JP2004512805A - １級アルコールの選択的酸化方法と新規な炭水化物アルデヒド - Google Patents
１級アルコールの選択的酸化方法と新規な炭水化物アルデヒド Download PDFInfo
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- JP2004512805A JP2004512805A JP2000601184A JP2000601184A JP2004512805A JP 2004512805 A JP2004512805 A JP 2004512805A JP 2000601184 A JP2000601184 A JP 2000601184A JP 2000601184 A JP2000601184 A JP 2000601184A JP 2004512805 A JP2004512805 A JP 2004512805A
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- 125000005842 heteroatom Chemical group 0.000 description 1
- WQZGKKKJIJFFOK-UHFFFAOYSA-N hexopyranose Chemical group OCC1OC(O)C(O)C(O)C1O WQZGKKKJIJFFOK-UHFFFAOYSA-N 0.000 description 1
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 229940050526 hydroxyethylstarch Drugs 0.000 description 1
- WCYJQVALWQMJGE-UHFFFAOYSA-M hydroxylammonium chloride Chemical compound [Cl-].O[NH3+] WCYJQVALWQMJGE-UHFFFAOYSA-M 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 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
- 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
- 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
- 230000001404 mediated effect Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 230000003278 mimic effect Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- GUQPPNZGDSQJGT-UHFFFAOYSA-N octadecane-1,9-diol Chemical compound CCCCCCCCCC(O)CCCCCCCCO GUQPPNZGDSQJGT-UHFFFAOYSA-N 0.000 description 1
- GDUWKVCUIFEAGC-UHFFFAOYSA-N octane-1,6-diol Chemical compound CCC(O)CCCCCO GDUWKVCUIFEAGC-UHFFFAOYSA-N 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- UKODFQOELJFMII-UHFFFAOYSA-N pentamethyldiethylenetriamine Chemical compound CN(C)CCN(C)CCN(C)C UKODFQOELJFMII-UHFFFAOYSA-N 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000003444 phase transfer catalyst Substances 0.000 description 1
- 229920000768 polyamine Polymers 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
- 238000006268 reductive amination reaction Methods 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000003270 steroid hormone Substances 0.000 description 1
- 150000003431 steroids Chemical class 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical class [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 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
- 239000002023 wood 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)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (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)
- Compounds Of Unknown Constitution (AREA)
- Steroid Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP99200536 | 1999-02-24 | ||
| PCT/NL2000/000117 WO2000050621A2 (en) | 1999-02-24 | 2000-02-24 | Process for producing nitrosoniom ions from a nitroxyl compound, their application in the selective oxidation of primary alcohols, and novel carbohydrate aldehydes |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2004512805A true JP2004512805A (ja) | 2004-04-30 |
| JP2004512805A5 JP2004512805A5 (enExample) | 2005-01-20 |
Family
ID=8239920
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000601184A Pending JP2004512805A (ja) | 1999-02-24 | 2000-02-24 | １級アルコールの選択的酸化方法と新規な炭水化物アルデヒド |
| JP2000600972A Pending JP2002537374A (ja) | 1999-02-24 | 2000-02-24 | ニトロソニウムイオンを生成する方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000600972A Pending JP2002537374A (ja) | 1999-02-24 | 2000-02-24 | ニトロソニウムイオンを生成する方法 |
Country Status (19)
| Country | Link |
|---|---|
| US (2) | US6875861B1 (enExample) |
| EP (2) | EP1173409B8 (enExample) |
| JP (2) | JP2004512805A (enExample) |
| KR (1) | KR20010102361A (enExample) |
| AT (1) | ATE308514T1 (enExample) |
| AU (2) | AU773835B2 (enExample) |
| BR (2) | BR0008478A (enExample) |
| CA (1) | CA2362717A1 (enExample) |
| CZ (1) | CZ20013042A3 (enExample) |
