DD146286A5 - Verfahren zur herstellung neuer substituierter phenoxybenzyloxycarbonylderivate - Google Patents

Verfahren zur herstellung neuer substituierter phenoxybenzyloxycarbonylderivate Download PDF

Info

Publication number: DD146286A5
Authority: DD; German Democratic Republic
Prior art keywords: spp; vinyl; halogen; berlin; fluoro
Prior art date: 1977-07-06

Application number

DD78215933A

Other languages

German (de)

English (en)

Inventor

Rainer Fuchs

Ingeborg Hammann

Wilhelm Stendel

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.)

1977-07-06

Filing date

1978-07-04

Publication date

1981-02-04

1978-07-04 Application filed by Bayer Ag filed Critical Bayer Ag

1981-02-04 Publication of DD146286A5 publication Critical patent/DD146286A5/de

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-1 PHENOXYBENZYLOXYCARBONYL Chemical class 0.000 title claims abstract description 36
238000000034 method Methods 0.000 title description 14
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 9
239000001257 hydrogen Substances 0.000 claims abstract description 9
229910052736 halogen Inorganic materials 0.000 claims abstract description 8
150000002367 halogens Chemical class 0.000 claims abstract description 8
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 7
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 6
125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims abstract description 5
125000000217 alkyl group Chemical group 0.000 claims abstract description 3
150000002825 nitriles Chemical group 0.000 claims abstract description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 2
239000000460 chlorine Substances 0.000 claims description 24
239000002904 solvent Substances 0.000 claims description 14
239000002253 acid Substances 0.000 claims description 12
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 8
229910052801 chlorine Inorganic materials 0.000 claims description 8
YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical class OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 claims description 7
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
229910052794 bromium Inorganic materials 0.000 claims description 4
125000005843 halogen group Chemical group 0.000 claims description 4
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238000002360 preparation method Methods 0.000 abstract description 3
102100029095 Exportin-1 Human genes 0.000 abstract 1
101100242909 Streptococcus pneumoniae (strain ATCC BAA-255 / R6) pbpA gene Proteins 0.000 abstract 1
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AGEZXYOZHKGVCM-UHFFFAOYSA-N benzyl bromide Chemical compound BrCC1=CC=CC=C1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 description 11
229920002554 vinyl polymer Polymers 0.000 description 11
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
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LDVNDECONPCEAK-UHFFFAOYSA-N [3-(4-fluorophenoxy)phenyl]methanol Chemical compound OCC1=CC=CC(OC=2C=CC(F)=CC=2)=C1 LDVNDECONPCEAK-UHFFFAOYSA-N 0.000 description 1
USWIQSJKSYQJHX-UHFFFAOYSA-N [phenoxy(phenyl)methyl] acetate Chemical class C=1C=CC=CC=1C(OC(=O)C)OC1=CC=CC=C1 USWIQSJKSYQJHX-UHFFFAOYSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
239000013543 active substance Substances 0.000 description 1
150000001447 alkali salts Chemical class 0.000 description 1
125000005037 alkyl phenyl group Chemical group 0.000 description 1
244000000054 animal parasite Species 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
XUHFBOUSHUEAQZ-UHFFFAOYSA-N bromobenzyl cyanide Chemical compound N#CC(Br)C1=CC=CC=C1 XUHFBOUSHUEAQZ-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
150000007942 carboxylates Chemical class 0.000 description 1
230000007681 cardiovascular toxicity Effects 0.000 description 1
238000012512 characterization method Methods 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
238000001035 drying Methods 0.000 description 1
244000078703 ectoparasite Species 0.000 description 1
230000012173 estrus Effects 0.000 description 1
ZFZXRNVTYVRULM-UHFFFAOYSA-N ethyl 3-formyl-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CCOC(=O)C1C(C=O)C1(C)C ZFZXRNVTYVRULM-UHFFFAOYSA-N 0.000 description 1
LDDOSDVZPSGLFZ-UHFFFAOYSA-N ethyl cyclopropanecarboxylate Chemical compound CCOC(=O)C1CC1 LDDOSDVZPSGLFZ-UHFFFAOYSA-N 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
150000003948 formamides Chemical class 0.000 description 1
239000003502 gasoline Substances 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
125000005059 halophenyl group Chemical group 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000000463 material Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
SYBYTAAJFKOIEJ-UHFFFAOYSA-N methyl iso-propyl ketone Natural products CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
230000003071 parasitic effect Effects 0.000 description 1
229960005235 piperonyl butoxide Drugs 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
238000007127 saponification reaction Methods 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Inorganic materials [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 1
CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000008096 xylene Substances 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (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)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

