NO793085L - Jordbruks-sulfonamider. - Google Patents
Jordbruks-sulfonamider.Info
- Publication number
- NO793085L NO793085L NO793085A NO793085A NO793085L NO 793085 L NO793085 L NO 793085L NO 793085 A NO793085 A NO 793085A NO 793085 A NO793085 A NO 793085A NO 793085 L NO793085 L NO 793085L
- Authority
- NO
- Norway
- Prior art keywords
- alkyl
- alkyl substituted
- connection according
- compounds
- methyl
- Prior art date
Links
- 229940124530 sulfonamide Drugs 0.000 title description 3
- 150000003456 sulfonamides Chemical class 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 54
- 229910052801 chlorine Inorganic materials 0.000 claims description 20
- 229910052739 hydrogen Inorganic materials 0.000 claims description 16
- -1 2-[(2-[(2-chloro-phenylsulfonylamino)-carbonylamino]-6-methylpyrimidin-4-yloxy)]-propanoic acid methyl ester Chemical group 0.000 claims description 14
- 229910052794 bromium Inorganic materials 0.000 claims description 14
- 229910052731 fluorine Inorganic materials 0.000 claims description 14
- 125000000217 alkyl group Chemical group 0.000 claims description 11
- 229910052760 oxygen Inorganic materials 0.000 claims description 10
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 9
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 4
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims description 2
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 claims description 2
- 125000004966 cyanoalkyl group Chemical group 0.000 claims description 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 2
- 230000008635 plant growth Effects 0.000 claims description 2
- 230000001105 regulatory effect Effects 0.000 claims description 2
- JHEGRLRLWOXEHG-UHFFFAOYSA-N 1-chloro-N-[4-methyl-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-yl]-6-sulfamoylcyclohexa-2,4-diene-1-carboxamide Chemical group ClC1(C(C=CC=C1)S(=O)(=O)N)C(=O)NC1=NC(=NC(=N1)OCC(F)(F)F)C JHEGRLRLWOXEHG-UHFFFAOYSA-N 0.000 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 33
- 241000196324 Embryophyta Species 0.000 description 21
- 238000000034 method Methods 0.000 description 19
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 17
- 238000002360 preparation method Methods 0.000 description 14
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- 239000007787 solid Substances 0.000 description 13
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- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 10
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- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
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- 125000004429 atom Chemical group 0.000 description 3
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- BQNXHDSGGRTFNX-UHFFFAOYSA-N n-methylpyrimidin-2-amine Chemical compound CNC1=NC=CC=N1 BQNXHDSGGRTFNX-UHFFFAOYSA-N 0.000 description 3
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- 229960000278 theophylline Drugs 0.000 description 3
- CHVQBEDBYMNJAX-UHFFFAOYSA-N 1-(2-chlorophenyl)sulfonyl-3-[4-(2-methoxyethoxy)-6-methylpyrimidin-2-yl]urea Chemical compound COCCOC1=CC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 CHVQBEDBYMNJAX-UHFFFAOYSA-N 0.000 description 2
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- 239000006185 dispersion Substances 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- RZILCCPWPBTYDO-UHFFFAOYSA-N fluometuron Chemical compound CN(C)C(=O)NC1=CC=CC(C(F)(F)F)=C1 RZILCCPWPBTYDO-UHFFFAOYSA-N 0.000 description 1
