NO763934L - - Google Patents

Info

Publication number: NO763934L
Authority: NO; Norway
Prior art keywords: group; lower alkyl; hydrogen atom; phenyl; carboxylate
Prior art date: 1974-09-10

Application number

NO763934A

Other languages

English (en)

Norwegian (no)

Inventor

K Kondo

K Matsui

A Negishi

Y Takahatake

Original Assignee

Sagami Chem Res

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.)

1974-09-10

Filing date

1976-11-18

Publication date

1976-03-11

1974-09-10 Priority claimed from JP10352174A external-priority patent/JPS5141316A/ja

1974-09-10 Priority claimed from JP10352074A external-priority patent/JPS5545062B2/ja

1974-09-26 Priority claimed from JP10997574A external-priority patent/JPS5545063B2/ja

1974-09-26 Priority claimed from JP10997674A external-priority patent/JPS5139624A/ja

1974-11-30 Priority claimed from JP13663274A external-priority patent/JPS5165710A/ja

1974-11-30 Priority claimed from JP13663174A external-priority patent/JPS5165734A/ja

1974-12-02 Priority claimed from JP13702674A external-priority patent/JPS5165735A/ja

1974-12-03 Priority claimed from JP13775274A external-priority patent/JPS5165714A/ja

1975-01-16 Priority claimed from JP50006429A external-priority patent/JPS5182216A/ja

1975-01-22 Priority claimed from JP50008673A external-priority patent/JPS5817735B2/ja

1975-01-31 Priority claimed from JP1238975A external-priority patent/JPS5821901B2/ja

1975-02-19 Priority claimed from JP50019918A external-priority patent/JPS5198213A/ja

1975-02-19 Priority claimed from JP1991775A external-priority patent/JPS5821902B2/ja

1975-02-24 Priority claimed from JP50021857A external-priority patent/JPS5198248A/ja

1975-03-11 Priority claimed from JP50028607A external-priority patent/JPS5822463B2/ja

1975-03-11 Priority claimed from JP50028606A external-priority patent/JPS5817451B2/ja

1975-06-04 Priority claimed from JP50066592A external-priority patent/JPS5819661B2/ja

1975-06-04 Priority claimed from JP6659375A external-priority patent/JPS5828263B2/ja

1975-09-09 Priority claimed from NO75753085A external-priority patent/NO147792C/no

