| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 161 | Composition for controlling harmful fungi and method for the same | JP2007266434 | 2007-10-12 | JP2008069168A | 2008-03-27 | BAYER HERBERT; SAUTER HUBERT; KOEHLE HARALD; RETZLAFF GUENTER; AMMERMANN EBERHARD; LORENZ GISELA; STRATHMANN SIEGFRIED; EICKEN KARL |
| PROBLEM TO BE SOLVED: To provide a composition improving possibility of controlling harmful fungi, especially Botrytis bacillus. SOLUTION: The invention relates to the composition for controlling harmful fungi comprising (A) at least a kind of active substances I represented by formula (1), wherein R' represents -N(OCH 3)-CO 2CH 3, and inhibits respiration of cytochrome complex III when R'' means a phenyloxymethylene, and (B) an amide compound represented by formula (2). COPYRIGHT: (C)2008,JPO&INPIT | ||||||
| 162 | Harmful bacteria-controlling agent for human containing bacillus thuringiensis | JP2006286093 | 2006-10-20 | JP2007291057A | 2007-11-08 | MOCHIZUKI MASAMI |
| <P>PROBLEM TO BE SOLVED: To provide a means for improving the balance of intestine flora, accelerating the control of the intestine, preventing or treating infectious diseases and capable of being used safely and simply for a human by inhibiting the proliferation of the harmful bacteria represented by pathogenic bacteria causing human infectious diseases and also inactivating a self-inducing factor of the bacteria. <P>SOLUTION: This controlling agent of harmful bacteria is provided by administering a medicine containing Bacillus thuringiensis to the human or ingesting a food containing the Bacillus thuringiensis to the human. <P>COPYRIGHT: (C)2008,JPO&INPIT | ||||||
| 163 | (HETERO)CYCLYLCARBOXANILIDE ZUR BEKÄMPFUNG VON SCHADPILZEN | EP04804217.0 | 2004-12-22 | EP1699752B1 | 2007-09-26 | GEWEHR, Markus; MÜLLER, Bernd; GROTE, Thomas; GRAMMENOS, Wassilios; TORMO I BLASCO, Jordi; SCHWÖGLER, Anja; RHEINHEIMER, Joachim; BLETTNER, Carsten; SCHÄFER, Peter; SCHIEWECK, Frank; WAGNER, Oliver; SPEAKMAN, John-Bryan; RETHER, Jan; STRATHMANN, Siegfried; STIERL, Reinhard |
| The invention relates to (hetero)cyclyl carboxanilides of general formula (I), wherein n represents 0, 1, 2, 3, or 4, m represents 1, 2, or 3, Y represents oxygen or sulfur, A represents optionally substituted phenyl or an at least monounsaturated, optionally substituted five-membered or six-membered heterocycle, and R1, R2, R3m, R4, R5, and R6 have the meanings indicated in claim 1, and the agriculturally useful salts thereof. The invention further relates to the use of said (hetero)cyclyl carboxanilides of general formula (I) and the agriculturally useful salts thereof as fungicides as well as plant protection agents containing the same. | ||||||
