; A는 비치환된 또는 C1-C3-알킬-치환된 C3-C5-알킬렌 또는 C4-C5-알켄일렌 사슬이며 그중 메틸렌기는 산소원자, 황원자, 술폭실기, 술포닐기 또는 -N(Ra)-로 치환되는데 Ra는 수소, C1-C4-알킬, C3-C6-알켄일 또는 C3-C6-알킨일이고, Z는 페닐, 3개의 질소원자와 하나의 산소 또는 황원자로 이루어지는 군으로부터 선택되는 1내지 3개의 헤테로 원자를 가지고 있는 5-원 헤테로 방향족 구조 또는 1내지 4개의 질소원자를 가지고 있는 6-원 헤테로 방향족구조이며; X는 아미녹 -NRaRb로서 Ra는 수소, C1-C4-알킬, C3-C6-알켄일 또는 C3-C6-알킨일이고, Rb는 수소, C1-C4-알킬, C3-C6-알켄일 또는 C1-C6-알킨일, C1-C6-아실 또는 벤조일(여기서 방향족 고리는 니트로, 시아노, 할로겐, C1-C4-알킬, C1-C|4-알콕시, C1-C4-알킬티오 및 C1-C4-할로알킬로 이루어지는 군으로부터 선택된 1내지 3개의 치환기로 치환될수 있다)이며: 니트로 시아노, 할로겐, C1-C4-알킬, 부분적으로 또는 완전히 할로겐화된 할로겐이며, C1-C4-알킬, C1-C4-알콕시, C1-C4-알킬티오 부분적으로 또는 완전히 할로겐화된 C1-C4-알콕시, 카르복실, C1-C4-알콕시카르보닐, 벤질옥시카르보닐 또는 페닐(여기서 방향족 라디칼은 부가적으로 다음 치환기; 니트로, 시아노, 할로겐, C1-C4-알킬, 부분적으로 또는 완전히 할로겐화된 C1-C4-알킬, C1-C4-알콕시, C1-C4-알킬티오 부분적으로 또는 완전히 할로겐화된 C1-C4-알콕시, 카르복실, C1-C4-알콕시카르보닐, 벤질옥시카르보닐 중 1개 내지 3개로 치환될 수 있다)이며; n은 0내지 3거나 또는 Z가 할로겐인 경우 1내지 5이고; R2는 C1-C4-알콕시-C1-C6-알킬 또는 C1-C4-알킬티오-C1-C6-알킬; C3-C7-시클로알킬 또는 C5-C7-시클롤알켄일 이들 기는 C1-C4-알킬, C1-C4-알콕시, C1-C|4-알킬티오, 부분적으로 또는 완전히 하로겐화된 C1-C4-알킬, 히들록시및 할로겐으로 이루어진 군으로부터 선택된 1개 내지 3개의 치환기로 치환될수 있으며; 산소 또는 황으로 이루어진 군으로부터 선택된 1개 내또는 2개의 헤테로 원자를 함유하는 5-원 포화 헤테로고리 구조로서 이헤테로구조는 부가적으로 C1-C4-알킬, C1-C4-알콕시, C1-C4-알킬티오 및 부분적으로 똔느 완전히 할로겐화된 C1-C4-알킬로 이루어진 군으로부터 선택된 1내지 3개의 라디칼로 치환될수 있고; 산소 및 황으로 이루어진 군으로부터 선택된 1 또는 2개의 헤테로 원자들을 함유하는 6-원자 또는 7-원자 포화 또는 단일-또는 이중-불포화 헤테로고리구조로서 이 헤테로고리 구조는 부가적으로 히드록실, 할로겐, C1-C4-알킬, C1-C4-알콕시, C1-C4-알킬티오, 부분적으로 또는 완전히 할로겐화된 C2-C6-알켄일 및 C1-C4-알콕-시C1-C4-알킬로 이루어진 군으로부터 선택된 1내지 3개의 라디칼로 치환될수 있고; 또는 R2는 페닐 또는 피리딜로서 이들 기는 부가적으로 할로겐, 니트로, 시아노, C1-C4-알킬, C1-C4-알콕시, 부분적으로 또는 완전히 할로겐화된 C1-C4-알킬, C3-C6-알켄일옥시, C3-C6-알킨일옥시 및 -NRaRb), RaRb는 상기 정의된 바와 같다)로 이루어지는 군으로부터 선택된 1내지 3개의 라디칼로 치환될수 있다
  3. 제1항에 있어서, Z가 페닐인 것을 특징으로 하는 시클로헥센온 옥심 에테르
  4. 제1항의 일반식(Ⅰ)의 화합물중 최소한 하나의 제초적 유효량과 비활성 첨가제를 함유하고 있는 제초조성물
  5. 바람직하지 않은 식물 및/또는 그것의 자생기를 제1항의 일반식(Ⅰ)의 시클로헥산온 유도체의 제초적 유효량으로 처리하는 것으로 이루어지는, 바람직하지 않은 식물의 성장 억제방법
  6. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019910007479A 1990-05-09 1991-05-09 시클로헥센온 옥심 에테르, 이것의 제조방법 및 이것을 제초제로서 사용하는 방법 Expired - Lifetime KR0175318B1 (ko)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
DE4014986A DE4014986A1 (de) 1990-05-09 1990-05-09 Cyclohexenonoximether, verfahren zu ihrer herstellung und ihre verwendung als herbizide
DEP4014986.2 1990-05-09
DE4033423A DE4033423A1 (de) 1990-10-20 1990-10-20 Cyclohexenonoximether, verfahren zu ihrer herstellung und ihre verwendung als herbizide
DEP40334236 1990-10-20
DEP4033423.6 1990-10-20

