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111. 发明授权

US4744817A Triazole derivatives 失效
标题翻译：三唑衍生物
公开(公告)号：US4744817A
公开(公告)日：1988-05-17
申请号：US835824
申请日：1986-03-03
申请人： Graham Holmwood , Karl H. Buchel , Paul Reinecke , Wilhelm Brandes , Gerd Hanssler
发明人： Graham Holmwood , Karl H. Buchel , Paul Reinecke , Wilhelm Brandes , Gerd Hanssler
IPC分类号： A01N43/653 , C07D249/08 , C07D521/00 , A61K31/41
CPC分类号： C07D231/12 , A01N43/653 , C07D233/56 , C07D249/08
摘要： Novel triazole of the formula ##STR1## in which R represents alkyl, cycloalkyl or the groupings ##STR2## wherein X.sup.1 represents hydrogen or halogen,X.sup.2 represents halogen,Y represents alkoxy, alkylthio, halogenoalkoxy, halogenoalkylthio, alkenyl, alkoxycarbonyl, cyano, optionally substituted phenyl, optionally substituted phenoxy, optionally substituted phenylthio, optionally substituted phenylalkoxy or optionally substituted phenylalkylthio andn represents the number 0, 1 or 2,Z represents halogen, alkyl, halogenoalkyl, halogenoalkoxy, halogenoalkylthio or phenyl andm represents the number 0, 1, 2, or 3,or addition products thereof with acids and metal salts, which exhibit fungicidal and plant growth-regulating activity.
摘要翻译：式中，R代表烷基，环烷基或基团的新型三唑，其中X 1代表氢或卤素，X 2代表卤素，Y代表烷氧基，烷硫基，卤代烷氧基，卤代烷硫基，烯基，烷氧基羰基，氰基，苯基，任选取代的苯氧基，任选取代的苯硫基，任选取代的苯基烷氧基或任选取代的苯基烷硫基，n表示数0,1或2，Z表示卤素，烷基，卤代烷基，卤代烷氧基，卤代烷硫基或苯基，m表示数， 2或3，或其与酸和金属盐的加成产物，其表现出杀真菌和植物生长调节活性。

112. 发明授权

US4740516A Substituted t-butanol fungicidal agents 失效
标题翻译：取代的叔丁醇杀真菌剂
公开(公告)号：US4740516A
公开(公告)日：1988-04-26
申请号：US826824
申请日：1986-02-06
申请人： Erik Regel , Karl H. Buchel , Paul Reinecke , Wilhelm Brandes
发明人： Erik Regel , Karl H. Buchel , Paul Reinecke , Wilhelm Brandes
IPC分类号： A01N31/14 , A01N31/00 , A01N31/02 , A01N33/04 , A01N33/08 , A01N43/48 , A01N43/50 , A01N43/56 , A01N43/64 , A01N43/653 , C07D249/08 , C07D303/22 , C07D303/24 , C07D303/34 , C07D303/36 , C07D521/00
CPC分类号： C07D303/22 , A01N43/50 , A01N43/56 , A01N43/653 , C07C323/00 , C07D231/12 , C07D233/56 , C07D249/08 , C07D303/24 , C07D303/34 , C07D303/36
摘要： A method of combating plant pathogenic fungi which comprises administering to such fungi or to a habitat thereof a plant pathogenic fungicidally effective amount of a substituted tert.-butanol derivative of the formula ##STR1## in which R.sup.1, R.sup.2 and R.sup.3 are identical or different and represent azolyl, optionally substituted phenoxy, optionally substituted phenylthio, alkylthio, alkenyl, alkinyl, optionally substituted phenylacetylenyl, alkylamino, dialkylamino, optionally substituted phenylamino, optionally substituted phenyl-N-alkyl-amino, optionally substituted cycloalkylamino, optionally substituted cycloalkyl-N-alkyl-amino, aminoethoxy, alkylaminoethoxy or dialkylaminoethoxy,or an acid addition salt or metal salt complex thereof.
摘要翻译：一种防治植物致病真菌的方法，其包括向所述真菌或其栖息地施用植物病原真菌有效量的式（I）的取代的叔丁醇衍生物，其中R 1，R 2和R 3相同任选取代的苯基乙酰基，烷基氨基，二烷基氨基，任选取代的苯基氨基，任选取代的苯基-N-烷基 - 氨基，任选取代的环烷基氨基，任选取代的环烷基 - N-烷基 - 氨基，氨基乙氧基，烷基氨基乙氧基或二烷基氨基乙氧基，或其酸加成盐或金属盐络合物。

