NO841017L - Fungicide triazolderivater - Google Patents

Fungicide triazolderivater

Info

Publication number: NO841017L
Authority: NO; Norway
Prior art keywords: compound; formula; salt; triazol; chlorophenyl
Prior art date: 1983-03-16

Application number

NO841017A

Other languages

English (en)

Norwegian (no)

Inventor

Kenneth Richardson

Subramaniyan Narayanaswami

Original Assignee

Pfizer

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.)

1983-03-16

Filing date

1984-03-15

Publication date

1984-09-17

1983-03-16 Priority claimed from GB838307232A external-priority patent/GB8307232D0/en

1983-05-07 Priority claimed from GB838312623A external-priority patent/GB8312623D0/en

1983-11-25 Priority claimed from GB838331475A external-priority patent/GB8331475D0/en

1984-03-15 Application filed by Pfizer filed Critical Pfizer

1984-09-17 Publication of NO841017L publication Critical patent/NO841017L/no

Links

230000000855 fungicidal effect Effects 0.000 title claims description 8
239000000417 fungicide Substances 0.000 title description 4
150000001875 compounds Chemical class 0.000 claims description 66
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 35
150000003839 salts Chemical class 0.000 claims description 28
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 24
-1 5-chloropyrid-2-yl Chemical group 0.000 claims description 22
239000000203 mixture Substances 0.000 claims description 22
NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 claims description 17
238000002360 preparation method Methods 0.000 claims description 14
229910000027 potassium carbonate Inorganic materials 0.000 claims description 12
238000000034 method Methods 0.000 claims description 11
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
206010017533 Fungal infection Diseases 0.000 claims description 7
208000031888 Mycoses Diseases 0.000 claims description 7
229910052794 bromium Inorganic materials 0.000 claims description 6
229910052801 chlorine Inorganic materials 0.000 claims description 6
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 6
125000001424 substituent group Chemical group 0.000 claims description 6
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 5
125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims description 4
125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 4
239000003085 diluting agent Substances 0.000 claims description 4
229910052731 fluorine Inorganic materials 0.000 claims description 4
229910052740 iodine Inorganic materials 0.000 claims description 4
125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 claims description 3
238000003898 horticulture Methods 0.000 claims description 3
125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims description 2
125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 claims description 2
125000006306 4-iodophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1I 0.000 claims description 2
125000004199 4-trifluoromethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C(F)(F)F 0.000 claims description 2
230000008635 plant growth Effects 0.000 claims description 2
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 57
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BPLKQGGAXWRFOE-UHFFFAOYSA-M trimethylsulfoxonium iodide Chemical compound [I-].C[S+](C)(C)=O BPLKQGGAXWRFOE-UHFFFAOYSA-M 0.000 description 8
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UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 6
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239000007858 starting material Substances 0.000 description 6
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238000002474 experimental method Methods 0.000 description 3
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FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
206010065764 Mucosal infection Diseases 0.000 description 1
241001537205 Paracoccidioides Species 0.000 description 1
241001507673 Penicillium digitatum Species 0.000 description 1
241001674048 Phthiraptera Species 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
241000221535 Pucciniales Species 0.000 description 1
241000813090 Rhizoctonia solani Species 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 1
241001238303 Turdus fuscater Species 0.000 description 1
201000007096 Vulvovaginal Candidiasis Diseases 0.000 description 1
241000222126 [Candida] glabrata Species 0.000 description 1
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
239000008272 agar Substances 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
230000000843 anti-fungal effect Effects 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000008280 blood Substances 0.000 description 1
210000004369 blood Anatomy 0.000 description 1
239000012267 brine Substances 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000000969 carrier Substances 0.000 description 1
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 1
125000000068 chlorophenyl group Chemical group 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
238000004040 coloring Methods 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
239000013078 crystal Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
DKWOHBPRFZIUQL-UHFFFAOYSA-N dimethyl-methylidene-oxo-$l^{6}-sulfane Chemical compound C[S+](C)([CH2-])=O DKWOHBPRFZIUQL-UHFFFAOYSA-N 0.000 description 1
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
239000003814 drug Substances 0.000 description 1
239000003937 drug carrier Substances 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
239000012259 ether extract Substances 0.000 description 1
238000000605 extraction Methods 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000012458 free base Substances 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
244000000004 fungal plant pathogen Species 0.000 description 1
239000000499 gel Substances 0.000 description 1
239000008103 glucose Substances 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
229910000042 hydrogen bromide Inorganic materials 0.000 description 1
238000012623 in vivo measurement Methods 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000000749 insecticidal effect Effects 0.000 description 1
238000007912 intraperitoneal administration Methods 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
238000002955 isolation Methods 0.000 description 1
239000008101 lactose Substances 0.000 description 1
231100000225 lethality Toxicity 0.000 description 1
229940057995 liquid paraffin Drugs 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000004949 mass spectrometry Methods 0.000 description 1
MXLMTQWGSQIYOW-UHFFFAOYSA-N methyl isopropyl carbinol Natural products CC(C)C(C)O MXLMTQWGSQIYOW-UHFFFAOYSA-N 0.000 description 1
238000004452 microanalysis Methods 0.000 description 1
239000008267 milk Substances 0.000 description 1
235000013336 milk Nutrition 0.000 description 1
210000004080 milk Anatomy 0.000 description 1
238000002156 mixing Methods 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
239000008194 pharmaceutical composition Substances 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
239000002689 soil Substances 0.000 description 1
241000894007 species Species 0.000 description 1
238000004611 spectroscopical analysis Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000000829 suppository Substances 0.000 description 1
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230000000699 topical effect Effects 0.000 description 1
210000003462 vein Anatomy 0.000 description 1
229940045860 white wax Drugs 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/36—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal
- C07C29/38—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal by reaction with aldehydes or ketones
- C07C29/40—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal by reaction with aldehydes or ketones with compounds containing carbon-to-metal bonds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Dentistry (AREA)
Zoology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Pest Control & Pesticides (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Plant Pathology (AREA)
Environmental Sciences (AREA)
Agronomy & Crop Science (AREA)
Plural Heterocyclic Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

