AR065276A1 - Herbicidas de n-oxidos de piridina sustituidos - Google Patents

Herbicidas de n-oxidos de piridina sustituidos

Info

Publication number
AR065276A1
AR065276A1 ARP080100559A ARP080100559A AR065276A1 AR 065276 A1 AR065276 A1 AR 065276A1 AR P080100559 A ARP080100559 A AR P080100559A AR P080100559 A ARP080100559 A AR P080100559A AR 065276 A1 AR065276 A1 AR 065276A1
Authority
AR
Argentina
Prior art keywords
alkyl
6alkyl
alkoxy
haloalkyl
halogen
Prior art date
Application number
ARP080100559A
Other languages
English (en)
Inventor
Thomas Paul Selby
Thomas Martin Stevenson
Brenton Todd Smith
Original Assignee
Du Pont
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Du Pont filed Critical Du Pont
Publication of AR065276A1 publication Critical patent/AR065276A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • 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
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4402—Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 2, e.g. pheniramine, bisacodyl
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines

Abstract

Reivindicacion 1: Un compuesto caracterizado porque se selecciona entre formula 1, sus N-oxidos y sales, en donde cada R1 es en forma independiente halogeno, ciano, hidroxi, amino, nitro, -CHO, -C(=O)OH, -C(=O)NH2, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-6, haloalquenilo C2-6, haloalquinilo C2-6, cicloalquilo C3-8, halocicloalquilo C3-8, alquilcicloalquilo C4-8, cicloalquilalquilo C4-8, cicloalquilcicloalquilo C6-8, halocicloalquilalquilo C4-8, alquilcicloalquilalquilo C5-8, cicloalquenilo C3-8, halocicloalquenilo C3-8, alcoxialquilo C2-6, cicloalcoxialquilo C4-8, alcoxialcoxialquilo C3-6, alquiltioalquilo C2-6, alquilsulfinilalquilo C2-6, alquilsulfonilalquilo C2-6, alquilaminoalquilo C2-6, dialquilaminoalquilo C3-6, haloalquilaminoalquilo C3-6, cicloalquilaminoalquilo C4-8, alquilcarbonilo C2-6, haloalquilcarbonilo C2-6, cicloalquilcarbonilo C4-8, alcoxicarbonilo C2-6, cicloalcoxicarbonilo C4-8, cicloalquilalcoxicarbonilo C5-8, alquilaminocarbonilo C2-6, dialquilaminocarbonilo C3-6, cicloalquilaminocarbonilo C4-8, haloalcoxialquilo C2-6, alcoxicarbonilalquilo C3-6, alcoxi C1-6, haloalcoxi C1-6, cicloalcoxi C3-8, halocicloalcoxi C3-8, cicloalquilalcoxi C4-8, alqueniloxi C2-6, haloalqueniloxi C2-6, alquiniloxi C3-6, haloalquiniloxi C3-6, alcoxialcoxi C2-6, alquilcarboniloxi C2-6, haloalquilcarboniloxi C2-6, cicloalquilcarboniloxi C4-8, alquilcarbonilalcoxi C3-6, alquiltio C1-6, haloalquiltio C1-6, cicloalquiltio C3-8, alquilsulfinilo C1-6, haloalquilsulfinilo C1-6, alquilsulfonilo C1-6, haloalquilsulfonilo C1-6, cicloalquilsulfonilo C3-8, trialquilsililo C3-8, alquilamino C1-6, dialquilamino C2-6, haloalquilamino C2-6, halodialquilamino C2-6, cicloalquilamino C3-8, alquilcarbonilamino