公开(公告)号：WO2007048735A3

公开(公告)日：2008-04-10

申请号：PCT/EP2006067480

申请日：2006-10-17

Applicant: BASF AG ,  WATERHOUSE STEVE ,  STIERL REINHARD ,  STAMMLER GERD

Inventor： WATERHOUSE STEVE ,  STIERL REINHARD ,  STAMMLER GERD

IPC: A01N47/24 ,  A01N25/00

CPC classification number: A01N47/24 ,  A01N37/38 ,  A01N37/50 ,  A01N43/40 ,  A01N43/54 ,  A01N43/88 ,  A01N61/00

Abstract: The present invention relates to a method of inducing plant tolerance to harmful fungi comprising the application to the plants, the soil, in which the plant grows or is to be grown and/or the seeds of the plant, of an effective amount of an active compound that inhibits the mitochondrial breathing chain at the level of the b/c 1 complex.

Abstract translation: 本发明涉及诱导植物对有害真菌的耐受性的方法，其包括施用植物，植物生长或将要生长的土壤和/或植物种子的有效量的活性物质 在b / c 1复合物的水平上抑制线粒体呼吸链的化合物。

公开(公告)号：WO2007065843A3

公开(公告)日：2007-11-15

申请号：PCT/EP2006069112

申请日：2006-11-30

Applicant: BASF AG ,  VOESTE DIRK ,  STRATHMANN SIEGFRIED ,  DOMBO PETER ,  STIERL REINHARD ,  GEWEHR MARKUS

Inventor： VOESTE DIRK ,  STRATHMANN SIEGFRIED ,  DOMBO PETER ,  STIERL REINHARD ,  GEWEHR MARKUS

IPC: A01N25/32 ,  A01N43/50 ,  A01N43/52 ,  A01N43/653 ,  A01N43/78 ,  A01N43/80 ,  A01N43/82 ,  A01N47/18 ,  A01N47/38 ,  A01N55/10 ,  A01P3/00 ,  A01P21/00

CPC classification number: A01N43/90 ,  A01N25/32 ,  A01N45/00 ,  A01N55/00 ,  A01N43/653 ,  A01N47/38 ,  A01N43/50 ,  A01N47/18 ,  A01N43/78 ,  A01N43/82 ,  A01N43/80 ,  A01N2300/00

Abstract: The invention relates to the use of gibberellin of formula (I), where R = H or OH and the dotted line indicates that at this ring position either a C- C single bond or a C=C double bond is present, as safener for at least one azol (2), selected from azaconazol, bitertanol, bromuconazol, cyproconazol, difenoconazol, diniconazol, enilconazol, epoxiconazol, fluquinconazol, fenbuconazol, flusilazol, flutriafol, hexaconazol, imibenconazol, ipconazol, metconazol, myclobutanil, penconazol, propiconazol, prothioconazol, simeconazol, triadimefon, triadimenol, tebuconazol, tetraconazol, triticonazol, prochloraz, pefurazoat, imazalil, triflumizol, cyazofamid, benomyl, carbendazim, thiabendazol, fuberidazol, ethaboxam, etridiazol, hymexazol, or the salts or adducts thereof, for the prevention fungal pests. The invention further relates to the use of compounds (I) and (2) in a method for the prevention of fungal pests with mixtures of compounds (I) and (2) and the use of compounds (I) and (2) for the production of such mixtures and agents comprising said mixtures.

