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    • 3. 发明授权
    • Fungicidal mixtures
    • US06346535B1
    • 2002-02-12
    • US09240412
    • 1999-01-29
    • Henry Van Tuyl CotterGunther ReichertEwald SieverdingPetrus Martinus Franciscus Emanuel Jegerings
    • Henry Van Tuyl CotterGunther ReichertEwald SieverdingPetrus Martinus Franciscus Emanuel Jegerings
    • A01N4354
    • A01N35/04A01N59/20A01N59/02A01N55/00A01N47/44A01N47/38A01N47/14A01N47/04A01N43/90A01N43/84A01N43/82A01N43/76A01N43/653A01N43/60A01N43/56A01N43/54A01N43/40A01N43/42A01N43/36A01N43/32A01N43/30A01N37/50A01N37/46A01N37/38A01N37/34A01N37/06A01N2300/00
    • The invention relates to a novel fungicidal composition comprising synergistically effective amounts of at least one benzophenone of formula I wherein R1 represents a halogen atom, an optionally substituted alkyl, alkanoyloxy or alkoxy group; or a hydroxy group, R2 represents a halogen atom or an optionally substituted alkyl group, R3 independently represents a halogen atom, an optionally substituted alkyl or alkoxy group or a nitro group; m is 0 or an integer of 1 to 3; R4 represents a halogen atom, a cyano, carboxy, hydroxy or nitro group or an optionally substituted alkyl, alkoxy, alkenyl, alkylthio, alkylsulphinyl, alkylsulphonyl or amino group; R5 represents an optionally substituted alkyl group; R6 represents a halogen atom or a nitro group, an optionally substituted alkyl, alkoxy, alkenyloxy, alkynyloxy, alkylthio, cycloalkyl, cycloalkyloxy, aryloxy group; R7 independently represents a halogen atom, an optionally substituted alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkoxy group; n is 0 or 1; and at least one fungicidally active ingredient selected from the groups consisting of (A), (B), (C), (D) and (E) wherein: (A) is an ergosterol biosynthesis inhibitor; (B) is a strobilurine derivative, (C) is a melanin biosynthesis inhibitor; (D) is a compound selected from the group consisting of acibenzolar, benomyl, captan, carboxin, chlorothalonil, copper, cyprodinil, dinocap, dithianon, dimethomorph, dodine, ethirimol, famoxadone, fenpiclonil, fluazinam, mancozeb, metalaxyl, pyrifenox, sulfur, vinclozolin and (E) is an azolopyrimidine of formula II  iwherein R8 and R9 each independently represent hydrogen or an optionally substituted alkyl, alkenyl, alkynyl, alkadienyl, aryl, heteroaryl, cycloalkyl, bicycloalkyl or heterocyclyl group, or R8 and R9 together with the interjacent nitrogen atom represent an optionally substituted heterocyclic ring, R10 represents hydrogen or an alkyl or aryl group, R11 represents a hydrogen or halogen atom or an alkyl or alkoxy group, L independently represents a halogen atom or an optionally substituted alkyl or alkoxy group, p is 0 or an integer from 1 to 5; and A represents N or CR2, wherein R12 has the meaning given for R10; together with a fungicidally acceptable carrier and/or surface active agent, and to a method of controlling the growth of phytopathogenic fungi which comprises applying synergistically effective amounts of the composition to the locus.
    • 4. 发明授权
    • Fungicidal mixtures
    • 杀菌混合物
    • US06521628B1
    • 2003-02-18
    • US09492440
    • 2000-01-27
    • Henry Van Tuyl CotterGunter ReichertEwald SieverdingPetrus Martinus Franciscus Emanuel Jegerings
    • Henry Van Tuyl CotterGunter ReichertEwald SieverdingPetrus Martinus Franciscus Emanuel Jegerings
    • A01N3744
    • A01N35/04A01N2300/00
    • The invention relates to a novel fungicidal composition comprising a fungicidally acceptable carrier and/or surface active agent together with, and synergistically effective amounts of (a) at least one benzophenone of formula I wherein R1, R2, R3, R4, R5, R6, R7, m and n have the meaning given; at least one fungicidal active ingredient selected from the following groups (A), (B), (C), (D) and (E): (A) an ergosterol biosynthesis inhibitor; (B) a strobilurine derivative, (C) a melanin biosynthesis inhibitor; (D) a compound selected from the group consisting of acibenzolar, benomyl, captan, carboxin, chlorothalonil, copper, cyprodinil, dinocap, dithianon, dimethomorph, dodine, ethirimol, famoxadone, fenpiclonil, fluazinam, mancozeb, metalaxyl, pyrifenox, sulfur, vinclozolin and (E) an azolopyrimidine of formula II in which R8, R9, R10, R11, A, L and p have the meaning given; and to a method of controlling the growth of phytopathogenic fungi at a locus which comprises applying synergistically effective amounts of (a) at least one benzophenones of formula I and (b) at least one fungicidal active ingredient selected from the groups (A), (B), (C), (D) and (E) to the locus.