1976-03-11 Publication of NO763934L publication Critical patent/NO763934L/no

1976-11-18 Application filed by Sagami Chem Res filed Critical Sagami Chem Res

1976-11-18 Priority to NO763934A priority Critical patent/NO763934L/no

Links

125000000217 alkyl group Chemical group 0.000 claims description 12
238000000034 method Methods 0.000 claims description 12
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
USPVNSDVCUTNJN-UHFFFAOYSA-N ethenyl cyclopropanecarboxylate Chemical compound C=COC(=O)C1CC1 USPVNSDVCUTNJN-UHFFFAOYSA-N 0.000 claims description 5
229910052736 halogen Inorganic materials 0.000 claims description 5
229910052739 hydrogen Inorganic materials 0.000 claims description 5
239000001257 hydrogen Substances 0.000 claims description 5
125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 4
125000003435 aroyl group Chemical group 0.000 claims description 4
125000003710 aryl alkyl group Chemical group 0.000 claims description 4
125000000753 cycloalkyl group Chemical group 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 3
125000002947 alkylene group Chemical group 0.000 claims description 2
125000004432 carbon atom Chemical group C* 0.000 claims description 2
125000002252 acyl group Chemical group 0.000 claims 2
125000003342 alkenyl group Chemical group 0.000 claims 2
125000000304 alkynyl group Chemical group 0.000 claims 2
125000003368 amide group Chemical group 0.000 claims 2
125000002560 nitrile group Chemical group 0.000 claims 2
YMGUBTXCNDTFJI-UHFFFAOYSA-M cyclopropanecarboxylate Chemical compound [O-]C(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-M 0.000 claims 1
125000005843 halogen group Chemical group 0.000 claims 1
238000006798 ring closing metathesis reaction Methods 0.000 claims 1
239000002917 insecticide Substances 0.000 description 7
VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 6
239000002728 pyrethroid Substances 0.000 description 6
VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 description 5
-1 dimethyl-vinyl group Chemical group 0.000 description 5
ROVGZAWFACYCSP-VUMXUWRFSA-N pyrethrin I Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 ROVGZAWFACYCSP-VUMXUWRFSA-N 0.000 description 5
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
150000002367 halogens Chemical group 0.000 description 4
239000000203 mixture Substances 0.000 description 4
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 3
238000010992 reflux Methods 0.000 description 3
WSNMPAVSZJSIMT-UHFFFAOYSA-N COc1c(C)c2COC(=O)c2c(O)c1CC(O)C1(C)CCC(=O)O1 Chemical compound COc1c(C)c2COC(=O)c2c(O)c1CC(O)C1(C)CCC(=O)O1 WSNMPAVSZJSIMT-UHFFFAOYSA-N 0.000 description 2
LTNDZDRYUXNFCU-NEWSRXKRSA-N Cinerin II Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]2[C@@H](C=C(C)OC(=O)C)C2(C)C LTNDZDRYUXNFCU-NEWSRXKRSA-N 0.000 description 2
241000238631 Hexapoda Species 0.000 description 2
241000124008 Mammalia Species 0.000 description 2
241001608567 Phaedon cochleariae Species 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
241000250966 Tanacetum cinerariifolium Species 0.000 description 2
239000002253 acid Substances 0.000 description 2
125000003158 alcohol group Chemical group 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
125000001589 carboacyl group Chemical group 0.000 description 2
230000015556 catabolic process Effects 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
SHCRDCOTRILILT-WOBDGSLYSA-N cinerin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C)C(=O)C1 SHCRDCOTRILILT-WOBDGSLYSA-N 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical group OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 description 2
238000006731 degradation reaction Methods 0.000 description 2
ORVPAYHEPQBFFC-UHFFFAOYSA-N ethyl 3-ethenyl-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CCOC(=O)C1C(C=C)C1(C)C ORVPAYHEPQBFFC-UHFFFAOYSA-N 0.000 description 2
WLLVIDYONYJCTH-UHFFFAOYSA-N ethyl 6-bromo-2,3,3-trimethylhex-4-enoate Chemical compound CCOC(=O)C(C)C(C)(C)C=CCBr WLLVIDYONYJCTH-UHFFFAOYSA-N 0.000 description 2
NNVHQXPXPLWGML-UHFFFAOYSA-N ethyl 6-bromo-3,3-dimethylhex-4-enoate Chemical compound CCOC(=O)CC(C)(C)C=CCBr NNVHQXPXPLWGML-UHFFFAOYSA-N 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
WKNSDDMJXANVMK-XIGJTORUSA-N jasmolin II Chemical compound C1C(=O)C(C\C=C/CC)=C(C)[C@H]1OC(=O)[C@H]1C(C)(C)[C@@H]1\C=C(/C)C(=O)OC WKNSDDMJXANVMK-XIGJTORUSA-N 0.000 description 2
229910052943 magnesium sulfate Inorganic materials 0.000 description 2
235000019341 magnesium sulphate Nutrition 0.000 description 2
229930014626 natural product Natural products 0.000 description 2
150000002825 nitriles Chemical class 0.000 description 2
LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 2
FMTFEIJHMMQUJI-NJAFHUGGSA-N 102130-98-3 Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]1[C@@H](C=C(C)C)C1(C)C FMTFEIJHMMQUJI-NJAFHUGGSA-N 0.000 description 1
125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
125000006024 2-pentenyl group Chemical group 0.000 description 1
239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
241000723353 Chrysanthemum Species 0.000 description 1
235000007516 Chrysanthemum Nutrition 0.000 description 1
FMTFEIJHMMQUJI-UHFFFAOYSA-N Cinerin I Natural products C1C(=O)C(CC=CC)=C(C)C1OC(=O)C1C(C)(C)C1C=C(C)C FMTFEIJHMMQUJI-UHFFFAOYSA-N 0.000 description 1
OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
NZKIRHFOLVYKFT-UHFFFAOYSA-N Jasmolin I Natural products C1C(=O)C(CC=CCC)=C(C)C1OC(=O)C1C(C)(C)C1C=C(C)C NZKIRHFOLVYKFT-UHFFFAOYSA-N 0.000 description 1
206010058667 Oral toxicity Diseases 0.000 description 1
235000017372 Piretro di Dalmazia Nutrition 0.000 description 1
VMORCWYWLVLMDG-YZGWKJHDSA-N Pyrethrin-II Natural products CC(=O)OC(=C[C@@H]1[C@H](C(=O)O[C@H]2CC(=O)C(=C2C)CC=CC=C)C1(C)C)C VMORCWYWLVLMDG-YZGWKJHDSA-N 0.000 description 1
241000700159 Rattus Species 0.000 description 1
ROVGZAWFACYCSP-MQBLHHJJSA-N [2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(C\C=C/C=C)C(=O)C1 ROVGZAWFACYCSP-MQBLHHJJSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
FMTFEIJHMMQUJI-DFKXKMKHSA-N cinerin I Chemical compound C1C(=O)C(C\C=C/C)=C(C)[C@H]1OC(=O)[C@H]1C(C)(C)[C@@H]1C=C(C)C FMTFEIJHMMQUJI-DFKXKMKHSA-N 0.000 description 1
150000001942 cyclopropanes Chemical class 0.000 description 1
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
239000012259 ether extract Substances 0.000 description 1
XXCGAENPCKWVAA-UHFFFAOYSA-N ethyl 3-ethenyl-1,2,2-trimethylcyclopropane-1-carboxylate Chemical compound CCOC(=O)C1(C)C(C=C)C1(C)C XXCGAENPCKWVAA-UHFFFAOYSA-N 0.000 description 1
239000000284 extract Substances 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
230000002140 halogenating effect Effects 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
239000005457 ice water Substances 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
NZKIRHFOLVYKFT-VUMXUWRFSA-N jasmolin I Chemical compound C1C(=O)C(C\C=C/CC)=C(C)[C@H]1OC(=O)[C@H]1C(C)(C)[C@@H]1C=C(C)C NZKIRHFOLVYKFT-VUMXUWRFSA-N 0.000 description 1
WKNSDDMJXANVMK-UHFFFAOYSA-N jasmolin II Natural products C1C(=O)C(CC=CCC)=C(C)C1OC(=O)C1C(C)(C)C1C=C(C)C(=O)OC WKNSDDMJXANVMK-UHFFFAOYSA-N 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
239000000463 material Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
231100000418 oral toxicity Toxicity 0.000 description 1
238000005949 ozonolysis reaction Methods 0.000 description 1
230000002085 persistent effect Effects 0.000 description 1
XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 description 1
229940015367 pyrethrum Drugs 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
229960002317 succinimide Drugs 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
239000000725 suspension Substances 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Landscapes

Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

NO763934A 1974-09-10 1976-11-18 NO763934L (tr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
NO763934A NO763934L (tr)	1974-09-10	1976-11-18

Applications Claiming Priority (20)

Application Number	Priority Date	Filing Date	Title
JP10352174A JPS5141316A (en)	1974-09-10	1974-09-10	Ganmaa harokarubonsanesuterunoseizohoho
JP10352074A JPS5545062B2 (tr)	1974-09-10	1974-09-10
JP10997574A JPS5545063B2 (tr)	1974-09-26	1974-09-26
JP10997674A JPS5139624A (en)	1974-09-26	1974-09-26	Ganmaa fuhowa epushiron harokarubonsanesuteru no seizoho
JP13663274A JPS5165710A (en)	1974-11-30	1974-11-30	Ganma fuhowakarubonsanesuteruno seizohoho
JP13663174A JPS5165734A (ja)	1974-11-30	1974-11-30	Shikuropuropankarubonsanesuteruo seizosuru hoho
JP13702674A JPS5165735A (ja)	1974-12-02	1974-12-02	Shikuropuropankarubonsanesuteruo seizosuru hoho
JP13775274A JPS5165714A (en)	1974-12-03	1974-12-03	Ganma fuhowa ipushiron harokarubonsanesuteruo seizosuru hoho
JP50006429A JPS5182216A (en)	1975-01-16	1975-01-16	Ganma harokarubonsanesuteruno seizoho
JP50008673A JPS5817735B2 (ja)	1975-01-22	1975-01-22	ガンマ − フホウワカルボンサンエステルノセイホウ
JP1238975A JPS5821901B2 (ja)	1975-01-31	1975-01-31	２−（２，２−ジクロルビニル）−３，３−ジメチルシクロプロパンカルボン酸エステルの製造方法
JP50019918A JPS5198213A (en)	1975-02-19	1975-02-19	arufua chikan ganma harokarubonsanesuteruno seizohoho
JP1991775A JPS5821902B2 (ja)	1975-02-19	1975-02-19	アルフア− チカンシクロプロパンカルボンサンエステルノセイゾウホウホウ
JP50021857A JPS5198248A (tr)	1975-02-24	1975-02-24
JP50028607A JPS5822463B2 (ja)	1975-03-11	1975-03-11	チカンビニルキオユウスルシクロプロパンカルボンサンユウドウタイノセイホウ
JP50028606A JPS5817451B2 (ja)	1975-03-11	1975-03-11	γ↓−クロル↓−δ↓−不飽和カルボン酸エステルの製法
JP50066592A JPS5819661B2 (ja)	1975-06-04	1975-06-04	ガンマ− − ハロ−カルボンサンエステルノセイゾウホウホウ
JP6659375A JPS5828263B2 (ja)	1975-06-04	1975-06-04	３３− ジメチル −２−（２２− ジハロビニル）シクロプロパンカルボンサンエステルノセイゾウホウホウ
NO75753085A NO147792C (no)	1974-09-10	1975-09-09	Fremgangsmaate for fremstilling av estere av dihalogen-vinylcyklopropankarboksylsyrer
NO763934A NO763934L (tr)	1974-09-10	1976-11-18

