DD248357A5 - Verfahren zur herstellung von 9,10-phenonthrendion-derivaten - Google Patents

Verfahren zur herstellung von 9,10-phenonthrendion-derivaten Download PDF

Info

Publication number: DD248357A5
Authority: DD; German Democratic Republic
Prior art keywords: general formula; phenanthrene; alkoxy; alkyl; starting material
Prior art date: 1985-06-04

Application number

DD86290957A

Other languages

German (de)

English (en)

Inventor

Pal Benko

Tibor Zsolnai

Marta Kiniczky

Laszlo Pallos

Iren Zsolnai

Peter Tetenyi

Jenoe Bernath

Original Assignee

��@��k��

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1985-06-04

Filing date

1986-06-04

Publication date

1987-08-05

1986-06-04 Application filed by ��@��k�� filed Critical ��@��k��

1987-08-05 Publication of DD248357A5 publication Critical patent/DD248357A5/de

Links

238000000034 method Methods 0.000 title claims abstract description 29
238000002360 preparation method Methods 0.000 title claims abstract description 22
150000001875 compounds Chemical class 0.000 claims abstract description 52
-1 nitro, amino Chemical group 0.000 claims abstract description 49
125000003545 alkoxy group Chemical group 0.000 claims abstract description 15
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 13
229910052784 alkaline earth metal Inorganic materials 0.000 claims abstract description 12
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 12
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims abstract description 7
239000003513 alkali Substances 0.000 claims abstract description 5
125000003282 alkyl amino group Chemical group 0.000 claims abstract description 5
125000004414 alkyl thio group Chemical group 0.000 claims abstract description 5
YNPNZTXNASCQKK-UHFFFAOYSA-N Phenanthrene Natural products C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 claims abstract description 3
125000000217 alkyl group Chemical group 0.000 claims description 15
239000007858 starting material Substances 0.000 claims description 13
150000002367 halogens Chemical group 0.000 claims description 12
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 9
239000000460 chlorine Substances 0.000 claims description 9
229910052736 halogen Inorganic materials 0.000 claims description 6
229910052801 chlorine Inorganic materials 0.000 claims description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
239000003960 organic solvent Substances 0.000 claims description 5
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 5
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
229910052783 alkali metal Inorganic materials 0.000 claims description 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
229910052794 bromium Inorganic materials 0.000 claims description 3
125000001309 chloro group Chemical group Cl* 0.000 claims description 3
239000012948 isocyanate Substances 0.000 claims description 3
150000002513 isocyanates Chemical class 0.000 claims description 3
239000012011 nucleophilic catalyst Substances 0.000 claims description 3
239000011593 sulfur Chemical group 0.000 claims description 3
229910052717 sulfur Chemical group 0.000 claims description 3
150000001340 alkali metals Chemical class 0.000 claims description 2
150000001342 alkaline earth metals Chemical class 0.000 claims description 2
125000005278 alkyl sulfonyloxy group Chemical group 0.000 claims description 2
125000005279 aryl sulfonyloxy group Chemical group 0.000 claims description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
229910052740 iodine Inorganic materials 0.000 claims description 2
229910052760 oxygen Inorganic materials 0.000 claims description 2
239000001301 oxygen Substances 0.000 claims description 2
150000003512 tertiary amines Chemical class 0.000 claims description 2
239000012442 inert solvent Substances 0.000 claims 1
238000004519 manufacturing process Methods 0.000 claims 1
230000000855 fungicidal effect Effects 0.000 abstract description 15
125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
125000005843 halogen group Chemical group 0.000 abstract 1
238000003898 horticulture Methods 0.000 abstract 1
238000002560 therapeutic procedure Methods 0.000 abstract 1
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239000004480 active ingredient Substances 0.000 description 14
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ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
238000004458 analytical method Methods 0.000 description 9
239000003795 chemical substances by application Substances 0.000 description 9
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
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LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
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239000000047 product Substances 0.000 description 6
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VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 6
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239000000969 carrier Substances 0.000 description 3
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238000002474 experimental method Methods 0.000 description 3
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238000001727 in vivo Methods 0.000 description 3
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ZEVCJZRMCOYJSP-UHFFFAOYSA-N sodium;2-(dithiocarboxyamino)ethylcarbamodithioic acid Chemical compound [Na+].SC(=S)NCCNC(S)=S ZEVCJZRMCOYJSP-UHFFFAOYSA-N 0.000 description 3
239000007787 solid Substances 0.000 description 3
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WRXXDADMLZZMRL-UHFFFAOYSA-N [1-(butylcarbamoyl)benzimidazol-2-yl] n-methylcarbamate Chemical compound C1=CC=C2N(C(=O)NCCCC)C(OC(=O)NC)=NC2=C1 WRXXDADMLZZMRL-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