C2-6, haloalquilcarbonilamino C2-6, alquilsulfonilamino C1-6 o haloalquilsulfonilamino C1-6; o fenilo, piridinilo, tienilo, naftalenilo o bencilo, cada uno opcionalmente sustituido con 1-3 sustituyentes seleccionados entre alquilo C1-4, haloalquilo C1-4, alcoxi C1-4, haloalcoxi C1-4, halogeno, hidroxi, amino, ciano y nitro; o dos R1 unidos a átomos de carbono contiguos del anillo se toman juntos para formar un anillo fusionado de 5 o 6 miembros que contiene átomos de carbono y opcionalmente entre 1 y 3 heteroátomos seleccionados entre O y N como miembros del anillo, e incluyendo opcionalmente entre 1 y 3 miembros del anillo seleccionados entre el grupo que consiste de C(=O), C(=S) y S(=O)p(=NR8)q; estando el anillo fusionado opcionalmente sustituido con 1-3 sustituyentes seleccionados entre alquilo C1-4, haloalquilo C1-4, alcoxi C1-4, haloalcoxi C1-4, halogeno, CN y NO2; m es 0, 1, 2, 3 o 4; W es O o NR7; n es 0 o 1; R2 H, halogeno, ciano, hidroxi, amino, nitro, -CHO, - C(=O)OH, -C(=O)NH2, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-6, haloalquenilo C2-6, haloalquinilo C2-6, cicloalquilo C3-8, halocicloalquilo C3-8, alquilcicloalquilo C4-8, cicloalquilalquilo C4-8, cicloalquilcicloalquilo C6-8, halocicloalquilalquilo C4-8, alquilcicloalquilalquilo C5-8, cicloalquenilo C3-8, halocicloalquenilo C3-8, alcoxialquilo C2-6, cicloalcoxialquilo C4-8, alcoxialcoxialquilo C3-6, alquiltioalquilo C2-6, alquilsulfinilalquilo C2-6, alquilsulfonilalquilo C2-6, alquilaminoalquilo C2-6, dialquilaminoalquilo C3-6, haloalquilaminoalquilo C3-6, cicloalquilaminoalquilo C4-8, alquilcarbonilo C2-6, haloalquilcarbonilo C2-6, cicloalquilcarbonilo C4-8, alcoxicarbonilo C2-6, cicloalcoxicarbonilo C4-8, cicloalquilalcoxicarbonilo C5-8, alquilaminocarbonilo C2-6, dialquilaminocarbonilo C3-6, cicloalquilaminocarbonilo C4-8, haloalcoxialquilo C2-6, alcoxicarbonilalquilo C3-6, alcoxi C1-6, haloalcoxi C1-6, cicloalcoxi C3-8, halocicloalcoxi C3-8, cicloalquilalcoxi C4-8, alqueniloxi C2-6, haloalqueniloxi C2-6, alquiniloxi C3-6, haloalquiniloxi C3-6, alcoxialcoxi C2-6, alquilcarboniloxi C2-6, haloalquilcarboniloxi C2-6, cicloalquilcarboniloxi C4-8, alquilcarbonilalcoxi C3-6, alquiltio C1-6, haloalquiltio C1-6, cicloalquiltio C3-8, alquilsulfinilo C1-6, haloalquilsulfinilo C1-6, alquilsulfonilo C1-6, haloalquilsulfonilo C1-6, cicloalquilsulfonilo C3-8, trialquilsililo C3-8, alquilamino C1-6, dialquilamino C2-6, haloalquilamino C2-6, halodialquilamino C2-6, cicloalquilamino C3-8, alquilcarbonilamino C2-6, haloalquilcarbonilamino C2-6, alquilsulfonilamino C1-6 o haloalquilsulfonilamino C1-6; R3 es H, halogeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6 o haloalquilo C1-6; o R2 y R3 se toman junto con el átomo de carbono al cual están unidos para formar un anillo carbocíclico