TW200814931A - Active compound combinations having insecticidal and acaricidal properties - Google Patents
Active compound combinations having insecticidal and acaricidal properties Download PDFInfo
- Publication number
- TW200814931A TW200814931A TW096121633A TW96121633A TW200814931A TW 200814931 A TW200814931 A TW 200814931A TW 096121633 A TW096121633 A TW 096121633A TW 96121633 A TW96121633 A TW 96121633A TW 200814931 A TW200814931 A TW 200814931A
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- Prior art keywords
- alkyl
- group
- alkoxy
- halogen
- substituted
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- A01N63/00—Biocides, pest repellants or attractants, or plant growth regulators containing microorganisms, viruses, microbial fungi, animals or substances produced by, or obtained from, microorganisms, viruses, microbial fungi or animals, e.g. enzymes or fermentates
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- A—HUMAN NECESSITIES
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- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
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Description
200814931 九、發明說明: 【發明所屬之技術領域】 本發明係關於新穎的活性化合物組合,其包括,第一, 已知的環狀酮烯醇類及,第二,有益的物種(天敵),該組合 5 極適於控制動物害蟲,例如,昆蟲及/或不想要的蟎類。 【先前技術】
10
已知某些環狀酮烯醇類具有殺昆蟲及殺蟎的特性氏?-八-528 156) 〇 WO 95/01971、EP-A_647 637、WO 96/1606卜 WO 96/20196、WO 96/25395、WO 96/35664、WO 97/02243、WO 97/01535、WO 97/36868、WO 97/43275、
WO 98/05638 、WO 98/06721 、WO 99/16748 、 WO 99/43649 > WO 99/48869 > WO 99/55673 > WO 00/42850 > WO 01/17972、WO 01/23354、WO 01/74770、WO 03/013249、WO 04/024688、WO 04/080962、WO 15 04/1 1 1042 、WO 05/092897、WO 06/000355 、WO 06/002824及WO 06/029799說明具有殺昆蟲及/或殺蟎特性 之其他酮烯醇類。此等物質之活性很好;然而,在低施用 率時有時並不令人滿意。 此外已知許多有益的物種被用於控制昆蟲及蜘蛛蟎類: 2〇 「認識與了解」;M.H.馬雷斯,W.J·拉芬伯格,由B,V,古 柏特出版,利德商業資訊(2003)。然而,有益物種本身之使 用上並非全然令人滿意。 【發明内容】 現今業已發現式(I)化合物 200814931
5其中,. X代表Q-C6-院基、_素、Cl_c6_院氧基或Ci_C3_a 烷基, φ Y代表氫、CVC6·炫基、齒素、Ci_c6•烧氧基或Ci_c3_幽 素烷基, 10 Z 代表C1_C6-烷基、鹵素或0卜(:6-烷氧基, η 代表數字0-3, Α代表氫或於各情況中任意地被齒素所取代之直鏈或分 支 cvc12-烧基、c3-c8-稀基、c3-C8-快基、c”Ci〇一院 氧基-C2-CV烧基、crc8-多院氧&_C2_C8_院基、 15 C1(^院基硫基-C2-C8·烧基或具有3-8個環原子之環院 φ 4 ’其可被氧及/或硫所插入,,及於各情況中任意地被 鹵素-、CpC6-烧基-、Ci-cv ii素烧基-、c卜cv炫氧 基-、CrCy鹵素烷氧基-或硝基_所取代之笨基或笨基_ Ci-C6-烧基, 20 B代表氫、Ci-C6-院基或Ci-C6-烧氧基-C2-C4-燒基, 或其中 i A及B與其等所連接之碳原子一起形成飽和或不飽和之3一 至8-員環,其任意地被氧及/或硫所挿入且任意地被齒 素、ci_c6-燒基、c〗-c6-院氧基、Ci-C4-_素院基、Ci_ 200814931 C^ii素烧氧基、Ci_C^烷基硫基或經任意取代之笨基 所取代或任意地經苯并-稠和, G代表氫(a)或代表基團
10 其中, R1代表於各情況中任意地被鹵素-所取代之c卜c2〇-烷 基、c2-c20-烯基、d-CV烷氧基-CrCV烷基、cr C8-烧基硫基-C2-C8-炫基、C1-C8-多烧氧基-C2-C8-燒基或具有3-8個環原子之環烷基,其可被氧及/或 15 硫原子所挿入, 代表任意地被鹵素-、硝基·、crc6-烷基-、Cpcv 着 烧氧基-、CVC6-鹵素烷基-或Crc6-鹵素烷氧基-所 取代之苯基, 代表任意地被ii素-、cvcv烷基-、crc6-烷氧基_ 2〇 、Ci-C6_鹵素烧基-或c〗-C6·鹵素烧氧基-所取代之 笨基-cvcv烷基, 代表於各情況中任意地被鹵素-及/或crc6-烷基-所 取代之吡啶基、嘧啶基、噻唑基或吡唑基, 代表任意地被鹵素-及/或CrC6_烷基_所取代之苯氧 200814931 基-q-cv院基, 2 R 代表於各情況中任意地被鹵素-所取代之Crc20-烷 基、c2-c20-烯基、crc8·烷氧基-C2-C8-烷基或CV C8-多烷氧基-C2-C8-烧基, 代表於各情況中任意地被鹵素·、硝基-、d-Cy烷 基-、C〗-C6-烧氧基-或Ci-C6-_素烧基-所取代之苯 基或节基, 3 R 代表任意地被_素-所取代之烷基,代表於各 情況中任意地被Crc4-烷基-、鹵素-、鹵素 烷基_、Ci-C4-烷氧基-、CrC4_鹵素烷氧基-、硝基-或氰基-所取代之苯基或苄基, R4及R5各自獨立代表於各情況中任意地被鹵素_所取 代之CrC8-烷基、CrCr烷氧基、CrCV烷基胺 基、二-(c〗-c8)-烷基胺基、cvcv烷基硫基、c2-C5-稀基硫基、C2-C5-快基硫基或C3-C7-環烧基硫 基,代表於各情況中任意地被鹵素-、硝基-、氰基一 、C1-C4-烧乳基-、C1-C4-鹵素烧氧基-、C1-C4-烧基 硫基-、C1-C4-鹵素烧基硫基-、C1-C4-烧基-或C!” c4-鹵素烷基-所取代之苯基、苯氧基或苯基硫基, R6及R7各自獨立代表於各情況中任意地被鹵素-所取 代之CpCw烷基、crc10-烷氧基、c3-c8-烯基或 Ci_Cg-烧氧基烧基,代表任意地被鹵素-、 Ci-cv鹵素烧基-、Ci-C6-统基-或cvcv烧氧基-所 取代之苯基,代表任意地被鹵素-、C1-C6-烧基-、 200814931
