HU200980B - Process for oxidation into carbonic acid of compositions containing methil-group in basical circumstances - Google Patents
Process for oxidation into carbonic acid of compositions containing methil-group in basical circumstances Download PDFInfo
- Publication number
- HU200980B HU200980B HU841499A HU149984A HU200980B HU 200980 B HU200980 B HU 200980B HU 841499 A HU841499 A HU 841499A HU 149984 A HU149984 A HU 149984A HU 200980 B HU200980 B HU 200980B
- Authority
- HU
- Hungary
- Prior art keywords
- copper
- methyl
- formula
- cobalt
- compound
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 21
- 238000007254 oxidation reaction Methods 0.000 title claims description 27
- 230000003647 oxidation Effects 0.000 title claims description 26
- 239000000203 mixture Substances 0.000 title claims description 12
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 title 1
- 239000010949 copper Substances 0.000 claims abstract description 24
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 21
- 229910052802 copper Inorganic materials 0.000 claims abstract description 21
- 229910017052 cobalt Inorganic materials 0.000 claims abstract description 18
- 239000010941 cobalt Substances 0.000 claims abstract description 18
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims abstract description 18
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims abstract description 15
- 229910052709 silver Inorganic materials 0.000 claims abstract description 15
- 239000004332 silver Substances 0.000 claims abstract description 15
- 238000002360 preparation method Methods 0.000 claims abstract description 4
- 150000001875 compounds Chemical class 0.000 claims description 20
- WXYKQNAKEPRCGF-UHFFFAOYSA-N 2-methylquinoline-3-carboxylic acid Chemical compound C1=CC=C2C=C(C(O)=O)C(C)=NC2=C1 WXYKQNAKEPRCGF-UHFFFAOYSA-N 0.000 claims description 17
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
- 239000005708 Sodium hypochlorite Substances 0.000 claims description 8
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 claims description 8
- 239000007864 aqueous solution Substances 0.000 claims description 6
- 239000000460 chlorine Substances 0.000 claims description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- 230000001590 oxidative effect Effects 0.000 claims description 5
- HNTZKNJGAFJMHQ-UHFFFAOYSA-N 2-methylpyridine-3-carboxylic acid Chemical compound CC1=NC=CC=C1C(O)=O HNTZKNJGAFJMHQ-UHFFFAOYSA-N 0.000 claims description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 claims description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical class OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 3
- 229910021592 Copper(II) chloride Inorganic materials 0.000 claims description 2
- 150000004678 hydrides Chemical class 0.000 claims 2
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 claims 1
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical class ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 claims 1
- 229910000104 sodium hydride Inorganic materials 0.000 claims 1
- 239000012312 sodium hydride Substances 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 abstract description 8
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 57
- 239000000243 solution Substances 0.000 description 42
- 239000011541 reaction mixture Substances 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 14
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 11
- JJLJMEJHUUYSSY-UHFFFAOYSA-L copper(II) hydroxide Inorganic materials [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 8
- 239000005749 Copper compound Substances 0.000 description 7
- 150000001880 copper compounds Chemical class 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- AEJIMXVJZFYIHN-UHFFFAOYSA-N copper;dihydrate Chemical compound O.O.[Cu] AEJIMXVJZFYIHN-UHFFFAOYSA-N 0.000 description 5
- 239000000706 filtrate Substances 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 238000004128 high performance liquid chromatography Methods 0.000 description 4
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- GJAWHXHKYYXBSV-UHFFFAOYSA-N quinolinic acid Chemical compound OC(=O)C1=CC=CN=C1C(O)=O GJAWHXHKYYXBSV-UHFFFAOYSA-N 0.000 description 4
