HU185400B - Compositions containing 2,2-dichloro-acetamide derivative as antidote and s-alkyl-thiocarbamate derivative as herbicide active substance together or the antidote without the active substance further process for preparing 2,2-dichloro-acetamide derivatives - Google Patents
Compositions containing 2,2-dichloro-acetamide derivative as antidote and s-alkyl-thiocarbamate derivative as herbicide active substance together or the antidote without the active substance further process for preparing 2,2-dichloro-acetamide derivatives Download PDFInfo
- Publication number
- HU185400B HU185400B HU803082A HU308280A HU185400B HU 185400 B HU185400 B HU 185400B HU 803082 A HU803082 A HU 803082A HU 308280 A HU308280 A HU 308280A HU 185400 B HU185400 B HU 185400B
- Authority
- HU
- Hungary
- Prior art keywords
- antidote
- formula
- propenyl
- dichloro
- alkyl
- Prior art date
Links
- 239000000729 antidote Substances 0.000 title claims abstract description 33
- 239000000203 mixture Substances 0.000 title claims abstract description 33
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 14
- 239000004009 herbicide Substances 0.000 title claims description 13
- WCGGWVOVFQNRRS-UHFFFAOYSA-N dichloroacetamide Chemical class NC(=O)C(Cl)Cl WCGGWVOVFQNRRS-UHFFFAOYSA-N 0.000 title description 10
- 239000013543 active substance Substances 0.000 title description 3
- 238000004519 manufacturing process Methods 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 12
- 238000002360 preparation method Methods 0.000 claims abstract description 10
- 238000000034 method Methods 0.000 claims abstract description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 12
- 239000004480 active ingredient Substances 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 5
- 239000005977 Ethylene Substances 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 150000001412 amines Chemical class 0.000 claims description 5
- FBCCMZVIWNDFMO-UHFFFAOYSA-N dichloroacetyl chloride Chemical compound ClC(Cl)C(Cl)=O FBCCMZVIWNDFMO-UHFFFAOYSA-N 0.000 claims description 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- 230000000885 phytotoxic effect Effects 0.000 claims description 4
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 claims description 4
- 239000003377 acid catalyst Substances 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 239000000969 carrier Substances 0.000 claims description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- 244000038559 crop plants Species 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims 4
- ZETHHMPKDUSZQQ-UHFFFAOYSA-N Betulafolienepentol Natural products C1C=C(C)CCC(C(C)CCC=C(C)C)C2C(OC)OC(OC)C2=C1 ZETHHMPKDUSZQQ-UHFFFAOYSA-N 0.000 claims 2
- PCSMJKASWLYICJ-UHFFFAOYSA-N Succinic aldehyde Chemical compound O=CCCC=O PCSMJKASWLYICJ-UHFFFAOYSA-N 0.000 claims 2
- HEOKFDGOFROELJ-UHFFFAOYSA-N diacetal Natural products COc1ccc(C=C/c2cc(O)cc(OC3OC(COC(=O)c4cc(O)c(O)c(O)c4)C(O)C(O)C3O)c2)cc1O HEOKFDGOFROELJ-UHFFFAOYSA-N 0.000 claims 2
- 239000004094 surface-active agent Substances 0.000 claims 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- -1 dioxane-2-ylmethyl Chemical group 0.000 abstract description 9
- 229940075522 antidotes Drugs 0.000 abstract description 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
- 241000196324 Embryophyta Species 0.000 description 10
- 230000003054 hormonal effect Effects 0.000 description 10
- 240000008042 Zea mays Species 0.000 description 9
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 9
- 239000002689 soil Substances 0.000 description 7
- OISQRMLHYOLTJL-UHFFFAOYSA-N 2,2-dichloro-n-(1,3-dioxolan-2-ylmethyl)-n-prop-2-enylacetamide Chemical compound ClC(Cl)C(=O)N(CC=C)CC1OCCO1 OISQRMLHYOLTJL-UHFFFAOYSA-N 0.000 description 5
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 235000005822 corn Nutrition 0.000 description 5
