AR057331A1 - Serin- amidas sustituidas con heteroaroilo - Google Patents
Serin- amidas sustituidas con heteroaroiloInfo
- Publication number
- AR057331A1 AR057331A1 ARP060102179A ARP060102179A AR057331A1 AR 057331 A1 AR057331 A1 AR 057331A1 AR P060102179 A ARP060102179 A AR P060102179A AR P060102179 A ARP060102179 A AR P060102179A AR 057331 A1 AR057331 A1 AR 057331A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- amino
- phenyl
- aminocarbonyl
- Prior art date
Links
- 125000000217 alkyl group Chemical group 0.000 abstract 39
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 33
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 22
- -1 C3-6 halogenalkynyl Chemical group 0.000 abstract 9
- 125000001188 haloalkyl group Chemical group 0.000 abstract 9
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 8
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 6
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 5
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 5
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 4
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 4
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 4
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 4
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 3
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 3
- 125000000304 alkynyl group Chemical group 0.000 abstract 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 3
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 abstract 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 3
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000006598 aminocarbonylamino group Chemical group 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 2
- 125000005020 hydroxyalkenyl group Chemical group 0.000 abstract 2
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 2
- 125000004434 sulfur atom Chemical group 0.000 abstract 2
- 125000004001 thioalkyl group Chemical group 0.000 abstract 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 abstract 1
- 125000006642 (C1-C6) cyanoalkyl group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 abstract 1
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 1
- 125000005089 alkenylaminocarbonyl group Chemical group 0.000 abstract 1
- 125000005090 alkenylcarbonyl group Chemical group 0.000 abstract 1
- 125000005092 alkenyloxycarbonyl group Chemical group 0.000 abstract 1
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 1
- 125000005103 alkyl silyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000005087 alkynylcarbonyl group Chemical group 0.000 abstract 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 abstract 1
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000005016 hydroxyalkynyl group Chemical group 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 125000006678 phenoxycarbonyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- 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
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/38—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Furan Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
