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Synthesis of a conformationally constrained delta-amino acid building block

机译:构象受限的δ-氨基酸构件的合成

摘要

Conformationally restricted amino acids are important components in peptidomimetics and drug design. Herein, we describe the synthesis of a novel, non-proteinogenic constrained delta amino acid containing a cyclobutane ring, cis-3(aminomethyl)cyclobutane carboxylic acid (ACCA). The synthesis of the target amino acid was achieved in seven steps, with the key reaction being a base induced intramolecular nucleophilic substitution. A small library of dipeptides was prepared through the coupling of ACCA with proteinogenic amino acids.
机译:构象受限的氨基酸是拟肽和药物设计中的重要组成部分。在这里,我们描述了一种新型的,非蛋白原的,受约束的δ氨基酸的合成,该氨基酸包含环丁烷环,顺式3(氨基甲基)环丁烷羧酸(ACCA)。目标氨基酸的合成分七个步骤完成,关键反应是碱基诱导的分子内亲核取代。通过ACCA与蛋白氨基酸的偶联,制备了一个小的二肽文库。

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