- 238000006114 decarboxylation reaction Methods 0.000 description 3
- 239000007800 oxidant agent Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- GWHJZXXIDMPWGX-UHFFFAOYSA-N 1,2,4-trimethylbenzene Chemical compound CC1=CC=C(C)C(C)=C1 GWHJZXXIDMPWGX-UHFFFAOYSA-N 0.000 description 2
- HPYNZHMRTTWQTB-UHFFFAOYSA-N 2,3-dimethylpyridine Chemical compound CC1=CC=CN=C1C HPYNZHMRTTWQTB-UHFFFAOYSA-N 0.000 description 2
- ONHGVIQHHDYDHI-UHFFFAOYSA-N 2-methylquinoline-3-carboxylic acid;hydrochloride Chemical compound Cl.C1=CC=C2C=C(C(O)=O)C(C)=NC2=C1 ONHGVIQHHDYDHI-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- ZWLPBLYKEWSWPD-UHFFFAOYSA-N o-toluic acid Chemical compound CC1=CC=CC=C1C(O)=O ZWLPBLYKEWSWPD-UHFFFAOYSA-N 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- -1 1,2,4-trimethylbenzoyl Chemical group 0.000 description 1
- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-Lutidine Substances CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 1
- JCNWMZGWLFRHEJ-UHFFFAOYSA-N 2-methylbenzoic acid Chemical compound CC1=CC=CC=C1C(O)=O.CC1=CC=CC=C1C(O)=O JCNWMZGWLFRHEJ-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
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- JFBJUMZWZDHTIF-UHFFFAOYSA-N chlorine chlorite Inorganic materials ClOCl=O JFBJUMZWZDHTIF-UHFFFAOYSA-N 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 150000001869 cobalt compounds Chemical class 0.000 description 1
- IUYLTEAJCNAMJK-UHFFFAOYSA-N cobalt(2+);oxygen(2-) Chemical compound [O-2].[Co+2] IUYLTEAJCNAMJK-UHFFFAOYSA-N 0.000 description 1
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(II) oxide Inorganic materials [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000002848 electrochemical method Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 229940100890 silver compound Drugs 0.000 description 1
- 150000003379 silver compounds Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B33/00—Oxidation in general
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/215—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of saturated hydrocarbyl groups
-
- 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/79—Acids; Esters
- C07D213/803—Processes of preparation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D215/54—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Pyridine Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
- Quinoline Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/485,769 US4623726A (en) | 1983-04-18 | 1983-04-18 | Method for oxidizing alkyl groups on pyridine, quinoline and benzene ring compounds to carboxylic acids under basic conditions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| HUT36771A HUT36771A (en) | 1985-10-28 |
| HU200980B true HU200980B (en) | 1990-09-28 |
Family
ID=23929381
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU841499A HU200980B (en) | 1983-04-18 | 1984-04-18 | Process for oxidation into carbonic acid of compositions containing methil-group in basical circumstances |
Country Status (16)
| Country | Link |
|---|---|
| US (2) | US4623726A (enExample) |
| EP (1) | EP0126893B1 (enExample) |
| JP (1) | JPS59199637A (enExample) |
| KR (2) | KR920003836B1 (enExample) |
| AR (1) | AR240910A1 (enExample) |
| AU (1) | AU566449B2 (enExample) |
| BR (1) | BR8401813A (enExample) |
| CA (1) | CA1261845A (enExample) |
| DE (1) | DE3478742D1 (enExample) |
| DK (3) | DK168211B1 (enExample) |
| ES (1) | ES8506573A1 (enExample) |
| HU (1) | HU200980B (enExample) |
| IE (1) | IE57308B1 (enExample) |
| IL (1) | IL71466A (enExample) |
| IN (1) | IN162865B (enExample) |
| ZA (1) | ZA842889B (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4816588A (en) * | 1986-09-12 | 1989-03-28 | American Cyanamid Company | Method for the preparation of pyridine-2,3-dicarboxylic acids |
| DE3706792A1 (de) * | 1987-03-03 | 1988-09-15 | Basf Ag | Verfahren zur herstellung von 7-chlor-chinolin-8-carbonsaeure |
| JP2743473B2 (ja) * | 1988-07-04 | 1998-04-22 | 日産化学工業株式会社 | ピラゾールカルボン酸類の製造方法 |
| US5202442A (en) * | 1988-07-04 | 1993-04-13 | Nissan Chemical Industries, Ltd. | Process for preparing pyrazolecarboxylic acid compounds |
| EP0388619B1 (en) * | 1989-03-22 | 1994-08-10 | American Cyanamid Company | Method for the sequential oxidation of substituted quinolines to produce substituted-pyridine-2,3-dicarboxylic acids |
