AR078783A1 - Compuestos heterociclicos pesticidas - Google Patents
Compuestos heterociclicos pesticidasInfo
- Publication number
- AR078783A1 AR078783A1 ARP100103933A ARP100103933A AR078783A1 AR 078783 A1 AR078783 A1 AR 078783A1 AR P100103933 A ARP100103933 A AR P100103933A AR P100103933 A ARP100103933 A AR P100103933A AR 078783 A1 AR078783 A1 AR 078783A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- thiocarbonyl
- alkylcarbonyl
- substituted
- amino
- Prior art date
Links
- 239000000575 pesticide Substances 0.000 title abstract 3
- 150000001875 compounds Chemical class 0.000 title 1
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 abstract 15
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 11
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 6
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 239000001257 hydrogen Substances 0.000 abstract 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 6
- 229910052760 oxygen Inorganic materials 0.000 abstract 6
- 229910052717 sulfur Inorganic materials 0.000 abstract 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 5
- 229910052799 carbon Inorganic materials 0.000 abstract 5
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 4
- 125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 abstract 4
- -1 nitro, cyano, hydroxy, mercapto Chemical class 0.000 abstract 4
- 229910052757 nitrogen Inorganic materials 0.000 abstract 4
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 abstract 3
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 3
- 125000004670 alkyl amino thio carbonyl group Chemical group 0.000 abstract 3
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 3
- 125000003636 chemical group Chemical group 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000005842 heteroatom Chemical group 0.000 abstract 3
- 125000005309 thioalkoxy group Chemical group 0.000 abstract 3
- 125000006569 (C5-C6) heterocyclic group Chemical group 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 abstract 2
- 125000000676 alkoxyimino group Chemical group 0.000 abstract 2
- 125000003282 alkyl amino group Chemical group 0.000 abstract 2
- 125000004471 alkyl aminosulfonyl group Chemical group 0.000 abstract 2
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 2
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 abstract 2
- 125000004414 alkyl thio group Chemical group 0.000 abstract 2
- 125000002947 alkylene group Chemical group 0.000 abstract 2
- 125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- HCMJWOGOISXSDL-UHFFFAOYSA-N (2-isothiocyanato-1-phenylethyl)benzene Chemical compound C=1C=CC=CC=1C(CN=C=S)C1=CC=CC=C1 HCMJWOGOISXSDL-UHFFFAOYSA-N 0.000 abstract 1
- 125000004641 (C1-C12) haloalkyl group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- IZXIZTKNFFYFOF-UHFFFAOYSA-N 2-Oxazolidone Chemical class O=C1NCCO1 IZXIZTKNFFYFOF-UHFFFAOYSA-N 0.000 abstract 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000000041 C6-C10 aryl group Chemical group 0.000 abstract 1
- 229930194542 Keto Natural products 0.000 abstract 1
- 239000003905 agrochemical Substances 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000005090 alkenylcarbonyl group Chemical group 0.000 abstract 1
- 125000004694 alkoxyaminocarbonyl group Chemical group 0.000 abstract 1
- 125000004695 alkoxyaminothiocarbonyl group Chemical group 0.000 abstract 1
