Concise, biomimetic total synthesis of d,l-marcfortine C
作者:Thomas J. Greshock、Alan W. Grubbs、Robert M. Williams
DOI:10.1016/j.tet.2007.03.016
日期:2007.7
A biomimetic total synthesis of the fungal metabolite marcfortine C utilizing an intramolecular Diels-Alder reaction is described. In addition, a key stereoselective oxaziridine-mediated oxidation/pinacolrearrangement of indole 24 was used to complete the total synthesis.
描述了利用分子内 Diels-Alder 反应对真菌代谢物 marcfortine C 进行仿生全合成。此外,吲哚24的关键立体选择性氧氮杂环丙烷介导氧化/频哪醇重排用于完成全合成。