DD78215933A 1977-07-06 1978-07-04 Verfahren zur herstellung neuer substituierter phenoxybenzyloxycarbonylderivate DD146286A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19772730515 DE2730515A1 (de)	1977-07-06	1977-07-06	Substituierte phenoxybenzyloxycarbonylderivate, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide

Publications (1)

Publication Number	Publication Date
DD146286A5 true DD146286A5 (de)	1981-02-04

Family

ID=6013281

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
DD78215933A DD146286A5 (de)	1977-07-06	1978-07-04	Verfahren zur herstellung neuer substituierter phenoxybenzyloxycarbonylderivate
DD78206509A DD139991A5 (de)	1977-07-06	1978-07-04	Insektizide und akarizide

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
DD78206509A DD139991A5 (de)	1977-07-06	1978-07-04	Insektizide und akarizide

Country Status (22)

Country	Link
US (2)	US4276306A (fr)
EP (2)	EP0011695B1 (fr)
JP (2)	JPS5414946A (fr)
AR (1)	AR227617A1 (fr)
AT (1)	AT361251B (fr)
AU (1)	AU520095B2 (fr)
BR (1)	BR7804334A (fr)
CA (1)	CA1254227C (fr)
CS (1)	CS199214B2 (fr)
DD (2)	DD146286A5 (fr)
DE (3)	DE2730515A1 (fr)
DK (1)	DK160300C (fr)
EG (1)	EG13788A (fr)
ES (2)	ES471461A1 (fr)
GR (1)	GR71682B (fr)
HU (1)	HU176473B (fr)
IL (1)	IL55061A (fr)
IT (1)	IT1097465B (fr)
PH (1)	PH16779A (fr)
PT (1)	PT68252A (fr)
TR (1)	TR20790A (fr)
ZA (1)	ZA783869B (fr)

