RU2003109610A - FUNGICID COMPOSITIONS - Google Patents

FUNGICID COMPOSITIONS

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Publication number
RU2003109610A
RU2003109610A RU2003109610/04A RU2003109610A RU2003109610A RU 2003109610 A RU2003109610 A RU 2003109610A RU 2003109610/04 A RU2003109610/04 A RU 2003109610/04A RU 2003109610 A RU2003109610 A RU 2003109610A RU 2003109610 A RU2003109610 A RU 2003109610A
Authority
RU
Russia
Prior art keywords
formula
compound
methyl
metalaxyl
ethyl
Prior art date
Application number
RU2003109610/04A
Other languages
Russian (ru)
Other versions
RU2270564C2 (en
Inventor
Козима НУНИНГЕР
Мартин Целлер
Original Assignee
Зингента Партисипейшнс Аг
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
Priority claimed from GBGB0022338.8A external-priority patent/GB0022338D0/en
Application filed by Зингента Партисипейшнс Аг filed Critical Зингента Партисипейшнс Аг
Publication of RU2003109610A publication Critical patent/RU2003109610A/en
Application granted granted Critical
Publication of RU2270564C2 publication Critical patent/RU2270564C2/en

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Claims (8)

1. Способ борьбы с фитопатогенными болезнями культурных растений, предусматривающий обработку культурных растений или места их произрастания, зараженных этой фитопатогенной болезнью, эффективным количеством композиции, содержащей1. A method of combating phytopathogenic diseases of cultivated plants, comprising treating cultivated plants or their growth sites infected with this phytopathogenic disease with an effective amount of a composition containing А) N-сульфонилвалинамид формулы IA) N-sulfonylvalinamide of the formula I
Figure 00000001
Figure 00000001
где R1 обозначает водород, С14алкил, С36циклоалкил или галофенил;where R 1 denotes hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl or halophenyl; R2 обозначает С14алкил,R 2 is C 1 -C 4 alkyl, в сочетанииin combination Б) либо с металаксилом формулы II, включая металаксил-М формулы IIаB) either with metalaxyl of formula II, including metalaxyl-M of formula IIa
Figure 00000002
Figure 00000002
Figure 00000003
Figure 00000003
либо с флуазинамом формулы IIIeither with fluazinam of the formula III
Figure 00000004
Figure 00000004
либо с манкоцебом формулы IVeither with mancozeb formula IV [-ScSNHCH2CH2NHCSSMn-]x[Zn]y, (IV)[-ScSNHCH 2 CH 2 NHCSSMn-] x [Zn] y , (IV) либо с хлорталонилом формулы Veither with chlorothalonil of formula V
Figure 00000005
Figure 00000005
либо со стробилурином формулы VIeither with strobilurin of formula VI
Figure 00000006
Figure 00000006
где Z обозначает CH или N;where Z is CH or N; R обозначаетR is
Figure 00000007
Figure 00000007
Figure 00000008
или
Figure 00000008
or
Figure 00000009
Figure 00000009
прежде всего со стробилуринами формул VIa, VIb или VIcprimarily with strobilurins of formulas VIa, VIb or VIc
Figure 00000010
Figure 00000010
Figure 00000011
Figure 00000011
Figure 00000012
Figure 00000012
либо с пираклостробином (BAS 500F) формулы VIIeither with pyraclostrobin (BAS 500F) of formula VII
Figure 00000013
Figure 00000013
либо с ацибензолар-S-метилом формулы VIIIeither with acibenzolar-S-methyl of formula VIII
Figure 00000014
Figure 00000014
либо с диметоморфом формулы IXeither with a dimetomorph of formula IX
Figure 00000015
Figure 00000015
либо с флудиоксонилом формулы Хeither with fludioxonil formula X
Figure 00000016
Figure 00000016
либо с цимоксанилом формулы XIeither with cymoxanil of formula XI
Figure 00000017
Figure 00000017
либо с имазалилом формулы XII, включая S-имазалил формулы ХIIаor with imazalil of formula XII, including S-imazalil of formula XIIa
