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1. 发明公开

EP4088575A1 VERFAHREN ZUR GLEICHZEITIGEN OPTIMIERUNG VON ÖKOLOGIE, ÖKONOMIE UND WIRKUNG BEI DER ANWENDUNG VON EPISYSTEMISCHEN STROBILURINFUNGIZIDEN 无效
公开(公告)号：EP4088575A1
公开(公告)日：2022-11-16
申请号：EP21020257.8
申请日：2021-05-14
申请人： Sauter, Hubert
发明人： Sauter, Hubert
IPC分类号： A01N37/50 , A01N43/40 , A01P3/00
摘要： Es wird ein einfaches und praktikables Verfahren beschrieben, das dem landwirtschaftlichen Anwender erhebliche Vorteile im Hinblick auf Wirkungsgrad, Ökonomie und Ökologie bei Fungizidbehandlungen mit episystemischen Strobilurinen, z.B. mit Kresoxim-methyl, Trifloxystrobin, Picoxystrobin, Triclopyricarb, Flufenoxistrobin oder Bifujunzhi bietet. Prinzip und Verfahren beruhen im Kern auf einer schlichten Vorverlegung der Behandlung vor bisher übliche, gewohnte und empfohlene Anwendungszeitpunkte. Hierdurch können kontraintuitiv überraschende Wirkungssteigerungen unter gleichzeitiger, ökonomisch und insbesondere ökologisch erwünschter Einsparung von Wirkstoff-Aufwandmengen bei gleichzeitigem Erhalt oder sogar Verbesserung des Wirkungsgrades erzielt werden.

2. 发明申请

WO2013092224A1 USE OF STROBILURIN TYPE COMPOUNDS FOR COMBATING PHYTOPATHOGENIC FUNGI RESISTANT TO QO INHIBITORS 审中-公开
标题翻译：使用抗菌素类化合物来抑制致病菌对真菌抑制剂的抗真菌性
公开(公告)号：WO2013092224A1
公开(公告)日：2013-06-27
申请号：PCT/EP2012/074586
申请日：2012-12-06
申请人： BASF SE , RHEINHEIMER, Joachim , TERTERYAN, Violeta , REDLICH, Stefan , KREMZOW, Doris , ROSENBAUM, Claudia , ROHRER, Sebastian Georgios , GRAMMENOS, Wassilios , PILGER, Christian , RÖHL, Franz , GEWEHR, Markus , STAMMLER, Gerd , MONTAG, Jurith , SAUTER, Hubert , BASF SCHWEIZ AG
发明人： RHEINHEIMER, Joachim , TERTERYAN, Violeta , REDLICH, Stefan , KREMZOW, Doris , ROSENBAUM, Claudia , ROHRER, Sebastian Georgios , GRAMMENOS, Wassilios , PILGER, Christian , RÖHL, Franz , GEWEHR, Markus , STAMMLER, Gerd , MONTAG, Jurith , SAUTER, Hubert
IPC分类号： A01N43/08 , A01N43/54 , A01N43/56 , A01N43/653 , A01N43/713 , A01N43/76 , A01N43/78 , A01N43/80 , A01N43/82 , A01N43/88 , A01N43/90 , A01N47/24 , A01P3/00 , A01N37/50 , A01N47/28
CPC分类号： A01N43/56 , A01N37/50 , A01N43/08 , A01N43/54 , A01N43/653 , A01N43/713 , A01N43/76 , A01N43/78 , A01N43/80 , A01N43/82 , A01N43/88 , A01N43/90 , A01N47/12 , A01N47/24 , A01N47/28 , C07D231/22 , C07D249/12
摘要： The present invention relates to the use of strobilurine type compounds of formula I and the N-oxides and the salts thereof for combating phytopathogenic fungi containing a mutation in the mitochondrial cytochrome b gene conferring resistance to Qo inhibitors, and to methods for combating such fungi. The invention also relates to novel compounds, processes for preparing these compounds, to compositions comprising at least one such compound, to plant health 10 applications, and to seeds coated with at least one such compound.
摘要翻译：本发明涉及式I的顺风草酸型化合物及其N-氧化物及其盐在与含有Qo抑制剂的线粒体细胞色素b基因中含有突变的植物病原性真菌中的用途以及与这些真菌相抗的方法。本发明还涉及新化合物，制备这些化合物的方法，包含至少一种这样的化合物的组合物，植物健康10种应用以及用至少一种这样的化合物包被的种子。

