AR112068A1 - SUBSTITUTED OXADIAZOLES TO COMBAT PHYTOPATOGENIC FUNGI - Google Patents
SUBSTITUTED OXADIAZOLES TO COMBAT PHYTOPATOGENIC FUNGIInfo
- Publication number
- AR112068A1 AR112068A1 ARP180101485A ARP180101485A AR112068A1 AR 112068 A1 AR112068 A1 AR 112068A1 AR P180101485 A ARP180101485 A AR P180101485A AR P180101485 A ARP180101485 A AR P180101485A AR 112068 A1 AR112068 A1 AR 112068A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- group
- heterocycle
- groups
- substituted
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/06—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
Abstract
Oxadiazoles sustituidos útiles en la agricultura y al uso de estos para controlar hongos fitopatógenos; un método para combatir hongos fitopatógenos dañinos, en donde el proceso comprende tratar los hongos, las plantas, el suelo o las semillas que se desean proteger del ataque fúngico, con una cantidad eficaz de al menos un compuesto y composiciones agroquímicas que comprenden al menos un compuesto. Reivindicación 1: Compuestos caracterizados por la fórmula (1), o los N-óxidos, o las sales de aquellos aceptables en la agricultura en donde: A es fenilo o un heterociclo aromático de 5 ó 6 miembros, en donde los átomos miembros del anillo del heterociclo aromático incluyen, además de los átomos de carbono, 1, 2, 3 ó 4 heteroátomos seleccionados de N, O y S como átomos miembros del anillo; y en donde el anillo de fenilo o el heterociclo aromático es no sustituido o sustituido con 1, 2, 3 ó 4 grupos RA idénticos o diferentes; en donde RA es halógeno, ciano, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alcoxi o C₁₋₆-haloalcoxi; B es un grupo divalente -C(R³)₂-C(R⁴)₂- o -C(R³)=C(R⁴)-; W es O ó S; V es un enlace simple directo o un grupo divalente -NR²-; R² es hidrógeno, C₁₋₆-alquilo, C₂₋₆-alquenilo, C₂₋₆-alquinilo, C₁₋₆-alcoxi, C₃₋₈-cicloalquilo, C₃₋₈-cicloalquenilo, C₃₋₈-cicloalquil-C₁₋₆-alquilo, fenil-C₁₋₄-alquilo, fenilo, formilo o N(R²ᵃ)₂; y en donde cualquiera de los grupos alifáticos o cíclicos es no sustituido o sustituido con 1, 2, 3 o hasta la máxima cantidad posible de radicales idénticos o diferentes seleccionados del grupo que consiste en halógeno, ciano, C₁₋₆-alquilo, C₃₋₈-cicloalquilo y C₁₋₆-alcoxi; y en donde R²ᵃ se selecciona independientemente del grupo que consiste en hidrógeno, OH, C₁₋₆-alquilo, C₂₋₆-alquenilo, C₂₋₆-alquinilo, C₃₋₈-cicloalquilo, C₃₋₈-cicloalquenilo, C₁₋₆-alcoxi, C₁₋₄-alcoxi-C₁₋₄-alquilo y C₁₋₆-alquiltio; R¹ es C₁₋₆-alquilo, C₃₋₈-cicloalquilo, C₃₋₈-cicloalquenilo, C₂₋₆-alquenilo, C₂₋₆-alquinilo, C₁₋₆-alcoxiimino-C₁₋₄-alquilo, C₂₋₆-alqueniloxiimino-C₁₋₄-alquilo, C₂₋₆-alquiniloxiimino-C₁₋₄-alquilo, fenil-C₁₋₄-alquilo, fenil-C₁₋₄-alquenilo, fenil-C₁₋₄-alquinilo, heteroaril-C₁₋₄-alquilo, fenilo, naftilo o un heterociclo mono- o bicíclico saturado, parcialmente insaturado o aromático de 3 a 10 miembros, en donde los átomos miembros del anillo de dicho heterociclo mono- o bicíclico incluyen, además de los átomos de carbono, otros 1, 2, 3 ó 4 heteroátomos seleccionados de N, O y S como átomos miembros del anillo; y en donde el grupo heteroarilo en el grupo heteroaril-C₁₋₄-alquilo es un heterociclo aromático de 5 ó 6 miembros, en donde los átomos miembros del anillo del anillo heterocíclico incluyen, además de los átomos de carbono, 1, 2, 3 ó 4 heteroátomos seleccionados de N, O y S como átomos miembros del anillo; y en donde cualquiera de los grupos alifáticos o cíclicos mencionados anteriormente es no sustituido o sustituido con 1, 2, 3 o hasta la máxima cantidad posible de grupos R¹ᵃ idénticos o diferentes; o R¹ es un carbociclo bicíclico de la fórmula (2), en donde Cᵃ y Cᵇ son átomos de carbono cabeza de puente; X es un enlace simple directo o un grupo divalente seleccionado del grupo que consiste en -CH₂-, -CH₂-CH₂-, -(CH₂)₃-, -(CH₂)₄-, -CH=CH-, -CH₂-CH=CH-, -CH=CH-CH₂- y -CH=CH-CH=CH-; Y y Z independientemente entre sí, son un grupo divalente seleccionado del grupo que consiste en -CH₂-, -CH₂-CH₂-, -(CH₂)₃-, -(CH₂)₄-, -CH=CH-, -CH₂-CH=CH-, -CH=CH-CH₂- y -CH=CH-CH=CH-; o R¹ es un carbociclo tricíclico de la fórmula (3), en donde Cᵃ y Cᵇ son átomos de carbono cabeza de puente; X es un enlace simple directo o un grupo divalente seleccionado del grupo que consiste en -CH₂-, -CH₂-CH₂-, -(CH₂)₃-, -(CH₂)₄-, -CH=CH-, -CH₂-CH=CH-, -CH=CH-CH₂- y -CH=CH-CH=CH-; Y y Z, independientemente entre sí, son un grupo divalente seleccionado del grupo que consiste en -CH₂-, -CH₂-CH₂-, -(CH₂)₃-, -(CH₂)₄-, -CH=CH-, -CH₂-CH=CH-, -CH=CH-CH₂- y -CH=CH-CH=CH-; y en donde los grupos Y y Z están unidos a átomos de carbono cabeza de puente Cᵃ y Cᵇ; T es un grupo divalente seleccionado del grupo que consiste en -CH₂-, -CH₂-CH₂-, -(CH₂)₃-, -(CH₂)₄-, -CH=CH-, -CH₂-CH=CH-, -CH=CH-CH₂- y -CH=CH-CH=CH-; y en donde el grupo T se une a un átomo de carbono en cada uno de los grupos Y y Z; y siempre que, si R¹ es un carbociclo tricíclico de la fórmula (3), en donde X es un enlace simple directo o un grupo divalente -CH₂-, los grupos T y Z, independientemente entre sí, son un grupo divalente seleccionado del grupo que consiste en -CH₂-CH₂-, -(CH₂)₃-, -(CH₂)₄-, -CH=CH-, -CH₂-CH=CH-, -CH=CH-CH₂- y -CH=CH-CH=CH-; y en donde los grupos de fórmula (2) ó (3) están conectados al grupo V a través de uno de los átomos de carbono del anillo; y en donde los grupos de fórmula (2) ó (3) son no sustituidos o sustituidos con 1, 2, 3, 4 o hasta la máxima cantidad posible de radicales seleccionados del grupo que consiste en oxo, hidroxi, halógeno, C₁₋₃-alquilo, C₁₋₃-haloalquilo, C₃₋₆-cicloalquilo, vinilideno y diclorovinilideno; o R¹ y R², junto con el átomo de nitrógeno al que están unidos, forman un heterociclo monocíclico o bicíclico saturado o parcialmente insaturado de 3 a 10 miembros, en donde el heterociclo incluye, además de un átomo de