Abstract translation: （1）式（I），其中R表示氢原子或羟基基团，虚线的赤霉Elling的使用表明，在该环任一C-C单键或C的位置是= C双键 如从戊环唑，双苯三唑醇，糠菌唑，环唑醇，醚唑，烯唑醇，恩康唑，氧唑菌，喹唑菌酮，腈苯唑，氟硅唑，粉唑醇，己唑醇，亚胺唑，种菌唑，叶菌唑，腈菌唑，戊菌唑，丙环唑选择用于（2）的至少一种唑类安全剂， 丙硫菌唑，硅氟唑，三唑酮，三唑醇，戊唑醇，四氟醚，戊叉，咪鲜胺，稻瘟酯，抑霉唑，氟菌唑，氰霜唑，苯菌灵，多菌灵，噻菌灵，麦穗宁，噻唑菌胺，土菌灵，恶霉灵，或其盐或加合物，其用于防治有害真菌，使用 式I化合物和（2）中，用于控制使用所述化合物的混合物我未有害真菌的方法 d（2）和使用所述化合物的I和（2）用于制备这样的混合物和包含这些混合物的组合物。

公开(公告)号：WO2007054469A3

公开(公告)日：2007-07-19

申请号：PCT/EP2006068098

申请日：2006-11-06

Applicant: BASF AG ,  YPEMA HENDRIK ,  HOPF ANDREAS ,  FROESE NATHAN ,  STIERL REINHARD

Inventor： YPEMA HENDRIK ,  HOPF ANDREAS ,  FROESE NATHAN ,  STIERL REINHARD

IPC: A01N37/46 ,  A01N43/653 ,  A01N47/24

CPC classification number: A01N47/24 ,  A01N37/46 ,  A01N43/653 ,  A01N2300/00

Abstract: Fungicidal mixtures, comprising (1) triticonazole of the formula I or salts or adducts thereof and (2) pyraclostrobin of the formula II and (3) at least one acylalanine selected from the group consisting of metalaxyl-M of the formula III and (4) kiralaxyl of the formula IV in a synergistically effective amount, methods for controlling harmful fungi using mixtures of the compounds I to III or I, II and IV and the use of the compounds I to III or I, II and IV for preparing such mixtures, and also compositions comprising such mixtures.

Abstract translation: 杀真菌混合物，其包含（1）式I的戊叉唑菌或其盐或加合物和（2）式II的唑菌胺酯和（3）至少一种选自式III的甲霜灵-M和 ）协同有效量的式IV的kiralaxyl，使用化合物I至III或I，II和IV的混合物防治有害真菌的方法以及化合物I至III或I，II和IV用于制备这样的混合物的用途 以及包含这种混合物的组合物。

公开(公告)号：WO2007017416A3

公开(公告)日：2007-05-10

申请号：PCT/EP2006064907

申请日：2006-08-01

Applicant: BASF AG ,  DIETZ JOCHEN ,  GEWEHR MARKUS ,  STRATHMANN SIEGFRIED ,  STIERL REINHARD ,  WERNER FRANK ,  SCHERER MARIA

Inventor： DIETZ JOCHEN ,  GEWEHR MARKUS ,  STRATHMANN SIEGFRIED ,  STIERL REINHARD ,  WERNER FRANK ,  SCHERER MARIA

IPC: A01N43/56 ,  A01N35/04 ,  A01N37/34 ,  A01N37/38 ,  A01N43/653 ,  A01N43/90 ,  A01N47/14 ,  A01N47/24 ,  A01N47/38 ,  A01P3/00

CPC classification number: A01N43/56 ,  A01N47/38 ,  A01N47/24 ,  A01N47/14 ,  A01N37/34 ,  A01N43/653 ,  A01N37/38 ,  A01N35/04 ,  A01N43/90

Abstract: The invention relates to fungicidal mixtures containing the following as active components: 1) at least one 1-methyl pyrazol-4-yl carboxylic acid anilide of formula (I), in which X = O or S, R 1 = C 1 -C 4 alkyl or C 1 -C 4 haloalkyl, R 2 = hydrogen or halogen, R 3 , R 4 and R 5 = independently of one another cyano, nitro, halogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkoxy or C 1 -C 4 alkylthio; and 2) at least one active ingredient II, selected from the active ingredient groups A) to F) in a synergistically active quantity: A) azoles; B) strobilurins; C) carboxamides; D) heterocyclic compounds; E) carbamates; F) other fungicides. The invention also relates to a method for controlling pathogenic fungi using mixtures of at least one compound I and at least one active ingredient II, to the use of the compound(s) I and active ingredients II for producing mixtures of this type and to agents and seeds containing said mixtures.