3. 发明申请

WO2003008417A1 SUBSTITUTED 6-(2-TOLYL)-TRIAZOLOPYRIMIDINES AS FUNGICIDES 审中-公开
标题翻译：取代的6-（2-三氟甲基） - 吡唑并嘧啶作为防腐剂
公开(公告)号：WO2003008417A1
公开(公告)日：2003-01-30
申请号：PCT/EP2002/007578
申请日：2002-07-08
申请人： BASF AKTIENGESELLSCHAFT , TORMO I BLASCO, Jordi , SAUTER, Hubert , MÜLLER, Bernd , GEWEHR, Markus , GRAMMENOS, Wassilios , GROTE, Thomas , GYPSER, Andreas , RHEINHEIMER, Joachim , ROSE, Ingo , SCHÄFER, Peter , SCHIEWECK, Frank , RACK, Michael , AMMERMANN, Eberhard , STRATHMANN, Siegfried , LORENZ, Gisela , STIERL, Reinhard
发明人： TORMO I BLASCO, Jordi , SAUTER, Hubert , MÜLLER, Bernd , GEWEHR, Markus , GRAMMENOS, Wassilios , GROTE, Thomas , GYPSER, Andreas , RHEINHEIMER, Joachim , ROSE, Ingo , SCHÄFER, Peter , SCHIEWECK, Frank , RACK, Michael , AMMERMANN, Eberhard , STRATHMANN, Siegfried , LORENZ, Gisela , STIERL, Reinhard
IPC分类号： C07D487/04
CPC分类号： C07D487/04 , A01N43/90
摘要： Substituted 6-(2-tolyl)-triazolopyrimidines of formula (I) in which R 1 and R 2 independently denote hydrogen or alkyl, alkenyl, alkynyl, or alkadienyl, haloalkyl, haloalkenyl, cycloalkyl, phenyl, naphthyl, or 5- or 6-membered heterocyclyl, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, or 5- or 6-membered heteroaryl, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, or where R 1 and R 2 radicals may be unsubstituted or substituted as defined in the description, or R 1 and R 2 together with the interjacent nitrogen atom represent a 5- or 6-membered heterocyclic ring, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, which may be substituted; R 3 is halogen, cyano, alkyl, alkoxy, haloalkyl, or C(=O)A, wherein A is hydrogen, hydroxy, alkyl, amino, or mono- or dialkyl-amino; n is an integer from 1 to 4; and X is halogen, cyano, alkyl, alkoxy, haloalkoxy or alkenyloxy; processes for their preparation, compositions containing them and to their use for combating phytopathogenic fungi.
摘要翻译：取代的式（I）的6-（2-甲苯基） - 三唑并嘧啶，其中R 1和R 2独立地表示氢或烷基，烯基，炔基或链二烯基，卤代烷基，卤代烯基，环烷基，苯基，萘基或含有一至四个氮原子或一至三个氮原子和一个硫或氧原子或含有一至四个氮原子或一至三个氮原子的五元或六元杂芳基的5-或6-元杂环基和一个硫或氧原子，或其中R 1和R 2基团可以是未被描述的或如说明书中定义的取代的那样，或者R 1和R 2与中间的氮原子一起表示5-或6 含有一至四个氮原子或一至三个氮原子和一个可被取代的硫或氧原子; R 3是卤素，氰基，烷基，烷氧基，卤代烷基或C（= O）A，其中A是氢，羟基，烷基，氨基或一或二烷基氨基; n是1至4的整数; X为卤素，氰基，烷基，烷氧基，卤代烷氧基或烯氧基; 其制备方法，含有它们的组合物及其用于对抗植物病原真菌的用途。