    • 本发明涉及一种新颖的杀真菌组合物,其包含杀真菌剂可接受的载体和/或表面活性剂以及协同有效量的(a)至少一种式I的二苯甲酮,其中R 1,R 2,R 3,R 4,R 5,R 6,R 7 ,m和n具有给定的含义; 至少一种选自以下组(A),(B),(C),(D)和(E):( A)麦角甾醇生物合成抑制剂的杀真菌活性成分;(B)嗜球果ur碱衍生物,(C) 黑色素生物合成抑制剂;(D)选自由以下物质组成的组的化合物:苯偶姻,苯菌灵,克拉曼,羧酸,百菌清,铜,嘧菌胺,二硝基,二噻吩,烯酰吗啉,十二烷,乙烯咪唑, ,硫,连环素和(E)式IIin的偶氮嘧啶,其中R8,R9,R10,R11,A,L和p具有给定的含义;以及一种控制植物病原真菌在一个位点生长的方法,其包括协同应用 有效量的(a)至少一种式I的二苯甲酮和(b)至少一种选自(A),(B),(C),(D)和(E)的杀真菌活性成分。
    • 7. 发明授权
    • Fungicidal mixtures
    • 杀菌混合物
    • US06699874B2
    • 2004-03-02
    • US10314594
    • 2002-12-10
    • Henry Van Tuyl CotterLeslie MayGunter ReichertEwald Sieverding
    • Henry Van Tuyl CotterLeslie MayGunter ReichertEwald Sieverding
    • A01N4354
    • A01N43/90A01N2300/00
    • Fungicidal compositions comprising an acceptable carrier and/or surface active agent and synergistically effective amounts of (a) at least one azolopyrimidine of formula I  in which R1, R2, L1, L2 and L3 have the meaning given in claim 1; and (b) at least one fungicidal active ingredient selected from benomyl, carboxin, captan, chlorothalonil, copper oxychloride, cyprodinil, dimethomorph, dithianon, dodine, famoxadone, fenhexamid, fenpiclonil, fenpropimorph, fluazinam, mancozeb, metalaxyl, pyrimethanil, quinoxifen, sulfur, triforine, vinclozolin, a fungicidal triazole derivative, and a synthetic strobilurine derivative. The invention also provides a method of controlling the growth of phytopathogenic fungi at a locus by applying synergistically effective amounts of at least one azolopyrimidine of formula I and at least one fungicidal active ingredient (b) to the locus.
    • 包含可接受的载体和/或表面活性剂和协同有效量的(a)至少一种R 1,R 2,L 1,L 2和L 3的式Iin的偶氮嘧啶的杀真菌组合物 >具有权利要求1中给出的含义; 和(b)至少一种杀真菌活性成分,其选自苯菌灵,呋喃丹,克拉曼,百菌清,氯氧化铜,西酞替尼,烯酰吗啉,二噻吩,十二烷,恶唑酮,芬己酰,芬替尼,芬卡芬,氟啶胺,代森锰锌,甲霜灵,嘧霉胺,喹喔啉, ,triperine,长春菌素,杀真菌三唑衍生物和合成次溴酸衍生物。 本发明还提供了一种通过将协同有效量的至少一种式I的偶氮嘧啶和至少一种杀真菌活性成分(b)施用于该基因座来控制植物病原真菌在一个场所生长的方法。
    • 10. 发明授权
    • Fungicidal mixtures
    • 杀菌混合物
    • US06656944B2
    • 2003-12-02
    • US09832964
    • 2001-04-11
    • Ewald SieverdingLeslie May
    • Ewald SieverdingLeslie May
    • A01N4354
    • A01N43/90A01N39/04A01N39/02A01N2300/00
    • The invention relates to fungicidal compositions comprising an acceptable carrier and/or surface active agent and synergistically effective amounts of (a) at least one azolopyrimidine of formula I  in which R1 through R2, L, A and n have the meaning given in claim 1; (b) and at least one melanin biosynthesis inhibitor (MBI), preferably a phenoxyamide of formula II  wherein R5 through R9, Y and m have the meaning given in claim 2; and to a method of controlling the growth of phythopathogenic fungi at a locus which comprises applying synergistically effective amounts of at least one azolopyrimidine of formula I (a) and at least one MBI (b) to the locus.
    • 本发明涉及包含可接受的载体和/或表面活性剂和协同有效量的(a)至少一种式Iin的至少一种氮杂嘧啶的杀真菌组合物,其中R 1至R 2,L,A和n具有其含义 在权利要求1中给出;(b)和至少一种黑色素生物合成抑制剂(MBI),优选式VII的苯氧基酰胺,其中R 5至R 9,Y和m具有权利要求2中给出的含义; 以及在一个场所控制植物病原真菌的生长的方法,其包括将协同有效量的至少一种式I(a)的偶氮嘧啶和至少一种MBI(b)施用于该基因座。