Procedimientos y productos intermediarios para su preparacion, así como el uso de esos compuestos o agentes que contienen estos compuestos, para el combate de plantas no deseadas. Reivindicacion 1: Serin-amidas sustituidas con heteroaroílo, caracterizadas porque tienen la formula en donde las variables tienen los siguientes significados: A es heteroarilo de 5 o 6 miembros con uno a cuatro átomos de N, o con uno a tres átomos de N y un átomo de O o S, o con un átomo de O o S, que puede estar parcial o totalmente halogenado y/o que puede llevar 1 a 3 radicales del grupo ciano, alquilo C1-6, cicloalquilo C3-6, halogenoalquilo C1-6, alcoxi C1-6, halogenoalcoxi C1-6 y alcoxi C1-6-alquilo C1-4; R1, R2 es H, hidroxi o alcoxi C1-6; R3 es alquilo C1-6, cianoalquilo C1-4 o halogenoalquilo C1-6; R4 es H, alquilo C1-6, cicloalquilo C3-6, alquenilo C3-6, alquinilo C3-6, halogenalquenilo C3-6, halogenalquinilo C3-6, formilo, alquil C1-6-carbonilo, cicloalquilcarbonilo C3-6, alquenilcarbonilo C2-6, alquinilcarbonilo C2-6, alcoxi C1-6-carbonilo, alqueniloxicarbonilo C3-6, alquinil C3-6-oxicarbonilo, alquil C1-6-aminocarbonilo, alquenilaminocarbonilo C3-6, alquinilaminocarbonilo C3-6, alquil C1-6-sulfonilaminocarbonilo, di(alquil C1-6)-aminocarbonilo, N-(alquenil C3-6)-N-(alquil C1-6)-aminocarbonilo, N-(alquinil C3-6)-N(alquilo C1-6)-aminocarbonilo, N-(alcoxi C1-6)-N-(alquil C1-6)-amino-carbonilo, N-(alquenil C3-6)-N-(alcoxi C1-6)-aminocarbonilo, N-(alquinil C3-6)- N-(alcoxi C1-6)-aminocarbonilo, di-(alquil C1-6)-aminotiocarbonilo, (alquil 1-6)cianoimino, (amino)cianoimino, [(alquil C1-6)amino]cianoimino, [di(alquil C1-6)amino]cianoimino, alquil C1-6-carbonil-alquilo C1-6, alcoxi C1-6-imino-alquilo C1-6, N- (alquil C1-6-amino)-imino-alquilo C1-6, N-(di-alquil C1-6-amino)-imino-alquilo C1-6, o tri-alquil C1-4-sililo, en donde los radicales alquilo, cicloalquilo y alcoxi mencionados pueden estar parcial o totalmente halogenados y/o pueden llevar 1 a 3 de los siguientes grupos: ciano, hidroxi, cicloalquilo C3-6, alcoxi C1-6-alquilo C1-4, alcoxi C1-4-alcoxi C1-4-alquilo C1-4, alcoxi C1-4, alquil C1-4-tio, di(alquil C1-4)-amino, alquilo C1-4-alcoxi C1-6-carbonilamino, alquil C1-4-carbonilo, hidroxicarbonilo, alcoxi C1-4-carbonilo, aminocarbonilo, alquil C1-4-aminocarbonilo, di(alquil C1-4)aminocarbonilo o alquil C1-4-carboniloxi; fenilo, fenil-alquilo C1-6, fenilcarbonilo, fenilcarbonil-alquilo C1-6, fenoxicarbonilo, fenilaminocarbonilo, fenilsulfonilaminocarbonilo, N-(alquilo C1-6)-N-(fenil)-aminocarbonilo, fenil-alquil C1-6-carbonilo, en donde el radical fenilo puede estar parcial o totalmente halogenado y/o puede llevar 1 a 3 de los siguientes grupos: nitro, ciano, alquilo C1-4, halogenalquilo C1-4, alcoxi C1-4 o halogenalcoxi C1-4, o SO2R7; R5 es H o alquilo C1-6; R6 es alquilo C1-6, alquenilo C2-6, alquinilo C2-6, halogenalquilo C1-6, halogenalquenilo C2-6, halogenalquinilo C2-6, cianoalquilo C1-6, cianoalquenilo C2-6, cianoalquinilo C2-6, hidroxialquilo C1-6, hidroxialquenilo C2-6, hidroxialquinilo C2-6, cicloalquilo C3-6, cicloalquenilo C3-6, heterociclilo de 3 a 6 miembros, heterociclil-alquilo C1-4 de 3 a 6 miembros, en donde los radicales cicloalquilo, cicloalquenilo o heterociclilo de 3 a 6 miembros antes mencionados peden estar parcial o totalmente halogenados y/o pueden llevar 1 a 3 radicales del grupo oxo, ciano, nitro, alquilo C1-6, halogenalquilo C1-6, hidroxi, alcoxi C1-6, halogenalcoxi C1-6, hidroxicarbonilo, alcoxi