4. 发明申请

WO2002083677A1 6-(2-CHLORO-6-FLUORO-PHENYL)-TRIAZOLOPYRIMIDINES 审中-公开
标题翻译： 6-（2-氯-6-氟 - 苯基）-TRIAZOLOPYRIMIDINES
公开(公告)号：WO2002083677A1
公开(公告)日：2002-10-24
申请号：PCT/EP2002/003830
申请日：2002-04-06
申请人： BASF AKTIENGESELLSCHAFT , TORMO I BLASCO, Jordi , SAUTER, Hubert , MÜLLER, Bernd , GEWEHR, Markus , GRAMMENOS, Wassilios , GROTE, Thomas , GYPSER, Andreas , RHEINHEIMER, Joachim , ROSE, Ingo , SCHÄFER, Peter , SCHIEWECK, Frank , AMMERMANN, Eberhard , STRATHMANN, Siegfried , LORENZ, Gisela , STIERL, Reinhard
发明人： TORMO I BLASCO, Jordi , SAUTER, Hubert , MÜLLER, Bernd , GEWEHR, Markus , GRAMMENOS, Wassilios , GROTE, Thomas , GYPSER, Andreas , RHEINHEIMER, Joachim , ROSE, Ingo , SCHÄFER, Peter , SCHIEWECK, Frank , AMMERMANN, Eberhard , STRATHMANN, Siegfried , LORENZ, Gisela , STIERL, Reinhard
IPC分类号： C07D487/04
CPC分类号： C07D487/04 , A01N43/90
摘要： 6-(2-Chloro-6-fluoro-phenyl)-triazolopyrimidines of formula (I), in which R 1 and R 2 independently denote hydrogen or alkyl, alkenyl, alkynyl, alkadienyl, or haloalkyl, cycloalkyl, bicycloalkyl, phenyl, naphthyl, or 5- or 6-membered heterocyclyl, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, or 5- or 6-membered heteroaryl, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, or where R 1 and R 2 radicals may be unsubstituted or partially or fully halogenated or may be substituted as defined in the description, R 1 and R 2 together with the interjacent nitrogen atom represent a 5- or 6-membered heterocyclic ring, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, which may be substituted; X is cyano, alkoxy, haloalkoxy or alkenyloxy; processes for their preparation, compositions containing them and to their use for combating phytopathogenic fungi.
摘要翻译：式（I）的6-（2-氯-6-氟 - 苯基） - 三唑并嘧啶，其中R 1和R 2独立地表示氢或烷基，烯基，炔基，链二烯基或卤代烷基，环烷基，双环烷基，含有1-4个氮原子或一至三个氮原子和一个硫或氧原子的苯基，萘基或5-或6-元杂环基，或含有1-4个氮原子或一个或四个氮原子的5-或6-元杂芳基 R 3和R 2基团可以是未被取代的或部分或完全卤化的或可以如说明书中所定义的取代，R 1和R 2都可以被取代，与相邻的氮原子一起表示含有一至四个氮原子或一至三个氮原子和一个可被取代的硫原子或氧原子的5-或6-元杂环; X是氰基，烷氧基，卤代烷氧基或烯氧基; 其制备方法，含有它们的组合物及其用于对抗植物病原真菌的用途。

