利用化学酶法全合成茜草霉素 A

0 CHEMISTRY, MULTIDISCIPLINARY Nature synthesis Pub Date : 2024-06-27 DOI:10.1038/s44160-024-00580-y
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引用次数: 0

摘要

由于茜草霉素 A 结构复杂,全合成茜草霉素 A 具有挑战性。现在,我们采用化学酶法实现了茜草霉素 A 的全合成,该方法结合了从头构建骨架和后期酶促氧化级联反应。在对一种关键酶进行合理的蛋白质工程设计后,最终产品以高产率获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Total synthesis of alchivemycin A using a chemoenzymatic strategy
Owing to its structural complexity, the total synthesis of alchivemycin A has proved challenging. Now, the total synthesis of alchivemycin A is achieved using a chemoenzymatic approach that combines de novo skeleton construction with a late-stage enzymatic oxidation cascade. Following rational protein engineering of a key enzyme, the final product is obtained in high yield.
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