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    Azolyl-derivatives endowed with antifungal activity
    4.
    发明授权
    Azolyl-derivatives endowed with antifungal activity 失效
    具有抗真菌活性的唑基衍生物

    公开(公告)号：US5036094A

    公开(公告)日：1991-07-30

    申请号：US408945

    申请日：1989-09-18

    申请人： Roberto Colle ,  Giovanni Camaggi ,  Franco Gozzo ,  Giuseppina Ratti ,  Luigi Mirenna ,  Carlo Garavaglia

    发明人： Roberto Colle ,  Giovanni Camaggi ,  Franco Gozzo ,  Giuseppina Ratti ,  Luigi Mirenna ,  Carlo Garavaglia

    IPC分类号： C07D317/00 ,  A01N43/50 ,  A01N43/653 ,  A01P3/00 ,  A61K20060101 ,  C07D20060101 ,  C07D249/08 ,  C07D317/22 ,  C07D405/06 ,  C07D409/06 ,  C07D521/00

    CPC分类号： C07D231/12 ,  A01N43/50 ,  A01N43/653 ,  C07D233/56 ,  C07D249/08 ,  C07D317/22

    摘要： Disclosed are compounds, having the general formula: ##STR1## wherein: m=0, 1, 2; n=0, 1 with the condition that when m=0, also n=0;p=0, 1; q=1, 2;X is either oxygen or sulphur;A=N, CH;R is H, CH.sub.3, F;R.sub.1 is selected from chlorine, bromine, fluorine, CF.sub.3, phe=nyl, C.sub.1 -C.sub.2 -alkoxy, C.sub.1 -C.sub.2 -haloalkoxy, alkylthio, haloalkyl=thio, wherein the halogen is Cl, Br, F;R.sub.2 is selected from H, chlorine, bromine, fluorine;R.sub.f is selected from the group formed by alkyls containing from 2 to 4 carbon atoms, and containing at least 4 atoms of halogen selected from F, Cl and Br, of which at least 3 are F atoms; alkenyls and alkynyls containing up to 4 carbon atoms, containing at least 2 F atoms and, optionally, other halogens selected between Cl and Br.The present invention relates to azolyl-derivatives, more particularly to substituted azolyldioxanes and azolyldioxolanes, endowed with high fungicidal activity, to the process for their preparation, and to their related use in the agrarian field.

    摘要翻译： 公开了具有以下通式的化合物：其中：m = 0,1,2; n = 0,1，条件是当m = 0时，n = 0; p = 0,1， q = 1,2; X是氧或硫; A = N，CH; R为H，CH 3，F; R 1选自氯，溴，氟，CF 3，phe = nyl，C 1 -C 2 - 烷氧基，C 1 -C 2卤代烷氧基，烷硫基，卤代烷基=硫代，其中卤素是Cl，Br，F; R2选自H，氯，溴，氟; Rf选自由含有2至4个碳原子的烷基形成的基团，并且含有至少4个选自F，Cl和Br的卤素，其中至少3个是F原子; 含有至多4个碳原子的烯基和炔基，其含有至少2个F原子，以及任选的选自Cl和Br之间的其它卤素。 本发明涉及唑类衍生物，更具体地涉及具有高杀真菌活性的取代的azolyldioxanes和azolyldioxolanes，其制备方法及其在土地领域的相关用途。

    Fungicidal azolyl-derivatives
    6.
    发明授权
    Fungicidal azolyl-derivatives 失效
    真菌化合物衍生物

    公开(公告)号：US5081141A

    公开(公告)日：1992-01-14

    申请号：US549648

    申请日：1990-07-06

    申请人： Roberto Colle ,  Francesco Corda ,  Giovanni Camaggi ,  Franco Gozzo ,  Luigi Mirenna ,  Carlo Garavaglia

    发明人： Roberto Colle ,  Francesco Corda ,  Giovanni Camaggi ,  Franco Gozzo ,  Luigi Mirenna ,  Carlo Garavaglia

    IPC分类号： C07D249/12 ,  A01N43/50 ,  A01N43/653 ,  A01P3/00 ,  C07C67/343 ,  C07C253/00 ,  C07D233/56 ,  C07D233/60 ,  C07D233/61 ,  C07D249/08 ,  C07D521/00

    CPC分类号： C07D231/12 ,  A01N43/50 ,  A01N43/653 ,  C07C255/00 ,  C07D233/56 ,  C07D249/08

    摘要： Disclosed are compounds having the formula: ##STR1## wherein: m=0, 1;n=0, 1;Z=CH, N;R.sub.1 is selected from chlorine, bromine, fluorine, CF.sub.3, phenyl, C.sub.1 -C.sub.2 -alkoxy, C.sub.1 -C.sub.2 -haloalkoxy, alkylthio, and haloalkylthio, wherein the halogen is Cl, Br, F;R.sub.2 is H, fluorine, chlorine, or bromine;R.sub.3 represents H, CH.sub.3, CN, or also F when m=1 or when n=1 and R.sub.4, R.sub.5 are H;R.sub.4, R.sub.5 are independently H or F;R.sub.3 and R.sub.4, furthermore, when m=0, may represent, taken together, a second bond between the two carbon atoms to which they are linked in formula (I); andR.sub.f is selected from the group consisting of polyfluoroalkyls, polyfluoroalkenyls and polyfluoroalkynyls containing up to 4 carbon atoms, containing at least 2 F atoms and, optionally, other halogens selected from Cl and Br.Anti-fungal compositions containing these new compounds.

    摘要翻译： 公开了具有下式的化合物：其中：m = 0,1; n = 0,1; Z = CH，N; R1选自氯，溴，氟，CF3，苯基，C1-C2-烷氧基，C1-C2-卤代烷氧基，烷硫基和卤代烷硫基，其中卤素为Cl，Br，F; R2是H，氟，氯或溴; 当m = 1或当n = 1且R 4，R 5为H时，R 3表示H，CH 3，CN或F。 R4，R5独立地为H或F; 此外，当m = 0时，R 3和R 4可以一起表示在式（I）中它们连接的两个碳原子之间的第二键; 并且Rf选自包含至少2个F原子的含有至多4个碳原子的多氟烷基，多氟烯基和多氟炔基，以及任选的选自Cl和Br的其它卤素。 含有这些新化合物的抗真菌组合物。