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US4200644A (en) *	1978-01-26	1980-04-29	Fmc Corporation	Arylthiovinylcyclopropanecarboxylate insecticides
DE2844271A1 (de) *	1978-10-11	1980-04-24	Bayer Ag	3-chlorostyryl-2,2-dimethyl-cyclopropancarbonsaeure-(4-fluoro-3-phenoxy- alpha -cyano-benzyl)-ester, verfahren zu ihrer herstellung und ihre verwendung als ektoparasitizide
DE2842542A1 (de) *	1978-09-29	1980-04-17	Bayer Ag	Substituierte bromostyryl-cyclopropancarbonsaeurephenoxybenzylester, verfahren zu ihrer herstellunnd ihre verwendung als insektizide und akarizide
DE2852028A1 (de) *	1978-12-01	1980-06-12	Bayer Ag	Mittel gegen keratinschaedlinge und verfahren zur behandlung von wolle mit diesen mitteln
IT1166681B (it) *	1979-03-09	1987-05-06	Montedison Spa	Piretroidi
CA1142953A (fr) *	1979-04-03	1983-03-15	Dale G. Brown	Methode de preparation d'esters pesticides a partir de certains acides carboxyliques a l'aide de catalyseurs a transfert de phase
DE2920947A1 (de) *	1979-05-23	1980-12-04	Bayer Ag	2-phenyl-alken-1-yl-cyclopropan- carbonsaeureester, verfahren zu ihrer herstellung sowie ihre verwendung als insektizide und akarizide und zwischenprodukte zu ihrer herstellung
DE2922481A1 (de) *	1979-06-01	1980-12-11	Bayer Ag	Elektroparasitizide mittel enthaltend substituierte phenoxybenzyloxycarbonylderivate, (ihio)phosphorsaeureester, verfahren zu ihrer herstellung und ihre verwendung als ektoparasitizide
FR2471187A1 (fr) *	1979-12-10	1981-06-19	Roussel Uclaf	Nouvelles compositions destinees a la lutte contre les parasites des animaux a sang chaud
FR2484256B1 (fr) *	1979-06-29	1986-10-24	Roussel Uclaf	Procede de lutte contre les parasites des animaux a sang chaud
US4296241A (en) *	1979-07-21	1981-10-20	Bayer Aktiengesellschaft	Preparation of 3-(2,2-dichlorovinyl)-2,2-dimethyl-cyclopropane-1-carboxylic acid derivatives
DE2929645A1 (de) *	1979-07-21	1981-02-12	Bayer Ag	Verfahren zur herstellung von 1,1- dichloralkenen
DE2936864A1 (de)	1979-09-12	1981-04-02	Bayer Ag, 5090 Leverkusen	(+-)-trans-3-(e, z-2-chlor-2-(4-chlorphenyl)-vinyl)-, 2,2-dimethyl-cyclopropan-carbonsaeure-(+-)-(alpha)-cyano-3-phenoxy-4-fluor-benzyl)-ester, die einzelnen e- und z-isomeren, verfahren zur herstellung dieser verbindungen und ihre verwendung als ektoparasitizide
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
DE3029426A1 (de) *	1980-08-02	1982-03-11	Bayer Ag, 5090 Leverkusen	Gegen zwecken wirksame pour-on-formulierungen
DE3033158A1 (de) *	1980-09-03	1982-04-01	Bayer Ag, 5090 Leverkusen	Optisch aktive isomere von trans-3-(2-chlor-2-(4-chlor-phenyl)-vinyl)-2,2-dimethyl-cyclopropan-1-carbonsaeure-((alpha)-cyano-4-fluor-3-phenoxy-benzyl)-ester, verfahren zu deren herstellung und deren verwendung als ektoparasitizide
JPS5786014A (en) *	1980-11-18	1982-05-28	Ishida Scales Mfg Co Ltd	Measuring or counting method by combination
US5286749A (en) *	1980-11-21	1994-02-15	Pitman-Moore Inc.	Control of sheep ectoparasites
DE3048021A1 (de) *	1980-12-19	1982-07-15	Bayer Ag, 5090 Leverkusen	Insektizide und akarizide mittel und ihre verwendung
JPS57169627A (en) *	1981-04-13	1982-10-19	Yamato Scale Co Ltd	Combination balance
JPS57175923A (en) *	1981-04-24	1982-10-29	Yamato Scale Co Ltd	Combined balance
DE3127752A1 (de) *	1981-07-14	1983-02-03	Bayer Ag, 5090 Leverkusen	Verfahren zur herstellung von permethrinsaeurementhylester
JPS5819516A (ja) *	1981-07-28	1983-02-04	Ishida Scales Mfg Co Ltd	複数の種類の品物の混合組合せ計量方法
JPS5892914A (ja) *	1981-11-30	1983-06-02	Ishida Scales Mfg Co Ltd	組合せ演算装置
DE3208334A1 (de) *	1982-03-09	1983-09-15	Bayer Ag, 5090 Leverkusen	Pestizide pour-on-formulierungen
JPS59622A (ja) *	1982-06-26	1984-01-05	Anritsu Corp	組合せ計量装置
DE3333657A1 (de) *	1983-09-17	1985-04-25	Bayer Ag, 5090 Leverkusen	Pyrethroide enthaltende formkoerper zur bekaempfung von ektoparasiten
DE3538688A1 (de) *	1985-10-31	1987-05-07	Bayer Ag	Verfahren zur bekaempfung von parasitosen bei bienen
NZ221534A (en) *	1986-08-27	1990-10-26	Montedison Spa	Derivatives of 2,2-dimethyl-cyclopropane carboxylic acid; insecticides and acaricides
DE3629387A1 (de) *	1986-08-29	1988-03-03	Bayer Ag	Verfahren zur diastereomerentrennung von cyclopropancarbonsaeureestern
JPH02100028U (fr) *	1989-01-25	1990-08-09
DE3906556A1 (de) *	1989-03-02	1990-09-06	Desowag Materialschutz Gmbh	Mittel oder konzentrat zum konservieren von holz oder holzwerkstoffen
DE3907069A1 (de) *	1989-03-04	1990-09-06	Basf Ag	Substituierte 2-phenyl-alk(en)yl-1-yl-cyclopropancarbonsaeurebenzylester, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung von schaedlingen
CN107365252A (zh) *	2016-05-11	2017-11-21	江苏优士化学有限公司	3-(2-氯-2-(4-氯苯基)乙烯基)-2,2-二甲基环丙烷羧酸的合成方法