Ci-C6_鹵素烷基-或烷氧基-所取代之苄基或 起代表5-至6-員%其任意地被氧或硫所掃入且其 可任意地被CrC6-烷基所取代, 與來自於蜘蛛目、蜱蟎亞綱、膜翅目、鞘翅目、脈翅目、 5缕翅目(Tysan〇Ptera)、異翅亞目、雙翅目、半翅目、革翅 目及寄蟎目之目或亞目的有益物種合併時具有極佳的殺昆 蟲及/或殺蟎特性。 ⑩ 令人驚奇地,根據本發明之活性化合物/有益物種組合 之殺昆蟲及/或殺蟎活性比個別活性化合物及單獨使用有益 10物種時之活性好。呈現不可預見的增強活性。 凰 再者,業已發現的是使用根據本發明之活性化合物/有 益物種組合可取代毒物學上及/或生態學上較不利之活性化 合物的施用而達到相當的活性,其對於使用者及/或環境安 全上尤其有利。此外,業已發現可減少喷霧施用。除了至 15 ^一種式(1)之活性化合物外,根據本發明之活性化合物/有 凰物種組合包括至少一種來自前文提及之目或亞目的有益 物種。 車乂佳者係使用活性化合物/有益物種組合其包括式⑴化 合物,其中基團係定義如下: 20 X且代表q-cv烷基、鹵素、d-cv烷氧基或c卜c2-鹵素 烷基, Μ Υ且代表氫、CVC4-烷基、鹵素、烷氧基或CKC2-鹵素燒基, z且代表CrQ-烧基、鹵素或crC4-烧氧基, 200814931 η 宜代表0或1, Α及Β與其等所連接之碳原子一起宜代表飽和之5-至6-員 環,其任意地被CrCzr烷基或CrC4-烷氧基所取代, G 宜代表氫(a)或代表基團 5 —CO—R1 (b) ^^0—R2 ⑹ 其中,
10 15
R1代表於各情況中任意地被鹵素-所取代之CrC16-烷 基、C2-C16-烯基、CrC6-烷氧基-C2-CV烷基-或具 有3至7個環原子之環烷基,其可被1至2個氧及/ 或硫原子所掃入’代表任意地被鹵素-、硝基-、Cl~ C4-烧基-、C1-C4"·烧氧基-、C1-C3-鹵素烧基-或C 1 ~ C3-鹵素烧氧基-所取代之苯基, R2代表於各情況中任意地被鹵素-所取代之CrC16-烷 基、c2-c16-烯基或CrC6-烷氧基-c2-c6-烷基, 代表於各情況中任意地被鹵素…硝基-、crc4-烷基-、 CrC4-烷氧基-或CrC4-鹵素烷基-所取代之苯基或苄 基。 特別佳者係使用活性化合物/有益物種組合其包括式(I-20 b-Ι)之二氫吱喃酮(dihydrofuranone)衍生物。
200814931 此外’活性化合物/有益物種組合亦可包括其他適當殺 真菌、殺滿或殺昆蟲活性添加的組成份。 較佳者係使用有益物種其來自胡蜂科、日光蜂科、紋翅 卵蜂科、跳小蜂科、纓小蜂科、姫小蜂科、亞洛西蜂科 5 (Alloxystidae)、黃蜂科(Megaspilidae)、小繭蜂科、花螢 科、瓢蟲科、郭公蟲科、草玲科、褐岭科、花墙科、盲虫春 科、球螋科、植綏蟎科、步行蟲科、隱翅蟲科、姬蜂科、 馨财繭蜂科、蜾藏科、細腰蜂科、寄生蠅科(丁achnihe)、食 財it科、廢蚊科、長鬚滿科、安吉瞒科(AngStic|ae)、恙蟎 1〇科、擬刺蝽象科、蝽象科、獵蝽科、粉蛉科、斑腹蠅科 (Chameiidae)、食蟲虻科、土棲蟎(s〇u mkes)、植綏蟎科 (Phytoseidae)、於一年生作物例如,蔬菜、瓜類、觀賞植 物、玉米中,以及於多年生植物例如,柑橘類果實、梨果 果實及果核果實、香料類、針葉植物及其他觀賞植物中, 15 且亦於造林中者。 僅以一般方式說明之所要保護的作物,將於下文中以更 洋細且特疋的方式說明。因此,至於用途,應瞭解蔬菜係 指,例如丄果實蔬菜及花芽群作為蔬菜,例如,青椒、紅 辣椒、蕃茄二茄子、小黃瓜、葫蘆、密生西葫蘆、蠶豆、 20花豆、蔓生菜豆、婉豆、朝鮮蓟; 以及多>葉蔬菜,例如,結球萵苣、菊苣、菊苣嫩葉、獨 行菜生菜野巨(field salad)、美生菜(iceberg iettuCe)、歐 洲並、疲菜、蒸菜; 以及塊災疏菜,根菜及莖菜,例如,根芹菜、根蒸菜、 200814931 胡蘿蔔、蕪菁、辣根、鴉葱、芦 椰’伽lm shoot)、竹筒’再者里鱗9心菜用甜菜⑽le beet)、 洲韭、旨S、大蒜; &爪采’例如’洋蔥、歐 以及蕓苔屬蔬菜,例如$ 藍、紅甘藍、白甘藍、綠甘藍^甘球花甘藍、球莖甘 球白菜。 敏葉甘藍、球子甘藍、結 橘; “、來姆、酸橙、金橘、薩摩蜜 10 15 20 及梨果果實,例如,頻果、梨及棍梓 如,桃、^桃、櫻桃、李、歐洲李、杏;果心果例 芒果以及木葡:之、蛇麻、油撖欖、茶,及熱帶作物,例如, 亡果、木瓜、無花果、鳳半 巧戈 子、可可、咖啡、牛油果^香無、權M、甜柿、椰 μη 果森枝、西番蓮、番石榴, 果巴HI仁及堅果仁’例如,棒子、胡桃、開心果、腰 諸、山核桃、灰胡桃、板栗、山核桃、澳洲胡 子二之有小果’例如,黑醋栗、醋栗、覆盆 ▲母、卓莓、紅越橘、奇異果、蔓越莓。 至於使用,應瞭解觀賞植物係指-年生及多年生栢物, 、康乃馨、非洲二年= 理花^d、水仙、白頭翁、馨粟花、孤挺花、大 里?匕杜病化、錦蔡, 以及例如’花壇植物、盆栽植物及灌木,例如,玫 -12- 200814931 瑰、,壽菊、三色莖、天竺葵、倒掛金鍾、木槿、菊花、 鳳仙花、仙客來、非洲紫羅蘭、向曰葵、秋海棠, 再者’例小樹叢及針葉植物,例如,無花果樹、 杜鸦花、雲杉樹、冷杉樹、松樹、紫杉樹、刺柏樹、石 5 松、夾竹桃。 至於使用,應瞭解香料係指—年生及多年生植物,例 如,洋菌香、紅辣椒、青椒、辣椒、香草、黑角蘭、百里 春香、丁香、杜松子、肉桂、龍蒿、芫荽、番紅花、薑。 來自於蜾贏科,特別佳者為:壺巢胡蜂,歐普洛蜂 10 (Oplomerus spp·),於作物例如,梨果果實、核果果實、蔬 菜、觀賞植物、針葉植物及香料中。 來自於泥蜂科’特別佳者為:多砂阿莫否拉蜂 (Ammophila sabulos)、砂地節腹泥蜂(CerceHs阶贿⑻,於 作物例如,梨果果實、核果果實、蔬菜、觀賞植物、針葉 15 植物及香料中。 來自於胡蜂科,特別佳者為:長足胡蜂(Polistes spp·)、大胡蜂、胡蜂(Dolichovespula spp·)、黃胡蜂 (Vespula spp·)、副胡蜂(Paravespula spp·),於作物例如, 梨果果實、核果果實、蔬菜、觀賞植物、針葉植物及香料 20 中。 來自於日光蜂科,特別佳者為:球蜂(Coccophagua spp·)、安卡西蜂(Encarsia spp·),例如,台灣安卡西蜂 (Encarsia Formosa)、寄生蜂(Aphytis spp·)、曰光蜂,例 如,日光小蜂、腹日光蜂(Aphelinus abdominalis)、爾莫西 -13- 200814931 蜂(Erelmocerus spp.),例如,艾氏爾莫西蜂(Erelmocerus erimicus)、曼氏爾莫西蜂(Erelmocerus mundus)、普洛斯蜂 (Prospaltella spp·),於作物例如,梨果果實、核果果實、蔬 菜、觀賞植物、針葉植物及香料中。 5 來自於赤眼蜂科’特別佳者為:赤眼蜂,例如,蕓苔 赤眼蜂,於作物例如,梨果果實、核果果實、蔬菜、觀賞 植物、針葉植物及香料中。 φ 來自於跳小蜂科,於作物例如,梨果果實、核果果 實、蔬菜、觀賞植物、針葉植物及香料中。 10 來自於纓小蜂科,於作物例如,梨果果實、核果果 實、蔬菜、觀賞植物、針葉植物及香料中。 