IL99868A - 2-(3-oxypyridinyl)-1,3-dioxolane and dioxane derivatives fungicidal compositions containing the same and methods for controlling fungi utilizing the same - Google Patents

2-(3-oxypyridinyl)-1,3-dioxolane and dioxane derivatives fungicidal compositions containing the same and methods for controlling fungi utilizing the same

Info

Publication number: IL99868A
Authority: IL; Israel
Prior art keywords: compound; hydrogen; structural formula; halogen; same
Prior art date: 1990-10-26

Application number

IL9986891A

Other languages

English (en)

Other versions

IL99868A0 (en

Original Assignee

Uniroyal Chemical Ltd

Uniroyal Chem Co Inc

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.)

1990-10-26

Filing date

1991-10-27

Publication date

1995-12-08

1991-10-27 Application filed by Uniroyal Chemical Ltd, Uniroyal Chem Co Inc filed Critical Uniroyal Chemical Ltd

1992-08-18 Publication of IL99868A0 publication Critical patent/IL99868A0/xx

1995-12-08 Publication of IL99868A publication Critical patent/IL99868A/en

Links

239000000203 mixture Substances 0.000 title claims abstract description 56
241000233866 Fungi Species 0.000 title claims abstract description 48
238000000034 method Methods 0.000 title claims abstract description 26
230000000855 fungicidal effect Effects 0.000 title description 10
150000002012 dioxanes Chemical class 0.000 title description 3
150000001875 compounds Chemical class 0.000 claims abstract description 106
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 23
239000001257 hydrogen Substances 0.000 claims abstract description 23
229910052736 halogen Inorganic materials 0.000 claims abstract description 19
150000002367 halogens Chemical group 0.000 claims abstract description 19
-1 nitro, cyano, phenyl Chemical group 0.000 claims abstract description 14
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 11
125000004953 trihalomethyl group Chemical group 0.000 claims abstract description 11
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 10
150000002431 hydrogen Chemical group 0.000 claims abstract description 10
230000003032 phytopathogenic effect Effects 0.000 claims abstract description 10
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims abstract description 9
239000000460 chlorine Chemical group 0.000 claims abstract description 8
229910052801 chlorine Inorganic materials 0.000 claims abstract description 8
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 7
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 7
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 5
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 5
229910052794 bromium Chemical group 0.000 claims abstract description 5
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 4
125000000217 alkyl group Chemical group 0.000 claims description 15
150000003839 salts Chemical class 0.000 claims description 13
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 9
125000003545 alkoxy group Chemical group 0.000 claims description 8
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
239000002253 acid Substances 0.000 claims description 7
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 5
125000001309 chloro group Chemical group Cl* 0.000 claims description 4
229940098779 methanesulfonic acid Drugs 0.000 claims description 4
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
150000007522 mineralic acids Chemical class 0.000 claims description 2
125000006004 trihaloethyl group Chemical group 0.000 claims 1
125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 2
125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
241000196324 Embryophyta Species 0.000 description 52
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
239000000243 solution Substances 0.000 description 19
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 18
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
239000000839 emulsion Substances 0.000 description 16
201000010099 disease Diseases 0.000 description 15
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 15
239000007788 liquid Substances 0.000 description 15
239000000417 fungicide Substances 0.000 description 14
241000209219 Hordeum Species 0.000 description 13
239000007787 solid Substances 0.000 description 13
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
GRFNBEZIAWKNCO-UHFFFAOYSA-N mhp Natural products OC1=CC=CN=C1 GRFNBEZIAWKNCO-UHFFFAOYSA-N 0.000 description 12
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 12
238000012360 testing method Methods 0.000 description 11
235000007340 Hordeum vulgare Nutrition 0.000 description 10
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 10
239000002689 soil Substances 0.000 description 10
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
241000221785 Erysiphales Species 0.000 description 9
239000002904 solvent Substances 0.000 description 9
240000008067 Cucumis sativus Species 0.000 description 8
238000002360 preparation method Methods 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 7
230000012010 growth Effects 0.000 description 7
239000004094 surface-active agent Substances 0.000 description 7
230000009885 systemic effect Effects 0.000 description 7
230000005764 inhibitory process Effects 0.000 description 6
238000011081 inoculation Methods 0.000 description 6
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 6
229910000027 potassium carbonate Inorganic materials 0.000 description 6
AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 6
238000003756 stirring Methods 0.000 description 6
FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical group CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 5
230000002411 adverse Effects 0.000 description 5
230000015572 biosynthetic process Effects 0.000 description 5
239000002270 dispersing agent Substances 0.000 description 5
239000000047 product Substances 0.000 description 5
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 5
244000046052 Phaseolus vulgaris Species 0.000 description 4
239000000969 carrier Substances 0.000 description 4
238000000576 coating method Methods 0.000 description 4
230000008018 melting Effects 0.000 description 4
238000002844 melting Methods 0.000 description 4
239000000843 powder Substances 0.000 description 4
125000001424 substituent group Chemical group 0.000 description 4
XKTYXVDYIKIYJP-UHFFFAOYSA-N 3h-dioxole Chemical compound C1OOC=C1 XKTYXVDYIKIYJP-UHFFFAOYSA-N 0.000 description 3
235000010799 Cucumis sativus var sativus Nutrition 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
238000005481 NMR spectroscopy Methods 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
239000000443 aerosol Substances 0.000 description 3
239000011248 coating agent Substances 0.000 description 3
150000004862 dioxolanes Chemical class 0.000 description 3
230000000694 effects Effects 0.000 description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
238000001914 filtration Methods 0.000 description 3
208000015181 infectious disease Diseases 0.000 description 3
238000010992 reflux Methods 0.000 description 3
150000000093 1,3-dioxanes Chemical class 0.000 description 2
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical class C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 description 2
229920001817 Agar Polymers 0.000 description 2
241000213004 Alternaria solani Species 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
241000315044 Passalora arachidicola Species 0.000 description 2
235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 2
239000008272 agar Substances 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
230000001627 detrimental effect Effects 0.000 description 2
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
235000013399 edible fruits Nutrition 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
230000007613 environmental effect Effects 0.000 description 2
238000009472 formulation Methods 0.000 description 2
230000002538 fungal effect Effects 0.000 description 2
239000007789 gas Substances 0.000 description 2
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
229910000041 hydrogen chloride Inorganic materials 0.000 description 2
239000000463 material Substances 0.000 description 2
238000001556 precipitation Methods 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
238000007363 ring formation reaction Methods 0.000 description 2
238000010079 rubber tapping Methods 0.000 description 2
239000008247 solid mixture Substances 0.000 description 2
241000894007 species Species 0.000 description 2
239000000725 suspension Substances 0.000 description 2
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 1
125000006091 1,3-dioxolane group Chemical class 0.000 description 1
