CN1038276A - 制备取代的苯基烷基甲酰胺的方法 - Google Patents

制备取代的苯基烷基甲酰胺的方法 Download PDF

Info

Publication number: CN1038276A
Authority: CN; China
Prior art keywords: compound; medicament; antifungal; general formula; formamido
Prior art date: 1988-05-18
Legal status (The legal status 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 status listed.): Pending

Application number

CN 89104607

Other languages

English (en)

Chinese (zh)

Inventor

米哈尔·米·鲍彼

瑟吉·米·维里西维奇

维拉·亚·埃里米纳

亚力山大·弗·波罗夫

塔特耶纳·伊·奥洛娃

法来里·帕·塔什

米里·格·普西金

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Vsesojuzny Nauchno-Issledovatelsky Institut Khimicheskikh Sredstv Zaschity Raste

Original Assignee

Vsesojuzny Nauchno-Issledovatelsky Institut Khimicheskikh Sredstv Zaschity Raste

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.)

1988-05-18

Filing date

1989-05-18

Publication date

1989-12-27

1988-05-18 Priority claimed from SU884443133A external-priority patent/RU1775394C/ru

1988-05-18 Priority claimed from SU884427664A external-priority patent/RU1775395C/ru

1989-05-18 Application filed by Vsesojuzny Nauchno-Issledovatelsky Institut Khimicheskikh Sredstv Zaschity Raste filed Critical Vsesojuzny Nauchno-Issledovatelsky Institut Khimicheskikh Sredstv Zaschity Raste

1989-12-27 Publication of CN1038276A publication Critical patent/CN1038276A/zh

Status Pending legal-status Critical Current

Links

UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 title claims abstract description 24
238000000034 method Methods 0.000 title claims abstract description 17
GKQIBHHDCVGBSA-UHFFFAOYSA-N C[NH3+].[NH-]C=O Chemical compound C[NH3+].[NH-]C=O GKQIBHHDCVGBSA-UHFFFAOYSA-N 0.000 title claims abstract description 8
125000000217 alkyl group Chemical group 0.000 title claims abstract description 8
238000002360 preparation method Methods 0.000 title claims abstract description 7
150000001875 compounds Chemical class 0.000 claims abstract description 30
-1 phenylalkyl ketone Chemical class 0.000 claims abstract description 10
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims abstract description 6
230000000843 anti-fungal effect Effects 0.000 abstract description 29
239000003814 drug Substances 0.000 abstract description 28
229940121375 antifungal agent Drugs 0.000 abstract description 15
239000013543 active substance Substances 0.000 abstract description 9
201000010099 disease Diseases 0.000 abstract description 7
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract description 7
235000013339 cereals Nutrition 0.000 abstract description 2
238000012360 testing method Methods 0.000 description 20
239000000463 material Substances 0.000 description 11
241000196324 Embryophyta Species 0.000 description 8
230000002902 bimodal effect Effects 0.000 description 8
230000000694 effects Effects 0.000 description 7
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
208000027418 Wounds and injury Diseases 0.000 description 6
230000006378 damage Effects 0.000 description 6
241000209140 Triticum Species 0.000 description 5
235000021307 Triticum Nutrition 0.000 description 5
239000000047 product Substances 0.000 description 5
240000005979 Hordeum vulgare Species 0.000 description 4
235000007340 Hordeum vulgare Nutrition 0.000 description 4
208000014674 injury Diseases 0.000 description 4
239000008177 pharmaceutical agent Substances 0.000 description 4
238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 4
229920001817 Agar Polymers 0.000 description 3
235000007199 Panicum miliaceum Nutrition 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
239000008272 agar Substances 0.000 description 3
244000022185 broomcorn panic Species 0.000 description 3
230000000855 fungicidal effect Effects 0.000 description 3
238000003306 harvesting Methods 0.000 description 3
239000000203 mixture Substances 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
238000001556 precipitation Methods 0.000 description 3
238000004659 sterilization and disinfection Methods 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
241000228245 Aspergillus niger Species 0.000 description 2
241000190150 Bipolaris sorokiniana Species 0.000 description 2
241000123650 Botrytis cinerea Species 0.000 description 2
241000235395 Mucor Species 0.000 description 2
206010052428 Wound Diseases 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000005660 chlorination reaction Methods 0.000 description 2
238000001816 cooling Methods 0.000 description 2
239000000645 desinfectant Substances 0.000 description 2
238000001914 filtration Methods 0.000 description 2
125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
230000035784 germination Effects 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
239000012074 organic phase Substances 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
230000001717 pathogenic effect Effects 0.000 description 2
239000000843 powder Substances 0.000 description 2
238000000926 separation method Methods 0.000 description 2
239000000243 solution Substances 0.000 description 2
239000003643 water by type Substances 0.000 description 2
238000009736 wetting Methods 0.000 description 2
ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical compound CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 1
ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
241000371644 Curvularia ravenelii Species 0.000 description 1
241000233866 Fungi Species 0.000 description 1
241000223218 Fusarium Species 0.000 description 1
241000223195 Fusarium graminearum Species 0.000 description 1
241000223221 Fusarium oxysporum Species 0.000 description 1
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 1
241001459558 Monographella nivalis Species 0.000 description 1
241001558145 Mucor sp. Species 0.000 description 1
241000736122 Parastagonospora nodorum Species 0.000 description 1
241000228168 Penicillium sp. Species 0.000 description 1
241000520648 Pyrenophora teres Species 0.000 description 1
241000221696 Sclerotinia sclerotiorum Species 0.000 description 1
241001533598 Septoria Species 0.000 description 1
RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical group O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 1
SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
229910052796 boron Inorganic materials 0.000 description 1
238000004364 calculation method Methods 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000013078 crystal Substances 0.000 description 1
239000002178 crystalline material Substances 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
230000006735 deficit Effects 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
239000012467 final product Substances 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
238000011081 inoculation Methods 0.000 description 1
239000007788 liquid Substances 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
239000006916 nutrient agar Substances 0.000 description 1
230000007170 pathology Effects 0.000 description 1
230000008654 plant damage Effects 0.000 description 1
238000012545 processing Methods 0.000 description 1
239000002994 raw material Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
230000002829 reductive effect Effects 0.000 description 1
238000011160 research Methods 0.000 description 1
238000005096 rolling process Methods 0.000 description 1
238000013077 scoring method Methods 0.000 description 1
230000007226 seed germination Effects 0.000 description 1
230000035939 shock Effects 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000002689 soil Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
230000001954 sterilising effect Effects 0.000 description 1
238000003756 stirring Methods 0.000 description 1
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000004809 thin layer chromatography Methods 0.000 description 1
230000009466 transformation Effects 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/12—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by halogen atoms or by nitro or nitroso groups
- C07C233/13—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by halogen atoms or by nitro or nitroso groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- 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
- A01N37/18—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 —CO—N<, e.g. carboxylic acid amides or imides; 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/16—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
- C07C233/17—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/18—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton

Landscapes

Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Environmental Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

CN 89104607 1988-05-18 1989-05-18 制备取代的苯基烷基甲酰胺的方法 Pending CN1038276A (zh)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
SU884443133A RU1775394C (ru)	1988-05-18	1988-05-18	1-(4-Хлор-или 2,4-дихлорфенил)-3-формамидо-4,4-диметилпентены-1, обладающие фунгицидной активностью
SU4427664		1988-05-18
SU884427664A RU1775395C (ru)	1988-05-18	1988-05-18	1-(2,4-Дихлорфенокси)-2-формамидо-3,3-диметилбутан, обладающий фунгицидной активностью
SU4443133		1988-05-18

Publications (1)

Publication Number	Publication Date
CN1038276A true CN1038276A (zh)	1989-12-27

Family

ID=26666163

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CN 89104607 Pending CN1038276A (zh)	1988-05-18	1989-05-18	制备取代的苯基烷基甲酰胺的方法

Country Status (11)

Country	Link
JP (1)	JPH02504281A (fr)
CN (1)	CN1038276A (fr)
AU (1)	AU3362489A (fr)
CH (1)	CH676597A5 (fr)
FR (1)	FR2631624A1 (fr)
GB (1)	GB2229437A (fr)
HU (1)	HUT49982A (fr)
NL (1)	NL8920256A (fr)
PL (1)	PL153872B1 (fr)
RO (1)	RO103770B1 (fr)
WO (1)	WO1989011472A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN110407681A (zh) *	2019-08-12	2019-11-05	海南大学	一种脱氢姜酮衍生物、其制备方法及应用

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2011790A (en) *	1934-03-13	1935-08-20	Gordon A Alles	1-(paramethoxyphenyl)-2-formylaminopropanes and method of preparing same
US2368073A (en) *	1943-04-12	1945-01-23	Commercial Solvents Corp	Process for preparing hydroxy amides
AT296242B (de) *	1969-07-21	1972-02-10	Boehringer Sohn Ingelheim	Verfahren zur Herstellung von neuen Formamidderivaten
US3835184A (en) *	1970-07-15	1974-09-10	Boehringer Sohn Ingelheim	Formamide derivatives
JPS4915768B1 (fr) *	1970-09-04	1974-04-17
US4147791A (en) *	1972-01-11	1979-04-03	Bayer Aktiengesellschaft	1-Substituted-1,2,4-triazole fungicidal compositions and methods for combatting fungi that infect or attack plants
US4160838A (en) *	1977-06-02	1979-07-10	Janssen Pharmaceutica N.V.	Antimicrobial and plant-growth-regulating triazole derivatives
DE2939350A1 (de) *	1979-09-28	1981-04-30	Basf Ag, 6700 Ludwigshafen	Glykoletheranilide, verfahren zu ihrer herstellung und diese enthaltende fungizide
DE3236522A1 (de) *	1982-05-18	1983-11-24	Bayer Ag, 5090 Leverkusen	Halogenpropargylformamide

