PH26304A - 6,7-dihydro-[1,2,4] triazolo-[1,5-a][1,3,5]triazine-2-sulfonamides and their use as herbicides and plant growth regulators - Google Patents
6,7-dihydro-[1,2,4] triazolo-[1,5-a][1,3,5]triazine-2-sulfonamides and their use as herbicides and plant growth regulators Download PDFInfo
- Publication number
- PH26304A PH26304A PH36251A PH36251A PH26304A PH 26304 A PH26304 A PH 26304A PH 36251 A PH36251 A PH 36251A PH 36251 A PH36251 A PH 36251A PH 26304 A PH26304 A PH 26304A
- Authority
- PH
- Philippines
- Prior art keywords
- dihydro
- triazine
- triazolo
- sulphonamide
- dimethyl
- Prior art date
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- 239000004009 herbicide Substances 0.000 title abstract description 7
- MDLJBXOSIGEKCK-UHFFFAOYSA-N 1,7-dihydro-[1,2,4]triazolo[1,5-a][1,3,5]triazine-2-sulfonamide Chemical class C1=NCN2NC(S(=O)(=O)N)=NC2=N1 MDLJBXOSIGEKCK-UHFFFAOYSA-N 0.000 title abstract 2
- 239000005648 plant growth regulator Substances 0.000 title description 4
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- 230000008635 plant growth Effects 0.000 claims abstract description 6
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- -1 nitro, methoxy Chemical group 0.000 claims description 14
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- 241001303487 Digitaria <clam> Species 0.000 description 1
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- 235000007351 Eleusine Nutrition 0.000 description 1
- 241000209215 Eleusine Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 241000221079 Euphorbia <genus> Species 0.000 description 1
- 241000234642 Festuca Species 0.000 description 1
- 241001290564 Fimbristylis Species 0.000 description 1
- 240000002727 Fimbristylis littoralis Species 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 241000748465 Galinsoga Species 0.000 description 1
- 241001101998 Galium Species 0.000 description 1
- JZNWSCPGTDBMEW-UHFFFAOYSA-N Glycerophosphorylethanolamin Natural products NCCOP(O)(=O)OCC(O)CO JZNWSCPGTDBMEW-UHFFFAOYSA-N 0.000 description 1
- ZWZWYGMENQVNFU-UHFFFAOYSA-N Glycerophosphorylserin Natural products OC(=O)C(N)COP(O)(=O)OCC(O)CO ZWZWYGMENQVNFU-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
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- 241000221024 Mercurialis Species 0.000 description 1
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- 235000006443 Panicum miliaceum subsp. miliaceum Nutrition 0.000 description 1
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- 241001330453 Paspalum Species 0.000 description 1
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- 244000064622 Physalis edulis Species 0.000 description 1
- 241000209048 Poa Species 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 241000205407 Polygonum Species 0.000 description 1
- 241000219295 Portulaca Species 0.000 description 1
- 241000857233 Rottboellia Species 0.000 description 1
- 240000009132 Sagittaria sagittifolia Species 0.000 description 1
- 241000202758 Scirpus Species 0.000 description 1
- 241000220261 Sinapis Species 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 235000002634 Solanum Nutrition 0.000 description 1
- 241000207763 Solanum Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- 244000062793 Sorghum vulgare Species 0.000 description 1
- 241000960310 Spergula Species 0.000 description 1
- 240000006694 Stellaria media Species 0.000 description 1
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical group O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 1
- 241000219873 Vicia Species 0.000 description 1
- 235000010716 Vigna mungo Nutrition 0.000 description 1
- 235000011453 Vigna umbellata Nutrition 0.000 description 1
- 241001506766 Xanthium Species 0.000 description 1
- ATBOMIWRCZXYSZ-XZBBILGWSA-N [1-[2,3-dihydroxypropoxy(hydroxy)phosphoryl]oxy-3-hexadecanoyloxypropan-2-yl] (9e,12e)-octadeca-9,12-dienoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(COP(O)(=O)OCC(O)CO)OC(=O)CCCCCCC\C=C\C\C=C\CCCCC ATBOMIWRCZXYSZ-XZBBILGWSA-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