| 164 | (HETERO)CYCLYLCARBOXAMIDE ZUR BEKÄMPFUNG VON SCHADPILZEN | EP05777428.3 | 2005-09-05 | EP1791427A1 | 2007-06-06 | GEWEHR, Markus; GROTE, Thomas; MÜLLER, Bernd; GRAMMENOS, Wassilios; SCHWÖGLER, Anja; RHEINHEIMER, Joachim; BLETTNER, Carsten; SCHÄFER, Peter; SCHIEWECK, Frank; WAGNER, Oliver; RETHER, Jan; STRATHMANN, Siegfried; STIERL, Reinhard; SCHERER, Maria |
| The invention relates to the use of (hetero)cyclylcarboxamides of general formula (I) and to the agriculturally useful salts thereof for controlling plant pathogenic fungi, the variables in formula (I) having the following designations: A represents phenyl or an at least monosaturated five-membered or six-membered heterocycle with 1, 2 or 3 heteroatoms as ring members selected from N, O, S, S(=O) and S(=O)2, where phenyl and the at least monosaturated five-membered or six-membered heterocycle can be unsubstituted or substituted according to the description; Y represents oxygen or sulphur; R1 represents H, OH, alkyl, cycloalkyl, alkoxy, halogenalkyl, halogencycloalkyl or halogenalkoxy; R2 and R3 represent H, halogen, nitro, CN, alkyl, cycloalkyl, alkenyl, alkinyl, alkoxy, halogenalkyl, halogencycloalkyl, halogenalkenyl, halogenalkinyl or halogenalkoxy; R4 represents halogen, nitro, CN, alkyl, cycloalkyl, alkenyl, alkinyl, alkoxy, halogenalkyl, halogencycloalkyl, halogenalkenyl, halogenalkinyl or halogenalkoxy; R5 represents hydrogen, halogen, nitro, CN, OH, alkyl, cycloalkyl, alkenyl, alkinyl, alkoxy, alkenyloxy, alkinyloxy, alkoxyalkoxy, halogenalkyl, halogencycloalkyl, halogenalkenyl, halogenalkinyl or halogenalkoxy; alkylthio, halogenalkylthio, alkylsulfinyl, halogenalkylsulfinyl, alkylsulfonyl, halogenalkylsulfonyl, -(CR6)=NOR7, -C(O)R8, NR9R10, -C(O)NR9R10, -C(S)NR9R10, phenyl or phenylalkyl, the phenyl ring in the last two radicals optionally comprising between 1 and 4 of the radicals cited for R4; R6, R7, R8, R9 and R10 have the designations cited in the description; the two radicals R4 and R5 bound to adjacent carbon atoms can also represent an alkylene chain with 3 to 5 members, wherein 1 or 2 non-adjacent CH2 groups can also be replaced by O or S, and part or all of