C1-6-carbonilo, hidroxicarbonil-alcoxi C1-6, alcoxi C1-6-carbonil-alcoxi C1-6, amino, alquil C1-6-amino, di(alquil C1-6)amino, alquil C1-6-sulfonilamino, halogenalquil C1-6-sulfonilamino, aminocarbonilamino, (alquil C1-6-amino)carbonilamino, di-(alquil C1-6)-aminocarbonilamino, arilo y aril(alquilo C1-6); alcoxi C1-6-alquilo C1-4, alquenil C2-6-oxi-alquilo C1-4, alquinil C2-6-oxi-alquilo C1-4, halogenalcoxi C1-6-alquilo C1-4, halogenalquenil C2-6-oxi-alquilo C1-4, halogenalquinil C2-6-oxi-alquilo C1-4, alcoxi C1-6-alcoxi C1-4-alquilo C1-4, alquil C1-6-tio-alquilo C1-4, alquenil C2-6-tio-alquilo C1-4, alquinil C2-6-tioalquilo C1-4, halogenalquil C1-6-tioalquilo C1-4, halogenalquenil C2-6-tioalquilo C1-4, halogenalquinil C2-6-tioalquilo C1-4, alquil C1-6-sulfinil-alquilo C1-4, halogenalquil C1-6-sulfinil-alquilo C1-4, alquil C1-4-sulfonil-alquilo C1-4, halogenalquil C1-6-sulfonil-alquilo C1-4, amino-alquilo C1-4, alquil C1-6-amino-alquilo C1-4, di-(alquil C1-6)amino-alquilo C1-4, alquil C1-6-sulfonilamino-alquilo C1-4, alquil C1-6-sulfonil-(alquil C1-6)-amino-alquilo C1-4, alquil C1-6-carbonilo, hidroxicarbonilo, alcoxi C1-6-carbonilo, aminocarbonilo, alquil C1-6-aminocarbonilo, di-(alquil C1-6)-aminocarbonilo, alquil C1-6-carbonil-alquilo C1-6, hidroxicarbonil-alquilo C1-4, alcoxi C1-6-carbonil-alquilo C1-4, halogenalcoxi C1-6-carbonil-alquilo C1-4, alquil C1-6-carboniloxi-alquilo C1-4, aminocarbonil- alquilo C1-4, alquil C1-6-aminocarbonil-alquilo C1-4, di(alquil C1-6)aminocarbonil-alquilo C1-4, formilamino-alquilo C1-4, alcoxi C1-6-carbonilamino-alquilo C1-4, alquil C1-6-carbonilamino-alquilo C1-4, alquil C1-6-carbonil-(alquil C1-6-amino)- alquilo C1-4, [(alquil C1-6)aminocarboniloxi]-alquilo C1-4, [di(-alquil C1-6)aminocarboniloxi]-alquilo C1-4, {di-[di-(alquil C1-6)amino]carboniloxi}-alquilo C1-4, [(alquil C1-6-amino)carbonilamino]-alquilo C1-4, [di-(alquil C1-6)aminocarbonilamino]- alquilo C1-4; fenil-alquilo C1-4, fenil-alquenilo C2-4, fenil-alquinilo C2-4, fenil-halogenalquilo C1-4, fenil-halogenalquenilo C2-4, fenil-halogenalquinilo C2-4, fenil-hidroxialquilo C1-4, fenil-hidroxialquenilo C2-4, fenil-hidroxialquinilo C2-4, fenilcarbonil-alquilo C1-4, fenilcarbonilamino-alquilo C1-4, fenilcarboniloxi-alquilo C1-4, fenilcarbonil-alquilo C1-4, feniloxi-alquilo C1-4, feniltio-alquilo C1-4, fenilsulfinil-alquilo C1-4, fenilsulfonil-alquilo C1-4, heteroaril-alquilo C1-4, heteroaril-alquenilo C2-4, heteroaril-alquinilo C2-4, heteroaril-halogenalquilo C1-4, heteroaril-halogenalquenilo C2-4, heteroaril-halogenalquinilo C2-4, heteroaril-hidroxialquilo C1-4, heteroaril-hidroxialquenilo C2-4, heteroaril-hidroxialquinilo C1-4, heteroarilcarbonil-alquilo C1-4, heteroarilcarboniloxi-alquilo C1-4, heteroariloxicarbonil-alquilo C1-4, heteroariloxi-alquilo C1-4, heteroariltio-alquilo C1-4, heteroarilsulfinil-alquilo C1-4, heteroarilsulfonil-alquilo C1-4, en donde los radicales fenilo y heteroarilo antes mencionados pueden estar parcial o totalmente halogenados y/o pueden llevar 1 a 3 radicales del grupo ciano, nitro, alquilo C1-6, halogenalquilo C1-6, hidroxi, alcoxi C1-6, halogenalcoxi C1-6, hidroxicarbonilo, alcoxi C1-6-carbonilo, hidroxicarbonil-alcoxi C1-6, alcoxi C1-6-carbonil-alcoxi C1-6, amino, alquil C1-6-amino, di-(alquil C1-6)amino, alquil C1-6-sulfonilamino, halogenalquil C1-6-sulfonilamino, (alquil C1-6-amino)carbonilamino, di-(alquil C1-6)- aminocarbonilamino, arilo y aril(alquilo C1-6); R7 alquilo C1-6, halogenalquilo C1-6 o fenilo; en donde el radical fenilo puede estar parcial o totalmente halogenado y/o puede llevar 1 a 3 de los siguientes grupos: alquilo C1-6, haloalquilo C1-6, o alcoxi C1-6; así como sus sales de utilidad en agricultura.