ES2063264T3 - Oxazolidinonas fungicidas. - Google Patents
Oxazolidinonas fungicidas.Info
- Publication number
- ES2063264T3 ES2063264T3 ES90303859T ES90303859T ES2063264T3 ES 2063264 T3 ES2063264 T3 ES 2063264T3 ES 90303859 T ES90303859 T ES 90303859T ES 90303859 T ES90303859 T ES 90303859T ES 2063264 T3 ES2063264 T3 ES 2063264T3
- Authority
- ES
- Spain
- Prior art keywords
- substituted
- ring
- alkyl
- phenyl
- cycloalkyl
- 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 - Lifetime
Links
- IZXIZTKNFFYFOF-UHFFFAOYSA-N 2-Oxazolidone Chemical compound O=C1NCCO1 IZXIZTKNFFYFOF-UHFFFAOYSA-N 0.000 title 1
- 239000000417 fungicide Substances 0.000 title 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 17
- 125000000217 alkyl group Chemical group 0.000 abstract 8
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 7
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 4
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 150000002367 halogens Chemical class 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical group C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 abstract 3
- -1 benzyl carbon Chemical compound 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical group C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 abstract 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000002837 carbocyclic group Chemical group 0.000 abstract 2
- 125000002541 furyl group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 2
- 125000001624 naphthyl group Chemical group 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000004076 pyridyl group Chemical group 0.000 abstract 2
- 125000001544 thienyl group Chemical group 0.000 abstract 2
- 125000006665 (C2 to C4) alkoxycarbonyl group Chemical group 0.000 abstract 1
- KAESVJOAVNADME-UHFFFAOYSA-N 1H-pyrrole Chemical group C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 abstract 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000006539 C12 alkyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 208000031888 Mycoses Diseases 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000004702 alkoxy alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- HRDXJKGNWSUIBT-UHFFFAOYSA-N methoxybenzene Chemical group [CH2]OC1=CC=CC=C1 HRDXJKGNWSUIBT-UHFFFAOYSA-N 0.000 abstract 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 abstract 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 125000005495 pyridazyl group Chemical class 0.000 abstract 1
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 1
- 125000000168 pyrrolyl group Chemical group 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D263/44—Two 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D263/46—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/10—Spiro-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Un procedimiento para reprimir enfermedades por hongos en plantas que comprende el tratamiento del lugar que se va a protegar con una cantidad efectiva de un compuesto de Fórmula I. en la que: A esOoNR 4 ; W esOoS; R 1 es H; C1 a C6 alquilo; C1 a C6 haloalquilo; C3 a C6 cicloalquilo; C2 a C6 alquenilo; C2 a C6 alquinilo; C2 a C6 alcoxialquilo; C1 a C3 alquilo sustituido con C3 a C6 cicloalquilo, fenilo o bencilo, en donde dicho anillo de fenilo o bencilo está sustituido en el anillo con R 6 , y el carbono bencílico está sustituido con R 7 ; R 2 es fenilo sustituido con R 5 y R 6 ; naftilo sustituido con 1 ó 2 grupos seleccionados de R 6 ; tienilo sustituido con R 5 y R 6 ; furilo sustituido con R 6 ; piridilo sustituido con uno de los siguientes: R 6 ; fenoxi sustituido con R 6 , o feniltio sustituido con R 6 ; C1 a C2 alquilo sustituido con fenoxi o feniltio, estando sustituidos dichos fenoxi o feniltio en el anillo con R 6 ; C1 a C6 alquilo; o C5 a C7 cicloalquilo; y R 1 y R 