JP2006514973A5 - - Google Patents
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- JP2006514973A5 JP2006514973A5 JP2004570084A JP2004570084A JP2006514973A5 JP 2006514973 A5 JP2006514973 A5 JP 2006514973A5 JP 2004570084 A JP2004570084 A JP 2004570084A JP 2004570084 A JP2004570084 A JP 2004570084A JP 2006514973 A5 JP2006514973 A5 JP 2006514973A5
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- Prior art keywords
- acid
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- 239000000178 monomer Substances 0.000 claims 6
- 239000000243 solution Substances 0.000 claims 5
- 239000002253 acid Substances 0.000 claims 4
- 239000011541 reaction mixture Substances 0.000 claims 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 3
- 239000002904 solvent Substances 0.000 claims 3
- BJHIKXHVCXFQLS-UYFOZJQFSA-N Fructose Chemical group OC[C@@H](O)[C@@H](O)[C@H](O)C(=O)CO BJHIKXHVCXFQLS-UYFOZJQFSA-N 0.000 claims 2
- BTCSSZJGUNDROE-UHFFFAOYSA-N GABA Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 claims 2
- GUBGYTABKSRVRQ-YOLKTULGSA-N Maltose Natural products O([C@@H]1[C@H](O)[C@@H](O)[C@H](O)O[C@H]1CO)[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 GUBGYTABKSRVRQ-YOLKTULGSA-N 0.000 claims 2
- SRBFZHDQGSBBOR-SQOUGZDYSA-N Xylose Natural products O[C@@H]1CO[C@@H](O)[C@@H](O)[C@@H]1O SRBFZHDQGSBBOR-SQOUGZDYSA-N 0.000 claims 2
- 229960003692 aminobutyric acid Drugs 0.000 claims 2
- 230000027455 binding Effects 0.000 claims 2
- 150000001720 carbohydrates Chemical class 0.000 claims 2
- 239000007822 coupling agent Substances 0.000 claims 2
- 239000003446 ligand Substances 0.000 claims 2
- 229940000687 6-Aminocaproic Acid Drugs 0.000 claims 1
- SLXKOJJOQWFEFD-UHFFFAOYSA-N Aminocaproic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 claims 1
- 229920000856 Amylose Polymers 0.000 claims 1
- GZCGUPFRVQAUEE-KCDKBNATSA-N D-(+)-Galactose Chemical group OC[C@@H](O)[C@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-KCDKBNATSA-N 0.000 claims 1
- GUBGYTABKSRVRQ-CUHNMECISA-N D-Cellobiose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-CUHNMECISA-N 0.000 claims 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical group OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 claims 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N D-sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims 1
- ASJSAQIRZKANQN-CRCLSJGQSA-N Deoxyribose Chemical compound OC[C@@H](O)[C@@H](O)CC=O ASJSAQIRZKANQN-CRCLSJGQSA-N 0.000 claims 1
- YTBSYETUWUMLBZ-IUYQGCFVSA-N Erythrose Chemical compound OC[C@@H](O)[C@@H](O)C=O YTBSYETUWUMLBZ-IUYQGCFVSA-N 0.000 claims 1
- 206010056474 Erythrosis Diseases 0.000 claims 1
- 239000005715 Fructose Chemical group 0.000 claims 1
- MSWZFWKMSRAUBD-GASJEMHNSA-N Galactosamine Chemical compound N[C@H]1C(O)O[C@H](CO)[C@H](O)[C@@H]1O MSWZFWKMSRAUBD-GASJEMHNSA-N 0.000 claims 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims 1
- DLRVVLDZNNYCBX-RTPHMHGBSA-N Isomaltose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)C(O)O1 DLRVVLDZNNYCBX-RTPHMHGBSA-N 0.000 claims 1
- AYRXSINWFIIFAE-SCLMCMATSA-N Isomaltose Natural products OC[C@H]1O[C@H](OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O)[C@@H](O)[C@@H](O)[C@@H]1O AYRXSINWFIIFAE-SCLMCMATSA-N 0.000 claims 1
- GUBGYTABKSRVRQ-UUNJERMWSA-N Lactose Natural products O([C@@H]1[C@H](O)[C@H](O)[C@H](O)O[C@@H]1CO)[C@H]1[C@@H](O)[C@@H](O)[C@H](O)[C@H](CO)O1 GUBGYTABKSRVRQ-UUNJERMWSA-N 0.000 claims 1
- JCQLYHFGKNRPGE-FCVZTGTOSA-N Lactulose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 JCQLYHFGKNRPGE-FCVZTGTOSA-N 0.000 claims 1
- OVRNDRQMDRJTHS-FMDGEEDCSA-N N-Acetylglucosamine Chemical group CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O OVRNDRQMDRJTHS-FMDGEEDCSA-N 0.000 claims 1
- 229950006780 N-Acetylglucosamine Drugs 0.000 claims 1
- BJHIKXHVCXFQLS-PUFIMZNGSA-N Psicose Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)C(=O)CO BJHIKXHVCXFQLS-PUFIMZNGSA-N 0.000 claims 1
- ZAQJHHRNXZUBTE-NQXXGFSBSA-N Ribulose Chemical compound OC[C@@H](O)[C@@H](O)C(=O)CO ZAQJHHRNXZUBTE-NQXXGFSBSA-N 0.000 claims 1