Figure 00000018
Figure 00000019
Figure 00000018
Figure 00000019
2. Способ по п.1, где компонент А) представляет собой соединение формулы I, где R1 обозначает водород, метил, этил, хлорфенил или бромфенил, или где R1 обозначает водород, этил, 4-хлорфенил или 4-бромфенил, или где R1 обозначает 4-хлорфенил, или где R2 обозначает метил или этил, или где R2 обозначает метил, или где R1 обозначает водород, этил, 4-хлорфенил или 4-бромфенил и R2 обозначает метил или этил, или где R1 обозначает 4-хлорфенил и R2 обозначает метил или этил.2. The method according to claim 1, where component A) is a compound of formula I, where R 1 is hydrogen, methyl, ethyl, chlorophenyl or bromophenyl, or where R 1 is hydrogen, ethyl, 4-chlorophenyl or 4-bromophenyl, or where R 1 is 4-chlorophenyl, or where R 2 is methyl or ethyl, or where R 2 is methyl, or where R 1 is hydrogen, ethyl, 4-chlorophenyl or 4-bromophenyl and R 2 is methyl or ethyl, or where R 1 is 4-chlorophenyl and R 2 is methyl or ethyl. 3. Способ по п.1 или 2, где компонент Б) выбирают из группы, включающей ацибензолар-S-метил, азоксистробин, хлороталонил, цимоксанил, диметоморф, флуазинам, флудиоксонил, имазалил, S-имазалил, манкоцеб, металаксил, металаксил-М, пикоксистробин, пираклостробин (BAS 500F) и трифлоксистробин.3. The method according to claim 1 or 2, where component B) is selected from the group consisting of acibenzolar-S-methyl, azoxystrobin, chlorothalonil, cymoxanil, dimethomorph, fluazinam, fludioxonil, imazalil, S-imazalil, mancozeb, metalaxyl, metalaxyl-M , picoxystrobin, pyraclostrobin (BAS 500F) and trifloxystrobin. 4. Способ по п.1 или 2, где компонент Б) представляет собой металаксил или металаксил-М.4. The method according to claim 1 or 2, where component B) is metalaxyl or metalaxyl-M. 5. Способ по любому из пп.1-4, где компонент А) выбирают из группы, включающей соединения I.01, I.11, I.12, I.13, I.14, I.15, I.17, I.19, I.20, I.21 и I.22.5. The method according to any one of claims 1 to 4, where component A) is selected from the group consisting of compounds I.01, I.11, I.12, I.13, I.14, I.15, I.17, I.19, I.20, I.21 and I.22. 6. Способ по п.5, где компонент А) представляет собой соединение I.13, или соединение I.14, или соединение I.15, или соединение I.17, или соединение I.19, или соединение I.20, или соединение I.21.6. The method according to claim 5, where component A) is a compound I.13, or a compound I.14, or a compound I.15, or a compound I.17, or a compound I.19, or a compound I.20, or Compound I.21. 7. Фунгицидная композиция, содержащая эффективную в качестве фунгицида комбинацию компонентов А) и Б) по п.1 в сочетании с приемлемым для сельского хозяйства носителем и необязательно поверхностно-активным веществом.7. A fungicidal composition containing a combination of components A) and B) effective as a fungicide according to claim 1 in combination with an agriculturally acceptable carrier and optionally a surfactant. 8. Композиция по п.7, где массовое соотношение А) к Б) составляет от 2000:1 до 1:1000.8. The composition according to claim 7, where the mass ratio of A) to B) is from 2000: 1 to 1: 1000.
RU2003109610/04A 2000-09-12 2001-09-10 Method for controlling of cultural plant phytopathogenic diseases and fungicide composition RU2270564C2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0022338.8A GB0022338D0 (en) 2000-09-12 2000-09-12 Organic Compounds
GB0022338.8 2000-09-12

Publications (2)

Publication Number Publication Date
RU2003109610A true RU2003109610A (en) 2004-09-20
RU2270564C2 RU2270564C2 (en) 2006-02-27