來自於姬蜂科’特別佳者為:球姬蜂(Cocdgomymus spp·)、4 尾姬蜂(Diadegma spp·)、網紋姬蜂(〇1丫0丨3 30口·)、 歐芬姬蜂(Ophion spp·)、瘤姬蜂(Pimpia spp.),於作物例 I5如’梨果果實、核果果實、蔬菜、觀賞植物、針葉植物及 香料中。 末自於姫小蜂科,特別佳者為:潛繩姬小蜂(Dyg|yphUS SPP·),例如,防治葉潛蠅(Dyglyphus isaea)、綠姬小蜂 (Eulophidae viridula)、花可普蜂(C〇ipodypeus fi〇TUS),於 2〇作物例如,梨果果實、核果果實、蔬菜、觀賞植物、針葉 植物,玉米及香料中。 來自於亞洛西蜂科(Alloxystidae),特別佳者為:亞洛 西蜂(Alloxysta spp·),於作物例如,梨果果實、核果果 實、蔬菜、觀賞植物、針葉植物及香料中。 -14- 200814931 來自於黃蜂科(Megaspilidae),特別佳者為:丹左蜂 (Dendrocerus spp·),於作物例如,梨果果實、核果果實、 蔬菜、觀賞植物、針葉植物及香料中。 來自於布拉康蜂科(Bracconidae),特別佳者為:財蜂、 5 布拉安蜂(Praon spp·)、潛蠅寄生蜂(Opius spp·)、鋪蜂 (Dacnusa spp·),例如,西伯利亞繭蜂(Dacnusa sibiria)、絨 繭蜂、囊蜂(Ascogaster spp·)、小繭蜂(Macrocentrus spp·), 於作物例如,梨果果實、核果果實、蔬菜、觀賞植物、針 _葉植物及香料中。 10 來自於财繭蜂科,特別佳者為:財蜂,例如,科爾曼 财蜂(Aphidius colemani)、艾維埘蜂(Aphidius ervi)、代瑞 蜂(Diaeretiella spp·)、來西費蜂(Lysiphlebus spp·),於作物 例如’梨果果實、核果果實、蔬菜、觀賞植物、針葉植物 及香料中。 I5 來自於瓢蟲科,特別佳者為:纖麗瓢蟲(Harmonia spp·)、胭脂蟲,例如,七星瓢蟲、高貴瓢蟲(Adalia spp·), ⑩例如,二點瓢蟲、卡維瓢蟲(Calvia spp·)、盔唇瓢蟲,例 如,畢氏盖唇瓢蟲(Chilocorus bipustulatus)、褐尾小黑瓢 蟲、蒙氏隱唇瓢蟲(Cryptolaemus montrouzieri)、艾索瓢蟲 20 (Exochomus spp.)、噬蟎瓢蟲(Stethorus spp·),例如,阿比 特褐尾小黑瓢蟲(Scymnus abietes)、金星褐尾小黑瓢蟲 (Scymnus interruptus)、安納提瓢蟲(Anatis spp.)、黑根瓢蟲 (Rhizobiusspp·)、茶瓢蟲(Theaspp·),於作物例如,梨果果 實、核果果實、疏菜、觀賞植物、針葉植物及香料中。 -15- 200814931 來自於隱翅蟲科(Staphylemidae),特別佳者為:阿蕊佳 蟲(Aleochara spp.)、亞利哥蟲(Aligota spp·)、瓔叟 (Philonthus spp·)、隱翅蟲(Staphylinus spp·),於作物例如, 梨果果實、核果果實、蔬菜、觀賞植物、針葉植物及香料 5 中。 來自於草蛉科,特別佳者為:草蛉(Chrysopa spp·),例 如,金眼草蛉、佩拉草蛉(Chrysopa perla)、普通草蛉、弗 馨拉瓦草蛉(Chrysopa flava)、大草蛉、草蛉(Chrysoperla spp·)、銀蠹蛾,例如,希萊銀蠹蛾(Chrysopidia ciliate)、 10 低草蛉(Hypochrysa spp.),例如,優低草蛉(Hypochrysa elegans),於作物例如,梨果果實、核果果實、蔬菜、觀賞 植物、針葉植物及香料中。 •來自於褐蛉科,特別佳者為:褐蛉,例如,窗格褐蛉 (Hemerobius fenestratus)、薄荷褐蛉(Hemerobius 15 humulinus)、小褐蛉(Hemerobius micans)、細 口褐蛉 (Hemerobius nitidulus),松褐蛉(Hemerobius pini)、棕邊翅 鲁褐蛉(Wesmaelius spp·),例如,裝甲形棕邊翅褐蛉 (Wesmaelius nervosus),於作物例如,梨果果實、核果果 實、蔬菜、觀賞植物、針葉植物及香料中。 20 來自於花蝽象科,特別佳者為:花蝽,例如,單花蝽 (Anthocoris nemoralis)、林花缚(Anthocoris nemorum)、花 蜂象,例如,大花蝽象(Orius majusculus)、 微小花蝽象 (Orius minutus)、光滑花蝽象(〇rius laevigatus)、隱花蝽象 (Orius insidiosus)、黑花蝽象(〇rius niger)、鄰花蝽象(Orius -16- 200814931 vicinus),於作物例如,梨果果實、核果果實、蔬菜、觀賞 植物、針葉植物及香料中。 來自於盲蝽科’特別佳者為:阿特脫蝽(Atractotomus spp·),例如,蘋果阿特脫蝽(Atractotomus mali)、網蝽 5 (Blepharidopterus spp·),例如,角網蝽(Blepharidopterus angulatus)、卡麥隆蝽(Camylomma spp·),例如,毛蕊卡麥 隆蝽(Camylomma verbasci)、迪拉歐蝽(Deraeocoris spp·)、 ⑩長冠蝽(Macrolophus spp.),例如,卡氏長冠蝽 (Macrolophus caliginosus),於作物例如,梨果果實、核果 10果實、蔬菜、觀賞植物、針葉植物及香料中。 來自於蝽象科,特別佳者為:阿馬蝽象(Arma spp,)、 刺益蝽,例如,斑腹刺益蝽,於作物例如,梨果果實、核 果果實、蔬菜、觀賞植物、針葉植物及香料中。 來自於擬刺蝽象科,特別佳者為:擬獵蝽,例如,無 15 翅擬獵蝽(Nabis apterus),於作物例如,梨果果實、核果果 實、蔬菜、觀賞植物、針葉植物及香料中。 ® 來自於獵蝽科,特別佳者為:飄浮獵蝽(Empicornis vagabundus)、臭獵蝽、臭蟲(Rhinocoris spp·),於作物例 如,梨果果實、核果果實、蔬菜、觀賞植物、針葉植物及 20香料中。 來自於寄繩科,特別佳者為:棕腹繩(Bessa fugax)、白 塞森繩(Cyzenius albicans)、吉普賽飛蛾(Compsileura concinnata)、艾洛迪亞蜂(Elodia tragica)、卵追寄繩 (Exorista larvarum)、拉緣寄蠅(1^口1^3(1111)丨3),於作物例 -17- 200814931 如,梨果果實、核果果實、蔬菜、觀賞植物、針葉植物及 香料中。 來自於食財虻科,特別佳者為:達西食蚜虻 (Dasysyrphus spp·)、細扁食对蠅、三角食财 it(Melangyna 5 triangulata)、小食財 it (Melanostoma spp·)、條背食财 fc (Metasyrphus spp.)、帕提食财it(Platycheirus spp,)、大食虫牙 虹:(Syrphus spp·),於作物例如,梨果果實、核果果實、蔬 _菜、觀賞植物、針葉植物及香料中。 來自於癭蚊科,特別佳者為:蚜食蚜虻(Aphidoletes 10 aphidimyza)、瘿蚊(Feltiella acarisuga),於作物例如,梨果 果實、核果果實、蔬菜、觀賞植物、針葉植物及香料中。 來自於植綏蟎科(Phytoseidae),特別佳者為:捕植虫高 (Amblyseius spp.)