5. 发明申请

WO1999031070A1 SUBSTITUTED PHENYLPYRAZOLONES, METHOD AND INTERMEDIATE PRODUCTS FOR THE PRODUCTION THEREOF, AND THEIR UTILIZATION FOR COMBATING PARASITIC FUNGI AND ANIMAL PARASITES 审中-公开
标题翻译：取代phenylpyrazolones，工艺和中间产品用于控制有害真菌有害动物的生产和使用
公开(公告)号：WO1999031070A1
公开(公告)日：1999-06-24
申请号：PCT/EP1998008179
申请日：1998-12-14
申请人： BASF AKTIENGESELLSCHAFT , MÜLLER, Bernd , SAUTER, Hubert , BAYER, Herbert , GEWEHR, Markus , GRAMMENOS, Wassilios , GROTE, Thomas , GYPSER, Andreas , PTOCK, Arne , RÖHL, Franz , GÖTZ, Norbert , GÖTZ, Roland , HARRIES, Volker , AMMERMANN, Eberhard , LORENZ, Gisela , STRATHMANN, Siegfried
发明人： BASF AKTIENGESELLSCHAFT
IPC分类号： C07D231/22
CPC分类号： C07D401/12 , A01N43/48 , C07C243/22 , C07D231/22 , C07D403/12 , C07D405/12 , C07D409/12 , C07D413/12 , C07D417/12
摘要： The invention relates to substituted phenylpyrazolones of formula (I) in which the substituents have the following meanings: Y represents halogen, alkyl, halogen alkyl or alkoxyl; n represents 0, 1 or 2, whereby the radical Y can be different when n = 2; E represents a group A (A), whereby # characterizes the bond with the phenyl ring; R represents halogen, cyano, alkyl or halogen alkyl; R represents hydrogen or alkyl; R represents alkyl or halogen alkyl; T represents a direct bond, oxygen or CH2O; Z represents a) when T represents oxygen or oxymethylene, a group X, N=CWR or N=C(R )-C(R )=NOR , whereby X represents optionally substituted heterocyclyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted arylmethylene or optionally substituted heteroarylmethylene; W represents optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkinyl, optionally substituted cycloalkyl, optionally substituted cycloalkenyl, optionally substituted heterocyclyl, optionally substituted aryl or optionally substituted heteroaryl; R represents hydrogen, cyano, alkyl, halognealkyl, alkoxyl, alkoxyl alkyl, cycloalkyl; R represents hydrogen, cyano, halogen, C(R )=NOR or W, OW, SW or NR W, whereby R represents hydrogen, alkyl, alkenyl or alkinyl; R represents hydrogen or alkyl; R represents hydrogen, optionally substituted alkyl, optionally substituted alkenyl or optionally substituted alkinyl, and b) when T represents a direct bond, Z represents a group W, CH2-CH2-W, CH=CH-W, CC-W, S-W, CH2-S-W, CH=N-O-CH2-W, CH2-O-C(=O)-W or CH2-O-C(CH3)=N-N=C(CH3)-W. The invention also relates to a method and intermediate products for the production of said phenylpyrazolones used for combating parasitic fungi and animal parasites.
摘要翻译：式的取代的phenylpyrazolones（I），其中取代基具有以下含义：Y是卤素，烷基，卤代烷基或烷氧基; n为0，1或2，其中基团Y是不同的，当n = 2; E为下式基团（A），其中＃表示连于苯环的; ř卤素，氰基，烷基或卤代烷基; [R 是氢或烷基; [R 烷基或卤代烷基; T是直接键，氧或CH 2 O; Z上）当T为氧或氧亚甲基是指基团X，N = CWR <1>或N = C（R <1>） - C（R <2>）= NOR <3>，其中X是未取代的或取代的。杂环基，未取代的或取代的。的芳基，未取代的或取代的。杂芳基，未取代的或取代的。芳亚甲基或未取代的或取代的。 Hetarylmethylen; W¯¯未取代或取代的。烷基，未取代或取代的。链烯基，未取代的或取代的。炔基，未取代的或取代的。环烷基，未取代的或取代的。环烯基，未取代的或取代的。杂环基，未取代的或取代的。芳基或未取代或取代的。杂芳基; [R <1>是氢，氰基，烷基，卤代烷基，烷氧基，烷氧基烷基，环烷基; [R <2>是氢，氰基，卤素，C（R ）= NOR <3>或W，OW，SW或NR W，其中R 是氢，烷基，烯基或炔基; [R 是氢或烷基; [R <3>为氢，未取代的或取代的。烷基，未取代或取代的。链烯基或未取代的或取代的。炔基，和b）当T表示直接键，一组W，CH2-CH2-W，CH = CH-W，CC-W，SW，CH2-SW，CH = NO-CH2-W，CH2-OC （= O）-W，或CH 2 OC（CH 3）= NN = C（CH 3）-W，它们的制备方法和它们在防治有害真菌和动物害虫中的用途的方法和中间体。