the hydrogens can be replaced by halogen; Ar represents phenyl, naphtyl or a five-membered or six-membered heteroaromatic radical with 1, 2 or 3 heteroatoms as ring members selected from N, O, and S, that can optionally also carry a fused benzene ring; and n represents 0, 1, 2, 3, or 4. The invention also relates to crop protection agents containing said compounds. | ||||||
| 165 | (HETERO)CYCLYLCARBOXANILIDE ZUR BEK MPFUNG VON SCHADPILZEN | EP04804217.0 | 2004-12-22 | EP1699752A1 | 2006-09-13 | GEWEHR, Markus; MÜLLER, Bernd; GROTE, Thomas; GRAMMENOS, Wassilios; TORMO I BLASCO, Jordi; SCHWÖGLER, Anja; RHEINHEIMER, Joachim; BLETTNER, Carsten; SCHÄFER, Peter; SCHIEWECK, Frank; WAGNER, Oliver; SPEAKMAN, John-Bryan; RETHER, Jan; STRATHMANN, Siegfried; STIERL, Reinhard |
| The invention relates to (hetero)cyclyl carboxanilides of general formula (I), wherein n represents 0, 1, 2, 3, or 4, m represents 1, 2, or 3, Y represents oxygen or sulfur, A represents optionally substituted phenyl or an at least monounsaturated, optionally substituted five-membered or six-membered heterocycle, and R1, R2, R3m, R4, R5, and R6 have the meanings indicated in claim 1, and the agriculturally useful salts thereof. The invention further relates to the use of said (hetero)cyclyl carboxanilides of general formula (I) and the agriculturally useful salts thereof as fungicides as well as plant protection agents containing the same. | ||||||
| 166 | 유해균 차단기능을 갖는 항균시트 및 그 제조방법 | KR1020080004035 | 2008-01-14 | KR101005291B1 | 2011-01-04 | 이춘구 |
| 본 발명은 유해균 차단기능을 갖는 항균시트(sheet)소재 및 그 제조방법에 관한 것이다. 본원은 유해균 차단기능을 갖는 항균 시트소재를 얻기 위한 수단으로 기본적으로 유해균 차단 기능물질로 소금을 이용하고자 하는 것이며, 소금을 이용하는 수단은 수용성바인더 100중량부를 기준하는 경우 용융소금 분말을 바인더 사용량의 25~100% 중량부의 비율로 혼합하고 이를 항균시트로 이용하고자 하는 섬유부직포나 합성수지시트 소재나 또는 지류(종이)에 함침 및/또는 도포시키는 수단을 포함하여 제공됨으로 유해균 차단기능을 갖는 항균시트소재를 얻고자 하는 기술에 관한 것이다. 항균시트, 소금, 섬유부직포, 합성수지시트, 지류(종이) | ||||||
| 167 | 유해 진균을 방제하기 위한 합성 및 생물학적 살진균제의 용도 | KR1020117025154 | 2010-03-25 | KR1020110132461A | 2011-12-07 | 셰러,마리아; 클라파흐,크리스틴; 하덴,에곤 |
| 본 발명은 유해 진균을 방제하기 위한 합성 살진균제 및 생물학적 방제제의 조합된 사용에 관한 것이다. 보다 구체적으로, 본 발명은, 1개 이상의 처리 블록에서 식물이 1종 이상의 합성 살진균제로 처리되고, 1개 이상의 처리 블록에서 식물이 1종 이상의 생물학적 방제제로 처리되되, 마지막 처리 블록이 1종 이상의 생물학적 방제제로의 1회 이상의 처리로 식물을 처리하는 것을 포함하는 2개 이상의 처리 블록을 포함하는, 유해 진균을 방제하기 위한 방법에 관한 것이다. | ||||||
| 168 | 유해 진균을 방제하기 위한 합성 및 생물학적 살진균제의 용도 | KR1020117025154 | 2010-03-25 | KR101737138B1 | 2017-05-17 | 셰러,마리아; 클라파흐,크리스틴; 하덴,에곤 |