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230000001476 alcoholic effect Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
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235000012211 aluminium silicate Nutrition 0.000 description 1
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IMHBYKMAHXWHRP-UHFFFAOYSA-N anilazine Chemical compound ClC1=CC=CC=C1NC1=NC(Cl)=NC(Cl)=N1 IMHBYKMAHXWHRP-UHFFFAOYSA-N 0.000 description 1
230000000843 anti-fungal effect Effects 0.000 description 1
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239000004305 biphenyl Substances 0.000 description 1
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239000000920 calcium hydroxide Substances 0.000 description 1
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239000001768 carboxy methyl cellulose Substances 0.000 description 1
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239000003995 emulsifying agent Substances 0.000 description 1
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238000011156 evaluation Methods 0.000 description 1
JFSPBVWPKOEZCB-UHFFFAOYSA-N fenfuram Chemical compound O1C=CC(C(=O)NC=2C=CC=CC=2)=C1C JFSPBVWPKOEZCB-UHFFFAOYSA-N 0.000 description 1
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239000011737 fluorine Substances 0.000 description 1
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150000008282 halocarbons Chemical class 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
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230000002401 inhibitory effect Effects 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
239000011630 iodine Substances 0.000 description 1
QPPQHRDVPBTVEV-UHFFFAOYSA-N isopropyl dihydrogen phosphate Chemical compound CC(C)OP(O)(O)=O QPPQHRDVPBTVEV-UHFFFAOYSA-N 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
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 1
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239000011572 manganese Substances 0.000 description 1
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VHOVSQVSAAQANU-UHFFFAOYSA-M mepiquat chloride Chemical compound [Cl-].C[N+]1(C)CCCCC1 VHOVSQVSAAQANU-UHFFFAOYSA-M 0.000 description 1
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229910052618 mica group Inorganic materials 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
239000011707 mineral Substances 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
HNHVTXYLRVGMHD-UHFFFAOYSA-N n-butyl isocyanate Chemical compound CCCCN=C=O HNHVTXYLRVGMHD-UHFFFAOYSA-N 0.000 description 1
125000002004 n-butylamino group Chemical group [H]N(*)C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
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VSIIXMUUUJUKCM-UHFFFAOYSA-D pentacalcium;fluoride;triphosphate Chemical compound [F-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O VSIIXMUUUJUKCM-UHFFFAOYSA-D 0.000 description 1
235000011197 perejil Nutrition 0.000 description 1
150000002987 phenanthrenes Chemical class 0.000 description 1
SBNFWQZLDJGRLK-UHFFFAOYSA-N phenothrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 SBNFWQZLDJGRLK-UHFFFAOYSA-N 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 1
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230000000885 phytotoxic effect Effects 0.000 description 1
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YEBIHIICWDDQOL-YBHNRIQQSA-N polyoxin Polymers O[C@@H]1[C@H](O)[C@@H](C(C=O)N)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 YEBIHIICWDDQOL-YBHNRIQQSA-N 0.000 description 1
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239000002689 soil Substances 0.000 description 1
238000007711 solidification Methods 0.000 description 1
230000008023 solidification Effects 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
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239000003381 stabilizer Substances 0.000 description 1
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125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
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239000004094 surface-active agent Substances 0.000 description 1
208000024891 symptom Diseases 0.000 description 1
239000000454 talc Substances 0.000 description 1
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239000003784 tall oil Substances 0.000 description 1
WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
229960002447 thiram Drugs 0.000 description 1
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
JARYYMUOCXVXNK-IMTORBKUSA-N validamycin Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-IMTORBKUSA-N 0.000 description 1
239000010455 vermiculite Substances 0.000 description 1
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235000019354 vermiculite Nutrition 0.000 description 1
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239000000080 wetting agent Substances 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C249/00—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C249/04—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton of oximes
- C07C249/12—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton of oximes by reactions not involving the formation of oxyimino groups
- 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
- A01N47/02—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 no bond to a nitrogen atom
- A01N47/06—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 no bond to a nitrogen atom containing —O—CO—O— groups; 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group; 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
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/22—Ortho- or ortho- and peri-condensed systems containing three rings containing only six-membered rings
- C07C2603/26—Phenanthrenes; Hydrogenated phenanthrenes

