ZA200209309B - Bidentate ligands useful in catalyst system. - Google Patents
Bidentate ligands useful in catalyst system. Download PDFInfo
- Publication number
- ZA200209309B ZA200209309B ZA200209309A ZA200209309A ZA200209309B ZA 200209309 B ZA200209309 B ZA 200209309B ZA 200209309 A ZA200209309 A ZA 200209309A ZA 200209309 A ZA200209309 A ZA 200209309A ZA 200209309 B ZA200209309 B ZA 200209309B
- Authority
- ZA
- South Africa
- Prior art keywords
- atoms
- bidentate ligand
- substituted
- group
- catalyst system
- Prior art date
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- 239000003446 ligand Substances 0.000 title claims abstract description 32
- 239000003054 catalyst Substances 0.000 title claims abstract description 24
- 125000001424 substituent group Chemical group 0.000 claims abstract description 22
- 238000006243 chemical reaction Methods 0.000 claims abstract description 20
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 19
- 238000005810 carbonylation reaction Methods 0.000 claims abstract description 18
- 150000001875 compounds Chemical class 0.000 claims abstract description 17
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims abstract description 16
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 16
- 229910002091 carbon monoxide Inorganic materials 0.000 claims abstract description 16
- 150000001450 anions Chemical class 0.000 claims abstract description 15
- 230000006315 carbonylation Effects 0.000 claims abstract description 14
- 229910052751 metal Inorganic materials 0.000 claims abstract description 13
- 239000002184 metal Substances 0.000 claims abstract description 13
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 11
- 238000000034 method Methods 0.000 claims abstract description 10
- 150000001768 cations Chemical class 0.000 claims abstract description 5
- 229910052787 antimony Inorganic materials 0.000 claims abstract description 4
- 229910052785 arsenic Inorganic materials 0.000 claims abstract description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 31
- 125000004429 atom Chemical group 0.000 claims description 20
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 125000004437 phosphorous atom Chemical group 0.000 claims description 7
- 125000006413 ring segment Chemical group 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 230000000269 nucleophilic effect Effects 0.000 claims description 3
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 18
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 17
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- VURFVHCLMJOLKN-UHFFFAOYSA-N diphosphane Chemical compound PP VURFVHCLMJOLKN-UHFFFAOYSA-N 0.000 description 12
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- 125000004122 cyclic group Chemical group 0.000 description 8
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- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
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- AMCBZAXVJIWQLI-UHFFFAOYSA-N ditert-butyl(4-ditert-butylphosphanylhexan-2-yl)phosphane Chemical compound CC(C)(C)P(C(C)(C)C)C(CC)CC(C)P(C(C)(C)C)C(C)(C)C AMCBZAXVJIWQLI-UHFFFAOYSA-N 0.000 description 1
- RAXUFDRKPWXAQH-UHFFFAOYSA-N ditert-butyl(4-ditert-butylphosphanylhexan-3-yl)phosphane Chemical compound CC(C)(C)P(C(C)(C)C)C(CC)C(CC)P(C(C)(C)C)C(C)(C)C RAXUFDRKPWXAQH-UHFFFAOYSA-N 0.000 description 1
- FKUZUFOPNKMYTE-UHFFFAOYSA-N ditert-butyl-(2-ditert-butylphosphanylcyclopentyl)phosphane Chemical compound CC(C)(C)P(C(C)(C)C)C1CCCC1P(C(C)(C)C)C(C)(C)C FKUZUFOPNKMYTE-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229940052303 ethers for general anesthesia Drugs 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 235000019256 formaldehyde Nutrition 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 229960004592 isopropanol Drugs 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- KWKAKUADMBZCLK-UHFFFAOYSA-N methyl heptene Natural products CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 1