6. 发明申请

WO1998017115A1 METHOD FOR CONTROLLING PARASITIC FUNGI IN CULTIVATED PLANTS 审中-公开
标题翻译：方法防治有害真菌在增产
公开(公告)号：WO1998017115A1
公开(公告)日：1998-04-30
申请号：PCT/EP1997005534
申请日：1997-10-08
申请人： BASF AKTIENGESELLSCHAFT , SCHMIDT, Ralf-Michael , SAUTER, Hubert , AMMERMANN, Eberhard , LORENZ, Gisela
发明人： BASF AKTIENGESELLSCHAFT
IPC分类号： A01N37/50
CPC分类号： A01N37/50
摘要： The invention relates to a method for controlling parasitic fungi in cultivated plants with modified pathogenic resistance against certain parasitic fungi, wherein the cultivated plants are treated with an active substance from the strobilurin class.
摘要翻译：一种用于控制作物植物有害真菌的方法具有修饰的某些有害真菌病原体抗性，其中所述作物植物与来自类嗜球果伞素的活性化合物处理。

7. 发明申请

WO1998008384A1 FUNGICIDAL MIXTURES 审中-公开
标题翻译：杀菌剂混合工
公开(公告)号：WO1998008384A1
公开(公告)日：1998-03-05
申请号：PCT/EP1997004540
申请日：1997-08-21
申请人： BASF AKTIENGESELLSCHAFT , MÜLLER, Bernd , SAUTER, Hubert , AMMERMANN, Eberhard , LORENZ, Gisela , STRATHMANN, Siegfried , SCHERER, Maria , SCHELBERGER, Klaus , LEYENDECKER, Joachim
发明人： BASF AKTIENGESELLSCHAFT
IPC分类号： A01N47/24
CPC分类号： A01N47/24 , A01N37/34 , A01N47/20 , A01N2300/00
摘要： The invention concerns a fungicidal mixture which contains in a synergistically effective amount: a) a carbamate of formula (I), in which X means CH and N, n stands for 0, 1 or 2 and R means halogen, C1-C4 alkyl and C1-C4 alkyl halide, wherein the R groups can be different when n stands for 2, one of its salts or adducts; and b) tetrachloroisophthalonitrile of formula (II).
摘要翻译：本发明涉及一种杀真菌混合物，其包含a）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卤代装置，其中基团R可以是不同的，如果n是2，或其盐或加合物，和b）含有式四氯（II）以协同有效量。

8. 发明申请

WO1997024317A1 IMINO OXYPHENYL ACETIC ACID DERIVATIVES, METHODS AND INTERMEDIATES FOR THEIR PREPARATION AND USE THEREOF 审中-公开
标题翻译： IMINOOXYPHENYLESSIGSÄUREDERIVATE，工艺和中间产品和使用
公开(公告)号：WO1997024317A1
公开(公告)日：1997-07-10
申请号：PCT/EP1996005642
申请日：1996-12-16
申请人： BASF AKTIENGESELLSCHAFT , GROTE, Thomas , SAUTER, Hubert , KIRSTGEN, Reinhard , BAYER, Herbert , MÜLLER, Ruth , MÜLLER, Bernd , OBERDORF, Klaus , GRAMMENOS, Wassilios , GÖTZ, Norbert , RACK, Michael , HARREUS, Albrecht , RÖHL, Franz , AMMERMANN, Eberhard , HARRIES, Volker , LORENZ, Gisela , STRATHMANN, Siegfried