de 3 a 8 miembros, opcionalmente sustituido con 1-3 sustituyentes seleccionados entre alquilo C1-4, haloalquilo C1-4, alcoxi C1-4, haloalcoxi C1-4, halogeno, hidroxi, amino, ciano y nitro; cada R4 y R5 es en forma independiente H, halogeno, ciano, hidroxi, amino, nitro, -CHO, C(=O)OH, -C(=O)NH2, C(=S)NH2, -C(=O)NHCN, -C(=O)NHOH, -SH, -SO2NH2, -SO2NHCN, -SO2NHOH, -OCN, -SCN, -SF5, -NHCHO, - NHNH2, -NHOH, -NHCN, -NHC(=O)NH2, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-6, haloalquenilo C2-6, haloalquinilo C2-6, cicloalquilo C3-8, halocicloalquilo C3-8, alquilcicloalquilo C4-8, cicloalquilalquilo C4-8, cicloalquilcicloalquilo C6-8, halocicloalquilalquilo C4-8, alquilcicloalquilalquilo C5-8, cicloalquenilo C3-8, halocicloalquenilo C3-8, alcoxialquilo C2-6, cicloalcoxialquilo C4-8, alcoxialcoxialquilo C3-6, alquiltioalquilo C2-6, alquilsulfinilalquilo C2-6, alquilsulfonilalquilo C2-6, alquilaminoalquilo C2-6, dialquilaminoalquilo C3-6, haloalquilaminoalquilo C3-6, cicloalquilaminoalquilo C4-8, alquilcarbonilo C2-6, haloalquilcarbonilo C2-6, cicloalquilcarbonilo C4-8, alcoxicarbonilo C2-6, cicloalcoxicarbonilo C4-8, cicloalquilalcoxicarbonilo C5-8, alquilaminocarbonilo C2-6, dialquilaminocarbonilo C3-6, cicloalquilaminocarbonilo C4-8, cianoalquilo C2-6, hidroxialquilo C1-6, cicloalquenilalquilo C4-8, haloalcoxialquilo C2-6, alcoxicarbonilalquilo C3-6, alcoxi C1-6, haloalcoxi C1-6, cicloalcoxi C3-8, halocicloalcoxi C3-8, cicloalquilalcoxi C4-8, alqueniloxi C2-6, haloalqueniloxi C2-6, alquiniloxi C3-6, haloalquiniloxi C3-6, alcoxialcoxi C2-6, alquilcarboniloxi C2-6, haloalquilcarboniloxi C2-6, cicloalquilcarboniloxi C4-8, alquilcarbonilalcoxi C3-6, alquiltio C1-6, haloalquiltio C1-6, cicloalquiltio C3-8, alquilsulfinilo C1-6, haloalquilsulfinilo C1-6, alquilsulfonilo C1-6, haloalquilsulfonilo C1-6, cicloalquilsulfonilo C3-8, trialquilsililo C3-8, halocicloalqueniloxi C3-8, haloalcoxialcoxi C2-6, alcoxihaloalcoxi C2-6, haloalcoxihaloalcoxi C2-6, alcoxicarbonilalcoxi C3-6, alquilaminosulfonilo C1-6, dialquilaminosulfonilo C2-6, halotrialquilsililo C3-8, alquilamino C1-6, dialquilamino C2-6, haloalquilamino C2-6, halodialquilamino C2-6, cicloalquilamino C3-8, alquilcarbonilamino C2-6, haloalquilcarbonilamino C2-6, alquilsulfonilamino C1-6 o haloalquilsulfonilamino C1-6; o fenilo, piridinilo, tienilo o bencilo, cada uno opcionalmente sustituido con 1-3 sustituyentes seleccionados entre alquilo C1-4, haloalquilo C1-4, alcoxi C1-4, haloalcoxi C1-4, halogeno, hidroxi, amino, ciano y nitro; R6 es H, hidroxi, amino, -C(=O)NH2, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-6, haloalquenilo C2-6, haloalquinilo C2-6, cicloalquilo C3-8, halocicloalquilo C3-8, alquilcicloalquilo C4-8, cicloalquilalquilo C4-8, cicloalquilcicloalquilo C6-8, halocicloalquilalquilo