CS212344B2 - Means for protection of plants against the fungous diseasesand method of making the active substances - Google Patents
Means for protection of plants against the fungous diseasesand method of making the active substances Download PDFInfo
- Publication number
- CS212344B2 CS212344B2 CS802192A CS219280A CS212344B2 CS 212344 B2 CS212344 B2 CS 212344B2 CS 802192 A CS802192 A CS 802192A CS 219280 A CS219280 A CS 219280A CS 212344 B2 CS212344 B2 CS 212344B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- carbon atoms
- radical containing
- radical
- formula
- halogen atom
- Prior art date
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- 239000013543 active substance Substances 0.000 title claims description 16
- 238000004519 manufacturing process Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 52
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 36
- 239000000203 mixture Substances 0.000 claims abstract description 26
- -1 nitro, hydroxyl Chemical group 0.000 claims abstract description 19
- 239000004480 active ingredient Substances 0.000 claims abstract description 17
- 125000005843 halogen group Chemical group 0.000 claims abstract description 12
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 11
- 125000001424 substituent group Chemical group 0.000 claims abstract description 11
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000001257 hydrogen Substances 0.000 claims abstract description 4
- 208000031888 Mycoses Diseases 0.000 claims abstract description 3
- 239000002253 acid Substances 0.000 claims description 7
- 239000011777 magnesium Substances 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- HXUIDZOMTRMIOE-UHFFFAOYSA-N 3-oxo-3-phenylpropionic acid Chemical class OC(=O)CC(=O)C1=CC=CC=C1 HXUIDZOMTRMIOE-UHFFFAOYSA-N 0.000 claims description 4
- 239000012442 inert solvent Substances 0.000 claims description 4
- 229910052749 magnesium Inorganic materials 0.000 claims description 4
- 239000011541 reaction mixture Substances 0.000 claims description 4
- 239000007858 starting material Substances 0.000 claims description 4
- 239000008346 aqueous phase Substances 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- 238000011065 in-situ storage Methods 0.000 claims description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims description 2
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- 239000012074 organic phase Substances 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 2
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 claims 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims 1
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- 230000000855 fungicidal effect Effects 0.000 abstract description 4
- UFECLJRYNAOWOI-UHFFFAOYSA-N 2-phenylpyran-4-one Chemical class O=C1C=COC(C=2C=CC=CC=2)=C1 UFECLJRYNAOWOI-UHFFFAOYSA-N 0.000 abstract description 2
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
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- 239000003795 chemical substances by application Substances 0.000 description 8
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 8
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- 239000002904 solvent Substances 0.000 description 7
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- RVDLHGSZWAELAU-UHFFFAOYSA-N 5-tert-butylthiophene-2-carbonyl chloride Chemical compound CC(C)(C)C1=CC=C(C(Cl)=O)S1 RVDLHGSZWAELAU-UHFFFAOYSA-N 0.000 description 2
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- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
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- 206010039509 Scab Diseases 0.000 description 2
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- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
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- 125000005336 allyloxy group Chemical group 0.000 description 2
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- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
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- 239000003112 inhibitor Substances 0.000 description 2
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 2
- 229920000940 maneb Polymers 0.000 description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
