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一种用于全合成银菌素类似物的色氨酸衍生物的简便方法。

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

作者信息

Chen Chou-Hsiung, Genapathy Sivaneswary, Fischer Peter M, Chan Weng C

机构信息

School of Pharmacy, Centre for Biomolecular Sciences, University of Nottingham, University Park, Nottingham NG7 2RD, UK.

出版信息

Org Biomol Chem. 2014 Dec 28;12(48):9764-8. doi: 10.1039/c4ob02107j.

Abstract

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)-methylbenzylamine and related derivatives. To illustrate the robustness of the 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.

摘要

已建立了一条从相应吲哚合成吲哚取代的(S)-色氨酸的简便路线,该路线采用了手性助剂促进的Strecker氨基酸合成策略。所评估的手性助剂试剂为(S)-甲基苄胺及其相关衍生物。为了说明该方法的稳健性,合成了八个光学纯的(S)-色氨酸类似物,随后将其用于强效抗菌剂阿吉林A及其类似物的汇聚合成。

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