、盲走蟎(Typhlodromus spp·)、捕植虫馬 (Phytoseiulus spp·),於作物例如,梨果果實、核果果實、 15蔬菜、觀賞植物及香料中。 ' 根據本發明之活性化合物/有益物種組合適用於护^制重力 響物害蟲,宜為節肢動物及線蟲類,特別是於葡萄栽與及& 果栽植中,於農業及園藝及於造林中發現之昆蟲類及/或^ 蛛類。其等於對抗通常為敏感及财受的種類,及對ρ 2〇或個別發展階段具有活性。前述害蟲包括: ~ 有 來自於等足目,例如,二櫛水潮轰、尋常平 婦。 ”蛛、氣 來自於倍足亞目,例如,斑點節Η #⑻ 心蛛⑴laniujus guttulatus) 〇 -18- 200814931 5 10 來自於唇足目 來自於綜合綱 來自於雙尾目 來自於彈尾目 來自於直翅目 蚱、群居蚱猛。 來自於緋蠊目 蠊及德國小蠊。 來自於革翅目 來自於等翅目 例如 例如 例如 例如 例如 食果土棲及家蚰蜓 無點家袖蜒。 西洋衣魚。 刺棘跳蟲。 ’家總蟀 螻蛄、亞洲飛蝗 螞 例如,東方蛸蠊、美洲大蠊、馬得拉蜡 例如 例如 歐洲球虫叟 白蟻 來自於風^目,例如 ▲ 人體虱、獸風、長顎風、咬虱 15 20 尾蝨 來自於缪翅目,例如,溫室條莉馬 及苜蓿薊馬。 來自於異翅亞目 擬網蝽、溫帶臭蟲、 來自於同翅目, 虱、棉财、甘藍虫牙 果綿财、桃大尾虫牙 虫牙、薄荷瘤額財、 蟬、李蜡蚧、盔蚧 盾蚧、粉蚧、木虱< 來自於鱗翅目 刺 芒薊馬、棕櫚薊馬 ’例如,中華褐盾蝽、中介紅蝽、甜菜 南美臭蟲、吸血撒培。 例如,夾癭粉虱、棉粉虱、溫室白粉 、余蘼隱瘤額蚜、蚕豆蚜、蘋果蚜、蘋 、大根瘤蚜、癭綿蚜、麥長管蚜、瘤額 粟縊管蚜、堞蟬、二葉堞蟬、黑尾堞 、稻灰飛虱、稻褐飛虱、紅圓蚧、春藤 例如 (Cheimatobia brumata) 紅鈐蟲、松尺蠖、冬天唇口蟲布蘭卡細峨(Lithocolletis 19- 200814931 blancardella)、櫻桃巢蛾、油菜菜蛾、天幕毛蟲、褐尾蠹、 毒蛾、棉葉穿孔潛峨、橘細潛蛾、夜蛾、切根蟲、褐夜 蛾、埃及金鋼鑽、棉鈐蟲、甘藍夜蛾、火焰夜蛾(Panolis flammea)、黏蟲、粉紋夜蛾、蘋果蠹蛾、粉蝶、稻螟、歐 5洲玉米填、地中海粉模、大蜡螟、袋衣蛾、網衣蛾、褐織 葉蛾、波那捲葉蛾(Cac〇ecia p〇dana)、網葉蛾(Capua reticulana)、雲杉捲葉蛾、葡萄果蠢蛾、廣葉捲蛾、櫟綠捲 馨葉蛾、稻縱捲螟、稻負泥蟲。 來自於勒翅目,例如,家倶竊蠢、穀橐、被覆豆象、大 10豆象、豕天牛、葉子曱蟲(Agelastica alni)、馬鈐薯曱蟲、 耳媧葉&、葉曱、洋菜藍跳曱、墨西哥豆瓢蟲、微點蟲 (Atomaria spp.)、鋸胸谷盜、象曱、谷象、縱槽象曱、香蕉 虫主基象曱、甘藍莢象甲、苜蓿葉象曱、皮蠢、斑皮蠹、圓 皮蠹、黑皮蠹、粉橐、綠甲(Meligethes aeneus)、蛛曱、金 15黃珠曱、麥珠甲、谷盜、黃粉甲、叩甲、金針蟲、鰓角金
龜、六月金龜、褐紐西蘭肋翅鰓角金龜、稻象曱。 來自於膜翅目,例如,鋸角葉蜂、葉蜂、田蟻、廚蟻、 大胡蜂。 來自於雙翅目,例如,伊蚊、按蚊、庫蚊、黃猩猩果 20蠅、家蠅、廄蠅、紅頭麗蠅、綠蠅、金蠅、疽蠅、胃蠅、 赤虱蠅、螯蠅、鼻蠅、皮蠅、牛虻、小捲葉蛾、艮毛蚋、 瑞典麥桿蠅、玻璃蠅、甜菜潛葉蠅、地中海實蠅、油撖欖 實繩、歐洲大蚊、種繩、潛繩。 來自於蚤目,例如,東方鼠蚤、毛列蚤。 -20- 200814931 來自於蛛形目,例如,中東金蠍、黑寡婦球腹蛛、粗腳 粉蟎、隱喙蜱、耳殘喙蜱、雞皮刺蟎、葡萄瘿蟎、橘 銹蟎、頭蜱、扇頭蜱、花蜱、璃眼蜱、硬蜱、癢蟎、恙 蟎、蚧蟎、線蟎、苜蓿苔蟎、爪蟎、紅葉蟎、半線蟎、短須 5 蟎。 虫植/勿-寄生性線蟲類包括,例如,根腐線蟲、穿孔線 ϋ線蟲、半穿透墊讀蟲、異皮線蟲、球皮線蟲、笑 籲月線触、蟲痳線蟲、長線蟲、劍線蟲、殘根線蟲、松材線 蟲。 ι〇 、活性化合物組合可轉化為習用調配物,例如,溶液、乳 濁液、可濕性粉末、懸浮液、粉末、粉屑、糊料、可溶性 孝刀末、顆粒、懸式乳濁濃縮物、注入活性化合物且微包膠 於聚合物質之天然及合成物質。 此等調配物係以已知的方式製造,例如,藉著將活性化 口物舁^充劑混合,其為液態溶劑及/或固態載體,任意地 用表面’舌丨生劑,其為乳化劑及/或分散劑,及/或泡珠形成 劑。 +士果所用的增充劑為水,亦可使用例如有機溶劑作為輔 助/合2。下列為基本上適當的液態溶劑:芳族類,例如, 20二:ϊ、甲苯或烷基萘、氣化芳族類及氣化脂族烴類,例 如氣笨、氣乙烯或二氣甲烷、脂族烴類,例如,環己烷或 鼠例如礦物油餘份、礦物油及植物油、醇類例如丁醇 一〜醇以及其荨之醚類及酯類、酮類例如丙酮、甲基乙 基酮、甲基異丁基酮或環己酮、強力極性溶劑例如二曱基 -21- 200814931 甲醯胺及二甲亞硪,或為水。 適當的固態載體為: 例如銨鹽及研碎之天然礦物例如高嶺土、触、 白堊、石英、活性白土、蒙脫土或石 =π 成物質,例如高度分散之石夕石及’以及研碎之合 10 15 石、大二的天然嚴石例如方解 類之人成顆粒,及;^=石或為無機和有機粉 米穗;桿及有適== 如,非離子性及陰離子性乳化劑,例如聚氧=申=:例 酸_、聚氧基伸乙基脂肪醇醚,例如烷^基二乙基月曰肪 驗、烧基磺酸醋類、烷基硫酸醋類、芳基::;:乙;=
蛋白質水解產物;適合的分散劑為:例如:木=亞= 鹽廢液及甲基纖維素。 个負京亞H 調配物中可使用的膠黏劑為,例 然與合成的聚合物,其可為粉末===纖維素及天 金合歡膠、聚乙烯醇及聚乙烯醋酸酯,二::例如 腦磷脂及卵磷脂及合成磷脂。並他 的2 4对爿曰例如 及植物油。 …-的添加物為礦物油 亦可使用染劑例如無機顏料,例如氧化鐵、 普魯士藍’及有機染劑例如茜素染料、; 花青染料,及微量養分例如鐵、铦伽k 了十及玉屬鈦 之鹽類。 M、硼、銅、鈷、銦及鋅 調配物通常包含0.1及95重量%間,較好為0.5及90% -22- 20 200814931 間之活性化合物。 根據本發明之活性化合物組合可以於市售可得之調配物 及以由此等調配物所製得之使用型式,以含有其他活性化 合物,例如,殺昆蟲劑、誘捕劑、殺菌劑、殺細菌劑、殺 5蟎劑、殺線蟲劑、殺真菌劑、生長_調節物質或除草劑之混 合物呈現。殺昆蟲劑包括,例如,磷酸化物類、胺基曱酸 化物類、羧酸化物類、氯化烴類、苯基脲類及尤其是由微 着生物所產生之物質。 含有其他已知活性化合物例如殺草劑或含有肥料及生長 10調節劑之混合物亦屬可能。 當用作為殺昆蟲劑時,根據本發明之活性化合物組合又 可於其等之市售可得之調配物以及於由此等調配物所製得 之使用型式,以含有協乘劑之混合物呈現。協乘劑為增加 =化合物作用之化合物,添加的協乘劑本身無需為具活 性去。 旦由市售可得之調配物所製得之使用型式的活性化合物含 ::在廣大乾圍間變化。使用型式中之活性化合物濃度可 為由0.0000001至95番吾〇/夕、、各a » 及1重細。 性化合物’宜為由。侧丨 20 化合物係以適合於使用型式之習用方式施用。 該活性化合物組合可如此的以濃 例如粉劑、粒劑、溶液、懸浮液、二= 製備,例如,藉著將活 前述調配物可依本身已知的方式 -23- 200814931 性化合物與至少一種溶劑或稀釋劑、乳化劑、分散劑及/或 結合劑或固定劑、防水劑混合,如果想要,與乾燥劑及 穩定劑混合,且如果想要,與染劑及色素及其他^作輔劑 混合。 根據本發明,亦可處理所有的植物及植物的一部分。應 暸解於本文中植物係指所有的植物及植物群,例如,邦^ 的及不想要的野生植物或作物植物(包括自然成長的作物植 物)。作物植物可為可藉由習用培植及最優化的方法或萨由 生物科技及遺傳工程方法或此等方法之組合所得到的 曰植 10物,包括基因轉移植物及包括栽培植物,其可以或不可以 被植物培育者之保證所保護者。應瞭解植物之一部分 所有的地上及地下部分及植物器官,例如,芽、葉了 曰 根,可提及為例的是葉、針、莖、桿、花、果實體、^ 15 及種子以及根、塊莖及塊根。植物之一部分亦包括收成的 植物及種植及生殖繁殖的物質,例如, 根、插枝及種子。 $田塊生、塊 根據本發明以活性化合物處理植物及植物之一部 據習用的處理方法直接或藉著作用於其地乂 儲存區域上,例如’藉由浸泡、喷m、菜董' f也或
