AR069835A1 - Azolilmetiloxiranos, su uso y agentes que los contienen - Google Patents
Azolilmetiloxiranos, su uso y agentes que los contienenInfo
- Publication number
- AR069835A1 AR069835A1 ARP080105548A ARP080105548A AR069835A1 AR 069835 A1 AR069835 A1 AR 069835A1 AR P080105548 A ARP080105548 A AR P080105548A AR P080105548 A ARP080105548 A AR P080105548A AR 069835 A1 AR069835 A1 AR 069835A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- phenyl
- alkoxy
- groups
- halogenoalkyl
- Prior art date
Links
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 12
- -1 C2-8 halogenoalkenyl Chemical group 0.000 abstract 11
- 125000001188 haloalkyl group Chemical group 0.000 abstract 9
- 125000003545 alkoxy group Chemical group 0.000 abstract 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 8
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 5
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 5
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 5
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 5
- 229910052736 halogen Inorganic materials 0.000 abstract 5
- 150000002367 halogens Chemical class 0.000 abstract 5
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 4
- 125000003282 alkyl amino group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 3
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- 241000233866 Fungi Species 0.000 abstract 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 2
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 1
- 125000002723 alicyclic group Chemical group 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract 1
- 125000005108 alkenylthio group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000005109 alkynylthio group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000002047 benzodioxolyl group Chemical group O1OC(C2=C1C=CC=C2)* 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
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000001768 cations Chemical class 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 239000010949 copper Substances 0.000 abstract 1
- 125000004465 cycloalkenyloxy group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000005366 cycloalkylthio group Chemical group 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 125000005347 halocycloalkyl 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
- 229910052742 iron Inorganic materials 0.000 abstract 1
- 229910052759 nickel Inorganic materials 0.000 abstract 1
- IBGCXOFOCKCBNQ-UHFFFAOYSA-N nitro cyanate Chemical compound [O-][N+](=O)OC#N IBGCXOFOCKCBNQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 230000003032 phytopathogenic effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000001425 triazolyl group Chemical group 0.000 abstract 1
- 229910052725 zinc Inorganic materials 0.000 abstract 1
- 239000011701 zinc Substances 0.000 abstract 1
Classifications
-
- 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
- C07D405/14—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 three or more hetero rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- 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
- C07D405/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Animal Behavior & Ethology (AREA)
- Communicable Diseases (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Epoxy Compounds (AREA)
Abstract