nitrógeno y uno o más átomos de carbono, ningún heteroátomo adicional o 1, 2 ó 3 heteroátomos seleccionados independientemente de N, O y S como átomos miembros del anillo; y en donde uno o dos grupos CH₂ del heterociclo se pueden reemplazar por uno o dos grupos seleccionados independientemente del grupo que consiste en -C(=O)- y -C(=S)-; y en donde el heterociclo es no sustituido o sustituido con 1, 2, 3, 4 o hasta la máxima cantidad posible de radicales idénticos o diferentes seleccionados del grupo que consiste en halógeno, ciano, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alcoxi y C₁₋₆-haloalcoxi; o R¹ y uno de los dos grupos R²ᵃ, junto con el átomo de nitrógeno al que R²ᵃ está unido, y junto con el átomo de nitrógeno del grupo -NR²-, forman un heterociclo mono- o bicíclico saturado o parcialmente insaturado de 3 a 10 miembros, en donde el heterociclo incluye, además de dos átomos de nitrógeno y uno o más átomos de carbono, ningún otro heteroátomo o 1, 2 ó 3 heteroátomos adicionales seleccionados independientemente de N, O y S como átomos miembros del anillo; y en donde el heterociclo es no sustituido o sustituido con 1, 2, 3, 4 o hasta la máxima cantidad posible de grupos R¹ᵃ idénticos o diferentes; R¹ᵃ es halógeno, oxo, ciano, NO₂, OH, SH, NH₂, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alcoxi, C₁₋₆-haloalcoxi, C₁₋₆-alquiltio, C₁₋₆-haloalquiltio, C₃₋₈-cicloalquilo, -NHSO₂-C₁₋₄-alquilo, (C=O)-C₁₋₄-alquilo, C(=O)-C₁₋₄-alcoxi, C₁₋₆-alquilsulfonilo, hidroxi-C₁₋₄-alquilo, C(=O)-NH₂, C(=O)-NH(C₁₋₄-alquilo), C₁₋₄-alquiltio-C₁₋₄-alquilo, amino-C₁₋₄-alquilo, C₁₋₄-alquilamino-C₁₋₄-alquilo, di-C₁₋₄-alquilamino-C₁₋₄-alquilo, aminocarbonil-C₁₋₄-alquilo o C₁₋₄-alcoxi-C₁₋₄-alquilo; R³, R⁴ se seleccionan, independientemente entre sí, del grupo que consiste en hidrógeno, halógeno, ciano, C₁₋₄-alquilo, C₁₋₄-haloalquilo, C₁₋₄-alcoxi y C₁₋₄-haloalcoxi; o, si B es -C(R³)₂-C(R⁴)₂-, dos radicales R³ y/o dos radicales R⁴, que están unidos al mismo átomo de carbono, junto con dicho átomo de carbono, forman un carbociclo saturado de 3 a 7 miembros o un heterociclo saturado de 3 a 6 miembros; en donde el heterociclo saturado incluye, además de los átomos de carbono, 1, 2 ó 3 heteroátomos seleccionados independientemente del grupo que consiste en N, O y S como átomos miembros del anillo; y en donde dicho átomo miembro del anillo de N se sustituye con el grupo RN; en donde RN es hidrógeno, C₁₋₆-alquilo o halógeno; y en donde el átomo miembro del anillo de S es no sustituido o sustituido con 1 ó 2 radicales oxo; y en donde uno o dos grupos CH₂ del carbociclo saturado o del heterociclo saturado se pueden reemplazar con uno o dos grupos seleccionados independientemente de -C(=O)- y -C(=S)-; y en donde los átomos miembros del anillo de carbono del carbociclo saturado o del heterociclo saturado son no sustituidos o sustituidos con una cantidad total de 1, 2, 3, 4 o hasta la máxima cantidad posible de radicales idénticos o diferentes seleccionados del grupo que consiste en halógeno, ciano, C₁₋₆-alquilo, C₁₋₆-alcoxi y C₃₋₈-cicloalquilo; o si B es -C(R³)₂-C(R⁴)₂-, un radical R³ y un radical R⁴, junto con los átomos de carbono a los que cada uno de ellos está unido, forman un carbociclo saturado de 3 a 7 miembros o un heterociclo saturado de 3 a 6 miembros; en donde el heterociclo saturado incluye, además de los átomos de carbono, 1, 2 ó 3 heteroátomos seleccionados, independientemente del grupo que consiste en N, O y S como átomos miembros del anillo; y en donde dicho átomo miembro del anillo de N se sustituye con el grupo RN; en donde RN es hidrógeno, C₁₋₆-alquilo o halógeno; y en donde el átomo miembro del anillo de S es no sustituido o sustituido con 1 ó 2 radicales oxo; y en donde uno o dos grupos CH₂ del carbociclo saturado o del heterociclo saturado se pueden reemplazar con uno o dos grupos seleccionados independientemente de -C(=O)- y -C(=S)-; y en donde los átomos miembros del anillo de carbono del carbociclo saturado o del heterociclo saturado, que están representados por radicales R³ y R⁴, son no sustituidos o sustituidos con una cantidad total de 1, 2, 3, 4 o hasta la máxima cantidad posible de radicales idénticos o diferentes seleccionados del grupo que consiste en halógeno, ciano, C₁₋₆-alquilo, C₁₋₆-alcoxi y C₃₋₈-cicloalquilo.Substituted oxadiazoles useful in agriculture and their use to control phytopathogenic fungi; a method for combating harmful phytopathogenic fungi, wherein the process comprises treating the fungi, plants, soil or seeds that are desired to be protected from fungal attack, with an effective amount of at least one compound and agrochemical compositions comprising at least one compound. Claim 1: Compounds characterized by formula (1), or N-oxides, or salts of those acceptable in agriculture wherein: A is phenyl or a 5- or 6-membered aromatic heterocycle, wherein the ring member atoms of the aromatic heterocycle include, in addition to carbon atoms, 1, 2, 3, or 4 heteroatoms selected from N, O, and S as ring member atoms; and wherein the phenyl ring or the aromatic heterocycle is unsubstituted or substituted with 1, 2, 3 or 4 identical or different RA groups; wherein RA is halogen, cyano, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₁₋₆-alkoxy, or C₁₋₆-haloalkoxy; B is a divalent group -C (R³) ₂-C (R⁴) ₂- or -C (R³) = C (R⁴) -; W is O or S; V is a direct single bond or a divalent group -NR²-; R² is hydrogen, C₁₋₆-alkyl, C₂₋₆-alkenyl, C₂₋₆-alkynyl, C₁₋₆-alkoxy, C₃₋₈-cycloalkyl, C₃₋₈-cycloalkenyl, C₃₋₈-cycloalkyl-C₁₋₆- alkyl, phenyl-C₁₋₄-alkyl, phenyl, formyl or N (R²ᵃ) ₂; and wherein any of the aliphatic or cyclic groups is unsubstituted or substituted with 1, 2, 3 or up to the maximum possible amount of identical or different radicals selected from the group consisting of halogen, cyano, C₁₋₆-alkyl, C₃₋ ₈-cycloalkyl and C₁₋₆-alkoxy; and wherein R²ᵃ is independently selected from the group consisting of hydrogen, OH, C₁₋₆-alkyl, C₂₋₆-alkenyl, C₂₋₆-alkynyl, C₃₋₈-cycloalkyl, C₃₋₈-cycloalkenyl, C₁₋₆- alkoxy, C₁₋₄-alkoxy-C₁₋₄-alkyl and C₁₋₆-alkylthio; R¹ is C₁₋₆-alkyl, C₃₋₈-cycloalkyl, C₃₋₈-cycloalkenyl, C₂₋₆-alkenyl, C₂₋₆-alkynyl, C₁₋₆-alkoxyimino-C₁₋₄-alkyl, C₂₋₆-alkenyloxyimino- C₁₋₄-alkyl, C₂₋₆-alkynyloxyimino-C₁₋₄-alkyl, phenyl-C₁₋₄-alkyl, phenyl-C₁₋₄-alkenyl, phenyl-C₁₋₄-alkynyl, heteroaryl-C₁₋₄-alkyl, phenyl, naphthyl, or a 3- to 10-membered saturated, partially unsaturated or aromatic mono- or bicyclic heterocycle, wherein the ring member atoms of said mono- or bicyclic heterocycle include, in addition to carbon atoms, other 1, 2, 3 or 4 heteroatoms selected from N, O and S as ring member atoms; and wherein the heteroaryl group in the heteroaryl-C₁₋₄-alkyl group is a 5- or 6-membered aromatic heterocycle, wherein the ring member atoms of the heterocyclic ring include, in addition to the carbon atoms, 1, 2, 3 or 4 heteroatoms selected from N, O and S as ring member atoms; and wherein any of the aliphatic or cyclic groups mentioned above is unsubstituted or substituted with 1, 2, 3 or up to the maximum possible amount of identical or different R¹ᵃ groups; or R¹ is a bicyclic carbocycle of formula (2), where Cᵃ and Cᵇ are bridgehead carbon atoms; X is a direct single bond or a divalent group selected from the group consisting of -CH₂-, -CH₂-CH₂-, - (CH₂) ₃-, - (CH₂) ₄-, -CH = CH-, -CH₂-CH = CH-, -CH = CH-CH₂- and -CH = CH-CH = CH-; Y and Z independently of each other, are a divalent group selected from the group consisting of -CH₂-, -CH₂-CH₂-, - (CH₂) ₃-, - (CH₂) ₄-, -CH = CH-, -CH₂- CH = CH-, -CH = CH-CH₂- and -CH = CH-CH = CH-; or R¹ is a tricyclic carbocycle of formula (3), where Cᵃ and Cᵇ are bridgehead carbon atoms; X is a direct single bond or a divalent group selected from the group consisting of -CH₂-, -CH₂-CH₂-, - (CH₂) ₃-, - (CH₂) ₄-, -CH = CH-, -CH₂-CH = CH-, -CH = CH-CH₂- and -CH = CH-CH = CH-; Y and Z, independently of each other, are a divalent group selected from the group consisting of -CH₂-, -CH₂-CH₂-, - (CH₂) ₃-, - (CH₂) ₄-, -CH = CH-, -CH₂ -CH = CH-, -CH = CH-CH₂- and -CH = CH-CH = CH-; and wherein the Y and Z groups are attached to Cᵃ and Cᵇ bridgehead carbon atoms; T is a divalent group selected from the group consisting of -CH₂-, -CH₂-CH₂-, - (CH₂) ₃-, - (CH₂) ₄-, -CH = CH-, -CH₂-CH = CH-, - CH = CH-CH₂- and -CH = CH-CH = CH-; and wherein the group T is attached to a carbon atom in each of the groups Y and Z; and provided that, if R¹ is a tricyclic carbocycle of formula (3), where X is a direct single bond or a divalent group -CH₂-, the groups T and Z, independently of each other, are a divalent group selected from the group consisting of -CH₂-CH₂-, - (CH₂) ₃-, - (CH₂) ₄-, -CH = CH-, -CH₂-CH = CH-, -CH = CH-CH₂- and -CH = CH- CH = CH-; and wherein the groups of formula (2) or (3) are connected to group V through one of the ring carbon atoms; and wherein the groups of formula (2) or (3) are unsubstituted or substituted with 1, 2, 3, 4 or up to the maximum possible amount of radicals selected from the group consisting of oxo, hydroxy, halogen, C₁₋₃ -alkyl, C₁₋₃-haloalkyl, C₃₋₆-cycloalkyl, vinylidene and dichlorovinylidene; or R¹ and R², together with the nitrogen atom to which they are attached, form a 3- to 10-membered saturated or partially unsaturated monocyclic or bicyclic heterocycle, wherein the heterocycle includes, in addition to a nitrogen atom and one or more atoms of carbon, no additional heteroatoms, or 1, 2, or 3 heteroatoms independently selected from N, O, and S as ring member atoms; and wherein one or two CH₂ groups of the heterocycle can be replaced by one or two groups independently selected from the group consisting of -C (= O) - and -C (= S) -; and wherein the heterocycle is unsubstituted or substituted with 1, 2, 3, 4 or up to the maximum possible amount of identical or different radicals selected from the group consisting of halogen, cyano, C₁₋₆-alkyl, C₁₋₆-haloalkyl , C₁₋₆-alkoxy and C₁₋₆-haloalkoxy; or R¹ and one of the two R²ᵃ groups, together with the nitrogen atom to which R²ᵃ is attached, and together with the nitrogen atom of the group -NR²-, form a saturated or partially unsaturated mono- or bicyclic heterocycle of 3 to 10 members, wherein the heterocycle includes, in addition to two nitrogen atoms and one or more carbon atoms, no other heteroatoms or 1, 2, or 3 additional heteroatoms independently selected from N, O, and S as ring member atoms; and wherein the heterocycle is unsubstituted or substituted with 1, 2, 3, 4 or up to the maximum possible number of identical or different R¹ᵃ groups; R¹ᵃ is halogen, oxo, cyano, NO₂, OH, SH, NH₂, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₁₋₆-alkoxy, C₁₋₆-haloalkoxy, C₁₋₆-alkylthio, C₁₋₆- haloalkylthio, C₃₋₈-cycloalkyl, -NHSO₂-C₁₋₄-alkyl, (C = O) -C₁₋₄-alkyl, C (= O) -C₁₋₄-alkoxy, C₁₋₆-alkylsulfonyl, hydroxy-C₁ ₋₄-alkyl, C (= O) -NH₂, C (= O) -NH (C₁₋₄-alkyl), C₁₋₄-alkylthio-C₁₋₄-alkyl, amino-C₁₋₄-alkyl, C₁₋ ₄-alkylamino-C₁₋₄-alkyl, di-C₁₋₄-alkylamino-C₁₋₄-alkyl, aminocarbonyl-C₁₋₄-alkyl or C₁₋₄-alkoxy-C₁₋₄-alkyl; R³, R⁴ are independently selected from the group consisting of hydrogen, halogen, cyano, C₁₋₄-alkyl, C₁₋₄-haloalkyl, C₁₋₄-alkoxy, and C₁₋₄-haloalkoxy; or, if B is -C (R³) ₂-C (R⁴) ₂-, two radicals R³ and / or two radicals R⁴, which are attached to the same carbon atom, together with said carbon atom, form a saturated carbocycle of 3 to 7 membered or a 3 to 6 membered saturated heterocycle; wherein the saturated heterocycle includes, in addition to carbon atoms, 1, 2, or 3 heteroatoms independently selected from the group consisting of N, O, and S as ring member atoms; and wherein said N ring member