-:塗抹且,於繁殖物質之情況時,特別是於種情: •時,可進-步進行單層或多層塗敷而進行。 I 誠如前文所提,根據本㈣可處理所 =分;=之具懸例中’係處理野生植物物種;栽: 植物,或其等由習用生物育種方法,例如雜交或原生= -24- 200814931 合,及其部份所獲得者。於另外較佳+ , 」)。「部分」或「植物之部分」或「植物部分 說明如前。 份,如果適當,可nrr栽培植物及其部 艚、。「都…「二 的方法(經基因改變的有機
J 詞業已 隹可^‘植物之植株,於每-情形中其係為市 "了仟或使用中者,係根據本發明來處理。
10 15
較適合根據本發明處理之基因轉移植物或栽培植物(亦 即那些藉由基因工程所得到者)包括所有的植物,其於基因 改貝中接X特別提供有利且有㈣性之基因物質給此等植 物。此等躲之㈣植物生長較佳、提高對高溫或低溫之 耐受性、提高對乾旱或對於水份或土壌鹽分含量之耐受 性、提高開花表現、較易收成、加速成熟、提高收穫量、 較佳品質及/或所收穫產物之營養價值較高、所收穫產物之 儲存%疋性及/或處理性較佳。另外及需特別強調此等特點 =植物物種或栽培植物’其等之位置及生長條件(土 μ = '、、生長期、養分)而定,根據本發明之處理亦可產 二南的加成(「協乘」)效應。因此,例如可降低施用率 ^或擴大侧譜及/或提高根據本發明所使狀物質及电 2活性、植物生長較佳、提高對高溫或低溫的耐受性, θ南對乾燥或對水分駐壤好含量的耐受性、提高開花 表現、較易收成、加速成熟、收穫量較高、品f較佳及 =穫產物之營養價值較高、收成產品的儲存安定性及/或 品處理性較佳’其超過了所實際預期的功效。 20 -25- 200814931 的實例為植物對抗動物及微生物蟲害,例如對抗昆蟲、蜗 類、植物性致病真菌、細菌及/或病毒之防禦力較佳,而且 提高植物對於某些除草活性化合物之耐受性。可提及為例 之基因轉移植物為重要的作物植物,例如榖類(小麥、稻 5米)、玉米、大豆、馬鈴薯、棉花、歐洲油菜以及果實植物 (含蘋果、梨子、柑橘及葡萄),且特別強調玉米、大豆、馬 鈴薯、棉花及歐洲油菜。需特別強調的特點為藉著在植物 0中所形成之毒素,特別為其等藉由來自蘇雲金芽孢桿菌於 植物中所形成之基因物質(例如,藉由基因CrylA(a)、 10 CrylA(b)、CrylA(c)、CryllA、CrylllA、CryIIIB2、Cry9c、 Cry2Ab、Cry3Bb及CrylF以及其組合)(下文中稱為「Bt植 物」)來提高植物對抗昆蟲的防禦力。又需特別強調的特點 為提高植物對於某些除草活性化合物,例如,咪唑咁酮 類、磺酿脲類、甘填散(glyphosate)或膦基三辛 15 (phosphinotricin)(例如,「PAT」基因)之财受性。於所討論 之議題中能提供所要之特點的基因亦可與其他基因合併出 ⑩現於基因轉移植物中。可提及為例之「Bt植物」為玉米變 種、棉花變種、大豆變種及馬鈐薯變種,其等係以yield GARD㊣(例如,玉米、棉花、大豆)、KnockOut⑧(例如,玉 20 米)、StarLink⑧(例如,玉米)、Bollgard®(棉花), Nucotn⑧(棉花)及NewLeaf®(馬鈴薯)之商標名販售。可提及 為例之除草劑-耐受性植物為玉米變種,棉花變種及大豆變 種,其等係以Roundup Ready®(對甘磷散具耐受性,例如 玉米、棉花、大豆),Liberty Link®(對膦基三辛具耐受性, -26- 200814931 例如,歐洲油菜),IMI®(對味。坐咐酮具耐受性)及STS®(對 磺醯脲類具耐受性,例如,玉米)之商標名販售。可提及為 例之除草劑-抗性植物(以習用方式育種對除草劑具耐受性之 植物)包括以Clearfield⑧(例如,玉米)商標名販售之變種。 當然,此等陳述亦適用於具有此等或仍待發展之基因特點 的栽培植物,該栽培植物將於未來發展及/或上市。
10 所列舉之植物可根據本發明以特別有利的方式用根據本 發明之活性化合物/有益物種組合處理。前文中所指明組合 之較佳範圍亦適合處理此等植物。需特別強調的是植物係 使用本文中所特別指明之活性化合物/有益物種組合處理。 根據本發明活性化合物/有益物種組合良好的殺昆蟲及 殺蟎作用可從下列實例來證明。雖然個別的活性化合物顯 示其等的作用微弱,該活性化合物/有益物種組合顯示出之 作用超過單一活性化合物作用。
-27- 200814931 【實施方式】
使用實例 實例A 於4個重複組中,於各情況中將5棵約10年大的蘋果 10 樹(樹冠高度約2.5米)''Braeburn"栽培種予以處理以對抗 紅蜘蛛歐洲紅葉蟎(PANOUL)。於本文中,將活性化合物(μ b-l)(24〇SC)及市售標準的艾妥沙唑(etoxaz〇ie) (11〇 sc)以所 指明之施用率使用壓力-可操作的背包喷霧器施用於出現掠 艮)生蜗烛女‘林捕植蜗(Ambiyseius anders〇ni) (ambLAN)者 上。水施用率為400公升/公頃。兩次施用之間隔為42天。 Λ估係在第一次處理前4天及處理後第6、29、43及63 =者#异在25個葉片上之成年料贼目 種作用之判斷桿準。 ”者之比㈣為支持有益物 15
'28- 200814931 施用率% PANOUL -4 d 6 d 29 d 43 d 63 d 艾妥少坐 0.05% 25 10 221 203 87 I-1-b 0.04% 36 13 111 52 0 未處理 39 39 411 288 3
施用率 % AMBLAN -4 d 6 d 29 d 43 d 63 d 艾妥沙唑 0.05% 1 5 18 52 86 I-l-b 0.04% 2 3 57 100 62 未處理 4 7 97 229 85
施用率 % 被捕食者/掠食者 -4 d 6 d 29 d 43 d 63 d 艾妥沙、坐 0.05% 25 2.0 12.3 3.9 1.01 I-l-b 0.04% 18 4.3 1.9 0.5 0.00 未處理 9.75 5.6 4.2 1.3 0.04 -29- 200814931 兩種活性化合物組合之殺死率的計算公式 含兩種活性化合物之給定組合的預期活性可計算(參看 S.R.柯比公式;「殺草劑組合物之計算的協乘及拮抗回 應」,雜草ϋ,第20-22頁,1967)如下: 5 若 X 為當活性化合物A以里ppm或克/公頃之施用率使用 時,以%表示未處理控制組的殺死率, ^ Y 為當活性化合物B以n ppm或克/公頃之施用率使用 時,以%表示未處理控制組的殺死率, 10 E 為當活性化合物A及B以m及E ppm或克/公頃之施用 率使用時,以%表示未處理控制組的殺死率,
X X Y 貝丨] E 二 X + Y —- 100 15 如果實際殺昆蟲之殺死率超過計算值時,則組合之殺死 率具超加成性,亦即,呈現協乘效應。於此情況中,實際 響所觀察到之殺死率必須超過使用上述期望殺死率(E)公式之 計算值。 -30- 200814931