| 본발명은유해진균을방제하기위한합성살진균제및 생물학적방제제의조합된사용에관한것이다. 보다구체적으로, 본발명은, 1개이상의처리블록에서식물이 1종이상의합성살진균제로처리되고, 1개이상의처리블록에서식물이 1종이상의생물학적방제제로처리되되, 마지막처리블록이 1종이상의생물학적방제제로의 1회이상의처리로식물을처리하는것을포함하는 2개이상의처리블록을포함하는, 유해진균을방제하기위한방법에관한것이다. | ||||||
| 169 | USE OF SYNTHETIC AND BIOLOGICAL FUNGICIDES IN COMBINATION FOR CONTROLLING HARMFUL FUNGI | PCT/EP2010/053867 | 2010-03-25 | WO2010108973A2 | 2010-09-30 | SCHERER, Maria; KLAPPACH, Kristin; HADEN, Egon |
The present invention relates to the combined use of synthetic fungicides and biological control agents for controlling harmful fungi. To be more precise, the invention relates to a method for controlling harmful fungi, which comprises at least two treatment blocks, where in at least one treatment block the plants are treated with at least one synthetic fungicide and in at least one treatment block the plants are treated with at least one biological control agent, with the proviso that the last treatment block comprises subjecting the plants to at least one treatment with at least one biological control agent. |
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| 170 | METHOD OF INDUCING RESISTANCE TO HARMFUL FUNGI | PCT/EP2006067480 | 2006-10-17 | WO2007048735A3 | 2008-04-10 | WATERHOUSE STEVE; STIERL REINHARD; STAMMLER GERD |
| 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/c1 complex. | ||||||
| 171 | TRIAZOLOPYRIMIDIN-VERBINDUNGEN UND IHRE VERWENDUNG ZUR BEKÄMPFUNG VON SCHADPILZEN | PCT/EP2005/006855 | 2005-06-24 | WO2006000436A1 | 2006-01-05 | BLETTNER, Carsten; SCHIEWECK, Frank; TORMO I BLASCO, Jordi; MÜLLER, Bernd; GEWEHR, Markus; GRAMMENOS, Wassilios; GROTE, Thomas; RHEINHEIMER, Joachim; SCHÄFER, Peter; SCHWÖGLER, Anja; WAGNER, Oliver; SPEAKMAN, John-Bryan; JABS, Thorsten; STRATHMANN, Siegfried; SCHÖFL, Ulrich; SCHERER, Maria; STIERL, Reinhard |
Die vorliegende Erfindung betrifft neue Triazolopyrimidin-Verbindungen der allgemeinen Formel (I), worin: X für Halogen, Cyano, C1-C4-Alkyl, C1-C4-Halogenalkyl, C1-C4-Alkoxy oder C1-C2-Halogenalkoxy steht; W Sauerstoff oder Schwefel bedeutet; Y für O-R4 oder eine Gruppe NR5R6 steht; A für eine chemische Bindung oder eine Gruppe CR7R8 steht; und die Variablen L, R1 bis R7 die in Anspruch 1 angegebenen Bedeutungen haben. Gegenstand der vorliegenden Erfindung ist weiterhin die Verwendung der Triazolopyrimidin-Verbindungen der allgemeinen Formel (I), ihrer Tautomere und deren landwirtschaftlich verträglichen Salze zur Bekämpfung von pflanzenpathogenen Pilzen (= Schadpilzen) sowie ein Verfahren zur Bekämpfung von pflanzenpathogenen Schadpilzen, das dadurch gekennzeichnet ist, dass man die Pilze, oder die vor Pilzbefall zu schützenden Materialien, Pflanzen, den Boden oder Saatgüter mit einer wirksamen Menge einer Verbindung der allgemeinen Formel (I), einem Tautomer von (I) und/oder mit einem landwirtschaftlich verträglichen Salz von (I) oder dessen Tautomer behandelt. |
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| 172 | ARYLKONDENSIERTE 3-ARYLPYRIDINVERBINDUNGEN UND IHRE VERWENDUNG ZUR BEKÄMPFUNG VON SCHADPILZEN | PCT/EP2004/007924 | 2004-07-15 | WO2005010000A2 | 2005-02-03 | WAGNER, Oliver; GROTE, Thomas; BLETTNER, Carsten; GEWEHR, Markus; GRAMMENOS, Wassilios; GYPSER, Andreas; MÜLLER, Bernd; RHEINHEIMER, Joachim; SCHÄFER, Peter; SCHIEWECK, Frank; SCHWÖGLER, Anja; TORMO I BLASCO, Jordi; AKERS, Alan; SPEAKMAN, John-Bryan; RACK, Michael; STIERL, Reinhard; SCHERER, Maria; STRATHMANN, Siegfried; SCHÖFL, Ulrich |
Die Erfindung betrifft bicyclische Verbindungen der allgemeinen Formel I, worin X, Y unabhängig voneinander für N oder C-R4 stehen; n für 1, 2, 3, 4 oder 5 steht; Ra für Halogen, Cyano, C1,-C6-Alkyl, C1,-C6-Alkoxy, C1,-C6-Halogenalkyl, C1,-C6-Halogenalkoxy, C2-C6-Alkenyl, C2-C6-Alkenyloxy oder C(O)R5 steht; R1 Halogen, Cyano, C1-C6-Alkyl, C1,-C6-Halogenalkyl, C2-C6-Alkenyl, C2-C6-Alkinyl, C3-C8-Cycloalkyl, das gegebenenfalls mit Alkyl und/oder Halogen ein- oder mehrfach substituiert ist, C5-C8 Cycloalkenyl, das gegebenenfalls mit Alkyl und/oder Halogen ein- oder mehrfach substituiert ist, OR6, SR6 oder NR7R8 bedeutet; R2 Halogen, Cyano, C1,-C6-Alkyl, C1,-C6-Halogenalkyl, C2-C6-Alkenyl, C2-C6-Alkinyl, C3-C8-Cycloalkyl, das gegebenenfalls mit Alkyl und/oder Halogen ein- oder mehrfach substituiert ist, C5-C8-Cycloalkenyl, das gegebenenfalls mit Alky und/oder Halogen ein- oder mehrfach substituiert ist, OR6, SR6 oder NR7R8 bedeutet; R3 für Wasserstoff, C1,-C6-Alkyl, C1-C6-Halogenalkyl oder C3-C6-Cycloalkyl, das gegebenenfalls mit Alkyl und/oder Halogen ein- oder mehrfach substituiert ist, steht; sowie die landwirtschaftlich verträglichen Salze von Verbindungen (I), Pflanzenschutzmittel, enthaltend wenigstens eine Verbindung der allgemeinen Formel (I) und/oder ein landwirtschaftlich verträgliches Salz von (I) und wenigstens einen flüssigen oder festen Trägerstoff sowie ein Verfahren zur Bekämpfung von pflanzenpathogenen Schadpilzen. |