atom is substituted with the group RN; wherein RN is hydrogen, C₁₋₆-alkyl, or halogen; and wherein the S ring member atom is unsubstituted or substituted with 1 or 2 oxo radicals; and wherein one or two CH₂ groups of the saturated carbocycle or saturated heterocycle can be replaced with one or two groups independently selected from -C (= O) - and -C (= S) -; and wherein the member atoms of the carbon ring of the saturated carbocycle or saturated heterocycle are unsubstituted or substituted with a total amount of 1, 2, 3, 4 or up to the maximum possible amount of identical or different radicals selected from the group consisting in halogen, cyano, C₁₋₆-alkyl, C₁₋₆-alkoxy and C₃₋₈-cycloalkyl; or if B is -C (R³) ₂-C (R⁴) ₂-, a radical R³ and a radical R⁴, together with the carbon atoms to which each of them is attached, form a saturated carbocycle of 3 to 7 members or a saturated 3- to 6-membered heterocycle; wherein the saturated heterocycle includes, in addition to carbon atoms, 1, 2, or 3 selected heteroatoms, independently from the group consisting of N, O, and S as ring member atoms; and wherein said N ring member atom is substituted with the group RN; wherein RN is hydrogen, C₁₋₆-alkyl, or halogen; and wherein the S ring member atom is unsubstituted or substituted with 1 or 2 oxo radicals; and wherein one or two CH₂ groups of the saturated carbocycle or saturated heterocycle can be replaced with one or two groups independently selected from -C (= O) - and -C (= S) -; and wherein the member atoms of the carbon ring of the saturated carbocycle or saturated heterocycle, which are represented by radicals R³ and R⁴, are unsubstituted or substituted with a total amount of 1, 2, 3, 4 or up to the maximum amount possible of identical or different radicals selected from the group consisting of halogen, cyano, C₁₋₆-alkyl, C₁₋₆-alkoxy, and C₃₋₈-cycloalkyl.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP17174262 | 2017-06-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR112068A1 true AR112068A1 (en) | 2019-09-18 |
Family
ID=58992751
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP180101485A AR112068A1 (en) | 2017-06-02 | 2018-06-01 | SUBSTITUTED OXADIAZOLES TO COMBAT PHYTOPATOGENIC FUNGI |
Country Status (2)
Country | Link |
---|---|
AR (1) | AR112068A1 (en) |
WO (1) | WO2018219797A1 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BR112019001229B1 (en) | 2016-07-22 | 2022-11-16 | Syngenta Participations Ag | OXADIAZOLE DERIVATIVE COMPOUND, AGROCHEMICAL COMPOSITION COMPRISING THE SAME, METHOD TO CONTROL OR PREVENT INFESTATION OF USEFUL PLANTS BY PHYTOPATHOGENIC MICRO-ORGANISMS AND USE OF THE SAID COMPOUND AS FUNGICIDE |
EP3713936B1 (en) | 2017-11-23 | 2021-10-20 | Basf Se | Substituted trifluoromethyloxadiazoles for combating phytopathogenic fungi |
WO2020078732A1 (en) * | 2018-10-17 | 2020-04-23 | Syngenta Crop Protection Ag | Microbiocidal oxadiazole derivatives |
WO2021175669A1 (en) * | 2020-03-04 | 2021-09-10 | Basf Se | Use of substituted 1,2,4-oxadiazoles for combating phytopathogenic fungi |
Family Cites Families (170)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3325503A (en) | 1965-02-18 | 1967-06-13 | Diamond Alkali Co | Polychloro derivatives of mono- and dicyano pyridines and a method for their preparation |
US3296272A (en) | 1965-04-01 | 1967-01-03 | Dow Chemical Co | Sulfinyl- and sulfonylpyridines |
SE8301957D0 (en) | 1983-04-08 | 1983-04-08 | Wso Cpu System Ab | Locking system |
DE3338292A1 (en) | 1983-10-21 | 1985-05-02 | Basf Ag, 6700 Ludwigshafen | 7-AMINO-AZOLO (1,5-A) -PYRIMIDINE AND FUNGICIDES CONTAINING THEM |
CA1249832A (en) | 1984-02-03 | 1989-02-07 | Shionogi & Co., Ltd. | Azolyl cycloalkanol derivatives and agricultural fungicides |
JPS61260075A (en) | 1985-05-15 | 1986-11-18 | Kuraray Co Ltd | Production of glycidic acid ester |
DE3545319A1 (en) | 1985-12-20 | 1987-06-25 | Basf Ag | ACRYLIC ACID ESTERS AND FUNGICIDES THAT CONTAIN THESE COMPOUNDS |
CN1015981B (en) | 1986-05-02 | 1992-03-25 | 施托福化学公司 | Fungicidal pyridyl imidates |
ATE82966T1 (en) | 1986-08-12 | 1992-12-15 | Mitsubishi Chem Ind | PYRIDINECARBOXAMIDE DERIVATIVES AND THEIR USE AS A FUNGICIDE. |
US4871753A (en) | 1986-12-12 | 1989-10-03 | Ciba-Geigy Corporation | 3-Phenyl-5-trifluoromethyl-1,2,4-oxadiazole compounds which are useful pesticides |
AU628229B2 (en) | 1989-11-10 | 1992-09-10 | Agro-Kanesho Co. Ltd. | Hexahydrotriazine compounds and insecticides |
US6395966B1 (en) | 1990-08-09 | 2002-05-28 | Dekalb Genetics Corp. | Fertile transgenic maize plants containing a gene encoding the pat protein |
JP2828186B2 (en) | 1991-09-13 | 1998-11-25 | 宇部興産株式会社 | Acrylate-based compounds, their preparation and fungicides |
EP1357189B1 (en) | 1992-07-01 | 2011-04-13 | Cornell Research Foundation Inc. | Elicitor of the hypersensitive response in plants |
US5952307A (en) | 1994-01-21 | 1999-09-14 | Georgia Tech Research Corp. | Basic α-aminoalkylphosphonate derivatives |
US5726159A (en) | 1994-03-04 | 1998-03-10 | Eli Lilly And Company | Antithrombotic agents |
AU1730497A (en) | 1996-02-17 | 1997-09-02 | Agrevo Uk Limited | Fungicidal 1,2,4-oxadiazoles and analogues |
DE19650197A1 (en) | 1996-12-04 | 1998-06-10 | Bayer Ag | 3-thiocarbamoylpyrazole derivatives |
CA2888685C (en) | 1997-04-03 | 2017-05-09 | T. Michael Spencer | Glyphosate resistant maize lines |
TW460476B (en) | 1997-04-14 | 2001-10-21 | American Cyanamid Co | Fungicidal trifluoromethylalkylamino-triazolopyrimidines |
ES2188016T3 (en) | 1997-09-18 | 2003-06-16 | Basf Ag | DERIVAQDO DE BENZAMIDOXIMA, INTERMEDIATE PRODUCTS AND PROCEDURE FOR OBTAINING AND EMPLOYMENT AS FUNGICIDES. |
DE19750012A1 (en) | 1997-11-12 | 1999-05-20 | Bayer Ag | Isothiazole carboxamides |
WO1999027783A1 (en) | 1997-12-04 | 1999-06-10 | Dow Agrosciences Llc | Fungicidal compositions and methods, and compounds and methods for the preparation thereof |