實例B 歐洲紅葉蟎試驗 溶劑: 7重量份二曱基曱醯胺 乳化劑: 2重量份烷基芳基聚乙二醇醚 5 將1重量份活性化合物與所述數量之溶劑及乳化劑混 合,且將濃縮物用含乳化劑的水予以稀釋至想要的濃度, 以製備適當的活性化合物製劑。 將被果樹蜘蛛蟎(歐洲紅葉蟎)感染之李樹(Prunus domestica)挿枝用所想要濃度的活性化合物製劑予以喷霧於 10 葉片的向上面上而處理。 於想要的一段時間後,添加既定量之掠食性蟎蟲派里盲 走蜗(Typhlodromus pyri) 〇 於想要的一段時間後,測定所殺死害蟲的百分比。 100%係指所有的蜘蛛蟎皆已被殺死;0%係指沒有蜘蛛蟎 〗5 被殺死。將测定的殺死率套進柯比公式中。 於此試驗中,例如,下列根據本發明之活性化合物/掠 食性蟎組合與組成份個別施用時相比較顯示出加強的協乘 活性: -31- 200814931
表B 植物-損害性昆蟲 歐洲紅葉滿-試驗 活性化合物 以ppm計之 濃度或動物數 7天後之殺死% 螺代克芬(spiro-diclofen) (Ex. I-b-1) 20 70 派里盲走蟎 約50-100個蛋 50 根據本發明 20+50-100 個蛋 實測值*計算值** 螺代克芬+ 派里盲走蟎 99 85 5 實測值* :實測的活性 計算值:使用柯比公式所計算的活性
-32- 200814931 實例c 臨界濃度試驗/ 土壤昆蟲-基因轉移植物之處理 試驗昆蟲:黑點葉曱(Diabrotica balteata) -土壤中之幼蟲 溶劑: 7重量份丙酮 5 乳化劑: 1重量份烷基芳基聚乙二醇醚 將1重量份活性化合物與指明述數量之溶劑混合,添加 指明數量之乳化劑混合且將濃縮物用水予以稀釋至想要的 濃度,以製備適當活性化合物之製劑。 將活性化合物之製劑倒在土壤上。於本文中,製劑中之 10活性化合物的濃度實質上係無關緊要的;只有每體積單位 土壤以重量計之活性化合物重量,其以ppm (毫克/公升)計 者,才重要。將土壤填充至0.25公升盆中,且將這些於20 °C靜置。 製備後立即將5個預先發芽的玉米栽培種YIELD 15 GUARD (美國孟山都公司之商標)放進各盆中。於2天後, 將適當的試驗昆蟲放進經處理的土壤内。又7天後,藉著 馨計算已發芽之玉米植株來測定活性化合物(1棵植物二20% 活性)之功效。 -33- 200814931
實例D 美洲菸葉蛾試驗-基因轉移植物之處理 溶劑: 7重量份丙酮 乳化劑: 1重量份烷基芳基聚乙二醇醚 5 將1重量份活性化合物與指定數量之溶劑及指定數量之 乳化劑混合,且將濃縮物用水稀釋至想要的濃度,以製備 適當的活性化合物製劑。 0 將栽培種Roundup Ready (美國孟山都公司之商標)之黃 豆芽(大豆)藉著滴進所想要濃度之活性化合物製劑而處理且 10 於葉片仍濕潤時用菸葉葉芽蟲美洲菸葉蛾予以污染。 於想要的一段時間後,測定所殺死的昆蟲數。 -34-
Claims (1)
- 200814931 十、申請專利範圍: 1. 一種活性化合物/有益物種組合’其包括式⑴化合物 G• #中, X代表crc6-烧基、_素、c卜c6-烧氧基或crc3-i| 10 素烷基, γ代表氫、Cl-C6·烷基、鹵素、C〗_c6•烷氧基或CV C3-鹵素院基, Z 代表CpC6-烧基、鹵素或Ci-Cg-燒氧基, η 代表數字0 - 3, 15 Α 代表氣或於各情況中任意地被ή素··所取代之直鍵或 φ 分支Ci-Cl2_烷基、C3-C8-烯基、c3-C8-炔基、c广 c10-烷氧基-C2-C8·烷基、crc8-多烷氧基-crc8-烷 基、C1-C丨〇-烧基硫基-(:2·〇ν院基或具有3至8個環 原子之環烷基,其可被氧及/或硫所插入及於各情況 20 中任意地被鹵素-、Ci-Cf烷基-、crC6-鹵素烷基· 、CpC6_烧氧基_、C1 鹵素烧氧基-或石肖基_戶斤取 代之苯基或苯基-C丨-c6-烷基, B 代表氮、C1-C6·烧基或C1-C6·烧氧基院基, 或其中 -35· 200814931 A及B與其等所連接之碳原子一起形成飽和或不飽和之 3-至8-員環,其任意地被氧及/或硫所挿入且任意地 被ή素、CrC6·院基、d-CV烧氧基、鹵素烷 基、CrC4_鹵素烷氧基、Cl-C4-烷基硫基或經任意 取代之苯基所取代或任意地經苯並_稠和, G 代表虱(a)或代表基團其中, r1代表於各情況中任意地被鹵素-所取代之CrC20_烷 基、C2-C2〇-烯基、crc8-烷氧基-crcv烷基-、Cr C8-烷基硫基_C2-C8-烷基、CrCV多烷氧基-c2-c8-烷基或具有3至8個環原子之環烷基其可被氧及/或 硫原子所挿入, 代表任意地被鹵素-、硝基-、CrC6-烷基-、〇卜(:6-烷氧基-、CrC6-鹵素烷基_或CpCy鹵素烷氧基-所 取代之苯基, 代表任意地被鹵素-、Ci_C6_烧基-、Ci-C6-:):完氧基-、cPc6-鹵素烷基-或crc6-鹵素烷氧基-所取代之 苯基胃c〗_c6_烷基, -36- 200814931 代表於各情況中任意地被鹵素-及/或CrCy烧基-所 取代之°比咬基、。密咬基、嗔峻基或咐嗤基’ 代表任意地被_素·及/或Ci_C6-烧基-所取代之本氧 基烧基, R2代表於各情況中任意地被鹵素-所取代之CpC^o-烷 基、c2-c20-烯基-、crc8-烷氧基-C2-C8-烷基或C】-c8-多烷氧基-c2-c8·烷基, 代表於各情況中任意地被鹵素-、石肖基-、C1-C6·院 基-'CpCy烷氧基-或Ci-C^-鹵素烷基-所取代之笨 基或+基, 3 R 代表任意地被ii素-所取代之烷基、代表於各 情況中任意地被CVCzr烷基-、鹵素」、CrC4-鹵素 烧基-、C1-C4-烧氧基-、C1-C4-鹵素烧氧基-、硝基-或氰基·所取代之苯基或苄基, 4 5 R及R各自獨立代表於各情況中任意地被_素_所取 代之C卜C8-烷基、Crc8-烷氧基、CrCs-烷基胺 基、二-(CVC8)-烷基胺基、crC8-烷基硫基、c2-Cr烯基硫基、C2-C5-炔基硫基或c3-cr環烷基硫 基’代表於各情況中任意地被鹵素-、硝基-、氰基-、cvcv烧氧基-、Cl-C4-鹵素烷氧基_、Ci_c4-烷基 硫基-、(VC4-鹵素烷基硫基-、Cl_c4-烷基-或 6 素烷基-所取代之苯基、笨氧基或苯基硫基, R及R各自獨立代表於各情況中任意地被鹵素-所取 代之CVCio-烷基、CVC10-烷氧基、C3-C8-稀基或 -37- 200814931 Ci-CV烧氧基-CpCV烧基,代表任意地被!素… Ci-C6-_素烷基-、CVCV烷基-或crC6-烷氧基··所 取代之苯基,代表任意地被_素·、CrC6_烷基… Ci-CV鹵素烧基-或CVC6·烷氧基-所取代之苄基或 5 一起代表5-至6-員環其任意地被氧或硫所揷入且其 可任意地被CpCy烷基所取代, 及來自於換蛛目、蜱蟎亞綱、膜翅目、鞘翅目、脈 Φ 翅目、纓翅目(Tysanoptera)、異翅亞目、雙翅目、 半翅目、革翅目及/或寄蟎目之目或亞目的有益物 10 種。 2·如申請專利範圍第1項之活性化合物/有益物種組合, 其中式(I)化合物之基團係定義如下: X代表q-cv烷基、鹵素、cvc4-烷氧基或 素炫*基’ 15 Υ代表氫、CrCV烷基、鹵素、crc4-烷氧基或Cl_ c2-i素烷基, ® z代表cvq-烧基、鹵素或crc4-烧氧基, η 代表0或1, Α及Β與其等所連接之碳原子一起代表飽和之5_至6_ 20 員環,其任意地被CrC4-烷基或CrC4-烷氧基所取 代, G代表氫⑻或代表基團 —CO—R1 (b) X R2 ⑹ -38- 200814931 其中, R1代表於各情況中任意地被鹵素-所取代之c〗-c16-烷 基、c2-c16-烯基、d-cv烷氧基-c2-c6-烷基-或具 有3至7個環原子之環烷基其可被1至2個氧及/或 硫原子所掃入, 代表任意地被鹵素…硝基·、CrC4-烷基-、C广C4-燒氧基-、CrC3-鹵素烷基-或crC3-鹵素烷氧基-所 取代之苯基, 2 10 R代表於各情況中任意地被!