JP2005501798A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2005501798A5 JP2005501798A5 JP2002555763A JP2002555763A JP2005501798A5 JP 2005501798 A5 JP2005501798 A5 JP 2005501798A5 JP 2002555763 A JP2002555763 A JP 2002555763A JP 2002555763 A JP2002555763 A JP 2002555763A JP 2005501798 A5 JP2005501798 A5 JP 2005501798A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- support
- integer selected
- subscript
- activator
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000012190 activator Substances 0.000 claims description 24
- 239000004793 Polystyrene Substances 0.000 claims description 14
- 125000005647 linker group Chemical group 0.000 claims description 12
- 239000000126 substance Substances 0.000 claims description 11
- 239000007787 solid Substances 0.000 claims description 10
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 9
- 125000003118 aryl group Chemical group 0.000 claims description 8
- 239000012038 nucleophile Substances 0.000 claims description 8
- 229920002223 polystyrene Polymers 0.000 claims description 8
- -1 polypropylene Polymers 0.000 claims description 7
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 claims description 7
- HBAHZZVIEFRTEY-UHFFFAOYSA-N 2-heptylcyclohex-2-en-1-one Chemical compound CCCCCCCC1=CCCCC1=O HBAHZZVIEFRTEY-UHFFFAOYSA-N 0.000 claims description 6
- 229920001367 Merrifield resin Polymers 0.000 claims description 6
- 230000002708 enhancing effect Effects 0.000 claims description 6
- 229920005990 polystyrene resin Polymers 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 125000003282 alkyl amino group Chemical group 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 2
- 125000004414 alkyl thio group Chemical group 0.000 claims description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000003153 chemical reaction reagent Substances 0.000 claims 9
- 238000000034 method Methods 0.000 claims 7
- 150000001875 compounds Chemical class 0.000 claims 3
- 229920001223 polyethylene glycol Polymers 0.000 claims 3
- 239000002202 Polyethylene glycol Substances 0.000 claims 2
- 150000001412 amines Chemical class 0.000 claims 2
- 150000001450 anions Chemical class 0.000 claims 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical class COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
- 239000005749 Copper compound Substances 0.000 claims 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical class O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 claims 1
- 239000004743 Polypropylene Substances 0.000 claims 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims 1
- 150000001639 boron compounds Chemical class 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 229920002678 cellulose Polymers 0.000 claims 1
- 239000001913 cellulose Substances 0.000 claims 1
- 239000005289 controlled pore glass Substances 0.000 claims 1
- 150000001880 copper compounds Chemical class 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 150000004795 grignard reagents Chemical class 0.000 claims 1
- 150000004678 hydrides Chemical class 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 150000002576 ketones Chemical class 0.000 claims 1
- 150000002642 lithium compounds Chemical class 0.000 claims 1
- 229910001510 metal chloride Inorganic materials 0.000 claims 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 claims 1
- 229920002401 polyacrylamide Polymers 0.000 claims 1
- 229920001155 polypropylene Polymers 0.000 claims 1
- 230000004224 protection Effects 0.000 claims 1
- 239000000741 silica gel Substances 0.000 claims 1
- 229910002027 silica gel Inorganic materials 0.000 claims 1
- 150000003377 silicon compounds Chemical class 0.000 claims 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
- 150000003573 thiols Chemical class 0.000 claims 1
- 150000003752 zinc compounds Chemical class 0.000 claims 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 15
