GB1521940A - Enolate salts - Google Patents

Enolate salts

Info

Publication number
GB1521940A
GB1521940A GB42535/77A GB4253577A GB1521940A GB 1521940 A GB1521940 A GB 1521940A GB 42535/77 A GB42535/77 A GB 42535/77A GB 4253577 A GB4253577 A GB 4253577A GB 1521940 A GB1521940 A GB 1521940A
Authority
GB
United Kingdom
Prior art keywords
enolate salts
enolate
salts
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.)
Expired
Application number
GB42535/77A
Other languages
English (en)
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.)
Commonwealth Scientific and Industrial Research Organization CSIRO
Original Assignee
Commonwealth Scientific and Industrial Research Organization CSIRO
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
Application filed by Commonwealth Scientific and Industrial Research Organization CSIRO filed Critical Commonwealth Scientific and Industrial Research Organization CSIRO
Publication of GB1521940A publication Critical patent/GB1521940A/en
Expired legal-status Critical Current

Links

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
    • C07D307/38—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 substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D307/40—Radicals substituted by oxygen atoms
    • C07D307/42—Singly bound oxygen atoms
    • 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
    • A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00—Carboxylic acid nitriles
    • 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
    • C07D307/38—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 substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D307/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
    • C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
    • C07D317/60—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Dentistry (AREA)
  • Wood Science & Technology (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Agronomy & Crop Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
  • Furan Compounds (AREA)
GB42535/77A 1975-11-26 1976-11-19 Enolate salts Expired GB1521940A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
AU407875 1975-11-26

Publications (1)

Publication Number Publication Date
GB1521940A true GB1521940A (en) 1978-08-16

Family

ID=3694538

Family Applications (2)

Application Number Title Priority Date Filing Date
GB42535/77A Expired GB1521940A (en) 1975-11-26 1976-11-19 Enolate salts
GB48335/76A Expired GB1521939A (en) 1975-11-26 1976-11-19 Insecticidal esters and intermediates for use in preparing the same

Family Applications After (1)

Application Number Title Priority Date Filing Date
GB48335/76A Expired GB1521939A (en) 1975-11-26 1976-11-19 Insecticidal esters and intermediates for use in preparing the same

Country Status (5)

Country Link
US (3) US4220591A (enExample)
JP (3) JPS5921858B2 (enExample)
CH (3) CH634818A5 (enExample)
DE (2) DE2660606C2 (enExample)
GB (2) GB1521940A (enExample)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6545173B1 (en) 1995-12-02 2003-04-08 Abbott Laboratories Process for the preparation of 1-aryl-1-cyanocyclobutane derivatives