| DE (1) | DE60023680T2 (enExample) |
| DK (1) | DK1173409T3 (enExample) |
| ES (1) | ES2255979T3 (enExample) |
| HU (2) | HUP0200203A2 (enExample) |
| MX (1) | MXPA01008603A (enExample) |
| NZ (1) | NZ513649A (enExample) |
| PL (2) | PL350567A1 (enExample) |
| RU (1) | RU2001125922A (enExample) |
| WO (2) | WO2000050388A1 (enExample) |
| ZA (2) | ZA200106737B (enExample) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE69713876T2 (de) | 1996-03-28 | 2003-02-13 | The Procter & Gamble Company, Cincinnati | Nassfestigkeit aufweisende papierprodukte aus aldehyd-funtionalisierten zellulosefasern und polymeren |
| 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 |
| MXPA00007979A (es) * | 1999-08-17 | 2002-03-08 | Nat Starch Chem Invest | Aldehidos de polisacaridos preparados por un metodo de oxidacion y usados como aditivos de resistencia en la fabricacion de papel. |
| 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 |
| 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 |
| 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 |
| 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 |
| JP5122821B2 (ja) | 2003-11-28 | 2013-01-16 | イーストマン ケミカル カンパニー | セルロースインターポリマー及び酸化方法 |
| 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 |
| WO2005059152A1 (en) * | 2003-12-18 | 2005-06-30 | 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 |
| WO2006121803A1 (en) | 2005-05-05 | 2006-11-16 | 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 |
| US8992728B2 (en) * | 2007-11-26 | 2015-03-31 | 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 |
| US8507256B2 (en) * | 2009-11-24 | 2013-08-13 | Foster-Miller, Inc. | Sorption reinforced catalytic coating system and method for the degradation of threat agents |
| US9446147B2 (en) * | 2011-02-24 | 2016-09-20 | The Ohio State University | Membrane stabilizing compositions and methods |
| CA2832624A1 (en) * | 2011-04-12 | 2012-10-18 | Evonik Degussa Gmbh | Continuously operable method for producing carbonyl compounds by means of a catalyst containing a nitroxyl radical |
| ES2734726T3 (es) * | 2014-03-11 | 2019-12-11 | Du Pont | Poli alfa-1,2-glucano oxidado como reforzante de detergente |
| BR112021014931A2 (pt) | 2019-01-31 | 2021-09-28 | Organofuel Sweden Ab | Processo para a produção de produtos de madeira oxidada |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3632802A (en) * | 1968-12-06 | 1972-01-04 | Univ Southern Illinois | Oxidation of carbohydrates |
| WO1995007303A1 (en) * | 1993-09-07 | 1995-03-16 | Nederlandse Organisatie Voor Toegepast-Natuurwetenschappelijk Onderzoek Tno | Method for oxidising carbohydrates |
| WO1996038484A1 (en) * | 1995-06-02 | 1996-12-05 | Coöperatieve Verkoop- En Productievereniging Van Aardappelmeel En Derivaten Avebe B.A. | Oxidized polymeric carbohydrate ethers for use as sequestering agent, and methods for the preparation thereof |
| WO1998055684A1 (de) * | 1997-06-05 | 1998-12-10 | Consortium für elektrochemische Industrie GmbH | Mehrkomponentensystem zum verändern, abbau oder bleichen von lignin, ligninhaltigen materialien oder ähnlichen stoffen sowie verfahren zu seiner anwendung |
| WO1999023117A1 (en) * | 1997-11-04 | 1999-05-14 | Valtion Teknillinen Tutkimuskeskus | Method for modification of cellulose |
| WO1999023240A1 (en) * | 1997-11-04 | 1999-05-14 | Valtion Teknillinen Tutkimuskeskus | Method of producing oxidized starch |
| JPH11158790A (ja) * | 1997-09-26 | 1999-06-15 | Consortium Elektrochem Ind Gmbh | リグニン、リグニン含有材料又は類似材料を変化させ、分解し又は漂白するための多成分系及びリグニン含有材料の脱リグニン化方法 |
| JP2000503075A (ja) * | 1996-01-12 | 2000-03-14 | ノボ ノルディスク アクティーゼルスカブ | セルラーゼ及びオキシドレダクターゼで処理した布帛 |
| JP2003521220A (ja) * | 1997-12-19 | 2003-07-15 | ノボ ノルディスク アクティーゼルスカブ | フェノール酸化酵素による多糖類の改良 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| NL9301905A (nl) * | 1993-11-04 | 1995-06-01 | Inst Voor Agrotech Onderzoek | Werkwijze voor het oxideren van koolhydraten. |
-
2000
- 2000-02-24 US US09/913,603 patent/US6875861B1/en not_active Expired - Fee Related
- 2000-02-24 AU AU28329/00A patent/AU773835B2/en not_active Ceased
- 2000-02-24 WO PCT/NL2000/000118 patent/WO2000050388A1/en not_active Ceased
- 2000-02-24 MX MXPA01008603A patent/MXPA01008603A/es not_active Application Discontinuation
- 2000-02-24 HU HU0200203A patent/HUP0200203A2/hu unknown
- 2000-02-24 JP JP2000601184A patent/JP2004512805A/ja active Pending
- 2000-02-24 PL PL00350567A patent/PL350567A1/xx not_active Application Discontinuation
- 2000-02-24 CA CA002362717A patent/CA2362717A1/en not_active Abandoned
- 2000-02-24 KR KR1020017010752A patent/KR20010102361A/ko not_active Withdrawn
- 2000-02-24 NZ NZ513649A patent/NZ513649A/en not_active IP Right Cessation
- 2000-02-24 PL PL00356989A patent/PL356989A1/xx not_active Application Discontinuation
- 2000-02-24 ES ES00906769T patent/ES2255979T3/es not_active Expired - Lifetime
- 2000-02-24 BR BR0008478-6A patent/BR0008478A/pt not_active IP Right Cessation
- 2000-02-24 EP EP00906769A patent/EP1173409B8/en not_active Expired - Lifetime
- 2000-02-24 EP EP00906768A patent/EP1177308A2/en not_active Withdrawn
- 2000-02-24 HU HU0105299A patent/HUP0105299A3/hu unknown
- 2000-02-24 JP JP2000600972A patent/JP2002537374A/ja active Pending
- 2000-02-24 RU RU2001125922/13A patent/RU2001125922A/ru unknown
- 2000-02-24 CZ CZ20013042A patent/CZ20013042A3/cs unknown
- 2000-02-24 US US09/914,182 patent/US6831173B1/en not_active Expired - Fee Related
- 2000-02-24 AU AU28328/00A patent/AU773792B2/en not_active Ceased
- 2000-02-24 DE DE60023680T patent/DE60023680T2/de not_active Expired - Lifetime
- 2000-02-24 AT AT00906769T patent/ATE308514T1/de not_active IP Right Cessation
- 2000-02-24 DK DK00906769T patent/DK1173409T3/da active
- 2000-02-24 WO PCT/NL2000/000117 patent/WO2000050621A2/en not_active Ceased
- 2000-02-24 BR BR0008474-3A patent/BR0008474A/pt not_active IP Right Cessation
-
2001
- 2001-08-15 ZA ZA200106737A patent/ZA200106737B/xx unknown
- 2001-08-20 ZA ZA200106850A patent/ZA200106850B/xx unknown
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| US3632802A (en) * | 1968-12-06 | 1972-01-04 | Univ Southern Illinois | Oxidation of carbohydrates |
| WO1995007303A1 (en) * | 1993-09-07 | 1995-03-16 | Nederlandse Organisatie Voor Toegepast-Natuurwetenschappelijk Onderzoek Tno | Method for oxidising carbohydrates |
| WO1996038484A1 (en) * | 1995-06-02 | 1996-12-05 | Coöperatieve Verkoop- En Productievereniging Van Aardappelmeel En Derivaten Avebe B.A. | Oxidized polymeric carbohydrate ethers for use as sequestering agent, and methods for the preparation thereof |
| JP2000503075A (ja) * | 1996-01-12 | 2000-03-14 | ノボ ノルディスク アクティーゼルスカブ | セルラーゼ及びオキシドレダクターゼで処理した布帛 |
| WO1998055684A1 (de) * | 1997-06-05 | 1998-12-10 | Consortium für elektrochemische Industrie GmbH | Mehrkomponentensystem zum verändern, abbau oder bleichen von lignin, ligninhaltigen materialien oder ähnlichen stoffen sowie verfahren zu seiner anwendung |
| JPH11158790A (ja) * | 1997-09-26 | 1999-06-15 | Consortium Elektrochem Ind Gmbh | リグニン、リグニン含有材料又は類似材料を変化させ、分解し又は漂白するための多成分系及びリグニン含有材料の脱リグニン化方法 |
| WO1999023117A1 (en) * | 1997-11-04 | 1999-05-14 | Valtion Teknillinen Tutkimuskeskus | Method for modification of cellulose |
| WO1999023240A1 (en) * | 1997-11-04 | 1999-05-14 | Valtion Teknillinen Tutkimuskeskus | Method of producing oxidized starch |
| JP2003521220A (ja) * | 1997-12-19 | 2003-07-15 | ノボ ノルディスク アクティーゼルスカブ | フェノール酸化酵素による多糖類の改良 |
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