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FR1507192A (fr) *	1966-08-26	1967-12-29	Roussel Uclaf	Nouvelles aryl allylsulfones et procédé de préparation
US3786052A (en) *	1966-08-26	1974-01-15	J Martel	Novel cyclopropanecarboxylic acids and esters
NL133054C (fr) *	1967-11-10
IL32569A (en) *	1968-07-12	1976-06-30	Roussel Uclaf	Process for the preparation of dimethyl cyclopropane carboxylic acid derivatives and some products resulting therefrom
US3666789A (en) *	1969-05-21	1972-05-30	Sumitomo Chemical Co	Cyclopropanecarboxylic acid esters
FR2067854A5 (en) *	1969-11-19	1971-08-20	Roussel Uclaf	Subst vinyl cyclo-propane-1-carboxylic acids insecticidal prepn
JPS5220473B1 (fr) *	1970-06-29	1977-06-03
JPS515450B1 (fr) *	1971-06-29	1976-02-20
US4024163A (en) *	1972-05-25	1977-05-17	National Research Development Corporation	Insecticides
FR2248264B1 (fr) *	1973-10-22	1977-05-27	Roussel Uclaf
IN142702B (fr) *	1974-09-10	1977-08-20	Sagami Chem Res
JPS5813522B2 (ja) *	1974-10-24	1983-03-14	住友化学工業株式会社	新しいシクロプロパンカルボン酸エステルを含有する殺虫、殺ダニ剤
US3966959A (en) *	1975-02-13	1976-06-29	American Cyanamid Company	Insecticidal and acaricidal, pyrethroid compounds
CH602005A5 (en)	1976-02-17	1978-07-14	Ciba Geigy Ag	(3)-Phenoxy-benzyl styryl-cyclopropane carboxylates
NL7701321A (nl) *	1976-02-17	1977-08-19	Ciba Geigy	Werkwijze voor de bereiding van een ester.
JPS5828264B2 (ja) *	1976-03-26	1983-06-15	財団法人相模中央化学研究所	ビニルシクロプロパンカルボン酸エステルの製造方法
ZA775160B (en) *	1976-08-27	1978-07-26	Fmc Corp	Insecticidal styryl- and substituted-styrylcyclopropanecarboxylates
US4157397A (en) *	1976-08-27	1979-06-05	Fmc Corporation	Insecticidal (β-phenylvinyl)cyclopropanecarboxylates
CA1260486A (fr) *	1976-08-27	1989-09-26	John F. Engel	Styrylcyclopropanecarboxylates et derive de substitution, insecticides
DE2848495A1 (de) *	1977-11-11	1979-05-17	Ciba Geigy Ag	Cyclopropankarbonsaeureester, verfahren zu ihrer herstellung und ihre verwendung in der schaedlingsbekaempfung
DE2800922A1 (de) *	1978-01-10	1979-07-19	Bayer Ag	Verfahren zur trennung stereoisomerer vinylcyclopropancarbonsaeuren
US4200644A (en) *	1978-01-26	1980-04-29	Fmc Corporation	Arylthiovinylcyclopropanecarboxylate insecticides
DE2810634A1 (de) *	1978-03-11	1979-09-20	Bayer Ag	Pentafluorbenzyloxycarbonylderivate, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide
US4358409A (en) *	1979-05-02	1982-11-09	Bayer Aktiengesellschaft	Preparation of styryl cyclopropane insecticide intermediates