发明人： BASF AKTIENGESELLSCHAFT
IPC分类号： C07C251/60
CPC分类号： C07C251/60 , C07C2601/10 , C07C2601/14
摘要： The invention relates to 2-imino oxyphenyl acetic acid derivatives of formula (I) in which the substituents and the index have the following meanings: R is C(CO2CH3)=NOCH3 (Ia), C(CONHCH3)=NOCH3 (Ib), C(CONH2)=NOCH3 (Ic), C(CO2CH3)=CHOCH3 (Id), or C(CO2CH3)=CHCH3 (Ie); R is cyano, nitro, halogen, alkyl, alkyl halide or alkoxy; m is 0,1 or 2; R is hydrogen, cyano, hydroxy, halogen, alkyl, alkyl halide, alkoxy alkyl, alkoxy, alkoxy halide, alkylthio, cyclopropyl, alkenyl, optionally substituted aryloxy alkyl, benzyl or benzyloxy; R is hydrogen, cyano, optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, heterocyclyl, aryl and hetaryl, optionally substituted alkoxy, alkenyloxy, alkinyloxy, cycloalkoxy, heterocyclyloxy, aryloxy and hetaryloxy, optionally substituted arylthio and hetarylthio; -Q-C(R )=N-Y -R or -Q-O-N=CR R ; R and R together with the carbon atom to which they are bound, are an optionally substituted four to eight-membered ring which can contain in addition to carbon atoms one or two oxygen atoms and/or sulphur atoms and/or NH- and/or N(C1-C4-alkyl)groups; wherein R and R are not simultaneously bound via heteroatoms to the carbon atom. The invention also relates to the salts of said derivatives, methods and intermediates for their preparation and use thereof.
摘要翻译：式（I），2-Iminooxyphenylessigsäurederivate其中取代基和指数具有以下含义：R t <1> C（CO 2 CH 3）= NOCH 3（Ia）中，C（CONHCH 3）= NOCH 3（Ib）中，C（CONH 2）= NOCH 3（Ic）中，C（CO2CH3）= CHOCH 3（同上）或C（CO2CH3）= CHCH3（IE）; [R <2>氰基，硝基，卤素，烷基，卤代烷基或烷氧基; m是0，1或2; [R <3>是氢，氰基，羟基，卤素，烷基，卤代烷基，烷氧基烷基，烷氧基，卤代烷氧基，烷硫基，环丙基，链烯基，未取代的或取代的。芳氧基烷基，苄基或苄氧基; [R <4>是氢，氰基，未取代的或取代的。烷基，烯基，炔基，环烷基，杂环基，芳基和杂芳基; 未取代的或取代的。烷氧基，烯氧基，炔氧基，环烷氧基，杂环氧基，芳氧基和杂芳氧基; 未取代的或取代的。芳和杂芳硫基; -Q-C（R <5>）= N-Y <1> -R <6>或-Q-O-N = CR <7> - [R <8>; [R <3>和R <4>的碳原子一起形成它们所连接的未取代或取代的。四到八位元环，其除了碳原子，一个或两个氧和/或硫原子和/或NH和/或N（C1-C4烷基）可以含有基团; 其中R <3>和R <4>不同时经由键合至的碳原子键合的杂原子; 和它们的盐，过程和它们的制备方法和它们的使用的中间体。

