CS268698B2 - Herbicide and method of its efficient substance production - Google Patents
Herbicide and method of its efficient substance production Download PDFInfo
- Publication number
- CS268698B2 CS268698B2 CS882923A CS292388A CS268698B2 CS 268698 B2 CS268698 B2 CS 268698B2 CS 882923 A CS882923 A CS 882923A CS 292388 A CS292388 A CS 292388A CS 268698 B2 CS268698 B2 CS 268698B2
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- Czechoslovakia
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- atom
- carbon atoms
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- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 31
- 238000000034 method Methods 0.000 title claims description 17
- 239000004009 herbicide Substances 0.000 title abstract 3
- 239000000126 substance Substances 0.000 title description 7
- 238000004519 manufacturing process Methods 0.000 title description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 47
- 239000000203 mixture Substances 0.000 claims abstract description 47
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 35
- 239000001257 hydrogen Substances 0.000 claims abstract description 30
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 25
- 125000005843 halogen group Chemical group 0.000 claims abstract description 25
- 125000001188 haloalkyl group Chemical group 0.000 claims abstract description 20
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 14
- 238000002360 preparation method Methods 0.000 claims abstract description 14
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 8
- 125000004438 haloalkoxy group Chemical group 0.000 claims abstract description 7
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 4
- 150000001875 compounds Chemical class 0.000 claims description 88
- 125000004432 carbon atom Chemical group C* 0.000 claims description 40
- 229910052801 chlorine Inorganic materials 0.000 claims description 32
- 125000001424 substituent group Chemical group 0.000 claims description 26
- 229910052731 fluorine Inorganic materials 0.000 claims description 24
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 23
- 239000004480 active ingredient Substances 0.000 claims description 22
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 17
- -1 diacetoxy Substances 0.000 claims description 17
- 125000001153 fluoro group Chemical group F* 0.000 claims description 16
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- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 6
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- 238000003556 assay Methods 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- YYRMJZQKEFZXMX-UHFFFAOYSA-N calcium;phosphoric acid Chemical class [Ca+2].OP(O)(O)=O.OP(O)(O)=O YYRMJZQKEFZXMX-UHFFFAOYSA-N 0.000 description 1
- 238000000160 carbon, hydrogen and nitrogen elemental analysis Methods 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 150000001989 diazonium salts Chemical class 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-O diazynium Chemical compound [NH+]#N IJGRMHOSHXDMSA-UHFFFAOYSA-O 0.000 description 1
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 description 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000003113 dilution method Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 235000012243 magnesium silicates Nutrition 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000008268 mayonnaise Substances 0.000 description 1
- 235000010746 mayonnaise Nutrition 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- VYQNWZOUAUKGHI-UHFFFAOYSA-N monobenzone Chemical compound C1=CC(O)=CC=C1OCC1=CC=CC=C1 VYQNWZOUAUKGHI-UHFFFAOYSA-N 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- YTNOCFWORLUHSA-UHFFFAOYSA-N n-(2,4-difluorophenyl)butanamide Chemical compound CCCC(=O)NC1=CC=C(F)C=C1F YTNOCFWORLUHSA-UHFFFAOYSA-N 0.000 description 1
- UHANVDZCDNSILX-UHFFFAOYSA-N n-phenylbutanamide Chemical compound CCCC(=O)NC1=CC=CC=C1 UHANVDZCDNSILX-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 150000005603 pentanoic acids Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical class [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000002426 superphosphate Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 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
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/32—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
- C07C235/38—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
-
- 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives thereof
-
- 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)
- 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)
- Cosmetics (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB878710362A GB8710362D0 (en) | 1987-05-01 | 1987-05-01 | Anilide herbicides |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CS292388A2 CS292388A2 (en) | 1989-07-12 |
| CS268698B2 true CS268698B2 (en) | 1990-04-11 |
Family
ID=10616695
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS882923A CS268698B2 (en) | 1987-05-01 | 1988-04-29 | Herbicide and method of its efficient substance production |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US4994616A (da) |
| EP (1) | EP0289100B1 (da) |
| JP (1) | JPS63297349A (da) |
| KR (1) | KR880013879A (da) |
| CN (1) | CN1015623B (da) |
| AT (1) | ATE74347T1 (da) |
| AU (1) | AU608836B2 (da) |
| BR (1) | BR8802065A (da) |
| CS (1) | CS268698B2 (da) |
| DE (1) | DE3869649D1 (da) |
| DK (1) | DK233788A (da) |
| ES (1) | ES2032948T3 (da) |
| FI (1) | FI882021A (da) |
| GB (1) | GB8710362D0 (da) |
| HU (1) | HU200593B (da) |
| MA (1) | MA21259A1 (da) |
| NZ (1) | NZ224427A (da) |
| OA (1) | OA08839A (da) |
| PH (1) | PH25696A (da) |
| PT (1) | PT87364B (da) |
| ZA (1) | ZA883067B (da) |
| ZW (1) | ZW4888A1 (da) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU640390B2 (en) * | 1990-07-27 | 1993-08-26 | Zeneca Limited | Amide derivatives |
| EP0665225B1 (en) * | 1994-02-01 | 1996-11-27 | Ube Industries, Ltd. | 4-Phenethylamino pyrimidine derivative, process for preparing the same and agricultural and horticultural chemical for controlling noxious organisms containing the same |
| HRP960302A2 (en) * | 1995-07-26 | 1998-04-30 | Ciba Geigy Ag | Process for the hydrogenation of imines |
| WO2016079521A1 (en) * | 2014-11-20 | 2016-05-26 | University College Cardiff Consultants Limited | Androgen receptor modulators and their use as anti-cancer agents |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3133119A (en) * | 1961-11-09 | 1964-05-12 | Givaudan Corp | Substituted acetanilides and propionanilides |
| GB1041982A (en) * | 1963-09-30 | 1966-09-07 | Boots Pure Drug Co Ltd | Herbicidal compounds and compositions |
| GB1588731A (en) * | 1977-03-09 | 1981-04-29 | Ici Ltd | Cotton desiccation with phenoxyalkanoic acids |
| GB2024213B (en) * | 1978-06-30 | 1982-09-08 | Ici Ltd | Dihalophenoxypropionic acids and their derivatives and their use as cotton desiccants |
| JPS5657752A (en) * | 1979-10-15 | 1981-05-20 | Sumitomo Chem Co Ltd | M-diaminobenzene derivative, its preparation, and herbicide constaining said compound as effective component |
| JPS5714506A (en) * | 1980-07-01 | 1982-01-25 | Ube Ind Ltd | Herbicide |
| IL64220A (en) * | 1980-11-21 | 1985-06-30 | May & Baker Ltd | Nicotinamide derivatives,their preparation and their use as herbicides |
| JPS57171904A (en) * | 1981-04-15 | 1982-10-22 | Mitsubishi Petrochem Co Ltd | Tri- or tetra-substituted phenoxycarboxylic acid anilide type herbicide |
| GB2108498B (en) * | 1981-10-20 | 1985-11-06 | Ube Industries | Phenoxyalkylamide derivative, process for preparing the same, herbicidal composition containing the same and method for controlling weeds by the use of the same |
| JPS60258150A (ja) * | 1984-06-06 | 1985-12-20 | Chugai Pharmaceut Co Ltd | アニリド系化合物、その製造法およびそれらを含有する除草剤 |
| JPH0657684B2 (ja) * | 1986-03-28 | 1994-08-03 | 宇部興産株式会社 | Ｎ―ベンジル２―（４―フルオル―３―トリフルオルメチルフェノキシ）ブタン酸アミド及びそれを含有する除草剤 |
-
1987
- 1987-05-01 GB GB878710362A patent/GB8710362D0/en active Pending
-
1988
- 1988-04-12 US US07/180,576 patent/US4994616A/en not_active Expired - Fee Related
- 1988-04-27 DE DE8888200831T patent/DE3869649D1/de not_active Expired - Lifetime
- 1988-04-27 ES ES198888200831T patent/ES2032948T3/es not_active Expired - Lifetime
- 1988-04-27 AT AT88200831T patent/ATE74347T1/de not_active IP Right Cessation
- 1988-04-27 EP EP88200831A patent/EP0289100B1/en not_active Expired - Lifetime
- 1988-04-28 DK DK233788A patent/DK233788A/da not_active Application Discontinuation
- 1988-04-28 JP JP63104463A patent/JPS63297349A/ja active Pending
- 1988-04-29 ZA ZA883067A patent/ZA883067B/xx unknown
- 1988-04-29 HU HU882224A patent/HU200593B/hu not_active IP Right Cessation
- 1988-04-29 KR KR1019880004940A patent/KR880013879A/ko not_active Application Discontinuation
- 1988-04-29 PT PT87364A patent/PT87364B/pt not_active IP Right Cessation
- 1988-04-29 ZW ZW48/88A patent/ZW4888A1/xx unknown
- 1988-04-29 NZ NZ224427A patent/NZ224427A/en unknown
- 1988-04-29 CN CN88102468A patent/CN1015623B/zh not_active Expired
- 1988-04-29 BR BR8802065A patent/BR8802065A/pt unknown
- 1988-04-29 CS CS882923A patent/CS268698B2/cs unknown
- 1988-04-29 MA MA21500A patent/MA21259A1/fr unknown
- 1988-04-29 AU AU15319/88A patent/AU608836B2/en not_active Ceased
- 1988-04-29 OA OA59341A patent/OA08839A/xx unknown
- 1988-04-29 PH PH36864A patent/PH25696A/en unknown
- 1988-04-29 FI FI882021A patent/FI882021A/fi not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| EP0289100A2 (en) | 1988-11-02 |
| BR8802065A (pt) | 1988-11-29 |
| CN88102468A (zh) | 1988-11-16 |
| KR880013879A (ko) | 1988-12-22 |
| US4994616A (en) | 1991-02-19 |
| DK233788A (da) | 1988-11-02 |
| DE3869649D1 (de) | 1992-05-07 |
| NZ224427A (en) | 1990-04-26 |
| MA21259A1 (fr) | 1988-12-31 |
| FI882021A0 (fi) | 1988-04-29 |
| PT87364A (pt) | 1989-05-31 |
| AU608836B2 (en) | 1991-04-18 |
| FI882021A (fi) | 1988-11-02 |
| PT87364B (pt) | 1992-08-31 |
| HU200593B (en) | 1990-07-28 |
| ES2032948T3 (es) | 1993-03-01 |
| EP0289100A3 (en) | 1989-10-18 |
| ZW4888A1 (en) | 1988-11-02 |
| EP0289100B1 (en) | 1992-04-01 |
| ATE74347T1 (de) | 1992-04-15 |
| CN1015623B (zh) | 1992-02-26 |
| AU1531988A (en) | 1988-11-03 |
| DK233788D0 (da) | 1988-04-28 |
| CS292388A2 (en) | 1989-07-12 |
| HUT48201A (en) | 1989-05-29 |
| PH25696A (en) | 1991-09-18 |
| GB8710362D0 (en) | 1987-06-03 |
| JPS63297349A (ja) | 1988-12-05 |
| OA08839A (en) | 1989-03-31 |
| ZA883067B (en) | 1988-12-28 |
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