- 239000000178 monomer Substances 0.000 description 9
- 230000003213 activating effect Effects 0.000 description 3
- 230000004913 activation Effects 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 150000001413 amino acids Chemical class 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 150000004985 diamines Chemical class 0.000 description 3
- 102000004196 processed proteins & peptides Human genes 0.000 description 3
- 108090000765 processed proteins & peptides Proteins 0.000 description 3
- 230000009257 reactivity Effects 0.000 description 3
- 230000008685 targeting Effects 0.000 description 2
- 125000004663 dialkyl amino group Chemical group 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26152501P | 2001-01-12 | 2001-01-12 | |
| PCT/US2002/000839 WO2002055026A2 (en) | 2001-01-12 | 2002-01-11 | Perfluoro sulfonyl halides and related species as polymer support modifiers |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005501798A JP2005501798A (ja) | 2005-01-20 |
| JP2005501798A5 true JP2005501798A5 (cg-RX-API-DMAC10.html) | 2005-05-26 |
| JP4349559B2 JP4349559B2 (ja) | 2009-10-21 |
Family
ID=22993697
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002555763A Expired - Fee Related JP4349559B2 (ja) | 2001-01-12 | 2002-01-11 | ポリマー支持体変性剤としてのハロゲン化パーフルオロスルホニルおよび関連する化学種 |
Country Status (15)
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1491888B1 (en) * | 2002-04-03 | 2008-09-17 | Mitsubishi Rayon Co., Ltd. | Microarray comprising gel having biosubstance fixed thereto as well as manufacture and use thereof |
| GB0317920D0 (en) | 2003-07-31 | 2003-09-03 | Amersham Plc | Solid-phase synthesis |
| RU2380685C1 (ru) * | 2008-11-07 | 2010-01-27 | Шлюмберже Текнолоджи Б.В. | Эталонный материал с порами контролируемого размера и формы и блок из фрагментов эталонного материала с порами контролируемого размера и формы |
| WO2012018709A2 (en) * | 2010-08-06 | 2012-02-09 | Arkema Inc. | Superacid functional compounds |
| EP3142709B1 (en) * | 2014-05-15 | 2025-07-30 | Mayo Foundation for Medical Education and Research | Synthesis sytem comprising a solution target for cyclotron production of radiometals and associated method |
| JP6912576B2 (ja) * | 2016-12-30 | 2021-08-04 | ダウ グローバル テクノロジーズ エルエルシー | 促進剤および酸化防止剤を含む樹脂 |
| CN116445941A (zh) * | 2023-04-28 | 2023-07-18 | 湖南法恩莱特新能源科技有限公司 | 含氟磺酸酯的制备方法及其电解液和电化学装置 |
| CN116554386B (zh) * | 2023-07-07 | 2023-09-29 | 国家电投集团氢能科技发展有限公司 | 全氟磺酰氟树脂的酯化方法和全氟磺酸树脂的制备方法 |
| CN120329653B (zh) * | 2025-05-19 | 2025-11-25 | 揭阳市恭发塑胶有限公司 | 一种安全抗菌pp材料及制备方法 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3028534A (en) * | 1960-03-02 | 1962-04-03 | Bendix Corp | Variably damped servo-control system |
| US4348310A (en) * | 1979-09-26 | 1982-09-07 | E. I. Du Pont De Nemours And Company | Solutions of sulfonyl fluoride compounds and fluoropolymers |
| US4414146A (en) * | 1982-05-05 | 1983-11-08 | Union Camp Corporation | Method of polymerizing rosin |
| US4522995A (en) * | 1983-05-02 | 1985-06-11 | E. I. Du Pont De Nemours And Company | Fluorinated alkyl ether-containing ethylenes, precursors thereto, and copolymers thereof with tetrafluoroethylene |
| US5235028A (en) * | 1990-08-31 | 1993-08-10 | University Of Minnesota | Polyethylene glycol derivatives for solid-phase applications |
| US5624711A (en) * | 1995-04-27 | 1997-04-29 | Affymax Technologies, N.V. | Derivatization of solid supports and methods for oligomer synthesis |
| DE69727374T2 (de) * | 1996-05-20 | 2004-11-11 | Smithkline Beecham Corp. | Silyl-linker für die organische synthese in fester phase von arylgruppen enthaltenden molekülen |
| DE19626762A1 (de) * | 1996-07-03 | 1998-01-08 | Basf Ag | Enzymatisch spaltbare Linker für Festphasensynthesen |
| US6392010B1 (en) * | 1996-12-19 | 2002-05-21 | Aventis Pharmaceuticals Inc. | Process for the solid phase synthesis of aldehyde, ketone, oxime, amine, hydroxamic acid and αβ-unsaturated carboxylic acid and aldehyde compounds |