1977
- 1977-07-06 DE DE19772730515 patent/DE2730515A1/de not_active Withdrawn
1978
- 1978-06-16 US US05/916,163 patent/US4276306A/en not_active Expired - Lifetime
- 1978-06-28 DE DE7979103787T patent/DE2861686D1/de not_active Expired
- 1978-06-28 EP EP79103787A patent/EP0011695B1/fr not_active Expired
- 1978-06-28 EP EP78100252A patent/EP0000345B1/fr not_active Expired
- 1978-06-28 DE DE7878100252T patent/DE2860574D1/de not_active Expired
- 1978-07-03 IL IL55061A patent/IL55061A/xx unknown
- 1978-07-03 CS CS784410A patent/CS199214B2/cs unknown
- 1978-07-04 CA CA 306758 patent/CA1254227C/fr not_active Expired
- 1978-07-04 DD DD78215933A patent/DD146286A5/de unknown
- 1978-07-04 AT AT484278A patent/AT361251B/de not_active IP Right Cessation
- 1978-07-04 IT IT25315/78A patent/IT1097465B/it active Protection Beyond IP Right Term
- 1978-07-04 PT PT68252A patent/PT68252A/pt unknown
- 1978-07-04 DD DD78206509A patent/DD139991A5/de not_active IP Right Cessation
- 1978-07-05 EG EG420/78A patent/EG13788A/xx active
- 1978-07-05 AR AR272845A patent/AR227617A1/es active
- 1978-07-05 BR BR7804334A patent/BR7804334A/pt unknown
- 1978-07-05 ZA ZA00783869A patent/ZA783869B/xx unknown
- 1978-07-05 JP JP8106878A patent/JPS5414946A/ja active Granted
- 1978-07-05 DK DK304178A patent/DK160300C/da not_active IP Right Cessation
- 1978-07-05 GR GR56693A patent/GR71682B/el unknown
- 1978-07-05 ES ES471461A patent/ES471461A1/es not_active Expired
- 1978-07-05 AU AU37787/78A patent/AU520095B2/en not_active Expired
- 1978-07-05 HU HU78BA3674A patent/HU176473B/hu not_active IP Right Cessation
- 1978-07-06 PH PH21337A patent/PH16779A/en unknown
- 1978-07-06 TR TR20790A patent/TR20790A/xx unknown
1979
- 1979-03-28 ES ES479021A patent/ES479021A1/es not_active Expired
1982
- 1982-06-24 US US06/391,732 patent/US4611009A/en not_active Expired - Lifetime
1986
- 1986-06-26 JP JP61148365A patent/JPS6248646A/ja active Granted

Also Published As

Publication number	Publication date
IL55061A0 (en)	1978-09-29
JPS6248646A (ja)	1987-03-03
JPS6218538B2 (fr)	1987-04-23
DK160300C (da)	1991-07-29
AT361251B (de)	1981-02-25
DK160300B (da)	1991-02-25
EP0011695A1 (fr)	1980-06-11
CA1254227C (fr)	1989-05-16
PH16779A (en)	1984-02-22
ES471461A1 (es)	1979-09-16
HU176473B (en)	1981-03-28
BR7804334A (pt)	1979-04-17
US4611009A (en)	1986-09-09
AR227617A1 (es)	1982-11-30
AU3778778A (en)	1980-01-10
PT68252A (de)	1978-08-01
US4276306A (en)	1981-06-30
ATA484278A (de)	1980-07-15
JPS5414946A (en)	1979-02-03
ZA783869B (en)	1979-07-25
GR71682B (fr)	1983-06-21
DD139991A5 (de)	1980-02-06
EP0000345A1 (fr)	1979-01-24
EP0000345B1 (fr)	1981-04-01
ES479021A1 (es)	1979-07-01
IT7825315A0 (it)	1978-07-04
CS199214B2 (en)	1980-07-31
JPH0127053B2 (fr)	1989-05-26
DK304178A (da)	1979-01-07
DE2860574D1 (en)	1981-04-23
EG13788A (en)	1982-03-31
IL55061A (en)	1985-04-30
DE2861686D1 (en)	1982-04-29
DE2730515A1 (de)	1979-01-18
AU520095B2 (en)	1982-01-14
EP0011695B1 (fr)	1982-03-24
IT1097465B (it)	1985-08-31
TR20790A (tr)	1982-08-16

