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A facile approach to tryptophan derivatives for the total synthesis of argyrin analogues

机译:一种用于色氨酸衍生物的简便方法,可用于精氨酸类似物的全合成

摘要

A facile route has been established for the synthesis of indole-substituted (S)-tryptophans from corresponding indoles, which utilizes a chiral auxiliary-facilitated Strecker amino acid synthesis strategy. The chiral auxiliary reagents evaluated were (S)-methylbenzylamineudand related derivatives. To illustrate the robustness ofudthe method, eight optically pure (S)-tryptophan analogues were synthesized, which were subsequently used for the convergent synthesis of a potent antibacterial agent, argyrin A and its analogues.
机译:已经建立了从相应的吲哚合成吲哚取代的(S)-色氨酸的简便途径,该途径利用了手性辅助促进的Strecker氨基酸合成策略。所评价的手性辅助试剂是(S)-甲基苄胺相关衍生物。为了说明该方法的鲁棒性,合成了八个光学纯的(S)-色氨酸类似物,随后将其用于有效合成的抗菌剂精氨酸A及其类似物的融合合成。

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