SU713526A3 - Фунгицидна композици - Google Patents

Фунгицидна композици Download PDF

Info

Publication number: SU713526A3
Authority: SU; USSR - Soviet Union
Prior art keywords: compound; hydrogen; dose; composition; compounds
Prior art date: 1973-01-12

Application number

SU741989304A

Other languages

English (en)

Russian (ru)

Inventor

Дебурж Жан-Клод

Голлиар Жан-Мишель

Тиолльер Жан-Пьер

Абблар Жан-Жорж

Лякруа Ги-Бернар

Пийон Даниель-Жан

Дюкре Жак-Жозеф

Тизи Андре

Original Assignee

Пепро,Сосьете Пур Ле Девелопман Э Ля Вант Де Спесиалите Шимик (Фирма)

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.)

1973-01-12

Filing date

1974-01-11

Publication date

1980-01-30

1974-01-11 Application filed by Пепро,Сосьете Пур Ле Девелопман Э Ля Вант Де Спесиалите Шимик (Фирма) filed Critical Пепро,Сосьете Пур Ле Девелопман Э Ля Вант Де Спесиалите Шимик (Фирма)

1980-01-30 Application granted granted Critical

1980-01-30 Publication of SU713526A3 publication Critical patent/SU713526A3/ru

Links

239000000203 mixture Substances 0.000 title claims description 13
230000000855 fungicidal effect Effects 0.000 claims abstract 5
239000000417 fungicide Substances 0.000 claims abstract 4
150000001875 compounds Chemical class 0.000 claims description 13
239000013543 active substance Substances 0.000 claims description 3
HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 claims description 3
239000000945 filler Substances 0.000 claims description 2
230000001225 therapeutic effect Effects 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims 3
239000001257 hydrogen Substances 0.000 claims 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims 3
AICOOMRHRUFYCM-ZRRPKQBOSA-N oxazine, 1 Chemical compound C([C@@H]1[C@H](C(C[C@]2(C)[C@@H]([C@H](C)N(C)C)[C@H](O)C[C@]21C)=O)CC1=CC2)C[C@H]1[C@@]1(C)[C@H]2N=C(C(C)C)OC1 AICOOMRHRUFYCM-ZRRPKQBOSA-N 0.000 claims 2
230000003449 preventive effect Effects 0.000 claims 2
231100000674 Phytotoxicity Toxicity 0.000 claims 1
239000000654 additive Substances 0.000 claims 1
230000000996 additive effect Effects 0.000 claims 1
239000012267 brine Substances 0.000 claims 1
JHRWWRDRBPCWTF-OLQVQODUSA-N captafol Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)C(Cl)Cl)C(=O)[C@H]21 JHRWWRDRBPCWTF-OLQVQODUSA-N 0.000 claims 1
125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 claims 1
239000003085 diluting agent Substances 0.000 claims 1
YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 claims 1
229920000940 maneb Polymers 0.000 claims 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
239000000575 pesticide Substances 0.000 claims 1
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 claims 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
125000005210 alkyl ammonium group Chemical group 0.000 abstract 1
125000000217 alkyl group Chemical group 0.000 abstract 1
150000001768 cations Chemical class 0.000 abstract 1
125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
239000002184 metal Substances 0.000 abstract 1
229910052751 metal Inorganic materials 0.000 abstract 1
238000012360 testing method Methods 0.000 description 14
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 9
239000000243 solution Substances 0.000 description 8
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
241000233866 Fungi Species 0.000 description 5
208000015181 infectious disease Diseases 0.000 description 5
238000000034 method Methods 0.000 description 5
239000000725 suspension Substances 0.000 description 5
241000219094 Vitaceae Species 0.000 description 4
240000006365 Vitis vinifera Species 0.000 description 4
239000013068 control sample Substances 0.000 description 4
235000021021 grapes Nutrition 0.000 description 4
239000000126 substance Substances 0.000 description 4
229920001817 Agar Polymers 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
241000196324 Embryophyta Species 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
235000014787 Vitis vinifera Nutrition 0.000 description 3
239000007900 aqueous suspension Substances 0.000 description 3
235000013339 cereals Nutrition 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
125000004122 cyclic group Chemical group 0.000 description 3
239000000843 powder Substances 0.000 description 3
239000000523 sample Substances 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000002689 soil Substances 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
206010003694 Atrophy Diseases 0.000 description 2
240000008067 Cucumis sativus Species 0.000 description 2
241000221779 Fusarium sambucinum Species 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
241001459558 Monographella nivalis Species 0.000 description 2
241001281803 Plasmopara viticola Species 0.000 description 2
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
241000233639 Pythium Species 0.000 description 2
241001518705 Sclerotinia minor Species 0.000 description 2
240000003768 Solanum lycopersicum Species 0.000 description 2
241000082085 Verticillium <Phyllachorales> Species 0.000 description 2