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| 173 | AZADIOXACYCLOALKENES AND THEIR USE FOR COMBATING HARMFUL FUNGI AND ANIMAL PESTS | PCT/EP2000/000013 | 2000-01-04 | WO00042039A1 | 2000-07-20 | |
| The invention relates to azadioxacycloalkenes of formula (I), in which the substituents and the index have the following meanings; Y represents N or CR, whereby R represents H, halogen or alkyl; n equals 0, 1, 2, 3 or 4, whereby the substituents R<1> can be different if n is greater than 1; R<1>n represents hydrogen or 1 to 4 substituents; R<2> represents hydrogen, nitro, cyano, halogen, alkyl, alkyl halide, alkoxy, alkylthio or alkoxycarbonyl; R<3> represents optionally substituted alkyl, cycloalkyl, aryl or hetaryl; A represents =N-OR<4>, =CH-OR<4> =CH-SR4 or =CH-R<5>, whereby R<4> represents C1-C4 alkyl or C1-C4 alkyl halide, and R<5> represents halogen or a group R<4>, and W represents optionally substituted alkylene. The invention also relates to a method for producing these compounds, to agents containing the same, and to their use for combating animal pests or harmful fungi. | ||||||
| 174 | PROCESS AND AGENTS FOR CONTROLLING HARMFUL FUNGI | PCT/EP1997002037 | 1997-04-22 | WO1997039630A1 | 1997-10-30 | BASF AKTIENGESELLSCHAFT |
| 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<1>R<2>, in which the substituents have the meanings given in the description. Also disclosed are processes for controlling harmful fungi by using said agents. | ||||||
| 175 | CARBAMOYL CARBOXYLIC ACID HYDRAZIDES AND THEIR USE AGAINST FUNGI | PCT/EP1995001924 | 1995-05-20 | WO1995033710A1 | 1995-12-14 | BASF AKTIENGESELLSCHAFT |
| Disclosed are carbamoyl carboxylic acid hydrazides (I) and their salts, wherein: R<1> is optionally substitued alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, aryl or heteroaryl or an optionally substituted non-aromatic carbo- or heterocycle, W<1>W<2>C=N-, where W<1> is optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, aryl or heteroaryl and W<2> is hydrogen or W<1>; R<2> is hydrogen or optionally halogenated alkyl or cycloalkyl; R<3> is optionally substituted alkyl, cycloalkyl or phenylalkyl; R<4> is hydrogen or one of the R<3> radicals, or R<3> and R<4> together with the C atom to which they are bound form an optionally substituted saturated carbo- or heterocycle; R<5> is one of the R<2> radicals; R<6> is optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, aryl or heteroaryl, an optionally sustituted