C4-8, alquilcicloalquilalquilo C5-8, cicloalquenilo C3-8, halocicloalquenilo C3-8, alcoxialquilo C2-6, cicloalcoxialquilo C4-8, alcoxialcoxialquilo C3-6, alquiltioalquilo C2-6, alquilsulfinilalquilo C2-6, alquilsulfonilalquilo C2-6, alquilaminoalquilo C2-6, dialquilaminoalquilo C3-6, haloalquilaminoalquilo C3-6, cicloalquilaminoalquilo C4-8, alquilcarbonilo C2-6, haloalquilcarbonilo C2-6, cicloalquilcarbonilo C4-8, alcoxicarbonilo C2-6, cicloalcoxicarbonilo C4-8, cicloalquilalcoxicarbonilo C5-8, alquilaminocarbonilo C2-6, dialquilaminocarbonilo C3-6, cicloalquilaminocarbonilo C4-8, cianoalquilo C2-6, haloalcoxialquilo C2-6, alcoxicarbonilalquilo C3-6, alquilsulfonilo C1-6, haloalquilsulfonilo C1-6, cicloalquilsulfonilo C3-8, alquilamino C1-6, dialquilamino C2-6, haloalquilamino C2-6, halodialquilamino C2-6, cicloalquilamino C3-8, alquilcarbonilamino C2-6, haloalquilcarbonilamino C2-6, alquilsulfonilamino C1-6 o haloalquilsulfonilamino C1-6; o fenilo, piridinilo, tienilo o bencilo, cada uno opcionalmente sustituido con 1-3 sustituyentes seleccionados entre alquilo C1-4, haloalquilo C1-4, alcoxi C1-4, haloalcoxi C1-4, halogeno, hidroxi, amino, ciano y nitro; o R5 y R6 se toman junto con los átomos a los cuales están unidos para formar un anillo fusionado que contiene entre 2 y 6 átomos de carbono y opcionalmente entre 1 y 3 heteroátomos seleccionados entre O y N como miembros del anillo además de los átomos a los cuales R5 y R6 están unidos, e incluyendo opcionalmente entre 1 y 3 miembros del anillo seleccionados entre el grupo que consiste de C(=O), C(=S) o S(=O)p(=NR8)q; estando el anillo fusionado opcionalmente sustituido con 1-3 sustituyentes seleccionados entre alquilo C1-2, halogeno, CN, NO2 y alcoxi C1-2; R7 es H, ciano, hidroxi, amino, alquilo C1-6, alquenilo C3-6, alquinilo C3-6, haloalquilo C1-6, haloalquilo C1-6, haloalquenilo C3-6, haloalquinilo C3-6, cicloalquilo C3-8, halocicloalquilo C3-8, alquilcicloalquilo C4-8, cicloalquilalquilo C4-8, cicloalquilcicloalquilo C6-8, halocicloalquilalquilo C4-8, alquilcicloalquilalquilo C5-8, cicloalquenilo C3-8, halocicloalquenilo C3-8, alcoxialquilo C2-6, alquilcarbonilo C2-6, haloalquilcarbonilo C2-6, alcoxicarbonilo C2-6, alquilaminocarbonilo C2-6, alcoxi C1-6, haloalcoxi C1-6, cicloalcoxi C3-8, halocicloalcoxi C3-8, cicloalquilalcoxi C4-8, alquilsulfonilo C1-6, haloalquilsulfonilo C1-6, cicloalquilsulfonilo C3-8, alquilamino C1-6, dialquilamino C2-6, haloalquilamino C2-6, halodialquilamino C2-6 o cicloalquilamino C3-6; o fenilo, piridinilo, tienilo, naftalenilo o bencilo, cada uno opcionalmente sustituido con 1-3 sustituyentes seleccionad
ARP080100559A 2007-02-09 2008-02-08 Herbicidas de n-oxidos de piridina sustituidos AR065276A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US90057907P 2007-02-09 2007-02-09