235000009754 Vitis X bourquina Nutrition 0.000 description 2
235000012333 Vitis X labruscana Nutrition 0.000 description 2
YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 2
239000008272 agar Substances 0.000 description 2
230000037444 atrophy Effects 0.000 description 2
DQTRYXANLKJLPK-UHFFFAOYSA-N chlorophosphonous acid Chemical compound OP(O)Cl DQTRYXANLKJLPK-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
238000001727 in vivo Methods 0.000 description 2
238000002955 isolation Methods 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 2
239000002904 solvent Substances 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 1
UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 1
101150111160 ALA1 gene Proteins 0.000 description 1
244000251953 Agaricus brunnescens Species 0.000 description 1
235000001674 Agaricus brunnescens Nutrition 0.000 description 1
VTBCDICMPMOJAN-UHFFFAOYSA-N CC(O1)=COP1=O Chemical compound CC(O1)=COP1=O VTBCDICMPMOJAN-UHFFFAOYSA-N 0.000 description 1
241001157813 Cercospora Species 0.000 description 1
241000530549 Cercospora beticola Species 0.000 description 1
235000009849 Cucumis sativus Nutrition 0.000 description 1
235000010799 Cucumis sativus var sativus Nutrition 0.000 description 1
241000371644 Curvularia ravenelii Species 0.000 description 1
208000004770 Fusariosis Diseases 0.000 description 1
241000223218 Fusarium Species 0.000 description 1
241000223221 Fusarium oxysporum Species 0.000 description 1
241000287828 Gallus gallus Species 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
241000736122 Parastagonospora nodorum Species 0.000 description 1
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
201000004681 Psoriasis Diseases 0.000 description 1
241001361634 Rhizoctonia Species 0.000 description 1
241000813090 Rhizoctonia solani Species 0.000 description 1
241000221662 Sclerotinia Species 0.000 description 1
241000221696 Sclerotinia sclerotiorum Species 0.000 description 1
241001533598 Septoria Species 0.000 description 1
244000269722 Thea sinensis Species 0.000 description 1
241000256856 Vespidae Species 0.000 description 1
241000700605 Viruses Species 0.000 description 1
CPGKMLVTFNUAHL-UHFFFAOYSA-N [Ca].[Ca] Chemical compound [Ca].[Ca] CPGKMLVTFNUAHL-UHFFFAOYSA-N 0.000 description 1
JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000002981 blocking agent Substances 0.000 description 1
229920005551 calcium lignosulfonate Polymers 0.000 description 1
RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
235000013330 chicken meat Nutrition 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
229940125904 compound 1 Drugs 0.000 description 1
229940125782 compound 2 Drugs 0.000 description 1
229940126214 compound 3 Drugs 0.000 description 1
235000005911 diet Nutrition 0.000 description 1
230000037213 diet Effects 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
239000012530 fluid Substances 0.000 description 1
238000000338 in vitro Methods 0.000 description 1
210000004283 incisor Anatomy 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000012423 maintenance Methods 0.000 description 1
238000002156 mixing Methods 0.000 description 1
230000017074 necrotic cell death Effects 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
210000000056 organ Anatomy 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
239000011148 porous material Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
238000012545 processing Methods 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
238000010298 pulverizing process Methods 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000011160 research Methods 0.000 description 1
239000004576 sand Substances 0.000 description 1
101150062190 sod1 gene Proteins 0.000 description 1
-1 sodium alkylaryl sulfonate Chemical class 0.000 description 1
238000009331 sowing Methods 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
230000004083 survival effect Effects 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
230000009885 systemic effect Effects 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
239000000080 wetting agent 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus as a ring member
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6571—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms
- C07F9/6574—Esters of oxyacids of phosphorus
- C07F9/65742—Esters of oxyacids of phosphorus non-condensed with carbocyclic rings or heterocyclic rings or ring systems

Landscapes

Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Pest Control & Pesticides (AREA)
Molecular Biology (AREA)
Agronomy & Crop Science (AREA)
Biochemistry (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

SU741989304A 1973-01-12 1974-01-11 Фунгицидна композици SU713526A3 (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR7301803A FR2213735A1 (en)	1973-01-12	1973-01-12	Fungicides for control of tobacco, vine and hop mildew - comprising 2-hydroxy-1,3,2-dioxaphospholone and 2-hydroxyethyl phosphonate

Publications (1)