non-aromatic carbo- or heterocycle or, when R<3> = isopropyl, hydrogen; R<7> is one of the R<6> radicals except hydrogen; X<1>, X<2> and X<3> are in each case oxygen or sulfur. Disclosed also are methods for their preparation, agents that contain them, their use and intermediate products (IV), wherein X<3> is oxygen and R<3> is a CH(CH3)2, CH2CH(CH3)2 or CH(CH3)C2H5 group. | ||||||
| 176 | 經取代之6-苯基-7-胺基-[1,2,4]-三唑并[1,5-a]嘧啶及彼等於控制有害真菌之用途 SUBSTITUTED 6-PHENYL-7-AMINO-[1,2,4]-TRIAZOLO[1,5-A] PYRIMIDINES AND THEIR USE FOR CONTROLLING HARMFUL FUNGI | TW096106679 | 2007-02-27 | TW200800026A | 2008-01-01 | 裘成 戴伊茲 DIETZ, JOCHEN; 湯瑪士 葛洛帝 GROTE, THOMAS; 瓦希琉斯 葛蘭梅諾 GRAMMENOS, WASSILIOS; 本德 慕勒 MUELLER, BERND; 珍 科拉司 龍門 LOHMANN, JAN KLAAS; 貞斯 仁諾爾 RENNER, JENS; 莎拉 奧舒尼德 ULMSCHNEIDER, SARAH |
| 本發明係關於式I之經取代6-苯基-7-胺基-【【1,2,4】】-三唑并【【1,5-a】】-嘧啶及其農業上可接受之鹽及彼等於控制有害真菌之用途。本發明亦係關於包含至少一種式I之經取代6-苯基-7-胺基-【【1,2,4】】-三唑并【【1,5-a】】嘧啶或其農業上可接受之鹽的組合物。096106679P01.bmp在式I中,取代基係定義如下:R^1係視情況經取代之C1-C8-烷基、C1-C8-鹵代烷基、C3-C8-環烷基、C3-C8-鹵代環烷基、C2-C8-烯基、C2-C8-鹵代烯基、C3-C6-環烯基、C3-C6-鹵代環烯基、C2-C8-炔基、C2-C8-鹵代炔基或苯基、基或一含有1、2、3或4個來自由O、N及S組成之群之雜原子之5或6員雜環,R^2 係氫或針對R^1所述基團中的一個,L^1係C1-C4-烷基或C1-C4-烷氧基,L^2係氟、氯或C1-C4-烷基,X係鹵素、氰基、C1-C4-烷基、C1-C4-鹵代烷基、C1-C4-烷氧基或C1-C2-鹵代烷氧基。 | ||||||
| 177 | 5,6-二烷基-7-胺基唑并嘧啶,彼等之製備及用於控制有害真菌之用途以及包含彼等化合物之組合物 5,6-DIALKYL-7-AMINOAZOLOPYRIMIDINES, THEIR PREPARATION AND THEIR USE FOR CONTROLLING HARMFUL FUNGI, AND COMPOSITIONS COMPRISING THESE COMPOUNDS | TW095106865 | 2006-03-01 | TW200714602A | 2007-04-16 | 彼德 夏菲爾 SCHAEFER, PETER; 伍都 亨格 HUENGER, UDO; 瑪麗亞 史奇勒 SCHERER, MARIA; 哈拉德 柯雷 KOEHLE, HARALD; 海穆特 希佛 SCHIFFER, HELMUT; 湯瑪士 葛洛帝 GROTE, THOMAS; 裘辰 戴茲 DIETZ, JOCHEN; 瓦希琉斯 葛蘭梅諾 GRAMMENOS, WASSILIOS; 珍 科拉司 龍門 LOHMANN, JAN KLAAS; 本德 慕勒 MUELLER, BERND; 裘秦 雷恩海默 RHEINHEIMER, JOACHIM; 法蘭克 史奇威克 SCHIEWECK, FRANK; 安亞 史奇伍革勒 SCHWOEGLER, ANJA |
| 本發明揭示式I之5,6-二烷基-7-胺基唑并嘧啶 095106865-p01.bmp 其中取代基定義如下:R@#1為鹵代烷基、鹵代烷氧烷基、烷氧鹵代烷基、烯基、鹵代烯基、炔基或鹵代炔基;R@#2為烷基、烷氧烷基、烯基或炔基;其中R@#1及/或R@#2可如說明書所述經取代;A為N或CH;且R@#3為CH@#3且,若A為CH,則又為氫;用於製備該等化合物之方法及中間物,包含彼等之組合物及彼等用於控制植物病原性有害真茵之用途。 095106865-p01.bmp | ||||||
| 178 | 5,6-二烷基-7-胺基唑并嘧啶,彼等之製備及用於控制有害真菌之用途以及包含彼等化合物之組合物 5,6-DIALKYL-7-AMINOAZOLOPYRIMIDINES, THEIR PREPARATION AND THEIR USE FOR CONTROLLING HARMFUL FUNGI, AND COMPOSITIONS COMPRISING THESE COMPOUNDS | TW095106804 | 2006-03-01 | TW200640927A | 2006-12-01 | 彼德 夏菲爾 SCHAEFER, PETER; 伍都 亨格 HUENGER, UDO; 瑪麗亞 史奇勒 SCHERER, MARIA; 哈拉德 柯雷 KOEHLE, HARALD; 海穆特 希佛 SCHIFFER, HELMUT; 湯瑪士 葛洛帝 GROTE, THOMAS; 裘辰 戴茲 DIETZ, JOCHEN; 瓦希琉斯 葛蘭梅諾 GRAMMENOS, WASSILIOS; 珍 科拉司 龍門 LOHMANN, JAN KLAAS; 本德 慕勒 MUELLER, BERND; 裘秦 雷恩海默 RHEINHEIMER, JOACHIM; 法蘭克 史奇威克 SCHIEWECK, FRANK; 安亞 史奇伍革勒 SCHWOEGLER, ANJA |