| AUPO440596A0 (en) * | 1996-12-30 | 1997-01-23 | Fujisawa Pharmaceutical Co., Ltd. | New compound |
| US6191231B1 (en) * | 1997-01-22 | 2001-02-20 | E. I. Du Pont De Nemours And Company | Grafting of polymers with fluorocarbon compounds |
| WO1998044329A2 (en) | 1997-03-28 | 1998-10-08 | Smithkline Beecham Corporation | Rink-chloride linker for solid phase organic synthesis of organic molecules |
| GB9716454D0 (en) * | 1997-08-05 | 1997-10-08 | Univ St Andrews | Polymer |
| US20030108944A1 (en) * | 1997-10-09 | 2003-06-12 | Klaus Haaf | Combinatorial preparations of phosphorus-containing active compounds and intermediates by solid phase synthesis |
-
2002
- 2002-01-11 MX MXPA03006228A patent/MXPA03006228A/es not_active Application Discontinuation
- 2002-01-11 US US10/044,784 patent/US20030124612A1/en not_active Abandoned
- 2002-01-11 KR KR10-2003-7009277A patent/KR20030078069A/ko not_active Ceased
- 2002-01-11 RU RU2003121311/04A patent/RU2291146C2/ru not_active IP Right Cessation
- 2002-01-11 EP EP02714736A patent/EP1352243A4/en not_active Withdrawn
- 2002-01-11 CA CA002434570A patent/CA2434570A1/en not_active Abandoned
- 2002-01-11 AU AU2002246986A patent/AU2002246986B2/en not_active Ceased
- 2002-01-11 CN CNB02806352XA patent/CN100480701C/zh not_active Expired - Fee Related
- 2002-01-11 HU HU0303192A patent/HUP0303192A2/hu unknown
- 2002-01-11 WO PCT/US2002/000839 patent/WO2002055026A2/en not_active Ceased
- 2002-01-11 JP JP2002555763A patent/JP4349559B2/ja not_active Expired - Fee Related
- 2002-01-11 CZ CZ20031921A patent/CZ20031921A3/cs unknown
- 2002-01-11 BR BR0206386-7A patent/BR0206386A/pt not_active IP Right Cessation
- 2002-01-11 IL IL15667702A patent/IL156677A0/xx unknown
- 2002-01-11 US US10/466,124 patent/US7700524B2/en not_active Expired - Fee Related
-
2003
- 2003-06-30 ZA ZA2003/05099A patent/ZA200305099B/en unknown
-
2010
- 2010-04-15 US US12/760,840 patent/US20110028751A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US6482912B2 (en) | Method of preparing aminofunctional alkoxy polysiloxanes | |
| RU2226535C2 (ru) | Компоненты катализаторов полимеризации олефинов | |
| JP2005501040A5 (cg-RX-API-DMAC10.html) | ||
| RU2538209C1 (ru) | Соединение, представляющее собой простой полиэфир, отверждающее средство, использующее соединение, представляющее собой простой полиэфир, и способ получения соединения, представляющего собой простой полиэфир | |
| US11041068B2 (en) | Solid support | |
| KR20130112721A (ko) | 분지형 헤테로―폴리에틸렌 글리콜 및 중간체 | |
| CN110511973A (zh) | 一种用于核酸原位合成的固相载体及其制备方法 | |
| KR20150102862A (ko) | 실세스퀴옥산 복합 고분자 및 이의 제조방법 | |
| JP6784932B2 (ja) | 生体機能性分子または薬物キャリアの化学修飾用生分解性ポリエチレングリコール誘導体 | |
| KR20150102860A (ko) | 실세스퀴옥산 복합 고분자 및 이의 제조방법 | |
| CN102168146A (zh) | 高特异性高灵敏度的基因芯片及其制备方法与应用 | |
| CN102757562B (zh) | 氨烷基封端的聚有机硅氧烷的制备方法 | |
| KR20150102861A (ko) | 실세스퀴옥산 복합 고분자 및 이의 제조방법 | |
| RU2003121311A (ru) | Перфторированные сульфонилгалогениды и аналогичные им соединения как модификаторы полимерных подложек | |
| JP6894747B2 (ja) | 重合体 | |
| AR032649A1 (es) | Compuesto apropiado como catalizador para la obtencion de un sistema catalitico, procedimientos para su obtencion y para la carbonilacion de compuestos olefinicamente insaturados | |
| JP2009516008A5 (cg-RX-API-DMAC10.html) | ||
| JP2009510221A5 (cg-RX-API-DMAC10.html) | ||
| ES2363122T3 (es) | Método para modificar un sistema macromolecular. | |
| US20060063147A1 (en) | Omega-amino-PEG-phosphoramidites and conjugates thereof | |
| JP4436057B2 (ja) | 含窒素有機珪素化合物、その製造方法およびシランカップリング剤 | |
| Ready et al. | Facile and Effective Synthesis of Siloxane‐Based Polyamines | |
| EP2104689B1 (en) | Polymeric substrates with fluoroalkoxycarbonyl groups for amine capture | |
| WO2009019901A1 (ja) | 任意の化合物が導入された新規核酸誘導体、及びその製造方法 | |
| JP6801152B2 (ja) | アミノアルキル及び不飽和末端を有する二官能性ポリ（アルキレンオキシド）並びにその誘導体 |