- DLCLIWPGKGWWND-UHFFFAOYSA-N 2,2-dichloro-n-(2,2-dimethoxyethyl)-n-prop-2-enylacetamide Chemical compound COC(OC)CN(CC=C)C(=O)C(Cl)Cl DLCLIWPGKGWWND-UHFFFAOYSA-N 0.000 description 4
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 4
- 235000013339 cereals Nutrition 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 235000009973 maize Nutrition 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 3
- RELPJIGBEFIKNK-UHFFFAOYSA-N 2,2-dichloro-n-(2,2-dimethoxyethyl)-n-methylacetamide Chemical compound COC(OC)CN(C)C(=O)C(Cl)Cl RELPJIGBEFIKNK-UHFFFAOYSA-N 0.000 description 2
- GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- OKUGPJPKMAEJOE-UHFFFAOYSA-N S-propyl dipropylcarbamothioate Chemical compound CCCSC(=O)N(CCC)CCC OKUGPJPKMAEJOE-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-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
- 230000000254 damaging effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 238000001228 spectrum Methods 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
- IEBNVYBKZGBTFL-UHFFFAOYSA-N 2,2-dichloro-n-(2,2-dimethoxyethyl)-n-propan-2-ylacetamide Chemical compound COC(OC)CN(C(C)C)C(=O)C(Cl)Cl IEBNVYBKZGBTFL-UHFFFAOYSA-N 0.000 description 1
- RMZCEMPARMLKJD-UHFFFAOYSA-N 2,2-dichloropent-4-enamide Chemical compound NC(=O)C(Cl)(Cl)CC=C RMZCEMPARMLKJD-UHFFFAOYSA-N 0.000 description 1
- HUMIEJNVCICTPJ-UHFFFAOYSA-N 2,2-dimethoxy-n-methylethanamine Chemical compound CNCC(OC)OC HUMIEJNVCICTPJ-UHFFFAOYSA-N 0.000 description 1
- QKWWDTYDYOFRJL-UHFFFAOYSA-N 2,2-dimethoxyethanamine Chemical compound COC(CN)OC QKWWDTYDYOFRJL-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- WARIWGPBHKPYON-UHFFFAOYSA-N Ethiolate Chemical compound CCSC(=O)N(CC)CC WARIWGPBHKPYON-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
- 239000012346 acetyl chloride Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 229940058963 dichloroacetamide derivative drug for amoebiasis and other protozoal diseases Drugs 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 230000004992 fission Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- KTSVVFZWNJVOSK-UHFFFAOYSA-N n,n-dimethylformamide;methanol;propan-2-one Chemical compound OC.CC(C)=O.CN(C)C=O KTSVVFZWNJVOSK-UHFFFAOYSA-N 0.000 description 1
- 230000017074 necrotic cell death Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
Classifications
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/14—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D317/28—Radicals substituted by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/04—1,3-Dioxanes; Hydrogenated 1,3-dioxanes
- C07D319/06—1,3-Dioxanes; Hydrogenated 1,3-dioxanes not condensed with other rings
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catching Or Destruction (AREA)
- Pretreatment Of Seeds And Plants (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10643379A | 1979-12-26 | 1979-12-26 | |
| US06/106,434 US4294764A (en) | 1979-12-26 | 1979-12-26 | N-(Optionally substituted 1,3-dioxolan- or dioxan-2-ylmethyl)-N-alkyl, alkenyl, or alkynyl-2,2-dichloroacetamides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HU185400B true HU185400B (en) | 1985-01-28 |
Family
ID=26803660
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU803082A HU185400B (en) | 1979-12-26 | 1980-12-22 | Compositions containing 2,2-dichloro-acetamide derivative as antidote and s-alkyl-thiocarbamate derivative as herbicide active substance together or the antidote without the active substance further process for preparing 2,2-dichloro-acetamide derivatives |
Country Status (17)
| Country | Link |
|---|---|
| EP (1) | EP0031686B1 (https=) |
| JP (1) | JPS6452704A (https=) |
| KR (1) | KR840001721B1 (https=) |
| AR (1) | AR226332A1 (https=) |
| AU (1) | AU522675B2 (https=) |
| BG (1) | BG36625A3 (https=) |