US6333449B1 (en) | 1998-11-03 | 2001-12-25 | Plant Genetic Systems, N.V. | Glufosinate tolerant rice |
AU1336200A (en) | 1998-11-03 | 2000-05-22 | Aventis Cropscience N.V. | Glufosinate tolerant rice |
WO2000029404A1 (en) | 1998-11-17 | 2000-05-25 | Kumiai Chemical Industry Co., Ltd. | Pyrimidinylbenzimidazole and triazinylbenzimidazole derivatives and agricultura/horticultural bactericides |
IT1303800B1 (en) | 1998-11-30 | 2001-02-23 | Isagro Ricerca Srl | DIPEPTID COMPOUNDS HAVING HIGH FUNGICIDE AND AGRICULTURAL USE. |
JP3417862B2 (en) | 1999-02-02 | 2003-06-16 | 新東工業株式会社 | Silica gel highly loaded with titanium oxide photocatalyst and method for producing the same |
AU770077B2 (en) | 1999-03-11 | 2004-02-12 | Dow Agrosciences Llc | Heterocyclic substituted isoxazolidines and their use as fungicides |
US6586617B1 (en) | 1999-04-28 | 2003-07-01 | Sumitomo Chemical Takeda Agro Company, Limited | Sulfonamide derivatives |
UA73307C2 (en) | 1999-08-05 | 2005-07-15 | Куміаі Кемікал Індастрі Ко., Лтд. | Carbamate derivative and fungicide of agricultural/horticultural destination |
US6509516B1 (en) | 1999-10-29 | 2003-01-21 | Plant Genetic Systems N.V. | Male-sterile brassica plants and methods for producing same |
US6506963B1 (en) | 1999-12-08 | 2003-01-14 | Plant Genetic Systems, N.V. | Hybrid winter oilseed rape and methods for producing same |
DE10021412A1 (en) | 1999-12-13 | 2001-06-21 | Bayer Ag | Fungicidal active ingredient combinations |
JP4880161B2 (en) | 2000-01-25 | 2012-02-22 | シンジェンタ パーティシペーションズ アクチェンゲゼルシャフト | Herbicidal formulation |
US6376548B1 (en) | 2000-01-28 | 2002-04-23 | Rohm And Haas Company | Enhanced propertied pesticides |
CN1114590C (en) | 2000-02-24 | 2003-07-16 | 沈阳化工研究院 | Unsaturated oximino ether bactericide |
BRPI0100752B1 (en) | 2000-06-22 | 2015-10-13 | Monsanto Co | DNA Molecules and Pairs of Molecules, Processes for Detecting DNA Molecules and for Creating a Glyphosate Tolerant Trait in Corn Plants, as well as DNA Detection Kit |
US6713259B2 (en) | 2000-09-13 | 2004-03-30 | Monsanto Technology Llc | Corn event MON810 and compositions and methods for detection thereof |
WO2002022583A2 (en) | 2000-09-18 | 2002-03-21 | E. I. Du Pont De Nemours And Company | Pyridinyl amides and imides for use as fungicides |
AU1536302A (en) | 2000-10-25 | 2002-05-06 | Monsanto Technology Llc | Cotton event pv-ghgt07(1445) and compositions and methods for detection thereof |
EP1417318B1 (en) | 2000-10-30 | 2011-05-11 | Monsanto Technology LLC | Canola event pv-bngt04(rt73) and compositions and methods for detection thereof |
CN100438865C (en) | 2000-11-17 | 2008-12-03 | 美国陶氏益农公司 | Compounds having fungicidal activity and processes to make and use same |
JP5034142B2 (en) | 2001-04-20 | 2012-09-26 | 住友化学株式会社 | Plant disease control composition |
EG26529A (en) | 2001-06-11 | 2014-01-27 | مونسانتو تكنولوجى ل ل سى | Cotton event mon 15985 and compositions and methods for detection thereof |
DE10136065A1 (en) | 2001-07-25 | 2003-02-13 | Bayer Cropscience Ag | pyrazolylcarboxanilides |
AR037228A1 (en) | 2001-07-30 | 2004-11-03 | Dow Agrosciences Llc | ACID COMPOUNDS 6- (ARIL OR HETEROARIL) -4-AMYNOPYCOLINIC, HERBICIDE COMPOSITION THAT UNDERSTANDS AND METHOD TO CONTROL UNWANTED VEGETATION |
FR2828196A1 (en) | 2001-08-03 | 2003-02-07 | Aventis Cropscience Sa | New iodochromone derivatives, useful for the prevention or cure of plant fungal disorders, especially in cereals, vines, fruits, legumes or ornamental plants |
US6818807B2 (en) | 2001-08-06 | 2004-11-16 | Bayer Bioscience N.V. | Herbicide tolerant cotton plants having event EE-GH1 |
WO2003016286A1 (en) | 2001-08-17 | 2003-02-27 | Sankyo Agro Company, Limited | 3-phenoxy-4-pyridazinol derivative and herbicide composition containing the same |
RU2004104638A (en) | 2001-08-20 | 2005-07-10 | Дайниппон Инк Энд Кемикалз, Инк. (Jp) | TETRAZOILOXYM DERIVATIVE AND AGRICULTURAL CHEMICALS CONTAINING IT AS AN ACTIVE INGREDIENT |
AU2002354251A1 (en) | 2001-12-21 | 2003-07-09 | Nissan Chemical Industries, Ltd. | Bactericidal composition |
TWI327462B (en) | 2002-01-18 | 2010-07-21 | Sumitomo Chemical Co | Condensed heterocyclic sulfonyl urea compound, a herbicide containing the same, and a method for weed control using the same |
DE10204390A1 (en) | 2002-02-04 | 2003-08-14 | Bayer Cropscience Ag | Disubstituted thiazolylcarboxanilides |
CA2477931C (en) | 2002-03-05 | 2011-02-01 | Josef Ehrenfreund | O-cyclopropyl-carboxanilides and their use as fungicides |
US7705216B2 (en) | 2002-07-29 | 2010-04-27 | Monsanto Technology Llc | Corn event PV-ZMIR13 (MON863) plants and compositions and methods for detection thereof |
GB0225129D0 (en) | 2002-10-29 | 2002-12-11 | Syngenta Participations Ag | Improvements in or relating to organic compounds |
GB0227966D0 (en) | 2002-11-29 | 2003-01-08 | Syngenta Participations Ag | Organic Compounds |
ATE553203T1 (en) | 2003-02-12 | 2012-04-15 | Monsanto Technology Llc | COTTON EVENT MON 88913 AND COMPOUNDS AND METHODS FOR DETECTING THERETO |
EP1597373B1 (en) | 2003-02-20 | 2012-07-18 | KWS Saat AG | Glyphosate-tolerant sugar beet |
WO2004083193A1 (en) | 2003-03-17 | 2004-09-30 | Sumitomo Chemical Company, Limited | Amide compound and bactericide composition containing the same |
CN1201657C (en) | 2003-03-25 | 2005-05-18 | 浙江省化工研究院 | Methoxy methyl acrylate compounds as bactericidal agent |
MXPA05011795A (en) | 2003-05-02 | 2006-02-17 | Dow Agrosciences Llc | Corn event tc1507 and methods for detection thereof. |
US7157281B2 (en) | 2003-12-11 | 2007-01-02 | Monsanto Technology Llc | High lysine maize compositions and event LY038 maize plants |
WO2005059103A2 (en) | 2003-12-15 | 2005-06-30 | Monsanto Technology Llc | Corn plant mon88017 and compositions and methods for detection thereof |
