AR076610A1 - Compuestos spiro epoxidos como intermediarios - Google Patents
Compuestos spiro epoxidos como intermediariosInfo
- Publication number
- AR076610A1 AR076610A1 ARP100101855A ARP100101855A AR076610A1 AR 076610 A1 AR076610 A1 AR 076610A1 AR P100101855 A ARP100101855 A AR P100101855A AR P100101855 A ARP100101855 A AR P100101855A AR 076610 A1 AR076610 A1 AR 076610A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- substituted
- haloalkyl
- alkoxy
- halogen
- Prior art date
Links
- -1 EPOXIDE COMPOUNDS Chemical class 0.000 title abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 17
- 229910052736 halogen Inorganic materials 0.000 abstract 10
- 150000002367 halogens Chemical class 0.000 abstract 10
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 abstract 7
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 7
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 7
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 7
- 229910052760 oxygen Inorganic materials 0.000 abstract 7
- 229910052717 sulfur Inorganic materials 0.000 abstract 7
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 6
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 6
- 125000004414 alkyl thio group Chemical group 0.000 abstract 6
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 6
- 125000001188 haloalkyl group Chemical group 0.000 abstract 6
- 239000001301 oxygen Substances 0.000 abstract 6
- 125000004434 sulfur atom Chemical group 0.000 abstract 6
- 125000003545 alkoxy group Chemical group 0.000 abstract 5
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 5
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 4
- 125000006705 (C5-C7) cycloalkyl group Chemical group 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 abstract 4
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 4
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 229920006395 saturated elastomer Polymers 0.000 abstract 3
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 2
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 2
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000003566 oxetanyl group Chemical group 0.000 abstract 2
- 125000006544 oxetanylalkyl group Chemical group 0.000 abstract 2
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- MILPANKGEKZHKH-UHFFFAOYSA-N 4-phenylthiane-3,5-dione Chemical class O=C1CSCC(=O)C1C1=CC=CC=C1 MILPANKGEKZHKH-UHFFFAOYSA-N 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000005280 halo alkyl sulfonyloxy group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000003107 substituted aryl group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/10—Spiro-condensed systems
-
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
- A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D309/08—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no 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
- C07D309/10—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/16—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D309/28—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
- C07D309/30—Oxygen atoms, e.g. delta-lactones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/32—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Pest Control & Pesticides (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pyrane Compounds (AREA)
- Furan Compounds (AREA)
- Epoxy Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Los compuestos son intermediarios adecuados en la preparacion de 4-fenil-3,5-pirandionas, 4-fenil-3,5-tiopirandionas y 6-fenilcicIohexan-1,3,5-trionas herbicidamente activas. Reivindicacion 1: Compuestos de la formula (1) donde R1 es halogeno, alquilo C1-4, haloalquilo C1-4, cicloalquilo C3-6, alcoxi C1-4, haloalcoxi C1-4, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4; R2 es hidrogeno, halogeno, metilsulfoniloxi, haloalquilsulfoniloxi C1-4, p-tolilsulfoniloxi, arilo opcionalmente sustituido o heteroarilo opcionalmente sustituido; r es 0, 1, 2 o 3; R3 si r es 1, es alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, alquiltio C1-6, alquilsulfinilo C1-6, alquilsulfonilo C1-6, ciano o nitro; o los sustituyentes R3, si r es 2 o 3, independientemente entre sí, son alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, alquiltio C1-6, alquilsulfinilo C1-6, alquilsulfonilo C1-6, ciano o nitro; Y es O, S, SO, SO2 o CO; R4, R5, R6 y R7, independientemente entre sí, son hidrogeno, alquilo C1-4, haloalquilo C1-4, alcoxi C1-4 alquilo C1-4, alquiltio C1-4 alquilo C1-4, alquilsulfinilo C1-4 alquilo C1-4, alquilsulfonilo C1-4 alquilo C1-4, ciclopropilo o ciclopropilo sustituido con alquilo C1 o C2, haloalquilo C1 o C2 o halogeno; ciclobutilo o ciclobutilo sustituido con alquilo C1 o C2; oxetanilo u oxetanilo sustituido con alquilo C1 o C2; cicloalquilo C5-7 o cicloalquilo C5-7 sustituido con alquilo C1 o C2 o haloalquilo C1 o C2, donde un grupo metileno del resto cicloalquilo se reemplaza opcionalmente por un átomo de oxígeno o azufre o un grupo sulfinilo o sulfonilo; cicloalquenilo C4-7 o cicloalquenilo C4-7 sustituido con alquilo C1 o C2 o haloalquilo C1 o C2, donde un grupo metileno del resto cicloalquenilo se reemplaza opcionalmente por un átomo de oxigeno o azufre o un grupo sulfinilo o sulfonilo; ciclopropilalquilo C1-5 o ciclopropilalquilo C1-5 sustituido con alquilo C1 o C2, haloalquilo C1 o C2 o halogeno; ciclobutilalquilo C1-5 o ciclobutilalquilo C1-5 sustituido con alquilo C1 o C2; oxetanilalquilo C1-5 u oxetanilalquilo C1-5 sustituido con alquilo C1 o C2; cicloalquilo C5-7 alquilo C1-5 o cicloalquilo C5-7 alquilo C1-5 sustituido con alquilo C1 o C2 o haloalquilo C1 o C2, donde un grupo metilo del resto cicloalquilo se reemplaza opcionalmente por un átomo de oxígeno o azufre o un grupo sulfinilo o sulfonilo; cicloalquenilo C4-7 alquilo C1-5 o cicloalquenilo C4-7 alquilo C1-5 el cual se encuentra sustituido con alquilo C1 o C2 o haloalquilo C1 o C2, donde un grupo metileno del resto cicloalquenilo se reemplaza opcionalmente por un átomo de oxígeno o azufre o un grupo sulfinilo o sulfonilo; fenilo o fenilo sustituido con alquilo C1-4, alcoxi C1-4, haloalquilo C1-4, halogeno, nitro, ciano, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4 o alquilcarbonilo C1-4 bencilo o bencilo sustituido con alquilo C1-4, alcoxi C1-4, haloalquilo C1-4, halogeno, nitro, ciano, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4 o alquilcarbonilo C1-4 heteroarilo o heteroarilo sustituido con alquilo C1-4, alcoxi C1-4, haloalquilo C1-4, halogeno, nitro, ciano, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4 o alquilcarbonilo C1-4; o R4 y R5, o R6 y R7, se unen para formar un anillo saturado o insaturado de 5 - 7 miembros donde un grupo metileno se reemplaza opcionalmente por un átomo de oxígeno o azufre, o un anillo saturado o insaturado de 5 - 7 miembros sustituido con alquilo C1 o C2, donde un grupo metileno del anillo se reemplaza opcionalmente por un átomo de oxígeno o azufre; o R4 y R7 se unen para formar un anillo saturado o insaturado de 5 - 7 miembros no sustituido o sustituido con alquilo C1 o C2, alcoxi C1 o C2, alcoxi C1 o C2 alquilo C1 o C2, hidroxi, halogeno, fenilo o fenilo sustituido con alquilo C1-4, alcoxi C1-4, haloalquilo C1-4, halogeno, nitro, ciano, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4 o alquilcarbonilo C1-4 heteroarilo o heteroarilo sustituido con alquilo C1-4, alcoxi C1-4, haloalquilo C1-4, halogeno, nitro, ciano, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4 o alquilcarbonilo C1-4.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0909303A GB0909303D0 (en) | 2009-05-29 | 2009-05-29 | Novel compounds |
| GB0921345A GB0921345D0 (en) | 2009-12-04 | 2009-12-04 | Novel compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR076610A1 true AR076610A1 (es) | 2011-06-22 |
Family
ID=42338979
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP100101855A AR076610A1 (es) | 2009-05-29 | 2010-05-28 | Compuestos spiro epoxidos como intermediarios |
Country Status (19)
| Country | Link |
|---|---|