Uso de los compuestos para combatir hongos fitopatogenos, composicion, semillas, procedimiento para combatir hongos, medicamento, procedimiento de obtencion de los compuestos e intermediarios. Reivindicacion 1: Azolilmetiloxiranos caracterizados porque tienen la formula (1) en la que las variables tienen los siguientes significados: A o B es un heterociclo saturado o parcialmente insaturado de tres, cuatro, cinco, seis, siete, ocho, nueve o diez miembros o un heterociclo aromático de cinco, seis, siete, ocho, nueve o diez miembros, cuyo heterociclo contiene cada vez uno, dos, tres o cuatro heteroátomos de los grupos O, N y S; y la respectiva otra variable B o A tiene uno de los significados arriba mencionados para A o B o es alquilo C1-8, halogenoalquilo C1-8, alquenilo C2-8, halogenoalquenilo C2-8, alquinilo C2-8, halogenoalquinilo C2-8, cicloalquilo C3-8, haIogenocicloalquilo C3-8, fenilo o benzodioxolilo; estando A y/o B, independientemente entre si, no sustituidos o sustituidos con uno, dos, tres o cuatro sustituyentes L independientemente seleccionados; L es halogeno, ciano, nitro, cianato (OCN), alquilo C1-8, halogenoalquilo C1-8, fenil-C1-6-alquiloxi, alquenilo C2-8, halogenoalquenilo C2-8, alquinilo C2-8, halogenoalquinilo C2-8, alcadienilo C4-10, halogenoalcadienilo C4-10, alcoxi C1-8, halogenoalcoxi C1-8, alquilcarboniloxi C1-8, alquilsulfoniloxi C1-8, alqueniloxi C2-8, halogenoalqueniloxi C2-8, alquiniloxi C2-8, halogenoalquiniloxi C2-8, cicloalquilo C3-8, haIogenocicloalquilo C3-8, cicloalquenilo C3-8, halogenocicloalquenilo C3-8, cicloalcoxi C3-8, cicloalqueniloxi C3-8, hidroxiimino-C1-8-alquilo, alquileno C1-6, oxi-C2-4-alquiIeno, oxi-C1-3-alquilenoxi, alcoximino C1-8-alquilo C1-8, alqueniloximino C2-8-alquilo C1-8, alquiniloximino C2-8-alquiIo C1-8, S(=O)nA1, C(=O)A2, C(=S)A2, NA3A4, fenilo, feniloxi o un heterociclo saturado, parcialmente insaturado o aromático de cinco o seis miembros, que contiene uno, dos, tres o cuatro heteroátomos del grupo O, N y S; donde N1, A2, A3, A4 significan: n 0, 1 o 2; A1 es hidrogeno, hidroxi, alquilo C1-8, halogenoalquilo C1-8, amino, alquilamino C1-8 o di-alquilamino C1-8, A2 uno de los grupos mencionados para A1 o alquenilo C2-8, halogenoalquenilo C2-8, alquinilo C2-8, halogenoalquinilo C2-8, alcoxi C1-8, halogenoalcoxi C1-8, alqueniloxi C2-8, halogenoalqueniloxi C2-8, aIquiniloxi C2-8, halogenoalquiniloxi C2-8, cicloalquilo C3-8, halogenocicloalquilo C3-8, cicloalcoxi C3-8 o halogenocicloalcoxi C3-8; A3, A4 significan independientemente entre si, hidrogeno, alquilo C1-8, halogenoalquilo C1-8, alquenilo C2-8, halogenoalquenilo C2-8, alquinilo C2-8, halogenoalquinilo C2-8, cicloalquilo C3-8, halogenocicloalquilo C3-8, cicloalquenilo C3-8, o halogenocicloalquenilo C3-8, pudiendo los grupos alifáticos y/o alicíclicos de las definiciones de los radicales L llevar a su vez uno, dos, tres o cuatro grupos iguales o diferentes de RL; RL es halogeno, ciano, nitro, alquilo C1-8, halogenoalquilo C1-8, alcoxi C1-8, halogenoalcoxi C1-8, cicloalquilo C3-8, halogenocicloalquilo C3-8, cicloalquenilo C3-8, cicloalcoxi C3-8, halogenocicloalcoxi C3-8; alquilcarbonilo C1-8, alquilcarboniloxi C1-8, alcoxicarbonilo C1-8, amino, alquilamino C1-8, di-alquilamino C1-8; D -S-R, donde R significa hidrogeno, alquilo C1-8, halogenoalquilo C1-8, alquenilo C2-8, halogenoalquenilo C2-8, alquinilo C2-8, halogenoalquinilo C2-8, C(=O)R3, C(=S)R3, SO2R4 o CN; donde R3 es hidrogeno, alquilo C1-8, halogenoalquilo