TWI355894B (en) | 2003-12-19 | 2012-01-11 | Du Pont | Herbicidal pyrimidines |
ATE473227T1 (en) | 2004-03-10 | 2010-07-15 | Basf Se | 5,6-DIALKYL-7-AMINO-TRIAZOLOPYRIMIDINES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR CONTROLLING HARMFUL FUNGI AND AGENTS CONTAINING SAME |
AU2005221808B8 (en) | 2004-03-10 | 2011-01-06 | Basf Se | 5,6-dialkyl-7-amino-triazolopyrimidines, method for their production, their use for controlling pathogenic fungi and agents containing said compounds |
EP2289311B1 (en) | 2004-03-25 | 2016-02-10 | Syngenta Participations AG. | Corn event MIR604 |
EP1737964A1 (en) | 2004-03-26 | 2007-01-03 | Dow AgroSciences LLC | Cry1f and cry1ac transgenic cotton lines and event-specific identification thereof |
WO2005120234A2 (en) | 2004-06-03 | 2005-12-22 | E.I. Dupont De Nemours And Company | Fungicidal mixtures of amidinylphenyl compounds |
EP1761498A1 (en) | 2004-06-18 | 2007-03-14 | Basf Aktiengesellschaft | 1-methyl-3-difluoromethyl-pyrazol-4-carbonic acid-(ortho-phenyl)-anilides, and use thereof as a fungicide |
WO2005123689A1 (en) | 2004-06-18 | 2005-12-29 | Basf Aktiengesellschaft | 1-methyl-3-trifluoromethyl-pyrazole-4-carboxylic acid (ortho-phenyl)-anilides and to use thereof as fungicide |
EP1623983A1 (en) | 2004-08-05 | 2006-02-08 | Santhera Pharmaceuticals (Deutschland) Aktiengesellschaft | Heterocyclic compounds useful as DPP-IV inhibitors |
GB0418048D0 (en) | 2004-08-12 | 2004-09-15 | Syngenta Participations Ag | Method for protecting useful plants or plant propagation material |
AR050891A1 (en) | 2004-09-29 | 2006-11-29 | Du Pont | EVENT DAS-59122-7 OF CORN AND METHODS FOR DETECTION |
WO2006087325A1 (en) | 2005-02-16 | 2006-08-24 | Basf Aktiengesellschaft | 5-alkoxyalkyl-6-alkyl-7-amino-azolopyrimidines, method for their production, their use for controlling pathogenic fungi and agents containing said substances |
DE102005007160A1 (en) | 2005-02-16 | 2006-08-24 | Basf Ag | Pyrazolecarboxylic acid anilides, process for their preparation and compositions containing them for controlling harmful fungi |
DE102005009458A1 (en) | 2005-03-02 | 2006-09-07 | Bayer Cropscience Ag | pyrazolylcarboxanilides |
EP1868426B1 (en) | 2005-03-16 | 2018-02-21 | Syngenta Participations AG | Corn event 3272 and methods of detection thereof |
ES2388548T3 (en) | 2005-04-08 | 2012-10-16 | Bayer Cropscience Nv | Elite event A2704-12 and methods and cases to identify this event in biological samples |
DK1871901T3 (en) | 2005-04-11 | 2011-10-17 | Bayer Bioscience Nv | Elite event A5547-127 and methods and sets for identifying such an event in biological samples |
AP2693A (en) | 2005-05-27 | 2013-07-16 | Monsanto Technology Llc | Soybean event MON89788 and methods for detection thereof |
AU2006254493B2 (en) | 2005-06-02 | 2010-12-09 | Syngenta Participations Ag | CE43- 67B, insecticidal transgenic cotton expressing CRY1AB |
BRPI0612637B1 (en) | 2005-07-07 | 2016-08-02 | Basf Ag | n-thio anthranilamide compounds, processes for preparing such compounds and a composition, use of such compounds, methods for controlling insects, mites or nematodes, for protection from developing plants from attack or insect infestation, mites or nematodes, and compositions |
CN1907024A (en) | 2005-08-03 | 2007-02-07 | 浙江化工科技集团有限公司 | Methoxyl group displacement methyl acrylate compound bactericidal agent |
EP1922409B1 (en) | 2005-08-08 | 2017-11-08 | Bayer CropScience NV | Herbicide tolerant cotton plants and methods for identifying same |
BR122015016965B8 (en) | 2006-01-13 | 2022-06-28 | Dow Agrosciences Llc | 6-(POLYSUBSTITUTED ARYL)-4-AMINOPICOLINATES, HERBICIDAL COMPOSITION, AND METHOD FOR CONTROL OF UNDESIRABLE VEGETATION |
US8124565B2 (en) | 2006-02-09 | 2012-02-28 | Syngenta Crop Protection, Inc. | Method of protecting a plant propagation material, a plant, and/or plant organs |
EP2017268B1 (en) | 2006-05-08 | 2013-01-16 | Kumiai Chemical Industry Co., Ltd. | 1,2-benzisothiazole derivative, and agricultural or horticultural plant disease-controlling agent |
EA022829B1 (en) | 2006-05-26 | 2016-03-31 | Монсанто Текнолоджи, Ллс | Transgenic plant or part thereof exhibiting resistance to insects in the lepidoptera family |
EP2468902B1 (en) | 2006-06-03 | 2015-06-17 | Syngenta Participations AG | Corn event MIR162 |
US7951995B2 (en) | 2006-06-28 | 2011-05-31 | Pioneer Hi-Bred International, Inc. | Soybean event 3560.4.3.5 and compositions and methods for the identification and detection thereof |
WO2008013622A2 (en) | 2006-07-27 | 2008-01-31 | E. I. Du Pont De Nemours And Company | Fungicidal azocyclic amides |
US7928296B2 (en) | 2006-10-30 | 2011-04-19 | Pioneer Hi-Bred International, Inc. | Maize event DP-098140-6 and compositions and methods for the identification and/or detection thereof |
BRPI0716347B8 (en) | 2006-10-31 | 2022-12-06 | Du Pont | ISOLATED POLYNUCLOTIDE, METHODS TO IDENTIFY WHETHER A BIOLOGICAL SAMPLE COMPRISES A POLYNUCLOTIDE, TO DETECT THE PRESENCE OF A POLYNUCLOTIDE, TO DETECT THE PRESENCE OF A SEQUENCE, TO SELECT SEEDS AND TO PRODUCE AN ALS INHIBITOR TOLERANT PAIR, DNA PRIMER PAIRS AND CONSTRUCTION OF AN EXPRESSION DNA |
EP1932843A1 (en) | 2006-12-14 | 2008-06-18 | sanofi-aventis | Sulfonyl-phenyl-2H-(1,2,4) oxadiazole-5-one derivatives, processes for their preparation and their use as pharmaceuticals |
BRPI0810786B1 (en) | 2007-04-05 | 2018-10-30 | Bayer Bioscience Nv | "method for producing a cotton plant or seed comprising an elite event, cotton genomic DNA, elite event identification kit, primer pair, specific probe, isolated nucleic acid molecule, isolated nucleic acid fragment, selection method and detection of seeds in relation to the presence of the elite event, method for determining the zygote state of a plant, plant material or seed comprising the elite event ". |