| US (2) | US8680299B2 (es) |
| EP (1) | EP2435415A1 (es) |
| JP (1) | JP5735491B2 (es) |
| KR (1) | KR20120018182A (es) |
| CN (1) | CN102448948B (es) |
| AP (1) | AP2011006038A0 (es) |
| AR (1) | AR076610A1 (es) |
| AU (1) | AU2010252000B2 (es) |
| BR (1) | BRPI1014691A2 (es) |
| CA (1) | CA2763830A1 (es) |
| CL (1) | CL2011003009A1 (es) |
| CO (1) | CO6470820A2 (es) |
| CU (1) | CU20110220A7 (es) |
| EA (1) | EA020243B1 (es) |
| EC (1) | ECSP11011485A (es) |
| IL (1) | IL216364A0 (es) |
| MX (1) | MX2011012533A (es) |
| TW (1) | TW201043608A (es) |
| WO (1) | WO2010136431A1 (es) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06100637B2 (ja) | 1985-06-05 | 1994-12-12 | 日本電気株式会社 | コンピユ−タ本体試験システム |
| EP2222657B1 (en) * | 2007-12-13 | 2012-09-12 | Syngenta Limited | Pyrandiones, thiopyrandiones and cyclohexantriones having herbicidal properties |
| WO2010136431A1 (en) * | 2009-05-29 | 2010-12-02 | Syngenta Limited | Spiro epoxides as intermediates |
| JP2013514343A (ja) | 2009-12-17 | 2013-04-25 | シンジェンタ リミテッド | 除草剤活性ピランジオンを含んでなる除草剤組成物、および除草剤活性ピランジオンの使用法 |
| WO2012175899A1 (en) | 2011-06-23 | 2012-12-27 | Syngenta Limited | Herbicidal composition comprising a pyrandione herbicide and a sulfonyl urea herbicide |
| GB201310047D0 (en) | 2013-06-05 | 2013-07-17 | Syngenta Ltd | Compounds |
| JP7355858B2 (ja) * | 2019-06-12 | 2023-10-03 | ヌーリオン ケミカルズ インターナショナル ベスローテン フェノーツハップ | 水性側流からカルボン酸を単離するための方法 |
| EP3983368B1 (en) | 2019-06-12 | 2023-08-02 | Nouryon Chemicals International B.V. | Process for the production of diacyl peroxides |
| US12209065B2 (en) | 2019-06-12 | 2025-01-28 | Nouryon Chemicals International B.V. | Process for the production of diacyl peroxides |
| US12215074B2 (en) | 2019-06-12 | 2025-02-04 | Nouryon Chemicals International B.V. | Process for the production of peroxyesters |
| ES2963382T3 (es) | 2019-06-12 | 2024-03-26 | Nouryon Chemicals Int Bv | Proceso para la producción de peróxidos de diacilo |
| CA3266992A1 (en) | 2022-09-14 | 2024-03-21 | Basf Se | USE OF AN ALKYLETHOLTER SULFATE TO IMPROVE THE EFFICACY OF HERBICIDES |
| EP4338592A1 (en) | 2022-09-15 | 2024-03-20 | Basf Se | Use of compound for improving the efficacy of herbicides |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2007331723B2 (en) * | 2006-12-14 | 2013-05-30 | Syngenta Limited | 4-phenyl-pyrane-3,5-diones, 4-phenyl-thiopyrane-3,5-diones and cyclohexanetriones as novel herbicides |
| GB0704652D0 (en) * | 2007-03-09 | 2007-04-18 | Syngenta Participations Ag | Novel herbicides |
| EP2222657B1 (en) * | 2007-12-13 | 2012-09-12 | Syngenta Limited | Pyrandiones, thiopyrandiones and cyclohexantriones having herbicidal properties |
| GB0900641D0 (en) * | 2009-01-15 | 2009-02-25 | Syngenta Ltd | Novel herbicides |
| WO2010136431A1 (en) * | 2009-05-29 | 2010-12-02 | Syngenta Limited | Spiro epoxides as intermediates |
-
2010
- 2010-05-25 WO PCT/EP2010/057121 patent/WO2010136431A1/en not_active Ceased
- 2010-05-25 BR BRPI1014691-1A patent/BRPI1014691A2/pt not_active Application Discontinuation
- 2010-05-25 CN CN201080023447.0A patent/CN102448948B/zh not_active Expired - Fee Related
- 2010-05-25 CA CA2763830A patent/CA2763830A1/en not_active Abandoned
- 2010-05-25 KR KR1020117029020A patent/KR20120018182A/ko not_active Withdrawn
- 2010-05-25 EP EP10720780A patent/EP2435415A1/en not_active Withdrawn
- 2010-05-25 AP AP2011006038A patent/AP2011006038A0/xx unknown
- 2010-05-25 US US13/375,223 patent/US8680299B2/en not_active Expired - Fee Related
- 2010-05-25 MX MX2011012533A patent/MX2011012533A/es active IP Right Grant
- 2010-05-25 EA EA201101675A patent/EA020243B1/ru not_active IP Right Cessation
- 2010-05-25 JP JP2012512334A patent/JP5735491B2/ja not_active Expired - Fee Related
- 2010-05-25 AU AU2010252000A patent/AU2010252000B2/en not_active Ceased
- 2010-05-27 TW TW099116933A patent/TW201043608A/zh unknown
- 2010-05-28 AR ARP100101855A patent/AR076610A1/es unknown
-
2011
- 2011-11-14 IL IL216364A patent/IL216364A0/en unknown
- 2011-11-24 CO CO11161433A patent/CO6470820A2/es active IP Right Grant