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- 239000012071 phase Substances 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
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- BCOSEZGCLGPUSL-UHFFFAOYSA-N 2,3,3-trichloroprop-2-enoyl chloride Chemical compound ClC(Cl)=C(Cl)C(Cl)=O BCOSEZGCLGPUSL-UHFFFAOYSA-N 0.000 description 1
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- 241000235349 Ascomycota Species 0.000 description 1
- 241000221198 Basidiomycota Species 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 239000001692 EU approved anti-caking agent Substances 0.000 description 1
- GKKZMYDNDDMXSE-UHFFFAOYSA-N Ethyl 3-oxo-3-phenylpropanoate Chemical compound CCOC(=O)CC(=O)C1=CC=CC=C1 GKKZMYDNDDMXSE-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 241000223194 Fusarium culmorum Species 0.000 description 1
- 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 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241001459558 Monographella nivalis Species 0.000 description 1
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 231100000674 Phytotoxicity Toxicity 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 241001123583 Puccinia striiformis Species 0.000 description 1
- CVQUWLDCFXOXEN-UHFFFAOYSA-N Pyran-4-one Chemical group O=C1C=COC=C1 CVQUWLDCFXOXEN-UHFFFAOYSA-N 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 241000221576 Uromyces Species 0.000 description 1
- 241000317942 Venturia <ichneumonid wasp> Species 0.000 description 1
- 241000228452 Venturia inaequalis Species 0.000 description 1
- 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 1
- WEVYAHXRMPXWCK-UHFFFAOYSA-N acetonitrile Substances CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000003302 alkenyloxy group Chemical group 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 125000005133 alkynyloxy group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 230000003266 anti-allergic effect Effects 0.000 description 1
- 230000000843 anti-fungal effect Effects 0.000 description 1
- 239000007798 antifreeze agent Substances 0.000 description 1
- 238000011483 antifungal activity assay Methods 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 238000003556 assay Methods 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
- 125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
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- WCRKIZKJGYWFDO-UHFFFAOYSA-N ethyl 5,6-dichloro-2-(4-fluorophenyl)-4-oxopyran-3-carboxylate Chemical compound O1C(Cl)=C(Cl)C(=O)C(C(=O)OCC)=C1C1=CC=C(F)C=C1 WCRKIZKJGYWFDO-UHFFFAOYSA-N 0.000 description 1
- KGCRMLQDXNUZCP-UHFFFAOYSA-N ethyl 5,6-dichloro-4-oxo-2-[3-(trifluoromethyl)phenyl]pyran-3-carboxylate Chemical compound O1C(Cl)=C(Cl)C(=O)C(C(=O)OCC)=C1C1=CC=CC(C(F)(F)F)=C1 KGCRMLQDXNUZCP-UHFFFAOYSA-N 0.000 description 1
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- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
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- 235000009566 rice Nutrition 0.000 description 1
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- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
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- 229910052623 talc Inorganic materials 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/34—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D309/36—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms
- C07D309/38—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms one oxygen atom in position 2 or 4, e.g. pyrones
-
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
- A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyrane Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7908569A FR2452487A1 (fr) | 1979-03-28 | 1979-03-28 | Nouveaux derives de la phenyl-2-pyrone-4 et leur utilisation comme fongicides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS212344B2 true CS212344B2 (en) | 1982-03-26 |
Family
ID=9223970
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS802192A CS212344B2 (en) | 1979-03-28 | 1980-03-28 | Means for protection of plants against the fungous diseasesand method of making the active substances |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US4297367A (de) |
| EP (1) | EP0017602B1 (de) |
| JP (1) | JPS55167286A (de) |
| AR (1) | AR223867A1 (de) |
| AT (1) | ATE1675T1 (de) |
| AU (1) | AU5681180A (de) |
| BG (1) | BG31478A3 (de) |
| BR (1) | BR8001870A (de) |
| CS (1) | CS212344B2 (de) |
| CU (1) | CU35252A (de) |
| DD (1) | DD149891A5 (de) |
| DE (1) | DE3060958D1 (de) |
| DK (1) | DK131880A (de) |
| ES (1) | ES8206508A1 (de) |
| FR (1) | FR2452487A1 (de) |
| GB (1) | GB2046264A (de) |
| GR (1) | GR67676B (de) |
| IL (1) | IL59608A0 (de) |
| MA (1) | MA18788A1 (de) |
| OA (1) | OA06498A (de) |
| PL (1) | PL223044A1 (de) |
| PT (1) | PT71022B (de) |
| SU (1) | SU938742A3 (de) |
| TR (1) | TR20293A (de) |
| ZA (1) | ZA801763B (de) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2494270A1 (fr) * | 1980-11-14 | 1982-05-21 | Rhone Poulenc Agrochimie | Nouveaux derives de la dihydro-2,3 pyrone-4, leur preparation, les compositions herbicides les contenant et leur utilisation pour le desherbage selectif des cultures |
| PH18960A (en) * | 1981-06-03 | 1985-11-26 | Ciba Geigy Ag | Novel 2-(phenoxyphenyl)-3-(carboxylic acid or ester)-5,6-dihydro-4-pyrone derivatives,compositions containing them as active ingredients and the use thereof for combating weeds |
| US5250566A (en) * | 1988-04-05 | 1993-10-05 | Board Of Trustees Operating Michigan State University | Method for controlling nematodes |
| ATE128128T1 (de) * | 1990-06-29 | 1995-10-15 | Upjohn Co | Antiatherosclerotische und antithrombotische 2- amino-6-phenyl-4h-pyran-4-one. |
| AU3419893A (en) * | 1991-12-23 | 1993-07-28 | Michigan State University | Method for controlling insects |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4060533A (en) * | 1976-06-25 | 1977-11-29 | Sandoz, Inc. | Pyranone carboxamides |
-
1979
- 1979-03-28 FR FR7908569A patent/FR2452487A1/fr active Granted
-
1980
- 1980-03-13 IL IL59608A patent/IL59608A0/xx unknown
- 1980-03-17 GR GR61459A patent/GR67676B/el unknown
- 1980-03-24 US US06/133,480 patent/US4297367A/en not_active Expired - Lifetime
- 1980-03-24 BG BG047105A patent/BG31478A3/xx unknown
- 1980-03-25 AU AU56811/80A patent/AU5681180A/en not_active Abandoned
- 1980-03-25 TR TR20293A patent/TR20293A/xx unknown
- 1980-03-25 ZA ZA00801763A patent/ZA801763B/xx unknown
- 1980-03-26 CU CU8035252A patent/CU35252A/es unknown
- 1980-03-26 AR AR280445A patent/AR223867A1/es active
- 1980-03-26 GB GB8010132A patent/GB2046264A/en not_active Withdrawn
- 1980-03-26 EP EP80420038A patent/EP0017602B1/de not_active Expired
- 1980-03-26 AT AT80420038T patent/ATE1675T1/de not_active IP Right Cessation
- 1980-03-26 DE DE8080420038T patent/DE3060958D1/de not_active Expired
- 1980-03-26 SU SU802898701A patent/SU938742A3/ru active
- 1980-03-27 ES ES489964A patent/ES8206508A1/es not_active Expired
- 1980-03-27 MA MA18987A patent/MA18788A1/fr unknown
- 1980-03-27 JP JP3964380A patent/JPS55167286A/ja active Pending
- 1980-03-27 PT PT71022A patent/PT71022B/pt unknown
- 1980-03-27 BR BR8001870A patent/BR8001870A/pt unknown
- 1980-03-27 DK DK131880A patent/DK131880A/da unknown
- 1980-03-27 PL PL22304480A patent/PL223044A1/xx unknown
- 1980-03-28 DD DD80220009A patent/DD149891A5/de unknown
- 1980-03-28 CS CS802192A patent/CS212344B2/cs unknown
- 1980-03-28 OA OA57067A patent/OA06498A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| FR2452487A1 (fr) | 1980-10-24 |
| BG31478A3 (en) | 1982-01-15 |
| CU35252A (en) | 1982-08-24 |
| PT71022A (fr) | 1980-04-01 |
| ZA801763B (en) | 1981-03-25 |
| AU5681180A (en) | 1980-10-02 |
| DK131880A (da) | 1980-09-29 |
| TR20293A (tr) | 1981-01-07 |
| ES489964A0 (es) | 1982-01-01 |
| OA06498A (fr) | 1981-07-31 |
| EP0017602B1 (de) | 1982-10-20 |
| MA18788A1 (fr) | 1980-10-01 |
| US4297367A (en) | 1981-10-27 |
| SU938742A3 (ru) | 1982-06-23 |
| FR2452487B1 (de) | 1982-01-08 |
| JPS55167286A (en) | 1980-12-26 |
| PL223044A1 (de) | 1981-02-13 |
| BR8001870A (pt) | 1980-11-18 |
| IL59608A0 (en) | 1980-06-30 |
| AR223867A1 (es) | 1981-09-30 |
| ES8206508A1 (es) | 1982-01-01 |
| ATE1675T1 (de) | 1982-11-15 |
| GR67676B (de) | 1981-09-04 |
| DD149891A5 (de) | 1981-08-05 |
| GB2046264A (en) | 1980-11-12 |
| DE3060958D1 (en) | 1982-11-25 |
| EP0017602A1 (de) | 1980-10-15 |
| PT71022B (fr) | 1981-06-25 |
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