- VUWZPRWSIVNGKG-UHFFFAOYSA-N fluoromethane Chemical compound F[CH2] VUWZPRWSIVNGKG-UHFFFAOYSA-N 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 231100000001 growth retardation Toxicity 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 208000006278 hypochromic anemia Diseases 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000010871 livestock manure Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- ALJNEKOPFWXIMZ-UHFFFAOYSA-N methyl 2-(2-amino-6-methylpyrimidin-4-yl)oxyacetate Chemical compound COC(=O)COC1=CC(C)=NC(N)=N1 ALJNEKOPFWXIMZ-UHFFFAOYSA-N 0.000 description 1
- BACHBFVBHLGWSL-UHFFFAOYSA-N methyl 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoate Chemical compound C1=CC(OC(C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-UHFFFAOYSA-N 0.000 description 1
- ZJZBLIANHDXKGW-UHFFFAOYSA-N methyl 2-[6-methyl-2-(thiophen-2-ylsulfonylcarbamoylamino)pyrimidin-4-yl]oxyacetate Chemical compound COC(=O)COC1=CC(C)=NC(NC(=O)NS(=O)(=O)C=2SC=CC=2)=N1 ZJZBLIANHDXKGW-UHFFFAOYSA-N 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
- FOXFZRUHNHCZPX-UHFFFAOYSA-N metribuzin Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1N FOXFZRUHNHCZPX-UHFFFAOYSA-N 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- JITOKQVGRJSHHA-UHFFFAOYSA-M monosodium methyl arsenate Chemical compound [Na+].C[As](O)([O-])=O JITOKQVGRJSHHA-UHFFFAOYSA-M 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- AVEVVDQCMKXKFZ-UHFFFAOYSA-N n,4-dimethyl-6-(2,2,2-trifluoroethoxy)pyrimidin-2-amine Chemical compound CNC1=NC(C)=CC(OCC(F)(F)F)=N1 AVEVVDQCMKXKFZ-UHFFFAOYSA-N 0.000 description 1
- ACTHAMCEAYJCSU-UHFFFAOYSA-N n-(2-chlorophenyl)sulfonyl-n-methylcarbamoyl chloride Chemical compound ClC(=O)N(C)S(=O)(=O)C1=CC=CC=C1Cl ACTHAMCEAYJCSU-UHFFFAOYSA-N 0.000 description 1
- WXVGCIXLCZOMKH-UHFFFAOYSA-N n-(benzenesulfonyl)-n-methylcarbamothioyl chloride Chemical class ClC(=S)N(C)S(=O)(=O)C1=CC=CC=C1 WXVGCIXLCZOMKH-UHFFFAOYSA-N 0.000 description 1
- FSOBYBLQJMGDTH-UHFFFAOYSA-N n-(sulfonylmethyl)carbamoyl chloride Chemical class ClC(=O)NC=S(=O)=O FSOBYBLQJMGDTH-UHFFFAOYSA-N 0.000 description 1
- WDDKTAPPTDUDGZ-UHFFFAOYSA-N n-methyl-n-thiophen-2-ylsulfonylcarbamoyl chloride Chemical class ClC(=O)N(C)S(=O)(=O)C1=CC=CS1 WDDKTAPPTDUDGZ-UHFFFAOYSA-N 0.000 description 1
- 230000017074 necrotic cell death Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 235000020030 perry Nutrition 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000019612 pigmentation Effects 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- LJXQPZWIHJMPQQ-UHFFFAOYSA-N pyrimidin-2-amine Chemical compound NC1=NC=CC=N1 LJXQPZWIHJMPQQ-UHFFFAOYSA-N 0.000 description 1
- 150000003230 pyrimidines Chemical class 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- QSAZNTFFELIFAJ-UHFFFAOYSA-N s-chloro carbamothioate Chemical class NC(=O)SCl QSAZNTFFELIFAJ-UHFFFAOYSA-N 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 230000007226 seed germination Effects 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000011593 sulfur Chemical group 0.000 description 1
- 239000004546 suspension concentrate Substances 0.000 description 1
- 150000004992 toluidines Chemical class 0.000 description 1
- 238000001665 trituration Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D521/00—Heterocyclic compounds containing unspecified hetero rings
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