Landscapes

Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Pharmacology & Pharmacy (AREA)
General Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Communicable Diseases (AREA)
Oncology (AREA)
Animal Behavior & Ethology (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

DD86290957A 1985-06-04 1986-06-04 Verfahren zur herstellung von 9,10-phenonthrendion-derivaten DD248357A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
HU852194A HU196288B (en)	1985-06-04	1985-06-04	Fungicides containing as active substance new derivatives of fenantren and process for production of the active substance

Publications (1)

Publication Number	Publication Date
DD248357A5 true DD248357A5 (de)	1987-08-05

Family

ID=10958225

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
DD86290957A DD248357A5 (de)	1985-06-04	1986-06-04	Verfahren zur herstellung von 9,10-phenonthrendion-derivaten
DD86301000A DD261083A5 (de)	1985-06-04	1986-06-04	Fungizide praeparate und verfahren zur bekaempfung von fungi-schaedlingen

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
DD86301000A DD261083A5 (de)	1985-06-04	1986-06-04	Fungizide praeparate und verfahren zur bekaempfung von fungi-schaedlingen

Country Status (26)

Country	Link
US (1)	US4746678A (sv)
JP (1)	JPS6248661A (sv)
KR (1)	KR870011083A (sv)
CN (1)	CN86103679A (sv)
AU (1)	AU589637B2 (sv)
BE (1)	BE904865A (sv)
BR (1)	BR8602608A (sv)
CH (1)	CH667645A5 (sv)
CS (1)	CS411386A2 (sv)
DD (2)	DD248357A5 (sv)
DE (1)	DE3618715A1 (sv)
DK (1)	DK262286A (sv)
ES (1)	ES8707711A1 (sv)
FI (1)	FI862382A (sv)
FR (1)	FR2582647B1 (sv)
GB (1)	GB2176186B (sv)
GR (1)	GR861451B (sv)
HU (1)	HU196288B (sv)
IL (1)	IL79029A0 (sv)
IT (1)	IT1204376B (sv)
NL (1)	NL8601435A (sv)
NO (1)	NO862231L (sv)
PL (1)	PL147246B1 (sv)
PT (1)	PT82713B (sv)
SE (1)	SE8602525L (sv)
SU (1)	SU1450737A3 (sv)

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DE3708320A1 (de) *	1987-03-14	1988-09-22	Bayer Ag	Benzaldoxim-derivate
EP1242363B1 (en) *	1999-12-21	2005-11-02	AstraZeneca AB	Cd45 inhibitors
WO2001045680A2 (en) *	1999-12-21	2001-06-28	Astrazeneca Ab	Cd45 inhibitors
KR20090104877A (ko) *	2007-01-23	2009-10-06	후지필름 가부시키가이샤	옥심 화합물, 감광성 조성물, 컬러 필터, 그 제조방법 및 액정표시소자
AR108745A1 (es) *	2016-06-21	2018-09-19	Syngenta Participations Ag	Derivados de oxadiazol microbiocidas
CN106565536B (zh) *	2016-07-15	2018-05-08	广西民族大学	异长叶烯酮肟醚衍生物及其制备方法和应用
CN110156867B (zh) *	2019-06-27	2022-03-25	南京神奇科技开发有限公司	一种氨基甲酸黄柏酮肟酯及其制备方法与应用
GB202014840D0 (en) *	2020-09-21	2020-11-04	Syngenta Crop Protection Ag	Microbiocidal compounds

