📜芥菜砜置于sodium Hydroxide,乙醇体系中,化学反应生成2,2'-磺酰基双乙醇 参考文献:Cashmore,Journal Of The Chemical Society,1923,Vol. 123,P. 1740 标题:Cashmore,Journal Of The Chemical Society,1923,Vol. 123,P. 1740
专利号:US-5278266-A 优先权日:1991-02-06 标 题 :Synthesis of poly(vinyl phosphonic acid) 发明人:BRAYBROOK JULIAN H; ELLIS JOHN 权利人:BRITISH TECH GROUP 摘要:Poly(vinyl phosphonic acid) is synthesized by polymerizing vinyl phosphonyl dichloride in the presence of a cross-linker such as formaldehyde or 1,3-butadiene di-epoxide, with a free-radical initiator. The product can be reacted with aluminosilicate glass to form an improved cement.
专利号:US-8541569-B2 优先权日:2008-09-06 标题:Phosphoramidites for synthetic RNA in the reverse direction, efficient RNA synthesis and convenient introduction of 3'-end ligands, chromophores and modifications of synthetic RNA 发明人:SRIVASTAVA SURESH C; SRIVASTAVA NAVEEN P 权利人:SRIVASTAVA SURESH C; SRIVASTAVA NAVEEN P; CHEMGENES CORP 摘要:The present invention provides building blocks and methods for synthesizing very pure RNA in a form that can efficiently be modified at the 3′ end. Reverse RNA monomer phosphoramidites have been developed for RNA synthesis in 5′→3′ direction, leading to very clean oligo synthesis that allows for the introduction of various modifications at the 3′-end cleanly and efficiently. Higher coupling efficiency per step have been observed during automated oligo synthesis with the reverse RNA amidites disclosed herein, resulting in a greater ability to achieve higher purity and produce very long oligonucleotides. The use of the reverse RNA phosphoramidites in the synthetic process of this invention leads to oligonucleotides free of N+1 species.
专利号:US-2009111737-A1 优先权日:1999-05-24 标题:Novel antibacterial agents 发明人:CHRISTENSEN BURTON G; MORAN EDMUND J; GRIFFIN JOHN H; JUDICE J KEVIN; MU YONGQI; PACE JOHN L; MAMMEN MATHAI; AGGEN JAMES 权利人:CHRISTENSEN BURTON G; MORAN EDMUND J; GRIFFIN JOHN H; JUDICE J KEVIN; MU YONGQI; PACE JOHN L; MAMMEN MATHAI; AGGEN JAMES 摘要:This invention relates to novel multibinding compounds (agents) that are antibacterial agents. The multibinding compounds of the invention comprise from 2-10 ligands covalently connected by a linker or linkers, wherein each of said ligands in their monovalent (i.e., unlinked) state have the ability to bind to a an enzyme involved in cell wall biosynthesis and metabolism, a precursor used in the synthesis of the bacterial cell wall and/or the bacterial cell surface thereby interfere with the synthesis and/or metabolism of the cell wall. In particular the multibinding compounds of the invention comprise from 2-10 ligands covalently connected by a linker or linkers, wherein each of said ligands hasn a ligand domain capable of binding to penicillin binding proteins, a transpeptidase enzyme, a substrate of a transpeptidase enzyme, a beta-lactamase enzyme, pencillinase enzyme, cephalosporinase enzyme, a transglycoslase enzyme, or a transglycosylase enzyme substrate; Preferably, the ligands are selected from the beta lactam or glycopeptide class of antibacterial agents.
专利号:US-2003036066-A1 优先权日:2000-09-08 标 题:Linker phosphoramidites for oligonucleotide synthesis 发明人:PON RICHARD T; YU SHUYAN 权利人:UNIV TECHNOLOGIES INT 摘要:A novel approach for combining the ease of cleavage of carboxylic acid linker arms with the single phosphoramidite coupling chemistry of the universal supports useful in oligonucleotide synthesis. There is disclosed a new class of phosphoramidite reagents, linker phosphoramidites, which contain a bifunctional linker arm with a protected nucleoside linked through a 3′-ester bond on one end and a reactive phosphoramidite group or other phosphate precursor group on the other end—see FIGS. 2 and 3. The phosphoramidite group on the linker phosphoramidite may be activated under the same conditions and has similar reactivity as conventional nucleoside-3′-phosphoramidite reagents lacking the intermediate linker arm. The 3′-ester linkage contained within the linker phosphoramidite has similar properties to the linkages on prederivatized supports. The ester linkage is stable to all subsequent synthesis steps, but upon treatment with a cleavage reagent, such as ammonium hydroxide, the ester linkage is hydrolyzed. This releases the oligonucleotide product with the desired 3′-hydroxyl terminus and leaves the phosphate portion of the reagent attached to the support, which is subsequently discarded.
专利号:JP-H10508827-A 优先权日:1994-08-17 标 题 :Solid support reagents for the synthesis of 3 'nitrogen-containing polynucleotides
专利号:WO-9320092-A1 优先权日:1992-04-03 标题 :Synthesis of oligonucleotides
参考标题:Synthesis Of Sulfoxides By The Hydrogen Peroxide Induced Oxidation Of Sulfides Catalyzed By Iron Tetrakis(Pentafluorophenyl)Porphyrin: Scope And Chemoselectivity 作者:Enrico Baciocchi,Maria Francesca Gerini,Andrea Lapi |发布日期:2004.5.1 摘要:The Oxidation Of Sulfides With H2O2 Catalyzed By Iron Tetrakis(Pentafluorophenyl)Porphyrin In Etoh Is An Efficient And Chemoselective Process. With A Catalyst Concentration 0.03−0.09% Of That Of The Substrate, Sulfoxides Are Obtained With Yields Generally Around 90−95% Of Isolated Product. With Vinyl And Allyl Sulfides, No Epoxidation Is Observed. With A Catalyst Concentration Between 0.09% And 0.25%