- 125000004685 alkoxythiocarbonyl group Chemical group 0.000 abstract 1
- 125000000002 alkyl sulfinylimino group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 1
- 244000000054 animal parasite Species 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 150000007982 azolidines Chemical class 0.000 abstract 1
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 abstract 1
- 125000005167 cycloalkylaminocarbonyl group Chemical group 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 1
- 125000000468 ketone group Chemical group 0.000 abstract 1
- RIFHJAODNHLCBH-UHFFFAOYSA-N methanethione Chemical group S=[CH] RIFHJAODNHLCBH-UHFFFAOYSA-N 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 125000004665 trialkylsilyl group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D263/10—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D263/12—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with radicals containing only hydrogen and carbon atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/06—Nitrogen directly attached to an aromatic ring system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D291/00—Heterocyclic compounds containing rings having nitrogen, oxygen and sulfur atoms as the only ring hetero atoms
- C07D291/02—Heterocyclic compounds containing rings having nitrogen, oxygen and sulfur atoms as the only ring hetero atoms not condensed with other rings
- C07D291/04—Five-membered rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Public Health (AREA)
- Agronomy & Crop Science (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Pest Control & Pesticides (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyrrole Compounds (AREA)
Abstract
La presente se refiere a pesticidas derivados de azolidina, así como a derivados de oxazolidinona y su uso como pesticidas para combatir parásitos animales que están presentes en el campo agroquímico y en el campo de la medicina veterinaria, respectivamente. Reivindicacion 1: Derivados de azolidina de formula (1) en la que R' representa alquilo C1-12 o haloalquilo C1-12 que pueden estar sustituidos I representa 0 o 1, G representa CH, CH2, N, O, S, C=O, C=S, o NR1; U representa CH, CH2, N, C=O, C=S, S=O, SO2 o NR1, con la condicion de que G y U no representan de forma simultánea CH2, y cuando G y U cada uno representan CH o N, un enlace entre G y U es un doble enlace; R1 y R2 cada uno de forma independiente representa hidrogeno, ciano, alquilo C1-12, cicloalquilo C3-8, cicloalquilo C3-8-alquiIo C1-12, alquenilo C2-6, alquinilo C2-6, alcoxi C1-12-carbonilo o tioalcoxi C1-12-carbonilo, en el que cada grupo del alquilo C1-2 al tioalcoxi C1-12-carbonilo descrito puede estar sustituido; R1 y R2 pueden formar un anillo hidrocarburo de 3-6 miembros con el átomo de carbono al que están unidos; X que puede ser igual o diferente representa hidrogeno, halogeno, nitro, ciano, hidroxi, mercapto, SF5, amino, alquilo C1-12, alcoxi C1-12, cicloalquilo C3-8, alquiltio C1-12, alquilsulfinilo C1-12, alquilsulfonilo C1-12, alquilsulfoniloxi C1-12, alquilaminosulfonilo C1-12, di(alquilo C1-12)amino-sulfonilo, alquilcarbonilamino C1-12, benzoilamino, tri(alquilo C1-12)sililo, o alcoxiimino C1-12, alquilsulfinilimino C1-12, alquilsulfonilimino C1-12, alcoxi C1-12-carbonilo, alquilcarbonilo