113. 发明授权

US4728356A Novel substituted azolylvinyl ketones and carbinols as fungicides and plant growth regulators 失效
标题翻译：新型取代的唑基乙烯基酮和甲醇作为杀真菌剂和植物生长调节剂
公开(公告)号：US4728356A
公开(公告)日：1988-03-01
申请号：US754788
申请日：1985-07-12
申请人： Hans-Ludwig Elbe , Wolf Reiser , Erik Regel , Karl H. Buchel , Paul Reinecke , Wilhelm Brandes , Klaus Lurssen , Paul-Ernst Frohberger
发明人： Hans-Ludwig Elbe , Wolf Reiser , Erik Regel , Karl H. Buchel , Paul Reinecke , Wilhelm Brandes , Klaus Lurssen , Paul-Ernst Frohberger
IPC分类号： A01N43/50 , A01N43/653 , C07D233/60 , C07D249/08 , C07D521/00
CPC分类号： C07D231/12 , A01N43/50 , A01N43/653 , C07D233/56 , C07D249/08
摘要： A substituted azolylvinyl ketone or carbinol of the formula ##STR1## in which R.sup.1 represents optionally substituted cycloalkyl with 3 to 5 carbon atoms, substituted cyclohexyl or the grouping ##STR2## wherein R.sup.3 represents optionally substituted phenyl, alkenyl, alkinyl, cyano or the grouping --Z--R.sup.4,whereinR.sup.4 represents alkyl, halogenoalkyl, optionally substituted phenyl or optionally substituted phenylalkyl andZ represents O, S, SO or SO.sub.2,n represents a number from 0 to 2,R.sup.2 represents alkyl, alkenyl, alkinyl, in each case optionally substituted phenyl or phenylalkyl, or in each case optionally substituted cycloalkyl, cycloalkylalkyl, cycloalkenyl, cycloalkenylalkyl, bicycloalkyl or bicycloalkenyl, but R.sup.2 does not represent optionally substituted phenyl at the same time as R.sup.1 represents optionally substituted cycloalkyl with 3 to 5 carbon atoms or substituted cyclohexyl or R.sup.3 represents optionally substituted phenyl,X represents the CO or CH(OH) group andY represents a nitrogen atom or the CH group,or an addition product thereof with an acid or metal salt.The products are active in combating fungi and in regulating the growth of plants.
摘要翻译：其中R 1表示任选取代的具有3至5个碳原子的环烷基，取代的环己基或基团，其中R 3表示任选取代的苯基，烯基，炔基，氰基或基团 - Z-R4，其中R4代表烷基，卤代烷基，任选取代的苯基或任选取代的苯基烷基，Z代表O，S，SO或SO 2，n代表0至2的数，R 2代表烷基，烯基，炔基，取代的苯基或苯基烷基，或者在每种情况下都是任选取代的环烷基，环烷基烷基，环烯基，环烯基烷基，双环烷基或双环烯基，但R 2不同时代表任选取代的苯基，其中R 1表示任选取代的具有3至5个碳原子的环烷基或取代的环己基或R 3表示任选取代的苯基，X表示CO或CH（OH）基团，Y表示氮气 m或CH基团，或其与酸或金属盐的加成产物。该产品在防治真菌和调节植物生长方面发挥积极作用。

