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    • 21. 发明申请
    • FUNGICIDAL MIXTURES III
    • 真菌混合物III
    • WO2009063076A2
    • 2009-05-22
    • PCT/EP2008065606
    • 2008-11-14
    • BASF SERENNER JENSULMSCHNEIDER SARAHDIETZ JOCHENHADEN EGON
    • RENNER JENSULMSCHNEIDER SARAHDIETZ JOCHENHADEN EGON
    • A01P3/00A01N37/34A01N37/50A01N43/40A01N43/50A01N43/54A01N43/653A01N43/88A01N47/04A01N47/12A01N47/14A01N47/24
    • A01N43/40A01N37/34A01N37/50A01N43/50A01N43/54A01N43/653A01N47/04A01N47/12A01N47/14A01N47/24A01N61/00A01N2300/00
    • The present invention relates to mixtures of fungicidally active compounds comprising at least one substituted 2-[hydroxyl(pyridine-3-yl)methyl]acrylate compound of the formula (I) wherein: R1 is H, C1-C6-alkyl, C1-C6-alkoxy-C1-C6-alkyl,C1-C6-haloalkyl, aryl or het- eroaryl, wherein the cyclic moieties of the last two radicals are unsubsti- tuted or substituted with 1, 2 or 3 radicals selected from halogen, C1-C4 alkyl, C2-C4-alkynyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-alkylthio, C1-C4- haloalkoxy, cyano and nitro; A is a covalent bond or C1-C4-alkylen, which is unsubstituted or which may carry a substitutent selected from C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and cyano; Ar is aryl or heteroaryl, wherein the cyclic moieties of the aromatic radicals are unsubstituted or substituted with 1, 2 or 3 radicals Ra, where the radicals Ra are identical or different and selected from halogen, C1-C4-alkyl, C2-C4- alkenyl, C2-C4-alkynyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-alkylthio, C1- C4-haloalkoxy, C1-C4-haloalkylthio, cyano, nitro, aryl, hetaryl, aryloxy, hetaryloxy, aryloxy-C1-C4-alkyl and hetaryloxy-C1-C4-alkyl, wherein the cyclic moieties of the six last mentioned radicals are unsubstituted or substi- tuted with 1, 2 or 3 radicals selected from halogen, C1-C4-alkyl, C1-C4- haloalkyl, C1-C4-alkoxy, C1-C4-alkylthio, C1-C4-haloalkoxy, cyano and nitro; or a salt thereof; and at least one further fungicidally active compound II.
    • 本发明涉及包含至少一种式(I)的取代的2- [羟基(吡啶-3-基)甲基]丙烯酸酯化合物的杀真菌活性化合物的混合物,其中:R1是H,C1-C6-烷基,C1- C 1 -C 6 - 烷氧基-C 1 -C 6烷基,C 1 -C 6卤代烷基,芳基或芳基,其中最后两个基团的环状部分未被取代或被1,2或3个选自卤素,C1- C4烷基,C2-C4-炔基,C1-C4-卤代烷基,C1-C4-烷氧基,C1-C4-烷硫基,C1-C4-卤代烷氧基,氰基和硝基; A是共价键或C1-C4-亚烷基,其是未取代的或可以携带选自C 1 -C 4 - 烷基,C 1 -C 4 - 卤代烷基,C 1 -C 4 - 烷氧基和氰基的取代基; Ar是芳基或杂芳基,其中芳族基团的环状部分是未取代的或被1,2或3个基团R a取代,其中基团R a相同或不同并且选自卤素,C 1 -C 4烷基,C 2 -C 4 - 烯基,C 2 -C 4 - 炔基,C 1 -C 4卤代烷基,C 1 -C 4 - 烷氧基,C 1 -C 4 - 烷硫基,C 1 -C 4卤代烷氧基,C 1 -C 4卤代烷硫基,氰基,硝基,芳基,杂芳基,芳氧基, 芳氧基-C 1 -C 4烷基和芳基氧基-C 1 -C 4 - 烷基,其中六个最后提到的基团的环状部分是未取代的或被1,2或3个选自卤素,C 1 -C 4 - 烷基,C 1 -C 4烷基的基团取代 C 1-4卤代烷基,C 1 -C 4 - 烷氧基,C 1 -C 4 - 烷硫基,C 1 -C 4卤代烷氧基,氰基和硝基; 或其盐; 和至少一种其它杀真菌活性化合物II。
    • 22. 发明申请
    • FUNGICIDAL MIXTURES I
    • 真菌混合物
    • WO2009063074A2
    • 2009-05-22
    • PCT/EP2008/065603
    • 2008-11-14