Publication Number	Publication Date
SU713526A3 true SU713526A3 (ru)	1980-01-30

Family

ID=9113510

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
SU741989304A SU713526A3 (ru)	1973-01-12	1974-01-11	Фунгицидна композици
SU762368855A SU620193A3 (ru)	1973-01-12	1976-06-17	Фунгицидное средство

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
SU762368855A SU620193A3 (ru)	1973-01-12	1976-06-17	Фунгицидное средство

Country Status (7)

Country	Link
AT (1)	AT332167B (de)
BE (1)	BE809660A (de)
CS (1)	CS194168B2 (de)
FR (1)	FR2213735A1 (de)
PL (1)	PL90905B1 (de)
SU (2)	SU713526A3 (de)
ZA (1)	ZA74185B (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR3143530B1 (fr)	2022-12-19	2024-11-01	Psa Automobiles Sa	Zone arrière de soubassement de structure de caisse de véhicule automobile

1973
- 1973-01-12 FR FR7301803A patent/FR2213735A1/fr active Granted
1974
- 1974-01-10 ZA ZA00740185A patent/ZA74185B/xx unknown
- 1974-01-11 BE BE139740A patent/BE809660A/xx not_active IP Right Cessation
- 1974-01-11 PL PL1974168053A patent/PL90905B1/pl unknown
- 1974-01-11 SU SU741989304A patent/SU713526A3/ru active
- 1974-01-11 AT AT24774*#A patent/AT332167B/de not_active IP Right Cessation
- 1974-01-14 CS CS74220A patent/CS194168B2/cs unknown
1976
- 1976-06-17 SU SU762368855A patent/SU620193A3/ru active

Also Published As

Publication number	Publication date
ZA74185B (en)	1975-08-27
FR2213735A1 (en)	1974-08-09
AT332167B (de)	1976-09-10
CS194168B2 (en)	1979-11-30
SU620193A3 (ru)	1978-08-15
PL90905B1 (en)	1977-02-28
FR2213735B1 (de)	1977-02-04
ATA24774A (de)	1975-12-15
BE809660A (fr)	1974-07-11

Publication	Publication Date	Title
RU2158510C2 (ru)	2000-11-10	Композиция для повышения устойчивости растений к болезням (варианты)
US4542023A (en)	1985-09-17	Fungicidal salts of organophosphorus derivatives
NO141971B (no)	1980-03-03	Fungicide preparater for kontroll av soppsykdommer i planter
SU511832A3 (ru)	1976-04-25	Фунгицид и микробицид
EA012413B1 (ru)	2009-10-30	Соли металлов дигидрожасмоновой кислоты, композиции, включающие их и производные бензойной кислоты, и их применение в сельском хозяйстве
SU713526A3 (ru)	1980-01-30	Фунгицидна композици
CA1118785A (en)	1982-02-23	New isothiouronium phosphite derivatives
DE2016351A1 (de)	1971-01-21	Phenoxyacetaldehyd athylenacetale, Ver fahren zu ihrer Herstellung und ihre Verwen dung als Herbicide
US4049801A (en)	1977-09-20	Phosphite compounds as fungicidal agents
JPS6239563A (ja)	1987-02-20	β−ニトロフエネチル誘導体および農園芸用殺菌剤
US3968208A (en)	1976-07-06	Fungicidal compositions
SU1055314A3 (ru)	1983-11-15	Фунгицидное средство
DE2112643C3 (de)	1981-02-19	Formamidin-Derivate und sie enthaltende Mittel
CH616687A5 (de)	1980-04-15
SU849976A3 (ru)	1981-07-23	Фунгицидоинсектицидное средство
SU843696A3 (ru)	1981-06-30	Гербицидный состав
JP3624209B2 (ja)	2005-03-02	農園芸用殺菌剤
EP0252983B1 (de)	1992-09-09	Salze der n-(vinyloxyäthyl)dithiokarbamidsäure, herstellungsverfahren und schädlingsbekämpfungsmittel
SU379071A1 (ru)		Фунгицид
SU681779A1 (ru)	1983-07-15	Ртутные соли @ -(1-окси-2,2,2-трихлорэтил)-лактамов,обладающие свойствами фунгицидов и протравителей сем н
US3859444A (en)	1975-01-07	Methods of killing bacteria using alkylthiosemicarbazides
KR850000493B1 (ko)	1985-04-11	1-옥소 이소인 돌린 유도체의 제법
GB2078740A (en)	1982-01-13	Complex salts of lactams or thiolactams and halides or nitrates of heavy metals
RU2322439C2 (ru)	2008-04-20	Производные 3-(2-феноксибензоил)пиридина и фунгицидная композиция на их основе
RU1781211C (ru)	1992-12-15	N,NЪ-Бис-(винилоксиэтил)тиурамдисульфид, про вл ющий фунгицидную и бактерицидную активность