114. 发明授权

US4666933A (O-substituted oximino)-pyrazolin-5-one pesticides 失效
标题翻译：（O-取代的肟基） - 吡唑啉-5-酮农药
公开(公告)号：US4666933A
公开(公告)日：1987-05-19
申请号：US875129
申请日：1986-06-17
申请人： Klaus Jelich , Wolfgang Kramer , Wilhelm Brandes , Gerd Hanssler , Paul Reinecke
发明人： Klaus Jelich , Wolfgang Kramer , Wilhelm Brandes , Gerd Hanssler , Paul Reinecke
IPC分类号： A01N43/56 , C07D231/46 , C07D405/06 , C07D405/12
CPC分类号： C07D405/06 , A01N43/56 , C07D231/46 , C07D405/12
摘要： Fungicidally active substituted pyrazolin-5-ones of the formula ##STR1## in which R.sup.1 is hydrogen or alkyl,R.sup.2 is hydrogen, alkyl, alkenyl, alkinyl, cyanoalkyl, hydroxyalkyl, alkoxyalkyl, hydroxycarbonylalkyl or alkoxycarbonylalkyl, aminocarbonylalkyl, alkylaminocarbonylalkyl or dialkylaminocarbonylalkyl, or in each case optionally substituted oxiranylmethyl, aralkyl or aryl, andR.sup.3 is alkyl, alkenyl, alkinyl, cyanoalkyl, hydroxyalkyl, alkoxyalkyl, hydroxycarbonylalkyl, alkoxycarbonylalkyl, cycloalkyl or cycloalkylalkyl, or in each case optionally substituted aralkyl, aryloxyalkyl or arylthioalkyl, but wherein R.sup.3 is methyl or ethyl only if R.sup.1 and/or R.sup.2 is not hydrogen or methyl.
摘要翻译： R 1为氢或烷基，R 2为氢，烷基，烯基，炔基，氰基烷基，羟基烷基，烷氧基烷基，羟基羰基烷基或烷氧基羰基烷基，氨基羰基烷基，烷基氨基羰基烷基或二烷基氨基羰基烷基的芳香族活性取代的吡唑啉-5-酮每种情况下任选取代的环氧乙烷基甲基，芳烷基或芳基，R 3是烷基，烯基，炔基，氰基烷基，羟基烷基，烷氧基烷基，羟基羰基烷基，烷氧基羰基烷基，环烷基或环烷基烷基，或在每种情况下任选取代的芳烷基，芳氧基烷基或芳硫基烷基，或仅在R 1和/或R 2不是氢或甲基时为乙基。

115. 发明授权

US4659723A Substituted azolylalkyl pyridinyl ethers 失效
标题翻译：取代的吡唑基烷基吡啶基醚
公开(公告)号：US4659723A
公开(公告)日：1987-04-21
申请号：US798525
申请日：1985-11-15
申请人： Karl H. Buchel , Udo Kraatz , Jorg Stetter , Paul Reinecke , Wilhelm Brandes
发明人： Karl H. Buchel , Udo Kraatz , Jorg Stetter , Paul Reinecke , Wilhelm Brandes
IPC分类号： A01N43/50 , A01N43/653 , C07D233/60 , C07D249/08 , C07D401/12 , C07D521/00 , A01N43/40
CPC分类号： C07D231/12 , A01N43/50 , A01N43/653 , C07D233/56 , C07D249/08
摘要： Novel substituted azolylalkyl pyridinyl ethers of the formula ##STR1## in which Az represents 1,2,4-triazolyl or imidazolyl,B represents the keto or the CH(OH) group,Y represents halogen, alkyl, alkoxy, alkylthio, alkylsulphonyl, halogenoalkyl, nitro, cyano, alkoxycarbonyl or optionally substituted phenylR represents optionally substituted aryl or the groupings ##STR2## wherein R.sup.1 represents optionally substituted aryl,X.sup.1 represents halogen andX.sup.2 represents hydrogen and halogen, andn represents the numbers 0, 1, 2 and 3,and their acid addition salts and metal salt complexes, are outstandingly effective as fungicides.
摘要翻译：新颖的取代的吡咯基烷基吡啶基醚，其中Az代表1,2,4-三唑基或咪唑基，B代表酮基或CH（OH）基团，Y代表卤素，烷基，烷氧基，烷硫基，烷基磺酰基，卤代烷基，硝基，氰基，烷氧基羰基或任选取代的苯基R代表任选取代的芳基或其中R 1表示任选取代的芳基，X 1表示卤素，X 2表示氢和卤素，n表示数字0,1,2和3的基团和它们的酸加成盐和金属盐络合物作为杀真菌剂是非常有效的。