C1-12, aminocarbonilo, alquilamino C1-12-carbonilo, amino-tiocarbonilo, alquilamino C1-12-tiocarbonilo, di(alquilo C1-12)amino-carbonilo o di(alquilo C1-12)amino-tiocarbonilo, en el que cada grupo de dicho alquilo C1-12 a di(alquilo C1-12)amino-tiocarbonilo puede estar sustituido; m representa 1, 2, 3 o 4; o el grupo químico (X)m-Q- representa un grupo cíclico aromático de 6 miembros que tiene la formula siguiente (2) en la que cada B1, B2, B3 y B4 representa cada uno de forma independiente C-X o N (nitrogeno), con la condicion de que solo dos de B1, B2, B3 y B4 puedan representar de forma simultánea N; Q representa un grupo heterocíclico de 5 miembros que contiene de 1 a 4 heteroátomos seleccionados de N, O y S; y en el que el grupo químico representa uno de los grupos siguientes (4) en las que A1, A2, A3 y A4 cada uno de forma independiente representa C-Y o N (nitrogeno) con la condicion de que solo dos de A1, A2, A3 y A4 pueden representar de forma simultánea N; cuando A1 y A2 representa C-Y, dos Y pueden formar un anillo de benceno o un anillo heteroaromático de 5 a 6 miembros con los átomos de carbono a los que están unidos; L representa un grupo químico (CR1R2) con n siendo 1, 2 o 3; R3 representa hidrogeno, amino, hidroxi, ciano, alquilo C1-12, alcoxi C1-12, alquilcarbonilamino C1-12, alquilamino C1-12, cicloalquilo C3-8, alquenilo C2-12, alquinilo C2-12, alquilcarbonilo C1-12, CH2-R5, C(=O)R5 o C(=S)R5, en el que cada grupo del alquilo C1-12 al alquilcarbonilo C1-12 descrito en el presente documento puede estar sustituido; R4 representa hidrogeno, ciano, formilo, tioformilo, alquilcarbonilo C1-12, alquilo C1-12-tiocarbonilo, alquilamino C1-12-carbonilo, alquilamino C1-12-tiocarbonilo, dialquilamino (numero total de carbonos) C2-24-carbonilo, dialquilamino (numero total de carbonos) C2-24-tiocarbonilo, alcoxiamino C1-12-carbonilo, alcoxiamino C1-12-tiocarbonilo, alcoxi C1-12-carbonilo, alcoxi C1-12-alquilcarbonilo C1-12, tioalcoxi C1-12-alquilcarbonilo C1-12, alquilsulfenilo C1-12-alquilcarbonilo C1-12, alquilsulfonilo C1-12-alquilcarbonilo C1-12, alcoxi C1-12-tiocarbonilo, tioalcoxi C1-12-carbonilo, tioalcoxi C1-12-tiocarbonilo, alquilsulfonilo C1-12, cicloalquilcarbonilo C3-8, cicloalquilo C3-8-alquilcarbonilo C1-12, alquenilo C2-12-carbonilo, alquinilo C2-12-carbonilo, cicloalquilamino C3-8-carbonilo, alquenilamino C2-12-carbonilo, alquinilamino C2-12-carbonilo, C(=O)R5 o C(=S)R5, en el que cada grupo del alquilcarbonilo C1-12 al alquinilamino C2-12-carbonilo descrito en el presente documento puede estar sustituido; o R3 y R4 pueden formar un heterociclo de 3 a 6 miembros con el átomo de nitrogeno al que están unidos, en el que el heterociclo puede estar sustituido con X, ceto, tioceto o nitroimino; R5 representa fenilo que puede estar sustituido o un grupo heterocíclico de 5 a 6 miembros que puede estar sustituido y contiene al menos un heteroátomo seleccionado de N, O y S; R6 y R7 cada uno de forma independiente representa hidrogeno, ciano, alquilo C1-12, cicloalquilo C3-8, alquenilo C2-6, alquinilo C2-6, alcoxi C1-12-carbonilo, alquilsulfonilo C1-12, arilo C6-10, aralquilo C7-9, un grupo heterocíclico de 5 a 6 miembros que contiene al menos un heteroátomo seleccionado de N, O y S, o alquilo C1-12-O-N=CH-, en el que cada grupo del alquilo C1-12 al alquilo C1-12-O-N=CH- descrito