9. 发明申请

WO1997016427A1 PYRIDYLACETIC ACID DERIVATIVES, PROCESS AND INTERMEDIATE PRODUCTS FOR THEIR PREPARATION, AND THEIR USE 审中-公开
标题翻译： PYRIDYLESSIGSÄUREDERIVATE，工艺和中间产品和使用
公开(公告)号：WO1997016427A1
公开(公告)日：1997-05-09
申请号：PCT/EP1996004576
申请日：1996-10-22
申请人： BASF AKTIENGESELLSCHAFT , MÜLLER, Bernd , SAUTER, Hubert , BAYER, Herbert , GRAMMENOS, Wassilios , GROTE, Thomas , KIRSTGEN, Reinhard , OBERDORF, Klaus , RÖHL, Franz , GÖTZ, Norbert , RACK, Michael , MÜLLER, Ruth , LORENZ, Gisela , AMMERMANN, Eberhard , STRATHMANN, Siegfried , HARRIES, Volker
发明人： BASF AKTIENGESELLSCHAFT
IPC分类号： C07D213/54
CPC分类号： C07D213/56 , A01N43/40 , C07D213/55
摘要： The invention concerns pyridylacetic acid derivatives of formula (I) in which the substituents and the index have the following meanings: X is NOCH3, CHOCH3 and CHCH3; Y is oxygen or NR ; R is hydrogen or alkyl; R is cyano, nitro, trifluoromethyl, halogen, alkyl and alkoxy; m is 0, 1 or 2; R is hydrogen or alkyl; R and R , independently of each other, stand for hydrogen, cyano, nitro, hydroxy, amino, halogen, optionally substituted alkyl, alkoxy, alkylthio, alkylamino, dialkylamino, alkenyl, alkenyloxy, alkenylthio, alkenylamino, N-alkenyl-N-alkylamino, alkinyl, alkinyloxy, alkinylthio, alkinylamino, N-alkinyl-N-alkylamino, cycloalkyl, cycloalkyloxy, cycloalkylthio, cycloalkylamino, N-cycloalkyl-N-alkylamino, cycloalkenyl, cycloalkenyloxy, cycloalkenylthio, cycloalkenylamino, N-cycloalkenyl-N-alkylamino, heterocyclyl, heterocyclyloxy, heterocyclylthio, heterocyclylamino, N-heterocyclyl-N-alkylamino, aryl, aryloxy, arylthio, arylamino, N-aryl-N-alkylamino, hetaryl, hetaryloxy, hetarylthio, hetarylamino or N-hetaryl-N-alkylamino; R is one of the groups mentioned under R or a CR =NOR group. The invention further concerns their salts, a process and intermediate products for their preparation and their use.
摘要翻译：式（I），其中取代基和指数具有以下含义的Pyridylessigsäurederivate：X是NOCH 3，CHOCH 3和CHCH 3; Y是氧或NR ; ř 中氢或烷基; R是氰基，硝基，三氟甲基，卤素，烷基和烷氧基; m是0，1或2; [R <1>是氢或烷基; [R <2>和R <3>独立地是氢，氰基，硝基，羟基，氨基，卤素，未取代或取代的。烷基，烷氧基，烷硫基，烷基氨基，二烷基氨基，烯基，烯氧基，烯硫基，链烯基，N-链烯基 - N-烷基氨基，炔基，炔氧基，炔硫基，炔基氨基，N-炔基 - N-烷基氨基，环烷基，环烷基氧基，环烷硫基，环烷基氨基， N-环烷基N-烷基氨基，环烯基，环烯氧基，环烯硫基，cycloalkenylamino，N-环烯基-N-烷基氨基，杂环基，杂环氧基，杂环硫基，杂环基氨基，N-杂环基 - N-烷基氨基，芳基，芳氧基，芳硫基，芳基氨基，N- 芳基-N-烷基氨基，杂芳基，杂芳氧基，杂芳硫基，Hetarylamino，N-杂芳基的N-烷基氨基; [R <4>是在R中<2>基团提到的或基团CR一个 = NOR ; 和它们的盐，过程和它们的制备方法和它们的使用的中间体。