- 2011-11-25 EC EC2011011485A patent/ECSP11011485A/es unknown
- 2011-11-28 CL CL2011003009A patent/CL2011003009A1/es unknown
- 2011-11-29 CU CU20110220A patent/CU20110220A7/es unknown
-
2014
- 2014-01-17 US US14/157,685 patent/US8987476B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EA020243B1 (ru) | 2014-09-30 |
| ECSP11011485A (es) | 2011-12-30 |
| CL2011003009A1 (es) | 2012-06-22 |
| KR20120018182A (ko) | 2012-02-29 |
| IL216364A0 (en) | 2012-01-31 |
| AP2011006038A0 (en) | 2011-12-31 |
| US20120077993A1 (en) | 2012-03-29 |
| US8680299B2 (en) | 2014-03-25 |
| WO2010136431A9 (en) | 2011-03-10 |
| EA201101675A1 (ru) | 2012-08-30 |
| WO2010136431A1 (en) | 2010-12-02 |
| EP2435415A1 (en) | 2012-04-04 |
| CU20110220A7 (es) | 2012-03-15 |
| CN102448948B (zh) | 2014-08-13 |
| CN102448948A (zh) | 2012-05-09 |
| AU2010252000B2 (en) | 2014-08-14 |
| JP2012528104A (ja) | 2012-11-12 |
| TW201043608A (en) | 2010-12-16 |
| US8987476B2 (en) | 2015-03-24 |
| US20140135508A1 (en) | 2014-05-15 |
| CA2763830A1 (en) | 2010-12-02 |
| MX2011012533A (es) | 2011-12-14 |
| AU2010252000A1 (en) | 2011-12-08 |
| JP5735491B2 (ja) | 2015-06-17 |
| BRPI1014691A2 (pt) | 2015-08-25 |
| CO6470820A2 (es) | 2012-06-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR076610A1 (es) | Compuestos spiro epoxidos como intermediarios | |
| AR064300A1 (es) | Pirandionas,tiopirandionas y ciclohexanotrionas como herbicidas | |
| AR087515A1 (es) | Compuestos de n-tio-antranilamida y sus usos como plaguicidas | |
| CO6170061A1 (es) | Compuestos de pirandiona, tiopirandiona y ciclohexantriona utiles como herbicidas, procesos para su preparacion, intermediarios utiles en su preparacion, metodos para controlar hierbas y malezas en cultivos de plantas utiles utilizando dichos herbici | |
| AR079224A1 (es) | Compuestos insecticidas basados en derivados de isoxazolina | |
| AR085903A1 (es) | Compuestos de pirazol sustituidos con halogeno | |
| AR082454A1 (es) | Proceso para producir compuestos aromaticos de carbonilo e imina | |
| PE20160608A1 (es) | Compuestos de quinolina selectivamente sustituida | |
| AR089644A1 (es) | Compuestos tipo anilina utiles como intermediarios para preparar insecticidas | |
| AR074909A1 (es) | Compuestos de imina para combatir plagas de invertebrados | |
| AR072459A1 (es) | DERIVADOS DE DIONAS CICLICAS ACTIVAS COMO HERBICIDAS, PROCESO DE PREPARACIoN Y COMPOSICIONES QUE COMPRENDEN DICHOS COMPUESTOS | |
| AR046020A1 (es) | Mimeticos de glucocorticoides, metodos de preparacion, composiciones farmaceuticas y usos de los mismos | |
| AR080233A1 (es) | Derivados de dihidrofurano como compuestos insecticidas | |
| PE20161035A1 (es) | Compuestos y usos de estos para la modulacion de la hemoglobina | |
| AR086587A1 (es) | Compuestos insecticidas | |
| AR068967A1 (es) | Compuestos de ciclohexandiona, proceso para la preparacion de los mismos, compuestos intermediarios, metodo de control de hierbas y malezas, y composicion herbicida | |
| PE20151605A1 (es) | Nuevos derivados de octahidro-pirrolo[3,4-c]-pirrol y analogos de los mismos como inhibidores de autotaxina | |
| PE20060932A1 (es) | Derivados de sulfonamidas como moduladores de receptores de glucocorticoides (gr) | |
| AR069596A1 (es) | Regulador del crecimiento de plantas | |
| AR076146A1 (es) | Derivados de isooxazol, composicion insecticida que los comprende y su uso en metodos de control de plagas. | |
| AR075040A1 (es) | Benzamida isoxazolinas y su uso como insecticidas. | |
| AR079205A1 (es) | Morfolinotiazoles como moduladores alostericos positivos alfa 7 | |
| AR081297A1 (es) | Derivados pirrolidina-diona espiroheterociclicos, procesos de preparacion, composiciones pesticidas y usos para combatir plagas | |
| AR083646A1 (es) | Compuestos de imina, composiciones veterinarias y agricolas que los contienen y su uso en el control de plagas de invertebrados | |
| AR068098A1 (es) | Derivados de ciclopentandiona como herbicidas |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |