HU191843B - Fungicide composition containing n-/2-methyl-5-chlorophenyl/-n-/methoxy-acetyl/-3-amino-1,3-oxazolidin-2-one as active agent - Google Patents
Fungicide composition containing n-/2-methyl-5-chlorophenyl/-n-/methoxy-acetyl/-3-amino-1,3-oxazolidin-2-one as active agent Download PDFInfo
- Publication number
- HU191843B HU191843B HU831871A HU187183A HU191843B HU 191843 B HU191843 B HU 191843B HU 831871 A HU831871 A HU 831871A HU 187183 A HU187183 A HU 187183A HU 191843 B HU191843 B HU 191843B
- Authority
- HU
- Hungary
- Prior art keywords
- compound
- formula
- amino
- methyl
- chlorophenyl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 32
- 230000000855 fungicidal effect Effects 0.000 title claims abstract description 16
- 239000000417 fungicide Substances 0.000 title description 4
- 239000013543 active substance Substances 0.000 title 1
- -1 2-methyl-5-chlorophenyl Chemical group 0.000 claims description 5
- 239000004094 surface-active agent Substances 0.000 claims description 5
- 239000004480 active ingredient Substances 0.000 claims description 3
- 239000000969 carrier Substances 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 3
- 239000003995 emulsifying agent Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 125000000129 anionic group Chemical group 0.000 claims 1
- 125000002091 cationic group Chemical group 0.000 claims 1
- 239000002270 dispersing agent Substances 0.000 claims 1
- 239000012634 fragment Substances 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 239000011435 rock Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 35
- 238000009472 formulation Methods 0.000 abstract description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 16
- 241000196324 Embryophyta Species 0.000 description 16
- 208000015181 infectious disease Diseases 0.000 description 9
- 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 9
- 206010017533 Fungal infection Diseases 0.000 description 7
- 241000233866 Fungi Species 0.000 description 7
- 208000031888 Mycoses Diseases 0.000 description 7
- 241001281803 Plasmopara viticola Species 0.000 description 7
- 239000011734 sodium Substances 0.000 description 7
- 229910052708 sodium Inorganic materials 0.000 description 7
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N Vilsmeier-Haack reagent Natural products CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 5
- 241000582441 Peronospora tabacina Species 0.000 description 5
- 230000001143 conditioned effect Effects 0.000 description 5
- 239000004495 emulsifiable concentrate Substances 0.000 description 5
- 238000011534 incubation Methods 0.000 description 5
- 230000003449 preventive effect Effects 0.000 description 5
- 241000219094 Vitaceae Species 0.000 description 4
- 239000007900 aqueous suspension Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000007429 general method Methods 0.000 description 4
- 235000021021 grapes Nutrition 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 239000004563 wettable powder Substances 0.000 description 4
- IGFHQQFPSIBGKE-UHFFFAOYSA-N 4-nonylphenol Polymers CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 241000208125 Nicotiana Species 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 230000035876 healing Effects 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Polymers CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000080 wetting agent Substances 0.000 description 3