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102005024599 | 2005-05-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR057331A1 true AR057331A1 (es) | 2007-11-28 |
Family
ID=36702367
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP060102179A AR057331A1 (es) | 2005-05-25 | 2006-05-24 | Serin- amidas sustituidas con heteroaroilo |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US7879761B2 (es) |
| EP (1) | EP1888532A1 (es) |
| JP (1) | JP4981037B2 (es) |
| CN (1) | CN101228133A (es) |
| AR (1) | AR057331A1 (es) |
| AU (1) | AU2006251302A1 (es) |
| BR (1) | BRPI0611498B1 (es) |
| CA (1) | CA2609243A1 (es) |
| EA (1) | EA013636B1 (es) |
| IL (1) | IL187502A0 (es) |
| MX (1) | MX2007014490A (es) |
| PE (1) | PE20070051A1 (es) |
| TW (1) | TW200716558A (es) |
| UA (1) | UA90720C2 (es) |
| UY (1) | UY29565A1 (es) |
| WO (1) | WO2006125687A1 (es) |
| ZA (1) | ZA200711009B (es) |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20060721A1 (es) * | 2004-09-16 | 2006-08-24 | Basf Ag | Serinamidas sustituidas por heteroaroilo |
| BRPI0710930A2 (pt) * | 2006-05-19 | 2012-02-14 | Basf Se | composto processo para preparar um composto, composição, processos para preparar composições e para combater vegetação indesejada, e, uso do composto |
| CN101578261B (zh) * | 2007-01-11 | 2014-04-16 | 巴斯夫欧洲公司 | 杂芳酰基取代的丝氨酰胺 |
| US8097712B2 (en) | 2007-11-07 | 2012-01-17 | Beelogics Inc. | Compositions for conferring tolerance to viral disease in social insects, and the use thereof |
| RU2011121521A (ru) * | 2008-10-31 | 2012-12-10 | Басф Се | Способ улучшения жизнеспособности растения |
| 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 |
| MX2012010479A (es) | 2010-03-08 | 2012-10-09 | Monsanto Technology Llc | Moleculas polinucleotidicas para regulacion genetica en plantas. |
| 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 |
| EP3296402B1 (en) | 2011-09-13 | 2020-04-15 | 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 |
| CN110066794A (zh) | 2011-09-13 | 2019-07-30 | 孟山都技术公司 | 用于杂草控制的方法和组合物 |
| CA2848576A1 (en) | 2011-09-13 | 2013-03-21 | Monsanto Technology Llc | Methods and compositions for weed control comprising topical application of 4-hydroxyphenyl-pyruvate-dioxygenase (hppd)-inhibiting polynucleotides |
| US10829828B2 (en) | 2011-09-13 | 2020-11-10 | Monsanto Technology Llc | Methods and compositions for weed control |
| MX362810B (es) | 2011-09-13 | 2019-02-13 | Monsanto Technology Llc | Metodos y composiciones para controlar malezas. |
| UA116092C2 (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 |
| MX362812B (es) | 2011-09-13 | 2019-02-13 | Monsanto Technology Llc | Metodos y composiciones para el control de malezas. |
| WO2013175480A1 (en) | 2012-05-24 | 2013-11-28 | A.B. Seeds Ltd. | Compositions and methods for silencing gene expression |