116. 发明授权

US4623653A Fungicidal compositions employing synergistic mixtures of a substituted 1-hydroxyethyl-triazole and triadimefon 失效
标题翻译：使用取代的1-羟乙基三唑和三唑酮的协同混合物的杀真菌组合物
公开(公告)号：US4623653A
公开(公告)日：1986-11-18
申请号：US644749
申请日：1984-08-27
申请人： Wilhelm Brandes , Gerd Hanssler , Paul Reinecke , Hans Scheinpflug , Graham Holmwood
发明人： Wilhelm Brandes , Gerd Hanssler , Paul Reinecke , Hans Scheinpflug , Graham Holmwood
IPC分类号： A01N47/04 , A01N35/08 , A01N37/00 , A01N43/653 , A01N43/66 , A01N43/78 , A01N43/80 , A01N43/84 , A01N43/90 , A01N47/02 , A01N47/14 , A01N47/18 , A01N47/30 , A01N47/32 , A01N47/38 , A01N47/44 , A01N55/02 , A01N57/14 , A01N59/02 , A01N43/64
CPC分类号： A01N47/14 , A01N43/653 , A01N43/66 , A01N47/02 , A01N47/32 , A01N59/02
摘要： Synergistic fungicidal compositions comprising(i) a substituted 1-hydroxyethyl-triazole of the formula ##STR1## in which R.sup.1, R.sup.2, X, Y and A have various meanings, or addition products thereof with acids or metal salts, and(ii) at least one of(A) wettable sulphur,(B) a polyhalogenoalkylthio derivative,(C) a quanidine derivative,(D) an aromatic acid lactone,(E) a dithiocarbamate,(F) a benzimidazole derivative,(G) an imidazole or triazole derivative,(H) a phosphoric acid ester,(I) a tetrahydroquinoline derivative,(J) an S, N-heterocyclic compound,(K) a urea derivative,(L) a sulphonamide derivative,(M) a polyhydroxyether derivative,(N) a triazine derivative,(O) a copper-hydroxy quinoline complex,(P) an N-formul derivative,(Q) a morpholine derivative,(R) a quinoxaline derivative, and(S) a dicarboxamide derivative.
摘要翻译：协同杀真菌组合物，其包含（i）式（Ⅰ）的取代的1-羟基乙基三唑，其中R1，R2，X，Y和A具有各种含义，或其与酸或金属盐的加成产物，和（ii）（A）可湿性硫，（B）多卤代烷硫基衍生物，（C）喹啉衍生物，（D）芳族酸内酯，（E）二硫代氨基甲酸酯，（F）苯并咪唑衍生物，（G）咪唑或三唑衍生物，（H）磷酸酯，（I）四氢喹啉衍生物，（J）S，N-杂环化合物，（K）脲衍生物，（L）磺酰胺衍生物，（M）聚羟基醚衍生物，（N）三嗪衍生物，（O）铜羟基喹啉络合物，（P）N-配位体衍生物，（Q）吗啉衍生物，（R）喹喔啉衍生物和（S）二甲酰胺衍生物。

117. 发明授权

US4568672A 3,6-Disubstituted 2-thioxo-1,3,5-thiadiazin-4-ones 失效
标题翻译： 3,6-二取代的2-硫代-1,3,5-噻二嗪-4-酮
公开(公告)号：US4568672A
公开(公告)日：1986-02-04
申请号：US644732
申请日：1984-08-27
申请人： Wilhelm Brandes , Rolf Bunnenberg , Gerd Hanssler , Paul Reinecke , Karlfried Wedemeyer
发明人： Wilhelm Brandes , Rolf Bunnenberg , Gerd Hanssler , Paul Reinecke , Karlfried Wedemeyer
IPC分类号： A01N43/88 , C07D285/34 , C07D319/00 , C07D417/12
CPC分类号： C07D417/12 , A01N43/88 , C07D285/34
摘要： 3,6-Disubstituted 2-thioxo-1,3,5-thiadiazin-4-ones of the formula ##STR1## in which R.sup.1 represents hydrogen; alkyl which is optionally monosubstituted or polysubstituted by identical or different substituents; alkenyl which is optionally monosubstituted or polysubstituted by identical or different substituents; alkinyl which is optionally monosubstituted or polysubstituted; cycloalkenyl or cycloalkyl which is optionally monosubstituted or polysubstituted by identical or different substituents; aryl or aralkyl which is optionally monosubstituted or polysubstituted by identical or different substituents; or a heterocyclic structure which is monosubstituted or polysubstituted by identical or different substituents;R.sup.2 represents alkenyl or alkyl which is optionally monosubstituted or polysubstituted by identical or different substituents; cycloalkenyl or cycloalkyl which is optionally monosubstituted or polysubstituted by identical or different substituents; aralkyl which is optionally monosubstituted or polysubstituted by identical or different substituents; or the fluorenyl radical; and X represents oxygen or sulphur.which possess fungicidal activity.
摘要翻译：具有式“IMAGE”的3,6-二取代的2-硫代-1,3,5-噻二嗪-4-酮，其中R 1表示氢; 任选被相同或不同取代基单取代或多取代的烷基; 任选被相同或不同取代基单取代或多取代的烯基; 任选单取代或多取代的炔基; 任选被相同或不同取代基单取代或多取代的环烯基或环烷基; 任选被相同或不同取代基单取代或多取代的芳基或芳烷基; 或被相同或不同取代基单取代或多取代的杂环结构; R 2表示任选被相同或不同取代基单取代或多取代的烯基或烷基; 任选被相同或不同取代基单取代或多取代的环烯基或环烷基; 任选被相同或不同取代基单取代或多取代的芳烷基; 或芴基; X表示氧或硫。具有杀菌活性。