|素-所取代之C!-C^烷 基、C2-C16-烯基或d-Cf烷氧基-c2-c6-烷基, 代表於各情況中任意地被鹵素-、石肖基-、C 1 -C4-貌 基-、C1-C4-烧氧基·或C1-C4-鹵素焼基-戶斤取代之苯 基或+基。 15如申請專利範圍第1項之活性化合物/有益物種組合, 其包括式(I-b-1)之化合物 204.:種如申請專利範圍第i項中所定義之活性化合物/有 ϋ物種組合用於控制動物害蟲上之用途。 -種用於控制動物害蟲之方法,其特徵在於將 利範圍第丨項所定義之活性化合物/有益物種組合;用 -39- 200814931 在動物害蟲及/或其等之棲息地上。 6· 8· 10 9· 種‘備杈此蟲及/或殺蟎組合物之方法,其特徵在於 將如申明專利範圍帛】項所定義之活性化合物/有益物 種組合與增充劑及/或表面活性劑混合。 :種精著使用如中請專利範圍第丨項之活性化合物/有 凰物種組合來降低噴霧施用(每季施用數)之方法。 一種藉著使用如申請專利範圍第 盈物種組合來降低收穫物質上及 /或殺蟎劑殘留物之方法。 1項之活性化合物/有 環境中之總殺昆蟲劑及 一種組成物,其包括如申請專利範圍第1項之活性化合 物/有益物種組合以用來控制動物害蟲。、丨-40- 200814931 七、指定代表圖: (一) 本案指定代表圖為:第(無)圖。 (二) 本代表圖之元件符號簡單說明: 無010 15 ®八、本案若有化學式時,請揭示最能顯示發明特徵的化學 式:
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| EP0809629B1 (de) * | 1995-02-13 | 2004-06-30 | Bayer CropScience AG | 2-phenylsubstituierte heterocyclische 1,3-ketoenole als herbizide und pestizide |
| AU5762696A (en) * | 1995-05-09 | 1996-11-29 | Bayer Aktiengesellschaft | Alkyl dihalogenated phenyl-substituted ketoenols useful as p esticides and herbicides |
| RU2195449C2 (ru) * | 1995-06-28 | 2002-12-27 | Байер Акциенгезельшафт | 2,4,5-тризамещенные фенилкетоенолы, промежуточные соединения для их получения, способ и средство для борьбы с насекомыми и паукообразными на их основе |
| DE59610095D1 (de) * | 1995-06-30 | 2003-03-06 | Bayer Cropscience Ag | Dialkyl-halogenphenylsubstituierte ketoenole zur verwendung als herbizide und pestizide |
| CN1535956A (zh) * | 1996-04-02 | 2004-10-13 | 取代的苯基酮烯醇杀虫剂及除草剂 | |
| AU2773397A (en) * | 1996-05-10 | 1997-12-05 | Bayer Aktiengesellschaft | New substituted pyridyl keto enols |
| ES2278856T3 (es) * | 1996-08-05 | 2007-08-16 | Bayer Cropscience Ag | Fenilcetoenoles 2- y 2,5-substituidos. |
| DE19632126A1 (de) * | 1996-08-09 | 1998-02-12 | Bayer Ag | Phenylsubstituierte cyclische Ketoenole |
| DE19808261A1 (de) * | 1998-02-27 | 1999-10-28 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| DE19813354A1 (de) * | 1998-03-26 | 1999-09-30 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| DE19818732A1 (de) * | 1998-04-27 | 1999-10-28 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| DE19939395A1 (de) * | 1998-10-23 | 2000-04-27 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE19901943A1 (de) * | 1999-01-20 | 2000-07-27 | Bayer Ag | Verwendung von 3-/2,4,6-Trimethylphenyl)-4-neopentylcarbonyloxy-5,5-tetramethylen- -dihydrofuran-2-on zur Bekämpfung der Weißen Fliege |
| PT1481970E (pt) * | 1999-09-07 | 2006-07-31 | Syngenta Participations Ag | Novos herbicidas |
| DE19946625A1 (de) * | 1999-09-29 | 2001-04-05 | Bayer Ag | Trifluormethylsubstituierte spirocyclische Ketoenole |
| US6689976B1 (en) * | 2002-10-08 | 2004-02-10 | Agilent Technologies, Inc. | Electrically isolated liquid metal micro-switches for integrally shielded microcircuits |
| DE10015310A1 (de) * | 2000-03-28 | 2001-10-04 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10016544A1 (de) * | 2000-04-03 | 2001-10-11 | Bayer Ag | C2-phenylsubstituierte Ketoenole |
| DE10139465A1 (de) * | 2001-08-10 | 2003-02-20 | Bayer Cropscience Ag | Selektive Herbizide auf Basis von substituierten, cayclischen Ketoenolen und Safenern |