1989
- 1989-02-17 NL NL8920256A patent/NL8920256A/nl not_active Application Discontinuation
- 1989-02-17 WO PCT/SU1989/000044 patent/WO1989011472A1/fr not_active Ceased
- 1989-02-17 AU AU33624/89A patent/AU3362489A/en not_active Abandoned
- 1989-02-17 JP JP1503855A patent/JPH02504281A/ja active Pending
- 1989-02-17 CH CH28090A patent/CH676597A5/de not_active IP Right Cessation
- 1989-05-17 HU HU245789A patent/HUT49982A/hu unknown
- 1989-05-17 PL PL27949089A patent/PL153872B1/pl unknown
- 1989-05-18 FR FR8906515A patent/FR2631624A1/fr not_active Withdrawn
- 1989-05-18 CN CN 89104607 patent/CN1038276A/zh active Pending
- 1989-05-18 RO RO13980489A patent/RO103770B1/ro unknown
1990
- 1990-01-17 GB GB9001044A patent/GB2229437A/en not_active Withdrawn

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN110407681A (zh) *	2019-08-12	2019-11-05	海南大学	一种脱氢姜酮衍生物、其制备方法及应用

Also Published As

Publication number	Publication date
WO1989011472A1 (fr)	1989-11-30
PL153872B1 (en)	1991-06-28
HUT49982A (en)	1989-12-28
FR2631624A1 (fr)	1989-11-24
GB9001044D0 (en)	1990-07-11
AU3362489A (en)	1989-12-12
CH676597A5 (fr)	1991-02-15
NL8920256A (nl)	1990-04-02
JPH02504281A (ja)	1990-12-06
RO103770B1 (en)	1993-04-15
PL279490A1 (en)	1990-01-08
GB2229437A (en)	1990-09-26

Legal Events

Date	Code	Title
1989-12-27	C06	Publication
1989-12-27	PB01	Publication
1992-02-26	C01	Deemed withdrawal of patent application (patent law 1993)
1992-02-26	WD01	Invention patent application deemed withdrawn after publication

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US8680337B2 (en)	2014-03-25	Process for the production of amides
CN1023224C (zh)	1993-12-22	制备1，5-二苯基-1h-1，2，4-三唑-3-甲酰胺衍生物的方法
CN1142746A (zh)	1997-02-12	保护植物免受真菌侵染的新方法
CN1810808A (zh)	2006-08-02	新型[1,2,3]噻二唑衍生物及其合成方法和用途
CN109535142A (zh)	2019-03-29	2-(1-吡唑基)嘧啶衍生物及其制备方法和应用
CN1057942A (zh)	1992-01-22	保护植物繁殖产品及由该产品获得植物的方法
CN1094890A (zh)	1994-11-16	土壤带有的真菌及其所致病害的预防、防治和改良的方法和组合物
CN1548425A (zh)	2004-11-24	取代的三唑甲酰胺
CN1281602C (zh)	2006-10-25	羧酸酯类除草剂
US4902337A (en)	1990-02-20	Herbicidal hydantoin derivatives
CN86102323A (zh)	1986-12-03	制备乙烯基环丙烷羧酸脂的方法
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CN118994175B (zh)	2025-09-16	3-螺环吲哚酮类衍生物及其制备方法和应用
CN87102978A (zh)	1988-10-05	1，5-二苯基-1h-1，2，4-三唑-3-甲酰胺衍生物及其除草的制剂
CN1491212A (zh)	2004-04-21	吡咯甲酰胺作为杀真菌剂的应用
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SK2082000A3 (en)	2001-02-12	4-cyano-4-deformylsordaricin derivatives, process for the preparation thereof and agricultural agent containing the same and use thereof
CN110386914A (zh)	2019-10-29	一种天然产物海杧果醛全合成方法及应用
JPH02504281A (ja)	1990-12-06	置換されたフェニルアルキルホルムアミド類及びそれらを基材とする殺カビ製剤
CN1760176A (zh)	2006-04-19	Z－2－氰基－3－(N－(S)－α－甲基对氟苄胺基)－2－戊烯酸乙氧乙酯合成及除草活性
CN86101647A (zh)	1986-11-26	S，s-二硫代叔丁基乙膦酸酯的制备及其作为农药的应用
CN1054593A (zh)	1991-09-18	新型烯丙基氨基乙基三唑的制备方法
KR930009820B1 (ko)	1993-10-11	2-퀴놀린온 유도체

CN1038276A - 制备取代的苯基烷基甲酰胺的方法 - Google Patents

Info

Links

Classifications

Landscapes

Applications Claiming Priority (4)

Publications (1)

Family

ID=26666163

Family Applications (1)

Country Status (11)

Cited By (1)

Family Cites Families (9)

Cited By (1)

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