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Publication number	Priority date	Publication date	Assignee	Title
NL275195A (sv) *	1961-02-28
US3547621A (en) *	1967-05-29	1970-12-15	Gulf Research Development Co	Method of combating weeds
GB1180846A (en) *	1967-08-08	1970-02-11	Agfa Gevaert Nv	Photopolymerisation of Ethylenically Unsaturated Organic Compounds

1985
- 1985-06-04 HU HU852194A patent/HU196288B/hu not_active IP Right Cessation
1986
- 1986-05-31 CN CN198686103679A patent/CN86103679A/zh active Pending
- 1986-06-03 CH CH2249/86A patent/CH667645A5/de not_active IP Right Cessation
- 1986-06-03 BE BE0/216735A patent/BE904865A/fr not_active IP Right Cessation
- 1986-06-04 DD DD86290957A patent/DD248357A5/de not_active IP Right Cessation
- 1986-06-04 GR GR861451A patent/GR861451B/el unknown
- 1986-06-04 GB GB8613531A patent/GB2176186B/en not_active Expired
- 1986-06-04 NO NO862231A patent/NO862231L/no unknown
- 1986-06-04 SU SU864027579A patent/SU1450737A3/ru active
- 1986-06-04 DD DD86301000A patent/DD261083A5/de not_active IP Right Cessation
- 1986-06-04 DE DE19863618715 patent/DE3618715A1/de not_active Withdrawn
- 1986-06-04 CS CS864113A patent/CS411386A2/cs unknown
- 1986-06-04 US US06/870,402 patent/US4746678A/en not_active Expired - Fee Related
- 1986-06-04 PL PL1986259870A patent/PL147246B1/pl unknown
- 1986-06-04 FI FI862382A patent/FI862382A/fi not_active IP Right Cessation
- 1986-06-04 IT IT20666/86A patent/IT1204376B/it active
- 1986-06-04 FR FR8608040A patent/FR2582647B1/fr not_active Expired
- 1986-06-04 SE SE8602525A patent/SE8602525L/sv not_active Application Discontinuation
- 1986-06-04 JP JP61130007A patent/JPS6248661A/ja active Pending
- 1986-06-04 DK DK262286A patent/DK262286A/da not_active Application Discontinuation
- 1986-06-04 IL IL79029A patent/IL79029A0/xx unknown
- 1986-06-04 BR BR8602608A patent/BR8602608A/pt unknown
- 1986-06-04 KR KR1019860004449A patent/KR870011083A/ko not_active Application Discontinuation
- 1986-06-04 PT PT82713A patent/PT82713B/pt unknown
- 1986-06-04 ES ES555709A patent/ES8707711A1/es not_active Expired
- 1986-06-04 AU AU58340/86A patent/AU589637B2/en not_active Ceased
- 1986-06-04 NL NL8601435A patent/NL8601435A/nl not_active Application Discontinuation

Also Published As

Publication number	Publication date
GR861451B (en)	1986-10-03
DD261083A5 (de)	1988-10-19
IL79029A0 (en)	1986-09-30
FR2582647B1 (fr)	1988-11-18
KR870011083A (ko)	1987-12-19
NL8601435A (nl)	1987-01-02
CN86103679A (zh)	1987-04-08
GB8613531D0 (en)	1986-07-09
SE8602525L (sv)	1986-12-05
CS411386A2 (en)	1989-09-12
GB2176186A (en)	1986-12-17
FI862382A (fi)	1986-12-05
PT82713A (en)	1986-07-01
PT82713B (en)	1987-10-14
IT1204376B (it)	1989-03-01
DE3618715A1 (de)	1986-12-04
DK262286A (da)	1986-12-05
AU5834086A (en)	1986-12-11
IT8620666A0 (it)	1986-06-04
SE8602525D0 (sv)	1986-06-04
NO862231D0 (no)	1986-06-04
BE904865A (fr)	1986-12-03
US4746678A (en)	1988-05-24
GB2176186B (en)	1989-07-05
PL147246B1 (en)	1989-05-31
HU196288B (en)	1988-11-28
ES555709A0 (es)	1987-08-16
BR8602608A (pt)	1987-02-03
HUT40551A (en)	1987-01-28
JPS6248661A (ja)	1987-03-03
FR2582647A1 (fr)	1986-12-05
DK262286D0 (da)	1986-06-04
NO862231L (no)	1986-12-05
ES8707711A1 (es)	1987-08-16
AU589637B2 (en)	1989-10-19
SU1450737A3 (ru)	1989-01-07
FI862382A0 (fi)	1986-06-04
CH667645A5 (de)	1988-10-31