- ORILYTVJVMAKLC-UHFFFAOYSA-N Adamantane Natural products C1C(C2)CC3CC1CC2C3 ORILYTVJVMAKLC-UHFFFAOYSA-N 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 244000061176 Nicotiana tabacum Species 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 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 2
- 230000003032 phytopathogenic effect Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000375 suspending agent Substances 0.000 description 2
- XVFXJNWHUFWYMQ-UHFFFAOYSA-N (5-chloro-2-methylphenyl)hydrazine Chemical compound CC1=CC=C(Cl)C=C1NN XVFXJNWHUFWYMQ-UHFFFAOYSA-N 0.000 description 1
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 1
- QBWKPGNFQQJGFY-QLFBSQMISA-N 3-[(1r)-1-[(2r,6s)-2,6-dimethylmorpholin-4-yl]ethyl]-n-[6-methyl-3-(1h-pyrazol-4-yl)imidazo[1,2-a]pyrazin-8-yl]-1,2-thiazol-5-amine Chemical compound N1([C@H](C)C2=NSC(NC=3C4=NC=C(N4C=C(C)N=3)C3=CNN=C3)=C2)C[C@H](C)O[C@H](C)C1 QBWKPGNFQQJGFY-QLFBSQMISA-N 0.000 description 1
- JHWLWOYSFJIYQV-UHFFFAOYSA-N 4-dodecylbenzenesulfonate;tris(2-hydroxyethyl)azanium Chemical compound OCC[NH+](CCO)CCO.CCCCCCCCCCCCC1=CC=C(S([O-])(=O)=O)C=C1 JHWLWOYSFJIYQV-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 241001223281 Peronospora Species 0.000 description 1
- 231100000674 Phytotoxicity Toxicity 0.000 description 1
- 241000233626 Plasmopara Species 0.000 description 1
- 241001281802 Pseudoperonospora Species 0.000 description 1
- 241000233639 Pythium Species 0.000 description 1
- NWGKJDSIEKMTRX-AAZCQSIUSA-N Sorbitan monooleate Polymers CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-AAZCQSIUSA-N 0.000 description 1
- NWGKJDSIEKMTRX-MDZDMXLPSA-N Sorbitan oleate Polymers CCCCCCCC\C=C\CCCCCCCC(=O)OCC(O)C1OCC(O)C1O NWGKJDSIEKMTRX-MDZDMXLPSA-N 0.000 description 1
- NWGKJDSIEKMTRX-BFWOXRRGSA-N [(2r)-2-[(3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] (z)-octadec-9-enoate Polymers CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)C1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-BFWOXRRGSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000012871 anti-fungal composition Substances 0.000 description 1
- 235000010216 calcium carbonate Nutrition 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 229940125810 compound 20 Drugs 0.000 description 1
- 229940125846 compound 25 Drugs 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 150000001879 copper Chemical class 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 244000038559 crop plants Species 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 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
- 239000003337 fertilizer Substances 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
- JAXFJECJQZDFJS-XHEPKHHKSA-N gtpl8555 Chemical compound OC(=O)C[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N[C@H](B1O[C@@]2(C)[C@H]3C[C@H](C3(C)C)C[C@H]2O1)CCC1=CC=C(F)C=C1 JAXFJECJQZDFJS-XHEPKHHKSA-N 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 235000014666 liquid concentrate Nutrition 0.000 description 1
- PKDHKQOKIXBGNG-UHFFFAOYSA-N n,n-dimethylformamide;1,2-xylene Chemical group CN(C)C=O.CC1=CC=CC=C1C PKDHKQOKIXBGNG-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D263/16—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
- C07D263/18—Oxygen atoms
- C07D263/20—Oxygen atoms attached in position 2
- C07D263/26—Oxygen atoms attached in position 2 with hetero atoms or acyl radicals directly attached to the ring nitrogen atom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT21507/82A IT1152196B (it) | 1982-05-27 | 1982-05-27 | Composto fungicida |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HU191843B true HU191843B (en) | 1987-04-28 |
Family
ID=11182826