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- AWUCVROLDVIAJX-UHFFFAOYSA-N alpha-glycerophosphate Natural products OCC(O)COP(O)(O)=O AWUCVROLDVIAJX-UHFFFAOYSA-N 0.000 description 1
- 229940115440 aluminum sodium silicate Drugs 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 150000008107 benzenesulfonic acids Chemical class 0.000 description 1
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
- 229940073608 benzyl chloride Drugs 0.000 description 1
- 235000021028 berry Nutrition 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- HCWYXKWQOMTBKY-UHFFFAOYSA-N calcium;dodecyl benzenesulfonate Chemical compound [Ca].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 HCWYXKWQOMTBKY-UHFFFAOYSA-N 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 238000001640 fractional crystallisation Methods 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 229910052987 metal hydride Inorganic materials 0.000 description 1
- 150000004681 metal hydrides Chemical class 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 229940042472 mineral oil Drugs 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
- RXPFZKKQXHCZFD-UHFFFAOYSA-N n-(2,6-dichlorophenyl)-5,6-dimethyl-7-sulfanylidene-[1,2,4]triazolo[1,5-a][1,3,5]triazine-2-sulfonamide Chemical compound N=1N2C(=S)N(C)C(C)=NC2=NC=1S(=O)(=O)NC1=C(Cl)C=CC=C1Cl RXPFZKKQXHCZFD-UHFFFAOYSA-N 0.000 description 1
- NSODMSASSLMUSD-UHFFFAOYSA-N n-methyl-1h-1,2,4-triazole-5-sulfonamide Chemical compound CNS(=O)(=O)C1=NC=NN1 NSODMSASSLMUSD-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
- 125000001624 naphthyl group Chemical group 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- WTJKGGKOPKCXLL-RRHRGVEJSA-N phosphatidylcholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCCCC WTJKGGKOPKCXLL-RRHRGVEJSA-N 0.000 description 1
- 229940067605 phosphatidylethanolamines Drugs 0.000 description 1
- 150000003905 phosphatidylinositols Chemical class 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 239000010773 plant oil Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000003223 protective agent Substances 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000000429 sodium aluminium silicate Substances 0.000 description 1
- 235000012217 sodium aluminium silicate Nutrition 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
- 229960000278 theophylline Drugs 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19863644343 DE3644343A1 (de) | 1986-12-19 | 1986-12-19 | 6,7-dihydro-(1,2,4)triazolo(1,5-a)(1,3,5) triazin-2-sulfonsaeureamide, verfahren zu ihrer herstellung und ihre verwendung als mittel mit herbizider und wachstumsregulierender wirkung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PH26304A true PH26304A (en) | 1992-04-29 |
Family
ID=6317131
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PH36251A PH26304A (en) | 1986-12-19 | 1987-12-17 | 6,7-dihydro-[1,2,4] triazolo-[1,5-a][1,3,5]triazine-2-sulfonamides and their use as herbicides and plant growth regulators |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US4859231A (xx) |
| EP (1) | EP0272628B1 (xx) |
| JP (1) | JPS63165385A (xx) |
| KR (1) | KR890008142A (xx) |
| CN (1) | CN87108134A (xx) |
| AT (1) | ATE75475T1 (xx) |
| AU (1) | AU603849B2 (xx) |
| BR (1) | BR8706931A (xx) |
| CA (1) | CA1305144C (xx) |
| DD (1) | DD264839A5 (xx) |
| DE (2) | DE3644343A1 (xx) |
| DK (1) | DK663387A (xx) |
| FI (1) | FI84726C (xx) |
| GR (1) | GR3004538T3 (xx) |
| HU (2) | HU206437B (xx) |
| IL (1) | IL84802A (xx) |
| PH (1) | PH26304A (xx) |
| SU (1) | SU1658808A3 (xx) |
| ZA (1) | ZA879531B (xx) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4954163A (en) * | 1983-11-14 | 1990-09-04 | The Dow Chemical Company | Substituted 1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamides, compositions containing them, and their utility as herbicides |
| DE3808122A1 (de) * | 1988-03-11 | 1989-09-21 | Bayer Ag | Triazolopyrimidin-2-sulfonamide |
| US5391759A (en) * | 1988-12-19 | 1995-02-21 | Dowelanco | Preparation of 5-acylamino-1,2,4-triazole-3-sulfonamides |