2 pueden tomarse conjuntamente, junto al carbono al que están unidos, para formar un anillo carbocíclico o heterocíclico (conteniendo O, N-R 7 ,oS)de5 a 7 átomos en el anillo en que el anillo heterocíclico puede estar fusionado con un anillo bencénico sustituido con R 5 o un anillo de tiofeno sustituido con R 6 , no estando unido el heteroátomo al centro espiro; y el anillo carbocíclico puede estar fusionado con 1 o 2 anillos bencénicos sustituidos con R 5 o con un anillo de tiofeno sustituido con R 6 ; R 3 es fenilo sustituido con R 10 ; bencilo sustituido en el carbono bencílico con un grupo seleccionado de R 7 y sustituido en el anillo de fenilo con R 10 ; naftilo sustituido con R 10 ; adicionalmente, R 3 puede ser tienilo sustituido con R 10 , furilo sustituido con R 10 , piridilo sustituido con R 10 , pirimidilo sustituido con R 10 , o piridazilo sustituido con R 10 ; oR 3 puede ser C2 a C10 alquilo o C5 a C7 cicloalquilo; R 4 es hidrógeno; formilo; C2 a C4 alquilcarbonilo; C2 a C4 haloalquilcarbonilo; C2 a C4 alcoxialquilcarbonilo; C2 a C4 alcoxicarbonilo; C2 a C5 alquilaminocarbonilo; C1 a C4 alquilsulfonilo; C1 a C4 alquilo; C4 a C6 cicloalquilo; fenilaminocarbonilo donde dicho fenilo está sustituido con R 10 ; yR 4 puede ser C3 a C4 alquenilo o C3 a C4 alquinilo; o R 3 y R 4 pueden tomarse conjuntamente, junto con el átomo de nitrógeno al que están unidos, para formar un anillo de pirrolidina, piperidina o pirrol sustituidos con R 10 , anillos que pueden estar fusionados a un anillo bencénico sustituido con R 10 ; R 5 es hidrógeno, halógeno, C1 a C12 alquilo; C1 a C12 haloalquilo; C1 a C12 alcoxi; C3 a C12 alquenilo; C3 a C12 haloalquenilo; C3 a C12 alqueniloxi; C3 a C12 alquinilo; C3 a C12 haloalquinilo; C3 a C12 alquiltio; C1 a C12 haloalquiltio; C1 a C12 haloalcoxi; C1 a C12 alquilsulfonilo; C1 a C12 haloalquilsulfonilo; nitro; fenilo sustituido con R 6 ; fenoxi sustituidoconR 6 ; feniltio sustituido con R 6 ; ciano;C3 a C12 alquiniloxi; C2 a C12 alcoxialquilo; C2 a C12 alcoxialcoxi; fenoximetilo sustituido en el anillo de fenilo con R 6 ; benciloxi sustituido en el anillo de fenilo con R 6 ; fenetiloxi sustituido en el anillo de fenilo con R 6 ; fenetilo sustituido en el anillo de fenilo con R 6 ; bencilo sustituido en el anillo de fenilo con R 6 ; C2 a C12 carboalcoxi; C5 a C6 cicloalquilo; NMe2; oNR 8 R 9 ; R 6 es hidrógeno; 1 a 2 halógenos; C1 a C4 alquilo; tri uorometilo; C1 a C4 alcoxi; metiltio; nitro; fenoxi; C2 a C6 cicloalquiloxi; o C6 a C6 cicloalquilo; R 7 es hidrógeno; o C1 a C4 alquilo; R 8 es H; o C1 a C4 alquilo; R 9 es H; fenilo sustituido con H; 1-2 halógenos; CF3; C1 a C2 alquilo; o C1 a C2 alcoxi; y R 10 es 0-2 grupos seleccionados de CF3; CF3O; NO2; CO2Me; halógeno; C1 a C5 alquilo; C1 a C5 alcoxi; o CN; a condición de que cuando el anillo R 3 es disustituido, uno de los grupos R 10 alquilo o alcoxi no son superiores a C1; con la condición de que, cuando A es oxígeno, R 3 es fenilo sustituido con R 10 .
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US34174289A | 1989-04-21 | 1989-04-21 | |
| US07/341,741 US4957933A (en) | 1989-04-21 | 1989-04-21 | Fungicidal oxazolidinones |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2063264T3 true ES2063264T3 (es) | 1995-01-01 |
Family
ID=26992641
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES90303859T Expired - Lifetime ES2063264T3 (es) | 1989-04-21 | 1990-04-10 | Oxazolidinonas fungicidas. |
Country Status (24)
| Country | Link |
|---|---|
| EP (2) | EP0393911B1 (es) |
| JP (1) | JP2963388B2 (es) |
| KR (1) | KR0148128B1 (es) |
| CN (2) | CN1028143C (es) |
| AT (1) | ATE110719T1 (es) |
| AU (1) | AU638460B2 (es) |
| BG (1) | BG60677B1 (es) |
| BR (1) | BR9007309A (es) |
| CZ (1) | CZ286037B6 (es) |
| DE (2) | DE69011930T2 (es) |