NO841017A 1983-03-16 1984-03-15 Fungicide triazolderivater NO841017L (no)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
GB838307232A GB8307232D0 (en)	1983-03-16	1983-03-16	Antifungal agents
GB838312623A GB8312623D0 (en)	1983-05-07	1983-05-07	Antifungal agents
GB838331475A GB8331475D0 (en)	1983-11-25	1983-11-25	Triazole antifungal agents

Publications (1)

Publication Number	Publication Date
NO841017L true NO841017L (no)	1984-09-17

Family

ID=27262010

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO841017A NO841017L (no)	1983-03-16	1984-03-15	Fungicide triazolderivater

Country Status (18)

Country	Link
EP (1)	EP0122056B1 (de)
KR (1)	KR880002275B1 (de)
AU (1)	AU575557B2 (de)
DD (1)	DD224850A5 (de)
DE (1)	DE3463269D1 (de)
DK (1)	DK159205C (de)
ES (1)	ES530587A0 (de)
FI (1)	FI78693C (de)
GR (1)	GR81884B (de)
HU (1)	HU194838B (de)
IE (1)	IE57100B1 (de)
IL (1)	IL71247A0 (de)
NO (1)	NO841017L (de)
NZ (1)	NZ207509A (de)
PH (1)	PH21437A (de)
PL (1)	PL143223B1 (de)
PT (1)	PT78243B (de)
YU (1)	YU45684A (de)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB8306351D0 (en) *	1983-03-08	1983-04-13	Ici Plc	Azole fungicides
DE3325313A1 (de) *	1983-07-13	1985-01-31	Bayer Ag, 5090 Leverkusen	Fungizide mittel, deren herstellung und verwendung
IE58738B1 (en) *	1984-09-05	1993-11-03	Ici Plc	Antifungal azole compounds
DE3440117A1 (de) *	1984-11-02	1986-05-15	Bayer Ag, 5090 Leverkusen	Substituierte azolylcyclopropyl-azolylmethyl-carbinol-derivate
JPS62201872A (ja) *	1986-02-28	1987-09-05	Shionogi & Co Ltd	アゾリルプロパノ−ル誘導体および抗真菌剤
DE3606947A1 (de) *	1986-03-04	1987-09-10	Basf Ag	Verfahren zur herstellung von phenoxyalkanoltriazolverbindungen und zwischenprodukte hierfuer
GB8716651D0 (en) *	1987-07-15	1987-08-19	Ici Plc	2-propanol derivatives
GB8819308D0 (en) *	1988-08-13	1988-09-14	Pfizer Ltd	Triazole antifungal agents
EP0548553A1 (de) *	1991-11-25	1993-06-30	Takeda Chemical Industries, Ltd.	Optisch aktive Azolverbindungen, ihre Herstellung und Anwendung
TW218017B (de) *	1992-04-28	1993-12-21	Takeda Pharm Industry Co Ltd
TW297813B (de) *	1993-09-24	1997-02-11	Takeda Pharm Industry Co Ltd
NZ270418A (en) *	1994-02-07	1997-09-22	Eisai Co Ltd	Polycyclic triazole & imidazole derivatives, antifungal compositions
TW318841B (de)	1995-02-17	1997-11-01	Takeda Pharm Industry Co Ltd

