CZ20013042A3 - Způsob selektivní oxidace primárních alkoholů - Google Patents
Způsob selektivní oxidace primárních alkoholů Download PDFInfo
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- CZ20013042A3 CZ20013042A3 CZ20013042A CZ20013042A CZ20013042A3 CZ 20013042 A3 CZ20013042 A3 CZ 20013042A3 CZ 20013042 A CZ20013042 A CZ 20013042A CZ 20013042 A CZ20013042 A CZ 20013042A CZ 20013042 A3 CZ20013042 A3 CZ 20013042A3
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- CZ
- Czechia
- Prior art keywords
- carbohydrate
- groups
- group
- aldehyde
- oxidation
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- 238000000034 method Methods 0.000 title claims abstract description 41
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- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- JYJIGFIDKWBXDU-MNNPPOADSA-N inulin Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)OC[C@]1(OC[C@]2(OC[C@]3(OC[C@]4(OC[C@]5(OC[C@]6(OC[C@]7(OC[C@]8(OC[C@]9(OC[C@]%10(OC[C@]%11(OC[C@]%12(OC[C@]%13(OC[C@]%14(OC[C@]%15(OC[C@]%16(OC[C@]%17(OC[C@]%18(OC[C@]%19(OC[C@]%20(OC[C@]%21(OC[C@]%22(OC[C@]%23(OC[C@]%24(OC[C@]%25(OC[C@]%26(OC[C@]%27(OC[C@]%28(OC[C@]%29(OC[C@]%30(OC[C@]%31(OC[C@]%32(OC[C@]%33(OC[C@]%34(OC[C@]%35(OC[C@]%36(O[C@@H]%37[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O%37)O)[C@H]([C@H](O)[C@@H](CO)O%36)O)[C@H]([C@H](O)[C@@H](CO)O%35)O)[C@H]([C@H](O)[C@@H](CO)O%34)O)[C@H]([C@H](O)[C@@H](CO)O%33)O)[C@H]([C@H](O)[C@@H](CO)O%32)O)[C@H]([C@H](O)[C@@H](CO)O%31)O)[C@H]([C@H](O)[C@@H](CO)O%30)O)[C@H]([C@H](O)[C@@H](CO)O%29)O)[C@H]([C@H](O)[C@@H](CO)O%28)O)[C@H]([C@H](O)[C@@H](CO)O%27)O)[C@H]([C@H](O)[C@@H](CO)O%26)O)[C@H]([C@H](O)[C@@H](CO)O%25)O)[C@H]([C@H](O)[C@@H](CO)O%24)O)[C@H]([C@H](O)[C@@H](CO)O%23)O)[C@H]([C@H](O)[C@@H](CO)O%22)O)[C@H]([C@H](O)[C@@H](CO)O%21)O)[C@H]([C@H](O)[C@@H](CO)O%20)O)[C@H]([C@H](O)[C@@H](CO)O%19)O)[C@H]([C@H](O)[C@@H](CO)O%18)O)[C@H]([C@H](O)[C@@H](CO)O%17)O)[C@H]([C@H](O)[C@@H](CO)O%16)O)[C@H]([C@H](O)[C@@H](CO)O%15)O)[C@H]([C@H](O)[C@@H](CO)O%14)O)[C@H]([C@H](O)[C@@H](CO)O%13)O)[C@H]([C@H](O)[C@@H](CO)O%12)O)[C@H]([C@H](O)[C@@H](CO)O%11)O)[C@H]([C@H](O)[C@@H](CO)O%10)O)[C@H]([C@H](O)[C@@H](CO)O9)O)[C@H]([C@H](O)[C@@H](CO)O8)O)[C@H]([C@H](O)[C@@H](CO)O7)O)[C@H]([C@H](O)[C@@H](CO)O6)O)[C@H]([C@H](O)[C@@H](CO)O5)O)[C@H]([C@H](O)[C@@H](CO)O4)O)[C@H]([C@H](O)[C@@H](CO)O3)O)[C@H]([C@H](O)[C@@H](CO)O2)O)[C@@H](O)[C@H](O)[C@@H](CO)O1 JYJIGFIDKWBXDU-MNNPPOADSA-N 0.000 description 1
- 229940029339 inulin Drugs 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229940099563 lactobionic acid Drugs 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- AIHDCSAXVMAMJH-GFBKWZILSA-N levan Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)OC[C@@H]1[C@@H](O)[C@H](O)[C@](CO)(CO[C@@H]2[C@H]([C@H](O)[C@@](O)(CO)O2)O)O1 AIHDCSAXVMAMJH-GFBKWZILSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000711 locust bean gum Substances 0.000 description 1
- 235000010420 locust bean gum Nutrition 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- MIVBAHRSNUNMPP-UHFFFAOYSA-N manganese(2+);dinitrate Chemical compound [Mn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MIVBAHRSNUNMPP-UHFFFAOYSA-N 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- LUEWUZLMQUOBSB-GFVSVBBRSA-N mannan Chemical class O[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@H](O[C@@H](O[C@H]3[C@H](O[C@@H](O)[C@@H](O)[C@H]3O)CO)[C@@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O LUEWUZLMQUOBSB-GFVSVBBRSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- SQDFHQJTAWCFIB-UHFFFAOYSA-N n-methylidenehydroxylamine Chemical compound ON=C SQDFHQJTAWCFIB-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- GUQPPNZGDSQJGT-UHFFFAOYSA-N octadecane-1,9-diol Chemical group CCCCCCCCCC(O)CCCCCCCCO GUQPPNZGDSQJGT-UHFFFAOYSA-N 0.000 description 1
- GDUWKVCUIFEAGC-UHFFFAOYSA-N octane-1,6-diol Chemical group CCC(O)CCCCCO GDUWKVCUIFEAGC-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 230000036284 oxygen consumption Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- UKODFQOELJFMII-UHFFFAOYSA-N pentamethyldiethylenetriamine Chemical compound CN(C)CCN(C)CCN(C)C UKODFQOELJFMII-UHFFFAOYSA-N 0.000 description 1
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical class OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000006268 reductive amination reaction Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000003270 steroid hormone Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000008362 succinate buffer Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229920001221 xylan Polymers 0.000 description 1
- 150000004823 xylans Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/24—Preparation of oxygen-containing organic compounds containing a carbonyl group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H1/00—Processes for the preparation of sugar derivatives
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P19/00—Preparation of compounds containing saccharide radicals
- C12P19/04—Polysaccharides, i.e. compounds containing more than five saccharide radicals attached to each other by glycosidic bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Microbiology (AREA)
- General Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Molecular Biology (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Saccharide Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Steroid Compounds (AREA)
- Compounds Of Unknown Constitution (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP99200536 | 1999-02-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CZ20013042A3 true CZ20013042A3 (cs) | 2002-02-13 |
Family
ID=8239920
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CZ20013042A CZ20013042A3 (cs) | 1999-02-24 | 2000-02-24 | Způsob selektivní oxidace primárních alkoholů |
Country Status (19)
| Country | Link |
|---|---|
| US (2) | US6875861B1 (enExample) |
| EP (2) | EP1173409B8 (enExample) |
| JP (2) | JP2002537374A (enExample) |
| KR (1) | KR20010102361A (enExample) |
| AT (1) | ATE308514T1 (enExample) |
| AU (2) | AU773792B2 (enExample) |
| BR (2) | BR0008474A (enExample) |
| CA (1) | CA2362717A1 (enExample) |
| CZ (1) | CZ20013042A3 (enExample) |
| DE (1) | DE60023680T2 (enExample) |
| DK (1) | DK1173409T3 (enExample) |
| ES (1) | ES2255979T3 (enExample) |
| HU (2) | HUP0105299A3 (enExample) |
| MX (1) | MXPA01008603A (enExample) |
| NZ (1) | NZ513649A (enExample) |
| PL (2) | PL356989A1 (enExample) |
| RU (1) | RU2001125922A (enExample) |
| WO (2) | WO2000050621A2 (enExample) |
| ZA (2) | ZA200106737B (enExample) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100304216B1 (ko) | 1996-03-28 | 2001-11-22 | 데이비드 엠 모이어 | 알데히드-작용화된셀룰로즈섬유및중합체로부터제조된습윤강도를갖는종이제품 |
| IL137887A0 (en) | 1999-08-17 | 2001-10-31 | Nat Starch Chem Invest | Polysaccharide aldehydes prepared by oxidation method and used as strength additives in papermaking |
| US6586588B1 (en) | 1999-08-17 | 2003-07-01 | National Starch And Chemical Investment Holding Corporation | Polysaccharide aldehydes prepared by oxidation method and used as strength additives in papermaking |
| US6228126B1 (en) | 1999-08-17 | 2001-05-08 | National Starch And Chemical Investment Holding Corporation | Paper prepared from aldehyde modified cellulose pulp and the method of making the pulp |
| US6368456B1 (en) | 1999-08-17 | 2002-04-09 | National Starch And Chemical Investment Holding Corporation | Method of making paper from aldehyde modified cellulose pulp with selected additives |
| US6695950B1 (en) | 1999-08-17 | 2004-02-24 | National Starch And Chemical Investment Holding Corporation | Aldehyde modified cellulose pulp for the preparation of high strength paper products |
| US6582559B2 (en) | 2000-05-04 | 2003-06-24 | Sca Hygiene Products Zeist B.V. | Aldehyde-containing polymers as wet strength additives |
| US6540876B1 (en) | 2000-05-19 | 2003-04-01 | National Starch And Chemical Ivnestment Holding Corporation | Use of amide or imide co-catalysts for nitroxide mediated oxidation |
| US7138035B2 (en) | 2001-05-08 | 2006-11-21 | National Starch And Chemical Investment Holding Corporation | Process for the selective modification of carbohydrates by peroxidase catalyzed oxidation |
| KR100395653B1 (ko) * | 2001-05-29 | 2003-08-21 | 주식회사 이제 | 카르복실 키토산의 제조방법 |
| US6919447B2 (en) | 2001-06-06 | 2005-07-19 | Weyerhaeuser Company | Hypochlorite free method for preparation of stable carboxylated carbohydrate products |
| KR20030000999A (ko) * | 2001-06-28 | 2003-01-06 | 장판식 | 키틴 또는 키토산내에서 1차 알콜기만을 선택적으로산화시키는 키틴 또는 키토산의 연속 산화방법 |
| US6916466B2 (en) | 2001-07-11 | 2005-07-12 | Sca Hygiene Products Ab | Coupling of modified cyclodextrins to fibers |
| EP1329498A1 (en) * | 2002-01-18 | 2003-07-23 | Nederlandse Organisatie voor Toegepast-Natuuurwetenschappelijk Onderzoek TNO | Process for cleaning filters |
| US6789744B2 (en) * | 2002-01-29 | 2004-09-14 | Valeo Electrical Systems, Inc. | Fluid heater with a variable mass flow path |
| US7001483B2 (en) | 2003-08-05 | 2006-02-21 | Weyerhaeuser Company | Apparatus for making carboxylated pulp fibers |
| US7125469B2 (en) * | 2003-10-16 | 2006-10-24 | The Procter & Gamble Company | Temporary wet strength resins |
| CN102276732B (zh) | 2003-11-28 | 2016-01-20 | 伊士曼化工公司 | 纤维素共聚体和氧化方法 |
| US20050121160A1 (en) * | 2003-12-08 | 2005-06-09 | Sca Hygiene Products Ab | Process for the separation of organic nitrosonium and/or hydroxylamine compounds by means of cation exchange resins and recovery and oxidation processes based thereon |
| US20050154206A1 (en) * | 2003-12-08 | 2005-07-14 | Sca Hygiene Products Ab | Process for the recovery of nitroxy compounds from organic solutions and oxidation process |
| US7517675B2 (en) | 2003-12-18 | 2009-04-14 | Cerestar Holding B.V. | Oxidation of carbohydrates by means of peroxidases and nitroxy radicals |
| EP1580228A1 (en) * | 2004-03-24 | 2005-09-28 | Nederlandse Organisatie voor toegepast-natuurwetenschappelijk onderzoek TNO | Process for gelatinising starch using a biodegradable polymer material bearing aldehyde groups |
| GB2417029A (en) | 2004-08-11 | 2006-02-15 | Sca Hygiene Prod Ab | Oxidation of hydroxyl groups using nitrosonium ions |
| JP4929581B2 (ja) * | 2004-11-01 | 2012-05-09 | 凸版印刷株式会社 | 水溶性ポリウロン酸の製造方法 |
| US7923231B2 (en) | 2004-12-17 | 2011-04-12 | Cargill, Incorporated | Production of glucuronic acid using myo-inositol oxygenase from cryptococcus neoformans |
| US7259218B2 (en) * | 2005-02-17 | 2007-08-21 | The Procter + Gamble Company | Processes for making temporary wet strength additives |
| CA2607004C (en) | 2005-05-05 | 2016-01-26 | Sensient Flavors Inc. | Production of beta-glucans and mannans |
| US7932548B2 (en) * | 2006-07-14 | 2011-04-26 | 4D-S Pty Ltd. | Systems and methods for fabricating self-aligned memory cell |
| EP2216345B1 (en) * | 2007-11-26 | 2014-07-02 | The University of Tokyo | Cellulose nanofiber, production method of same and cellulose nanofiber dispersion |
| DE102009002811A1 (de) * | 2009-05-05 | 2010-11-11 | Evonik Degussa Gmbh | Enzymatisches Verfahren zur Herstellung von Aldehyden |
| US8507255B2 (en) * | 2009-11-24 | 2013-08-13 | Foster-Miller, Inc. | Coating system comprising synzyme for degradation of threat agents |
| US9446147B2 (en) * | 2011-02-24 | 2016-09-20 | The Ohio State University | Membrane stabilizing compositions and methods |
| CN103459398B (zh) * | 2011-04-12 | 2016-06-15 | 赢创德固赛有限公司 | 借助含有氮氧自由基的催化剂制造羰基化合物的可连续运行的方法 |
| MX2016011467A (es) * | 2014-03-11 | 2016-11-16 | Du Pont | Poli alfa-1,3-glucano oxidado como mejorador de detergente. |
| KR20210136010A (ko) | 2019-01-31 | 2021-11-16 | 오르가노퓨얼 스웨덴 에이비 | 산화된 목재 생성물을 생산하는 공정 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3632802A (en) * | 1968-12-06 | 1972-01-04 | Univ Southern Illinois | Oxidation of carbohydrates |
| JPS5054684A (enExample) | 1973-09-14 | 1975-05-14 | ||
| FR2545101B1 (fr) * | 1983-04-29 | 1985-08-16 | Agronomique Inst Nat Rech | Procede de modification des pectines de betterave, produits obtenus et leurs applications |
| US4983748A (en) | 1984-08-17 | 1991-01-08 | National Starch And Chemical Investment Holding Corporation | Acetals useful for the preparation of polysaccharide derivatives |
| DE3705785A1 (de) | 1987-02-24 | 1988-09-01 | Basf Ag | Verfahren zur herstellung von polyenaldehyden |
| NL194919C (nl) * | 1993-09-07 | 2003-07-04 | Tno | Werkwijze voor het oxideren van koolhydraten. |
| NL9301905A (nl) * | 1993-11-04 | 1995-06-01 | Inst Voor Agrotech Onderzoek | Werkwijze voor het oxideren van koolhydraten. |