Publications (2)

Publication Number Publication Date
KR910019996A true KR910019996A (ko) 1991-12-19
KR0175318B1 KR0175318B1 (ko) 1999-02-18

Family

ID=25893053

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019910007479A Expired - Lifetime KR0175318B1 (ko) 1990-05-09 1991-05-09 시클로헥센온 옥심 에테르, 이것의 제조방법 및 이것을 제초제로서 사용하는 방법

Country Status (11)

Country Link
US (1) US5190573A (ko)
EP (1) EP0456112B1 (ko)
JP (1) JP3083865B2 (ko)
KR (1) KR0175318B1 (ko)
AT (1) ATE110708T1 (ko)
BR (1) BR9101868A (ko)
CA (1) CA2041835C (ko)
DE (1) DE59102689D1 (ko)
ES (1) ES2058983T3 (ko)
RU (1) RU2092484C1 (ko)
UA (1) UA34414C2 (ko)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4014984A1 (de) * 1990-05-09 1991-11-14 Basf Ag Cyclohexenonoximether, verfahren und zwischenprodukte zu ihrer herstellung und ihre verwendung als herbizide
US5604183A (en) * 1991-08-09 1997-02-18 Basf Aktiengesellschaft Cyclohexenone oxime ethers
DE4201720A1 (de) * 1992-01-23 1993-07-29 Basf Ag Thiochromenonderivate als antidots und sie enthaltende herbizide mittel
DE4204204A1 (de) * 1992-02-13 1993-08-19 Basf Ag Mischungen aus optisch aktiven cyclohexenonoximethern, verfahren und zwischenprodukte zu ihrer herstellung und ihre verwendung als herbizide
DE4204203A1 (de) * 1992-02-13 1993-08-19 Basf Ag Cyclohexenonoximether, verfahren zu ihrer herstellung und ihre verwendung als herbizide
DE4204206A1 (de) * 1992-02-13 1993-08-19 Basf Ag Mischungen aus optisch aktiven cyclohexenonoximethern, verfahren und zwischenprodukte zu ihrer herstellung und ihre verwendung als herbizide
DE4204205A1 (de) * 1992-02-13 1993-08-19 Basf Ag Cyclohexenonoximether, verfahren zu ihrer herstellung und ihre verwendung als herbizide
DE4227896A1 (de) * 1992-08-22 1994-02-24 Basf Ag Cyclohexenonoximether, ihre Herstellung und ihre Verwendung
DE4244390A1 (de) * 1992-12-29 1994-06-30 Basf Ag Verfahren zur Herstellung von Oximino-Derivaten und neue Oximino-Derivate
WO1994026696A1 (en) * 1993-05-11 1994-11-24 Dunlena Pty. Limited Herbicidal cyclohexanes
DE19510183A1 (de) * 1994-03-31 1995-10-05 Basf Ag 5-(Sulf-/Carbamoylmethyl)-cyclohexenonoximether
CA2187440A1 (en) * 1994-04-08 1995-10-19 John J. Kilama Herbicidal bicyclic and tricyclic imides
DE4415871A1 (de) * 1994-05-05 1995-11-09 Basf Ag O-(Oxyimino)ethyl-Cyclohexenonoximether und deren Verwendung als Herbizide
DE19506570A1 (de) * 1995-02-24 1996-08-29 Basf Ag 5-Tetrahydropyranon-Cyclohexenonoximether und deren Verwendung als Herbizide
RO119106B1 (ro) * 1995-09-20 2004-04-30 Basf Aktiengesellschaft Compoziţie erbicidă şi utilizarea acesteia
DE19545212A1 (de) * 1995-12-05 1997-06-12 Basf Ag Cyclohexenonoximether-Metallsalze
CA2277019A1 (en) * 1997-01-09 1998-07-16 Basf Aktiengesellschaft 5-(dioxabicyclohept-6-yl)-cyclohexenone oxime ethers, their preparation and their use
DE10045131A1 (de) * 2000-09-13 2002-03-21 Basf Ag Verfahren zur Herstellung eines Cyclohexenonoximether-Lithiumsalzes, damit erhältliche Produkte, deren Verwendung sowie entsprechende Pflanzenschutzmittel
DE10142336A1 (de) * 2001-08-30 2003-03-20 Bayer Cropscience Ag Selektive Herbizide enthaltend ein Tetrazolinon-Derivat
EP1382247A1 (en) 2002-07-18 2004-01-21 Bayer CropScience GmbH Combinations of cyclohexanedione oxime herbicides and safeners
EP2052605A1 (de) 2007-10-24 2009-04-29 Bayer CropScience AG Herbizid-Kombination
DE102008037632A1 (de) 2008-08-14 2010-02-18 Bayer Cropscience Ag Herbizid-Kombination mit Dimethoxytriazinyl-substituierten Difluormethansulfonylaniliden
TR201900122T4 (tr) * 2009-10-28 2019-02-21 Dow Agrosciences Llc Fluroksipir ve profoksidim içeren sinerjistik herbisit bileşimi.
DE102013006328A1 (de) * 2013-04-11 2014-10-16 Daimler Ag Halteanordnung eines Stoßfängers an einem Bauelement eines Personenkraftwagens sowie Leuchteinheit für einen Personenkraftwagen
CN115417791B (zh) * 2022-09-23 2023-10-27 郑州手性药物研究院有限公司 一种肟醚类1,3-环己二酮化合物及其合成方法和应用