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)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Fats And Perfumes (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/946,176 US4214890A (en) | 1978-09-27 | 1978-09-27 | Herbicidal pyrimidine and triazine sulfonamides |
| US6320879A | 1979-08-07 | 1979-08-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO793085L true NO793085L (no) | 1980-03-28 |
Family
ID=26743162
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO793085A NO793085L (no) | 1978-09-27 | 1979-09-26 | Jordbruks-sulfonamider. |
Country Status (17)
| Country | Link |
|---|---|
| EP (1) | EP0009419B1 (fr) |
| BR (1) | BR7906134A (fr) |
| CA (1) | CA1114820A (fr) |
| CS (1) | CS208677B2 (fr) |
| DE (1) | DE2967559D1 (fr) |
| DK (1) | DK349479A (fr) |
| EG (1) | EG13798A (fr) |
| ES (1) | ES484495A1 (fr) |
| FI (1) | FI793012A (fr) |
| GR (1) | GR70682B (fr) |
| IL (1) | IL58330A0 (fr) |
| NO (1) | NO793085L (fr) |
| NZ (1) | NZ191682A (fr) |
| PL (1) | PL118737B1 (fr) |
| PT (1) | PT70236A (fr) |
| TR (1) | TR21078A (fr) |
| YU (1) | YU233379A (fr) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4655822A (en) * | 1977-10-06 | 1987-04-07 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
| BR8007727A (pt) * | 1979-11-30 | 1981-06-09 | Du Pont | Composto agricola,composicao apropriada e processo para o controle do crescimento de vegetacao indesejada |
| ZA806970B (en) * | 1979-11-30 | 1982-06-30 | Du Pont | Agricultural sulfonamides |
| DK465580A (da) * | 1979-11-30 | 1981-05-31 | Du Pont | Sulfonamider og deres anvendelse i prae- og postemergens-herbicider og eller plantevaekstreguleringsmidler |
| US4398939A (en) * | 1980-06-03 | 1983-08-16 | E. I. Du Pont De Nemours And Company | Herbicidal thiophenesulfonamides |
| US4368069A (en) * | 1980-07-11 | 1983-01-11 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
| CA1330438C (fr) * | 1980-07-17 | 1994-06-28 | Willy Meyer | N-phenylsulfonyl-n'-pyrimidinyl-et triazinylurees |
| US4391627A (en) * | 1980-07-25 | 1983-07-05 | E. I. Du Pont De Nemours And Company | Herbicidal benzothiophene and benzofuran sulfonamides |
| US4371391A (en) * | 1980-09-15 | 1983-02-01 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
| US4441910A (en) * | 1981-03-24 | 1984-04-10 | E. I. Du Pont De Nemours And Company | Thiophene or furan herbicides |
| US4443243A (en) * | 1981-07-16 | 1984-04-17 | Ciba-Geigy Corporation | N-Phenylsulfonyl-N-triazinylureas |
| US4545811A (en) * | 1981-08-06 | 1985-10-08 | Ciba-Geigy Corporation | N-Phenylsulfonyl-N'-triazinyl-ureas |
| US4528024A (en) * | 1981-09-09 | 1985-07-09 | E. I. Du Pont De Nemours And Company | Herbicidal alkyl sulfones |
| US4579584A (en) * | 1981-10-13 | 1986-04-01 | Ciba-Geigy Corporation | N-phenylsulfonyl-N'-triazinylureas |
| CA1221698A (fr) * | 1981-12-07 | 1987-05-12 | Rafael Shapiro | N-arylsulfonyl-n'-pyrimidinyl- et triazinylurees |
| US4478635A (en) * | 1982-01-11 | 1984-10-23 | Ciba-Geigy Corporation | N-Arylsulfonyl-N'-pyrimidinylureas |
| MA19680A1 (fr) * | 1982-01-11 | 1983-10-01 | Novartis Ag | N- arylsulfonyl - n' - pyrimidinylurees. |
| JP2961267B2 (ja) * | 1982-06-01 | 1999-10-12 | イー・アイ・デユポン・ドウ・ヌムール・アンド・カンパニー | イミダゾール又はピラゾール誘導体 |
| MA19797A1 (fr) * | 1982-06-14 | 1983-12-31 | Ciba Geigy Ag | N-heterocyclosulfonyl -n- pyrimidinyl et triazinylurees . |
