首页> 外文期刊>Tetrahedron >Total synthesis of the antifungal dilactones UK-2A and UK-3A: The determination of their relative and absolute configurations, analog synthesis and antifungal activities.
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Total synthesis of the antifungal dilactones UK-2A and UK-3A: The determination of their relative and absolute configurations, analog synthesis and antifungal activities.

机译:抗真菌双内酯UK-2A和UK-3A的全合成:确定其相对和绝对构型,类似物合成和抗真菌活性。

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The synthesis of the antifungal dilactones, UK-2A and UK-3A, is described. In addition to providing a workable synthetic route to these potent antifungal antibiotics, this has allowed us to determine the assignment of the relative and absolute configurations in the nine-membered ring. Furthermore, UK-2A analogs were also synthesized and evaluated their antifungal activities and cytotoxic activities along with UK-2A, (2R, 3R, 4S, 7R)-UK-2A, UK-3A, (2R, 3R, 4S, 7R)-UK-3A, and antimycin A. The structural requirements for the selective cytotoxicity against yeasts and filamentous fungi will also be suggested. (C) 1998 Elsevier Science Ltd. All rights reserved. [References: 33]
机译:描述了抗真菌双内酯UK-2A和UK-3A的合成。除了为这些有效的抗真菌抗生素提供可行的合成途径外,这还使我们能够确定九元环中相对构型和绝对构型的分配。此外,UK-2A类似物还与UK-2A,(2R,3R,4S,7R)-UK-2A,UK-3A,(2R,3R,4S,7R)一起合成并评估了其抗真菌活性和细胞毒性活性。 -UK-3A和抗霉素A。还将提出针对酵母和丝状真菌的选择性细胞毒性的结构要求。 (C)1998 Elsevier ScienceLtd。保留所有权利。 [参考:33]

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