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Basic Concepts of using Solid Phase Synthesis to Build Small Organic Molecules using 2-Chlorotrityl Chloride Resin

机译:使用固相合成使用2-氯邻苯二甲酰氯树脂构建小的有机分子的基本概念

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Solid Phase Synthesis (SPS) is a chemical strategy that was developed and refined by Bruce Merrifield in the early 1960s and later led to a Nobel Prize in 1984. This discovery paved the way for chemists to be able to construct proteins with high yields, less timeconsuming purification and much faster synthetic routes. The strategy utilizes an insoluble solid polystyrene cross-linked support resin, 2-chlorotrityl-chloride (2-CCR), to form an ester linkage with an acid so proteins or small molecules can be built from the N terminal one amino acid at a time. This same chemistry can be employed to construct peptidomimetics and small non-peptide molecules. This chemistry is especially useful for building molecules that require temporary protection of a carboxylic acid during the synthetic route. This article will provide the basic concepts and considerations when practicing SPS for small non-peptide molecule construction. Significant considerations in employing this chemistry include: resin selection, swelling of resin, coupling agents, solvents, mechanism, loading of resin, nucleophilic substitution, and cleavage from resin support, amine protecting groups, general reaction techniques as well as purification of final product.
机译:固相合成(SPS)是一种化学策略,由布鲁斯·梅里菲尔德(Bruce Merrifield)在1960年代初期开发和改进,后来又在1984年获得了诺贝尔奖。这项发现为化学家们能够以高产量,更少的成本构建蛋白质铺平了道路。耗时的纯化和更快的合成路线。该策略利用不溶性固体聚苯乙烯交联的支持树脂2-氯三苯甲基氯(2-CCR)与酸形成酯键,因此可以一次从N个末端的一个氨基酸构建蛋白质或小分子。可以使用相同的化学方法来构建拟肽和小的非肽分子。对于在合成途径中需要暂时保护羧酸的分子,该化学方法特别有用。本文将为小型非肽分子构建实践SPS时提供基本概念和注意事项。采用该化学方法的重要考虑因素包括:树脂选择,树脂溶胀,偶联剂,溶剂,机理,树脂负载量,亲核取代和从树脂载体上裂解,胺保护基,通用反应技术以及最终产物的纯化。

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