| EP0098569A3 (fr) * | 1982-07-08 | 1984-12-19 | Hoechst Aktiengesellschaft | Sulfonylurées substituées par un hétérocycle, procédé pour leur préparation et leur utilisation dans l'agriculture |
| US4515626A (en) * | 1982-10-06 | 1985-05-07 | Ciba Geigy Corporation | N-(Cyclopropyl-triazinyl-n'-(arylsulfonyl) ureas having herbicidal activity |
| GR79414B (fr) * | 1982-10-29 | 1984-10-22 | Du Pont | |
| AU581865B2 (en) * | 1983-11-15 | 1989-03-09 | E.I. Du Pont De Nemours And Company | Herbicidal substituted-thiophene sulfonamides |
| US4588432A (en) * | 1984-02-27 | 1986-05-13 | E. I. Du Pont De Nemours And Company | Herbicidal selenylsulfonamides |
| AU585761B2 (en) * | 1984-03-07 | 1989-06-22 | E.I. Du Pont De Nemours And Company | Herbicidal fluoroethoxy triazines |
| US4609398A (en) * | 1984-06-29 | 1986-09-02 | E. I. Du Pont De Nemours And Company | Herbicidal fluoroethoxy triazines |
| US4689069A (en) * | 1984-08-08 | 1987-08-25 | E. I. Du Pont De Nemours And Company | Herbicidal acetylenic pyrimidines and triazines |
| JPH05501415A (ja) * | 1990-03-07 | 1993-03-18 | フセソユーズヌイ、ナウチノ―イスレドワーチェルスキー、インスチツート、ヒミチェスキフ、スレドストフ、ザスチトイ、ラステヌイ | 置換フェニルスルホニルトリアジニル尿素、その塩並びにそれに基づく植物成長促進及び阻害用薬剤 |
| WO1991013880A1 (fr) * | 1990-03-07 | 1991-09-19 | Vsesojuzny Nauchno-Issledovatelsky Institut Khimicheskikh Sredstv Zaschity Rasteny | Phenylsulfonyltriazinyluree substituee, et ses sels, et agent de stimulation et de suppression de la croissance des plantes a base de ces substances |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| OA05625A (fr) * | 1976-04-07 | 1981-04-30 | Du Pont | N-(hétérocyclique aminocarbonyl) aryl sulfonamides herbicides, compositions les contenant et procédés les utilisant . |
| US4257802A (en) * | 1977-10-06 | 1981-03-24 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
-
1979
- 1979-08-21 DK DK349479A patent/DK349479A/da not_active Application Discontinuation
- 1979-09-25 BR BR7906134A patent/BR7906134A/pt unknown
- 1979-09-25 CA CA336,331A patent/CA1114820A/fr not_active Expired
- 1979-09-26 NO NO793085A patent/NO793085L/no unknown
- 1979-09-26 CS CS796511A patent/CS208677B2/cs unknown
- 1979-09-26 DE DE7979302014T patent/DE2967559D1/de not_active Expired
- 1979-09-26 PL PL1979218523A patent/PL118737B1/pl unknown
- 1979-09-26 EP EP79302014A patent/EP0009419B1/fr not_active Expired
- 1979-09-26 IL IL58330A patent/IL58330A0/xx unknown
- 1979-09-26 EG EG568/79A patent/EG13798A/xx active
- 1979-09-26 YU YU02333/79A patent/YU233379A/xx unknown
- 1979-09-26 ES ES484495A patent/ES484495A1/es not_active Expired
- 1979-09-26 NZ NZ191682A patent/NZ191682A/xx unknown
- 1979-09-27 FI FI793012A patent/FI793012A/fi not_active Application Discontinuation
- 1979-09-27 TR TR21078A patent/TR21078A/xx unknown
- 1979-09-27 PT PT70236A patent/PT70236A/pt unknown
- 1979-09-27 GR GR60123A patent/GR70682B/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ES484495A1 (es) | 1980-09-01 |
| FI793012A (fi) | 1980-03-28 |
| DE2967559D1 (en) | 1986-02-13 |
| CA1114820A (fr) | 1981-12-22 |
| TR21078A (tr) | 1983-06-23 |
| PT70236A (en) | 1979-10-01 |
| EG13798A (en) | 1982-09-30 |
| YU233379A (en) | 1983-02-28 |
| EP0009419B1 (fr) | 1986-01-02 |
| GR70682B (fr) | 1982-12-20 |
| CS208677B2 (en) | 1981-09-15 |
| BR7906134A (pt) | 1980-05-27 |
| DK349479A (da) | 1980-03-28 |
| EP0009419A1 (fr) | 1980-04-02 |
| PL118737B1 (en) | 1981-10-31 |
| IL58330A0 (en) | 1979-12-30 |
| NZ191682A (en) | 1983-07-29 |
| PL218523A1 (fr) | 1980-06-16 |
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