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通过折叠途径实现骨架多样性:吲哚生物碱类骨架的合成

Skeletal diversity via a folding pathway: synthesis of indole alkaloid-like skeletons.

作者信息

Oguri Hiroki, Schreiber Stuart L

机构信息

Howard Hughes Medical Institute, Department of Chemistry and Chemical Biology, Harvard University; Broad Institute of Harvard and MIT, Cambridge, Massachusetts 02138, USA.

出版信息

Org Lett. 2005 Jan 6;7(1):47-50. doi: 10.1021/ol047945w.

Abstract

Inspired by the skeletal diversity of naturally occurring indole alkaloids and the rich potential of chemistry developed by Padwa and co-workers, we conceived a pathway entailing six modes of intramolecular reactions leading to indole alkaloid-like skeletons. In this context, an efficient folding pathway via a rhodium-catalyzed tandem cyclization-cycloaddition involving three of the modes has been developed (two of which are shown above) that affords densely functionalized compounds with three distinct skeletons in a stereocontrolled manner.

摘要

受天然存在的吲哚生物碱骨架多样性以及Padwa及其同事所开发化学方法的丰富潜力启发,我们构想了一条涉及六种分子内反应模式的途径,可导向吲哚生物碱类骨架。在此背景下,已开发出一条通过铑催化串联环化-环加成反应的高效折叠途径(其中涉及三种反应模式,上述展示了其中两种),该途径能以立体控制的方式提供具有三种不同骨架的高度官能化化合物。

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