- KJALUUCEMMPKAC-UHFFFAOYSA-N methyl pent-3-enoate Chemical class COC(=O)CC=CC KJALUUCEMMPKAC-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 150000002941 palladium compounds Chemical class 0.000 description 1
- GTCCGKPBSJZVRZ-UHFFFAOYSA-N pentane-2,4-diol Chemical compound CC(O)CC(C)O GTCCGKPBSJZVRZ-UHFFFAOYSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 1
- 150000003057 platinum Chemical class 0.000 description 1
- 229920001470 polyketone Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
- HHVIBTZHLRERCL-UHFFFAOYSA-N sulfonyldimethane Chemical compound CS(C)(=O)=O HHVIBTZHLRERCL-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000007970 thio esters Chemical group 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 125000005490 tosylate group Chemical group 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/50—Organo-phosphines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6571—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms
- C07F9/657163—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms the ring phosphorus atom being bound to at least one carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/49—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide
- C07C45/50—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide by oxo-reactions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/36—Preparation of carboxylic acid esters by reaction with carbon monoxide or formates
- C07C67/38—Preparation of carboxylic acid esters by reaction with carbon monoxide or formates by addition to an unsaturated carbon-to-carbon bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/50—Organo-phosphines
- C07F9/5027—Polyphosphines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6568—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms
- C07F9/65683—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms the ring phosphorus atom being part of a phosphine
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP00304171 | 2000-05-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200209309B true ZA200209309B (en) | 2003-07-29 |
Family
ID=8172999
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200209309A ZA200209309B (en) | 2000-05-17 | 2002-11-15 | Bidentate ligands useful in catalyst system. |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US6639091B2 (de) |
| EP (1) | EP1282629B2 (de) |
| JP (1) | JP5390734B2 (de) |
| KR (1) | KR100744207B1 (de) |
| CN (1) | CN1216889C (de) |
| AT (1) | ATE258936T1 (de) |
| AU (2) | AU7404601A (de) |
| BR (1) | BRPI0110882B1 (de) |
| CA (1) | CA2408862C (de) |
| DE (1) | DE60101963T3 (de) |
| ES (1) | ES2210170T5 (de) |
| MX (1) | MXPA02011237A (de) |
| MY (1) | MY127093A (de) |
| TW (1) | TWI287017B (de) |
| WO (1) | WO2001087899A1 (de) |
| ZA (1) | ZA200209309B (de) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6184431B1 (en) * | 1999-08-23 | 2001-02-06 | Shell Oil Company | Process for separating internal and alpha olefins from saturated compounds |
| CA2419271C (en) * | 2000-08-14 | 2010-01-19 | Sasol Technology (Proprietary) Limited | Production of oxygenated products |
| WO2002064250A2 (en) * | 2001-01-31 | 2002-08-22 | Shell Internationale Research Maatschappij B.V. | Process for the carbonylation of ethylenically unsaturated compounds, bidentate diphosphine composition used in this process and processes for preparation of this bidentate diphosphine composition |