| US5002641A (en) * | 1990-06-28 | 1991-03-26 | Reilly Industries, Inc. | Electrochemical synthesis of niacin and other N-heterocyclic compounds |
| EP0743279A1 (en) * | 1995-05-16 | 1996-11-20 | The Procter & Gamble Company | Process for the manufacture of hypochlorite bleaching compositions |
| US5928559A (en) * | 1995-05-16 | 1999-07-27 | The Procter & Gamble Company | Process for the manufacture of hypochlorite bleaching compositions |
| PL236815B1 (pl) | 2015-11-09 | 2021-02-22 | Wojciech Bukowski | Zastosowanie preparatu antybakteryjnego i antygrzybicznego |
| EP3782985A1 (en) | 2019-08-19 | 2021-02-24 | BASF Agrochemical Products B.V. | Process for manufacturing 5-methoxymethylpyridine-2,3-dicarboxylic acid derivatives |
| CN117143012B (zh) * | 2023-07-21 | 2026-06-05 | 江西帝劢药业有限公司 | 一种喹啉酸的合成方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2515593A (en) | 1947-02-03 | 1950-07-18 | Shell Dev | Production of pyridine-carboxylic acids |
| US2513099A (en) | 1947-09-09 | 1950-06-27 | Allied Chem & Dye Corp | Oxidation of heterocyclic aromatic nitrogen compounds |
| US2793213A (en) | 1954-07-23 | 1957-05-21 | Allied Chem & Dye Corp | Process for preparing pyridine carboxylic acids |
| US4450055A (en) * | 1983-03-30 | 1984-05-22 | Celanese Corporation | Electrogenerative partial oxidation of organic compounds |
| US4496440A (en) * | 1984-06-04 | 1985-01-29 | The Dow Chemical Company | Oxidation of hydrophobic --CH2 OH compounds at oxidized nickel anodes |
-
1983
- 1983-04-18 US US06/485,769 patent/US4623726A/en not_active Expired - Lifetime
-
1984
- 1984-03-28 DE DE8484103414T patent/DE3478742D1/de not_active Expired
- 1984-03-28 EP EP84103414A patent/EP0126893B1/en not_active Expired
- 1984-03-30 IN IN211/CAL/84A patent/IN162865B/en unknown
- 1984-04-08 IL IL71466A patent/IL71466A/xx not_active IP Right Cessation
- 1984-04-16 ES ES531657A patent/ES8506573A1/es not_active Expired
- 1984-04-16 CA CA000452079A patent/CA1261845A/en not_active Expired
- 1984-04-17 IE IE946/84A patent/IE57308B1/en not_active IP Right Cessation
- 1984-04-17 AR AR296332A patent/AR240910A1/es active
- 1984-04-17 AU AU26897/84A patent/AU566449B2/en not_active Expired
- 1984-04-17 DK DK198084A patent/DK168211B1/da not_active IP Right Cessation
- 1984-04-17 JP JP59075903A patent/JPS59199637A/ja active Granted
- 1984-04-17 BR BR8401813A patent/BR8401813A/pt not_active IP Right Cessation
- 1984-04-17 ZA ZA842889A patent/ZA842889B/xx unknown
- 1984-04-17 KR KR1019840002011A patent/KR920003836B1/ko not_active Expired
- 1984-04-18 HU HU841499A patent/HU200980B/hu unknown
-
1986
- 1986-08-25 US US06/900,462 patent/US4750978A/en not_active Expired - Lifetime
-
1991
- 1991-10-11 KR KR1019910017899A patent/KR920000693B1/ko not_active Expired
-
1993
- 1993-06-22 DK DK074193A patent/DK170154B1/da not_active IP Right Cessation
- 1993-06-22 DK DK074093A patent/DK168623B1/da not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| US4623726A (en) | 1986-11-18 |
| BR8401813A (pt) | 1984-11-27 |
| IL71466A0 (en) | 1984-07-31 |
| US4750978A (en) | 1988-06-14 |
| DK170154B1 (da) | 1995-06-06 |
| DK168211B1 (da) | 1994-02-28 |
| JPS59199637A (ja) | 1984-11-12 |
| AR240910A2 (es) | 1991-03-27 |
| DK168623B1 (da) | 1994-05-09 |
| DK74193D0 (da) | 1993-06-22 |
| HUT36771A (en) | 1985-10-28 |
| AU2689784A (en) | 1984-10-25 |
| JPH0582372B2 (enExample) | 1993-11-18 |
| KR840008460A (ko) | 1984-12-15 |
| DK74193A (da) | 1993-06-22 |
| IE57308B1 (en) | 1992-07-15 |
| KR920003836B1 (ko) | 1992-05-15 |
| DK198084A (da) | 1984-10-19 |
| AU566449B2 (en) | 1987-10-22 |
| IE840946L (en) | 1984-10-18 |
| IN162865B (enExample) | 1988-07-16 |
| AR240910A1 (es) | 1991-03-27 |
| DE3478742D1 (en) | 1989-07-27 |
| ES531657A0 (es) | 1985-08-01 |
| EP0126893B1 (en) | 1989-06-21 |
| ZA842889B (en) | 1984-11-28 |
| CA1261845A (en) | 1989-09-26 |
| IL71466A (en) | 1989-12-15 |
| KR920000693B1 (ko) | 1992-01-20 |
| EP0126893A1 (en) | 1984-12-05 |
| ES8506573A1 (es) | 1985-08-01 |
| DK74093D0 (da) | 1993-06-22 |
| DK74093A (da) | 1993-06-22 |
| DK198084D0 (da) | 1984-04-17 |
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