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重氮酰胺A的化学与生物学:第二次全合成及生物学研究

Chemistry and biology of diazonamide A: second total synthesis and biological investigations.

作者信息

Nicolaou K C, Hao Junliang, Reddy Mali V, Rao Paraselli Bheema, Rassias Gerasimos, Snyder Scott A, Huang Xianhai, Chen David Y-K, Brenzovich William E, Giuseppone Nicolas, O'Brate Aurora, Giannakakou Paraskevi

机构信息

Contribution from the Department of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.

出版信息

J Am Chem Soc. 2004 Oct 13;126(40):12897-906. doi: 10.1021/ja040093a.

Abstract

As an especially unique target for chemical synthesis, diazonamide A has the potential to be constructed through a plethora of synthetic routes, each attended by different challenges and opportunities for discovery. In this article, we detail our second total synthesis of diazonamide A through a sequence entirely distinct from that employed in our first campaign, one whose success required the development of several special strategies and tactics. We also disclose our complete studies regarding the chemical biology of diazonamide A and its structural congeners, and more fully delineate the scope of our protocol for Robinson-Gabriel cyclodehydration using pyridine-buffered POCl(3).

摘要

作为化学合成中一个特别独特的目标,重氮酰胺A有潜力通过大量的合成路线来构建,每条路线都伴随着不同的挑战和发现机会。在本文中,我们详细介绍了重氮酰胺A的第二次全合成,该合成路线与我们首次合成中所采用的路线完全不同,此次成功合成需要开发几种特殊的策略和方法。我们还披露了关于重氮酰胺A及其结构类似物化学生物学的完整研究,并更全面地描述了我们使用吡啶缓冲的POCl₃进行罗宾逊 - 加布里埃尔环脱水反应方案的适用范围。

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