118. 发明授权

US4563447A Combating fungi with 4-piperidino methyl-1,3-dioxolanes 失效
标题翻译：用4-哌啶子基甲基-1,3-二氧戊环杀灭真菌
公开(公告)号：US4563447A
公开(公告)日：1986-01-07
申请号：US630487
申请日：1984-07-13
申请人： Wolfgang Kramer , Joachim Weissmuller , Dieter Berg , Paul Reinecke , Gerd Hanssler , Wilhelm Brandes
发明人： Wolfgang Kramer , Joachim Weissmuller , Dieter Berg , Paul Reinecke , Gerd Hanssler , Wilhelm Brandes
IPC分类号： A01N43/40 , C07D317/00 , C07D317/16 , C07D317/28 , C07D405/06 , C07D405/14
CPC分类号： C07D405/06 , A01N43/40 , C07D317/16 , C07D317/28 , C07D405/14
摘要： Substituted 4-piperidinomethyl-1,3-dioxolanes of the formula ##STR1## in which R.sup.1 is tetrahydronaphthyl, decahydronaphthyl, optionally substituted naphthyl, optionally substituted cycloalkyl or cycloalkenyl, optionally substituted phenyl, or alkyl which is substituted by in each case optionally substituted phenyl, phenoxy, phenylthio, cyclohexyl, cyclohexyloxy or cyclohexylthio,R.sup.2 is hydrogen or methyl,R.sup.3 is hydrogen or an acyl radicalor plant-tolerated addition products thereof with acids or metal salts, which possess fungicidal activity.
摘要翻译：取代的式“IMAGE”的4-哌啶甲基-1,3-二氧戊烷，其中R 1是四氢萘基，十氢萘基，任选取代的萘基，任选取代的环烷基或环烯基，任选取代的苯基或被各种情况下被取代的任选取代的苯基，苯氧基，苯硫基，环己基，环己氧基或环己基硫基，R2是氢或甲基，R3是氢或具有杀真菌活性的酸或其盐的酰基或植物耐受的加成产物。