| DE10239479A1 (de) * | 2002-08-28 | 2004-03-04 | Bayer Cropscience Ag | Substituierte spirocyclische Ketoenole |
| DE10311300A1 (de) * | 2003-03-14 | 2004-09-23 | Bayer Cropscience Ag | 2,4,6-Phenylsubstituierte cyclische Ketoenole |
| DE10326386A1 (de) * | 2003-06-12 | 2004-12-30 | Bayer Cropscience Ag | N-Heterocyclyl-phenylsubstituierte cyclische Ketoenole |
| DE10330723A1 (de) * | 2003-07-08 | 2005-02-03 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10353281A1 (de) * | 2003-11-14 | 2005-06-16 | Bayer Cropscience Ag | Wirkstoffkombination mit insektiziden und akariziden Eigenschaften |
| DE102004011006A1 (de) * | 2004-03-06 | 2005-09-22 | Bayer Cropscience Ag | Suspensionskonzentrate auf Ölbasis |
| DE102004014620A1 (de) * | 2004-03-25 | 2005-10-06 | Bayer Cropscience Ag | 2,4,6-phenylsubstituierte cyclische Ketoenole |
| DE102004030753A1 (de) * | 2004-06-25 | 2006-01-19 | Bayer Cropscience Ag | 3'-Alkoxy spirocyclische Tetram- und Tretronsäuren |
| DE102004032420A1 (de) * | 2004-07-05 | 2006-01-26 | Bayer Cropscience Ag | Verwendung von 3-(2,4,6-Trimethylphenyl)-4-neopentylcarbonyloxy-5,5-tetramethylen-Δ3-dihydrofuran-2-on zur Bekämpfung von Psylliden |
| DE102004044827A1 (de) * | 2004-09-16 | 2006-03-23 | Bayer Cropscience Ag | Jod-phenylsubstituierte cyclische Ketoenole |
| DE102005008033A1 (de) * | 2005-02-22 | 2006-08-24 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006007882A1 (de) * | 2006-02-21 | 2007-08-30 | Bayer Cropscience Ag | Cycloalkyl-phenylsubstituierte cyclische Ketoenole |
| DE102006025874A1 (de) * | 2006-06-02 | 2007-12-06 | Bayer Cropscience Ag | Alkoxyalkyl-substituierte cyclische Ketoenole |
| DE102006027731A1 (de) * | 2006-06-16 | 2007-12-20 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006027732A1 (de) * | 2006-06-16 | 2008-01-10 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006033154A1 (de) * | 2006-07-18 | 2008-01-24 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102007001866A1 (de) * | 2007-01-12 | 2008-07-17 | Bayer Cropscience Ag | Spirocyclische Tetronsäure-Derivate |
| EP2008517A1 (de) * | 2007-06-29 | 2008-12-31 | Bayer CropScience AG | Akarizide Wirkstoffkombinationen |
-
2006
- 2006-06-16 DE DE102006027730A patent/DE102006027730A1/de not_active Withdrawn
-
2007
- 2007-06-05 US US12/304,958 patent/US20100056620A1/en not_active Abandoned
- 2007-06-05 MX MX2008015840A patent/MX2008015840A/es not_active Application Discontinuation
- 2007-06-05 KR KR1020097000779A patent/KR20090020699A/ko not_active Withdrawn
- 2007-06-05 JP JP2009514670A patent/JP2009539900A/ja not_active Withdrawn
- 2007-06-05 WO PCT/EP2007/004971 patent/WO2007144089A1/de not_active Ceased
- 2007-06-05 EP EP07725839A patent/EP2034843A1/de not_active Withdrawn
- 2007-06-05 CN CNA2007800221765A patent/CN101466267A/zh active Pending
- 2007-06-15 TW TW096121633A patent/TW200814931A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MX2008015840A (es) | 2009-01-09 |
| DE102006027730A1 (de) | 2007-12-20 |
| EP2034843A1 (de) | 2009-03-18 |
| JP2009539900A (ja) | 2009-11-19 |
| KR20090020699A (ko) | 2009-02-26 |
| CN101466267A (zh) | 2009-06-24 |
| US20100056620A1 (en) | 2010-03-04 |
| WO2007144089A1 (de) | 2007-12-21 |
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