- CZMRCDWAGMRECN-GDQSFJPYSA-N Sucrose Natural products O([C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](CO)O1)[C@@]1(CO)[C@H](O)[C@@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-GDQSFJPYSA-N 0.000 claims 1
- 229960003487 Xylose Drugs 0.000 claims 1
- 229960002684 aminocaproic acid Drugs 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 claims 1
- 239000001913 cellulose Substances 0.000 claims 1
- 229920002678 cellulose Polymers 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 238000001035 drying Methods 0.000 claims 1
- BJHIKXHVCXFQLS-PYWDMBMJSA-N keto-D-sorbose Chemical compound OC[C@@H](O)[C@H](O)[C@@H](O)C(=O)CO BJHIKXHVCXFQLS-PYWDMBMJSA-N 0.000 claims 1
- 239000008101 lactose Substances 0.000 claims 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N lactose Chemical compound 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](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 claims 1
- SQVRNKJHWKZAKO-OQPLDHBCSA-N sialic acid Chemical group CC(=O)N[C@@H]1[C@@H](O)C[C@@](O)(C(O)=O)OC1[C@H](O)[C@H](O)CO SQVRNKJHWKZAKO-OQPLDHBCSA-N 0.000 claims 1
- 238000000638 solvent extraction Methods 0.000 claims 1
- 239000005720 sucrose Substances 0.000 claims 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N α-D-galactose Chemical group OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 claims 1
- LKDRXBCSQODPBY-DPYQTVNSSA-N β-D-tagatopyranose Chemical compound OC[C@@]1(O)OC[C@@H](O)[C@H](O)[C@@H]1O LKDRXBCSQODPBY-DPYQTVNSSA-N 0.000 claims 1
Claims (1)
- 式1：
の重合性モノマーを調製するための方法であって、
当該方法は、重合性モノマー酸塩化物をアルカリの溶液中に溶かし、スペーサーの水性溶液を別個に調製し、当該重合性モノマー酸塩化物の溶液を当該スペーサーの溶液に対して滴下して加えて混合物を獲得し、未反応のモノマー酸塩化物を溶媒抽出によって除去し、当該反応混合物を酸性化し、そして当該反応混合物を溶媒抽出し、非溶媒を使用することで当該抽出物を沈殿させてモノマー−スペーサー結合体を獲得し、そして当該モノマースペーサー結合体を真空下で乾燥させ、そして当該結合体を有機溶媒中に溶かし、この溶液に対して炭水化物リガンドを添加して反応混合物を獲得し、この反応混合物に対してカップリング剤を添加し、当該反応を生じさせて、未反応のカップリング剤を除去し、透明な溶液を溶媒により処理し重合性モノマーを獲得することを含んで成る方法。
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/IN2003/000115 WO2004087725A1 (en) | 2003-03-31 | 2003-03-31 | Polymerizable monomers and process of preparation thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006514973A JP2006514973A (ja) | 2006-05-18 |
| JP2006514973A5 true JP2006514973A5 (ja) | 2006-06-29 |
Family
ID=33104964
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004570084A Pending JP2006514973A (ja) | 2003-03-31 | 2003-03-31 | 重合性モノマー及びそれらの調製する方法 |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP1615940A1 (ja) |
| JP (1) | JP2006514973A (ja) |
| CN (1) | CN1823080A (ja) |
| AU (1) | AU2003226635A1 (ja) |
| WO (1) | WO2004087725A1 (ja) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101812490B (zh) * | 2009-02-20 | 2013-09-11 | 元智大学 | 一种微生物生产葡萄糖胺的方法 |
| CN102002077B (zh) * | 2010-01-26 | 2014-08-27 | 深圳伯美生物医药有限公司 | 一种唾液酸-蛋氨酸锌新型偶联物、制备工艺及其应用 |
| CN107602634A (zh) * | 2017-09-19 | 2018-01-19 | 佛山科学技术学院 | 一种三糖的合成方法 |
| CN111333158B (zh) * | 2020-03-12 | 2023-04-07 | 江苏美淼环保科技有限公司 | 抑菌型abs异相离子交换膜及其制备方法和应用 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU5874794A (en) * | 1992-12-21 | 1994-07-19 | University Of Iowa Research Foundation, The | Sugar-based polymers |
| EP0668294B1 (de) * | 1994-02-15 | 1999-08-18 | Novartis AG | Ungesättigte Kohlenhydratderivate, Polymere davon und deren Verwendung |
| US5891862A (en) * | 1996-03-15 | 1999-04-06 | Geltex Pharmaceuticals, Inc. | Polyvalent polymers for the treatment of rotavirus infection |
| DE19854186A1 (de) * | 1998-11-24 | 2000-05-25 | Wacker Chemie Gmbh | Grenzflächenaktive Organosiliciumverbindungen |
-
2003
- 2003-03-31 EP EP03816519A patent/EP1615940A1/en not_active Withdrawn
- 2003-03-31 AU AU2003226635A patent/AU2003226635A1/en not_active Abandoned
- 2003-03-31 CN CN03826558.3A patent/CN1823080A/zh active Pending
- 2003-03-31 JP JP2004570084A patent/JP2006514973A/ja active Pending
- 2003-03-31 WO PCT/IN2003/000115 patent/WO2004087725A1/en active Application Filing
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