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU831871A HU191843B (en) | 1982-05-27 | 1983-05-26 | Fungicide composition containing n-/2-methyl-5-chlorophenyl/-n-/methoxy-acetyl/-3-amino-1,3-oxazolidin-2-one as active agent |
Country Status (20)
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8504181D0 (en) * | 1985-02-19 | 1985-03-20 | Sandoz Ltd | Fungicides |
| US7901701B2 (en) * | 2007-10-29 | 2011-03-08 | Lignotech Usa, Inc. | Methods for producing dried pesticide compositions |
| US20100278890A1 (en) * | 2009-04-29 | 2010-11-04 | Lignotech Usa, Inc. | Use of Lignosulfonates in Suspo-emulsions for Producing Pesticide Compositions |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH646158A5 (en) * | 1979-08-16 | 1984-11-15 | Sandoz Ag | Fungicides |
| IT1123564B (it) * | 1979-09-07 | 1986-04-30 | Montedison Spa | N-aril-n-acil-3-ammino-ossazolidin-2-oni fungicidi |
| DE3030026A1 (de) * | 1980-08-08 | 1981-03-26 | Sandoz-Patent-GmbH, 79539 Lörrach | Fungizide |
| DE3231605A1 (de) * | 1981-02-05 | 1983-02-10 | Sandoz Ag | Fungizide |
| DE3231606A1 (de) * | 1981-02-09 | 1983-02-10 | Sandoz Ag | Fungizide |
-
1982
- 1982-05-27 IT IT21507/82A patent/IT1152196B/it active
-
1983
- 1983-05-24 NZ NZ204342A patent/NZ204342A/en unknown
- 1983-05-24 NL NL8301827A patent/NL8301827A/nl not_active Application Discontinuation
- 1983-05-24 TR TR22255A patent/TR22255A/xx unknown
- 1983-05-24 DE DE19833318762 patent/DE3318762A1/de active Granted
- 1983-05-24 CH CH2804/83A patent/CH656381A5/fr not_active IP Right Cessation
- 1983-05-24 AT AT0188083A patent/AT381004B/de not_active IP Right Cessation
- 1983-05-24 ZA ZA833753A patent/ZA833753B/xx unknown
- 1983-05-25 FR FR8308589A patent/FR2527604B1/fr not_active Expired
- 1983-05-25 AU AU14983/83A patent/AU554684B2/en not_active Ceased
- 1983-05-25 CA CA000428822A patent/CA1214100A/en not_active Expired
- 1983-05-25 GR GR71458A patent/GR79237B/el unknown
- 1983-05-25 PT PT76758A patent/PT76758B/pt unknown
- 1983-05-25 IL IL68776A patent/IL68776A/xx unknown
- 1983-05-25 JP JP58090869A patent/JPS58216174A/ja active Granted
- 1983-05-26 ES ES522726A patent/ES8407031A1/es not_active Expired
- 1983-05-26 BE BE0/210855A patent/BE896852A/fr not_active IP Right Cessation
- 1983-05-26 GB GB08314666A patent/GB2121040B/en not_active Expired
- 1983-05-26 HU HU831871A patent/HU191843B/hu not_active IP Right Cessation
- 1983-05-27 MX MX8310632U patent/MX7296E/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IT1152196B (it) | 1986-12-31 |
| GB2121040B (en) | 1985-09-11 |
| IT8221507A0 (it) | 1982-05-27 |
| GR79237B (enrdf_load_stackoverflow) | 1984-10-22 |
| GB2121040A (en) | 1983-12-14 |
| ATA188083A (de) | 1986-01-15 |
| NZ204342A (en) | 1986-05-09 |
| JPH049789B2 (enrdf_load_stackoverflow) | 1992-02-21 |
| PT76758B (en) | 1986-03-11 |
| PT76758A (en) | 1983-06-01 |
| ZA833753B (en) | 1984-02-29 |
| ES522726A0 (es) | 1984-09-01 |
| TR22255A (tr) | 1986-11-25 |
| DE3318762C2 (enrdf_load_stackoverflow) | 1991-10-24 |
| AU1498383A (en) | 1983-12-01 |
| DE3318762A1 (de) | 1983-12-01 |
| MX7296E (es) | 1988-04-25 |
| IL68776A (en) | 1987-09-16 |
| NL8301827A (nl) | 1983-12-16 |
| GB8314666D0 (en) | 1983-06-29 |
| CH656381A5 (fr) | 1986-06-30 |
| BE896852A (fr) | 1983-11-28 |
| AU554684B2 (en) | 1986-08-28 |
| FR2527604A1 (fr) | 1983-12-02 |
| ES8407031A1 (es) | 1984-09-01 |
| AT381004B (de) | 1986-08-11 |
| CA1214100A (en) | 1986-11-18 |
| FR2527604B1 (fr) | 1986-11-14 |
| JPS58216174A (ja) | 1983-12-15 |
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