CS215146B2 - Fungicide means - Google Patents
Fungicide means Download PDFInfo
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- CS215146B2 CS215146B2 CS8143A CS4381A CS215146B2 CS 215146 B2 CS215146 B2 CS 215146B2 CS 8143 A CS8143 A CS 8143A CS 4381 A CS4381 A CS 4381A CS 215146 B2 CS215146 B2 CS 215146B2
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- 230000000855 fungicidal effect Effects 0.000 title claims description 8
- 239000000417 fungicide Substances 0.000 title description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 7
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 3
- 150000002367 halogens Chemical class 0.000 claims abstract description 3
- 239000000203 mixture Substances 0.000 claims description 20
- 239000004480 active ingredient Substances 0.000 claims description 14
- 150000003839 salts Chemical class 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
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- 241000196324 Embryophyta Species 0.000 abstract description 10
- 150000001875 compounds Chemical class 0.000 description 33
- -1 azolyl-silyl glycol ethers Chemical class 0.000 description 17
- 239000000243 solution Substances 0.000 description 14
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 10
- 239000013543 active substance Substances 0.000 description 10
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- 239000000428 dust Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 125000006260 ethylaminocarbonyl group Chemical group [H]N(C(*)=O)C([H])([H])C([H])([H])[H] 0.000 description 1
- AWYFNIZYMPNGAI-UHFFFAOYSA-L ethylenebis(dithiocarbamate) Chemical compound [S-]C(=S)NCCNC([S-])=S AWYFNIZYMPNGAI-UHFFFAOYSA-L 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- WHDGWKAJBYRJJL-UHFFFAOYSA-K ferbam Chemical compound [Fe+3].CN(C)C([S-])=S.CN(C)C([S-])=S.CN(C)C([S-])=S WHDGWKAJBYRJJL-UHFFFAOYSA-K 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- UYJUZNLFJAWNEZ-UHFFFAOYSA-N fuberidazole Chemical compound C1=COC(C=2NC3=CC=CC=C3N=2)=C1 UYJUZNLFJAWNEZ-UHFFFAOYSA-N 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- CKAPSXZOOQJIBF-UHFFFAOYSA-N hexachlorobenzene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl CKAPSXZOOQJIBF-UHFFFAOYSA-N 0.000 description 1
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Substances C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 1
- WJZHMLNIAZSFDO-UHFFFAOYSA-N manganese zinc Chemical compound [Mn].[Zn] WJZHMLNIAZSFDO-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- XXZBIMWVXSTERN-UHFFFAOYSA-N n-[butyl(dimethyl)silyl]acetamide Chemical compound CCCC[Si](C)(C)NC(C)=O XXZBIMWVXSTERN-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- OYRIKLVYHTWHCZ-UHFFFAOYSA-N n-cyclohexyl-2,5-dimethylfuran-3-carboxamide Chemical compound O1C(C)=CC(C(=O)NC2CCCCC2)=C1C OYRIKLVYHTWHCZ-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- WDFKBRQZGBFDAB-UHFFFAOYSA-N n-triethylsilylacetamide Chemical compound CC[Si](CC)(CC)NC(C)=O WDFKBRQZGBFDAB-UHFFFAOYSA-N 0.000 description 1
