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首页> 外文期刊>Journal of Applied Polymer Science >SYNTHESIS, CHARACTERIZATION AND APPLICATION OF TETRAETHYLENE GLYCOL DIACRYLATE CROSSLINKED POLYSTYRENE SUPPORT FOR GEL PHASE PEPTIDE SYNTHESIS
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SYNTHESIS, CHARACTERIZATION AND APPLICATION OF TETRAETHYLENE GLYCOL DIACRYLATE CROSSLINKED POLYSTYRENE SUPPORT FOR GEL PHASE PEPTIDE SYNTHESIS

机译:四乙撑乙二醇双丙烯酸酯交联聚苯乙烯支持凝胶相肽的合成,表征及应用

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Styrene and tetraethylene glycol diacrylate (TTEGDA) were copolymerized by the free radical aqueous suspension polymerization technique, employing toluene as the monomer diluent at 80 degrees C. The resulting beads were functionalized by chloromethylation. The co-polymer was characterized by IR and high-resolution solid-state C-13-NMR techniques. Scanning electron microscopy was employed to observe shape, size, and morphological features of the crosslinked bead copolymer. The swelling capacities of the copolymer were measured in various solvents. Reactivity of the amino functionalized polymer was compared with divinylbenzene-polystyrene (I'S) resin. Stability of the copolymer was tested under various peptide synthetic conditions. High capacity chloromethyl TTEGDA-crosslinked PS was employed as a solid support in the synthesis of the hydrophobic peptide Boc(Ala-Leu-Ala)(4)-OMe. The coupling and deprotection steps in the synthetic scheme proceeded in near quantitative yields, supporting the positive role of the flexible and hydrophilic crosslinking agent. The fully protected 12-residue peptide was cleaved from the support by a transesterification procedure in 85% overall yield and characterized by thin-layer chromatography, amino acid analysis, and H-1-NMR. (C) 1996 John Wiley & Sons, Inc. [References: 40]
机译:苯乙烯和四甘醇二丙烯酸二酯(TTEGDA)通过自由基水悬浮聚合技术,在80℃下使用甲苯作为单体稀释剂进行共聚。通过氯甲基化将所得的珠粒官能化。通过IR和高分辨率固态C-13-NMR技术表征共聚物。使用扫描电子显微镜观察交联的珠状共聚物的形状,尺寸和形态特征。在各种溶剂中测量共聚物的溶胀能力。将氨基官能化聚合物的反应性与二乙烯基苯-聚苯乙烯(I'S)树脂进行了比较。在各种肽合成条件下测试共聚物的稳定性。高容量的氯甲基TTEGDA交联的PS被用作疏水肽Boc(Ala-Leu-Ala)(4)-OMe的合成的固体支持物。合成方案中的偶联和脱保护步骤以接近定量的产率进行,支持了柔性和亲水性交联剂的积极作用。通过酯交换方法以85%的总收率将完全保护的12残基肽从支持物上切割下来,并通过薄层色谱,氨基酸分析和H-1-NMR进行表征。 (C)1996 John Wiley&Sons,Inc. [参考:40]

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