C1-8, alcoxi C1-8, halogenoalcoxi C1-8 o NA3A4; y R4 significa aIquilo C1-8, fenil-C1-8-alquilo o fenilo, estando los grupos fenilo cada vez no sustituidos o sustituidos por uno, dos o tres grupos independientemente seleccionados de halogeno y alquilo C1-4; un grupo D1 teniendo A y B tienen las definiciones arriba indicadas; un grupo D2 donde representa el lugar de enlace con el anillo triazol y Q, R1 y R2;significan: Q es O o S; R1 y R2 significan, independientemente entre si, alquilo C1-8, halogenoalquilo C1-8, alcoxi C1-8, alcoxi C1-8-alcoxi C1-8, halogenoalcoxi C1-8, alcoxi C1-8-alquilo C1-8, alquiltio C1-8, alqueniltio C2-8, alquiniltio C2-8, cicloalquilo C3-8, cicloalquiltio C3-8, fenilo, fenil-C1-4-alquilo, fenoxi, feniltio, fenil-C1-4-alcoxi o NR5R6, donde R5 es H o alquilo C1-8 y R6 es alquilo C1-8, fenil-C1-4-alquilo o fenilo o R5 y R6 representan juntos una cadena alquileno con 4 o 5 átomos de C o un radical de la formula -CH2-CH2-O-CH2-CH2- o -CH2-CH2-NR7-CH2-CH2-, donde R7 es H o alquilo C1-4, estando los grupos aromáticos en los radicales arriba mencionados, cada vez independientemente entre si, no sustituidos o sustituidos por 1, 2 o 3 grupos seleccionados de halogeno y alquilo C1-4 o un grupo SM, donde M significa un cation de metal alcalino, un equivalente de un cation de metal alcalinotérreo, un equivalente de un cation de cobre, cinc, hierro o níquel o un cation de amonio de la formula Z1-N+(Z2)(Z3)(Z4), donde Z1 y Z2 significan independientemente H o alquilo C1-8; Z3 y Z4 significan independientemente H, alquilo C1-8, bencilo o fenilo; estando los grupos fenilo cada vez sin sustituir o sustituidos por 1, 2 o 3 grupos independientemente seleccionados de halogeno y alquilo C1-4, y sus sales agronomicamente compatibles.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07123735 | 2007-12-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR069835A1 true AR069835A1 (es) | 2010-02-24 |
Family
ID=39500033
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080105548A AR069835A1 (es) | 2007-12-19 | 2008-12-18 | Azolilmetiloxiranos, su uso y agentes que los contienen |
Country Status (6)
| Country | Link |
|---|---|
| AR (1) | AR069835A1 (es) |
| CL (1) | CL2008003866A1 (es) |
| PE (1) | PE20091178A1 (es) |
| TW (1) | TW200932116A (es) |
| UY (1) | UY31563A1 (es) |
| WO (1) | WO2009077497A2 (es) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010535156A (ja) | 2007-08-03 | 2010-11-18 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | ウイルスポリメラーゼ阻害剤 |
| US8476257B2 (en) | 2007-12-19 | 2013-07-02 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
| WO2011069916A1 (de) | 2009-12-08 | 2011-06-16 | Basf Se | Triazolverbindungen, ihre verwendung als fungizide sowie sie enthaltende mittel |
| WO2011069894A1 (de) | 2009-12-08 | 2011-06-16 | Basf Se | Triazolverbindungen, ihre verwendung sowie sie enthaltende mittel |
| US20120289706A1 (en) | 2009-12-18 | 2012-11-15 | Basf Se | Method for Producing Triazolinthione Derivatives and Intermediates Thereof |
| AU2011229200A1 (en) | 2010-03-16 | 2012-10-11 | Basf Se | A process using Grignard reagents |
| EP2621922A1 (en) | 2010-09-30 | 2013-08-07 | Basf Se | A process for the synthesis of thio-triazolo-group containing compounds |
| WO2012130823A1 (en) | 2011-03-30 | 2012-10-04 | Basf Se | Suspension concentrates |
| WO2012146598A1 (en) | 2011-04-28 | 2012-11-01 | Basf Se | Process for the preparation of 2-substituted 4-amino-2,4-dihydro-[1,2,4]triazole-3-thiones |