| DK (1) | DK0393911T3 (es) |
| ES (1) | ES2063264T3 (es) |
| FI (1) | FI914927A0 (es) |
| HU (1) | HU214551B (es) |
| IE (1) | IE66407B1 (es) |
| IL (1) | IL94152A (es) |
| NL (1) | NL350010I2 (es) |
| NO (1) | NO914117L (es) |
| NZ (1) | NZ233374A (es) |
| RO (1) | RO111765B1 (es) |
| RU (1) | RU2092051C1 (es) |
| UA (1) | UA35548C2 (es) |
| WO (1) | WO1990012791A1 (es) |
| YU (1) | YU80390A (es) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1991019703A2 (en) * | 1990-06-11 | 1991-12-26 | E.I. Du Pont De Nemours And Company | Fungicidal iminooxazolidinones |
| WO1992016515A1 (en) * | 1991-03-15 | 1992-10-01 | E.I. Du Pont De Nemours And Company | Fungicidal 4-thioxooxazolidin-2-ones and 4-iminooxazolindin-2-ones |
| AU647599B2 (en) * | 1991-03-27 | 1994-03-24 | Sankyo Company Limited | New thiazolidinone and oxazolidinone derivatives, their preparation and their use as vasodilators |
| FR2685328B1 (fr) * | 1991-12-20 | 1995-12-01 | Rhone Poulenc Agrochimie | Derives de 2-imidazoline-5-ones et 2-imidazoline-5-thiones fongicides. |
| WO1993018016A1 (en) * | 1992-03-11 | 1993-09-16 | E.I. Du Pont De Nemours And Company | Fungicidal oxazolidinones |
| WO1993022299A1 (en) * | 1992-04-24 | 1993-11-11 | E.I. Du Pont De Nemours And Company | Fungicidal oxazolidinones |
| EP0642502B1 (en) * | 1992-05-22 | 2000-07-12 | E.I. Du Pont De Nemours And Company | Fungicidal imidazolinones |
| HU215699B (hu) * | 1992-11-13 | 1999-02-01 | E. I. Du Pont De Nemours And Co. | Eljárás 2,4-oxazolidin-dionok és intermedierjeik előállítására |
| HUP9800413A3 (en) * | 1995-03-08 | 1998-07-28 | Du Pont | Fungicide composition containing 5-methyl-5-(4-phenoxyphenyl)-3-phenylamino-2,4-oxazolidinedione and triazole-derivative compound as active ingredients and use thereof |
| CZ296513B6 (cs) * | 1995-07-12 | 2006-03-15 | E. I. Du Pont De Nemours And Company | Synergická fungicidní kompozice |
| GB9607784D0 (en) * | 1996-04-15 | 1996-06-19 | Zeneca Ltd | Fungicides |
| GB9607785D0 (en) * | 1996-04-15 | 1996-06-19 | Zeneca Ltd | Fungicides |
| CA2280809C (en) * | 1997-03-05 | 2007-04-24 | Novartis Ag | Fungicidal compositions based on metalyxyl |
| FR2771898B1 (fr) * | 1997-12-04 | 2000-01-07 | Rhone Poulenc Agrochimie | Composition fongicide et/ou bactericide synergique |
| US6090806A (en) * | 1998-08-31 | 2000-07-18 | American Cyanamid Company | Fungicidal mixtures |
| DE10347090A1 (de) | 2003-10-10 | 2005-05-04 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| DE10349501A1 (de) | 2003-10-23 | 2005-05-25 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| DE102004021532A1 (de) * | 2004-05-03 | 2005-12-08 | Degussa Ag | Dispersion mit insektizider Wirkung |
| DE102005015677A1 (de) | 2005-04-06 | 2006-10-12 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| DE102005026482A1 (de) | 2005-06-09 | 2006-12-14 | Bayer Cropscience Ag | Wirkstoffkombinationen |
| EA201270781A1 (ru) | 2005-06-09 | 2013-09-30 | Байер Кропсайенс Аг | Комбинации биологически активных веществ |
| DE102007045920B4 (de) | 2007-09-26 | 2018-07-05 | Bayer Intellectual Property Gmbh | Synergistische Wirkstoffkombinationen |
| CN101555207B (zh) * | 2008-04-10 | 2012-10-17 | 上海生农生化制品有限公司 | 一种对苯氧基苯基乳酸酯化高收率的方法 |
| MX2011009732A (es) | 2009-03-25 | 2011-09-29 | Bayer Cropscience Ag | Combinaciones de principios activos sinergicas. |
| KR20120051015A (ko) | 2009-07-16 | 2012-05-21 | 바이엘 크롭사이언스 아게 | 페닐 트리아졸을 함유하는 상승적 활성 물질 배합물 |
| CN103396410A (zh) * | 2013-08-07 | 2013-11-20 | 北京金五元科技发展有限责任公司 | 吡噁唑菌酮的合成及作为农用杀菌剂的应用 |
| CN104472502A (zh) * | 2014-11-27 | 2015-04-01 | 广东中迅农科股份有限公司 | 一种含有噁唑菌酮和咯菌腈的杀菌组合物 |
| CN104488888A (zh) * | 2014-12-03 | 2015-04-08 | 广东中迅农科股份有限公司 | 一种含有噁唑菌酮和苯锈啶的杀菌组合物 |
| EP2910126A1 (en) | 2015-05-05 | 2015-08-26 | Bayer CropScience AG | Active compound combinations having insecticidal properties |