en el presente documento puede estar sustituido; o R6 y R7 juntos pueden formar alquileno C2-6; preferentemente R6 y R7 juntos pueden formar alquileno C4-5; Y que puede ser igual o diferente representa hidrogeno, halogeno, nitro, ciano, hidroxi, mercapto, amino, alquilo C1-12, cicloalquilo C3-8, alcoxi C1-12, alquiltio C1-12, alquilsulfinilo C1-12, alquilsulfonilo C1-12, alquilsulfoniloxi C1-12, alquilaminosulfonilo C1-12, dialquilamino C2-24 (numero total de carbonos)-sulfonilo, alquilcarbonilamino C1-6, benzoilamino, trialquilsililo-C1-12, alcoxiimino C1-12, alquilsulfinilimino C1-12, alquilsulfonilimino C1-12, alcoxi C1-12-carbonilo, alquilcarbonilo C1-12, aminocarbonilo, alquilamino C1-12-carbonilo, amino-tiocarbonilo, alquilamino C1-12-tiocarbonilo, dialquilamino C2-24 (numero total de carbonos)-carbonilo o dialquilamino C2-24 (numero total de carbonos)-tiocarbonilo, en el que cada grupo del amino al dialquilamino C2-24 (numero total de carbonos)-tiocarbonilo descrito en el presente documento puede estar sustituido.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2009250744A JP2011093855A (ja) | 2009-10-30 | 2009-10-30 | 殺虫性オキサゾリジノン誘導体 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR078783A1 true AR078783A1 (es) | 2011-11-30 |
Family
ID=43430262
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP100103933A AR078783A1 (es) | 2009-10-30 | 2010-10-26 | Compuestos heterociclicos pesticidas |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US20110152332A1 (es) |
| JP (2) | JP2011093855A (es) |
| KR (1) | KR20120113723A (es) |
| CN (1) | CN102666505A (es) |
| AR (1) | AR078783A1 (es) |
| BR (1) | BR112012010238A2 (es) |
| MX (1) | MX2012005066A (es) |
| TW (1) | TW201127292A (es) |
| UY (1) | UY32982A (es) |
| WO (1) | WO2011051455A1 (es) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI487486B (zh) | 2009-12-01 | 2015-06-11 | Syngenta Participations Ag | 以異唑啉衍生物為主之殺蟲化合物 |
| JP2012232910A (ja) * | 2011-04-28 | 2012-11-29 | Bayer Cropscience Ag | 殺虫性アリルヘテロサイクル誘導体 |
| US20140171475A1 (en) * | 2011-05-31 | 2014-06-19 | Sumitomo Chemical Company, Limited | Animal ectoparasite-controlling agent |
| WO2013087710A2 (en) | 2011-12-14 | 2013-06-20 | Syngenta Participations Ag | Pesticidal mixtures |
| JP2015515454A (ja) * | 2012-03-14 | 2015-05-28 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングＢａｙｅｒ Ｉｎｔｅｌｌｅｃｔｕａｌ Ｐｒｏｐｅｒｔｙ ＧｍｂＨ | 殺有害生物性アリールピロリジン類 |
| WO2014019609A1 (en) | 2012-07-31 | 2014-02-06 | Syngenta Participations Ag | Methods of pest control in soybean |
| US20150152070A1 (en) | 2012-08-03 | 2015-06-04 | Syngenta Paricipations Ag | Methods of pest control in soybean |
| AU2013326600B2 (en) | 2012-10-02 | 2017-03-30 | Bayer Cropscience Ag | Heterocyclic compounds as pesticides |
| WO2014114250A1 (en) | 2013-01-23 | 2014-07-31 | Syngenta Participations Ag | Pyrazoline derivatives as insecticidal compounds |
| WO2020113094A1 (en) | 2018-11-30 | 2020-06-04 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1992000964A1 (en) | 1990-07-05 | 1992-01-23 | Nippon Soda Co., Ltd. | Amine derivative |
| AU2002258633A1 (en) * | 2001-03-28 | 2002-10-15 | Bristol-Myers Squibb Company | Cyanamide, alkoxyamino, and urea derivatives of 1,3-benzodiazapines as hiv reverse transcriptase inhibitors |