Families Citing this family (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU4244478A (en) * 1977-12-19 1979-06-28 Commw Scient Ind Res Org Cyclobutane carboxylic acids and esters and insecticides
AU526817B2 (en) * 1978-06-21 1983-02-03 Ici Australia Limited Pesticides
DE2965744D1 (en) * 1978-10-27 1983-07-28 Ici Plc Process for separating optical isomers of substituted cyclopropane carboxylic acids; amine salts of substituted cyclopropane carboxylic acids; a substituted cyclopropane carboxylic acid
AU525002B2 (en) 1978-12-04 1982-10-14 Commonwealth Scientific And Industrial Research Organisation Insecticidal substituted cyclopropane and cyclobutane derivatives
JPS6016922B2 (ja) * 1980-04-25 1985-04-30 日本化薬株式会社 殺虫組成物
DE3025218A1 (de) * 1980-07-03 1982-02-11 Bayer Ag, 5090 Leverkusen 1-aryl-cyclopropan-1-carbonsaeureester, verfahren zu deren herstellung und deren verwendung in schaedlingsbekaempfungsmitteln
US4390715A (en) * 1980-07-18 1983-06-28 Commonwealth Scientific And Industrial Research Organization Pentafluorobenzyl esters
JPS57144208A (en) * 1981-03-04 1982-09-06 Nippon Kayaku Co Ltd Insecticide composition
JPS57144207A (en) * 1981-03-04 1982-09-06 Nippon Kayaku Co Ltd Expellent against noxious insect for rice plant
US4362744A (en) * 1981-03-19 1982-12-07 Fmc Corporation Trans-3-substituted-1-indanol insecticidal ester derivatives
JPS57167906A (en) * 1981-04-08 1982-10-16 Nippon Kayaku Co Ltd Insecticidal composition
DE3128444A1 (de) * 1981-07-18 1983-02-03 Bayer Ag, 5090 Leverkusen Substituierte phenyl-cyclopropancarbonsaeureester, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
US4418202A (en) * 1981-12-21 1983-11-29 Emery Industries, Inc. 2-Vinyl- and 2-ethylcyclopropane monocarboxylates
EP0291626A3 (en) 1982-11-22 1989-05-31 E.I. Du Pont De Nemours And Company Process for the preparation of optically-active cyanomethyl esters
JPS59155350A (ja) * 1983-02-24 1984-09-04 Nippon Kayaku Co Ltd 高活性なα−シアノ−ｍ−フエノキシベンジル−２，２−ジクロル−１−（ｐ−エトキシフエニル）シクロプロパンカルボン酸エステルの光学異性体混合物、その製造方法およびそれを有効成分として含有する殺虫剤
NZ207293A (en) * 1983-03-02 1987-03-31 Commw Scient Ind Res Org Cyclobutane carboxylic acid esters and pesticidal compositions
US4704156A (en) * 1986-05-07 1987-11-03 Eli Lilly And Company Method for plant growth regulation
DE3824433A1 (de) * 1988-07-19 1990-01-25 Bayer Ag, 5090 Leverkusen Fluorcyclopropyl-derivate
DE3824432A1 (de) * 1988-07-19 1990-03-22 Bayer Ag 2,2-difluorcyclopropyl-derivate
US5264632A (en) * 1988-07-19 1993-11-23 Bayer Aktiengesellschaft 2,2-difluorocyclopropyl derivatives
JPH03236364A (ja) * 1990-08-09 1991-10-22 Nippon Kayaku Co Ltd 高活性なα―シアノ―ｍ―フェノキシベンジル―２，２―ジクロル―１―（ｐ―エトキシフェニル）シクロプロパンカルボン酸エステルの光学異性体混合物、その製造方法およびそれを有効成分として含有する殺虫剤
DE4041540A1 (de) * 1990-12-22 1992-06-25 Huels Chemische Werke Ag Verfahren zur herstellung von 2-phenylcyclopropancarbonsaeurebutylestern
DE4142190A1 (de) * 1991-12-20 1993-06-24 Bayer Ag Verfahren zur herstellung von optisch aktiven (alpha)-hydroxycarbonsaeuren
US5352820A (en) * 1993-06-28 1994-10-04 Levin Jeremy I Expedient route to aryl propenoic esters
DE10007411A1 (de) 2000-02-18 2001-08-23 Bayer Ag Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
AR029677A1 (es) * 2000-06-29 2003-07-10 Bayer Ag Combinaciones de compuestos activos con propiedades insecticidas y acaricidas
DE102004001271A1 (de) 2004-01-08 2005-08-04 Bayer Cropscience Ag Wirkstoffkombinationen mit insektiziden Eigenschaften
DE102004006324A1 (de) * 2004-02-10 2005-08-25 Bayer Cropscience Ag Wirkstoffkombinationen mit insektiziden Eigenschaften
CN1332930C (zh) * 2005-08-05 2007-08-22 中国科学院上海有机化学研究所 制备乙氰菊酯前体的方法
US20090281157A1 (en) * 2006-07-11 2009-11-12 Bayer Cropscience Ag Active Ingredient Combinations With Insecticidal and Acaricidal Properties
DE102006046688B3 (de) * 2006-09-29 2008-01-24 Siemens Ag Kälteanlage mit einem warmen und einem kalten Verbindungselement und einem mit den Verbindungselementen verbundenen Wärmerohr
EP2068633A1 (de) * 2006-09-30 2009-06-17 Bayer CropScience Aktiengesellschaft Suspensionskonzentrate zur verbesserung der wurzelaufnahme von agrochemischen wirkstoffen
CN1970535B (zh) * 2006-12-01 2012-05-30 中国科学院上海有机化学研究所 乙氰菊酯的光活异构体的制备方法
EP2039248A1 (de) * 2007-09-21 2009-03-25 Bayer CropScience AG Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
DE102007045953B4 (de) 2007-09-26 2018-07-05 Bayer Intellectual Property Gmbh Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
CA2723616C (en) * 2008-05-07 2017-10-31 Bayer Cropscience Ag Synergistic combinations comprising a sulfoximine insecticide
EP2127522A1 (de) 2008-05-29 2009-12-02 Bayer CropScience AG Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
KR101647706B1 (ko) 2009-03-25 2016-08-11 바이엘 인텔렉쳐 프로퍼티 게엠베하 살충 및 살비성을 지니는 활성 성분 배합물
EP2382865A1 (de) 2010-04-28 2011-11-02 Bayer CropScience AG Synergistische Wirkstoffkombinationen

