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    44.
    发明专利
    未知

    公开(公告)号：DK1039805T3

    公开(公告)日：2002-11-25

    申请号：DK98964520

    申请日：1998-12-15

    Applicant: BASF AG

    Inventor： SCHELBERGER KLAUS ,  SCHERER MARIA ,  EICKEN KARL ,  HAMPEL MANFRED ,  AMMERMANN EBERHARD ,  LORENZ GISELA ,  STRATHMANN SIEGFRIED

    IPC: A01N37/18 ,  A01N37/20 ,  A01N37/40 ,  A01N43/40 ,  A01N43/50 ,  A01N43/76 ,  A01N47/12 ,  A01N47/14 ,  A01N57/12

    Abstract: Fungicidal mixture comprises: (1) an amide compound of formula (I) and (2) one or more compounds (II), (III), (IV), (V), (VI) or (VII). Fungicidal mixture comprises: (1) an amide compound of formula (I); and (2) a second component comprising: (i) a dithiocarbamate selected from mancozeb, maneb, metiram and zineb; (ii) the carbamate compound propamocarb (III); (iii) an N-acetonyl-benzamide compound of formula (IV), or a salt or adduct; (iv) a phosphorus compound of formula (V); (v) the compound famoxadone (VI); and/or (vi) a heterocyclic compound of formula (VII). A = Ar or Het (both optionally substituted by 1-3 alkyl, halo, CHF2, CF3, (halo)alkoxy, alkylthio, alkylsulfinyl or alkylsulfonyl; R = H; R = phenyl (optionally substituted by 1-3 Q and optionally fused to a group M); or cycloalkyl (optionally substituted by 1-3 Q); M = a saturated 5-membered ring which may contain an O or S atom and is optionally substituted by one or more alkyl; Ar = an aryl group; Het = an aromatic or non-aromatic, 5-6 membered heterocycle which contains 1-3 N, O or S atoms; Q = alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkenyl, cycloalkyloxy, cycloalkenyloxy, phenyl or halo; in Q, the (cyclo)aliphatic residues are optionally halogenated, the cycloaliphatic residues are optionally substituted by 1-3 alkyl, and the phenyl is optionally substituted by 1-5 halo and/or 1-3 (halo)alkyl, (halo)alkoxy or (halo)alkylthio; R , R = halo or T; R = CN, T, U, V or OT; R = H or T; R = 2-4C alkyl; R = thiocyano, isothiocyano or halo; Y = H, a metal atom from main groups I or III of the periodic table, or a group NR R R R ; R = H; 1-8C alkyl (optionally substituted by halo or a NO2 group); 2-8C alkenyl or 2-8C alkynyl (both optionally substituted by a NO2 group); 1-8C alkoxy(1-8C)alkyl; 2-8C alkenyl(1-8C)alkyl; 6-14C aryl (optionally substituted); 3-7C cycloalkyl; 1-4C alkylaryl; or a 5-6 membered heterocyclic group which contains 1 heteroatom (selected from N, O and S) and which is linked to the O atom directly or via an aliphatic chain; R -R = T or 1-4C hydroxyalkyl; R -R = H, 1-6C (halo)alkyl, 2-6C alkenyl, 2-6C alkynyl, TOCO, TCO, formyl(3-7C)cycloalkyl,6-14C aryl (optionally substituted by T, TO, NO2 or halo), 1-6C alkoxy, 2-6C alkoxyalkyl, 2-6C alkylthioalkyl, di(1-4C alkyl)aminoalkyl, pyridyl, furyl, thiazolyl or thienyl; W = O, S or S(O); T = 1-4C alkyl; U = 2-4C alkenyl; V = 2-4C alkynyl.

    46.
    发明专利
    未知

    公开(公告)号：DK1041883T3

    公开(公告)日：2002-10-14

    申请号：DK98966339

    申请日：1998-12-15

    Applicant: BASF AG

    Inventor： SCHELBERGER KLAUS ,  SCHERER MARIA ,  EICKEN KARL ,  HAMPEL MANFRED ,  AMMERMANN EBERHARD ,  LORENZ GISELA ,  STRATHMANN SIEGFRIED

    IPC: A01N43/40 ,  A01N43/84

    Abstract: Fungicidal mixtures comprising as active componentsa) an amide compound of the formula Iin whichA is an aryl group or an aromatic or non-aromatic, 5- or 6-membered heterocycle which has from 1 to 3 hetero atoms selected from O, N and S;where the aryl group or the heterocycle may or may not have 1, 2 or 3 substituents which are selected, independently of one another, from alkyl, halogen, CHF2, CF3, alkoxy, haloalkoxy, alkylthio, alkylsulfynyl and alkylsulfonyl;R is a hydrogen atom;R is a phenyl or cycloalkyl group which may or may not have 1, 2 or 3 substituents which are selected, independently of one another, from alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkenyl, cycloalkyloxy, cyclo-alkenyloxy, phenyl and halogen, where the aliphatic and cycloaliphatic radicals may be partially or fully halogenated and/or the cycloaliphatic radicals may be substituted by from 1 to 3 alkyl groups and where the phenyl group may have from 1 to 5 halogen atoms and/or from 1 to 3 substituents which are selected, independently of one another, from alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio and haloalkylthio, and where the amidic phenyl group may or may not be condensed with a saturated 5-membered ring which may or may not be substituted by one or more alkyl groups and/or may have a hetero atom selected from O and S, andb) a morpholine or piperidine derivative II selected from the group of the compounds IIa, IIb, IIc, IId [sic] and IIe [sic]in a synergistically effective amount.

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