Publications (1)

Publication Number	Publication Date
NO763934L true NO763934L (tr)	1976-03-11

Family

ID=27586372

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO763934A NO763934L (tr)	1974-09-10	1976-11-18

Country Status (1)

Country	Link
NO (1)	NO763934L (tr)

1976
- 1976-11-18 NO NO763934A patent/NO763934L/no unknown

Publication	Publication Date	Title
SU1344244A3 (ru)	1987-10-07	Способ получени пергалоидалкилвинилциклопропанкарбоксилатов
US3666789A (en)	1972-05-30	Cyclopropanecarboxylic acid esters
DE2365555C2 (tr)	1987-10-15
EP0020685B1 (en)	1983-06-15	Insecticidal cyclopropanecarboxylates from substituted (1,1'-biphenyl)-3-ylmethyl compounds
US3318766A (en)	1967-05-09	Chrysanthemum carboxylic acid maleimidomethyl ester insecticidal compositions
SE430298B (sv)	1983-11-07	Insekticid komposition
US3876681A (en)	1975-04-08	Novel cyclopropanecarboxylate
EP0050454B1 (en)	1984-08-29	New cyclopropanecarboxylates, their production and insecticide containing them as an active ingredient
CA1084943A (en)	1980-09-02	Pesticidal m-phenoxybenzyl esters of 2,2- dimethylspiro 2,4 heptane-1-carboxylic acid derivatives
US3966963A (en)	1976-06-29	Insecticidal composition containing cyclopropane-carboxylate
US3636059A (en)	1972-01-18	Cyclopentenolone esters
NO763934L (tr)	1976-03-11
NO153098B (no)	1985-10-07	3-substituerte 2,2-dimethyl-cyclopropancarboxylsyrer og lavere alkylestere derav som er anvendelige som utgangsmaterialer ved fremstilling av pyrethroider med insekticid virkning
WO1982002321A1 (en)	1982-07-22	(+)-4-substituted-2-indanols and insecticidal ester derivatives
AU595796B2 (en)	1990-04-12	Novel carboxylic acid esters, methods for production thereof and insecticides containing them as the active ingredient
US4179446A (en)	1979-12-18	Sex pheromone produced by the female Japanese beetle: specificity of male response to enantiomers
US4997855A (en)	1991-03-05	Vinyl fluorides and pesticidal uses
US3857858A (en)	1974-12-31	Cyclopropane carboxylic acid esters
JPS6051452B2 (ja)	1985-11-14	置換イソ吉草酸およびそのエステル
US4758590A (en)	1988-07-19	Method for control of soil-borne insects
US4309555A (en)	1982-01-05	Novel cyclopropane derivatives
US3711555A (en)	1973-01-16	Aryl allyl sulfones
KR820000803B1 (ko)	1982-05-11	2,2-디메틸-시클로프로판 카복실산의 에스테르의 제조방법
HU194800B (en)	1988-03-28	Process for preparing novel esters formed by cyclopropanecarboxylic acids and unsaturated aliphatic alcohols
US4239773A (en)	1980-12-16	Insecticidal esters of certain substituted 7-oxabicyclo[2.2.1]2,5-heptadiene methanols