Publications (1)

Publication Number Publication Date
AR065276A1 true AR065276A1 (es) 2009-05-27

Family

ID=39690673

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP080100559A AR065276A1 (es) 2007-02-09 2008-02-08 Herbicidas de n-oxidos de piridina sustituidos

Country Status (17)

Country Link
US (1) US20100298141A1 (es)
EP (1) EP2120939A2 (es)
JP (1) JP2010518084A (es)
KR (1) KR20090110374A (es)
AR (1) AR065276A1 (es)
AU (1) AU2008216859A1 (es)
BR (1) BRPI0806366A2 (es)
CA (1) CA2675200A1 (es)
CL (1) CL2008000376A1 (es)
CO (1) CO6230985A2 (es)
IL (1) IL199764A0 (es)
MX (1) MX2009008325A (es)
NZ (1) NZ578196A (es)
RU (1) RU2009133794A (es)
UY (1) UY30898A1 (es)
WO (1) WO2008100426A2 (es)
ZA (1) ZA200905133B (es)

Families Citing this family (54)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8097712B2 (en) 2007-11-07 2012-01-17 Beelogics Inc. Compositions for conferring tolerance to viral disease in social insects, and the use thereof
US8962584B2 (en) 2009-10-14 2015-02-24 Yissum Research Development Company Of The Hebrew University Of Jerusalem, Ltd. Compositions for controlling Varroa mites in bees
US9121022B2 (en) 2010-03-08 2015-09-01 Monsanto Technology Llc Method for controlling herbicide-resistant plants
MX348495B (es) 2011-09-13 2017-06-14 Monsanto Technology Llc Metodos y composiciones para el control de malezas.
UA116090C2 (uk) 2011-09-13 2018-02-12 Монсанто Текнолоджи Ллс Спосіб та композиція для боротьби з бур'янами (варіанти)
US10806146B2 (en) 2011-09-13 2020-10-20 Monsanto Technology Llc Methods and compositions for weed control
CN103975068A (zh) 2011-09-13 2014-08-06 孟山都技术公司 用于杂草控制的方法和组合物
WO2013040021A1 (en) 2011-09-13 2013-03-21 Monsanto Technology Llc Methods and compositions for weed control
AU2012308686B2 (en) 2011-09-13 2018-05-10 Monsanto Technology Llc Methods and compositions for weed control
US10760086B2 (en) 2011-09-13 2020-09-01 Monsanto Technology Llc Methods and compositions for weed control
US10829828B2 (en) 2011-09-13 2020-11-10 Monsanto Technology Llc Methods and compositions for weed control
AU2012308694B2 (en) 2011-09-13 2018-06-14 Monsanto Technology Llc Methods and compositions for weed control
AU2012308659B2 (en) 2011-09-13 2017-05-04 Monsanto Technology Llc Methods and compositions for weed control
EP2816896B1 (de) * 2012-02-21 2016-09-07 Bayer Intellectual Property GmbH Herbizid wirksame sulfinimidoyl- und sulfonimidoylbenzoylderivate
AR091143A1 (es) 2012-05-24 2015-01-14 Seeds Ltd Ab Composiciones y metodos para silenciar la expresion genetica
US10683505B2 (en) 2013-01-01 2020-06-16 Monsanto Technology Llc Methods of introducing dsRNA to plant seeds for modulating gene expression
BR112015015975A2 (pt) 2013-01-01 2018-11-06 A. B. Seeds Ltd. moléculas de dsrna isoladas e métodos de uso das mesmas para silenciamento das moléculas alvo de interesse.
UY35385A (es) 2013-03-13 2014-09-30 Monsanto Technology Llc ?métodos y composiciones para el control de malezas?.
AU2014249015B2 (en) 2013-03-13 2020-04-16 Monsanto Technology Llc Methods and compositions for weed control
US10568328B2 (en) 2013-03-15 2020-02-25 Monsanto Technology Llc Methods and compositions for weed control
US9850496B2 (en) 2013-07-19 2017-12-26 Monsanto Technology Llc Compositions and methods for controlling Leptinotarsa
RU2703498C2 (ru) 2013-07-19 2019-10-17 Монсанто Текнолоджи Ллс Композиции и способы борьбы с leptinotarsa
EP3062619B1 (en) 2013-10-22 2019-07-24 Dow AgroSciences LLC Pesticidal compositions and related methods
