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Exploring the post-polymerization modification of side-chain amino acid containing polymers via Michael addition reactions

机译:通过迈克尔加成反应探索含侧链氨基酸的聚合物的聚合后修饰

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An efficacious protocol for the aza-Michael addition of a C-terminus modified phenylalanine side-chain containing polymer (Michael donor) was demonstrated with various Michael acceptors. The aza-Michael addition reactions were carried out at 50 degrees C in anhydrous methanol, which is a protic solvent, to enhance the advancement of the reactions. H-1 and inverse gated C-13 NMR spectroscopy were utilized to qualitatively deliver comprehensive data on the reaction progress. Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF) provided quantitative information about the modification of the polymer. The extent of change in the aza-Michael addition varied with different Michael acceptors and decreased in the order of acrylate > acrylamide > methacrylate. The present study opens up a library of polymers with functional modifications in the side-chain. (C) 2015 Elsevier B.V. All rights reserved.
机译:用多种迈克尔受体证明了一种有效的方案,该方案用于将C末端修饰的含苯丙氨酸侧链的聚合物(迈克尔供体)进行氮杂-迈克尔加成。氮杂-迈克尔加成反应在50℃下在作为质子溶剂的无水甲醇中进行,以增强反应的进行。使用H-1和反门C-13 NMR光谱定性地提供有关反应进程的全面数据。基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF)提供了有关聚合物改性的定量信息。氮杂-迈克尔加成的变化程度随不同的迈克尔受体而变化,并且以丙烯酸酯>丙烯酰胺>甲基丙烯酸酯的顺序降低。本研究建立了在侧链中具有功能修饰的聚合物库。 (C)2015 Elsevier B.V.保留所有权利。

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