| WO2012146535A1 (en) | 2011-04-28 | 2012-11-01 | Basf Se | Process for the preparation of 2-substituted 2,4-dihydro-[1,2,4]triazole-3-thiones |
| WO2014095381A1 (en) | 2012-12-19 | 2014-06-26 | Basf Se | Fungicidal imidazolyl and triazolyl compounds |
| EP2746255A1 (en) | 2012-12-19 | 2014-06-25 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
| EP2746256A1 (en) | 2012-12-19 | 2014-06-25 | Basf Se | Fungicidal imidazolyl and triazolyl compounds |
| EP2746277A1 (en) | 2012-12-19 | 2014-06-25 | Basf Se | Fungicidal imidazolyl and triazolyl compounds |
| EP2746279A1 (en) | 2012-12-19 | 2014-06-25 | Basf Se | Fungicidal imidazolyl and triazolyl compounds |
| WO2014095249A1 (en) | 2012-12-19 | 2014-06-26 | Basf Se | Fungicidal imidazolyl and triazolyl compounds |
| EP2746264A1 (en) | 2012-12-19 | 2014-06-25 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
| EP2746259A1 (en) | 2012-12-21 | 2014-06-25 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
| EP2746260A1 (en) | 2012-12-21 | 2014-06-25 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
| EP2746258A1 (en) | 2012-12-21 | 2014-06-25 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
| EP2746257A1 (en) | 2012-12-21 | 2014-06-25 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
| US20200029564A1 (en) * | 2016-09-29 | 2020-01-30 | Bayer Cropscience Aktiengesellschaft | Novel 5-substituted imidazolylmethyloxirane derivatives |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3218129A1 (de) * | 1982-05-14 | 1983-11-17 | Basf Ag, 6700 Ludwigshafen | Azolylmethyloxirane, ihre herstellung und verwendung als arzneimittel |
| DE3805684A1 (de) * | 1988-02-24 | 1989-09-07 | Basf Ag | Azolylmethylcycloalkyloxirane, ihre herstellung und verwendung als pflanzenschutzmittel |
| IL95493A0 (en) * | 1989-09-09 | 1991-06-30 | Basf Ag | Azolylmethyloxiranes,their manufacture and their use as fungicides |
| DE19520097A1 (de) * | 1995-06-01 | 1996-12-05 | Bayer Ag | Triazolylmethyl-oxirane |
| DE19617461A1 (de) * | 1996-05-02 | 1997-11-06 | Bayer Ag | Acylmercapto-triazolyl-Derivate |
| AU9441898A (en) * | 1997-10-08 | 1999-04-27 | Bayer Aktiengesellschaft | Method for producing triazolinthion derivatives |
| DE19744400A1 (de) * | 1997-10-08 | 1999-04-15 | Bayer Ag | Verfahren zur Herstellung von Triazolinthion-Derivaten |
| DE19744401A1 (de) * | 1997-10-08 | 1999-04-15 | Bayer Ag | Verfahren zur Herstellung von Triazolinthion-Derivaten |
| US7910614B2 (en) * | 2006-07-25 | 2011-03-22 | Basf Se | Azolylmethyloxiranes, use thereof for controlling plant pathogenic fungi, and agents containing the same |
-
2008
- 2008-12-15 WO PCT/EP2008/067539 patent/WO2009077497A2/de not_active Ceased
- 2008-12-18 AR ARP080105548A patent/AR069835A1/es not_active Application Discontinuation
- 2008-12-19 CL CL2008003866A patent/CL2008003866A1/es unknown
- 2008-12-19 PE PE2008002153A patent/PE20091178A1/es not_active Application Discontinuation
- 2008-12-19 UY UY31563A patent/UY31563A1/es unknown
- 2008-12-19 TW TW097149852A patent/TW200932116A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CL2008003866A1 (es) | 2009-11-27 |
| WO2009077497A3 (de) | 2010-01-28 |
| WO2009077497A2 (de) | 2009-06-25 |
| TW200932116A (en) | 2009-08-01 |
| PE20091178A1 (es) | 2009-09-03 |
| UY31563A1 (es) | 2009-07-17 |
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