CS203938B2 - Herbicide means and method of making the active substances - Google Patents
Herbicide means and method of making the active substances Download PDFInfo
- Publication number
- CS203938B2 CS203938B2 CS788213A CS821378A CS203938B2 CS 203938 B2 CS203938 B2 CS 203938B2 CS 788213 A CS788213 A CS 788213A CS 821378 A CS821378 A CS 821378A CS 203938 B2 CS203938 B2 CS 203938B2
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- Czechoslovakia
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- formula
- compound
- alkyl
- atom
- compounds
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- 230000002363 herbicidal effect Effects 0.000 title claims description 14
- 239000013543 active substance Substances 0.000 title claims description 7
- 239000004009 herbicide Substances 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 66
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 11
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 10
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 8
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 8
- 239000001301 oxygen Substances 0.000 claims abstract description 7
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 4
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 3
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 3
- 238000000034 method Methods 0.000 claims description 40
- 239000000203 mixture Substances 0.000 claims description 31
- 239000004480 active ingredient Substances 0.000 claims description 16
- 238000002360 preparation method Methods 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 239000003960 organic solvent Substances 0.000 claims description 8
- 229910052717 sulfur Chemical group 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 6
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- 125000004434 sulfur atom Chemical group 0.000 claims description 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 2
- 125000006569 (C5-C6) heterocyclic group Chemical group 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
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- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 240000006694 Stellaria media Species 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- 235000007244 Zea mays Nutrition 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000000202 analgesic effect Effects 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 230000000843 anti-fungal effect Effects 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 239000007798 antifreeze agent Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- KGNDCEVUMONOKF-UGPLYTSKSA-N benzyl n-[(2r)-1-[(2s,4r)-2-[[(2s)-6-amino-1-(1,3-benzoxazol-2-yl)-1,1-dihydroxyhexan-2-yl]carbamoyl]-4-[(4-methylphenyl)methoxy]pyrrolidin-1-yl]-1-oxo-4-phenylbutan-2-yl]carbamate Chemical compound C1=CC(C)=CC=C1CO[C@H]1CN(C(=O)[C@@H](CCC=2C=CC=CC=2)NC(=O)OCC=2C=CC=CC=2)[C@H](C(=O)N[C@@H](CCCCN)C(O)(O)C=2OC3=CC=CC=C3N=2)C1 KGNDCEVUMONOKF-UGPLYTSKSA-N 0.000 description 1
- 229920005551 calcium lignosulfonate Polymers 0.000 description 1
- RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
- QFBYMGFVUNJGQE-UHFFFAOYSA-N carbonyl dichloride;n,n-diethylethanamine Chemical compound ClC(Cl)=O.CCN(CC)CC QFBYMGFVUNJGQE-UHFFFAOYSA-N 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- FLGZHHJNRZUPIL-UHFFFAOYSA-N chromene-4-thione Chemical class C1=CC=C2C(=S)C=COC2=C1 FLGZHHJNRZUPIL-UHFFFAOYSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 229940126208 compound 22 Drugs 0.000 description 1
- 229940125833 compound 23 Drugs 0.000 description 1