Publication	Publication Date	Title
DE2804299C2 (sv)	1987-10-29
EP0165448B1 (de)	1991-10-16	1-Heteroaryl-4-aryl-pyrozolin-5-one
EP0006540B1 (de)	1981-10-07	N-Dichloracetyl-1,2,3,4-tetrahydro-chinaldin, Verfahren zu dessen Herstellung und dessen Verwendung zur Verhütung von Herbizidschäden an Kulturpflanzen sowie selektive herbizide Mittel auf Basis von N-Dichloracetyl-1,2,3,4-tetrahydro-chinaldin und herbizid wirksamen Acetaniliden oder Thiolcarbamaten
EP0013360B1 (de)	1982-04-07	N-substituierte Carbonsäureanilide, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Fungizide
EP0430033A2 (de)	1991-06-05	Mikrobizide Mittel
EP0130366B1 (de)	1991-01-30	Arylalkylimidazolium- und -triazoliumsalze, Verfahren zu ihrer Herstellung und ihre Verwendung als Mikrozide
DE2600799A1 (de)	1977-07-14	Acylierte triazolyl-0,n-acetale, verfahren zu ihrer herstellung und ihre verwendung als fungizide
DD248357A5 (de)	1987-08-05	Verfahren zur herstellung von 9,10-phenonthrendion-derivaten
CH623575A5 (sv)	1981-06-15
CH637386A5 (de)	1983-07-29	Benzoxazol- und benzothiazolderivate.
DE69017971T2 (de)	1995-07-20	Biozide Verbindungen.
DE2643403A1 (de)	1977-04-07	Mikrobizide mittel
CH635580A5 (de)	1983-04-15	Mikrobizide mittel.
DE2759121A1 (de)	1978-07-13	Fungizides mittel, verwendung von n-benzoylanthranilsaeureestern zur bekaempfung pflanzenpathogener pilze, n-benzoylanthranilsaeureester und verfahren zu ihrer herstellung
DE3003933A1 (de)	1981-08-13	(beta) -imidazolylalkohole, verfahren zu ihrer herstellung, diese enthaltende fungizide und verfahren zur bekaempfung von pilzen mit ihnen
DD157292A5 (de)	1982-11-03	Mittel zur behandlung von pilzinfektionen
EP0075172B1 (de)	1985-05-29	N-Sulfenylierte Benzylsulfonamide, ein Verfahren und ihre Verwendung als Mikrobizide
DE2604761A1 (de)	1977-08-11	Acylierte imidazolyl-o,n-acetale, verfahren zu ihrer herstellung und ihre verwendung als fungizide
EP0019858A2 (de)	1980-12-10	N-Oximinoalkyl-anilide, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Fungizide
EP0155574B1 (de)	1988-08-24	Pyridiniumsalze und diese enthaltende Fungizide und Bakterizide
EP0094566B1 (de)	1986-03-12	Dibenzofuranoxyalkyl-imidazoliumsalze, Verfahren zu ihrer Herstellung und ihre Verwendung als Mikrozide
DE3102907A1 (de)	1982-04-08	"benzoxazolonderivate, verfahren zur herstellung derselben sowie zubereitungen, die diese derivate enthalten"
EP0096280A2 (de)	1983-12-21	Alkylen(cycloalkylen)-bis-heterocyclyl-biguanide
EP0003975B1 (de)	1981-05-13	Dichlormaleinsäurediamid-Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide
EP0025019B1 (de)	1983-02-09	Sulfinyl- und Sulfonylacetanilide, Verfahren zu deren Herstellung und deren Verwendung als Mikrobizide

Legal Events

Date	Code	Title	Description
1994-11-24	ENJ	Ceased due to non-payment of renewal fee