Family

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RU2003109610/04A RU2270564C2 (en) 2000-09-12 2001-09-10 Method for controlling of cultural plant phytopathogenic diseases and fungicide composition

Country Status (23)

Country Link
EP (1) EP1317178B1 (en)
JP (1) JP2004518623A (en)
KR (1) KR20030029977A (en)
CN (1) CN1455641A (en)
AR (1) AR030637A1 (en)
AT (1) ATE266316T1 (en)
AU (2) AU2002212227B2 (en)
BR (1) BR0113815A (en)
CA (1) CA2421226A1 (en)
CR (1) CR6915A (en)
DE (1) DE60103292T2 (en)
EC (1) ECSP034508A (en)
ES (1) ES2217194T3 (en)
GB (1) GB0022338D0 (en)
GT (1) GT200100182A (en)
HU (1) HUP0301024A3 (en)
IL (1) IL154573A0 (en)
MX (1) MXPA03002117A (en)
PL (1) PL360142A1 (en)
RU (1) RU2270564C2 (en)
TW (1) TWI220381B (en)
WO (1) WO2002021918A1 (en)
ZA (1) ZA200301569B (en)

Families Citing this family (12)

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Publication number Priority date Publication date Assignee Title
CN100340167C (en) * 2002-12-06 2007-10-03 陶氏农业科学公司 Synergistic compositions
BRPI0418640A (en) * 2004-03-16 2007-05-29 Syngenta Partcipations Ag pesticide composition and method for seed treatment
BRPI0519234A2 (en) * 2004-12-23 2009-01-06 Basf Ag fungicidal mixtures to combat phytopathogenic harmful fungi, agent, process to combat phytopathogenic harmful fungi, seeds, and, use of compounds
EP2036438A1 (en) * 2007-09-12 2009-03-18 Bayer CropScience AG Post-harvest treatment
CN101708003B (en) * 2009-12-23 2013-02-27 深圳诺普信农化股份有限公司 Sterilizing composition containing active ester
CN101889573B (en) * 2010-03-02 2013-01-02 陕西美邦农资贸易有限公司 Sterilizing composite with imazaril and azoxystrobin
CN102150656B (en) * 2010-12-06 2012-10-10 北京颖泰嘉和生物科技有限公司 Bactericide composition, preparation and application thereof
CN102204535A (en) * 2011-04-12 2011-10-05 陕西汤普森生物科技有限公司 Antibacterial composition containing picoxystrobin and chlorothalonil
BR112014016890B1 (en) 2012-01-24 2019-05-07 Sumitomo Chemical Company, Limited Composition and methods for plant disease control
CN102578127A (en) * 2012-02-06 2012-07-18 山东禾宜生物科技有限公司 Bactericide for controlling cucumber downy mildew
CN103329938B (en) * 2013-07-09 2015-02-04 四川大学 Pesticide composition and applications thereof in preventing and controlling saffron crocus corm rot
CN109310088A (en) * 2016-06-17 2019-02-05 因多菲尔实业有限公司 A kind of Fungicidal mixture

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL178747B1 (en) * 1994-05-04 2000-06-30 Novartis Ag Amides of n-sulphonyl and n-sulphinyl amino acids as microbisidal agents
ES2186145T3 (en) * 1997-02-25 2003-05-01 Syngenta Participations Ag AMIDAS OF N-SULFONIL AND N-SULFINIL AMINO ACIDS AS MICROBICIDES.
GT199800109A (en) * 1997-08-06 2000-01-13 DERIVATIVES OF N-SULFONILGLICINALQUINILOXIFENETILAMIDA MICROBICIDAS.
GB9804265D0 (en) * 1998-02-27 1998-04-22 Ciba Geigy Ag Organic compounds
GB9826649D0 (en) * 1998-12-03 1999-01-27 Novartis Ag Organic compounds
TW564244B (en) * 1999-01-11 2003-12-01 Novartis Ag Novel propargylether derivatives

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