- 229940125851 compound 27 Drugs 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 235000008504 concentrate Nutrition 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- RVGAEGHWOZOGRZ-UHFFFAOYSA-N cyclohexanone;oxirane Chemical compound C1CO1.O=C1CCCCC1 RVGAEGHWOZOGRZ-UHFFFAOYSA-N 0.000 description 1
- 101150047356 dec-1 gene Proteins 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012156 elution solvent Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- OWFXIOWLTKNBAP-UHFFFAOYSA-N isoamyl nitrite Chemical compound CC(C)CCON=O OWFXIOWLTKNBAP-UHFFFAOYSA-N 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 229910052622 kaolinite Inorganic materials 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 239000008268 mayonnaise Substances 0.000 description 1
- 235000010746 mayonnaise Nutrition 0.000 description 1
- HAMGRBXTJNITHG-UHFFFAOYSA-N methyl isocyanate Chemical compound CN=C=O HAMGRBXTJNITHG-UHFFFAOYSA-N 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- QYCUCSXZEFALJL-UHFFFAOYSA-N n-(6-tert-butyl-4-sulfanylidenechromen-3-yl)acetamide Chemical compound C1=C(C(C)(C)C)C=C2C(=S)C(NC(=O)C)=COC2=C1 QYCUCSXZEFALJL-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- 235000014483 powder concentrate Nutrition 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- ARENMZZMCSLORU-UHFFFAOYSA-N propan-2-yl naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)OC(C)C)=CC=CC2=C1 ARENMZZMCSLORU-UHFFFAOYSA-N 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 208000017520 skin disease Diseases 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- 238000001665 trituration Methods 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D335/00—Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom
- C07D335/04—Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D335/06—Benzothiopyrans; Hydrogenated benzothiopyrans
-
- 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
-
- 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<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/22—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Pyrane Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7738152A FR2411186A1 (fr) | 1977-12-12 | 1977-12-12 | Nouveaux derives d'ureido-3 (thio)chromones et compositions herbicides les contenant |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS203938B2 true CS203938B2 (en) | 1981-03-31 |
Family
ID=9198974
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS788213A CS203938B2 (en) | 1977-12-12 | 1978-12-11 | Herbicide means and method of making the active substances |
Country Status (31)
| Country | Link |
|---|---|
| US (1) | US4259506A (de) |
| JP (1) | JPS54130573A (de) |
| AR (1) | AR220162A1 (de) |
| AT (1) | AT362189B (de) |
| AU (1) | AU4239978A (de) |
| BE (1) | BE872689A (de) |
| BG (1) | BG30162A3 (de) |
| BR (1) | BR7808132A (de) |
| CA (1) | CA1101419A (de) |
| CS (1) | CS203938B2 (de) |
| CU (1) | CU34993A (de) |
| DD (1) | DD140327A5 (de) |
| DE (1) | DE2853587A1 (de) |
| DK (1) | DK556778A (de) |
| ES (1) | ES475875A1 (de) |
| FR (1) | FR2411186A1 (de) |
| GB (1) | GB2009740B (de) |
| GR (1) | GR65330B (de) |
| IL (1) | IL56180A0 (de) |
| IT (1) | IT7852251A0 (de) |
| LU (1) | LU80635A1 (de) |
| NL (1) | NL7811866A (de) |
| NZ (1) | NZ189139A (de) |
| OA (1) | OA06126A (de) |
| PH (1) | PH13707A (de) |
| PL (1) | PL211651A1 (de) |
| PT (1) | PT68892A (de) |
| SE (1) | SE7812723L (de) |
| SU (1) | SU814277A3 (de) |
| TR (1) | TR20073A (de) |