| DE3916469A1 (de) * | 1989-05-20 | 1990-11-22 | Basf Ag | Sulfonamide |
| JP4565018B2 (ja) * | 2007-05-22 | 2010-10-20 | 国立大学法人静岡大学 | 植物生長調節剤及び植物生長調節方法 |
| CN103281905B (zh) | 2010-12-21 | 2016-10-19 | 拜尔作物科学有限合伙公司 | 芽孢杆菌属的砂纸突变体及其用于增进植物生长、促进植物健康及控制疾病和害虫的方法 |
| EP2755485A1 (en) | 2011-09-12 | 2014-07-23 | Bayer Cropscience LP | Methods of enhancing health and/or promoting growth of a plant and/or of improving fruit ripening |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2236340A1 (de) * | 1972-07-25 | 1974-02-07 | Bayer Ag | S-triazolo eckige klammer auf 1,5-d eckige klammer zu -as-triazin-derivate, verfahren zu ihrer herstellung und ihre verwendung als herbizide |
| GB1579932A (en) * | 1976-05-12 | 1980-11-26 | Ici Ltd | Herbicidal triazolotriazines |
| DD205905A1 (de) * | 1982-08-17 | 1984-01-11 | Univ Rostock | Verfahren zur herstellung von substituierten 1,2,4-triazolo (2,3-a)-1,3,5-triazinen |
| US4565815A (en) * | 1982-12-30 | 1986-01-21 | Biomeasure, Inc. | Pyrazolo[1,5-a]-1,3,5-triazines |
| EP0142152B1 (en) * | 1983-11-14 | 1991-03-20 | The Dow Chemical Company | Novel substituted 1,2,4-triazolo- [1,5-a] pyrimidine-2-sulfonamides and compositions and methods of controlling undesired vegetation and suppressing the nitrification of ammonium nitrogen in soil |
| GR850161B (xx) * | 1984-01-26 | 1985-05-21 | Dow Chemical Co | |
| US4685958A (en) * | 1986-05-06 | 1987-08-11 | The Dow Chemical Company | Sulfonamides derived from substituted 2-amino-1,2,4-triazolo[1,5-a]-1,3,5-triazines and compositions and methods of controlling undesired vegetation |
-
1986
- 1986-12-19 DE DE19863644343 patent/DE3644343A1/de not_active Withdrawn
-
1987
- 1987-12-11 IL IL84802A patent/IL84802A/xx unknown
- 1987-12-15 FI FI875501A patent/FI84726C/fi not_active IP Right Cessation
- 1987-12-16 JP JP62316378A patent/JPS63165385A/ja active Pending
- 1987-12-16 DK DK663387A patent/DK663387A/da not_active Application Discontinuation
- 1987-12-16 DD DD87310561A patent/DD264839A5/de not_active IP Right Cessation
- 1987-12-17 DE DE8787118740T patent/DE3778666D1/de not_active Expired - Lifetime
- 1987-12-17 PH PH36251A patent/PH26304A/en unknown
- 1987-12-17 EP EP87118740A patent/EP0272628B1/de not_active Expired - Lifetime
- 1987-12-17 AT AT87118740T patent/ATE75475T1/de active
- 1987-12-18 HU HU875865A patent/HU206437B/hu unknown
- 1987-12-18 CN CN198787108134A patent/CN87108134A/zh active Pending
- 1987-12-18 HU HU875856A patent/HUT45851A/hu unknown
- 1987-12-18 US US07/135,142 patent/US4859231A/en not_active Expired - Fee Related
- 1987-12-18 SU SU874203886A patent/SU1658808A3/ru active
- 1987-12-18 ZA ZA879531A patent/ZA879531B/xx unknown
- 1987-12-18 BR BR8706931A patent/BR8706931A/pt unknown
- 1987-12-18 CA CA000554861A patent/CA1305144C/en not_active Expired - Lifetime
- 1987-12-18 AU AU82825/87A patent/AU603849B2/en not_active Ceased
- 1987-12-19 KR KR870014566A patent/KR890008142A/ko not_active Application Discontinuation
-
1992
- 1992-05-08 GR GR920400798T patent/GR3004538T3/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| HU206437B (en) | 1992-11-30 |
| SU1658808A3 (ru) | 1991-06-23 |
| DE3778666D1 (de) | 1992-06-04 |
| ZA879531B (en) | 1988-06-15 |
| AU603849B2 (en) | 1990-11-29 |
| HUT45851A (en) | 1988-09-28 |
| KR890008142A (ko) | 1989-07-10 |
| JPS63165385A (ja) | 1988-07-08 |
| FI875501A (fi) | 1988-06-20 |
| CA1305144C (en) | 1992-07-14 |
| FI84726B (fi) | 1991-09-30 |
| DE3644343A1 (de) | 1988-06-30 |
| EP0272628A2 (de) | 1988-06-29 |
| DK663387A (da) | 1988-06-20 |
| US4859231A (en) | 1989-08-22 |
| FI875501A0 (fi) | 1987-12-15 |
| GR3004538T3 (xx) | 1993-04-28 |
| BR8706931A (pt) | 1988-07-26 |
| IL84802A (en) | 1991-11-21 |
| AU8282587A (en) | 1988-06-23 |
| CN87108134A (zh) | 1988-12-28 |
| FI84726C (fi) | 1992-01-10 |
| DK663387D0 (da) | 1987-12-16 |
| EP0272628B1 (de) | 1992-04-29 |
| IL84802A0 (en) | 1988-06-30 |
| DD264839A5 (de) | 1989-02-15 |
| ATE75475T1 (de) | 1992-05-15 |
| EP0272628A3 (en) | 1989-08-23 |
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