WO2015061163A1 (en) 2013-10-22 2015-04-30 Dow Agrosciences Llc Pesticidal compositions and related methods
JP2016538265A (ja) 2013-10-22 2016-12-08 ダウ アグロサイエンシィズ エルエルシー 相乗的有害生物防除組成物および関連する方法
KR20160074620A (ko) 2013-10-22 2016-06-28 다우 아그로사이언시즈 엘엘씨 상승작용적 살충 조성물 및 관련 방법
AR098088A1 (es) 2013-10-22 2016-05-04 Dow Agrosciences Llc Composiciones plaguicidas sinérgicas y métodos relacionados
MX2016005317A (es) 2013-10-22 2016-08-12 Dow Agrosciences Llc Composiciones pesticidas y metodos relacionados.
AR098092A1 (es) 2013-10-22 2016-05-04 Dow Agrosciences Llc Composiciones plaguicidas sinérgicas y los métodos relacionados
US9549560B2 (en) * 2013-10-22 2017-01-24 Dow Agrosciences Llc Pesticidal compositions and related methods
JP2016535025A (ja) 2013-10-22 2016-11-10 ダウ アグロサイエンシィズ エルエルシー 相乗的有害生物防除組成物および関連する方法
MX2016005325A (es) 2013-10-22 2016-08-08 Dow Agrosciences Llc Composiciones pesticidas sinergicas y metodos relacionados.
CN105848482A (zh) 2013-10-22 2016-08-10 美国陶氏益农公司 协同杀虫组合物和相关方法
KR20160074628A (ko) 2013-10-22 2016-06-28 다우 아그로사이언시즈 엘엘씨 상승작용적 살충 조성물 및 관련 방법
AR098097A1 (es) 2013-10-22 2016-05-04 Dow Agrosciences Llc Composiciones plaguicidas sinérgicas y métodos relacionados
CA2926647A1 (en) 2013-10-22 2015-04-30 Dow Agrosciences Llc Pesticidal compositions and related methods
AU2014340443B2 (en) 2013-10-22 2017-06-08 Dow Agrosciences Llc Synergistic pesticidal compositions and related methods
NZ719688A (en) 2013-10-22 2017-06-30 Dow Agrosciences Llc Pesticidal compositions and related methods
RU2016119569A (ru) 2013-10-22 2017-11-28 ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи Синергетические пестицидные композиции и относящиеся к ним способы
AU2014341879B2 (en) 2013-11-04 2020-07-23 Beeologics, Inc. Compositions and methods for controlling arthropod parasite and pest infestations
UA119253C2 (uk) 2013-12-10 2019-05-27 Біолоджикс, Інк. Спосіб боротьби із вірусом у кліща varroa та у бджіл
AU2015206585A1 (en) 2014-01-15 2016-07-21 Monsanto Technology Llc Methods and compositions for weed control using EPSPS polynucleotides
WO2015153339A2 (en) 2014-04-01 2015-10-08 Monsanto Technology Llc Compositions and methods for controlling insect pests
AU2015280252A1 (en) 2014-06-23 2017-01-12 Monsanto Technology Llc Compositions and methods for regulating gene expression via RNA interference
US11807857B2 (en) 2014-06-25 2023-11-07 Monsanto Technology Llc Methods and compositions for delivering nucleic acids to plant cells and regulating gene expression
RU2021123470A (ru) 2014-07-29 2021-09-06 Монсанто Текнолоджи Ллс Композиции и способы борьбы с насекомыми-вредителями
WO2016118762A1 (en) 2015-01-22 2016-07-28 Monsanto Technology Llc Compositions and methods for controlling leptinotarsa
UY36703A (es) 2015-06-02 2016-12-30 Monsanto Technology Llc Composiciones y métodos para la administración de un polinucleótido en una planta
WO2016196782A1 (en) 2015-06-03 2016-12-08 Monsanto Technology Llc Methods and compositions for introducing nucleic acids into plants
CN110041249A (zh) * 2019-05-22 2019-07-23 南京合巨药业有限公司 一种4-叔丁基-2-氯吡啶和4-叔丁基-2,6-二氯-吡啶的制备方法
US20220267279A1 (en) * 2019-07-30 2022-08-25 Adama Agan Ltd. Process and intermediates for the preparation of pyroxasulfone
CN113135867B (zh) * 2020-06-02 2022-09-23 山东润博生物科技有限公司 S-（5,5-二甲基-4,5-二氢异恶唑-3-基）乙硫酸乙酯及其合成方法和应用
CN113754647B (zh) * 2020-06-02 2023-02-17 山东润博生物科技有限公司 一种砜吡草唑及其中间体的合成方法
EP4177245A1 (en) * 2020-07-10 2023-05-10 Adama Agan Ltd. Process and intermediates for the preparation of fenoxasulfone