| ZA (1) | ZA786920B (de) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4614745A (en) * | 1984-04-24 | 1986-09-30 | Ciba-Geigy Corporation | Anti-allergic 3-(carboxycarbonyl)amino benzothiopyran-4-one derivatives, compositions, and method of use therefor |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2624664A (en) * | 1950-02-25 | 1953-01-06 | Monsanto Chemicals | Herbicides |
| IL41839A (en) * | 1972-04-13 | 1975-04-25 | Basf Ag | The use of cyclic sulfonium salts for regulating plant growth |
| FR2259589A1 (en) * | 1974-02-04 | 1975-08-29 | Ferlux | 2-Acylamino-chromones - with cardiac stimulant, analgesic and antiinflammatory, and some with normolipaemic activity |
-
1977
- 1977-12-12 FR FR7738152A patent/FR2411186A1/fr active Granted
-
1978
- 1978-11-30 ES ES475875A patent/ES475875A1/es not_active Expired
- 1978-12-05 NL NL7811866A patent/NL7811866A/xx not_active Application Discontinuation
- 1978-12-07 US US05/967,098 patent/US4259506A/en not_active Expired - Lifetime
- 1978-12-11 PH PH21921A patent/PH13707A/en unknown
- 1978-12-11 DD DD78209662A patent/DD140327A5/de unknown
- 1978-12-11 IT IT7852251A patent/IT7852251A0/it unknown
- 1978-12-11 PL PL21165178A patent/PL211651A1/xx unknown
- 1978-12-11 IL IL56180A patent/IL56180A0/xx unknown
- 1978-12-11 CS CS788213A patent/CS203938B2/cs unknown
- 1978-12-11 AU AU42399/78A patent/AU4239978A/en active Pending
- 1978-12-11 CA CA317,682A patent/CA1101419A/en not_active Expired
- 1978-12-11 JP JP15358678A patent/JPS54130573A/ja active Pending
- 1978-12-11 PT PT68892A patent/PT68892A/pt unknown
- 1978-12-11 GB GB7847919A patent/GB2009740B/en not_active Expired
- 1978-12-11 CU CU34993A patent/CU34993A/es unknown
- 1978-12-11 ZA ZA00786920A patent/ZA786920B/xx unknown
- 1978-12-11 AT AT881378A patent/AT362189B/de not_active IP Right Cessation
- 1978-12-11 LU LU80635A patent/LU80635A1/fr unknown
- 1978-12-11 NZ NZ189139A patent/NZ189139A/xx unknown
- 1978-12-11 DK DK556778A patent/DK556778A/da not_active Application Discontinuation
- 1978-12-11 SE SE7812723A patent/SE7812723L/xx unknown
- 1978-12-12 BR BR7808132A patent/BR7808132A/pt unknown
- 1978-12-12 BG BG041702A patent/BG30162A3/xx unknown
- 1978-12-12 BE BE192264A patent/BE872689A/xx unknown
- 1978-12-12 AR AR274758A patent/AR220162A1/es active
- 1978-12-12 TR TR20073A patent/TR20073A/xx unknown
- 1978-12-12 DE DE19782853587 patent/DE2853587A1/de not_active Withdrawn
- 1978-12-12 OA OA56678A patent/OA06126A/xx unknown
- 1978-12-12 GR GR57853A patent/GR65330B/el unknown
-
1979
- 1979-04-06 SU SU792745951A patent/SU814277A3/ru active
Also Published As
| Publication number | Publication date |
|---|---|
| GB2009740B (en) | 1982-03-17 |
| NZ189139A (en) | 1980-08-26 |
| CA1101419A (en) | 1981-05-19 |
| FR2411186A1 (fr) | 1979-07-06 |
| FR2411186B1 (de) | 1980-10-17 |
| SU814277A3 (ru) | 1981-03-15 |
| ATA881378A (de) | 1980-09-15 |
| PL211651A1 (de) | 1980-06-16 |
| SE7812723L (sv) | 1979-06-13 |
| ES475875A1 (es) | 1979-04-16 |
| ZA786920B (en) | 1979-12-27 |
| AR220162A1 (es) | 1980-10-15 |
| AT362189B (de) | 1981-04-27 |
| JPS54130573A (en) | 1979-10-09 |
| GR65330B (en) | 1980-08-13 |
| PH13707A (en) | 1980-09-08 |
| IL56180A0 (en) | 1979-03-12 |
| TR20073A (tr) | 1980-07-08 |
| BG30162A3 (en) | 1981-04-15 |
| LU80635A1 (fr) | 1980-07-21 |
| BR7808132A (pt) | 1979-08-07 |
| OA06126A (fr) | 1981-06-30 |
| DK556778A (da) | 1979-08-02 |
| NL7811866A (nl) | 1979-06-14 |
| GB2009740A (en) | 1979-06-20 |
| IT7852251A0 (it) | 1978-12-11 |
| US4259506A (en) | 1981-03-31 |
| PT68892A (fr) | 1980-02-07 |
| AU4239978A (en) | 1979-06-21 |
| CU34993A (en) | 1981-12-04 |
| DD140327A5 (de) | 1980-02-27 |
| BE872689A (fr) | 1979-06-12 |
| DE2853587A1 (de) | 1979-06-28 |
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