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4440566A (en) * 1982-08-05 1984-04-03 Chevron Research Company Herbicidal substituted 2-(1-(oxyamino)-alkylidene)-cyclohexane-1,3-diones
NZ202284A (en) * 1981-11-20 1986-06-11 Ici Australia Ltd 2-(1-(alkoxyimino)alkyl)-3-hydroxy-5-poly(methyl)phenyl-cyclohex-2-en-1-ones and herbicidal compositions
NZ207964A (en) * 1983-05-06 1987-03-31 Ici Australia Ltd 5-heteroaryl-cyclohexane-1,3-dione derivatives
DE3514798A1 (de) * 1984-08-22 1986-03-06 Bayer Ag, 5090 Leverkusen 2,4-bis-(alkoximinoalkyl)-cyclohexan-1,3-dione
DE3437238A1 (de) * 1984-10-11 1986-04-17 Basf Ag, 6700 Ludwigshafen Neue verbindungen, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses
DE3536117A1 (de) * 1985-10-10 1987-04-16 Basf Ag Cyclohexenonderivate, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses
DE3600642A1 (de) * 1986-01-11 1987-07-16 Basf Ag Cyclohexenonderivate, verfahren zu ihrer herstellung und ihre verwendung als herbizide mittel
DE3609181A1 (de) * 1986-03-19 1987-09-24 Basf Ag Cyclohexenonderivate, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwachstums
DE3808072A1 (de) * 1988-03-11 1989-09-21 Basf Ag Cyclohexenonverbindungen, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses
US5034047A (en) * 1988-09-30 1991-07-23 Basf Aktiengesellschaft Cyclohexenone derivatives and their use as herbicides
DE3838309A1 (de) * 1988-11-11 1990-05-31 Basf Ag Cyclohexenonoximether, verfahren zu ihrer herstellung und ihre verwendung als herbizid

Also Published As

Publication number Publication date
EP0456112A1 (de) 1991-11-13
CA2041835C (en) 2001-11-27
EP0456112B1 (de) 1994-08-31
JP3083865B2 (ja) 2000-09-04
UA34414C2 (uk) 2001-03-15
US5190573A (en) 1993-03-02
DE59102689D1 (de) 1994-10-06
ES2058983T3 (es) 1994-11-01
KR0175318B1 (ko) 1999-02-18
ATE110708T1 (de) 1994-09-15
JPH04225943A (ja) 1992-08-14
RU2092484C1 (ru) 1997-10-10
CA2041835A1 (en) 1991-11-10
BR9101868A (pt) 1991-12-17