| CN105541743A (zh) * | 2015-12-10 | 2016-05-04 | 上海生农生化制品有限公司 | 一种双联类噁唑菌酮化合物及其合成方法 |
| CN107540626A (zh) * | 2016-06-23 | 2018-01-05 | 华东理工大学 | 噁唑菌酮的多晶型及其制备方法 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2037717A (en) * | 1932-11-09 | 1936-04-21 | Du Pont | Xanthates and method of making same |
| US2891855A (en) | 1954-08-16 | 1959-06-23 | Geigy Ag J R | Compositions and methods for influencing the growth of plants |
| US3054794A (en) * | 1958-01-17 | 1962-09-18 | Us Vitamin Pharm Corp | Process for preparing 3-(aminoalkyl)-oxazolidine-2, 4-diones |
| US2928840A (en) * | 1958-11-26 | 1960-03-15 | Us Vitamin Pharm Corp | 3-(o-substituted phenyl) oxazolidinediones and process therefor |
| US3235361A (en) | 1962-10-29 | 1966-02-15 | Du Pont | Method for the control of undesirable vegetation |
| US3309192A (en) | 1964-12-02 | 1967-03-14 | Du Pont | Method of controlling seedling weed grasses |
| US3773782A (en) * | 1971-10-18 | 1973-11-20 | J Zielinski | Thiophosphates of acylated 3-amino-2-oxazolidones |
| DE2324591C2 (de) * | 1973-05-16 | 1985-12-12 | Basf Ag, 6700 Ludwigshafen | Oxazolidin-Derivate |
| US4150144A (en) * | 1977-02-15 | 1979-04-17 | Ciba-Geigy Corporation | 3-Phenyl-oxazolidine-2,4-dione microbicides |
| DE3682275D1 (de) * | 1985-10-11 | 1991-12-05 | Sagami Chem Res | Oxazolidindionabkoemmlinge, deren herstellungsverfahren und unkrautvertilgungsmittel, die diese enthalten. |
| GB8612630D0 (en) | 1986-05-23 | 1986-07-02 | Ici Plc | Biocides |
| US4957933A (en) | 1989-04-21 | 1990-09-18 | E. I. Du Pont De Nemours And Company | Fungicidal oxazolidinones |
| ES2224428T3 (es) | 1997-09-26 | 2005-03-01 | Celltech Pharma Europe Limited | Composicion farmnaceutica para el tratamiento de la enfermedad inflmatoria intestinal. |
-
1990
- 1990-04-10 KR KR1019910701399A patent/KR0148128B1/ko not_active Expired - Lifetime
- 1990-04-10 EP EP90303859A patent/EP0393911B1/en not_active Expired - Lifetime
- 1990-04-10 BR BR909007309A patent/BR9007309A/pt not_active IP Right Cessation
- 1990-04-10 AU AU56554/90A patent/AU638460B2/en not_active Ceased
- 1990-04-10 FI FI914927A patent/FI914927A0/fi not_active Application Discontinuation
- 1990-04-10 ES ES90303859T patent/ES2063264T3/es not_active Expired - Lifetime
- 1990-04-10 EP EP90907560A patent/EP0469061A1/en active Pending
- 1990-04-10 DE DE69011930T patent/DE69011930T2/de not_active Expired - Lifetime
- 1990-04-10 RU SU905010194A patent/RU2092051C1/ru active
- 1990-04-10 WO PCT/US1990/002076 patent/WO1990012791A1/en not_active Ceased
- 1990-04-10 DK DK90303859.4T patent/DK0393911T3/da active
- 1990-04-10 RO RO148595A patent/RO111765B1/ro unknown
- 1990-04-10 UA UA5010194A patent/UA35548C2/uk unknown
- 1990-04-10 HU HU904470A patent/HU214551B/hu unknown
- 1990-04-10 AT AT90303859T patent/ATE110719T1/de not_active IP Right Cessation
- 1990-04-10 DE DE2001199034 patent/DE10199034I2/de active Active
- 1990-04-19 NZ NZ233374A patent/NZ233374A/xx unknown
- 1990-04-20 IE IE141090A patent/IE66407B1/en not_active IP Right Cessation
- 1990-04-20 CZ CS901984A patent/CZ286037B6/cs not_active IP Right Cessation
- 1990-04-20 IL IL9415290A patent/IL94152A/en not_active IP Right Cessation
- 1990-04-21 CN CN90103920A patent/CN1028143C/zh not_active Expired - Lifetime
- 1990-04-23 YU YU00803/90A patent/YU80390A/xx unknown
-
1991
- 1991-10-18 BG BG95344A patent/BG60677B1/xx unknown
- 1991-10-18 NO NO91914117A patent/NO914117L/no unknown
-
1993
- 1993-12-23 CN CN93121368A patent/CN1058841C/zh not_active Expired - Lifetime
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1996
- 1996-04-01 JP JP8101941A patent/JP2963388B2/ja not_active Expired - Lifetime
-
2003
- 2003-01-22 NL NL350010C patent/NL350010I2/nl unknown
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