| 本發明提供式I之5,6–二烷基–7–胺基唑并嘧啶095106804-p01.bmp其中取代基定義如下：R^1為烷基或烷氧烷基，其中該等脂族基團可如說明書中定義經取代；R^2為CHR^xCH3、環丙基、CH＝CH2或CH2CH＝CH2；R^x為氫、CH3或CH2CH3或鹵代甲基；A為N或CH；R^3為甲基，且若A為CH，則又為氫；製備該等化合物之方法及中間物，包含彼等之組合物及彼等用於控制植物病原性有害真菌之用途。095106804-p01.bmp | ||||||
| 179 | 7-胺基-6-雜芳基-1,2,4-三唑并[1,5-a]嘧啶化合物及彼等於控制有害真菌之用途 7-AMINO-6-HETARYL-1,2,4-TRIAZOLO[1,5-A]PYRIMIDINE COMPOUNDS AND THEIR USE FOR CONTROLLING HARMFUL FUNGI | TW094144942 | 2005-12-16 | TW200637864A | 2006-11-01 | 奧利佛 瓦格諾 WAGNER, OLIVER; 湯瑪士 葛洛帝 GROTE, THOMAS; 裘秦 雷恩海默 RHEINHEIMER, JOACHIM; 芭芭拉 納維 NAVE, BARBARA; 雷恩哈德 史堤爾 STIERL, REINHARD |
| 本發明係關於新穎7–胺基–6–雜芳基–1,2,4–三唑并〔1,5–a〕嘧啶化合物，及其農業上可接受之鹽，且亦關於其控制有害真菌之用途，以及包含至少一種此類化合物作為活性成份之作物保護組合物。該新穎7–胺基–6–雜芳基–1,2,4–三唑并〔1,5–a〕嘧啶化合物可藉由式I描述094144942-p01.bmp其中在式I中之取代基R^1、R^2、Het、X及Y均如下文定義：Het為6–員雜芳族基團，選自包括啶基、嗒基、基、1,2,4–三基及1,3,5–三基，其中6–員雜芳族基團可具有1,2或3個相同或不同取代基L，R^1、R^2互相獨立為氫、C1–C8–烷基、C1–C8–鹵烷基、C1–C8–烷氧基、C3–C8–環烷基、C3–C8–環烷氧基、C5–C10–雙環烷基、C3–C8–鹵環烷基、C2@eB!–C8–烯基、C2–C8–烯氧基、C4–C10–烷二烯基、C2–C8–鹵烯基、C3–C8–環烯基、C3–C8–鹵環烯基、C2–C8–炔基、C2–C8–炔氧基、C2–C8–鹵炔基、NH2、C1–C8–烷胺基、二–C1–C8–烷胺基、苯基、基，或五–或六–員飽和、部份不飽和或芳族雜環，X為氫、鹵素、OH、氰基、C1–C4–烷基等，Y為氫、鹵素、氰基、C1–C4–烷基等。094144942-p01.bmp | ||||||
| 180 | 6-(2-氯-4-烷氧苯基)三唑并嘧啶,其製備方法及其於控制有害真菌之用途,以及包含此等化合物之組合物 6-(2-CHLORO-4-ALKOXYPHENYL)TRIAZOLOPYRIMIDINES, THEIR PREPARATION AND THEIR USE FOR CONTROLLING HARMFUL FUNGI, AND COMPOSITIONS COMPRISING THESE COMPOUNDS | TW093139403 | 2004-12-17 | TW200531975A | 2005-10-01 | 喬狄 托默I 布拉斯柯 BLASCO, JORDI TORMO I; 卡斯登 布雷特諾 BLETTNER, CARSTEN; 本德 慕勒 MUELLER, BERND; 馬庫斯 吉維爾 GEWEHR, MARKUS; 瓦希琉斯 葛蘭梅諾 GRAMMENOS, WASSILIOS; 湯瑪士 葛洛帝 GROTE, THOMAS; 裘秦 雷恩海默 RHEINHEIMER, JOACHIM; 彼德 夏菲爾 SCHAEFER, PETER; 法蘭克 史奇威克 SCHIEWECK, FRANK; 安亞 史奇伍革勒 SCHWOEGLER, ANJA; 奧利佛 瓦格諾 WAGNER, OLIVER; 瑪麗亞 史奇勒 SCHERER, MARIA; 希格佛雷德 史揣斯曼 STRATHMANN, SIEGFRIED; 歐里齊 史丘佛 SCHOEFL, ULRICH; 雷恩哈德 史堤爾 STIERL, REINHARD |
| 式I之經取代的三唑并嘧啶093139403-p01.bmp其中取代基係定義如下：L為氫，氯或溴；R^1,R^2為氫，烷基，鹵烷基，環烷基，鹵環烷基，烯基，鹵烯基，環烯基，鹵環烯基，炔基，鹵炔基或苯基，基或五–或六–員環之飽和，部份不飽和或芳族的雜環，其含有一到四個由O，N和S組成之群的雜原子，R^1和R^2和其所連接的氮原子也可以一齊為透過N連接之五–或六–員的雜環基或雜芳基，並且可含有為環成員之另一由O，N和S組成之群的雜原子，和／或可如說明書中所定義為經取代者；R^3為烷基，鹵烷基，鹵烯基，炔基，鹵炔基，環烷基，鹵環烷基或苯烷基；R^1,R^2和／或R^3可如說明書中所定義為經取代者；X為鹵素，氰基，烷基，鹵烷基，烷氧基或鹵烷氧基；製備彼等化合物之方法和中間物，包含其等之組合物，以及其等用於控制植物致病之有害真菌的用途。093139403-p01.bmp | ||||||
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