JZYJCPDIYHVNKR-UHFFFAOYSA-N 2-(bromomethyl)-2-(2-bromophenyl)-1,3-dioxolane Chemical compound C=1C=CC=C(Br)C=1C1(CBr)OCCO1 JZYJCPDIYHVNKR-UHFFFAOYSA-N 0.000 description 1
KTBBVIQIYGLVMD-UHFFFAOYSA-N 2-(bromomethyl)-2-[4-[3-(trifluoromethyl)phenoxy]phenyl]-1,3-dioxolane Chemical compound FC(F)(F)C1=CC=CC(OC=2C=CC(=CC=2)C2(CBr)OCCO2)=C1 KTBBVIQIYGLVMD-UHFFFAOYSA-N 0.000 description 1
WFNWWGSTRUUCRD-UHFFFAOYSA-N 3-[[2-(4-bromophenyl)-1,3-dioxolan-2-yl]methoxy]pyridine;methanesulfonic acid Chemical compound CS(O)(=O)=O.C1=CC(Br)=CC=C1C1(COC=2C=NC=CC=2)OCCO1 WFNWWGSTRUUCRD-UHFFFAOYSA-N 0.000 description 1
RYIIDFFVBUDIAW-UHFFFAOYSA-N 3-[[2-(4-phenylphenyl)-1,3-dioxolan-2-yl]methoxy]pyridine Chemical compound O1CCOC1(C=1C=CC(=CC=1)C=1C=CC=CC=1)COC1=CC=CN=C1 RYIIDFFVBUDIAW-UHFFFAOYSA-N 0.000 description 1
PVJIOHORCFOVST-UHFFFAOYSA-N 3-[[4,5-dimethyl-2-(4-phenylphenyl)-1,3-dioxolan-2-yl]methoxy]pyridine Chemical compound O1C(C)C(C)OC1(C=1C=CC(=CC=1)C=1C=CC=CC=1)COC1=CC=CN=C1 PVJIOHORCFOVST-UHFFFAOYSA-N 0.000 description 1
SRLXKWCLAGDKAM-UHFFFAOYSA-N 3-tetradecoxypyridine Chemical class CCCCCCCCCCCCCCOC1=CC=CN=C1 SRLXKWCLAGDKAM-UHFFFAOYSA-N 0.000 description 1
125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 description 1
241001530056 Athelia rolfsii Species 0.000 description 1
241000228438 Bipolaris maydis Species 0.000 description 1
241001480061 Blumeria graminis Species 0.000 description 1
241000123650 Botrytis cinerea Species 0.000 description 1
241000221787 Erysiphe Species 0.000 description 1
241000896222 Erysiphe polygoni Species 0.000 description 1
241000223221 Fusarium oxysporum Species 0.000 description 1
241000896246 Golovinomyces cichoracearum Species 0.000 description 1
241001330975 Magnaporthe oryzae Species 0.000 description 1
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
241000233622 Phytophthora infestans Species 0.000 description 1
241000221696 Sclerotinia sclerotiorum Species 0.000 description 1
241000221577 Uromyces appendiculatus Species 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
239000013543 active substance Substances 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
AGEZXYOZHKGVCM-UHFFFAOYSA-N benzyl bromide Chemical class BrCC1=CC=CC=C1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
125000000319 biphenyl-4-yl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 1
238000009835 boiling Methods 0.000 description 1
125000004799 bromophenyl group Chemical group 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
238000004113 cell culture Methods 0.000 description 1
239000003610 charcoal Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000000151 deposition Methods 0.000 description 1
239000003599 detergent Substances 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
229940113088 dimethylacetamide Drugs 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
125000000532 dioxanyl group Chemical group 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
230000035784 germination Effects 0.000 description 1
239000008187 granular material Substances 0.000 description 1
230000009036 growth inhibition Effects 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000008263 liquid aerosol Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
BLTAPEIEHGWKKN-UHFFFAOYSA-N methanesulfonate;pyridin-1-ium Chemical compound CS(O)(=O)=O.C1=CC=NC=C1 BLTAPEIEHGWKKN-UHFFFAOYSA-N 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
239000011707 mineral Substances 0.000 description 1
230000017066 negative regulation of growth Effects 0.000 description 1
238000005580 one pot reaction Methods 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000006072 paste Substances 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
230000002265 prevention Effects 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
238000012552 review Methods 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
238000007711 solidification Methods 0.000 description 1
230000008023 solidification Effects 0.000 description 1
239000007921 spray Substances 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid group Chemical class S(O)(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
239000010455 vermiculite Substances 0.000 description 1
229910052902 vermiculite Inorganic materials 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings

Landscapes

Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Plural Heterocyclic Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

IL9986891A 1990-10-26 1991-10-27 2-(3-oxypyridinyl)-1,3-dioxolane and dioxane derivatives fungicidal compositions containing the same and methods for controlling fungi utilizing the same IL99868A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US07/603,969 US5071862A (en)	1990-10-26	1990-10-26	2-(3-oxypyridinyl)-1,3-dioxolane and dioxane compounds, compositions containing same and process for controlling fungi using same

Publications (2)

Publication Number	Publication Date
IL99868A0 IL99868A0 (en)	1992-08-18
IL99868A true IL99868A (en)	1995-12-08

Family

ID=24417636

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL9986891A IL99868A (en)	1990-10-26	1991-10-27	2-(3-oxypyridinyl)-1,3-dioxolane and dioxane derivatives fungicidal compositions containing the same and methods for controlling fungi utilizing the same

Country Status (14)

Country	Link
US (1)	US5071862A (de)
EP (1)	EP0555365B1 (de)
CN (1)	CN1062907A (de)
AT (1)	ATE115578T1 (de)
AU (1)	AU9017891A (de)
CA (1)	CA2094799A1 (de)
DE (1)	DE69105995T2 (de)
DK (1)	DK0555365T3 (de)
IE (1)	IE913733A1 (de)
IL (1)	IL99868A (de)
MX (1)	MX9101775A (de)
WO (1)	WO1992007848A1 (de)
YU (1)	YU171391A (de)
ZA (1)	ZA918572B (de)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5660981A (en) *	1994-06-06	1997-08-26	E. I. Du Pont De Nemours And Company	Selection of diagnostic genetic markers in microorganisms and use of a specific marker for detection of salmonella
US5580544A (en) *	1995-03-29	1996-12-03	Uniroyal Chemical Company, Inc.	Paste formulation useful for seed treatment and foliar treatment of plants
US5719103A (en) *	1996-05-02	1998-02-17	Uniroyal Chemical Company, Inc.	Powder formulation useful for seed treatment and foliar treatment of plants
GB9919558D0 (en) *	1999-08-18	1999-10-20	Hoechst Schering Agrevo Gmbh	Fungicidal compounds
US7081436B2 (en)	2001-01-26	2006-07-25	General Electric Company	Paste formulation for seed treatment of plants

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4143144A (en) *	1978-03-23	1979-03-06	The Dow Chemical Company	Ethers of 4-halomethylpyridines
US4590198A (en) *	1983-02-24	1986-05-20	Chugai Seiyaku Kabushiki Kaisha	Fungicidal isonicotinanllide retals, their compositions and method of using them
DE3476543D1 (en) *	1983-05-19	1989-03-09	Ciba Geigy Ag	Microbicides

1990
- 1990-10-26 US US07/603,969 patent/US5071862A/en not_active Expired - Fee Related
1991
- 1991-10-22 DK DK92900034.7T patent/DK0555365T3/da active
- 1991-10-22 AT AT92900034T patent/ATE115578T1/de not_active IP Right Cessation
- 1991-10-22 DE DE69105995T patent/DE69105995T2/de not_active Expired - Fee Related
- 1991-10-22 WO PCT/US1991/007801 patent/WO1992007848A1/en not_active Ceased
- 1991-10-22 EP EP92900034A patent/EP0555365B1/de not_active Expired - Lifetime
- 1991-10-22 CA CA002094799A patent/CA2094799A1/en not_active Abandoned
- 1991-10-22 AU AU90178/91A patent/AU9017891A/en not_active Abandoned
- 1991-10-25 YU YU171391A patent/YU171391A/sh unknown
- 1991-10-25 MX MX9101775A patent/MX9101775A/es unknown
- 1991-10-25 IE IE373391A patent/IE913733A1/en unknown
- 1991-10-26 CN CN91111447A patent/CN1062907A/zh active Pending
- 1991-10-27 IL IL9986891A patent/IL99868A/en not_active IP Right Cessation
- 1991-10-28 ZA ZA918572A patent/ZA918572B/xx unknown

Also Published As

Publication number	Publication date
CA2094799A1 (en)	1992-04-27
IL99868A0 (en)	1992-08-18
MX9101775A (es)	1992-06-05
YU171391A (sh)	1994-01-20
EP0555365B1 (de)	1994-12-14
DE69105995T2 (de)	1995-05-11
WO1992007848A1 (en)	1992-05-14
EP0555365A1 (de)	1993-08-18
IE913733A1 (en)	1992-05-22
US5071862A (en)	1991-12-10
ATE115578T1 (de)	1994-12-15
AU9017891A (en)	1992-05-26
DE69105995D1 (de)	1995-01-26
DK0555365T3 (da)	1995-05-15
ZA918572B (en)	1992-08-26
CN1062907A (zh)	1992-07-22

Legal Events

Date	Code	Title	Description
1996-06-18	FF	Patent granted
1998-10-30	RH	Patent void

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