Abstract translation: 一种杀真菌混合物，其包含作为活性组分：1）式中的至少一个-1-甲基吡唑-4-基甲酰苯胺（I），其中X = O或S，R ^{1 = C _{1 -C 4 烷基或C 1 -C 4 卤代烷基，R 2 是氢或卤素，R 3 ，R 4 和R 5 =独立地是氰基，硝基，卤素，C 1 -C 4 烷基，C 1 -C 4 卤代烷基，C 1 -C 4 烷氧基，C 1 -C 4 - 卤代烷氧基或C 1 -C 4 烷硫基; 和2）至少一种选自活性化合物组A）到F）中选择的活性化合物II：A）唑类; B）嗜球果伞素; C）羧酸酰胺; D）杂环化合物; E）氨基甲酸酯; F）其他杀菌剂; 在协同有效量，用于控制使用至少一种化合物I和至少一种活性化合物II，使用了化合物（S）1与活性化合物II在制备该类混合物和组合物和种子，其包含这些混合物的混合物防治有害真菌的方法。}}

公开(公告)号：WO2007009969A2

公开(公告)日：2007-01-25

申请号：PCT/EP2006064322

申请日：2006-07-17

Applicant: BASF AG ,  SEMAR MARTIN ,  CHRISTEN THOMAS ,  SCHERER MARIA ,  STIERL REINHARD ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  BEDFORD JOHN

Inventor： SEMAR MARTIN ,  CHRISTEN THOMAS ,  SCHERER MARIA ,  STIERL REINHARD ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  BEDFORD JOHN

CPC classification number: A01N43/653 ,  A01N2300/00

Abstract: The invention relates to the combined use of metconazole and epoxiconazole for reducing or preventing the contamination of cereals with mycotoxins formed by mould fungus producing trichothecene.

Abstract translation: 本发明涉及联合使用环戊唑菌和氧唑菌以减少或防止由生产单端孢霉菌的霉菌产生的霉菌毒素污染谷类。

公开(公告)号：WO2005095404A3

公开(公告)日：2006-04-06

申请号：PCT/EP2005003208

申请日：2005-03-26

Applicant: BASF AG ,  BLETTNER CARSTEN ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  GROTE THOMAS ,  HUENGER UDO ,  MUELLER BERND ,  NIEDENBRUECK MATTHIAS ,  RHEINHEIMER JOACHIM ,  SCHAEFER PETER ,  SCHIEWECK FRANK ,  SCHWOEGLER ANJA ,  WAGNER OLIVER ,  RACK MICHAEL ,  NAVE BARBARA ,  SCHERER MARIA ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  STIERL REINHARD

Inventor： BLETTNER CARSTEN ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  GROTE THOMAS ,  HUENGER UDO ,  MUELLER BERND ,  NIEDENBRUECK MATTHIAS ,  RHEINHEIMER JOACHIM ,  SCHAEFER PETER ,  SCHIEWECK FRANK ,  SCHWOEGLER ANJA ,  WAGNER OLIVER ,  RACK MICHAEL ,  NAVE BARBARA ,  SCHERER MARIA ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  STIERL REINHARD

IPC: C07D487/04 ,  A01N43/90

CPC classification number: A01N43/90 ,  C07D487/04

Abstract: The invention relates to the 6-(2-fluorophenyl)-triazolopyrimidines of formula (I), wherein the substituents are defined as follows: R

Abstract translation: 本申请公开了式-6-（2-氟苯基） - 三唑并嘧啶予其中的取代基具有下列含义：R t

公开(公告)号：WO2005095405A3

公开(公告)日：2005-12-22

申请号：PCT/EP2005004187

申请日：2005-03-29

Applicant: BASF AG ,  BLETTNER CARSTEN ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  GROTE THOMAS ,  HUENGER UDO ,  MUELLER BERND ,  NIEDENBRUECK MATTHIAS ,  RHEINHEIMER JOACHIM ,  SCHAEFER PETER ,  SCHIEWECK FRANK ,  SCHWOEGLER ANJA ,  WAGNER OLIVER ,  RACK MICHAEL ,  NAVE BARBARA ,  SCHERER MARIA ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  STIERL REINHARD

