식물 병원균인 피시움 미리오틸륨 균주 및 이를 이용한 잡초의 생물학적 방제 방법
    1.
    发明授权
    식물 병원균인 피시움 미리오틸륨 균주 및 이를 이용한 잡초의 생물학적 방제 방법 失效
    식물병원균인피시움미리오틸륨균주및이를이용한잡초의생물학적방제방

    公开(公告)号:KR100457069B1

    公开(公告)日:2004-11-10

    申请号:KR1020010054440

    申请日:2001-09-05

    Abstract: PURPOSE: Provided are a novel Pythium myriotylum strain, a pathogen of plants, and a method for the biological control of weeds using same, thereby effectively and selectively removing weeds from a rice field. CONSTITUTION: The novel strain, Pythium myriotylum MD2(KCTC 10034BP) is used for selectively controlling weeds selected from American black cherry, Monochoria vaginalis, yellow birtch, Chondostereum purpureum, Northern joint vetch, Colletotrichum gloeosporioides f. sp. aeschynomene, Morrenia odorata, Phyrophthora palmivora, Poa annua, Pseudomonas gladioli, etc.

    Abstract translation: 用途:提供了一种新型的Pythium myriotylum菌株,植物病原体,以及使用它的生物防治杂草的方法,由此有效地选择性地从稻田中除去杂草。 组成:新菌株Pythium myriotylum MD2(KCTC 10034BP)用于选择性控制选自美国黑樱桃,Monochoria vaginalis,黄色birtch,Chondostereum purpureum,Northern joint vetch,Colletotrichum gloeosporioides f。 SP。 aeschynomene,Morrenia odorata,Phyrophthora palmivora,Poa annua,唐菖蒲假单胞菌等

    케토미움 글로보숨 F0142 및 이에 의해 생산된 케토비리딘 A 및 B를 이용한 식물병의 생물학적 방제 방법
    2.
    发明公开
    케토미움 글로보숨 F0142 및 이에 의해 생산된 케토비리딘 A 및 B를 이용한 식물병의 생물학적 방제 방법 失效
    使用全氟辛酸F0142和其生产的乙酰胆碱酯酶A和B的植物病害生物控制方法

    公开(公告)号:KR1020030050072A

    公开(公告)日:2003-06-25

    申请号:KR1020010080458

    申请日:2001-12-18

    Abstract: PURPOSE: A method for biological control of plant diseases using Chaetomium globosum F0142 and chaetoviridins A and B produced by the same is provided, thereby effectively controlling plant diseases. CONSTITUTION: A method for biological control of plant diseases using Chaetomium globosum F0142(KCTC 0957BP) and chaetoviridins A and B produced by the same comprises spraying the cultured medium, mycelia or spores of Chaetomium globosum F0142, or chaetoviridins A and B isolated from the Chaetomium globosum cultured medium to plants, wherein the plant disease is rice blast disease, late blight, leaf rust or phytophthora blight. The chaetoviridins A and B are represented by the formula(1) and (2) respectively, and purified by extraction of Chaetomium globosum F0142(KCTC 0957BP) with ethyl acetate, first silica gel column chromatography, thin layer chromatography and second silica gel column chromatography, sequentially.

    Abstract translation: 目的:提供使用球毛壳菌F0142和由其生产的凝血酶原A和B的植物病害生物防治方法,从而有效控制植物病害。 构成:使用球毛壳菌F0142(KCTC 0957BP)和由其产生的切杆菌素A和B的植物病害的生物防治方法包括喷洒球形梭菌F0142的培养培养基,菌丝体或孢子,或从毛壳菌分离的凝血因子A和B 球藻培养基至植物,其中植物病是稻瘟病,晚疫病,叶锈病或疫病疫苗。 川to嗪A和B分别由式(1)和(2)表示,并用乙酸乙酯萃取球毛壳菌F0142(KCTC 0957BP),首先用硅胶柱层析,薄层色谱和第二次硅胶柱色谱法提纯 ,顺序。

    4H, 6H-푸로[3,4-c]이소옥사졸 유도체와 그 제조방법
    3.
    发明授权
    4H, 6H-푸로[3,4-c]이소옥사졸 유도체와 그 제조방법 失效
    4H,OH-FURO [3,4-C]异噻唑衍生物及其制备方法

    公开(公告)号:KR1019950005734B1

    公开(公告)日:1995-05-29

    申请号:KR1019920009552

    申请日:1992-06-02

    Abstract: The preparation method of isooxazol (I) dervatives which has antifungal activity consists of 1) reacting nitro-olefin and alcohol with basic catalyst to form nitro compounds, 2) dehydrating nitro compounds with triethylamine and phenylisocyanate to form cycles as (I) in benzene or dichlromethane. Derivatives of (I) are R1 = propyl or isopropyl, R2 = H or methyl, R3 = H, methyl, ethyl, phenyl, phenyl chloride, aldehyde, or oxime.