10. 发明申请

WO1997006678A1 FUNGICIDAL MIXTURES 审中-公开
标题翻译： OXIMETHERCARBONSÄUREAMIDS与吡咯衍生物杀菌剂MIXTURES
公开(公告)号：WO1997006678A1
公开(公告)日：1997-02-27
申请号：PCT/EP1996003358
申请日：1996-07-31
申请人： BASF AKTIENGESELLSCHAFT , SCHWALGE, Barbara , MÜLLER, Ruth , BAYER, Herbert , SAUTER, Hubert , SAUR, Reinhold , SCHELBERGER, Klaus , AMMERMANN, Eberhard , LORENZ, Gisela , STRATHMANN, Siegfried
发明人： BASF AKTIENGESELLSCHAFT
IPC分类号： A01N37/50
CPC分类号： A01N37/50 , A01N55/00 , A01N47/38 , A01N43/653 , A01N43/50 , A01N2300/00
摘要： A fungicidal mixture contains synergistically effective amounts of (a) an oximether carboxylic acid amide having the formula (I), in which R stands for hydrogen or halogen, and (b) an azol derivative (II) selected from the group of compounds II.1 to II.17, namely 1-(2 RS ,4 RS ;2 RS ,4 SR )-4-brom-2-(2,4-dichlorophenyl)tetrahydrofuryl)-1H-1,2,4-triazol (II.1), 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H,1,2,4-triazol-1-yl)-butan-2-ol (II.2), (+/-)-4-chloro-4-(4-methyl-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-2-yl)-phenyl-4-chlorophenylether (II.3); (E)-(R,S)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol (II.4); (Z)-2-(1H-1,2,4-triazol-1-ylmethyl)-2-(4-fluorophenyl)-3-(2-chlorophenyl)-oxirane (II.5); 4-(4-chlorophenyl)-2-phenyl-2-(1H-1,2,4-triazolylmethyl)-butyronitril (II.6); 3-(2,4-dichlorophenyl)-6-fluoro-2-(1H-1,2,4-triazol-1-yl)quinazolin-4-(3H)-one (II.7); bis(4-fluorophenyl)(methyl)(1H-1,2,4-triazol-1-yl-methyl)silane (II.8); (R,S)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)-hexan-2-ol (II.9); (1 RS ,5 RS ;1 RS ,5 RS )-5-(4-chlorobenzyl)-2,2-dimethyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol (II.10); N-propyl-N-(2-(2,4,6-trichlorophenoxy)ethyl)imidazol-1-carboxamide (II.11); (+/-)-1-(2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-yl-methyl)-1H-1,2,4-triazol (II.12); (R,S)-1-(4-chlorophenyl)-4,4-dimethyl-3-(1H,1,2,4-triazol-1-ylmethyl)-pentan-3-ol (II.13); (+/-)-2-(2,4-dichlorophenyl)-3-(1H-1,2,4-triazol-yl)-propyl-1,1,2,2-tetrafluorethylether (II.14); (E)-1-1(1-((4-chloro-2-(trifluoromethyl)-phenyl)imino)-2-propoxyethyl)-1H-imidazol (II.15); (RS)-2,4'-difluoro- alpha -(1H-1,2,4-triazol-1-ylmethyl)-benzyhdryl-alcohol (II.16); 2-p-chlorophenyl-2-(1H-1,2,4-triazol-1-ylmethyl)-hexanenitril (II.17).
摘要翻译：含有a）式（I），其中R代表氢或卤素的肟醚甲酰胺的杀真菌混合物，和b）从该组化合物中选择的吡咯衍生物II II.1到II.17：1 - [（2- RS ，4 RS 2 RS ，4 SR ） - 4-溴-2-（2,4-二氯苯基）四氢呋喃基〕-1H-1,2,4-三唑（II.1）; 2-（4-氯苯基）-3-环丙基-1-（1H-1,2,4-三唑-1-基） - 丁-2-醇（II.2）; （+/-） - 4-氯-4- [4-甲基-2-（1H-1,2,4-三唑-1-基甲基）-1,3-二氧戊环-2-基] - 苯基-4- 氯苯基醚（II.3）; （E） - （R，S）-1-（2,4-二氯苯基）-4,4-二甲基-2-（1H-1,2,4-三唑-1-基）戊-1-烯-3- 醇（II.4）; （Z）-2-（1H-1,2,4-三唑-1-基甲基）-2-（4-氟苯基）-3-（2-氯苯基） - 环氧乙烷（II.5）; 4-（4-氯苯基）-2-苯基-2-（1H-1,2,4-三唑基甲基）丁腈（II.6）; 3-（2,4-二氯苯基）-6-氟-2-（1H-1,2,4-三唑-1-基）喹唑啉-4（3H） - 酮（II.7）; 双（4-氟苯基）（甲基）（1H-1,2,4-三唑-1-基 - 甲基）硅烷（II.8）; （R，S）-2-（2,4-二氯苯基）-1-（1H-1,2,4-三唑-1-基） - 己-2-醇（II.9）; （1 RS 5 RS 1 RS 5 SR ） - 5-（4-氯苄基） - 2,2-二甲基-1-（1H-1,2,4-三唑-1-基甲基）环戊醇（II.10）; N-丙基-N- [2-（2,4,6-三氯苯氧基）乙基]咪唑-1-羧酰胺（II.11）; （+/-） - 1- [2-（2,4-二氯苯基）-4-丙基-1,3-二氧戊环-2-基 - 甲基] -1H-1,2,4-三唑（.12） ; （R，S）-1-（4-氯苯基）-4,4-二甲基-3-（1H-1,2,4-三唑-1-基甲基）戊烷-3-醇（二，13）; （+/-） - 2-（2,4-二氯苯基）-3-（1H-1,2,4-三唑基） - 丙基-1,1,2,2-四氟乙基醚（二.14）; 和（E）-1- [1 - [[4-氯-2-（三氟甲基]苯基]亚氨基] -2-丙氧基乙基] -1H-咪唑（II.15），（RS）-2,4' 二氟α - （1H-1,2,4-三唑-1-基甲基） - 二苯甲基醇（二，16）; 2-对氯苯基-2-（1H-1,2,4-三唑-1- 在协同有效量基甲基）-hexanenitril（二.17）。

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