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

被引:31
|
作者
Chen, Chou-Hsiung [1 ]
Genapathy, Sivaneswary [1 ]
Fischer, Peter M. [1 ]
Chan, Weng C. [1 ]
机构
[1] Univ Nottingham, Ctr Biomol Sci, Sch Pharm, Nottingham NG7 2RD, England
关键词
IMMUNOSUPPRESSIVE CYCLIC-PEPTIDES; BACTERIAL PROTEIN-SYNTHESIS; EFFICIENT METHOD; DEBENZYLATION; MYXOBACTERIA; INHIBITORS; ACIDS;
D O I
10.1039/c4ob02107j
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
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)-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.
引用
收藏
页码:9764 / 9768
页数:5
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