| EP1385517A1 (en) * | 2001-04-16 | 2004-02-04 | University Of Virginia Patent Foundation | Novel oral general anesthetics and metabolitically resistant anticonvulsants |
| WO2004018410A1 (ja) * | 2002-08-26 | 2004-03-04 | Nissan Chemical Industries, Ltd. | 置換ベンズアニリド化合物及び有害生物防除剤 |
| JP2005272452A (ja) * | 2004-02-23 | 2005-10-06 | Nissan Chem Ind Ltd | 置換ベンズアニリド化合物及び有害生物防除剤 |
| DK1731512T3 (en) | 2004-03-05 | 2015-01-05 | Nissan Chemical Ind Ltd | Isoxazoline-substituted benzamide AND INSTRUMENTS FOR COMBATING HARMFUL ORGANISMS |
| MX2007004710A (es) | 2004-10-20 | 2007-06-14 | Kumiai Chemical Industry Co | Derivado de sulfuro de 3-triazolilfenilo e insecticida/acaricida/ nematicida que contiene el mismo como ingrediente activo. |
| DE102005008021A1 (de) * | 2005-02-22 | 2006-08-24 | Bayer Cropscience Ag | Spiroketal-substituierte cyclische Ketoenole |
| JP5007788B2 (ja) * | 2005-05-16 | 2012-08-22 | 日産化学工業株式会社 | ジヒドロアゾール置換ベンズアミド化合物及び有害生物防除剤 |
| TWI398433B (zh) | 2006-02-10 | 2013-06-11 | Dow Agrosciences Llc | 殺蟲性之ｎ-取代（６-鹵烷基吡啶-３-基）烷基磺醯亞胺 |
| PL1997813T3 (pl) | 2006-03-10 | 2010-10-29 | Nissan Chemical Ind Ltd | Podstawiony związek izoksazolinowy i środek zwalczający szkodniki |
| DE102006015468A1 (de) | 2006-03-31 | 2007-10-04 | Bayer Cropscience Ag | Substituierte Enaminocarbonylverbindungen |
| DE102006015467A1 (de) | 2006-03-31 | 2007-10-04 | Bayer Cropscience Ag | Substituierte Enaminocarbonylverbindungen |
| DE102006015470A1 (de) | 2006-03-31 | 2007-10-04 | Bayer Cropscience Ag | Substituierte Enaminocarbonylverbindungen |
| MX2008013305A (es) | 2006-04-20 | 2008-10-27 | Du Pont | Agentes heterociclicos de cinco miembros para el control de plagas de invertebrados. |
| TWI381811B (zh) | 2006-06-23 | 2013-01-11 | Dow Agrosciences Llc | 用以防治可抵抗一般殺蟲劑之昆蟲的方法 |
| JP5164510B2 (ja) | 2006-10-06 | 2013-03-21 | 日本曹達株式会社 | 含窒素複素環化合物および有害生物防除剤 |
| DE102006057036A1 (de) | 2006-12-04 | 2008-06-05 | Bayer Cropscience Ag | Biphenylsubstituierte spirocyclische Ketoenole |
| JP2008266230A (ja) | 2007-04-23 | 2008-11-06 | Bayer Cropscience Ag | 殺虫性アリールピロリジン類 |
-
2009
- 2009-10-30 JP JP2009250744A patent/JP2011093855A/ja active Pending
-
2010
- 2010-10-26 AR ARP100103933A patent/AR078783A1/es unknown
- 2010-10-27 UY UY0001032982A patent/UY32982A/es not_active Application Discontinuation
- 2010-10-29 JP JP2012535852A patent/JP2013509383A/ja not_active Withdrawn
- 2010-10-29 MX MX2012005066A patent/MX2012005066A/es not_active Application Discontinuation
- 2010-10-29 WO PCT/EP2010/066480 patent/WO2011051455A1/en active Application Filing
- 2010-10-29 CN CN2010800494247A patent/CN102666505A/zh active Pending
- 2010-10-29 KR KR1020127013856A patent/KR20120113723A/ko not_active Application Discontinuation
- 2010-10-29 TW TW099137097A patent/TW201127292A/zh unknown
- 2010-10-29 BR BR112012010238A patent/BR112012010238A2/pt not_active IP Right Cessation
- 2010-11-01 US US12/917,116 patent/US20110152332A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| TW201127292A (en) | 2011-08-16 |
| JP2013509383A (ja) | 2013-03-14 |
| MX2012005066A (es) | 2012-06-13 |
| WO2011051455A1 (en) | 2011-05-05 |
| JP2011093855A (ja) | 2011-05-12 |
| US20110152332A1 (en) | 2011-06-23 |
| UY32982A (es) | 2011-05-31 |
| BR112012010238A2 (pt) | 2015-09-29 |
| CN102666505A (zh) | 2012-09-12 |
| KR20120113723A (ko) | 2012-10-15 |
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