| BR (1) | BR8008247A (https=) |
| CA (1) | CA1178286A (https=) |
| DE (1) | DE3071807D1 (https=) |
| ES (1) | ES8205751A1 (https=) |
| HU (1) | HU185400B (https=) |
| IL (1) | IL61739A (https=) |
| PT (1) | PT72281B (https=) |
| RO (1) | RO81053A (https=) |
| SU (1) | SU1440323A3 (https=) |
| YU (1) | YU42546B (https=) |
| ZW (1) | ZW31080A1 (https=) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4561876A (en) * | 1980-04-28 | 1985-12-31 | Stauffer Chemical Co. | Haloalkylcarbonylamino-1,3-dioxane herbicide antidotes |
| JPH05275958A (ja) * | 1992-03-25 | 1993-10-22 | Murata Mfg Co Ltd | ノイズフィルタ |
| DE59408196D1 (de) | 1993-03-22 | 1999-06-10 | Novartis Ag | Selektiv-herbizides Mittel |
| EE9500018A (et) | 1994-06-03 | 1995-12-15 | Ciba-Geigy Ag | Selektiivne herbitsiid ja meetod selle kasutamiseks |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US113464A (en) * | 1871-04-04 | Improvement in cutter-heads | ||
| US4137070A (en) * | 1971-04-16 | 1979-01-30 | Stauffer Chemical Company | Herbicide compositions |
| US3859308A (en) * | 1973-05-07 | 1975-01-07 | Velsicol Chemical Corp | Heterocyclic anilids |
| US3948950A (en) * | 1973-05-07 | 1976-04-06 | Velsicol Chemical Corporation | Heterocyclic anilids |
| US3894048A (en) * | 1973-05-07 | 1975-07-08 | Velsicol Chemical Corp | Dithiepanyl anilids |
| US3900497A (en) * | 1973-05-07 | 1975-08-19 | Velsicol Chemical Corp | Dithianyl anilids |
| US3894046A (en) * | 1973-05-07 | 1975-07-08 | Velsicol Chemical Corp | Dithiolanyl anilids |
| US4116670A (en) * | 1977-04-04 | 1978-09-26 | Velsicol Chemical Company | Dioxane substituted amides |
| US4155745A (en) * | 1978-04-04 | 1979-05-22 | Stauffer Chemical Company | Certain 2-(chloroacetylamino)methyl-1,3-dioxolanes, thioxalanes or dithiolanes as herbicides |
-
1980
- 1980-11-19 CA CA000364989A patent/CA1178286A/en not_active Expired
- 1980-12-09 AU AU65195/80A patent/AU522675B2/en not_active Ceased
- 1980-12-16 BR BR8008247A patent/BR8008247A/pt not_active IP Right Cessation
- 1980-12-16 ZW ZW310/80A patent/ZW31080A1/xx unknown
- 1980-12-17 IL IL61739A patent/IL61739A/xx unknown
- 1980-12-19 DE DE8080304610T patent/DE3071807D1/de not_active Expired
- 1980-12-19 EP EP80304610A patent/EP0031686B1/en not_active Expired
- 1980-12-22 AR AR283748A patent/AR226332A1/es active
- 1980-12-22 HU HU803082A patent/HU185400B/hu not_active IP Right Cessation
- 1980-12-23 PT PT72281A patent/PT72281B/pt not_active IP Right Cessation
- 1980-12-23 YU YU3255/80A patent/YU42546B/xx unknown
- 1980-12-24 BG BG050137A patent/BG36625A3/xx unknown
- 1980-12-24 ES ES498146A patent/ES8205751A1/es not_active Expired
- 1980-12-24 KR KR1019800004957A patent/KR840001721B1/ko not_active Expired
- 1980-12-25 SU SU803222445A patent/SU1440323A3/ru active
- 1980-12-26 RO RO80102971A patent/RO81053A/ro unknown
-
1988
- 1988-03-15 JP JP63061735A patent/JPS6452704A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| DE3071807D1 (en) | 1986-12-04 |
| YU325580A (en) | 1983-12-31 |
| CA1178286A (en) | 1984-11-20 |
| BR8008247A (pt) | 1981-07-07 |
| SU1440323A3 (ru) | 1988-11-23 |
| ES498146A0 (es) | 1982-06-16 |
| PT72281A (en) | 1981-01-01 |
| ES8205751A1 (es) | 1982-06-16 |
| JPS6452704A (en) | 1989-02-28 |
| EP0031686A1 (en) | 1981-07-08 |
| RO81053B (ro) | 1983-01-30 |
| KR840001721B1 (ko) | 1984-10-17 |
| IL61739A0 (en) | 1981-01-30 |
| YU42546B (en) | 1988-10-31 |
| IL61739A (en) | 1984-06-29 |
| JPH0251899B2 (https=) | 1990-11-08 |
| PT72281B (en) | 1981-11-06 |
| AU6519580A (en) | 1981-07-02 |
| RO81053A (ro) | 1983-02-01 |
| KR830004211A (ko) | 1983-07-06 |
| ZW31080A1 (en) | 1981-01-21 |
| AR226332A1 (es) | 1982-06-30 |
| AU522675B2 (en) | 1982-06-17 |
| EP0031686B1 (en) | 1986-10-29 |
| BG36625A3 (en) | 1984-12-16 |
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