| US10683505B2 (en) | 2013-01-01 | 2020-06-16 | Monsanto Technology Llc | Methods of introducing dsRNA to plant seeds for modulating gene expression |
| MX375327B (es) | 2013-01-01 | 2025-03-06 | A B Seeds Ltd | Métodos para introducir dsrna en semillas de plantas para modular la expresión genética. |
| WO2014164797A2 (en) | 2013-03-13 | 2014-10-09 | Monsanto Technology Llc | Methods and compositions for weed control |
| CN105074008A (zh) | 2013-03-13 | 2015-11-18 | 孟山都技术有限公司 | 用于杂草控制的方法和组合物 |
| US10568328B2 (en) | 2013-03-15 | 2020-02-25 | Monsanto Technology Llc | Methods and compositions for weed control |
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| CA2918387C (en) | 2013-07-19 | 2021-11-02 | Monsanto Technology Llc | Compositions and methods for controlling leptinotarsa |
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| UA119253C2 (uk) | 2013-12-10 | 2019-05-27 | Біолоджикс, Інк. | Спосіб боротьби із вірусом у кліща varroa та у бджіл |
| UA121462C2 (uk) | 2014-01-15 | 2020-06-10 | Монсанто Текнолоджі Елелсі | Спосіб та композиція для боротьби із бур'янами з використанням полінуклеотидів epsps |
| EP3420809A1 (en) | 2014-04-01 | 2019-01-02 | Monsanto Technology LLC | Compositions and methods for controlling insect pests |
| EP3158067B1 (en) | 2014-06-23 | 2020-08-12 | Monsanto Technology LLC | Compositions and methods for regulating gene expression via rna interference |
| EP3161138A4 (en) | 2014-06-25 | 2017-12-06 | Monsanto Technology LLC | Methods and compositions for delivering nucleic acids to plant cells and regulating gene expression |
| WO2016018887A1 (en) | 2014-07-29 | 2016-02-04 | Monsanto Technology Llc | Compositions and methods for controlling insect pests |
| CN105801485B (zh) * | 2014-12-29 | 2018-04-24 | 浙江省化工研究院有限公司 | 一类苯基连吡唑酰胺衍生物、其制备方法及应用 |
| CA2974101A1 (en) | 2015-01-22 | 2016-07-28 | Monsanto Technology Llc | Compositions and methods for controlling leptinotarsa |
| WO2016196738A1 (en) | 2015-06-02 | 2016-12-08 | Monsanto Technology Llc | Compositions and methods for delivery of a polynucleotide into a plant |
| CN108024517A (zh) | 2015-06-03 | 2018-05-11 | 孟山都技术公司 | 用于将核酸引入到植物中的方法和组合物 |
| TN2017000544A1 (en) | 2015-07-31 | 2019-04-12 | Pfizer | 1,1,1-trifluoro-3-hydroxypropan-2-yl carbamate derivatives and 1,1,1-trifluoro-4-hydroxybutan-2-yl carbamate derivatives as magl inhibitors |
| RU2720203C1 (ru) | 2017-01-20 | 2020-04-27 | Пфайзер Инк. | 1,1,1-трифтор-3-гидроксипропан-2-илкарбаматные производные как ингибиторы magl |
| MX2019008690A (es) | 2017-01-23 | 2019-09-18 | Pfizer | Compuestos espiro heterociclicos como inhibidores de magl. |
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| JPS63301868A (ja) | 1987-06-01 | 1988-12-08 | Nippon Kayaku Co Ltd | N−(2−クロロイソニコチノイル)アミノ酸誘導体およびそれを有効成分とする農園芸用殺菌剤 |
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| JPH02172956A (ja) | 1988-12-23 | 1990-07-04 | Sumitomo Pharmaceut Co Ltd | エリスロ―3―(3,4―ジヒドロキシフェニル)セリン誘導体の新規製造法 |
| US4904674A (en) * | 1989-08-16 | 1990-02-27 | Hoechst-Roussel Pharmaceuticals Inc. | 1-(Benzo[b]thienyl)-2-(thienyl)ethenes and related compounds useful as anti-inflammatory agents |
| JP2543771B2 (ja) * | 1989-12-12 | 1996-10-16 | 四国化成工業株式会社 | 4(5)―カルバモイル―イミダゾ―ル化合物の合成方法及び新規化合物 |
| DE4011172A1 (de) * | 1990-04-06 | 1991-10-10 | Degussa | Verbindungen zur bekaempfung von pflanzenkrankheiten |