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4394155A (en) * 1981-02-05 1983-07-19 Uniroyal, Inc. Substituted pyridine 1-oxide herbicides
UA78071C2 (en) * 2002-08-07 2007-02-15 Kumiai Chemical Industry Co Herbicidal composition

Also Published As

Publication number Publication date
JP2010518084A (ja) 2010-05-27
MX2009008325A (es) 2009-08-12
NZ578196A (en) 2011-01-28
AU2008216859A1 (en) 2008-08-21
CA2675200A1 (en) 2008-08-21
IL199764A0 (en) 2010-04-15
KR20090110374A (ko) 2009-10-21
ZA200905133B (en) 2010-09-29
EP2120939A2 (en) 2009-11-25
RU2009133794A (ru) 2011-03-20
BRPI0806366A2 (pt) 2011-09-06
WO2008100426A3 (en) 2008-10-23
CO6230985A2 (es) 2010-12-20
CL2008000376A1 (es) 2008-08-18
WO2008100426A2 (en) 2008-08-21
UY30898A1 (es) 2008-09-30
US20100298141A1 (en) 2010-11-25

Similar Documents

Publication Publication Date Title
AR065276A1 (es) Herbicidas de n-oxidos de piridina sustituidos
ECSP099639A (es) Compuestos amino-5-[-4-(difluorometoxi)fenil sustituido]-5-fenilimidazolona como inhibidores de ?-secretasa
RU2017123114A (ru) 3-оксо-3-(ариламино)пропионаты, способ их получения и их применение в получении пирролидинонов
AR110398A1 (es) Herbicidas de nitrona
RU2017134973A (ru) Бутиролактоны в качестве гербицидов
AR089415A1 (es) Derivados de heteroarilpiperidina y de heteroarilpiperazina como funguicidas
AR104866A1 (es) Amidas cíclicas sustituidas como herbicidas
AR098673A1 (es) Herbicidas de pirrolidinona
AR101102A1 (es) Herbicidas de piperidinona
AR074411A1 (es) Compuestos heterociclicos fungicidas
JP2013501063A5 (es)
AR104618A1 (es) Herbicidas derivados de compuestos bicíclicos sustituidos con arilo
AR070680A1 (es) Derivados herbicidas de piridazinona
JP2017522374A5 (es)
RU2016118768A (ru) Композиции, пригодные для лечения расстройств, связанных с kit
PE20090151A1 (es) Derivados de pirimidinona y metodos para su uso
TW200740773A (en) Diaminopyrimidines as P2X3 and P2X2/3 modulators
AR059622A1 (es) Quinolonas utiles como inhibidores de la sintetasa del oxido nitrico inducibles
AR105544A1 (es) Compuestos de n-carboxamida cíclica útiles como herbicidas
JP2011507893A5 (es)
RU2006120441A (ru) Комбинация действующих веществ с инсектицидными свойствами
JP2013528602A5 (es)
AR076798A1 (es) Pirazinilpirazoles y composiciones que comprenden dichos compuestos
TW200612965A (en) Methods for preparing p2x7 inhibitors
WO2008122767A3 (en) 2, 6, 9-substituted purine derivatives having anti proliferative properties

Legal Events

Date Code Title Description
FB Suspension of granting procedure