119. 发明授权

US4562198A Combating fungi with substituted azolyl-tetrahydro-furan-2-ylidene-methane derivatives 失效
标题翻译：用真空灭菌与取代的吡唑并四氢呋喃-2-亚基甲烷衍生物
公开(公告)号：US4562198A
公开(公告)日：1985-12-31
申请号：US658344
申请日：1984-10-05
申请人： Hans-Ludwig Elbe , Manfred Jautelat , Karl H. Buchel , Wilhelm Brandes , Gerd Hanssler , Paul Reinecke
发明人： Hans-Ludwig Elbe , Manfred Jautelat , Karl H. Buchel , Wilhelm Brandes , Gerd Hanssler , Paul Reinecke
IPC分类号： A01N43/50 , A01N43/64 , A01N43/653 , C07C17/00 , C07C17/278 , C07C45/00 , C07C45/59 , C07C45/63 , C07C45/71 , C07C49/16 , C07C49/175 , C07C67/00 , C07C313/00 , C07C323/22 , C07D233/60 , C07D249/08 , C07D307/28 , C07D405/06 , C07D521/00 , C07F1/08 , C07F3/02 , C07F3/06 , C07F13/00 , C07F15/02 , C07F15/04
CPC分类号： C07D231/12 , A01N43/50 , A01N43/653 , C07C17/00 , C07C17/278 , C07C323/00 , C07C45/59 , C07C45/63 , C07C45/71 , C07C49/16 , C07D233/56 , C07D249/08 , C07D307/28
摘要： Azolyl-tetrahydrofuran-2-ylidene-methanes of the formula ##STR1## in which A represents a nitrogen atom or the CH group;X represents oxygen, sulphur or the SO or SO.sub.2 group;R represents optionally substituted aryl;R.sup.1 and R.sup.6 are identical or different and represent hydrogen, alkyl, halogenoalkyl or halogen, a maximum of up to 3 substituents representing halogen or halogenoalkyl, with the proviso that R.sup.1 and R.sup.2 are not at the same time methyl if X represents oxygen;R.sup.1 and R.sup.2, together with the carbon atom to which they are bonded, represent optionally substituted cycloalkyl orR.sup.2 and R.sup.3, together with the carbon atoms to which they are bonded, represent optionally substituted cycloalkyl,or addition products thereof with acids or metal salts. Some new intermediates are also shown. The end products are fungicides.
摘要翻译：其中A表示氮原子或CH基团的式（I）的唑基 - 四氢呋喃-2-亚基 - 甲烷; X表示氧，硫或SO或SO2基团; R代表任选取代的芳基; R1和R6相同或不同，代表氢，烷基，卤代烷基或卤素，最多可含3个代表卤素或卤代烷基的取代基，条件是如果X表示氧，则R1和R2不同时为甲基; R 1和R 2与它们所键合的碳原子一起代表任选取代的环烷基或R 2和R 3与它们所键合的碳原子一起代表任选取代的环烷基，或其与酸或金属盐的加成产物。还显示了一些新的中间体。最终产品是杀真菌剂。

120. 发明授权

US5240952A Fungicidal agents 失效
标题翻译：杀真菌剂
公开(公告)号：US5240952A
公开(公告)日：1993-08-31
申请号：US885417
申请日：1992-05-19
申请人： Wilhelm Brandes , Gerd Hanssler , Paul Reinecke , Hans Scheinpflug , Graham Holmwood
发明人： Wilhelm Brandes , Gerd Hanssler , Paul Reinecke , Hans Scheinpflug , Graham Holmwood
IPC分类号： A01N43/653 , A01N43/66 , A01N59/02 , C07D521/00
CPC分类号： C07D249/08 , A01N43/653 , A01N43/66 , A01N59/02 , C07D231/12 , C07D233/56
摘要： A fungicidal composition comprising a fungicidally effective amount of (i) a substituted 1-hydroxyethyl-triazole of the formula ##STR1## in which A is --CH.sub.2 CH.sub.2 -- or --CH.dbd.CH--,or an addition product thereof with an acid or metal salt, and (ii) at least one member selected from the group consisting ofA) wettable sulphur,B) a polyhalogenoalkylthio derivative,C) a guanidine derivative,D) an aromatic carboxylic acid derivative,E) a dithocarbamate,F) a benzimidazole derivative,G) an imidazole or triazole derivative,H) a phosphoric acid ester,I) a tetrahydroquinoline derivative,J) an S,N-heterocyclene compound,K) a urea derivative,L) a sulphonamide derivative,M) a polyhydroxy ether derivative,N) a triazine derivative,O) a copper complex salt,P) an N-formyl derivative,Q) a morpholine derivative,R) a quinoxaline derivative, andS) a dicarboximide derivative.
摘要翻译：一种杀真菌组合物，其包含杀真菌有效量的（i）其中A是-CH 2 CH 2 - 或-CH = CH-的式“IMAGE”的取代的1-羟乙基三唑或其与酸或金属盐的加成产物，和（ii）至少一种选自A）可湿性硫，B）多卤代烷硫基衍生物，C）胍衍生物，D）芳族羧酸衍生物，E）二氨基甲酸酯，F）苯并咪唑衍生物，G）咪唑或三唑衍生物，H）磷酸酯，I）四氢喹啉衍生物，J）S，N-杂环烯化合物，K）脲衍生物，L）磺酰胺衍生物，M）多羟基醚衍生物，N）三嗪衍生物，O）铜络合盐，P）N-甲酰基衍生物，Q）吗啉衍生物，R）喹喔啉衍生物和S）二羧酰亚胺衍生物。

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