Inventor： BLETTNER CARSTEN ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  GROTE THOMAS ,  HUENGER UDO ,  MUELLER BERND ,  NIEDENBRUECK MATTHIAS ,  RHEINHEIMER JOACHIM ,  SCHAEFER PETER ,  SCHIEWECK FRANK ,  SCHWOEGLER ANJA ,  WAGNER OLIVER ,  RACK MICHAEL ,  NAVE BARBARA ,  SCHERER MARIA ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  STIERL REINHARD

IPC: A01N43/90 ,  C07D487/04

CPC classification number: A01N43/90 ,  C07D487/04

Abstract: The invention relates to 6-(2,6-dichlorophenyl)-triazolopyrimidines of formula (I) wherein the substituents have the following designations: R and R represent hydrogen, alkyl, halogenalkyl, cycloalkyl, halogencycloalkyl, alkenyl, halogenalkenyl, cycloalkenyl, halogencycloalkenyl, alkinyl, halogenalkinyl or phenyl, naphthyl, or a five-membered or six-membered saturated, partially unsaturated or aromatic heterocycle containing between one and four heteroatoms from the group containing O, N or S; R and R can also form, together with the nitrogen atom to which they are bound, a five-membered or six-membered heterocycle or heteroaryl which is bound by N and contains between one and three other heteroatoms from the group containing O, N and S as a cyclic member and is substituted according to the description; and X represents alkyl, cyano, alkoxy, halogenalkoxy, alkenyloxy or halogenalkenyloxy, but does not represent C1-C4 alkyl when R and R together represent piperidin-1-yl or 4-methylpiperidin-1-yl. The invention also relates to a method for producing said compounds, agents containing the same, and the use thereof for controlling plant pathogenic fungi.

Abstract translation: 6-（2,6-二氯苯基） - 三唑并嘧啶的式（I）的其中取代基具有以下含义：R t <1>，R <2>是氢，烷基，卤代烷基，环烷基，卤代环烷基，烯基，卤代烯基，环烯基，卤代环烯基 基，炔基，卤代炔基，或苯基，萘基，或含有选自O，N，或S，R <1>和R <2>也可以，一起一至四个杂原子的五元或六元饱和，部分不饱和或芳族杂环 形成一个五元或六元杂环基或杂芳基的氮原子与它们所连接，这是经N个附接和选自O，N和S的一至三个另外的杂原子作为环成员，并且可以根据该描述被取代; X为烷基，氰基，烷氧基，卤代烷氧基，烯氧基或卤代链烯氧基，其中X不为C1-C4烷基，当R <1>和R <2>是常见的哌啶-1-基或4-甲基 - 哌啶-1-基; 一种用于制备这些化合物，含有它们和它们在防治植物病原性有害真菌的用途的组合物的过程。

公开(公告)号：WO2005110080A2

公开(公告)日：2005-11-24

申请号：PCT/EP2005005070

申请日：2005-05-11

Applicant: BASF AG ,  BLETTNER CARSTEN ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  GROTE THOMAS ,  HUENGER UDO ,  MUELLER BERND ,  NIEDENBRUECK MATTHIAS ,  RHEINHEIMER JOACHIM ,  SCHAEFER PETER ,  SCHIEWECK FRANK ,  SCHWOEGLER ANJA ,  WAGNER OLIVER ,  NAVE BARBARA ,  SCHERER MARIA ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  STIERL REINHARD