AP3195A (en) | 2007-06-11 | 2015-03-31 | Bayer Cropscience Nv | Insect resistant cotton plants and methods for identifying same |
AU2008321220A1 (en) | 2007-11-15 | 2009-05-22 | Monsanto Technology Llc | Soybean plant and seed corresponding to transgenic event MON87701 and methods for detection thereof |
RU2010128006A (en) | 2007-12-10 | 2012-01-20 | Актелион Фармасьютиклз Лтд (Ch) | THIOPHENE DERIVATIVES AS SIPI / EDGI AGONISTS |
ES2632135T3 (en) | 2008-01-15 | 2017-09-11 | Bayer Intellectual Property Gmbh | Pesticide composition comprising a tetrazolyl oxime derivative and an active substance pesticide or insecticide |
EP2562162B1 (en) | 2008-01-22 | 2015-08-19 | Dow AgroSciences LLC | N-cyano-4-amino-5-fluoro-pyrimidine derivatives as fungicides |
MX2010008977A (en) | 2008-02-14 | 2010-11-22 | Pioneer Hi Brend International Inc | Plant genomic dna flanking spt event and methods for identifying spt event. |
CA2712445C (en) | 2008-02-15 | 2018-11-06 | Monsanto Technology Llc | Soybean plant and seed corresponding to transgenic event mon87769 and methods for detection thereof |
HUE029544T2 (en) | 2008-02-29 | 2017-03-28 | Monsanto Technology Llc | Corn plant event MON87460 and compositions and methods for detection thereof |
CA2738474C (en) | 2008-09-29 | 2020-05-12 | Monsanto Technology Llc | Soybean transgenic event mon87705 and methods for detection thereof |
UA110320C2 (en) | 2008-12-16 | 2015-12-25 | Syngenta Participations Ag | Corn event 5307 |
GB0823002D0 (en) | 2008-12-17 | 2009-01-28 | Syngenta Participations Ag | Isoxazoles derivatives with plant growth regulating properties |
CA2748973A1 (en) | 2009-01-07 | 2010-07-15 | Basf Agrochemical Products B.V. | Soybean event 127 and methods related thereto |
CN101906075B (en) | 2009-06-05 | 2012-11-07 | 中国中化股份有限公司 | E-type phenyl acrylic acid ester compound containing substituted anilino pyrimidine group and applications thereof |
JP2013526832A (en) | 2009-08-19 | 2013-06-27 | ダウ アグロサイエンシィズ エルエルシー | AAD-1 event DAS-40278-9, related transgenic corn lines and their event-specific identification |
US8470840B2 (en) | 2009-09-01 | 2013-06-25 | Dow Agrosciences, Llc. | Synergistic fungicidal compositions containing a 5-fluoropyrimidine derivative for fungal control in cereals |
ES2866126T3 (en) | 2009-09-17 | 2021-10-19 | Monsanto Technology Llc | MON 87708 GM soy event and procedures for its use |
RU2764586C2 (en) | 2009-11-23 | 2022-01-18 | Монсанто Текнолоджи Ллс | Transgenic event mon 87427 of maize and relative development scale |
BR112012012511A2 (en) | 2009-11-24 | 2015-09-15 | Dow Agrosciences Llc | event 416 of the aad-12 gene related to transgenic soybean strains and their event-specific identification |
PL2512226T3 (en) | 2009-12-17 | 2019-10-31 | Pioneer Hi Bred Int | Maize event dp-004114-3 and methods for detection thereof |
BR112012015626B1 (en) | 2009-12-22 | 2017-09-19 | Mitsui Chemicals Agro, Inc | COMPOSITION OF CONTROL OF PLANT DISEASE AND METHOD FOR CONTROLLING THE DISEASE BY THE APPLICATION OF THE SAME |
NZ600926A (en) | 2010-01-04 | 2013-07-26 | Nippon Soda Co | Nitrogen-containing heterocyclic compound and agricultural/horticultural germicide |
ES2605490T3 (en) | 2010-04-28 | 2017-03-14 | Sumitomo Chemical Company, Limited | Composition of plant disease control and its use |
KR101941297B1 (en) | 2010-06-04 | 2019-01-22 | 몬산토 테크놀로지 엘엘씨 | Transgenic brassica event mon 88302 and methods of use thereof |
BR112013009001A2 (en) | 2010-10-12 | 2016-07-05 | Monsanto Technology Llc | soybean plant and seed corresponding to mon87712 transgenic event and methods for detecting them |
TWI667347B (en) | 2010-12-15 | 2019-08-01 | 瑞士商先正達合夥公司 | Soybean event syht0h2 and compositions and methods for detection thereof |
IT1403275B1 (en) | 2010-12-20 | 2013-10-17 | Isagro Ricerca Srl | HIGH-ACTIVITY INDANYLANILIDES FUNGICIDE AND THEIR PHYTOSANITARY COMPOSITIONS |
CN103597079B (en) | 2011-03-30 | 2017-04-05 | 孟山都技术公司 | Cotton transgenic event MON88701 and its using method |
TWI583308B (en) | 2011-05-31 | 2017-05-21 | 組合化學工業股份有限公司 | Method for controlling rice disease |
EP2532233A1 (en) | 2011-06-07 | 2012-12-12 | Bayer CropScience AG | Active compound combinations |
AU2012275393B2 (en) | 2011-06-30 | 2017-06-08 | Forage Genetics International, Llc | Alfalfa plant and seed corresponding to transgenic event KK 179-2 and methods for detection thereof |
US9056843B2 (en) | 2011-07-08 | 2015-06-16 | Novartis Ag | Trifluoromethyl-oxadiazole derivatives and their use in the treatment of disease |
HUE027461T2 (en) | 2011-07-13 | 2016-09-28 | Basf Agro Bv | Fungicidal substituted 2-[2-halogenalkyl-4-(phenoxy)-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds |
US9173402B2 (en) | 2011-07-15 | 2015-11-03 | Basf Se | Fungicidal alkyl-substituted 2[2-chloro-4-(4-chioro-phenoxy)-phenyl]-1[1,2,4]triazol-1-yl-ethanol compounds |
BR102012019434B1 (en) | 2011-07-26 | 2021-11-09 | Dow Agrosciences Llc | PEST, INSECT, MOLECULE AND DIAGNOSTIC DNA SEQUENCE CONTROL METHODS FOR THE SOYBEAN EVENT 9582.814.19.1 |
US20140179519A1 (en) | 2011-08-12 | 2014-06-26 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
EA201400212A1 (en) | 2011-08-12 | 2014-07-30 | Басф Се | N-THIOANTRANILAMIDE COMPOUNDS AND THEIR APPLICATION AS PESTICIDES |
JP6005652B2 (en) | 2011-09-26 | 2016-10-12 | 日本曹達株式会社 | Agricultural / horticultural fungicide composition |
JP5993860B2 (en) | 2011-09-29 | 2016-09-14 | 三井化学アグロ株式会社 | Method for producing 4,4-difluoro-3,4-dihydroisoquinoline derivative |
DK2793579T6 (en) | 2011-12-21 | 2018-05-28 | Basf Se | APPLICATION OF STROBILUR TYPE-COMPOUNDS TO COMBAT PHYTOPATHOGENIC Fungi RESISTANT TO QO INHIBITORS |
US9605273B2 (en) | 2012-01-23 | 2017-03-28 | Dow Agrosciences Llc | Herbicide tolerant cotton event pDAB4468.19.10.3 |
TWI568721B (en) | 2012-02-01 | 2017-02-01 | 杜邦股份有限公司 | Fungicidal pyrazole mixtures |