| DE10148712A1 (de) | 2001-10-02 | 2003-04-17 | Basf Ag | Diphosphin |
| CA2466252A1 (en) | 2001-11-09 | 2003-05-15 | Shell Internationale Research Maatschappij B.V. | Bidentate ligands for the carbonylation of unsaturated compounds |
| US6806391B2 (en) | 2002-07-31 | 2004-10-19 | Shell Oil Company | Process for the carbonylation of ethylenically unsaturated compounds and bidentate diphosphine composition used in this process |
| US7084089B2 (en) | 2002-07-31 | 2006-08-01 | Shell Oil Company | Process for the carbonylation of ethylenically unsaturated compounds, bidentate diphosphine composition used in this process and a process for preparation of this bidentate diphosphine composition |
| JP2006500414A (ja) | 2002-09-26 | 2006-01-05 | シエル・インターナシヨナル・リサーチ・マートスハツペイ・ベー・ヴエー | 第一級アルコールの製造方法 |
| US7250538B2 (en) | 2002-09-26 | 2007-07-31 | Shell Oil Company | Process for the hydroformylation of an ethylenically unsaturated compound |
| GB0403592D0 (en) | 2004-02-18 | 2004-03-24 | Lucite Int Uk Ltd | A catalyst system |
| US7265242B2 (en) * | 2004-02-26 | 2007-09-04 | Shell Oil Company | Process for the carbonylation of ethylenically or acetylenically unsaturated compounds |
| US7013601B2 (en) * | 2004-07-22 | 2006-03-21 | Coastal Planters, Llc | Plant container with hanger |
| GB0516556D0 (en) * | 2005-08-12 | 2005-09-21 | Lucite Int Uk Ltd | Improved catalyst system |
| KR101633325B1 (ko) | 2005-11-17 | 2016-06-24 | 루사이트 인터내셔널 유케이 리미티드 | 에틸렌성 불포화 화합물의 카르보닐화 |
| GB0607494D0 (en) * | 2006-04-13 | 2006-05-24 | Lucite Int Uk Ltd | Metal complexes |
| GB2437930A (en) * | 2006-05-10 | 2007-11-14 | Lucite Int Uk Ltd | Mixing apparatus |
| ES2729615T3 (es) | 2006-12-02 | 2019-11-05 | Lucite Int Uk Ltd | Nuevos ligandos de carbonilación y su uso en la carbonilación de compuestos etilénicamente insaturados |
| KR100985955B1 (ko) * | 2008-03-25 | 2010-10-06 | 김경수 | 피부 미용기 |
| GB0812297D0 (en) * | 2008-07-04 | 2008-08-13 | Lucite Int Uk Ltd | Novel carbonylation ligand sand thier use of in the carbonylation of ethylenically unsaturated compounds |
| US20100069679A1 (en) * | 2008-09-12 | 2010-03-18 | Eastman Chemical Company | Acetylene tolerant hydroformylation catalysts |
| EP2213644A1 (de) | 2009-01-28 | 2010-08-04 | Hexion Specialty Chemicals Research Belgium S.A. | Verfahren zur Herstellung eines Allylarylethers durch katalytische Allylierung |
| EP2213645A1 (de) | 2009-01-28 | 2010-08-04 | Hexion Specialty Chemicals Research Belgium S.A. | Verfahren zur Herstellung eines Allylarylethers durch katalytische O-Allylierung |
| EP2213643A1 (de) | 2009-01-28 | 2010-08-04 | Hexion Specialty Chemicals Research Belgium S.A. | Verfahren zur Herstellung eines Allylarylethers durch katalytische O-Allylierung |
| GB201000078D0 (en) | 2010-01-05 | 2010-02-17 | Lucite Int Uk Ltd | Process for the carbonylation of ethylenically unsaturated compounds, novel carbonylation ligands and catalyst systems incorporatng such ligands |
| US9540440B2 (en) | 2013-10-30 | 2017-01-10 | Cytomx Therapeutics, Inc. | Activatable antibodies that bind epidermal growth factor receptor and methods of use thereof |
| WO2015089283A1 (en) | 2013-12-11 | 2015-06-18 | Cytomx Therapeutics, Inc. | Antibodies that bind activatable antibodies and methods of use thereof |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2880222A (en) * | 1957-02-06 | 1959-03-31 | Ernst A H Friedheim | Organic dithiol derivatives |
| US3035052A (en) * | 1959-03-02 | 1962-05-15 | Ernst A H Friedheim | Arsenic-containing derivatives of dimercapto-succinic acid |
| GB1127965A (en) | 1965-11-26 | 1968-09-25 | Shell Int Research | Ditertiary phosphines and application thereof as catalyst components for alcohol production |