Similar Documents

Publication Publication Date Title
KR910019996A (ko) 시클로헥센온 옥심 에테르, 그것의 제조방법 및 제초제로서의 이용
KR910009640A (ko) 헤테로고리옥시 페녹시아세트산유도체 및 제초제로서의 그의 용도
DK117087A (da) Heterocycliske forbindelser, deres fremstilling oganvendelse som insekticider
KR900004718A (ko) 방향족 카르복실산유도체 및 바람직하지 않은 식물생장을 억제하는 이들 화합물의 용도
KR910019994A (ko) 시클로헥센온 옥심 에테르, 이들의 제조방법, 이들의 제조를 위한 중간체 및 이들의 제초제로서의 용도
KR930009997A (ko) 히드록시피리돈카르복스아미드, 그의 제조 방법 및 용도
GB1503077A (en) Quaternary imidazolium compounds and their use as microbicides
FI844225A0 (fi) Griseolinsyraderivat och deras anvaendning.
KR830004266A (ko) 호모세린 유도체의 제조방법과 살균제로서의 사용
JPS5283432A (en) Preparation and applications of 3-(2-aryl-2-propyl) urea derivatives
KR910019995A (ko) 시클로헥센온 옥심 에테르, 이들의 제조 및 제초제로서 이들의 사용
SU940629A3 (ru) Способ регулировани роста растений
ES468658A1 (es) Un procedimiento para preparar 4-alcohiltio-2-trifluorome- tilalcanosulfonanilidas y sus derivados
ATE112769T1 (de) Benzoxazepinderivate.
ES364921A1 (es) Procedimiento para la preparacion de nuevos derivados de s-triacina.
FI853866A0 (fi) 2-pyridin-tiol-derivat, foerfarande foer framstaellning av dessa samt farmaceutiska foereningar innehaollande dessa.
KR870000298A (ko) 심장혈관의 병 치료용 1,4-디하이드로피리딘 유도체의 제법
FI875749A0 (fi) Amider av eikosatetraynolsyra och deras anvaendning i laekemedel och kosmetik.
SE8001981L (sv) Kompositioner for behandling av glaukom
ES8502700A1 (es) Procedimiento para la fabricacion de derivados de tetrahidrobenzotiazol.
KR900003153A (ko) 신규 치환 2-아릴옥시 및 2-아릴티오트리아진 유도체, 그의 제조방법 및 제초제 및 식물 성장 조절제로서 그의 용도
ES352463A1 (es) Procedimiento de obtencion de un producto para combatir ma-lezas, especialmente para empleo en la viticultura.
KR950026860A (ko) 4-히드록시 피라졸을 함유한 프로페노익 에스테르 유도체
KR920000707A (ko) 제초성 화합물
JPS54122727A (en) Fungicidal, antiseptic, anti-termitic agent

Legal Events

Date Code Title Description
PA0109 Patent application

Patent event code: PA01091R01D

Comment text: Patent Application

Patent event date: 19910509

PG1501 Laying open of application
A201 Request for examination
PA0201 Request for examination

Patent event code: PA02012R01D

Patent event date: 19960201

Comment text: Request for Examination of Application

Patent event code: PA02011R01I

Patent event date: 19910509

Comment text: Patent Application

E902 Notification of reason for refusal
PE0902 Notice of grounds for rejection

Comment text: Notification of reason for refusal

Patent event date: 19980526

Patent event code: PE09021S01D

E701 Decision to grant or registration of patent right
PE0701 Decision of registration

Patent event code: PE07011S01D

Comment text: Decision to Grant Registration

Patent event date: 19980821

GRNT Written decision to grant
PR0701 Registration of establishment

Comment text: Registration of Establishment

Patent event date: 19981110

Patent event code: PR07011E01D

PR1002 Payment of registration fee

Payment date: 19981110

End annual number: 3

Start annual number: 1

PG1601 Publication of registration
PR1001 Payment of annual fee

Payment date: 20011024

Start annual number: 4

End annual number: 4

PR1001 Payment of annual fee

Payment date: 20021022

Start annual number: 5

End annual number: 5

PR1001 Payment of annual fee

Payment date: 20031106

Start annual number: 6

End annual number: 6

PR1001 Payment of annual fee

Payment date: 20041025

Start annual number: 7

End annual number: 7

PR1001 Payment of annual fee

Payment date: 20051025

Start annual number: 8

End annual number: 8

PR1001 Payment of annual fee

Payment date: 20061026

Start annual number: 9

End annual number: 9

PR1001 Payment of annual fee

Payment date: 20071026

Start annual number: 10

End annual number: 10

PR1001 Payment of annual fee

Payment date: 20081024

Start annual number: 11

End annual number: 11

PR1001 Payment of annual fee

Payment date: 20091022

Start annual number: 12

End annual number: 12

FPAY Annual fee payment

Payment date: 20101108

Year of fee payment: 13

PR1001 Payment of annual fee

Payment date: 20101108

Start annual number: 13

End annual number: 13

EXPY Expiration of term
PC1801 Expiration of term

Termination date: 20121009

Termination category: Expiration of duration