PE20190343A1 (en) | 2012-02-27 | 2019-03-07 | Bayer Ip Gmbh | ACTIVE COMPOUND COMBINATIONS |
JP6107377B2 (en) | 2012-04-27 | 2017-04-05 | 住友化学株式会社 | Tetrazolinone compounds and uses thereof |
WO2013169923A2 (en) | 2012-05-08 | 2013-11-14 | Monsanto Technology Llc | Corn event mon 87411 |
CN103387541B (en) | 2012-05-10 | 2016-02-10 | 中国中化股份有限公司 | A kind of preparation method of substituted pyrazolecarboxylic ether compound |
WO2014026327A1 (en) | 2012-08-15 | 2014-02-20 | Merck Sharp & Dohme Corp. | 4-heteroaryl substituted benzoic acid compounds as rorgammat inhibitors and uses thereof |
WO2014060177A1 (en) | 2012-10-16 | 2014-04-24 | Syngenta Participations Ag | Fungicidal compositions |
US20150361446A1 (en) | 2013-01-25 | 2015-12-17 | Pioneer-Hi-Bred International and E.I. Dupont De Nemours & Company | Maize event dp-033121-3 and methods for detection thereof |
CN105264078A (en) | 2013-05-02 | 2016-01-20 | 杰.尔.辛普洛公司 | Potato cultivar e12 |
EA036941B1 (en) | 2013-06-14 | 2021-01-18 | Монсанто Текнолоджи Ллс | Soybean transgenic event mon87751 and methods for detection and use thereof |
BR112016007566A2 (en) | 2013-10-09 | 2017-09-12 | Monsanto Technology Llc | mon87403 transgenic corn event and methods for detecting it |
EP3062686B1 (en) | 2013-10-28 | 2019-05-08 | Dexcom, Inc. | Devices used in connection with continuous analyte monitoring that provide the user with one or more notifications, and related methods |
EP2865265A1 (en) | 2014-02-13 | 2015-04-29 | Bayer CropScience AG | Active compound combinations comprising phenylamidine compounds and biological control agents |
PE20161403A1 (en) | 2014-03-20 | 2016-12-29 | Monsanto Technology Llc | MON 87419 TRANSGENIC CORN EVENT AND METHODS FOR ITS USE |
UA121116C2 (en) | 2014-06-06 | 2020-04-10 | Басф Се | Use of substituted oxadiazoles for combating phytopathogenic fungi |
WO2016183445A1 (en) | 2015-05-14 | 2016-11-17 | J.R. Simplot Company | Potato cultivar v11 |
MX2018003845A (en) | 2015-10-02 | 2018-06-18 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives. |
PL3356358T3 (en) | 2015-10-02 | 2020-11-02 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
WO2017062825A1 (en) | 2015-10-08 | 2017-04-13 | J.R. Simplot Company | Potato cultivar y9 |
EP3358970A4 (en) | 2015-10-08 | 2019-03-06 | J.R. Simplot Company | Potato cultivar x17 |
US20180319753A1 (en) | 2015-10-28 | 2018-11-08 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
EP3371177A1 (en) | 2015-11-02 | 2018-09-12 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
US20180317488A1 (en) | 2015-11-03 | 2018-11-08 | Basf Se | Use of Substituted Oxadiazoles for Combating Phytopathogenic Fungi |
WO2017076935A1 (en) | 2015-11-04 | 2017-05-11 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
EP3370525A1 (en) | 2015-11-04 | 2018-09-12 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
CR20180310A (en) | 2015-11-05 | 2018-11-30 | Basf Se | OXADIAZOLS REPLACED TO COMBAT HONGOD PHYTOOPATHOGENS |
AR106679A1 (en) | 2015-11-13 | 2018-02-07 | Basf Se | OXADIAZOLS REPLACED TO FIGHT FITOPATHOGEN FUNGI |
WO2017081309A1 (en) | 2015-11-13 | 2017-05-18 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
EP3373732A1 (en) | 2015-11-13 | 2018-09-19 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
EP3373733A1 (en) | 2015-11-13 | 2018-09-19 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
KR20180083417A (en) | 2015-11-19 | 2018-07-20 | 바스프 에스이 | Substituted oxadiazoles for combating phytopathogenic fungi |
MX2018006244A (en) | 2015-11-19 | 2018-11-09 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi. |
-
2018
- 2018-05-25 WO PCT/EP2018/063766 patent/WO2018219797A1/en active Application Filing
- 2018-06-01 AR ARP180101485A patent/AR112068A1/en unknown
Also Published As
Publication number | Publication date |
---|---|
WO2018219797A1 (en) | 2018-12-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR108696A1 (en) | OXADIAZOLS REPLACED TO FIGHT FITOPATHOGEN FUNGI | |
AR100770A1 (en) | USE OF SUBSTITUTED OXADIAZOLS TO COMBAT PHYTOPATHOGENIC FUNGI | |
AR112068A1 (en) | SUBSTITUTED OXADIAZOLES TO COMBAT PHYTOPATOGENIC FUNGI | |
AR108118A1 (en) | OXADIAZOLS REPLACED TO FIGHT FITOPATHOGEN FUNGI | |
AR106947A1 (en) | OXADIAZOLS REPLACED TO FIGHT FITOPATHOGEN FUNGI | |
AR106679A1 (en) | OXADIAZOLS REPLACED TO FIGHT FITOPATHOGEN FUNGI | |
AR113865A1 (en) | MICROBICIDE DERIVATIVES OF PHENYLAMIDINE | |
AR111850A1 (en) | SUBSTITUTED TRIFLUOROMETILOXADIAZOLS TO FIGHT FITOPATHOGEN FUNGI | |
AR111365A1 (en) | OXADIAZOLS REPLACED TO FIGHT FITOPATHOGEN FUNGI | |
AR111427A1 (en) | DERIVATIVES OF SUCCINIMIDA REPLACED | |
AR106763A1 (en) | OXADIAZOLS REPLACED TO FIGHT FITOPATHOGEN FUNGI | |
PE20181453A1 (en) | SUBSTITUTE OXADIAZOLES TO COMBAT PHYTOPATOGENIC FUNGI | |
AR111371A1 (en) | OXADIAZOLS REPLACED TO FIGHT FITOPATHOGEN FUNGI | |
AR100315A1 (en) | PIRIDINE SUBSTITUTED COMPOUNDS THAT HAVE HERBICITY ACTION | |
AR110366A1 (en) | ACTIVE COMPOUND COMBINATIONS | |
UY38490A (en) | DERIVATIVES OF THIAZOL FUNGICIDE CONTAINING AN N-CARBONYL GROUP | |
AR113842A1 (en) | THIAZOL DERIVATIVES MICROBIOCIDES | |
AR107955A1 (en) | DERIVATIVES OF PIRIDINO- / PIRIMIDINO-PIRIDINA, WITH HERBICITY ACTIVITY | |
AR106405A1 (en) | MICROBIOCIDES PHENYLAMIDINE DERIVATIVES | |
AR120074A1 (en) | FUSED HETEROCYCLIC COMPOUNDS AND THEIR USE AS PEST CONTROL AGENTS | |
AR118051A1 (en) | HETEROCYCLIC COMPOUNDS FOR THE CONTROL OF INVERTEBRATE PESTS | |
AR112219A1 (en) | SUBSTITUTED TRIFLUOROMETILOXADIAZOLES TO COMBAT PHYTOPATOGENIC FUNGI | |
AR118054A1 (en) | HERBICIDE COMPOUNDS | |
CL2022001312A1 (en) | Pyrimidone derivatives containing two fused bicyclic rings | |
AR107835A1 (en) | SPIROCYCLES DERIVATIVES AND THEIR USE IN THE COMBAT OF INVESTED PESTS |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FB | Suspension of granting procedure |