- BLUMSOONSFWPGU-UHFFFAOYSA-N n-trimethylsilylbenzamide Chemical compound C[Si](C)(C)NC(=O)C1=CC=CC=C1 BLUMSOONSFWPGU-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000004533 oil dispersion Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229960003540 oxyquinoline Drugs 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- KNCYXPMJDCCGSJ-UHFFFAOYSA-N piperidine-2,6-dione Chemical compound O=C1CCCC(=O)N1 KNCYXPMJDCCGSJ-UHFFFAOYSA-N 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- FGVVTMRZYROCTH-UHFFFAOYSA-N pyridine-2-thiol N-oxide Chemical compound [O-][N+]1=CC=CC=C1S FGVVTMRZYROCTH-UHFFFAOYSA-N 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical class [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002210 silicon-based material Substances 0.000 description 1
- PYODKQIVQIVELM-UHFFFAOYSA-M sodium;2,3-bis(2-methylpropyl)naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CC(C)C)C(CC(C)C)=CC2=C1 PYODKQIVQIVELM-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- BCNZYOJHNLTNEZ-UHFFFAOYSA-N tert-butyldimethylsilyl chloride Chemical compound CC(C)(C)[Si](C)(C)Cl BCNZYOJHNLTNEZ-UHFFFAOYSA-N 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 description 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19803000140 DE3000140A1 (de) | 1980-01-04 | 1980-01-04 | Fungizide azolyl-silyl-glykolether, ihre herstellung und verwendung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS215146B2 true CS215146B2 (en) | 1982-07-30 |
Family
ID=6091506
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS8143A CS215146B2 (en) | 1980-01-04 | 1981-01-04 | Fungicide means |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US4330535A (pt) |
| EP (1) | EP0031962B1 (pt) |
| JP (1) | JPS56100791A (pt) |
| AR (1) | AR226333A1 (pt) |
| AT (1) | ATE2433T1 (pt) |
| AU (1) | AU6591580A (pt) |
| BR (1) | BR8008546A (pt) |
| CA (1) | CA1154776A (pt) |
| CS (1) | CS215146B2 (pt) |
| DD (1) | DD155132A5 (pt) |
| DE (2) | DE3000140A1 (pt) |
| ES (1) | ES8201171A1 (pt) |
| FI (1) | FI803759L (pt) |
| GR (1) | GR71007B (pt) |
| IE (1) | IE50679B1 (pt) |
| IL (1) | IL61717A0 (pt) |
| NO (1) | NO803522L (pt) |
| NZ (1) | NZ195927A (pt) |
| PL (1) | PL124967B2 (pt) |
| PT (1) | PT72220B (pt) |
| RO (2) | RO86277B (pt) |
| SU (1) | SU953969A3 (pt) |
| ZA (1) | ZA816B (pt) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4510136A (en) * | 1981-06-24 | 1985-04-09 | E. I. Du Pont De Nemours And Company | Fungicidal 1,2,4-triazole derivatives |
| US4496551A (en) * | 1981-06-24 | 1985-01-29 | E. I. Du Pont De Nemours And Company | Fungicidal imidazole derivatives |
| US4533659A (en) * | 1982-06-09 | 1985-08-06 | Ciba-Geigy Corporation | Microbicidal 2-(1H-1,2,4-triazolylmethyl-1'-yl)-2-siloxy-2-phenyl-acetates |
| DE3421649A1 (de) * | 1984-06-09 | 1985-12-12 | Bayer Ag, 5090 Leverkusen | Mono- und bistrimethylsilylamino-triazinone |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2208329A1 (de) | 1971-02-23 | 1972-09-07 | Agripat S.A., Basel (Schweiz) | Verfahren zur Herstellung neuer herbizid wirksamer s-Triazin-Derivate |
| DE2720868A1 (de) | 1977-05-10 | 1978-11-23 | Bayer Ag | Antimikrobielle mittel |