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB2078719B (en) *	1980-06-02	1984-04-26	Ici Ltd	Heterocyclic compounds
EP0069442B1 (de) *	1981-06-06	1985-02-20	Pfizer Limited	Fungizide Mittel, Verfahren zu deren Herstellung, und diese enthaltende pharmazeutische Zusammenstellungen
US4510148A (en) *	1982-06-12	1985-04-09	Pfizer Inc.	2-Heterocyclic-1,3-bis(1H-1,2,4-triazol-1-yl)-propan-2-ols as antifungal agents
DE3307218A1 (de) *	1983-03-02	1984-09-06	Bayer Ag, 5090 Leverkusen	Substituierte diazolylalkyl-carbinole, verfahren zu ihrer herstellung und ihre verwendung als antimykotische mittel
GB8306351D0 (en) *	1983-03-08	1983-04-13	Ici Plc	Azole fungicides
DE3325313A1 (de) *	1983-07-13	1985-01-31	Bayer Ag, 5090 Leverkusen	Fungizide mittel, deren herstellung und verwendung

1984
- 1984-02-29 DK DK135084A patent/DK159205C/da not_active IP Right Cessation
- 1984-03-13 EP EP84301670A patent/EP0122056B1/de not_active Expired
- 1984-03-13 PT PT78243A patent/PT78243B/pt active IP Right Revival
- 1984-03-13 DE DE8484301670T patent/DE3463269D1/de not_active Expired
- 1984-03-14 ES ES530587A patent/ES530587A0/es active Granted
- 1984-03-14 YU YU00456/84A patent/YU45684A/xx unknown
- 1984-03-14 PL PL1984246664A patent/PL143223B1/pl unknown
- 1984-03-14 PH PH30391A patent/PH21437A/en unknown
- 1984-03-15 NZ NZ207509A patent/NZ207509A/en unknown
- 1984-03-15 GR GR74120A patent/GR81884B/el unknown
- 1984-03-15 AU AU25636/84A patent/AU575557B2/en not_active Expired - Fee Related
- 1984-03-15 DD DD84260944A patent/DD224850A5/de unknown
- 1984-03-15 IE IE652/84A patent/IE57100B1/en not_active IP Right Cessation
- 1984-03-15 NO NO841017A patent/NO841017L/no unknown
- 1984-03-15 IL IL71247A patent/IL71247A0/xx unknown
- 1984-03-15 FI FI841056A patent/FI78693C/fi not_active IP Right Cessation
- 1984-03-15 HU HU841027A patent/HU194838B/hu unknown
- 1984-03-16 KR KR1019840001330A patent/KR880002275B1/ko active IP Right Grant

Also Published As

Publication number	Publication date
YU45684A (en)	1986-06-30
PL143223B1 (en)	1988-01-30
EP0122056B1 (de)	1987-04-22
PH21437A (en)	1987-10-20
PL246664A1 (en)	1985-07-16
PT78243B (en)	1986-08-12
ES8603243A1 (es)	1985-12-16
AU575557B2 (en)	1988-08-04
FI78693C (fi)	1989-09-11
NZ207509A (en)	1986-07-11
FI841056A0 (fi)	1984-03-15
DK159205B (da)	1990-09-17
IL71247A0 (en)	1984-06-29
DK135084D0 (da)	1984-02-29
DE3463269D1 (en)	1987-05-27
PT78243A (en)	1984-04-01
DK159205C (da)	1991-03-04
DK135084A (da)	1984-09-17
FI78693B (fi)	1989-05-31
GR81884B (de)	1984-12-12
AU2563684A (en)	1984-09-20
IE57100B1 (en)	1992-04-22
KR840008017A (ko)	1984-12-12
DD224850A5 (de)	1985-07-17
HU194838B (en)	1988-03-28
FI841056A (fi)	1984-09-17
KR880002275B1 (ko)	1988-10-21
ES530587A0 (es)	1985-12-16
IE840652L (en)	1984-09-16
EP0122056A1 (de)	1984-10-17

Publication	Publication Date	Title
US4616027A (en)	1986-10-07	Antifungal 1-aryl-1-fluoroalkyl-2-(1H-1,2,4-triazol-1-yl)ethanols
NO832083L (no)	1983-12-12	Triazol-antisoppmidler
NO841017L (no)	1984-09-17	Fungicide triazolderivater
US4960782A (en)	1990-10-02	Triazole antifungal agents
CA1287059C (en)	1991-07-30	Bis-triazole derivatives having antifungal activity
US4767777A (en)	1988-08-30	Triazole antifungal agents
EP0195557B1 (de)	1988-10-05	Antifungale Triazole
EP0115416B1 (de)	1988-06-29	Fungizide Triazole
EP0100193B1 (de)	1986-01-02	Antifungi Triazolverbindungen
US4992454A (en)	1991-02-12	Antifungal 1,3-bis (1H-1,2,4-triazol-1-yl)-2-aryl butan-2-ols and derivatives thereof
EP0110570A2 (de)	1984-06-13	Antifungische Triazole
EP0101212B1 (de)	1987-01-28	Antifungische Triazole
EP0113509A2 (de)	1984-07-18	1,3-Bis(triazolyl)-2-Amino-2-Aryl-Propan-Derivate, diese enthaltende pharmazeutische fungizide Zusammenstellungen
NO843198L (no)	1985-02-11	Fungicide triazolderivater