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1. 发明申请

WO1997010716A1 HARMFUL FUNGI CONTROL WITH AN ACTIVE SUBSTANCE INHIBITING RESPIRATION BY INHIBITING THE CYTOCHROME COMPLEX III, COMBINED WITH AN AMIDE 审中-公开
标题翻译：与一个呼吸AM细胞色素复合物III抑制剂与A中的组合AMID有害蘑菇阵法
公开(公告)号：WO1997010716A1
公开(公告)日：1997-03-27
申请号：PCT/EP1996004151
申请日：1996-09-23
申请人： BASF AKTIENGESELLSCHAFT , BAYER, Herbert , SAUTER, Hubert , KÖHLE, Harald , RETZLAFF, Günter , AMMERMANN, Eberhard , LORENZ, Gisela , STRATHMANN, Siegfried , EICKEN, Karl
发明人： BASF AKTIENGESELLSCHAFT
IPC分类号： A01N61/00
CPC分类号： A01N43/40 , A01N61/00 , A01N37/50 , A01N2300/00
摘要： The invention pertains to agents intended for use against harmful fungi and containing as active substances at least one compound which inhibits respiration by inhibiting the cytochrome complex III, and at least one amide compound of formula (II) A-CO-NR R in which A, R and R have the meanings indicated in the description. The proposed agents are especially suitable for use against Botrytis.
摘要翻译：本发明涉及组合物，用于控制其包含作为活性成分的至少一种化合物，其抑制对细胞色素复合物III呼吸有害真菌，和式中的至少一种酰胺化合物（II）A-CO-NR <1> [R <2>，其中A，R <1>和R <2>具有说明书中给出的含义。本发明的组合物可用于灰霉病的控制特别有用的。

2. 发明申请

WO1997011606A1 COMBATTING PARASITIC FUNGI WITH A COMBINATION OF AN ACTIVE AGENT INHIBITING RESPIRATION IN THE CYTOCHROME COMPLEX III AND OF FENAZAQUINE 审中-公开
标题翻译：与一个呼吸AM细胞色素复合物的组合有害蘑菇阵法III-抑制与喹螨醚剂
公开(公告)号：WO1997011606A1
公开(公告)日：1997-04-03
申请号：PCT/EP1996004013
申请日：1996-09-12
申请人： BASF AKTIENGESELLSCHAFT , BAYER, Herbert , SAUTER, Hubert , AMMERMANN, Eberhard , LORENZ, Gisela , STRATHMANN, Siegfried , KÖHLE, Harald , RETZLAFF, Günter
发明人： BASF AKTIENGESELLSCHAFT
IPC分类号： A01N43/54
CPC分类号： A01N43/54 , A01N61/00 , A01N43/56 , A01N37/50 , A01N2300/00
摘要： The present invention relates to means for combatting parasitic fungi, containing as the active agents at least one compound which prevents respiration in the cytochrome complex III and fenazaquine. The means of the invention may be used in particular in combatting botrytis.
摘要翻译：本发明涉及组合物，用于控制其包含作为活性成分的至少一种化合物，其抑制对细胞色素复合物III，以及喹螨醚呼吸有害真菌。本发明的组合物可用于灰霉病的控制特别有用的。

3. 发明申请

WO1997039630A1 PROCESS AND AGENTS FOR CONTROLLING HARMFUL FUNGI 审中-公开
标题翻译：手段与方法防治有害真菌
公开(公告)号：WO1997039630A1
公开(公告)日：1997-10-30
申请号：PCT/EP1997002037
申请日：1997-04-22
申请人： BASF AKTIENGESELLSCHAFT , EICKEN, Karl , AMMERMANN, Eberhard , STRATHMANN, Siegfried , LORENZ, Gisela , KÖHLE, Harald , RETZLAFF, Günter
发明人： BASF AKTIENGESELLSCHAFT
IPC分类号： A01N43/58
CPC分类号： A01N43/56 , A01N43/58 , A01N61/00 , A01N43/78 , A01N43/76 , A01N43/40 , A01N43/32 , A01N43/16 , A01N43/08 , A01N37/22 , A01N37/18 , A01N2300/00
摘要： Agents for controlling harmful fungi contain in a solid or liquid carrier pyridabene of formula (a), fenpyroxymate of formula (b) or tebufenpyrade of formula (c), and at least one amide compound of formula (I) A-CO-NR R , in which the substituents have the meanings given in the description. Also disclosed are processes for controlling harmful fungi by using said agents.
摘要翻译：本发明涉及一种药剂防治有害真菌，其在式（a）或式Fenpyroxymat（b）或式（c）和式（I）的至少一种酰胺化合物的吡螨胺A-CO的固体或液体载体哒 NR <1> [R <2>包括，其中取代基具有本说明书中给出的含义，和用于控制使用这些试剂有害真菌的方法。