Publication	Publication Date	Title
EP0000345B1 (fr)	1981-04-01	Dérivés phénoxybenzyloxycarbonyles substitués, leur procédé de préparation et leur utilisation comme insecticides et acaricides
EP0008340A1 (fr)	1980-03-05	Esters d'acide cyclopropane carboxylique substitué par fluoroalcényl, produits intermédiaires, préparation des composés et leur utilisation comme insecticides et/ou acaricides
EP0019787B1 (fr)	1984-03-14	Esters d'acides 2-phénylalcén-1-yl-cyclopropane carboxyliques, procédé pour leur préparation et application comme insecticides et acaricides; intermédiaires pour leur préparation
CH631430A5 (de)	1982-08-13	Verfahren zur herstellung vinylsubstituierter cyclopropancarbonsaeureester.
CH630889A5 (de)	1982-07-15	Verfahren zur herstellung neuer substituierter phenoxybenzyloxycarbonylderivate, und ihre verwendung als insektizide und akarizide.
DE2615435C2 (de)	1984-02-09	Substituierte Phenoxybenzyloxycarbonylderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide und Akarizide
EP0001064B1 (fr)	1982-07-07	Derivés oxycarbonyles de phénoxybenzyles fluores; alcools phénoxybenzyliques fluorés et halogénures phénoxybenzyliques fluorés, procédés pour leur préparation et leur application
EP0004022B1 (fr)	1981-09-16	Dérivés pentafluorobenzyloxycarbonylés, méthode de préparation et leur utilisation comme insecticides et acaricides
EP0019090B1 (fr)	1983-05-18	Dérivés substitués de l'acide styrylcyclopropanecarboxylique, procédé pour leur préparation, leur utilisation, insecticides et acaricides, leur fabrication et procédé pour combattre les insectes
EP0033160B1 (fr)	1985-05-02	Esters substitués d'acide 3-(1,2-dibromo-alkyl)-2,2-diméthyl-cyclopropan-1-carboxylique, procédé et produits intermédiaires pour leur préparation et leur utilisation comme insecticides
EP0009708B1 (fr)	1984-11-21	Esters m-phénoxybenzyliques d'acides bromostyrylcyclopropane carboxyliques (I), procédés pour leur préparation, produits intermédiaires obtenus ainsi que leur préparation, compositions contenant les esters (I), utilisation des esters (I) et procédé de préparation des compositions insecticides ou acaricides
DE3012642A1 (de)	1981-10-08	3-carbamoyl-4-hydroxy-cumarine, verfahren zu ihrer herstellung als schaedlingsbekaepfungsmittel
EP0001566B1 (fr)	1980-11-26	Dérivés d'acides cyclobutane carboxyliques, leurs procédés de préparation, et leur application comme insecticides
DE3318572A1 (de)	1983-12-01	Neue pestizide und verfahren zu ihrer herstellung
DD153318A5 (de)	1982-01-06	Schaedlingsbekaempfungsmittel
DE3019552A1 (de)	1981-11-26	3-(2-chlor-3,3,4,4,4-pentafluor-1-butenyl)-2,2-dimethyl-cyclopropancarbonsaeureester, verfahren zu deren herstellung und deren verwendung in schaedlingsbekaempfungsmitteln
EP0076961A1 (fr)	1983-04-20	(6-Phénoxy-2-pyridinyl)méthyl esters d'acides vinylcyclopropane carboxyliques substitués, procédé pour leur préparation, et leur utilisation comme pesticides
EP0020954A1 (fr)	1981-01-07	Esters fluorés d'acides oxyalcénylcyclopropanecarboxyliques, procédé pour leur préparation, produits intermédiaires, leur préparation, insecticides et acaricides contenant les produits finals, leur préparation et leur utilisation
DE3323118A1 (de)	1984-01-12	Substituierte allylbenzylester von cyclopropan- und anderen carbonsaeuren
EP0095636A1 (fr)	1983-12-07	Iminoesters N-substitués, procédé de préparation et utilisation comme insecticide
DE3222910A1 (de)	1983-12-22	Allenyl-benzylester, verfahren zu ihrer herstellung sowie ihre verwendung zur schaedlingsbekaempfung
DD202494A5 (de)	1983-09-21	Schaedlingsbekaempfungsmittel
DE2933600A1 (de)	1981-04-09	Substituierte 2-carbamoyloximinobutane, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
EP0006456A1 (fr)	1980-01-09	Esters de l'acide spiropentane carboxylique, procédé pour leur préparation, compositions insecticides et acaricides, utilisation des esters de l'acide spiropentane carboxylique pour la lutte contre les insectes ou les araignées et procédé pour la préparation d'insecticides ou d'acaricides
DE2458626A1 (de)	1976-06-16	Benzisoxazolo-thionophosphor(phosphon)-saeureester, verfahren zu ihrer herstellung sowie ihre verwendung als insektizide und akarizide