| JPH03294253A (ja) | 1990-04-12 | 1991-12-25 | Shionogi & Co Ltd | 消化管ホルモン拮抗物質 |
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| US5658885A (en) | 1993-04-27 | 1997-08-19 | The Dupont Merck Pharmaceutical Company | Amidino and guanidino substituted boronic acid inhibitors of trypsin-like enzymes |
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| CA2467665A1 (en) * | 2001-11-29 | 2003-06-05 | Basf Aktiengesellschaft | 2,w-diaminocarboxylic acid compounds |
| DE10204951A1 (de) | 2002-02-06 | 2003-08-14 | Basf Ag | Phenylalaninderivate als Herbizide |
| AR046792A1 (es) | 2003-12-19 | 2005-12-21 | Basf Ag | Fenilalanina-amidas sustituidas por heteroaroilo, un procedimiento para su preparacion, utilizacion de las mismas como herbicidas y productos fitosa-nitarios que los contienen como principio activo |
| CN1894202A (zh) | 2003-12-19 | 2007-01-10 | 巴斯福股份公司 | 苯甲酰基取代的苯基丙氨酸酰胺 |
| US8202843B2 (en) * | 2004-02-27 | 2012-06-19 | Rib-X Pharmaceuticals, Inc. | Macrocyclic compounds and methods of making and using the same |
| PE20060721A1 (es) * | 2004-09-16 | 2006-08-24 | Basf Ag | Serinamidas sustituidas por heteroaroilo |
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2006
- 2006-03-29 CA CA002609243A patent/CA2609243A1/en not_active Abandoned
- 2006-03-29 UA UAA200714187A patent/UA90720C2/ru unknown
- 2006-03-29 US US11/915,227 patent/US7879761B2/en not_active Expired - Fee Related
- 2006-03-29 EP EP06725384A patent/EP1888532A1/de not_active Withdrawn
- 2006-03-29 JP JP2008512789A patent/JP4981037B2/ja not_active Expired - Fee Related
- 2006-03-29 EA EA200702443A patent/EA013636B1/ru not_active IP Right Cessation
- 2006-03-29 MX MX2007014490A patent/MX2007014490A/es not_active Application Discontinuation
- 2006-03-29 AU AU2006251302A patent/AU2006251302A1/en not_active Abandoned
- 2006-03-29 CN CNA2006800271632A patent/CN101228133A/zh active Pending
- 2006-03-29 BR BRPI0611498A patent/BRPI0611498B1/pt not_active IP Right Cessation
- 2006-03-29 WO PCT/EP2006/061128 patent/WO2006125687A1/de not_active Ceased
- 2006-04-14 TW TW095113549A patent/TW200716558A/zh unknown
- 2006-05-24 AR ARP060102179A patent/AR057331A1/es unknown
- 2006-05-24 PE PE2006000547A patent/PE20070051A1/es not_active Application Discontinuation
- 2006-05-25 UY UY29565A patent/UY29565A1/es unknown
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2007
- 2007-11-20 IL IL187502A patent/IL187502A0/en unknown
- 2007-12-19 ZA ZA200711009A patent/ZA200711009B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PE20070051A1 (es) | 2007-02-01 |
| JP2008542231A (ja) | 2008-11-27 |
| EP1888532A1 (de) | 2008-02-20 |
| CA2609243A1 (en) | 2006-11-30 |
| ZA200711009B (en) | 2009-11-25 |
| CN101228133A (zh) | 2008-07-23 |
| EA200702443A1 (ru) | 2008-06-30 |
| IL187502A0 (en) | 2008-03-20 |
| AU2006251302A1 (en) | 2006-11-30 |
| US7879761B2 (en) | 2011-02-01 |
| MX2007014490A (es) | 2008-02-11 |
| WO2006125687A1 (de) | 2006-11-30 |
| BRPI0611498B1 (pt) | 2015-10-13 |
| UA90720C2 (en) | 2010-05-25 |
| US20080200338A1 (en) | 2008-08-21 |
| BRPI0611498A2 (pt) | 2011-02-22 |
| JP4981037B2 (ja) | 2012-07-18 |
| EA013636B1 (ru) | 2010-06-30 |
| UY29565A1 (es) | 2006-12-29 |
| TW200716558A (en) | 2007-05-01 |
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