Inventor： BLETTNER CARSTEN ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  GROTE THOMAS ,  HUENGER UDO ,  MUELLER BERND ,  NIEDENBRUECK MATTHIAS ,  RHEINHEIMER JOACHIM ,  SCHAEFER PETER ,  SCHIEWECK FRANK ,  SCHWOEGLER ANJA ,  WAGNER OLIVER ,  NAVE BARBARA ,  SCHERER MARIA ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  STIERL REINHARD

IPC: A01N20060101 ,  A01N43/90 ,  A01N

CPC classification number: A01N43/90 ,  A01N59/06 ,  A01N59/02 ,  A01N57/12 ,  A01N47/38 ,  A01N47/34 ,  A01N47/24 ,  A01N47/04 ,  A01N43/50 ,  A01N43/76 ,  A01N43/653 ,  A01N43/36 ,  A01N43/40 ,  A01N43/32 ,  A01N37/48 ,  A01N37/46 ,  A01N37/38 ,  A01N37/34 ,  A01N2300/00

Abstract: The invention relates to fungicidal mixtures containing in the form of active components 1) 5-methyl-7-amino-triazolopyrimidine of formula (I), wherein R is alkyl, halogenalkyl, alkenyl or cyclopentyl, R is hydrogen or alkyl, R and R together with the nitrogen atom to which they are bound may form a piperidinyl cycle substitutable by a methyl group, L is fluorine or chlorine, L , L are independently from each other hydrogen, fluorine or chlorine and 2) at least one type of active substance selected from groups A) azoles, B) strobilurins, C) acyl alanines, D) amine derivatives, E) anilinopyrimidines; F) dicarboximides; G) cinnamic acid amides and analogues thereof, H) antibiotics, K) dithiocarbamates, L) heterocyclic compounds, M) sulphur and copper fungicides, N) nitrophenyl derivatives, O) phenylpyrroles, P) sulfenic acid derivatives, Q) other fungicides and R) growth retardants according to the descriptions, wherein said mixtures contain the compounds in a synergically efficient amount. Novel triazolopyrimidines, methods for controlling pathogenic fungi using the mixtures of the compound (I) with active substances of the groups A) and R), the use the compounds (I) with the active substances of the groups A) and R) for producing said mixtures and agents containing said mixtures are also disclosed.

Abstract translation: 一种杀真菌混合物，其包含作为活性组分：1）式（I）的5-甲基-7-氨基三唑并嘧啶，其中R <1>是烷基，卤代烷基，链烯基或环戊基; [R <2>是氢或烷基; [R <1>和R <2>也可以与氮原子一起与它们所连接的形式，其可以由甲基取代的哌啶环; →<1>是氟或氯; →<2>，L <3>独立地是氢，氟或氯; 和2）选自组A）唑类中的至少一种活性化合物; B）嗜球果伞素; C）酰基丙氨酸类; D）胺衍生物; E）苯胺基嘧啶; F）二甲酰亚胺; G）肉桂酸和类似物; 1H）抗生素; K）二硫代氨基甲酸酯; L）杂环化合物; M）硫和铜杀真菌剂; N）硝基苯基衍生物; O）苯基吡咯; P）Sulfensäurederivate; Q）其他杀菌剂; R）Wachstumsretardantien; 根据描述; 在协同有效量; 新的三唑并嘧啶，用于控制使用I化合物的混合物与基团A），以R的活性成分）包含这些混合物的有害真菌及其制造这样的混合物使用I化合物与基团A）至R）的活性成分和组合物的方法 ，

公开(公告)号：WO2004045282A3

公开(公告)日：2004-07-29

申请号：PCT/EP0312772

申请日：2003-11-14

Applicant: BASF AG ,  TORMO I BLASCO JORDI ,  GROTE THOMAS ,  AMMERMANN EBERHARD ,  STIERL REINHARD ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH

Inventor： TORMO I BLASCO JORDI ,  GROTE THOMAS ,  AMMERMANN EBERHARD ,  STIERL REINHARD ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH

IPC: A01N43/90

CPC classification number: A01N43/90 ,  A01N43/40 ,  A01N2300/00

Abstract: Disclosed are fungicidal mixtures containing a synergistically effective amount of A) a triazolopyrimidine of formula (I), and B) amide compounds of formula (II), wherein X and X represent halogen, nitro, cyano, alkyl, alkenyl, alkinyl, haloalkyl, haloalkenyl, haloalkinyl, alkoxy, haloalkoxy, haloalkylthio, alkylsulfinyl, or alkylsulfonyl, x represents 1, 2, 3, or 4, and y represents 1, 2, 3, 4, or 5. Also disclosed are methods for controlling destructive fungi by means of mixtures of compounds (I) and (II), agents containing said mixtures, and the use of compounds (I) and (II) for producing such mixtures.

Abstract translation: 一种杀真菌混合物摘要杀真菌混合物，其包含A中的式（I）的三唑并嘧啶，和B.酰胺化合物的式（II），其中X <1>和X <2>是卤素，硝基，氰基，烷基，烯基，炔基，卤代烷基的 卤代烯基，卤代炔基，烷氧基，卤代烷氧基，卤代烷硫基，烷基亚磺酰基或烷基磺酰基; X 1，2，3或4; 和y是1，2，3，4或5; 在协同有效量，用于控制使用（I）和化合物的混合物防治有害真菌的方法（II），含有它们的用于制造这种混合物使用的化合物（I）和（II）的试剂。

公开(公告)号：WO0249438A3

公开(公告)日：2003-08-21

申请号：PCT/EP0114635

申请日：2001-12-13

Applicant: BASF AG ,  MUELLER BERND ,  PTOCK ARNE ,  AMMERMANN EBERHARD ,  STIERL REINHARD ,  LORENZ GISELA ,  STRATHMANN SIEGFRIED ,  SCHERER MARIA ,  SCHELBERGER KLAUS ,  LEYENDECKER JOACHIM

Inventor： MUELLER BERND ,  PTOCK ARNE ,  AMMERMANN EBERHARD ,  STIERL REINHARD ,  LORENZ GISELA ,  STRATHMANN SIEGFRIED ,  SCHERER MARIA ,  SCHELBERGER KLAUS ,  LEYENDECKER JOACHIM

IPC: A01N43/653 ,  A01N43/50 ,  A01N43/56 ,  A01N43/80 ,  A01N47/24

CPC classification number: A01N47/24 ,  A01N43/90 ,  A01N43/50 ,  A01N2300/00

Abstract: The invention relates to a fungicidal mixture containing, A) carbamates of formula (I) wherein X, represents CH and N, n represents 0, 1 or 2 and R represents halogen, C1-C4-alkyl and C1-C4-halogenalkyl, wherein the radicals R can be different if n represents 2, a salt thereof or adduct, and B) imidazole derivatives of formula (II) wherein R and R represent halogen and phenyl which can be substituted by halogen or alkyl, or R and R together with the bridging C=C-double bond form a 3.4-difluoromethylene dioxy phenyl group; R represents cyano or halogen, and R represents dialkylamino or isoxazole-4-yl which can include two alkyl radicals in a synergistically active quantity. The invention also relates to a method for combating harmful fungi with mixtures of compounds I and II and the use thereof for producing said mixtures.

Abstract translation: 一种杀真菌混合物，包含：A）通式（I的氨基甲酸酯），其中X为CH和N，n是0，1或2，R是卤素，C1-C4烷基和C1-C4卤代烷基，其中所述基团 中，R是不同的，如果n为2，其盐或加合物的一个，和B）下式的咪唑衍生物（II），其中R <1>和R <2>是可被卤素或烷基取代的卤素和苯基， 或R <1>和R <2>与桥接C一起= C双键形成3,4- Difluormethylendioxyphenyl基; [R <4>二烷基氨基或异恶唑-4-基，其可带有两个烷基基团，意味着<3>是氰基或卤素，和R，以协同有效量，用于控制使用I和II和使用的化合物的混合物防治有害真菌的方法 化合物I和II在制备该类混合物。