4. 发明申请

WO1997039628A1 PROCESS AND AGENTS FOR CONTROLLING HARMFUL FUNGI 审中-公开
标题翻译：手段与方法防治有害真菌
公开(公告)号：WO1997039628A1
公开(公告)日：1997-10-30
申请号：PCT/EP1997002036
申请日：1997-04-22
申请人： BASF AKTIENGESELLSCHAFT , WAGNER, Oliver , EICKEN, Karl , AMMERMANN, Eberhard , LORENZ, Gisela , STRATHMANN, Siegfried , KÖHLE, Harald , RETZLAFF, Günter
发明人： BASF AKTIENGESELLSCHAFT
IPC分类号： A01N37/24
CPC分类号： A01N37/24 , A01N43/78 , A01N43/76 , A01N43/56 , A01N43/40 , A01N43/32 , A01N43/16 , A01N43/08 , A01N37/22 , A01N37/18 , A01N2300/00
摘要： Agents for controlling harmful fungi contain in a solid or liquid carrier: (a) at least one p-hydroxyaniline derivative of formula (I); and (b) at least one amide compound of formula (II) A - CO - NR - R , in which the substituents have the meanings given in the description. Also disclosed are processes for controlling harmful fungi by means of such agents.
摘要翻译：本发明涉及组合物在防治有害真菌，包含在固体或液体载体中的式（I a）的至少一个p-羟基苯胺衍生物），b）式中的至少一种酰胺化合物（II）：A - CO - NR <8> - [R <9>，其中取代基如说明书中所定义; 和用于控制使用这种组合物有害真菌的方法。

5. 发明申请

WO1997008952A1 FUNGICIDAL AGENTS AND METHOD 审中-公开
标题翻译：手段与方法防治有害真菌
公开(公告)号：WO1997008952A1
公开(公告)日：1997-03-13
申请号：PCT/EP1996003861
申请日：1996-09-03
申请人： BASF AKTIENGESELLSCHAFT , EICKEN, Karl , KÖHLE, Harald , RETZLAFF, Günter , AMMERMANN, Eberhard , LORENZ, Gisela , STRATHMANN, Siegfried
发明人： BASF AKTIENGESELLSCHAFT
IPC分类号： A01N43/54
CPC分类号： A01N43/54 , A01N43/78 , A01N43/76 , A01N43/56 , A01N43/40 , A01N43/32 , A01N43/18 , A01N43/16 , A01N43/10 , A01N43/08 , A01N2300/00
摘要： The invention concerns fungicidal agents which contain as active substances fenazaquine and at least one amide compound of formula (I), A - CO - NR R , in which A, R and R have the meanings given in the description. The agents according to the invention can be used in particular against botrytis.
摘要翻译：本发明涉及组合物在防治有害真菌，作为活性成分，喹螨醚和式（I）的至少一种酰胺化合物A - CO - NR <1> [R <2>包含其中A，R <1>和R <2>中，具有说明书中给出的含义。本发明的组合物可用于灰霉病的控制特别有用的。