| JPS58103537A (ja) * | 1981-12-15 | 1983-06-20 | Adeka Argus Chem Co Ltd | 安定化された合成樹脂組成物 |
| DE4026406A1 (de) * | 1990-08-21 | 1992-02-27 | Basf Ag | Rhodiumhydroformylierungskatalysatoren mit bis-phosphit-liganden |
| EP0495548B1 (de) † | 1991-01-15 | 1995-09-13 | Shell Internationale Researchmaatschappij B.V. | Verfahren zur Karbonylierung von Olefin |
| SG45352A1 (en) * | 1991-01-15 | 1998-01-16 | Shell Int Research | Carbonylation of olefins |
| CA2086285A1 (en) * | 1992-12-24 | 1994-06-25 | Colleen Elizabeth Micklethwaite | Process for the preparation of vicinally-disubstituted bis(diorganophosphino) compounds |
| DE69414578T2 (de) * | 1993-08-19 | 1999-05-20 | Shell Int Research | Hydroformylierungs verfahren |
| GB9425911D0 (en) * | 1994-12-22 | 1995-02-22 | Ici Plc | Process for the carbonylation of olefins and catalyst system for use therein |
| US5495041A (en) | 1995-02-22 | 1996-02-27 | Dsm N.W. | Process for the preparation of a pentenoate ester |
| FR2761071B1 (fr) † | 1997-03-20 | 1999-12-03 | Synthelabo | Derives de quinolein-2(1h)-one et de dihydroquinolein-2(1h)- one, leur preparation et leur application en therapeutique |
| US6156934A (en) * | 1997-03-26 | 2000-12-05 | Shell Oil Company | Diphosphines |
| DE19840253A1 (de) | 1998-09-03 | 2000-03-09 | Basf Ag | Verfahren zur Herstellung von Cyanvaleriansäure oder -estern |
-
2001
- 2001-05-15 MY MYPI20012269 patent/MY127093A/en unknown
- 2001-05-16 DE DE60101963T patent/DE60101963T3/de not_active Expired - Lifetime
- 2001-05-16 KR KR1020027015277A patent/KR100744207B1/ko active IP Right Grant
- 2001-05-16 AU AU7404601A patent/AU7404601A/xx active Pending
- 2001-05-16 EP EP01940491A patent/EP1282629B2/de not_active Expired - Lifetime
- 2001-05-16 ES ES01940491T patent/ES2210170T5/es not_active Expired - Lifetime
- 2001-05-16 BR BRPI0110882A patent/BRPI0110882B1/pt not_active IP Right Cessation
- 2001-05-16 CN CN018095658A patent/CN1216889C/zh not_active Expired - Lifetime
- 2001-05-16 MX MXPA02011237A patent/MXPA02011237A/es active IP Right Grant
- 2001-05-16 CA CA2408862A patent/CA2408862C/en not_active Expired - Lifetime
- 2001-05-16 AT AT01940491T patent/ATE258936T1/de active
- 2001-05-16 JP JP2001584292A patent/JP5390734B2/ja not_active Expired - Fee Related
- 2001-05-16 AU AU2001274046A patent/AU2001274046B2/en not_active Ceased
- 2001-05-16 WO PCT/EP2001/005625 patent/WO2001087899A1/en active IP Right Grant
- 2001-05-17 US US09/860,015 patent/US6639091B2/en not_active Expired - Lifetime
- 2001-07-03 TW TW090116261A patent/TWI287017B/zh not_active IP Right Cessation
-
2002
- 2002-11-15 ZA ZA200209309A patent/ZA200209309B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MXPA02011237A (es) | 2003-04-25 |
| EP1282629B2 (de) | 2007-04-11 |
| EP1282629B1 (de) | 2004-02-04 |
| KR20020094051A (ko) | 2002-12-16 |
| KR100744207B1 (ko) | 2007-07-30 |
| CA2408862A1 (en) | 2001-11-22 |
| DE60101963D1 (de) | 2004-03-11 |
| EP1282629A1 (de) | 2003-02-12 |
| AU7404601A (en) | 2001-11-26 |
| JP2003533534A (ja) | 2003-11-11 |
| JP5390734B2 (ja) | 2014-01-15 |
| WO2001087899A1 (en) | 2001-11-22 |
| MY127093A (en) | 2006-11-30 |
| DE60101963T2 (de) | 2004-12-23 |
| AU2001274046B2 (en) | 2004-05-06 |
| CN1216889C (zh) | 2005-08-31 |
| DE60101963T3 (de) | 2007-10-18 |
| BRPI0110882B1 (pt) | 2015-12-22 |
| ES2210170T5 (es) | 2007-11-01 |
| ES2210170T3 (es) | 2004-07-01 |
| US20020016484A1 (en) | 2002-02-07 |
| BR0110882A (pt) | 2003-06-10 |
| ATE258936T1 (de) | 2004-02-15 |
| TWI287017B (en) | 2007-09-21 |
| CA2408862C (en) | 2010-02-16 |
| CN1429228A (zh) | 2003-07-09 |
| US6639091B2 (en) | 2003-10-28 |
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