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH407989A (de) * 1960-03-25 1966-02-28 Ceskoslovenska Akademie Ved Verfahren zur Herstellung von 2,2-Dihalogencyclopropancarbonsäuren
US3068283A (en) * 1960-12-05 1962-12-11 Smith Kline French Lab (2-phenylcyclopropyl)-ureas, and 2-phenylcyclopropylcarbamoylamines
GB1168797A (en) * 1965-12-09 1969-10-29 Nat Res Dev Cyclopropane Carboxylic Acid Derivatives and their use as Insecticides
US3442935A (en) * 1967-06-30 1969-05-06 Exxon Research Engineering Co Direct production of acrylate esters from acrylic acids
US3669989A (en) * 1968-06-13 1972-06-13 Sumitomo Chemical Co Cyclopropanecarboxylic acid esters
US3674832A (en) * 1968-08-22 1972-07-04 Schering Corp Cyclopropane carboxylic acid derivatives
US3666789A (en) * 1969-05-21 1972-05-30 Sumitomo Chemical Co Cyclopropanecarboxylic acid esters
NL7112938A (enExample) * 1970-09-30 1972-04-05
GB1323183A (en) * 1971-01-14 1973-07-11 Bdh Pharmaceuticals Ltd Cyclopropane esters and acids thereof
JPS515450B1 (enExample) * 1971-06-29 1976-02-20
US3857880A (en) * 1971-07-20 1974-12-31 Schering Corp Cyclopropane carboxylic acid derivatives
US3803254A (en) * 1972-07-27 1974-04-09 Mitsubishi Chem Ind Process for producing oligomers of unsaturated compounds
SU655700A1 (ru) * 1976-01-04 1979-04-05 Предприятие П/Я А-3103 Способ получени алкиловых эфиров -фенилакриловой кислоты
GB1580193A (en) * 1976-04-22 1980-11-26 Nat Res Dev Phenyl acetic acid derivatives
US4105780A (en) * 1977-03-03 1978-08-08 American Cyanamid Company Insecticidal and acaricidal m-phenoxybenzyl esters of 2,2-difluoro-1,3-benzodioxole-5-(α-alkyl)acetic acids

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6545173B1 (en) 1995-12-02 2003-04-08 Abbott Laboratories Process for the preparation of 1-aryl-1-cyanocyclobutane derivatives

Also Published As

Publication number Publication date
JPS56142237A (en) 1981-11-06
JPS5283354A (en) 1977-07-12
CH634818A5 (de) 1983-02-28
JPS6021574B2 (ja) 1985-05-28
US4262014A (en) 1981-04-14
GB1521939A (en) 1978-08-16
JPS5921858B2 (ja) 1984-05-22
CH634817A5 (de) 1983-02-28
JPS5521011B2 (enExample) 1980-06-06
US4309350A (en) 1982-01-05
DE2660606C2 (de) 1984-08-02
DE2653189A1 (de) 1977-06-08
DE2653189C2 (de) 1985-02-14
JPS5470423A (en) 1979-06-06
US4220591A (en) 1980-09-02
CH634816A5 (de) 1983-02-28

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Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]
PE20 Patent expired after termination of 20 years

Effective date: 19961118