6. 发明申请

WO1996003047A1 METHOD OF COMBATING HARMFUL FUNGI 审中-公开
标题翻译：方法防治有害真菌
公开(公告)号：WO1996003047A1
公开(公告)日：1996-02-08
申请号：PCT/EP1995002744
申请日：1995-07-13
申请人： BASF AKTIENGESELLSCHAFT , KÖHLE, Harald , AMMERMANN, Eberhard , LORENZ, Gisela , RÖHL, Franz , BAYER, Herbert , SAUTER, Hubert , EICKEN, Karl
发明人： BASF AKTIENGESELLSCHAFT
IPC分类号： A01N61/00
CPC分类号： A01N37/50 , A01N47/20 , A01N61/00 , A01N43/78 , A01N43/40 , A01N43/32 , A01N43/14 , A01N43/08 , A01N37/40 , A01N37/28 , A01N37/22 , A01N2300/00
摘要： The invention concerns a method of combating harmful fungi which is characterized in that the fungi, their biosphere or the materials, plants, seeds, soils, surfaces or areas to be protected from fungal infection are treated simultaneously together or separately or successively with an active substance I which inhibits the respiration of cytochrome complex III and a) with an active substance of formula IIA, R -CO-NR -OR , in which the substituents have the following meanings: R is hydrogen, alkyl, alkenyl or alkynyl, cycloalkyl or cycloalkenyl, optionally substituted aryl, hetaryl, heterocyclyl, arylcarbonyl or hetarylcarbonyl, R , R designate hydrogen, alkyl or aryl, or b) with an active substance of formula IIB, R -CO-NR -R , in which the substituents have the following meanings: R is optionally substituted phenyl, furyl, dihydropyranyl, oxathi-inyl, oxathi-inyl dioxide, pyridyl or thiazolyl; R is hydrogen, alkyl or alkoxy; R is optionally substituted phenyl or cyclohexyl, and mixtures suitable therefor.
摘要翻译：一种用于防治有害真菌的方法，其特征在于所述真菌，其栖息地或从真菌侵染同时或单独处理要保护的材料，植物，种子，土壤，区域或空间或依次与活性成分（I）时，呼吸的细胞色素复合物（III）抑制，并且a）将式的化合物（IIA）R <1> -CO-NR <2> -OR <3>处理，其中取代基具有以下含义：R t <1>是氢烷基，烯基或炔基，环烷基或环烯基，未取代的或取代的。芳基，杂芳基，杂环基，芳基羰基或hetarylcarbonyl，R <2>，R <3>是氢，烷基或芳基，或（b）式的化合物IIB）R -CO-NR的 [R 处理，其中取代基具有以下含义：R t 中未取代的或取代的。苯基，呋喃基，二氢吡喃基，oxathiinyl，Oxathiinyldioxid，吡啶基或噻唑基; [R 是氢，烷基或烷氧基; [R 未取代的或取代的。苯基或环己基，以及它们的混合物适用于该目的。

7. 发明申请

WO1998008386A1 AGENTS FOR CONTROLLING HARMFUL FUNGI 审中-公开
标题翻译：用于控制有害真菌
公开(公告)号：WO1998008386A1
公开(公告)日：1998-03-05
申请号：PCT/EP1997004679
申请日：1997-08-27
申请人： BASF AKTIENGESELLSCHAFT , MÜLLER, Ruth , BAYER, Herbert , SAUTER, Hubert , EICKEN, Karl , WETTERICH, Frank , AMMERMANN, Eberhard , LORENZ, Gisela , STRATHMANN, Siegfried , SCHERER, Maria , SCHELBERGER, Klaus , MÜLLER, Bernd , LEYENDECKER, Joachim
发明人： BASF AKTIENGESELLSCHAFT
IPC分类号： A01N47/24
CPC分类号： A01N47/12 , A01N47/24 , A01N37/52 , A01N2300/00
摘要： Agents for controlling harmful fungi contain in a solid or liquid carrier (a) at least one compound of formula (I), in which M and M have different meanings, and (b) at least one valine amide of formula (II), in which R stands for C3-C4-alkyl and R stands for naphthyl or phenyl, the phenyl radical being substituted at position 4 by a halogen atom, a C1-C4-alkyl or C1-C4-alkoxy group. Also disclosed is a process for controlling harmful fungi by using these agents.
摘要翻译：本发明涉及一种药剂防治有害真菌，含有固体或液体载体中的）式（I中的至少一种化合物），其中M <1>和M <2>具有不同的含义，以及b）式中的至少一个缬氨酰胺（ II）其中R <1>是C3-C4烷基，并且R <2>为萘基或苯基的装置，其中所述苯基在4-位被卤素原子取代的C1-C4烷基或C1-C4烷氧基是; 和控制使用这些药物有害真菌的方法。

8. 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。

9. 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。

10. 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。

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