    • BASF SERENNER, JensULMSCHNEIDER, SarahDIETZ, JochenHADEN, Egon
    • RENNER, JensULMSCHNEIDER, SarahDIETZ, JochenHADEN, Egon
    • A01N43/40A01P3/00A01N37/34A01N37/50A01N43/653A01N43/84A01N43/90A01N47/04A01N47/12A01N47/14A01N47/18
    • A01N43/40A01N2300/00
    • The present invention relates to mixtures of fungicidally active compounds comprising at least one substituted 3-hydroxymethylpyridin compound formula I and at least one further fungicidally active compound II. wherein: X is O, S or NR4; R 1 is d-C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, aryl-C 1 -C 4 -alkyl, aryloxy-C 1 -C 4 -alkyl, arylthio-C 1 -C 4 -alkyl, aryl or heteroaryl, wherein the cyclic moieties of the last five radicals are unsubstituted or substituted with 1, 2 or 3 radicals selected from halogen, C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl, C 2 -C 4 - alkynyl, C 1 -C 4 -haloalkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -haloalkoxy, C 1 -C 4 -haloalkylthio, cyano and nitro; R 2 is H or C 1 -C 4 -alkyl; R 3 is C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, aryl-C 1 -C 4 -alkyl, aryloxy-C 1 -C 4- alkyl, arylthio-C 1 -C 4 -alkyl, aryl or heteroaryl, wherein the cyclic moieties of the last five radicals are unsubstituted or substituted with 1, 2 or 3 radicals selected from halogen, C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl, C 2 -C 4 - alkynyl, C 1 -C 4 -haloalkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -haloalkoxy, C 1 -C 4 -haloalkylthio, cyano and nitro; R 4 is H, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, aryl-C 1 -C 6 -alkyl, aryloxy-C 1 -C 4 -alkyl, arylthio-C 1 -C 4 -alkyl, aryl or heteroaryl, wherein the cyclic moieties of the last five radicals are unsubstituted or substituted with 1, 2 or 3 radicals selected from halogen, C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl, C 2 -C 4 - alkynyl, C 1 -C 4 -haloalkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -haloalkoxy, C 1 -C 4 -haloalkylthio, cyano and nitro.
    • 本发明涉及杀真菌活性化合物的混合物,其包含至少一种取代的3-羟甲基吡啶化合物式I和至少一种其它杀真菌活性化合物II。 其中:X是O,S或NR4; R 1是C 1 -C 6 - 烷基,C 1 -C 6烷氧基-C 1 -C 6烷基,C 1 -C 6卤代烷基,芳基-C 1 -C 4烷基,芳氧基-C 1 -C 4烷基,芳硫基-C 1 -C 4 - 烷基,芳基或杂芳基,其中最后五个基团的环状部分是未取代的或被1,2或3个选自卤素,C 1 -C 4 - 烷基,C 2 -C 4 - 烯基,C 2 -C 4 - 炔基,C 1 -C 4 - C 1 -C 4 - 卤代烷基,C 1 -C 4 - 烷氧基,C 1 -C 4 - 烷硫基,C 1 -C 4卤代烷氧基,C 1 -C 4卤代烷硫基,氰基和硝基; R2是H或C1-C4-烷基; R 3是C 1 -C 6烷基,C 1 -C 6烷氧基-C 1 -C 6烷基,C 1 -C 6卤代烷基,芳基-C 1 -C 4烷基,芳氧基-C 1 -C 4烷基,芳硫基-C 1 -C 4烷基, 芳基或杂芳基,其中最后五个基团的环状部分是未取代的或被1,2或3个选自卤素,C 1 -C 4 - 烷基,C 2 -C 4 - 烯基,C 2 -C 4 - 炔基,C 1 -C 4 - 卤代烷基,C 1 -C 4 - 烷氧基,C 1 -C 4 - 烷硫基,C 1 -C 4卤代烷氧基,C 1 -C 4卤代烷硫基,氰基和硝基; R 4是H,C 1 -C 6烷基,C 1 -C 6烷氧基-C 1 -C 6烷基,C 1 -C 6卤代烷基,芳基-C 1 -C 6烷基,芳氧基-C 1 -C 4烷基,芳硫基-C 1 -C 4 - 烷基,芳基或杂芳基,其中最后五个基团的环状部分是未取代的或被1,2或3个选自卤素,C 1 -C 4 - 烷基,C 2 -C 4 - 烯基,C 2 -C 4 - 炔基,C 1 -C 4 - C 1 -C 4 - 卤代烷基,C 1 -C 4 - 烷氧基,C 1 -C 4 - 烷硫基,C 1 -C 4卤代烷氧基,C 1 -C 4卤代烷硫基,氰基和硝基。