| NL1000495C2 (nl) * | 1995-06-02 | 1996-12-03 | Avebe Coop Verkoop Prod | Geoxideerde polymere koolhydraatethers voor toepassing als sequestreer- middel, alsmede werkwijzen ter bereiding daarvan. |
| EP0935692B1 (en) * | 1996-01-12 | 2002-11-27 | Novozymes A/S | Fabric treated with cellulase and oxidoreductase |
| DE19723629B4 (de) * | 1997-06-05 | 2008-12-11 | Wacker Chemie Ag | Verfahren zum Behandeln von Lignin, ligninhaltigen Materialien oder ähnlichen Stoffen |
| EP0905306A1 (de) * | 1997-09-26 | 1999-03-31 | Consortium für elektrochemische Industrie GmbH | Mehrkomponentensystem zum Verändern, Abbau oder Bleichen von Lignin, ligninhaltigen Materialien sowie Verfahren zu seiner Anwendung |
| FI974139A7 (fi) * | 1997-11-04 | 1999-05-05 | Valtion Teknillinen Tutkimuskeskus | Menetelmä selluloosan modifioimiseksi |
| FI105690B (fi) * | 1997-11-04 | 2000-09-29 | Valtion Teknillinen | Menetelmä hapetetun tärkkelyksen valmistamiseksi |
| KR20010024767A (ko) * | 1997-12-19 | 2001-03-26 | 한센 핀 베네드 | 페놀 산화효소에 의한 다당류의 변형 |
-
2000
- 2000-02-24 CA CA002362717A patent/CA2362717A1/en not_active Abandoned
- 2000-02-24 EP EP00906769A patent/EP1173409B8/en not_active Expired - Lifetime
- 2000-02-24 WO PCT/NL2000/000117 patent/WO2000050621A2/en not_active Ceased
- 2000-02-24 DK DK00906769T patent/DK1173409T3/da active
- 2000-02-24 EP EP00906768A patent/EP1177308A2/en not_active Withdrawn
- 2000-02-24 AU AU28328/00A patent/AU773792B2/en not_active Ceased
- 2000-02-24 AT AT00906769T patent/ATE308514T1/de not_active IP Right Cessation
- 2000-02-24 PL PL00356989A patent/PL356989A1/xx not_active Application Discontinuation
- 2000-02-24 NZ NZ513649A patent/NZ513649A/en not_active IP Right Cessation
- 2000-02-24 WO PCT/NL2000/000118 patent/WO2000050388A1/en not_active Ceased
- 2000-02-24 AU AU28329/00A patent/AU773835B2/en not_active Ceased
- 2000-02-24 HU HU0105299A patent/HUP0105299A3/hu unknown
- 2000-02-24 ES ES00906769T patent/ES2255979T3/es not_active Expired - Lifetime
- 2000-02-24 US US09/913,603 patent/US6875861B1/en not_active Expired - Fee Related
- 2000-02-24 KR KR1020017010752A patent/KR20010102361A/ko not_active Withdrawn
- 2000-02-24 JP JP2000600972A patent/JP2002537374A/ja active Pending
- 2000-02-24 JP JP2000601184A patent/JP2004512805A/ja active Pending
- 2000-02-24 BR BR0008474-3A patent/BR0008474A/pt not_active IP Right Cessation
- 2000-02-24 BR BR0008478-6A patent/BR0008478A/pt not_active IP Right Cessation
- 2000-02-24 DE DE60023680T patent/DE60023680T2/de not_active Expired - Lifetime
- 2000-02-24 US US09/914,182 patent/US6831173B1/en not_active Expired - Fee Related
- 2000-02-24 CZ CZ20013042A patent/CZ20013042A3/cs unknown
- 2000-02-24 RU RU2001125922/13A patent/RU2001125922A/ru unknown
- 2000-02-24 HU HU0200203A patent/HUP0200203A2/hu unknown
- 2000-02-24 MX MXPA01008603A patent/MXPA01008603A/es not_active Application Discontinuation
- 2000-02-24 PL PL00350567A patent/PL350567A1/xx not_active Application Discontinuation
-
2001
- 2001-08-15 ZA ZA200106737A patent/ZA200106737B/xx unknown
- 2001-08-20 ZA ZA200106850A patent/ZA200106850B/xx unknown
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