| JPS6053018B2 (ja) * | 1977-09-07 | 1985-11-22 | 住友化学工業株式会社 | アゾ−ル系化合物、その製造法および該化合物からなる殺菌剤 |
| DE2758784A1 (de) | 1977-12-29 | 1979-07-12 | Basf Ag | Triazolyl-glykolaether |
| US4150122A (en) * | 1978-01-05 | 1979-04-17 | E. I. Du Pont De Nemours And Company | Substituted carbamates |
| DE2801579A1 (de) | 1978-01-14 | 1979-07-19 | Basf Ag | Triazolyl-glykolaether |
-
1980
- 1980-01-04 DE DE19803000140 patent/DE3000140A1/de not_active Withdrawn
- 1980-11-06 GR GR63301A patent/GR71007B/el unknown
- 1980-11-21 NO NO803522A patent/NO803522L/no unknown
- 1980-12-03 FI FI803759A patent/FI803759L/fi not_active Application Discontinuation
- 1980-12-08 US US06/213,791 patent/US4330535A/en not_active Expired - Lifetime
- 1980-12-11 CA CA000366586A patent/CA1154776A/en not_active Expired
- 1980-12-12 DD DD80226024A patent/DD155132A5/de unknown
- 1980-12-15 IL IL61717A patent/IL61717A0/xx unknown
- 1980-12-16 RO RO110909A patent/RO86277B/ro unknown
- 1980-12-16 RO RO80102866A patent/RO81430A/ro unknown
- 1980-12-18 PT PT72220A patent/PT72220B/pt unknown
- 1980-12-23 NZ NZ195927A patent/NZ195927A/xx unknown
- 1980-12-24 JP JP18218380A patent/JPS56100791A/ja active Pending
- 1980-12-27 DE DE8080108221T patent/DE3061931D1/de not_active Expired
- 1980-12-27 EP EP80108221A patent/EP0031962B1/de not_active Expired
- 1980-12-27 AT AT80108221T patent/ATE2433T1/de not_active IP Right Cessation
- 1980-12-29 BR BR8008546A patent/BR8008546A/pt unknown
- 1980-12-29 ES ES498209A patent/ES8201171A1/es not_active Expired
- 1980-12-30 AR AR283830A patent/AR226333A1/es active
- 1980-12-30 SU SU803223401A patent/SU953969A3/ru active
- 1980-12-31 AU AU65915/80A patent/AU6591580A/en not_active Abandoned
-
1981
- 1981-01-02 PL PL1981229046A patent/PL124967B2/pl unknown
- 1981-01-02 ZA ZA00810006A patent/ZA816B/xx unknown
- 1981-01-02 IE IE1/81A patent/IE50679B1/en unknown
- 1981-01-04 CS CS8143A patent/CS215146B2/cs unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PT72220A (en) | 1981-01-01 |
| FI803759L (fi) | 1981-07-05 |
| IE810001L (en) | 1981-07-04 |
| US4330535A (en) | 1982-05-18 |
| BR8008546A (pt) | 1981-07-21 |
| PT72220B (en) | 1981-11-02 |
| AU6591580A (en) | 1981-07-09 |
| ZA816B (en) | 1982-02-24 |
| SU953969A3 (ru) | 1982-08-23 |
| EP0031962A2 (de) | 1981-07-15 |
| ATE2433T1 (de) | 1983-03-15 |
| RO86277A (ro) | 1985-03-15 |
| CA1154776A (en) | 1983-10-04 |
| NO803522L (no) | 1981-07-06 |
| GR71007B (pt) | 1983-03-31 |
| RO81430B (ro) | 1983-06-30 |
| PL124967B2 (en) | 1983-03-31 |
| DE3000140A1 (de) | 1981-07-09 |
| AR226333A1 (es) | 1982-06-30 |
| RO86277B (ro) | 1985-03-31 |
| IE50679B1 (en) | 1986-06-11 |
| RO81430A (ro) | 1983-07-07 |
| EP0031962A3 (en) | 1981-10-07 |
| IL61717A0 (en) | 1981-01-30 |
| DE3061931D1 (en) | 1983-03-17 |
| PL229046A2 (pt) | 1981-09-04 |
| JPS56100791A (en) | 1981-08-12 |
| NZ195927A (en) | 1983-03-15 |
| DD155132A5 (de) | 1982-05-19 |
| EP0031962B1 (de) | 1983-02-09 |
| ES498209A0 (es) | 1981-12-01 |
| ES8201171A1 (es) | 1981-12-01 |
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