    Abstract translation: 具有抗真菌活性的异恶唑(I)衍生物的制备方法包括:1)使硝基烯烃和醇与碱性催化剂反应生成硝基化合物,2)用三乙胺和异氰酸苯酯脱水硝基化合物,形成(I)在苯或 dichlromethane。 (I)的衍生物是R1 =丙基或异丙​​基,R2 = H或甲基,R3 = H,甲基,乙基,苯基,苯基氯,醛或肟。

    4-아졸일-2-퀴놀리논 유도체 및 이를 포함하는 살균제조성물
    5.
    发明授权
    4-아졸일-2-퀴놀리논 유도체 및 이를 포함하는 살균제조성물 失效
    4-아졸일-2-퀴놀리논유도체및이를포함하는살균제조성물

    公开(公告)号:KR100417705B1

    公开(公告)日:2004-02-11

    申请号:KR1020010044459

    申请日:2001-07-24

    Abstract: PURPOSE: An agricultural or horticultural fungicide composition containing a 4-azoyl-2-quinolinone derivative is provided which exhibits a preventive effect and treating effect against various fungi, in particular, excellent selective bactericidal activity against any plant pathogenic bacteria. CONSTITUTION: The titled composition contains a 4-azoyl-2-quinolinone derivative of formula(1) as an active component. In formula, X is O or S, Y is CH or N, R1 is C1-5 alkyl, R2, R3, R4 and R5 are the same or different, each differently H, H, C1-3 alkyl, C1-3 alkoxy, phenyl or NO2.

    Abstract translation: 目的:提供一种含有4-偶氮基-2-喹啉酮衍生物的农业或园艺杀菌剂组合物,它对各种真菌具有预防效果和治疗效果,特别是对任何植物病原菌具有优异的选择性杀菌活性。 组成:标题组合物含有式(1)的4​​-苯甲酰基-2-喹啉酮衍生物作为活性组分。 式中,X为O或S,Y为CH或N,R 1为C 1-5烷基,R 2,R 3,R 4和R 5相同或不同,各自不同为H,H,C 1-3烷基,C 1-3烷氧基 ,苯基或NO 2。

    신규의 4-아졸일 퀴놀린 유도체 및 이를 포함하는 조성물
    6.
    发明授权
    신규의 4-아졸일 퀴놀린 유도체 및 이를 포함하는 조성물 失效
    新型4-氨基喹啉衍生物及其组合物

    公开(公告)号:KR100266964B1

    公开(公告)日:2000-09-15

    申请号:KR1019980024301

    申请日:1998-06-26

    Abstract: 본 발명은 우수한 살균력을 가지는 하기 일반식 (I)로 표시되는 신규의 4-아졸일 퀴놀린 유도체 및 이를 포함하는 살균제 조성물에 관한 것이다.
    (I)
    상기식에서,
    W는 CH 또는 질소 원자이고,
    R
    1 , R
    2 , R
    3 및 R
    4 는 같거나 서로 다르며, 각각 독립적으로 수소 원자, 할로겐 원자, C
    1 -C
    5 알킬, C
    1 -C
    3 알콕시, C
    1 -C
    3 할로알킬, C
    1 -C
    4 알킬티오, 페닐, CN 또는 NO
    2 이고,
    R
    5 는 C
    1 -C
    4 알콕시, C
    1 -C
    4 알킬티오, C
    1 -C
    4 알킬설피닐, C
    1 -C
    4 알킬설포닐, 알릴옥시, 프로파길옥시, 염소원자이다.

    신규의 4-아졸일 퀴놀린 유도체 및 이를 포함하는 조성물
    7.
    发明公开
    신규의 4-아졸일 퀴놀린 유도체 및 이를 포함하는 조성물 失效
    新型4-氨基喹啉衍生物及其组合物

    公开(公告)号:KR1020000003147A

    公开(公告)日:2000-01-15

    申请号:KR1019980024301

    申请日:1998-06-26

    Abstract: PURPOSE: Novel 4-azolyl quinoline derivatives are prepared. The composition containing these derivatives exhibits a bactericidal effect on vegetable pathogen. CONSTITUTION: The derivatives of the formula (I), wherein: W is CH or N; R1, R2, R3 and R4 are the same or not, H, halogen, C1-C5 alkyl, C1-C3 alkoxy; C1-C3 haloalkyl, C1-C4 alkylthio, phenyl, CN, or NO2; R5 is C1-C4 alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, allyloxy, propargyloxy, chloro) such as 3-aryl-4-(1,2,4-triazol-1-yl)-quinoline and 3-aryl-4-(1,3-imidazol-1-yl) quinoline are prepared. Thus, 2,4-dichloro-3-(2,4-dichlorophenyl)-6-fluoro-quinoline of 1.08g, potassium carbonate of 0.77g, and triazole of 0.8g are stirred in dimethylformamide for 5 hours at 80°C to give 2-chloro-3-(2,4-dichloro phenyl)-6-fluoro-4-(1,2,4-triazol-1-yl) quinoline of 0.73g.

    Abstract translation: 目的:制备新型4-唑基喹啉衍生物。 含有这些衍生物的组合物对植物病原体表现出杀菌作用。 构成:式(I)的衍生物,其中:W是CH或N; R 1,R 2,R 3和R 4相同或不同,为H,卤素,C 1 -C 5烷基,C 1 -C 3烷氧基; C 1 -C 3卤代烷基,C 1 -C 4烷硫基,苯基,CN或NO 2; R5是C1-C4烷氧基,烷硫基,烷基亚磺酰基,烷基磺酰基,烯丙氧基,炔丙氧基,氯),例如3-芳基-4-(1,2,4-三唑-1-基) - 喹啉和3-芳基-4- 1,3-咪唑-1-基)喹啉。 因此,将1.08g的2,4-二氯-3-(2,4-二氯苯基)-6-氟 - 喹啉,0.77g的碳酸钾和0.8g的三唑在80℃下在二甲基甲酰胺中搅拌5小时至 得到0.73g的2-氯-3-(2,4-二氯苯基)-6-氟-4-(1,2,4-三唑-1-基)喹啉。

    옥심기를 측쇄로 하는 신규의 프로페노익 에스테르 및아미드 유도체, 이의 제조방법 그리고 이를 함유하는살균제 조성물
    10.
    发明授权
    옥심기를 측쇄로 하는 신규의 프로페노익 에스테르 및아미드 유도체, 이의 제조방법 그리고 이를 함유하는살균제 조성물 失效
    옥심기를측쇄로하는신규의프로페노익스르르르및미미,,살균살균살균

    公开(公告)号:KR100379761B1

    公开(公告)日:2003-04-11

    申请号:KR1020000070103

    申请日:2000-11-23

    Abstract: PURPOSE: Provided are novel propanoic ester and amide derivatives having an oxime group as a branched chain, which are excellent in disinfecting activity, a preparation thereof, and a disinfectant composition containing the propanoic ester and amide derivatives. CONSTITUTION: The propaonic ester and amide derivatives represented by the formula 1 are produced by a process comprising the steps of: reacting a bromine compound represented by the formula 2 and 2,3-butanedione monoxime represented by the formula 3 in the presence of a base to produce an oxime-based ketone compound; reducing the oxime-based ketone compound or condensing the oxime-based ketone compound with a hydroxyl amine to produce an oxime-based alcohol compound or a dioxime-based compound; reacting the oxime-based alcohol compound or the dioxime-based compound with a propanyl fluoride compound in the presence of a base. In the formula, R1 is trifluoromethyl, R2 is a phenyl group, X is CH or N, and Y is O or NH.

    Abstract translation: 目的:提供具有肟基作为支链的新型丙酸酯和酰胺衍生物,其消毒活性极好,其制备和含有丙酸酯和酰胺衍生物的消毒剂组合物。 构成:由式1代表的丙酸酯和酰胺衍生物通过包括以下步骤的方法制备:使式2代表的溴化合物和式3代表的2,3-丁二酮单肟在碱存在下反应 制造肟类酮化合物; 还原所述肟类酮化合物或使所述肟类酮化合物与羟基胺缩合以制备肟类醇类化合物或二肟类化合物; 使肟基醇化合物或二肟基化合物与丙基氟化物在碱存在下反应。 在该式中,R1是三氟甲基,R2是苯基,X是CH或N,并且Y是O或NH。

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